Diaryl benzopyran derivatives and cyclooxygenase-2 inhibitor containing it

专利摘要:
PURPOSE: Title compound is provided which has a good COX-2 inhibition effect. CONSTITUTION: The diarylbenzopyran derivatives(formula I; X is O, NR5 or S(O)n; R5 is hydrogen, C1- C6 lower alkyl pr NR6R7; R6 and R7 are same or not, hydrogen or C1- C6 lower alkyl group; n is integer of 0- 2; Y is O, S, H2 or N(OR6); R1 and R2 are same or not, H, halogen, C1- C6 lower alkyl, trifluoromethyl, alkoxy, hydroxy, nitro, S(O)nR5 or NR8R9; R8 and R9 are same or not H, C1- C6 lower alkyl or methylsulfonyl group; R4 is oxazolyl, benzo£b|thienyl, benzodioxanyl, naphthyl, thiazolyl, indanyl, indolyl, etc. and formula II; R10- R14 are same or not, H, halogen, C1- C6 lower alkyl, phenyl, alkoxy, hydroxy, nitro, S(O)nR5, NR6R7, etc.) and their pharmaceutical salt and cyclooxygenase-2 inhibitor containing formula I. are provided.
公开号:KR20000014628A
申请号:KR1019980034131
申请日:1998-08-22
公开日:2000-03-15
发明作者:강선화；노민수；이창훈；주영협
申请人:서경배；주식회사 태평양；
IPC主号:

专利说明:

Diarylbenzopyran Derivatives and Cyclooxygenase-2 Inhibitor Compositions Containing the Same
The present invention relates to a diarylbenzopyran derivative represented by the following general formula (I) and a pharmaceutically acceptable salt thereof, and a cyclooxygenase-2 inhibitor composition containing these in an effective amount. It is about.
(Ⅰ)
In the above formula,
X is O, NR ⁵ or S (O) n,
Wherein n is 0, 1 or 2,
R ⁵ is hydrogen, lower alkyl having 1 to 6 carbon atoms or NR ⁶ R ⁷ group,
Wherein R ⁶ and R ⁷ are the same as or different from each other and are hydrogen or a lower alkyl group having 1 to 6 carbon atoms.
Y is O, S, H ₂ or N (OR ⁶ ),
Wherein R ⁶ is the same as defined in X above.
R ¹ and R ² are the same as or different from each other, and are hydrogen, halogen, lower alkyl having 1 to 6 carbon atoms, trifluoromethyl, alkoxy, hydroxy, nitro, nitrile or carboxyl group,
R ³ is hydrogen, halogen, lower alkyl, trifluoromethyl, alkoxy, hydroxy, nitro, nitrile, carboxyl, S (O) nR ⁵ or NR ⁸ R ⁹ ,
Wherein n and R ⁵ are the same as defined above in X,
R ⁸ and R ⁹ are the same as or different from each other and are hydrogen, a lower alkyl or methylsulfonyl group having 1 to 6 carbon atoms.
R ⁴ is oxazolyl, benzo [b] thienyl, benzodioxyl, naphthyl, tetrahydronaphthyl, thiazolyl, indanyl, indolyl, pyrroyl, oxocyclopentenyl, oxohydrofuryl, benzofuranyl , Dihydrobenzofuranyl, pyrazinyl, phenylethynyl, phenylethenyl, dihydrobenzopyranyl, dihydrobenzothiopyranyl or a substituent having the following structures.

Wherein R ¹⁰ to ¹⁴ are the same as or different from each other, and are hydrogen, halogen, lower alkyl having 1 to 6 carbon atoms, phenyl, trifluoromethyl, alkoxy, hydroxy, hydroxyalkyl, nitro, S (O) nR ⁵ , NR ⁶ R ⁷ , trifluoromethoxy, nitrile, carboxyl, acetyl, morpholino and formyl groups.
Wherein n, R⁵, R⁶or R⁷Is X and R³As defined in.

Wherein R ¹⁵ is hydrogen, halogen, lower alkyl having 1 to 6 carbon atoms, phenyl, trifluoromethyl, alkoxy, hydroxy, nitro, S (O) nR ⁵ , NR ⁶ R ⁷ , trifluoromethoxy, nitrile, Carboxyl, acetyl, morpholino, and formyl groups.
Wherein n, R⁵, R⁶or R⁷Is X and R³As defined in.
or
Wherein R ^16-18 are the same as or different from each other, hydrogen, halogen, lower alkyl having 1 to 6 carbon atoms, phenyl, trifluoromethyl, alkoxy, hydroxy, nitro, S (O) nR ⁵ , NR ⁶ R ⁷ , Trifluoromethoxy, nitrile, carboxyl, acetyl, morpholino, and formyl groups.
Wherein n, R⁵, R⁶or R⁷Is X and R³As defined in.
, or
Wherein R ¹⁹ is the same as or different from each other, hydrogen, halogen, lower alkyl having 1 to 6 carbon atoms, phenyl, trifluoromethyl, alkoxy, hydroxy, nitro, S (O) nR ⁵ , NR ⁶ R ⁷ , tri Fluoromethoxy, nitrile, carboxyl, acetyl, morpholino and formyl groups.
Wherein n, R⁵, R⁶or R⁷Is X and R³As defined in.
or
Wherein R ²⁰ is hydrogen, halogen, lower alkyl of 1 to 6 carbon atoms, phenyl, trifluoromethyl, alkoxy, hydroxy, nitro, NR ⁶ R ⁷ , trifluoromethoxy, nitrile, carboxyl, acetyl, morpholy Furnace, formyl, S (O) nR ⁵ .
Wherein n, R⁵, R⁶or R⁷Is X and R³As defined in.
or
Wherein R ²¹ to ²³ silver hydrogen, halogen, lower alkyl of 1 to 6 carbon atoms, phenyl, trifluoromethyl, alkoxy, hydroxy, nitro, NR ⁶ R ⁷ , trifluoromethoxy, nitrile, carboxyl, acetyl, Morpholino, formyl, S (O) nR ⁵ .
Wherein n, R⁵, R⁶or R⁷Is X and R³As defined in.
Non-steroidal antiinflammatory drugs (NSAIDs) are the most widely used drugs in the world, but there are problems that cause serious side effects such as gastrointestinal tract and neurotoxicity. This drug inhibits the action of prostaglandin synthase, cyclooxygenase (hereinafter referred to as "COX"), and thus inhibits prostaglandin biosynthesis not only in inflammatory sites but also in the stomach and kidneys. Because. However, COX is known that COX-1 and COX-2 are present as isoenzymes. COX-1 is present in normal cells and is known to maintain cellular normality, regulate normal gastric acid, and renal function. COX-2 is used for inflammation and pain. Since it is expressed at the site and known as an enzyme involved in pathology, the toxicity of the nonsteroidal anti-inflammatory agent is due to the inhibitory effect of coexisting COX-1.
Thus, instead of nonsteroidal anti-inflammatory agents, as can be seen from Nature, 367, 215 (1994), they may have suitable anti-inflammatory, analgesic, antipyretic and gastrointestinal and renal toxicity reductions and bleeding time reduction and potential anti-cancer effects. We tried to use a selective inhibitor of COX-2 which can reduce the effects of mechanism-related side effects and reduce the asthma-induced effects on asthmatic patients who are sensitive to existing nonsteroidal anti-inflammatory drugs. These selective inhibitors of COX-2 can be used to inhibit smooth muscle contraction, to treat Alzheimer's disease and to treat osteoporosis in postmenopausal women.
Accordingly, studies on selective inhibitors of COX-2 have been actively conducted, for example, WO 9606840, Bioorg. Med. Chem. Lett. 5, 2377 (1995) and the like disclose a COX-2 inhibitor having a heterocyclic compound as a basic structure.
However, the inventors of the present invention have made diaryl benzopyran derivatives as a new compound which is not structurally similar to these known compounds, and has been studied to produce a novel compound capable of selectively inhibiting the action of COX-2. It was found that has a very good COX-2 inhibitory effect was completed the present invention.
Accordingly, it is an object of the present invention to provide diarylbenzopyran derivatives represented by the general formula (I) and pharmaceutically acceptable salts thereof.
Another object of the present invention is to provide a cyclooxygenase-2 inhibitor composition containing an effective amount of the compound of formula (I) and a pharmaceutically acceptable salt thereof.
Other objects, features and applications of the present invention will become apparent to those skilled in the art by the following detailed description.
Hereinafter, the present invention will be described in detail.
Diarylbenzopyran derivatives of the present invention and pharmaceutically acceptable salts thereof selectively inhibit the action of COX-2, which is involved in the biosynthesis of prostaglandin, which plays a more important role in the progression of inflammation than COX-1. It is effective to suppress it.
Diarylbenzopyran derivatives of the invention useful as COX-2 selective inhibitors are represented by the following general formula (I).
(Ⅰ)
In the above formula,
X is O, NR ⁵ or S (O) n,
Wherein n is 0, 1 or 2,
R ⁵ is hydrogen, lower alkyl having 1 to 6 carbon atoms or NR ⁶ R ⁷ group,
Wherein R ⁶ and R ⁷ are the same as or different from each other and are hydrogen or a lower alkyl group having 1 to 6 carbon atoms.
Y is O, S, H ₂ or N (OR ⁶ ),
Wherein R ⁶ is the same as defined in X above.
R ¹ and R ² are the same as or different from each other, and are hydrogen, halogen, lower alkyl having 1 to 6 carbon atoms, trifluoromethyl, alkoxy, hydroxy, nitro, nitrile or carboxyl group,
R ³ is hydrogen, halogen, lower alkyl, trifluoromethyl, alkoxy, hydroxy, nitro, nitrile, carboxyl, S (O) nR ⁵ or NR ⁸ R ⁹ ,
Wherein n and R ⁵ are the same as defined above in X,
R ⁸ and R ⁹ are the same as or different from each other and are hydrogen, a lower alkyl or methylsulfonyl group having 1 to 6 carbon atoms.
R ⁴ is oxazolyl, benzo [b] thienyl, benzodioxyl, naphthyl, tetrahydronaphthyl, thiazolyl, indanyl, indolyl, pyrroyl, oxocyclopentenyl, oxohydrofuryl, benzofuranyl , Dihydrobenzofuranyl, pyrazinyl, phenylethynyl, phenylethenyl, dihydrobenzopyranyl, dihydrobenzothiopyranyl or a substituent having the following structures.
Wherein R ¹⁰ to ¹⁴ are the same as or different from each other, and are hydrogen, halogen, lower alkyl having 1 to 6 carbon atoms, phenyl, trifluoromethyl, alkoxy, hydroxy, hydroxyalkyl, nitro, S (O) nR ⁵ , NR ⁶ R ⁷ , trifluoromethoxy, nitrile, carboxyl, acetyl, morpholino and formyl groups.
Wherein n, R⁵, R⁶or R⁷Is X and R³As defined in.
Wherein R ¹⁵ is hydrogen, halogen, lower alkyl having 1 to 6 carbon atoms, phenyl, trifluoromethyl, alkoxy, hydroxy, nitro, S (O) nR ⁵ , NR ⁶ R ⁷ , trifluoromethoxy, nitrile, Carboxyl, acetyl, morpholino, and formyl groups.
Wherein n, R⁵, R⁶or R⁷Is X and R³As defined in.
or
Wherein R ^16-18 are the same as or different from each other, hydrogen, halogen, lower alkyl having 1 to 6 carbon atoms, phenyl, trifluoromethyl, alkoxy, hydroxy, nitro, S (O) nR ⁵ , NR ⁶ R ⁷ , Trifluoromethoxy, nitrile, carboxyl, acetyl, morpholino, and formyl groups.
Wherein n, R⁵, R⁶or R⁷Is X and R³As defined in.
, or
Wherein R ¹⁹ is the same as or different from each other, hydrogen, halogen, lower alkyl having 1 to 6 carbon atoms, phenyl, trifluoromethyl, alkoxy, hydroxy, nitro, S (O) nR ⁵ , NR ⁶ R ⁷ , tri Fluoromethoxy, nitrile, carboxyl, acetyl, morpholino and formyl groups.
Wherein n, R⁵, R⁶or R⁷Is X and R³As defined in.
or
Wherein R ²⁰ is hydrogen, halogen, lower alkyl of 1 to 6 carbon atoms, phenyl, trifluoromethyl, alkoxy, hydroxy, nitro, NR ⁶ R ⁷ , trifluoromethoxy, nitrile, carboxyl, acetyl, morpholy Furnace, formyl, S (O) nR ⁵ .
Wherein n, R⁵, R⁶or R⁷Is X and R³As defined in.
or
Wherein R ²¹ to ²³ silver hydrogen, halogen, lower alkyl of 1 to 6 carbon atoms, phenyl, trifluoromethyl, alkoxy, hydroxy, nitro, NR ⁶ R ⁷ , trifluoromethoxy, nitrile, carboxyl, acetyl, Morpholino, formyl, S (O) nR ⁵ .
Wherein n, R⁵, R⁶or R⁷Is X and R³As defined in.
In addition, the diarylbenzopyran derivative of the general formula (I) may form a pharmaceutically acceptable salt, which is generally an alkali metal salt and an acid addition salt or a base addition salt. Salt, which is non-toxic and therefore pharmaceutically acceptable. Pharmaceutically acceptable acid addition salts of formula (I) are those derived from organic or inorganic acids. Inorganic acids used in the present invention include, for example, hydrochloric acid, bromic acid, iodic acid, nitric acid, carbonic acid, sulfuric acid, phosphoric acid, and the like. Organic acids include formic acid, acetic acid, propionic acid, succinic acid, aspartic acid, ascorbic acid, benzoic acid, benzenesulfonic acid, ethylsulfonic acid, methanesulfonic acid, p-toluenesulfonic acid, salicylic acid and the like.
Pharmaceutically acceptable base addition salts of general formula (I) are metal salts derived from aluminum, calcium, lithium, magnesium, potassium, sodium and zinc or N, N'-dibenzylethylenediamine, choline, chloroprop Organic salts derived from Chloroprocaine, diethanolamine, ethylenediamine, N-methylglucamine and procaine.
The diarylbenzopyran derivatives (I) of the present invention are not particularly limited, but are useful for the treatment of inflammation-related diseases such as, for example, for the treatment of inflammation, analgesics for the treatment of pain and headache or antipyretics for the treatment of fever. Do. For example, the compounds of the present invention are not particularly limited, but are useful for the treatment of arthritis such as rheumatoid arthritis, ankylosing spondylitis, gouty arthritis, osteoarthritis and the like. The compounds of the invention are also useful for the treatment of asthma, bronchitis, dysmenorrhea, tendinitis, bursitiis, and skin-related diseases such as psoriasis, eczema, burns and dermatitis. The compounds of the present invention are also useful for the treatment of diseases such as peptic ulcer, gastritis, local enteritis, ulcerative enteritis, colon diverticulitis, gastrointestinal bleeding. In addition, the compounds of the present invention can be used in the treatment of cancer by inhibiting cell culture modification and metastatic cancer growth, and exhibit abnormalities in the proliferation involving cyclooxygenase in diabetic retinal abnormalities and cancerous angiogenesis. It can be used for the treatment and prevention of diseases. It is also effective in the treatment of Alzheimer's disease and in the prevention of osteoporosis and the treatment of glaucoma.
In addition, the diarylbenzopyran derivative (I) of the present invention has high activity against COX-2 and specificity to COX-2 compared to COX-1, and thus may be used as an alternative to nonsteroidal anti-inflammatory drugs. In particular, it can be used as a substitute for nonsteroidal anti-inflammatory drugs in patients who have a history of recurrence in the gastrointestinal system such as hypoprothrombinemia, hemophilia or kidney disease, preoperative conditions, and cohesion problems with other bleeding problems, such as when taking anticoagulants. have.
As described above, the compound of the present invention can be usefully used in the treatment of warm-blooded rats, mice, horses, cows, sheep, dogs, cats, etc. in addition to being useful for treating human diseases. .
The compounds of the present invention can also be used as complete or partial replacements for formulations comprising conventional nonsteroidal anti-inflammatory agents. That is, the diarylbenzopyran derivative (I) and pharmaceutically acceptable salts thereof include other pain relief agents including acetoaminophen or phenacetin; Potentiators, including caffeine; H ₂ -antagonist; Aluminum hydroxide, magnesium hydroxide, simethicone, phenylephrine, phenylpropanolamine, pseudophedrine, oxymetazoline, ephinephrine, naphazoline ), Decongestant including xylometazoline, propylhexedrine or levodesoxyephedrine; Antitussives including codeine, hydrocodone, caramiphene, carbetapentane or dextramethorphan; Prostaglandins including misoprostol, enprostil, rioprostil, ornoprostol or rosaprostol; diuretic; It can be used with one or several ingredients, such as antihistamines, which do not have a calming or calming effect.
In the present invention, preferred compounds of the general formula (I) include the following compounds.
2- (4- (methylsulfonyl) phenyl) -3-phenyl-4H-1-benzopyran-4-one
3- (4-aminophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (4- (methylthio) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (4-nitrophenyl) -4H-1-benzopyran-4-one
3- (4-ethoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (2-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (2-chlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-cyanophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4- (N, N-dimethylamino) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4- (N-methylamino) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2- (methylthio) phenyl) -4H-1-benzopyran-4-one
3- (2,5-dichlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (3- (methylthio) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (4-trifluoromethoxyphenyl) -4H-1-benzopyran-4-one
3- (3-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-isopropylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (2,6-dichlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-t-butylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-ethylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-hydroxymethylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-isobutylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-n-butoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (4-morpholinophenyl) -4H-1-benzopyran-4-one
3- (2- (methylsulfinyl) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (4-trifluoromethylphenyl) -4H-1-benzopyran-4-one
3- (3- (methylsulfinyl) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-hydroxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (2,3-difluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-chloro-3-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3,5-difluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-hydroxy-3-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3,4-dihydroxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4- (methylsulfinyl) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-hydroxy-3-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (2,6-difluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,5,6-trifluorophenyl) -4H-1-benzopyran-4-one
3- (2-hydroxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (2,4-dimethoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (2,4-difluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (2,4-dichlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-acetylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-chloro-2-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (2,4-dimethylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-formylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (pentafluorophenyl) -4H-1-benzopyran-4-one
3- (4-chloro-3-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3,4-dimethoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,4,6-trichlorophenyl) -4H-1-benzopyran-4-one
3- (4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3,4-dichlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,4,5-trichlorophenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,3,4,5-tetrafluorophenyl) -4H-1-benzopyran-4-one
3- (2-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3,5-dichlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,3,4-trifluorophenyl) -4H-1-benzopyran-4-one
3- (4-chlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,4,5-trifluorophenyl) -4H-1-benzopyran-4-one
3- (4-chloro-3-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
6-chloro-3- (4-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (3-nitrophenyl) -4H-1-benzopyran-4-one
3- (3,4-difluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (1-naphthyl) -4H-1-benzopyran-4-one
3- (3-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3,4-dimethylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (2-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3-chloro-4-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,3,5,6-tetrafluorophenyl) -4H-1-benzopyran-4-one
3- (4-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3-fluoro-4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-bromophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (2,3-dichlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-Fluoro-3-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3-chlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-Fluoro-3- (methylthio) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (5-methyl-2-thienyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3-fluoro-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-Fluoro-3-hydroxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylthio) phenyl) -3- (4-trifluoromethylphenyl) -4H-1-benzopyran-4-one
3- (4-Fluoro-3-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (2,5-difluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3-bromo-4- (methylthio) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,5,6-trichlorophenyl) -4H-1-benzopyran-4-one
3- (3-chloro-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
6,8-dichloro-3- (4-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3-ethyl-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,3,4-trichlorophenyl) -4H-1-benzopyran-4-one
3- (3-fluoro-4- (methylthio) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3-chloro-4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3-methyl-4- (methylthio) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-methyl-3-nitrophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-fluoro-2-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3-chloro-4- (methylthio) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (3,4,5-trichlorophenyl) -4H-1-benzopyran-4-one
3- (2,4-dimethyl-3-thienyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-chloro-3- (methylthio) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3-hydroxy-3-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2-oxazolyl) -4H-1-benzopyran-4-one
3- (4-methoxy-3-propylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (2-fluoro-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,3,4,5-tetrachlorophenyl) -4H-1-benzopyran-4-one
3- (4-methoxy-3-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (2-chloro-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-Fluoro-2-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3-hydroxy-4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (5-chloro-2-thienyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3-amino-4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3-methoxy-4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
6-Fluoro-2- (4-fluorophenyl) -3- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (2-fluoro-4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3-bromo-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-chloro-2-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (2,5-dichloro-3-thienyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3,5-dimethyl-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3-fluoro-4-hydroxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (2-chloro-4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (5-bromo-2-furyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (3,4,5-trifluorophenyl) -4H-1-benzopyran-4-one
3- (3,5-dichloro-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-chloro-3-hydroxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3-chloro-4-methoxy-5-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (5-chloro-2-furyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3,5-difluoro-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2-naphthyl) -4H-1-benzopyran-4-one
3- (4-methyl-1,3-benzodioxol-5-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,4,6-trifluorophenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,3,4,6-tetrafluorophenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (pentachlorophenyl) -4H-1-benzopyran-4-one
3- (2-benzothienyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3-biphenyl-2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (1,2,3,4-tetrahydronaphth-6-6yl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,3,4,6-tetrachlorophenyl) -4H-1-benzopyran-4-one
3- (6-methoxy-2-naphthyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2-pyridyl) -4H-1-benzopyran-4-one
3- (1,4-benzodioxan-6-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,3,5,6-tetrachlorophenyl) -4H-1-benzopyran-4-one
3- (1,3-benzodioxol-5-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-methyl-1,3-benzodioxol-6-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2-thiazolyl) -4H-1-benzopyran-4-one
3- (5-bromo-2-thienyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (5-benzothienyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (benzofuran-2-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2-thienyl) -4H-1-benzopyran-4-one
3- (benzofuran-5-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (2,3-dihydrobenzofuran-5-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3,4-dihydro-2H-1-benzopyran-6-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3,4-dihydro-2H-1-benzothiopyran-6-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2-pyrazinyl) -4H-1-benzopyran-4-one
3- (6-methyl-3-pyridyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (4-pyridyl) -4H-1-benzopyran-4-one
3- (2,5-dimethyl-3-furyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (5-methyl-2-furyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (2-furyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (5-Indanyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4-methylphenyl) -3- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4-fluorophenyl) -6-methyl-3- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4-fluorophenyl) -6-methoxy-3- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3-phenylethynyl-4H-1-benzopyran-4-one
8-Fluoro-3- (3-fluorophenyl) -5-hydroxy-2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2-phenylethenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (3-oxocyclopent-1 (5) -enyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2-oxocyclopent-1 (5) -enyl) -4H-1-benzopyran-4-one
3- (4-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran
3- (3-fluorophenyl) -5-hydroxy-2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3-fluorophenyl) -5-methoxy-2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (5-oxo-4-hydro-2-furyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (5-oxo-4-hydro-3-furyl) -4H-1-benzopyran-4-one
3- (4-aminophenyl) -2- (4-aminosulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-methylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,5-dichlorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-bromophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,4-dihydroxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-fluoro-2-methoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3-phenyl-4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,4-difluorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-chloro-3-fluorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,5-dichlorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-t-butylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-chloro-4-fluorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,4-dichlorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-chlorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,6-difluorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-chlorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-chlorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-hydroxy-4-methylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4- (N, N-dimethylamino) phenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-ethylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-ethoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,3-difluorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-fluorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-chloro-4-methylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-fluorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,5-difluorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-hydroxymethylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-isobutylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,4-difluorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-fluoro-4-methoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-methylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4- (methylthio) phenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-methoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4- (N-methylamino) phenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2- (methylthio) phenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2- (methylsulfinyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-chloro-4-hydroxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3- (methylsulfinyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4- (methylsulfinyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-methylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-chloro-4-methoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-methoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,5,6-trifluorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,3,4,5-tetrafluorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-methoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-morpholinophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-hydroxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-nitrophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-trifluoromethylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-trifluoromethoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-hydroxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-isopropylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (1,3-benzodioxol-5-yl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-n-butoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,4-dichlorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,6-dichlorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-fluorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,3-dichlorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,5-difluorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,4-dimethoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,4-dimethoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,4,5-trifluorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,4-dimethylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,4-dimethylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-bromo-4- (methylthio) phenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-cyanophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-chloro-3-methylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,3,4,6-tetrafluorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-chloro-4-methoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-fluoro-3-methoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-ethyl-4-methoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-hydroxy-3-methoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,3,4-trifluorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-fluoro-4-methylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-fluoro-2-methylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-fluoro-4-hydroxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,5,6-trichlorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-fluoro-4- (methylthio) phenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-methyl-1,3-benzodioxol-5-yl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-fluoro-3-hydroxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-chloro-3- (methylthio) phenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-methyl-4- (methylthio) phenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-fluoro-3- (methylthio) phenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-chloro-4- (methylthio) phenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-methyl-3-nitrophenyl) -4H-1-benzopyran-4-one
3- (3-amino-4-methylphenyl) -2- (4- (aminosulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-hydroxy-3-methylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-methoxy-3-methylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-methoxy-3-propylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-fluoro-4-methoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-chloro-2-methoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,4,6-trichlorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-fluoro-4-methylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-thiazolyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-fluoro-3-methylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (pentafluorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-chloro-4-methylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-chloro-2-methylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-bromo-4-methoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,5-dimethyl-4-methoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-chloro-4-methoxy-5-methylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,5-dichloro-4-methoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,5-difluoro-4-methoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,4,6-trifluorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-methoxy-4-methylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,4,5-trifluorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-pyridyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-chloro-3-hydroxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (benzofuran-5-yl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,3,5,6-tetrafluorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,4,5-trichlorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,4,5-trichlorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,3,4,5-tetrachlorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (5-chloro-2-furyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-hydroxy-4-methoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,3,4,6-tetrachlorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-chloro-3-methoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,3,5,6-tetrachlorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (pentachlorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3-biphenyl-4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (1,2,3,4-tetrahydronaphth-6-6yl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-naphthyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (6-methoxy-2-naphthyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-phenylethenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (1,4-benzodioxan-6-yl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-methyl-1,3-benzodioxol-6-yl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-oxazolyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-thienyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (5-bromo-2-thienyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (5-chloro-2-thienyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,4-dimethyl-3-thienyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,5-dichloro-3-thienyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (5-methyl-2-thienyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (5-benzothienyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,3,4-trichlorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-benzothienyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (benzofuran-2-yl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,3-dihydrobenzofuran-5-yl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,4-dihydro-2H-1-benzopyran-6-yl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,4-dihydro-2H-1-benzothiopyran-6-yl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-pyrazinyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (6-methyl-3-pyridyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-pyridyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,5-dimethyl-3-furyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (5-methyl-2-furyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (5-bromo-2-furyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-furyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (5-indanyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -8-fluoro-3- (3-fluorophenyl) -5-hydroxy-4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-oxocyclopent-1- (5) enyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-oxocyclopent-1- (5) enyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-fluorophenyl) -5-hydroxy-4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-fluorophenyl) -5-methoxy-4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (5-oxo-4-hydro-2-furyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (5-oxo-4-hydro-3-furyl) -4H-1-benzopyran-4-one
3- (4-ethoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3-phenyl-4H-1-benzopyran-4-thione
3- (4- (methylsulfinyl) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-aminophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-methoxy-3-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3,4-dimethoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4- (N-methylamino) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-cyanophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4- (N, N-dimethylamino) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (4- (methylthio) phenyl) -4H-1-benzopyran-4-thione
3- (3- (methylsulfinyl) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (4-nitrophenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (4-trifluoromethylphenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (4-trifluoromethoxyphenyl) -4H-1-benzopyran-4-thione
3- (2-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-isopropylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (2,6-dichlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-t-butylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-ethylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-hydroxymethylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-isobutylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (4-morpholinophenyl) -4H-1-benzopyran-4-thione
3- (4-hydroxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2,4,6-trichlorophenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2,3,5,6-tetrafluorophenyl) -4H-1-benzopyran-4-thione
3- (4-n-butoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (2-hydroxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (2,5-dichlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (2,3-difluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-chloro-3-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (3,4,5-trifluorophenyl) -4H-1-benzopyran-4-thione
3- (4-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3,5-difluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3,4-dihydroxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2,3,4,5-tetrafluorophenyl) -4H-1-benzopyran-4-thione
3- (2-chlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (2,6-difluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2,3,4-trifluorophenyl) -4H-1-benzopyran-4-thione
3- (2,4-dimethoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3-fluoro-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (2,4-dimethylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2,4,5-trifluorophenyl) -4H-1-benzopyran-4-thione
3- (3,4-difluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3,4-dimethylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2,3,5,6-tetrachlorophenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (pentafluorophenyl) -4H-1-benzopyran-4-thione
3- (2,4-dichlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (2-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (3-nitrophenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (1-naphthyl) -4H-1-benzopyran-4-thione
3- (2-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3-chloro-4-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-chloro-2-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -6-nitro-4H-1-benzopyran-4-thione
3- (4-chlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-bromophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (2,3-dichlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
6-chloro-3- (4-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2-oxazolyl) -4H-1-benzopyran-4-thione
3- (3-chlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylthio) phenyl) -3- (4-trifluoromethylphenyl) -4H-1-benzopyran-4-thione
3- (2,5-difluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3-bromo-4- (methylthio) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (pentachlorophenyl) -4H-1-benzopyran-4-thione
3- (3-chloro-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2,5,6-trifluorophenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2,3,4,6-tetrafluorophenyl) -4H-1-benzopyran-4-thione
3- (3-ethyl-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3-fluoro-4- (methylthio) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3-chloro-4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3-methyl-4- (methylthio) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-methyl-3-nitrophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-Fluoro-2-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3-chloro-4- (methylthio) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
6,8-dichloro-3- (4-fluoromethyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-methoxy-3-propylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (2-Fluoro-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2- (methylthio) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2- (methylthio) phenyl) -4H-1-benzopyran-4-thione
3- (4-hydroxy-3-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (2-chloro-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (2- (methylsulfinyl) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-Fluoro-2-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3-amino-4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
6-Fluoro-2- (4-fluorophenyl) -3- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (2-fluoro-4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (2,5-dichloro-3-thienyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-Fluoro-3-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3-bromo-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-chloro-2-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3,5-dimethyl-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (2-chloro-4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3,5-dichloro-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (5-bromo-2-furyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3-chloro-4-methoxy-5-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3,5-difluoro-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2,4,6-trifluorophenyl) -4H-1-benzopyran-4-thione
3- (2,4-difluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (3,4,5-trichlorophenyl) -4H-1-benzopyran-4-thione
3- (3,5-dichlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3,4-dichlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2,5,6-trichlorophenyl) -4H-1-benzopyran-4-thione
3- (3-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2,3,4,5-tetrachlorophenyl) -4H-1-benzopyran-4-thione
3- (2-benzothienyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3-biphenyl-2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (1,2,3,4-tetrahydronaphth-6-6yl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2-naphthyl) -4H-1-benzopyran-4-thione
3- (6-methoxy-2-naphthyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (1,4-benzodioxan-6-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (1,3-benzodioxol-5-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-methyl-1,3-benzodioxol-6-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-methyl-1,3-benzodioxol-5-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2-thiazolyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2,4,5-trichlorophenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2-thienyl) -4H-1-benzopyran-4-thione
3- (5-bromo-2-thienyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2,3,4,6-tetrachlorophenyl) -4H-1-benzopyran-4-thione
3- (5-chloro-2-thienyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (2,4-dimethyl-2-thienyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (5-methyl-2-thienyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (5-benzothienyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (benzofuran-2-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (benzofuran-5-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (2,3-dihydrobenzofuran-5-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3,4-dihydro-2H-1-benzopyran-6-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3,4-dihydro-2H-1-benzothiopyran-6-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2-pyrazinyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2-pyridyl) -4H-1-benzopyran-4-thione
3- (6-methyl-3-pyridyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (4-pyridyl) -4H-1-benzopyran-4-thione
3- (2,5-dimethyl-3-furyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (5-methyl-2-furyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (5-chloro-2-furyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2,3,4-trichlorophenyl) -4H-1-benzopyran-4-thione
3- (2-furyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (5-Indanyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4-methylphenyl) -3- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4-fluorophenyl) -6-methyl-3- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4-fluorophenyl) -6-methoxy-3- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3-phenylethynyl-4H-1-benzopyran-4-thione
8-Fluoro-3- (3-fluorophenyl) -5-hydroxy-2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2-phenylethenyl) -4H-1-benzopyran-4-thione
3- (3-fluorophenyl) -5-hydroxy-2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3-fluorophenyl) -5-methoxy-2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-aminophenyl) -2- (4-aminosulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-bromophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-t-butylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2-chlorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-cyanophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-chloro-4-hydroxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-chlorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4- (N, N-dimethylamino) phenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-fluorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2-chloro-4-methoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-ethylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2-fluoro-4-methylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-ethoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,5-dichlorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-fluorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2-fluorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-hydroxymethylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-isobutylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-methylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4- (methylthio) phenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2-methoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2- (methylthio) phenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4- (N-methylamino) phenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3- (methylsulfinyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-methylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2-methylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-hydroxy-4-methylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-methoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-methoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-morpholinophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2-hydroxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-nitrophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-trifluoromethylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,3,5,6-tetrafluorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3,4,5-trifluorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-trifluoromethoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-hydroxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-isopropylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3,5-dichlorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,3,5,6-tetrachlorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3,4,5-trichlorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-n-butoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3,4-dichlorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,3,4-trifluorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,3,4,5-tetrafluorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,6-dichlorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,3-difluorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,5-difluorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2- (methylsulfinyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,4-difluorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,6-difluorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3,5-difluorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3,4-dihydroxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,4-dimethoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3,4-dimethoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,4-dimethylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3,4-dimethylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-bromo-4- (methylthio) phenyl) -4H-1-benzopyran-4
2- (4- (aminosulfonyl) phenyl) -3- (3-methoxy-4-methylphenyl) -4H-1-benzopyran-4-thione-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-chloro-4-fluorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-chloro-3-methylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,4-dimethyl-3-thienyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4- (methylsulfinyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-chloro-4-methoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-ethyl-4-methoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,3,4-trichlorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,3,4,5-tetrachlorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-fluoro-2-methoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (5-chloro-2-thienyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,5-dichloro-3-thienyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-fluoro-3-methylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2-oxazolyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2-thienyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-fluoro-4-methoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-fluoro-4- (methylthio) phenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-methyl-4- (methylthio) phenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-fluoro-4-hydroxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-fluoro-4-methylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3-phenyl-4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-fluoro-3-methoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-chloro-3-fluorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-chloro-3-methoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-chloro-4- (methylthio) phenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-fluoro-3-hydroxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-chloro-3- (methylthio) phenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-fluoro-3- (methylthio) phenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-chloro-3-hydroxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,3-dichlorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-hydroxy-4-methylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-methyl-3-nitrophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-hydroxy-4-methoxyphenyl) -4H-1-benzopyran-4-thione
3- (3-amino-4-methylphenyl) -2- (4- (aminosulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-hydroxy-3-methoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (5-methyl-2-furyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2-fluoro-4-methoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-chlorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-chloro-3-methoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-fluoro-3-methylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (1,3-benzodioxol-5-yl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-chloro-4-methylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2-chloro-4-methylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-chloro-2-methylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-bromo-4-methoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3,5-dimethyl-4-methoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-chloro-4-methoxy-5-methylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3,5-dichloro-4-methoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3,5-difluoro-4-methoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,4,6-trifluorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3-biphenyl-4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (1,2,3,4-tetrahydronatthi-6-yl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,4,6-trichlorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,3,4,6-tetrafluorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,4,5-trifluorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,5,6-trifluorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,4-dichlorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,3,4,6-tetrachlorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,4,5-trichlorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,5,6-trichlorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (pentachlorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (5-chloro-2-furyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (pentafluorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2-naphthyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3,4-difluorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (6-methoxy-2-naphthyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2-phenylethenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (1,4-benzodioxan-6-yl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-methyl-1,3-benzodioxol-6-yl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-methyl-1,3-benzodioxol-5-yl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2-thiazolyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (5-bromo-2-thienyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (5-methyl-2-thienyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (5-benzothienyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-methoxy-3-methylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-methoxy-3-propylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (benzofuran-2-yl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (benzofuran-5-yl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,3-dihydrobenzofuran-5-yl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3,4-dihydro-2H-1-benzopyran-6-yl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3,4-dihydro-2H-1-benzothiopyran-6-yl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2-pyrazinyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2-pyridyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (6-methyl-3-pyridyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-pyridyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,5-dimethyl-3-furyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (5-bromo-2-furyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2-benzothienyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2-furyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (5-indanyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -8-fluoro-3- (3-fluorophenyl) -5-hydroxy-4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-fluorophenyl) -5-hydroxy-4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-fluorophenyl) -5-methoxy-4H-1-benzopyran-4-thione
3- (4- (methylsulfonyl) phenyl) -2-phenyl-4H-1-benzothiopyran-4-one
2- (4-bromophenyl) -3- (4-fluorophenyl) -4H-1-benzothiopyran-4-one
3- (4-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one-1,1-dioxide
2- (4-bromophenyl) -3- (4-fluorophenyl) -4H-1-benzothiopyran-4-thione
3- (3,5-difluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-thione
3- (4-aminophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-bromophenyl) -2- (4-fluorophenyl) -4H-1-benzothiopyran-4-one
3- (4-t-butylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (2-chlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3-chlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-cyanophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-chlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4- (N, N-dimethylamino) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-ethylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-ethoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-isobutylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (4- (methylthio) phenyl) -4H-1-benzothiopyran-4-one
3- (2-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4- (N-methylamino) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2- (methylthio) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (3- (methylthio) phenyl) -4H-1-benzothiopyran-4-one
3- (2- (methylsulfinyl) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3- (methylsulfinyl) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4- (methylsulfinyl) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (2-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (4-morpholinophenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (4-nitrophenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (4-trifluoromethylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (4-trifluoromethoxyphenyl) -4H-1-benzothiopyran-4-one
3- (4-hydroxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-isobutylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-n-butoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3,4-dichlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (2,4-dichlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (2,6-dichlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (2,5-dichlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (2,3-difluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (2,5-difluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-fluorophenyl) -2- (4- (methylthio) phenyl) -4H-1-benzothiopyran-4-one
3- (2,4-difluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (2,6-difluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3,4-dihydroxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (2,4-dimethoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3,4-dimethoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (2,4-dimethylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3,4-dimethylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3-bromo-4- (methylthio) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-Fluoro-3-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-chloro-3-hydroxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-chloro-3-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3-chloro-4-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-chloro-3-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-chloro-2-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (2-Fluoro-4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (3,4,5-trifluorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,4,5-trifluorophenyl) -4H-1-benzothiopyran-4-one
3- (3-chloro-4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3-chloro-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3-ethyl-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-Fluoro-2-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-Fluoro-2-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3-fluoro-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3-fluoro-4- (methylthio) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3-Fluoro-4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-Fluoro-3- (methylthio) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-Fluoro-3-hydroxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-chloro-3-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3-chloro-4-hydroxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3-methyl-4- (methylthio) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3-chloro-4- (methylthio) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-chloro-3- (methylthio) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3-hydroxy-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-hydroxy-3-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3-hydroxy-4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-methyl-3-nitrophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (2-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-hydroxymethylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3-amino-4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (2-benzothienyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (benzofuran-2-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-hydroxy-3-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-methoxy-3-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (2-chloro-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,5,6-trifluorophenyl) -4H-1-benzothiopyran-4-one
3- (4-Fluoro-3-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (2-chloro-4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-chloro-2-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3-bromo-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3,5-dimethyl-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3-methoxy-4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3-chloro-4-methoxy-5-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3,5-dichloro-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3,5-difluoro-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,4,6-trifluorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,3,4-trichlorophenyl) -4H-1-benzothiopyran-4-one
3- (3-fluoro-4-hydroxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (3,4,5-trichlorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,4,5-trichlorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (pentafluorophenyl) -4H-1-benzothiopyran-4-one
3-biphenyl-2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (1,2,3,4-tetrahydronaphth-6-yl) -4H-1-benzothiopyran-4-one
3- (5-bromo-2-furyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2-naphthyl) -4H-1-benzothiopyran-4-one
3- (6-methoxy-2-naphthyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2-phenylethenyl) -4H-1-benzothiopyran-4-one
3- (1,4-benzodioxan-6-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-methoxy-3-propylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (2-Fluoro-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (1,3-benzodioxol-5-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-methyl-1,3-benzodioxol-6-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-methyl-1,3-benzodioxol-5-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2-thiazolyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2-oxazolyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2-thienyl) -4H-1-benzothiopyran-4-one
3- (5-bromo-2-thienyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (5-chloro-2-thienyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (2,4-dimethyl-3-thienyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (2,5-dimethyl-3-thienyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (5-methyl-2-thienyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (5-benzothienyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (benzofuran-5-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (2,3-dihydrobenzofuran-5-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3,4-dihydro-2H-1-benzopyran-6-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3,4-dihydro-2H-1-benzothiopyran-6-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,5,6-trichlorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (pentachlorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2-pyrazinyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2-pyridyl) -4H-1-benzothiopyran-4-one
3- (6-methyl-3-pyridyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (4-pyridyl) -4H-1-benzothiopyran-4-one
3- (2,5-dimethyl-3-furyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (5-methyl-2-furyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,4,6-trichlorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,3,4-trifluorophenyl) -4H-1-benzothiopyran-4-one
3- (5-chloro-2-furyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (2-furyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (2-indanyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-aminophenyl) -2- (4-aminosulfonyl) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,6-difluorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-bromophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-t-butylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-chlorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,5-dichlorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-cyanophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-chlorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4- (N, N-dimethylamino) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-ethylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-ethoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-fluorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-hydroxymethylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-isobutylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-methylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4- (methylthio) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-methoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4- (N-methylamino) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2- (methylsulfinyl) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3- (methylsulfinyl) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4- (methylsulfinyl) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-methylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-methylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,5-difluorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-methoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-methoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-morpholinophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-nitrophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-trifluoromethylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-methoxy-4-methylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-fluoro-3-hydroxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-trifluoromethoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-hydroxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-isopropylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-n-butoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,4-dichlorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-chloro-4-methoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,4-dichlorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,3-difluorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-chlorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,4-difluorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,5-difluorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,4-dihydroxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,4-dimethoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,4-dimethoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,4-dimethylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,4-dimethylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-bromo-4- (methylthio) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-chloro-3-fluorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-chloro-3-hydroxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-chloro-4-fluorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-chloro-3-methylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-chloro-4-methylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3-phenyl-4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-chloro-4-methoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,4,5-trifluorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-chloro-4-hydroxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-ethyl-4-methoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-fluoro-2-methoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-fluoro-2-methylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-benzothienyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (benzofuran-2-yl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-fluoro-4-methoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-fluoro-4- (methylthio) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (6-methyl-3-pyridyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-pyridyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-chloro-3-methoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,4,5-trichlorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,5-dichloro-3-thienyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-methyl-4- (methylthio) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-chloro-4- (methylthio) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,6-dichlorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,5,6-trichlorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-chloro-3- (methylthio) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-hydroxy-4-methylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (5-chloro-2-furyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-fluoro-3-methoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-methyl-3-nitrophenyl) -4H-1-benzothiopyran-4-one
3- (3-amino-4-methylphenyl) -2- (4- (aminosulfonyl) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-hydroxy-3-methylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,3,4-trichlorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-methoxy-3-methylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-fluoro-3- (methylthio) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-hydroxy-4-methoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-fluoro-4-hydroxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-methoxy-3-propylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-hydroxy-3-methoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-fluorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (5-bromo-2-furyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-fluorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-fluoro-4-methoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-chloro-2-methoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-chloro-4-methoxy-5-methylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-fluoro-4-methylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-fluoro-3-methylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-chloro-4-methylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-chloro-2-methylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-fluoro-4-methylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3-biphenyl-4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-bromo-4-methoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,5-dimethyl-4-methoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,5-dichloro-4-methoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,5-difluoro-4-methoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,4,6-trifluorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,4-dihydro-2H-1-benzopyran-6-yl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,4,6-trichlorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,3,4-trifluorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,4,5-trichlorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (pentafluorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (1,2,3,4-tetrahydronaphth-6-6yl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-naphthyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (6-methoxy-2-naphthyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-phenylethenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (1,4-benzodioxan-6-yl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (1,3-benzodioxol-5-yl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-methyl-1,3-benzodioxol-6-yl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-thiazolyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,5,6-trifluorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-oxazolyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-thienyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,4,5-trichlorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (pentachlorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (5-bromo-2-thienyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-methyl-1,3-benzodioxol-5-yl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (5-chloro-2-thienyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,4-dimethyl-3-thienyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (5-methyl-2-thienyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (5-benzothienyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (benzofuran-5-yl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,3-dihydrobenzofuran-5-yl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,4-dihydro-2H-1-benzothiopyran-6-yl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-pyrazinyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-pyridyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,5-dimethyl-3-furyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (5-methyl-2-furyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-furyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (5-indanyl) -4H-1-benzothiopyran-4-one
3- (4-Fluorophenyl) -N-methyl-2- (4- (methylsulfonyl) phenyl) -quinolin-4-one
3- (2-Fluorophenyl) -N-methyl-2- (4- (methylsulfonyl) phenyl) -quinolin-4-one
3- (4-Fluorophenyl) -N-methyl-2- (4- (methylsulfonyl) phenyl) -quinolin-4-thione
3- (2-Fluorophenyl) -N-methyl-2- (4- (methylsulfonyl) phenyl) -quinolin-4-thione
3- (4-Fluorophenyl) -N-methyl-2- (4- (methylsulfinyl) phenyl) -quinolin-4-one
3- (4-Fluorophenyl) -N-methyl-2-phenyl-quinolin-4-one
N-methyl-3- (4- (methylsulfonyl) phenyl) -2-phenylquinolin-4-one
3- (4-Fluorophenyl) -2- (4- (methylsulfonyl) phenyl-quinolin-4-one
Diarylbenzopyran derivatives of the present invention may be prepared according to Schemes 1 to 7. Unless otherwise specified in the schemes, R ¹ , R ² , R ³ and R ⁴ are as defined in general formula (I).
Scheme 1 shows a six step reaction to prepare a diarylbenzopyran derivative. In step 1, substituted acetophenone (1) and substituted aldehyde (2) are condensed under potassium hydroxide basic conditions to prepare chalcone (3). In step 2, the chalcone (3) is cyclized using a catalytic amount of iodine to produce the flavone derivative (4) (Indian J. Chem., 25B, 759 (1986)). A suitable solvent in this reaction is dimethyl sulfoxide (DMSO). In step 3, the flavone derivatives 4 are reacted with iodine at 78 ° C. in the presence of a base such as lithium diisopropylamide (LDA) (J. Chem. Soc. Perkin Trans. I. 799 (1985)). ), Reflux in a chloroform solvent in the presence of N-bromosuccinimide (NBS) to prepare a 3-halogenated flavone derivative (5). In step 4, when R ³ is a methylthio (CH ₃ S) group, 3-halogenated flavone (5) is oxidized to oxone (potassium peroxymonosulfate; oxone) or 3-chloroperoxybenzoic acid (MCPBA). Methyl sulfone or methyl sulfoxide flavone derivative (6) is prepared. In step 5, the substituted flavone derivative (6) is cross-coupling with boronic acid (7) substituted with R ⁴ group under palladium catalysis (Synth. Commun., 11, 513 (1981)). A benzopyran derivative (8) in which the 3-position of benzopyran is substituted with the R ⁴ group is prepared. In step 6, the substituted benzopyran derivative (8) was replaced with Lawson reagent (2,4-bis (4-methoxyphenyl) -1,3-dithia-2,4-diphosphentan-2,4-disulfide; Org. Synth. Coll., 7, 372 (1990)) or phosphorus pentasulfide (P ₂ S ₅ ) to prepare substituted benzopyrantion (9) derivatives.
Scheme 2 is a modified process for preparing diarylbenzopyran derivatives in a four step reaction.
In step 1, the flavone derivative (4) prepared in step 2 of Scheme 1 was iodinated with ammonium cerium (IV) nitrate (CAN) under iodine conditions to prepare 3-iodinated flavone derivative (10). do. In step 2, the 3-iodinated flavone derivative (10) is cross-reacted with boronic acid (7) substituted with R ⁴ group under palladium catalysis to prepare a flavone derivative (11) substituted with R ⁴ group. In step 3, when R ⁴ is a p-methylthiophenyl (p-CH ₃ SPh) group, the substituted flavone derivative (11) is oxidized with oxone or MCPBA so that the 3-position is methylsulfonylphenyl or methylsulfinyl. A flavone derivative (12) substituted with phenyl is prepared. In step 4, the substituted flavone derivative 12 is reacted with Lawson's reagent or phosphorus pentasulfide to prepare a substituted benzopyrantion derivative (13).
Scheme 3 is a modified seven-step reaction for preparing a diarylbenzopyran derivative.
In step 1, substituted thiophenol and substituted ethylbenzoyl acetate (J. Am. Chem. Soc., 37, 1258 (1915)) were heated under polyphosphoric acid (PPA) conditions to obtain a thioflavone derivative (14). (J. Med. Chem., 21,643 (1978)). In step 2, the ioflavone derivative 14 is iodinated under CAN and iodine conditions to prepare a 3-iodinated thioflavone derivative 15. In step 3, 3-iodinated thioflavone derivative (15) was cross-reacted with boronic acid (7) substituted with R ⁴ group under palladium catalysis to prepare a thioflavone derivative (16) with 3-position substituted R ⁴ group. do. In the fourth step, when the R ³ group is bromine, it is substituted with hexamethylphosphoramide (HMPA) solvent with methanethiol sodium salt (Synthesis, 475 (1982)), and then oxidized to benzopyran at the 2-position of methylthiol. Nilo prepares a benzothiopyran derivative (17) in which the 3-position is substituted with an R ⁴ group.
In step 5, the substituted benzothiopyran derivative (17) is oxidized with oxone or MCPBA to prepare a benzothiopyran derivative (18) in which the 2-position of benzopyran is substituted with methylsulfonylphenyl or methylsulfinylphenyl. In step 6, the substituted benzothiopyran derivative (18) is oxidized with MCPBA to prepare a substituted benzothiopyran-4-one-1,1-dioxide derivative (19). In step 7, the substituted benzothiopyran-4-one-1,1-dioxide derivative (19) is reacted with Lawson's reagent or phosphorus pentasulfide to replace the substituted benzothiopyran-4-thione-1,1-dioxide derivative (20 ).
Scheme 4 is a six-step reaction with a modified process for preparing the diarylbenzopyran derivatives.
In step 1, substituted acetoaminophenone (21) and substituted aldehyde (2) are condensed under basic conditions of potassium hydroxide to prepare aminochalcon (22). In step 2, aminochalcone 22 is cyclized using catalytic amount of phosphoric acid to prepare aminoflavone derivatives 23 (J. Org. Chem., 55, 1757 (1990)). In step 3, the aminoflavone derivative 23 is dehydrogenated under thallium (III) salt conditions to prepare a substituted quinoline-4-one derivative 24 (Synth. Commun., 23, 277 (1993)). In step 4, when the R ³ group is a methylthio group, the substituted quinoline-4-one derivative (24) is oxidized to oxone to quinoline in which the 2-position of the quinoline-4-one is substituted with methylsulfonylphenyl or methylsulfinylphenyl. A 4-one derivative 25 is prepared. In step 5, the substituted quinolin-4-one derivative 25 is iodinated under CAN and iodine conditions to prepare a substituted 3-iodine-quinolin-4-one derivative 26. In step 6, the substituted 3-iodine-quinolin-4-one derivative (26) is cross-reacted with boronic acid (7) substituted with the R ⁴ group under palladium catalysis, whereby the 3-position of the quinoline-4-one is R. A quinolin-4-one derivative (27) substituted with ⁴ groups is prepared.
Scheme 5 is a modified five-step reaction for preparing a diarylbenzopyran derivative.
In the first step, anhydrous N-methyl isatoic acid and p-bromoacetophenone were reacted under LDA conditions (J. Heterocycl. Chem. 727 (1982)) to give 2- (4-bromophenyl) -N-methyl-quinoline Prepare the 4-one 28. In step 2, 2- (4-bromophenyl) -N-methyl-quinolin-4-one (28) was substituted with methanethiol sodium salt under HMPA solvent and then oxidized to 2- (4- (methylthio) Phenyl) -N-methyl-quinolin-4-one 29 is prepared. In step 3, 2- (4- (methylthio) phenyl) -N-methyl-quinolin-4-one (29) is oxidized with oxone to give 2- (4- (methylsulfonyl) phenyl) -N-methyl- Prepare Quinolin-4-one (30). In step 4, 2- (4- (methylsulfonyl) phenyl) -N-methyl-quinolin-4-one (30) is iodinated under CAN and iodine conditions and substituted 3-iodine-2- (4- (methyl Sulfonyl) phenyl) -N-methyl-quinolin-4-one (31) is prepared. In step 5, 3-iodine-2- (4- (methylsulfonyl) phenyl) -N-methyl-quinolin-4-one (31) is crosslinked with boronic acid (7) substituted with R ⁴ group under palladium catalysis. The pairing reaction yields 2- (4- (methylsulfonyl) phenyl) -N-methyl-quinolin-4-one (32) in which the 3-position is substituted with an R ⁴ group.
Scheme 6 is a modified process for preparing diarylbenzopyran derivatives in an eight step reaction.
In step 1, substituted acetophenone (1) is acylated with substituted benzoyl chloride (33) under pyridine basic conditions and then transferred under potassium hydroxide conditions to prepare dione (34) (Org. Synth. Coll. 4). , 478 (1963)). In step 2, dione 34 is heated under sulfuric and acetic acid conditions to prepare flavone derivatives 4. In step 3, the flavone derivative (4) is brominated with bromine and pyridine to prepare 3-brominated flavone derivative (35). In step 4, the 3-brominated flavone derivative 34 is cross-coupled with boronic acid (7) substituted with an R ⁴ group under palladium catalysis to prepare a flavone derivative (11) having a 3-position substituted with an R ⁴ group. In step 5, when R ³ is a nitro group, a benzopyran derivative (37) in which 2-position of benzopyran is replaced with p-aminophenol and 3-position of R ⁴ group is reduced by tin chloride. In step 6, the substituted benzopyran derivatives 37 are diazotized, then xanthate substituted, and hydrolyzed with potassium carbonate to prepare a thiol derivative 38. In step 7, a thiol derivative 38 is prepared by sulfonyl chloride (Chem. Lett. 1483 (1992)) by radical reaction of a benzopyran derivative (38) in which the 2-position of benzopyran is substituted with thiophenol. The benzopyran derivative (39) in which the 2-position of benzopyran is substituted with sulfonamide phenol is prepared by treating with ammonia water. In step 8, a benzopyranthione derivative (40) is prepared by reacting a benzopyran derivative (39) substituted with sulfonamide phenol with Lawson reagent or phosphorus penta sulfide (40). On the other hand, when the flavone derivative (11) substituted in the 3-position R ⁴ group prepared in step ⁴ is reacted with Lawson reagent or phosphorus penta sulfide to prepare a substituted benzopyrantion derivative (36).
Scheme 7 is a one-step reaction in a modified process for preparing the diarylbenzopyran derivatives.
In step 1, the substituted 3-iodinated flavone derivative (10) is cross-linked with an arylethynyl compound under palladium catalysis to prepare 3-arylethynylated flavone derivative (41).
Alternatively, the substituted 3-iodinated flavone derivative (10) is reacted under styrene compound, palladium acetate and phosphine reagent conditions to prepare 3-arylethenylflavone derivative (42).
Hereinafter, the present invention will be described in detail with reference to Examples and Test Examples, but the present invention is not limited only to these examples.
Example 1 3- (4-fluorophenyl) -2- (4-methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
Stage 1; 2'-hydroxy-4- (methylthio) chalcone
2'-hydroxyacephenone (10.88 g, 80 mmol) and 4- (methylthio) benzaldehyde (12.16 g, 80 mmol) were added to ethanol (120 mL), stirred at 0 ° C. to dissolve, and then potassium hydroxide ( 8.96 g, 2.0 equivalents) dissolved in water (40 mL) was slowly added dropwise and stirred at room temperature for about 1 day. After completion of the reaction, the mixture was acidified with 3N hydrochloric acid (88 mL) and extracted twice with dichloromethane (100 mL). Then, the organic extract was washed with saturated sodium chloride solution, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to recrystallize the solid obtained by dichloromethane and petroleum ether to give 42.01 g (65%) of the title compound. .
mp 98-100 ℃
¹ H NMR (CDCl ₃ , 300 MHz): δ7.94-7.86 (2H, m), 7.65-7.47 (6H, m), 7.29-7.25 (2H, m), 7.05-6.72 (2H, m), 2.53 ( 3H, s)
IR (KBr) 2911, 1658, 1433, 1306, 1090, 1013 cm ^-1
Step 2: 2- (4- (methylthio) phenyl) -4H-1-benzopyran-4-one
2'-hydroxy-4- (methylthio) chalcone (9.5 g, 35.15 mmol) prepared in step 1 was dissolved in dimethyl sulfoxide (DMSO; 100 mL) and a catalytic amount of iodine crystals, and stirred at 180 ° C. for 30 minutes. It was. After completion of the reaction by TLC, the reaction solution was added to an excess of ice water (about 300 mL), stirred for 10 minutes, extracted twice with dichloromethane (100 mL), and the organic extract was washed with saturated sodium thiosulfate solution to give a brown color. Iodine component was removed. Then, the organic extract was washed again with saturated sodium chloride solution, dried over anhydrous magnesium sulfate, filtered, concentrated under reduced pressure, and the resulting solid was recrystallized from dichloromethane and petroleum ether to give 7.54 g (80%) of the title compound. Obtained.
mp: 110-112 degreeC
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.25 to 8.22 (m, 1H), 7.86 to 7.83 (m, 2H), 7.73 to 7.62 (1H, m), 7.58 to 7.55 (m, 1H), 7.45 to 7.40 (1H, m), 7.37-7.73 (2H, m), 6.83 (1H, s), 2.55 (3H, s)
IR (KBr) 1654, 1594, 1464, 1379, 1099 cm ^-1
Step 3: 3-iodine-2- (4- (methylthio) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylthio) phenyl) -4H-1-benzopyran-4-one (0.20 g, 0.75 mmol) prepared in step 2 was dissolved in anhydrous tetrahydrofuran (THF; 15 mL), and argon Under stirring, 2M LDA solution (0.38 mL, 1 equiv) was added dropwise at -78 ° C with a syringe, followed by stirring for 15 minutes. Iodine (0.19 g, 0.75 mmol) dissolved in anhydrous THF (5 mL) was slowly added dropwise, followed by reaction for 12 hours while gradually raising the temperature. After completion of the reaction, saturated sodium thiosulfate solution was added to the reaction mixture, stirred for 1 hour, and then extracted twice with dichloromethane (30 mL). Then, the organic extract was washed with saturated sodium chloride solution, dried over anhydrous magnesium sulfate, filtered, concentrated under reduced pressure, and separated by column chromatography (hexane: ethyl acetate = 7: 1) to give 0.23 g of the title compound ( 78%) was obtained.
mp 150-152 ℃
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.30-8.27 (1H, m), 7.77-7.74 (2H, m), 7.73-7.70 (1H, m), 7.51-7.44 (2H, m), 7.38- 7.35 (2H, m), 2.57 (3H, s)
IR (KBr) 3032, 2912, 1646, 1599, 1490, 1330, 1060, 752 cm ^-1
Step 4: 3-iodine-2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran
3-Iodine-2- (4-methylthio) phenyl) -4H-1-benzopyran-4-one (0.34 g, 0.86 mmol) prepared in step 3 was diluted with methanol (10 mL) and THF (10 mL). Dissolved in a mixed solution of and oxone (1.59g, 2.59mmol) dissolved in water (10ml) at 0 ℃ was added dropwise and stirred for 3 hours. Then, the reaction solution was filtered under reduced pressure, extracted twice with dichloromethane (20 mL), and the organic extract was washed with saturated sodium chloride solution and dried over anhydrous magnesium sulfate. The solution was filtered, concentrated under reduced pressure, and recrystallized with dichloromethane and petroleum ether to obtain 0.33 g (90%) of the title compound.
mp 164-165 deg.
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.33-8.29 (1H, m), 8.15-8.12 (2H, m), 8.03-7.99 (2H, m), 7.80-7.74 (1H, m), 7.53- 7.49 (2H, m), 3.16 (3H, s)
IR (KBr) 1643, 1470, 1301, 1151, 960, 750 cm ^-1
Step 5: 3- (4-fluorophenyl) -2- (4-methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3-Iodine-2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one (0.085 g, 0.20 mmol) and 4-fluorobenzeneboronic acid (0.036 g) prepared in step 4 were prepared. , 0.26 mmol) was dissolved in a mixed solution of toluene (1 mL) and ethanol (1 mL), 2 M sodium carbonate (0.61 mL) was added, followed by tetrakis (triphenylphosphine) palladium (0.014 g, 0.012 mmol). Put and stirred for 4 hours at 90 ℃. Then, the reaction solution was concentrated under reduced pressure, dissolved in dichloromethane (10 ml), washed with water and saturated sodium chloride solution, and the organic layer was dried over anhydrous magnesium sulfate. The solution was filtered, concentrated under reduced pressure and separated by column chromatography (hexane: ethyl acetate = 1: 1) to afford 0.046 g (59%) of the title compound.
mp 208-210 ° C
¹ H NMR (CDCl ₃ , 300 MHz) δ 8.32 to 8.30 (1H, m), 7.90 to 7.87 (2H, d), 7.79 to 7.73 (1H, m), 7.62 to 7.60 (2H, d), 7.57 to 7.54 (1H, d), 7.51-7.46 (1H, m), 7.21-7.16 (2H, m), 7.07-7.01 (2H, m), 3.07 (3H, s)
IR (KBr) 3017, 2922, 1640, 1509, 1468, 1378, 1290, 1230, 1155, 1142, 770 cm ^-1
Example 2 2- (4- (methylsulfonyl) phenyl) -3-phenyl-4H-1-benzopyran-4-one
The title compound was obtained in the same manner as in Example 1 except that benzeneboronic acid was used instead of 4-fluorobenzeneboronic acid in Step 5 of Example 1.
mp 208-209 ° C
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.34-8.31 (1H, m), 7.88-7.85 (2H, m), 7.79-7.74 (1H, m), 7.64-7.55 (3H, m), 7.51- 7.46 (1H, m), 7.36-7.33 (3H, m), 7.23-7.20 (2H, m), 3.06 (3H, s)
IR (KBr) 3020, 2923, 1621, 1467, 1378, 1295, 1152 cm ^-1
Example 3 6-Chloro-3- (4-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
The title compound was obtained in the same manner as in Example 1, except that 5-chloro-2'-hydroxyacetophenone was used instead of 2'-hydroxyacetophenone in Step 1 of Example 1.
mp 247 ~ 250 ℃
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.27 to 8.25 (1H, m), 7.91 to 7.87 (2H, m), 7.72 to 7.68 (1H, m), 7.61 to 7.58 (2H, m), 7.54 to 7.50 (1H, m), 7.20-7.15 (2H, m), 7.08-7.01 (2H, m), 3.07 (3H, s)
IR (KBr) 3025, 2926, 1642, 1308, 1154 cm ^-1
Example 4 6,8-dichloro-3- (4-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
The title compound was obtained in the same manner as in Example 1, except that 3,5-dichloro-2'-hydroxyacetophenone was used instead of 2'-hydroxyacetophenone in Step 1 of Example 1. .
mp 190 ~ 192 ℃
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.17 to 8.15 (1H, m), 7.92 to 7.89 (2H, m), 7.81 to 7.79 (1H, m), 7.67 to 7.63 (2H, m), 7.22 to 7.16 (2H, m), 7.11-7.04 (2H, m), 3.07 (3H, s)
IR (KBr) 3074, 2925, 2751, 1641, 1597, 1559, 1307, 1226, 1142 cm ^-1
Example 5 3- (4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
The title compound was obtained in the same manner as in Example 1 except that p-tolylboronic acid was used instead of 4-fluorobenzeneboronic acid in step 5 of Example 1.
mp 225 ℃
¹ H NMR (CDCl ₃ , 300 MHz) δ 8.32 to 8.29 (1H, m), 7.88 to 7.85 (2H, d), 7.77 to 7.71 (1H, m), 7.64 to 7.82 (2H, d), 7.56 to 7.44 (2H, m), 7.16 to 7.07 (4H, m), 3.06 (3H, s), 2.36 (3H, s)
IR (KBr) 1644, 1377, 1297 cm ^-1
Example 6 2- (4- (methylsulfonyl) phenyl) -3- (3-nitrophenyl) -4H-1-benzopyran-4-one
The title compound was obtained in the same manner as in Example 1 except that 3-nitrobenzeneboronic acid was used instead of 4-fluorobenzeneboronic acid in Step 5 of Example 1.
mp 223-224 ° C
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.33 to 8.30 (1H, m), 8.22 to 8.18 (1H, m), 8.10 (1H, m), 7.93 to 7.90 (2H, m), 7.83 to 7.77 ( 1H, m), 7.63-7.49 (6H, m), 3.06 (3H, s)
IR (KBr) 3080, 2914, 1640, 1526, 1462, 1350, 1143 cm ^-1
Example 7 3- (2,4-dichlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
The title compound was obtained in the same manner as in Example 1, except that 2,4-dichlorobenzeneboronic acid was used instead of 4-fluorobenzeneboronic acid in Step 5 of Example 1.
mp 172-175 ° C
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.32-8.29 (1H, m), 7.93-7.91 (2H, m), 7.81-7.75 (1H, m), 7.66-7.63 (2H, m), 7.59- 7.47 (3H, m), 7.26 to 7.33 (1H, m), 7.11 to 7.09 (1H, d), 3.07 (3H, s)
IR (KBr) 1642, 1472, 1302, 1145, 774 cm ^-1
Example 8 3- (2-benzo [b] thienyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
The title compound was obtained in the same manner as in Example 1 except that in the fifth step of Example 1, benzo [b] thiophene-2-boronic acid was used instead of 4-fluorobenzeneboronic acid.
mp 158-160 ℃
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.35-8.31 (1H, m), 7.93-7.90 (2H, m), 7.83-7.79 (2H, m), 7.75-7.68 (2H, m), 7.57- 7.50 (3H, m), 7.34-7.31 (2H, m), 7.21 (1H, s), 3.06 (3H, s)
IR (KBr) 3065, 2924, 1649, 1465, 1372, 1308, 1152 cm ^-1
Example 9 2- (4- (methylsulfonyl) phenyl) -3- (2-thiophene) -4H-1-benzopyran-4-one
The title compound was obtained in the same manner as in Example 1 except that thiophene-2-boronic acid was used instead of 4-fluorobenzeneboronic acid in step 5 of Example 1.
mp 165-167 ° C
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.33-8.30 (1H, m), 8.15-8.12 (2H, m), 8.02-7.99 (2H, m), 7.95-7.73 (1H, m), 7.80- 7.72 (2H, m), 7.55-7.46 (3H, m), 3.16 (3H, s)
IR (KBr) 1668, 1300, 1157 cm ^-1
Example 10 3- (4-acetylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
The title compound was obtained in the same manner as in Example 1 except that 4-acetylbenzeneboronic acid was used instead of 4-fluorobenzeneboronic acid in Step 5 of Example 1.
mp 239 ℃
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.33 to 8.30 (1H, m), 7.95 to 7.86 (4H, m), 7.81 to 7.75 (1H, m), 7.63 to 7.59 (2H, m), 7.56 ( 1H, s), 7.53 to 7.47 (1H, m), 7.36 to 7.32 (2H, m), 3.07 (3H, s), 2.62 (3H, s)
IR (KBr) 1690, 1646, 1376, 1142 cm ^-1
Example 11 3- (4-formylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
The title compound was obtained in the same manner as in Example 1 except that 4-formylbenzeneboronic acid was used instead of 4-fluorobenzeneboronic acid in step 5 of Example 1.
mp 189-190 ° C
¹ H NMR (CDCl ₃ , 300 MHz) δ 10.03 (1H, s), 8.33 to 8.29 (1H, m), 7.90 to 7.84 (4H, m), 7.80 to 7.75 (1H, m), 7.63 to 7.60 (2H , m), 7.57 (1H, s), 7.53-7.48 (2H, m), 7.43-7.39 (2H, m), 3.07 (3H, s)
IR (KBr) 2925, 1642, 1466, 1379, 1301, 1143 cm ^-1
Example 12 3- (4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
The title compound was obtained in the same manner as in Example 1 except that 4-methoxybenzeneboronic acid was used instead of 4-fluorobenzeneboronic acid in step 5 of Example 1.
mp 212-213 ° C
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.32-8.29 (1H, m), 7.89-7.86 (2H, d), 7.77-7.71 (1H, m), 7.65-7.82 (2H, d), 7.56- 7.53 (1H, d), 7.47 (1H, t), 7.14 to 7.11 (2H, d), 6.89 to 6.66 (2H, d), 3.82 (3H, s), 3.06 (3H, s)
IR (KBr) 3006, 2915, 1632, 1608, 1513, 1465, 1376, 1300, 1141 cm ^-1
Example 13 3- (3,4-dichlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
The title compound was obtained in the same manner as in Example 1, except that 3,4-dichlorobenzeneboronic acid was used instead of 4-fluorobenzeneboronic acid in step 5 of Example 1.
mp 164-165 deg.
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.31 to 8.28 (1H, m), 7.95 to 7.92 (2H, m), 7.80 to 7.74 (1H, m), 7.65 to 7.82 (2H, m), 7.58 to 7.50 (2H, m), 7.41-7.37 (2H, m), 7.03-7.00 (1H, m), 3.08 (3H, s)
IR (KBr) 1643, 1619, 1470, 1301, 1151 cm ^-1
Example 14 3- (2-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
The title compound was obtained in the same manner as in Example 1 except that 2-fluorobenzeneboronic acid was used instead of 4-fluorobenzeneboronic acid in step 5 of Example 1.
mp 180 ~ 181 ℃
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.33 to 8.30 (1H, m), 7.90 to 7.87 (2H, m), 7.79 to 7.74 (1H, m), 7.66 to 7.63 (2H, m), 7.58 to 7.46 (2H, m), 7.40-7.72 (1H, m), 7.24-7.20 (3H, m), 3.06 (3H, s)
IR (KBr) 3089, 2931, 1640, 1469, 1376, 1300, 1142, 769 cm ^-1
Example 15 2- (4- (methylsulfonyl) phenyl) -3- (1-naphthyl) -4H-1-benzopyran-4-one
The title compound was obtained in the same manner as in Example 1, except that 1-natylboronic acid was used instead of 4-fluorobenzeneboronic acid in step 5 of Example 1.
mp 193-194 ° C
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.34-8.30 (1H, m), 7.91-7.77 (3H, m), 7.74-7.61 (4H, m), 7.54-7.43 (5H, m), 7.44- 7.36 (1H, m), 7.20-7.17 (1H, m), 2.96 (3H, s)
IR (KBr) 2925, 1638, 1464, 1317, 1156, 764 cm ^-1
Example 16 3- (2,3-dichlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
The title compound was obtained in the same manner as in Example 1, except that 2,3-dichlorobenzeneboronic acid was used instead of 4-fluorobenzeneboronic acid in Step 5 of Example 1.
mp 135-137 ℃
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.33 to 8.29 (1H, m), 7.92 to 7.89 (2H, m), 7.79 to 7.75 (1H, m), 7.66 to 7.63 (2H, m), 7.60 to 7.57 (1H, m), 7.53-7.47 (2H, m), 7.21-7.15 (1H, m), 7.06-7.03 (1H, m), 3.06 (3H, s)
IR (KBr) 1646, 1607, 1468, 1381, 1309, 1145, 772 cm ^-1
Example 17 3- (3-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
Stage 1; 3-bromo-2- (4- (methylthio) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylthio) phenyl) -4H-1-benzopyran-4-one (0.50 g, 1.86 mmol) and NBS (0.36 g, 2.05 mmol) were dissolved in chloroform (30 mL) and warmed for 5 hours. It was refluxed. The reaction mixture was then washed with saturated sodium bicarbonate solution and saturated sodium chloride solution, dried over anhydrous magnesium sulfate, filtered, concentrated under reduced pressure, and separated by column chromatography (hexane: ethyl acetate = 4: 1). 0.60 g (93%) of the title compound were obtained.
mp 162-163 degreeC
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.30 to 8.27 (1H, m), 7.84 to 7.80 (2H, m), 7.74 to 7.69 (1H, m), 7.51 to 7.43 (2H, m), 7.38 to 7.34 (2H, m), 2.55 (3H, s)
IR (KBr) 1658, 1611, 1463, 1331, 1065, 753 cm ^-1
Two steps; 3-bromo-2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3-bromo-2- (4- (methylthio) phenyl) prepared in step 1 instead of 3-iodine-2- (4- (methylthio) phenyl) -4H-1-benzopyran-4-one Oxidation reaction was carried out in the same manner as in Example 4, except that -4H-1-benzopyran-4-one (0.6 g, 0.86 mmol) was used to obtain 0.59 g (90%) of the title compound. .
mp 211-213 ° C
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.34-8.30 (1H, m), 8.15-8.05 (4H, m), 7.80-7.74 (1H, m), 7.54-7.49 (2H, m), 3.15 ( 3H, s)
IR (KBr) 1646, 1310, 1146, 1075 cm ^-1
Three steps; 3- (3-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3-Bromo-2- (4- (methyl (4- (methyl) sulfonyl) phenyl) -4H-1-benzopyran and 4-fluorobenzeneboronic acid In the same manner as in Example 5, except that sulfonyl) phenyl) -4H-1-benzopyran (0.18 g, 0.47 mmol) and m-tolylboronic acid (0.071 g, 0.52 mmol) were used. This gave 0.13 g (70%) of the title compound.
mp 178-179 ℃
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.31 to 8.29 (1H, m), 7.87 to 7.84 (2H, m), 7.76 to 7.72 (1H, m), 7.64 to 7.61 (2H, m), 7.56 to 7.44 (2H, m), 7.22-7.06 (2H, m), 6.96-6.93 (1H, m), 3.05 (3H, s), 2.31 (3H, s)
IR (KBr) 2920, 1639, 1465, 1377, 1299, 1149, 771 cm ^-1
Example 18 3- (2-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
The title compound was obtained in the same manner as step 3 of Example 17, except that o-tolylboronic acid was used instead of m-tolylboronic acid.
mp 190 ~ 191 ℃
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.32-8.29 (1H, m), 7.86-7.83 (2H, m), 7.79-7.74 (1H, m), 7.60-7.57 (3H, m), 7.51- 7.46 (1H, m), 7.28-7.26 (2H, m), 7.18-7.16 (1H, m), 7.01-6.99 (1H, m), 3.04 (3H, s), 2.15 (3H, s)
IR (KBr) 1618, 1376, 1324, 1156, 766 cm ^-1
Example 19 3- (3-chlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
The title compound was obtained in the same manner as step 3 of Example 17, except that 3-chlorobenzeneboronic acid was used instead of m-tolylboronic acid.
mp 195-196 ℃
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.32 to 8.27 (1H, m), 7.91 to 7.89 (2H, m), 7.80 to 7.74 (1H, m), 7.64 to 7.71 (2H, m), 7.58 to 7.49 (2H, m), 7.31-7.28 (2H, m), 7.26-7.25 (1H, m), 7.07-70.5 (1H, m), 3.07 (3H, s)
IR (KBr) 1645, 1466, 1377, 1141 cm ^-1
Example 20 3- (3-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
The title compound was obtained in the same manner as step 3 of Example 17, except that 3-fluorobenzeneboronic acid was used instead of m-tolylboronic acid.
mp 225 ℃
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.36 to 8.33 (1H, m), 7.91 to 7.89 (2H, m), 7.80 to 7.73 (1H, m), 7.64 to 7.61 (2H, m), 7.58 to 7.46 (2H, m), 7.34-7.28 (2H, m), 7.08-6.97 (2H, m), 3.07 (3H, s)
IR (KBr) 3022, 1646, 1468, 1379, 1296, 1142, 770 cm ^-1
Example 21 3- (3-Chloro-4-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
The title compound was obtained in the same manner as Step 3 of Example 17, except that 3-chloro-4-fluorobenzeneboronic acid was used instead of m-tolylboronic acid.
mp 196 ℃
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.32-8.25 (1H, m), 7.94-7.91 (2H, m), 7.80-7.75 (1H, m), 7.65-7.71 (2H, m), 7.58- 7.47 (2H, m), 7.34-7.31 (1H, m), 7.13-7.01 (2H, m), 3.08 (3H, s)
IR (KBr) 1618, 1466, 1375, 1301, 1144, 761 cm ^-1
Example 22 3- (4-Fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -6-nitro-4H-1-benzopyran-4-one
Step 1: 3-bromo-2- (4- (methylsulfonyl) phenyl) -6-nitro-4H-1-benzopyran-4-one
Condensation reaction of 5-nitro-2'-hydroxyacetophenone in place of 2'-hydroxyacetophenone in Step 1 of Example 1 to prepare 2-hydroxy-5-nitro-4- (methylthio) chalcone Subsequently, cyclization was carried out in the same manner as in step 2 of Example 1 in the presence of a catalytic amount of iodine to prepare 2- (4- (methylthio) phenyl) -6-nitro-4H-1-benzopyran-4-one. . Subsequently, 2-bromo-2 using 2-N- (4- (methylthio) phenyl) -6-nitro-4H-l-benzopyran-4-one in the same manner as in Example 17 using NBS -(4- (methylthio) phenyl) -6-nitro-4H-1-benzopyran-4-one was prepared and the title compound was obtained using oxone in the same manner as in step 2 of Example 17.
mp 210-212 ° C
¹ H NMR (CDCl ₃ , 300 MHz): δ 9.19 to 9.18 (1H, m), 8.62 to 8.57 (1H, m), 8.20 to 8.07 (4H, m), 7.72 to 7.68 (1H, m), 3.16 ( 3H, s)
IR (KBr) 1659, 1531, 1324, 1220, 1147 cm ^-1
Step 2: 3- (4-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -6-nitro-4H-1-benzopyran-4-one
In step 5 of Example 1, instead of 3-iodine-2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one and 4-fluorobenzeneboronic acid (0.036 g, 0.26 mmol) 3-Bromo-2- (4- (methylsulfonyl) phenyl) -6-nitro-4H-1-benzopyran-4-one (0.047 g, 0.47 mmol) prepared in step 1 and 4-fluorobenzene Except for using boronic acid (0.019g, 0.13mmol) in the same manner as in step 5 of Example 1 to obtain 0.03g (65%) of the title compound.
mp 228-230 ℃
¹ H NMR (CDCl ₃ , 300 MHz): δ 9.15-9.13 (1H, m), 8.60-8.56 (1H, m), 7.93-7.90 (2H, m), 7.37-7.70 (1H, m), 7.64- 7.60 (2H, m), 7.22-7.17 (2H, m), 7.10-7.03 (2H, m), 3.08 (3H, s)
IR (KBr) 3079, 2815, 1652, 1621, 1524, 1342, 1233, 1143, 934, 844, 771 cm ^-1
Example 23 3- (4-chlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
Stage 1; 3- (4-chlorophenyl) -2- (4- (methylthio) phenyl) -4H-1-benzopyran-4-one
In the fifth step of Example 1 3-bromo-2- instead of 3-iodine-2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one and 4-fluorobenzeneboronic acid Example except that (4- (methylthio) phenyl) -4H-1-benzopyran-4-one (0.1 g, 0.29 mmol) and 4-chlorobenzeneboronic acid (0.05 g, 0.32 mmol) are used The same procedure as in step 5 of 1 was carried out to obtain 0.02 g (20%) of the title compound.
mp 145-147 ℃
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.30-8.26 (1H, m), 7.73-7.72 (1H, m), 7.55-7.44 (3H, m), 7.33-7.29 (3H, m), 7.20- 7.12 (4H, m), 2.48 (3H, s)
IR (KBr) 1636, 1594, 1465, 1092 cm ^-1
Two steps; 3- (4-chlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-chlorophenyl) -2- (4- (methyl) prepared in step 1 instead of 3-iodine-2- (4- (methylthio) phenyl) -4H-1-benzopyran-4-one Oxidation reaction was carried out in the same manner as in Example 4, except that thio) phenyl) -4H-1-benzopyran-4-one (0.05 g, 0.12 mmol) was used. %) Was obtained.
mp 187-188 ° C
¹ H NMR (CDCl ₃ , 300 MHz) δ 8.32 to 8.28 (1H, m), 7.91 to 7.89 (2H, m), 7.79 to 7.73 (1H, m), 7.63 to 7.61 (2H, m), 7.57 to 7.46 (2H, m), 7.34-7.27 (2H, m), 7.17-7.14 (2H, m), 3.08 (3H, s)
IR (KBr) 3083, 2926, 1617, 1465, 1377, 1301, 1157, 1091, 770 cm ^-1
Example 24 3- (4-bromophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-bromophenyl) -2- (4- (methylthio) phenyl)-instead of 3-iodine-2- (4- (methylthio) phenyl) -4H-1-benzopyran-4-one Oxidation reaction was carried out in the same manner as in Example 4, except that 4H-1-benzopyran-4-one (0.06 g, 0.14 mmol) was used to obtain 0.059 g (90%) of the title compound. .
mp 168-170 degreeC
¹ H NMR (CDCl ₃ , 300 MHz); δ 8.32 to 8.28 (1H, m), 7.92 to 7.89 (2H, m), 7.77 to 7.73 (1H, m), 7.63 to 7.46 (6H, m), 7.11 to 7.08 (2H, m), 3.08 (3H , s)
IR (KBr) 3027, 2925, 1640, 1465, 1375, 1300, 1142, 772 cm ^-1
Example 25 2- (4- (methylthio) phenyl) -3- (4-trifluoromethylphenyl) -4H-1-benzopyran-4-one
3-bromo-2 in place of 3-iodine-2- (4- (methylsulfonyl) phenyl) -4H-1-] benzopyran-4-one and 4-fluorobenzeneboronic acid in step 5 of Example 1 -(4- (methylthio) phenyl) -4H-1-benzopyran-4-one (0.1 g, 0.32 mmol) and 4-trifluoromethylbenzeneboronic acid (0.066 g, 0.35 mmol) are used Was carried out in the same manner as in the fifth step of Example 1 to obtain 0.05g (40%) of the title compound.
mp 189-192 ℃
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.31 to 8.27 (1H, m), 7.77 to 7.70 (1H, m), 7.61 to 7.74 (3H, m), 7.49 to 7.43 (1H, m), 7.39 to 7.36 (2H, m), 7.31-7.28 (2H, m), 7.15-7.71 (2H, m), 2.48 (3H, s)
IR (KBr) 2870, 1663, 1425, 1295, 1010 cm ^-1
Example 26 2- (4- (methylsulfonyl) phenyl) -3- (4-trifluoromethylphenyl) -4H-1-benzopyran-4-one
2- (4- (methylthio) phenyl) -3- (4-trifluoromethylphenyl) -instead of 3-iodine-2- (4- (methylthio) phenyl) -4H-1-benzopyran-4-one Oxidation reaction was carried out in the same manner as in Example 4, except that 4H-1-benzopyran-4-one (0.027 g, 0.065 mmol) was used to obtain 0.03 g (100%) of the title compound. .
mp 213-216 ° C
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.33-8.29 (1H, m), 7.92-7.88 (2H, m), 7.81-7.75 (1H, m), 7.63-7.47 (6H, m), 7.37-7.74 (2H, m), 3.08 (3H, s)
IR (KBr) 2927, 1641, 1455, 1378, 1325, 1143, 1109, 1017, 771 cm ^-1
Example 27 3- (3,5-dichlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
Stage 1; 3- (3,5-dichlorophenyl) -2- (4- (methylthio) phenyl) -4H-1-benzopyran-4-one
In the fifth step of Example 1 3-bromo-2- instead of 3-iodine-2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one and 4-fluorobenzeneboronic acid Except that (4- (methylthio) phenyl) -4H-1-benzopyran-4-one (0.1 g, 0.29 mmol) and 3,5-dichlorobenzeneboronic acid (0.067 g, 0.35 mmol) are used In the same manner as in the fifth step of Example 1, 0.043 g (36%) of the title compound was obtained.
mp 198-200 ℃
¹ H NMR (CDCl ₃ , 300 MHz); δ 8.29 to 8.25 (1H, m), 7.77 to 7.70 (1H, m), 7.57 to 7.43 (2H, m), 7.35 to 7.74 (5H, m), 6.94 to 6.72 (1H, m), 6.75 to 6.74 (1H, m), 2.50 (3H, s)
IR (KBr) 2880, 1650, 1430, 1253, 950 cm ^-1
2 step; 3- (3,5-dichlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3,5-dichlorophenyl) -2- (4- prepared in step 1 above instead of 3-iodine-2- (4- (methylthio) phenyl) -4H-1-benzopyran-4-one Oxidation reaction was carried out in the same manner as in Example 4, except that (methylthio) phenyl) -4H-1-benzopyran-4-one (0.04 g, 0.096 mmol) was used. (47%) was obtained.
mp 258-260 ° C
¹ H NMR (CDCl ₃ , 300 MHz); δ 8.32 to 8.28 (1H, m), 7.97 to 7.73 (2H, m), 7.81 to 7.75 (1H, m), 7.66 to 7.72 (2H, m), 7.59 to 7.48 (2H, m), 7.35 to 7.33 (1H, m), 7.11-7.10 (2H, m), 3.08 (3H, s)
IR (KBr) 3011, 2920, 1628, 1580, 1453, 1373, 1305, 1299, 1155, 961, 764 cm ^-1
Example 28 3- (4-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-Fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one (0.45 g, 1.14 mmol) prepared in Example 1 was used as Lawson. In the reagent (0.23 g, 0.57 mmol) and toluene (10 mL) solvent was heated to reflux for 1 hour. Then, the reaction solution was concentrated under reduced pressure, and then separated by column chromatography (hexane: ethyl acetate: dichloromethane = 1: 1: 1) to obtain 0.4 g (85%) of the title compound.
mp 203-205 ° C
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.67-8.64 (1H, m), 7.88-7.85 (2H, d), 7.80-77.7591H, m), 7.60-77.5 (2H, d), 7.55 (1H) , s), 7.51 to 7.46 (1H, m), 7.16 to 7.02 (4H, m), 3.06 (3H, s)
IR (KBr) 2929, 1605, 1589, 1536, 1508, 1459, 1400, 1377, 1314, 1297, 1254, 1151, 833 cm ^-1
Example 29 3-phenyl-2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
Except for using 2- (4- (methylsulfonyl) phenyl) -3-phenyl-4H-1-benzopyran-4-one (0.19 g, 0.49 mmol) prepared in Example 1 above. The title compound was obtained in the same manner as the Example 28.
mp 204-206 ° C
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.68 to 8.65 (1H, m), 7.84 to 7.81 (2H, d), 7.80 to 7.74 (1H, m), 7.60 to 7.58 (2H, d), 7.55 ( 1H, s), 7.50-7.45 (1H, m), 7.36-7.74 (3H, m), 7.18-7.15 (2H, m), 3.04 (3H, s)
IR (KBr) 2931, 1589, 1455, 1375, 1298, 1150 cm ^-1
Example 30 3- (3,4-dichlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3,4-dichlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one (0.07 g, 0.16 mmol) prepared in Example 13 was used. The title compound was obtained in the same manner as in Example 28, except that the title compound was obtained.
mp 168 ℃
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.65 to 8.60 (1H, m), 7.93 to 7.90 (2H, m), 7.82 to 7.76 (1H, m), 7.63 to 7.60 (2H, m), 7.58 to 7.41 (3H, m), 7.28 (1H, d), 7.03-6.99 (1H, m), 3.07 (3H, s)
IR (KBr) 1591, 1463, 1319, 1243, 1153, 774 cm ^-1
Example 31 3- (4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
Except that 3- (4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one (0.065 g, 0.17 mmol) prepared in Example 5 was used. Then, the title compound was obtained in the same manner as in Example 28.
mp 204-205 ° C
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.68-8.64 (1H, m), 7.84-7.82 (2H, d), 7.78-7.73 (1H, m), 7.61-7.59 (2H, d), 7.57- 7.44 (2H, m), 7.17-7.15 (2H, d), 7.05-7.02 (2H, d), 3.05 (3H, s), 2.37 (3H, s)
IR (KBr) 2918, 1593, 1370, 1298, 1251, 1149 cm ^-1
Example 32 3- (4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one (0.064 g, 0.16 mmol) prepared in Example 12 was used. A title compound was obtained in the same manner as in Example 28, except that the title compound was obtained.
mp 199 ℃
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.68-8.65 (1H, d), 7.86-7.83 (2H, d), 7.78-7.72 (1H, m), 7.62-7.59 (2H, d), 7.56-7.44 (2H, m), 7.09 to 7.06 (2H, d), 6.89 to 6.07 (2H, d), 3.83 (3H, s), 3.05 (3H, s)
IR (KBr) 1590, 1510, 1459, 1297, 1152 cm ^-1
Example 33 3- (2-Fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
Except for using 3- (2-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one (0.025, 0.064 mmol) prepared in Example 14. Then, the title compound was obtained in the same manner as in Example 28.
mp 198-200 ℃
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.67 to 8.64 (1H, d), 7.88 to 7.85 (2H, d), 7.80 to 7.75 (1H, m), 7.66 to 7.63 (2H, d), 7.57 to 7.55 (1H, d), 7.50-7.45 (1H, t), 7.36 (1H, m), 7.14-7.06 (3H, m), 3.05 (3H, s)
IR (KBr) 3088, 1591, 1537, 1465, 1460, 1376, 1152, 757 cm ^-1
Example 34 3- (3-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one (0.108 g, 0.27 mmol) prepared in Example 20 was used. The title compound was obtained in the same manner as in Example 28 except for the above.
mp 212 ℃
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.65-8.63 (1H, m), 7.87-7.85 (2H, m), 7.80-7.74 (1H, m), 7.63-7.55 (3H, m), 7.50-7.45 (1H, m), 7.36-7.28 (1H, m), 7.08-7.02 (1H, m), 6.96-6.89 (2H, m), 3.05 (3H, s)
IR (KBr) 3032, 1591, 1297, 1261, 1127 cm ^-1
Example 35 3- (2,3-dichlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (2,3-dichlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one (0.075 g, 0.17 mmol) prepared in Example 16 was used. The title compound was obtained in the same manner as in Example 28, except that the title compound was obtained.
mp 191-192 ℃
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.65-8.63 (1H, m), 7.91-7.89 (2H, m), 7.82-7.72 (1H, m), 7.67-7.74 (2H, m), 7.59- 7.56 (1H, m), 7.52-7.46 (2H, m), 7.22-7.16 (1H, m), 7.05-7.02 (1H, m), 3.06 (3H, s)
IR (KBr) 1594, 1542, 1457, 1296, 1152 cm ^-1
Example 36 3- (3-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
Except that 3- (3-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one (0.115 g, 0.29 mmol) prepared in Example 17 was used. Then, the title compound was obtained in the same manner as in Example 28.
mp 201-202 ° C
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.68 to 8.64 (1H, m), 7.85 to 7.82 (2H, m), 7.57 to 7.54 (1H, m), 7.49 to 7.44 (1H, m), 7.26 to 7.16 (2H, m), 6.97-6.94 (2H, m), 3.04 (3H, s), 2.30 (3H, s)
IR (KBr) 1607, 1539, 1458, 1374, 1299, 1264, 1152 cm ^-1
Example 37 3- (3-chlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3-chlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one (0.08 g, 0.19 mmol) prepared in Example 19 was used. The title compound was obtained in the same manner as in Example 28 except for the above.
mp 196-198 ℃
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.64-8.61 (1H, m), 7.88-7.85 (2H, m), 7.77-7.74 (1H, m), 7.61-7.55 (3H, m), 7.50- 7.45 (1H, m), 7.34-7.44 (2H, m), 7.17-7.16 (1H, m), 7.06-7.03 (1H, m), 3.05 (3H, s)
IR (KBr) 1589, 1249, 1152 cm ^-1
Example 38 3- (2-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
Except that 3- (2-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one (0.043, 0.11 mmol) prepared in Example 18 was used. The title compound was obtained in the same manner as in Example 28.
mp 234 ℃
¹ H NMR (CDCl ₃ , 300 MHz) δ 8.68 to 8.64 (1H, m), 7.85 to 7.82 (2H, m), 7.81 to 7.78 (1H, m), 7.61 to 7.58 (2H, m), 7.51 to 7.48 ( 1H, m), 7.33-7.16 (4H, m), 7.01-6.99 (1H, m), 3.04 (3H, s), 2.08 (3H, s)
IR (KBr) 2913, 1590, 1541, 1458, 1298, 1253, 1150 cm ^-1
Example 39 6-Fluoro-2- (4-fluorophenyl) -3- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
Stage 1; 4,5'-difluoro-2'-hydroxychalcone
5-Fluoro-2'-hydroxyacetophenone (3.08g, 20mmol) and 4-fluoroaldehyde (2.48g, 20mmol) were added to ethanol (30ml), stirred at 0 ° C, and dissolved, followed by potassium hydroxide. (2.24 g, 2.0 equiv) dissolved in water (10 mL) was slowly added dropwise and stirred at room temperature for about 1 day. After completion of the reaction, the mixture was acidified with 3N hydrochloric acid (22 mL) and extracted twice with dichloromethane (30 mL). Then, the organic extract was washed with saturated sodium chloride solution, dried over anhydrous magnesium sulfate, filtered, concentrated under reduced pressure, and the resulting solid was recrystallized with dichloromethane and petroleum ether to obtain 2.2 g (43%) of the title compound. It was.
mp 182-183 ° C
¹ H NMR (CDCl ₃ , 300 MHz); δ12.5 (1H, s), 7.92 (1H, d, J = 16 Hz), 7.71 to 7.75 (2H, m), 7.60 to 7.55 (1H, m), 7.47 (1H, d, J = 16 Hz), 7.29 ~ 7.22 (1H, m), 7.18-7.72 (2H, m), 7.03-6.98 (1H, m)
IR (KBr) 1648, 1581, 1168, 831 cm ^-1
Two steps; 2- (4-fluorophenyl) -6-fluor-4H-1-benzopyran-4-one
The 4,5'-difluoro-2'-hydroxychalcone (0.46g, 1.77mmol) prepared in step 1 and the catalytic amount of iodine crystals were dissolved in DMSO (5ml) and stirred at 180 ° C for 30 minutes. After confirming the reaction by TLC, the reaction solution was added to an excess of ice water (about 30 mL), stirred for 10 minutes, extracted twice with dichloromethane (10 mL), and the organic extract was washed with saturated sodium thiosulfate solution to give a brown color. Iodine component was removed. Then, the organic extract was washed with saturated sodium chloride solution and dried over anhydrous magnesium sulfate. The solution was filtered and concentrated under reduced pressure, and the resulting solid was recrystallized from dichloromethane and petroleum ether to give 0.46 g (100%) of the title compound.
mp 171-174 deg.
¹ H NMR (CDCl ₃ , 300 MHz): δ 7.96-7.85 (3H, m), 7.61-7.72 (1H, m), 7.47-7.40 (1H, m), 7.27-7.20 (2H, m), 6.77 (1H) , s),
IR (KBr) 1652, 1597, 1472, 1379, 1092, 775 cm ^-1
Three steps; 2- (4-Fluorophenyl) -6-fluor-3-iodine-4H-1-benzopyran-4-one
2- (4-Fluorophenyl) -6-fluoro-4H-1-benzopyran-4-one (0.2 g, 0.77 mmol) prepared in step 2 was dissolved in acetonitrile (6 mL), and iodine (0.24g, 0.95mmol) and CAN (0.48g, 0.88mmol) were added thereto, and the mixture was stirred at 60 ° C for 19 hours. The reaction temperature of this solution was lowered to room temperature, diluted with dichloromethane (20 ml), washed with saturated sodium thiosulfate solution and saturated sodium chloride solution, and dried over anhydrous magnesium sulfate. Then, the solution was filtered, concentrated under reduced pressure, and then separated by column chromatography (hexane: ethyl acetate = 6: 1) to give 0.093 g (31%) of the title compound.
mp 168-170 degreeC
¹ H NMR (CDCl ₃ , 300 MHz): δ7.94-7.90 (1H, m), 7.83-7.78 (2H, m), 7.54-7.42 (2H, m), 7.26-7.20 (2H, m)
IR (KBr) 1642, 1503, 1445, 1320, 1058, 829 cm ^-1
4 steps; 2- (4-fluorophenyl) -6-fluoro-3- (4- (methylthio) phenyl) -4H-1-benzopyran-4-one
2- (4-Fluorophenyl) -6-fluoro-3-iodine-4H-1-benzopyran-4-one (0.14 g, 0.36 mmol) and 4- (methylthio) benzoic acid (0.058) prepared in step 3 g, 0.35 mmol) was dissolved in a mixed solution of toluene (1 mL) and ethanol (1 mL), 2 M sodium carbonate (0.93 mL) was added, followed by tetrakis (triphenylphosphine) palladium (0.021 g, 0.018 mmol). Was added and stirred at 90 ° C. for 9 hours. Then, the reaction solution was concentrated under reduced pressure, dissolved in dichloromethane (10 ml), washed with water and saturated sodium chloride solution, and the organic layer was dried over anhydrous magnesium sulfate. The solution was filtered, concentrated under reduced pressure and separated by column chromatography (hexane: ethyl acetate = 6: 1) to give 0.056 g (41%) of the title compound.
mp 174-175 ° C
¹ H NMR (CDCl ₃ , 300 MHz): δ7.94-7.89 (1H, m), 7.57-7.52 (1H, m), 7.47-7.39 (3H, m), 7.22-7.10 (4H, m), 7.03- 6.96 (2H, m), 2.48 (3H, s)
IR (KBr) 1626, 1493, 1237, 1096 cm ^-1
5 steps; 6-Fluoro-2- (4-fluorophenyl) -3- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4-fluorophenyl) -6-fluoro-3- (4- (methylthio) phenyl) -4H-1-benzopyran-4-one (0.02 g, 0.053 mmol) prepared in step 4 was prepared by methanol. (1.5 mL) and THF (1.5 mL) were dissolved in a mixed solution, and oxone (0.036 g, 0.058 mmol) dissolved in water (1.5 mL) at 0 ° C. was added dropwise and stirred for about 1 day. Then, the reaction solution was filtered under reduced pressure, extracted twice with dichloromethane (10 mL), and the organic extract was washed with saturated sodium chloride solution and dried over anhydrous magnesium sulfate. The solution was filtered, concentrated under reduced pressure, and recrystallized from dichloromethane and petroleum ether to give 0.012 g (55%) of the title compound.
mp 192-193 ℃
¹ H NMR (CDCl ₃ , 300 MHz): δ7.94-7.89 (3H, m), 7.61-7.56 (1H, m), 7.52-7.47 (1H, m), 7.46-7.42 (2H, m), 7.39- 7.33 (2H, m), 7.05-6.98 (2H, m), 3.07 (3H, s)
IR (KBr) 3037, 2928, 1639, 1489, 1369, 1306, 1152, 929, 774 cm ^-1
Example 40 2- (4-methylphenyl) -3- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
In step 1 of Example 39, 2-hydroxyacetophenone (12.3 g, 90 mmol) and p-tolualdehyde (10.8 g, 90 mmol) were used in place of 5-fluoro-2'-hydroxyacetophenone and 4-fluoroaldehyde. Except that, the title compound was obtained in the same manner as in Example 39.
mp 201-203 ℃
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.30-8.27 (1H, m), 7.90-7.86 (2H, m), 7.78-7.70 (1H, m), 7.58-7.55 (1H, m), 7.49- 7.43 (3H, m), 7.26-7.72 (2H, m), 7.12-7.09 (2H, m), 3.05 (3H, s), 2.35 (3H, s)
IR (KBr) 2923, 1638, 1468, 1377, 1300, 1151, 769 cm ^-1
Example 41 2- (4-Fluorophenyl) -6-methyl-3- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2-hydroxy-5-methylacetophenone (6 g, 40 mmol) and 4-fluorbenzaldehyde (5 g, 40 mmol) instead of 5-fluoro-2'-hydroxyacetophenone and 4-fluoroaldehyde in step 1 of Example 39 The title compound was obtained in the same manner as in Example 39 except for using.
mp 230 ~ 231 ℃
¹ H NMR (CDCl ₃ , 300 MHz) δ 8.08 to 8.06 (1H, m), 7.93 to 7.89 (2H, m), 7.59 to 7.56 (1H, m), 7.49 to 7.43 (3H, m), 7.39 to 7.74 ( 2H, m), 7.05-6.98 (2H, m), 3.07 (3H, s), 2.51 (3H, s)
IR (KBr) 2923, 1637, 1489, 1367, 1305, 1150, 777 cm ^-1
Example 42 2- (4-Fluorophenyl) -6-methoxy-3- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
In step 1 of Example 39, 2-hydroxy-5-methoxyacetophenone (2 g, 12 mmol) and 4-fluorbenzaldehyde (1.5 g, instead of 5-fluoro-2'-hydroxyacetophenone and 4-fluoroaldehyde) 12 mmol) was used in the same manner as in Example 39 to obtain the title compound.
mp 220-222 ℃
¹ H NMR (CDCl ₃ , 300 MHz): δ7.93-7.89 (2H, m), 7.66-7.74 (1H, m), 7.54-7.44 (3H, m), 7.40-7.73 (3H, m), 7.05- 6.98 (2H, m), 3.94 (3H, s), 3.08 (3H, s)
IR (KBr) 2923, 1634, 1489, 1367, 1313, 1237, 1152, 933 cm ^-1
Example 43 2- (4- (methylsulfonyl) phenyl) -3-phenylethynyl-4H-1-benzopyran-4-one
Toluene (5 ml) of 3-iodine-2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one (0.1 g, 0.23 mmol) prepared in step 4 of Example 1 was prepared. It was dissolved in and tetrakis (triphenylphosphine) palladium (0.002g, 0.01 equivalent) and phenylethynyltributyltin (0.145g, 0.35mol) were added at room temperature and stirred at 85 ° C for 3.5 hours. Then, the reaction solution was cooled to room temperature, diluted with dichloromethane, washed three times with aqueous potassium fluoride solution and once with aqueous sodium bicarbonate solution, and then the organic layer was dried over anhydrous magnesium sulfate. The solution was filtered, dried and separated by column chromatography (dichloromethane) to afford 0.02 g (22%) of the title compound.
mp 220-222 ℃
¹ H NMR (CDCl ₃ , 300 MHz): δ8.50 to 8.47 (2H, m), 8.43 to 8.30 (1H, m), 8.16 to 8.13 (2H, m), 7.80 to 7.44 (1H, m), 7.59 to 7.47 (4H, m), 7.38-7.74 (3H, m), 3.15 (3H, s)
IR (KBr) 3026, 2922, 1641, 1465, 1304, 1143, 964 cm ^-1
Example 44 2- (4- (methylsulfonyl) phenyl) -3-phenylethenyl-4H-1-benzopyran-4-one
Styrene (0.03 g, 0.28 mmol), palladium acetate (0.001 g, 0.02 equiv) and triparatolylphosphine (0.009 g, 0.12 equiv) were dissolved in dimethylformamide (DMF; 1 mL), followed by triethylamine ( Triethylamine; 0.03 g, 1.32 eq.) And 3-iodine-2- (4-methylsulfonyl) phenyl) -4H-1-benzopyran-4-one (0.1 g, prepared in Step 4 of Example 1). 0.23 mmol) was added and stirred at 100 ° C. for 4 hours. Then, the reaction solution was cooled to room temperature, diluted with dichloromethane, washed with water and saturated aqueous sodium chloride solution, and then the organic layer was dried over anhydrous magnesium sulfate. The solution was filtered, dried and separated by column chromatography (dichloromethane) to give 0.06 g (65%) of the title compound.
mp 169-170 ° C
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.35-8.32 (1H, m), 8.15-8.11 (2H, m), 8.02-7.97 (3H, m), 7.75-7.70 (1H, m), 7.52- 7.45 (2H, m), 7.40-7.28 (5H, m), 6.75 (1H, d, J = 16 Hz), 3.16 (3H, s)
IR (KBr) 3024, 2926, 1643, 1548, 1464, 1404, 1319, 1154, 958 cm ^-1
Example 45 3- (4- (methylsulfonyl) phenyl) -2-phenyl-4H-1-benzothiopyran-4-one
Stage 1; 3-iodine-2-phenyl-4H-1-benzothiopyran-4-one
2-phenyl-4H-1-benzothiopyran-4-one (0.50 g, 2.10 mmol) was dissolved in acetonitrile (8 mL), followed by iodine (0.64 g, 2.51 mmol) and CAN (1.27 g, 2.30 mmol). Added and warmed to reflux for 18 hours. Then, the reaction temperature was lowered to room temperature, diluted with dichloromethane (20 mL), washed with cooled saturated sodium thiosulfate solution and saturated sodium chloride solution, and dried over anhydrous magnesium sulfate. The solution was filtered and concentrated under reduced pressure to give 0.62 g (81%) of the title compound.
mp 140 ℃
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.80 to 8.36 (1H, m), 7.85 to 7.25 (8H, m)
IR (KBr) 1620, 1520, 1275, 1098, 730 cm ^-1
Two steps; 3- (4- (methylthio) phenyl) -2-phenyl-4H-1-benzothiopyran-4-one
3-iodine-2-phenyl-4H-1-benzothiopyran-4-one (0.23 g, 0.63 mmol) and 4- (methylthio) benzeneboronic acid (0.15 g, 0.91 mmol) prepared in step 1 were prepared. Dissolve in a mixed solution of toluene (8 ml) and ethanol (8 ml), add 2 M sodium carbonate (0.82 ml), add tetrakis (triphenylphosphine) palladium (0.03 g, 0.024 mmol), and add 5 at 100 ° C. Stir for hours. Then, the reaction solution was concentrated under reduced pressure, dissolved in dichloromethane (50 mL), washed with water and saturated sodium chloride solution, and the organic layer was dried over anhydrous magnesium sulfate. The solution was filtered, concentrated under reduced pressure and separated by column chromatography (dichloromethane) to obtain 0.075 g (33%) of the title compound.
mp 195-197 ℃
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.60 to 8.56 (1H, m), 7.65 to 7.52 (3H, m), 7.30 to 7.72 (4H, m), 7.12 to 7.01 (4H, m), 2.43 ( 3H, s)
IR (KBr) 1650, 1595, 1454, 1320, 1070 cm ^-1
Three steps; 3- (4- (methylsulfonyl) phenyl) -2-phenyl-4H-1-benzothiopyran-4-one
3- (4- (methyl) prepared in step 2 instead of 2- (4-fluorophenyl) -6-fluoro-3- (4- (methylthio) phenyl) -4H-1-benzopyran-4-one The title compound was prepared in the same manner as in Example 5, except that thio) phenyl) -2-phenyl-4H-1-benzothiopyran-4-one (0.06 g, 0.17 mmol) was used. Obtained.
mp 264-266 ℃
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.60 to 8.57 (1H, m), 7.81 to 7.77 (2H, m), 7.70 to 7.59 (3H, m), 7.35 to 7.27 (4H, m), 7.24 to 7.17 (3H, m), 3.02 (3H, s)
IR (KBr) 3141, 2921, 1608, 1535, 1307, 1147, 755 cm ^-1
Example 46 2- (4-Bromophenyl) -3- (4-fluorophenyl) -4H-1-benzothiopyran-4-one
Stage 1; 2- (4-bromophenyl) -4H-1-benzothiopyran-4-one
Ethyl p-bromobenzoyl acetate (1.0 g, 3.69 mmol) and thiophenol (0.325 g, 2.94 mmol) were preheated with PPA (4.0 g) at 85 ° C. and vigorously stirred for 30 minutes. Then, after raising the reaction temperature to 95 ℃, and further stirred for 30 minutes, ice water (100ml) was added again and stirred for another 1 hour, and then the precipitate was filtered. The precipitate was washed with water and petroleum ether and then recrystallized with acetone to give 0.936 g (75%) of the title compound.
mp 165-167 ° C
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.57 to 8.54 (1H, d), 7.67 to 7.55 (7H, m), 7.22 (1H, s)
IR (KBr) 3017, 1630, 1582, 1482, 1328, 777 cm ^-1
Two steps; 2- (4-bromophenyl) -3-iodine-4H-1-benzothiopyran-4-one
2- (4-bromophenyl) -4H-1-benzothiopyran-4-one (0.3 g, 0.95 mmol) prepared in step 1 instead of 2-phenyl-4H-1-benzothiopyran-4-one ), But the title compound was obtained in the same manner as the Step 1 of Example 44 above.
mp 200-201 ℃
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.64-8.61 (1H, m), 7.68-7.58 (5H, m), 7.34-7.31 (2H, m)
IR (KBr) 3082, 1627, 1586, 1477, 1293, 738 cm ^-1
Three steps; 2- (4-bromophenyl) -3- (4-fluorophenyl) -4H-1-benzothiopyran-4-one
2- (4-bromophenyl) -3-iodine prepared in step 2 instead of 3-iodine-2-phenyl-4H-1-benzothiopyran-4-one and 4- (methylthio) benzeneboronic acid Same method as step 2 of Example 44, except that -4H-1-benzothiopyran-4-one (0.025 g, 0.056 mmol) and 4-fluorobenzeneboronic acid (0.087 g, 0.62 mmol) are used To give the title compound.
mp 191-192 ℃
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.58-8.56 (1H, d), 7.67-7.57 (3H, m), 7.42-7.39 (2H, m), 7.11-7.04 (4H, m), 6.97- 6.91 (2H, m)
IR (KBr) 1689, 1601, 1344, 1206, 813 cm ^-1
Example 47 3- (4-fluorophenyl) -2- (4- (methylthio) phenyl) -4H-1-benzothiopyran-4-one
2- (4-bromophenyl) -3- (4-fluorophenyl) -4H-1-benzothiopyran-4-one (0.20 g, 0.51 mmol) prepared in Example 46 was diluted with dichloromethane (10 mL). ), HMPA (0.5 mL) was added thereto, and sodium thiomethoxide (0.039 g, 0.56 mmol) was added to the solution, and the mixture was warmed to reflux for 3 hours. Then, the reaction solution was cooled to room temperature, diluted with water, extracted with dichloromethane, and dried over magnesium sulfate. The solution was filtered, concentrated under reduced pressure and separated by column chromatography (hexane: ethyl acetate = 8: 1) to give 0.155 g (80%) of the title compound.
mp 168-170 degreeC
¹ H NMR (CDCl ₃ , 300 MHz) δ 8.58 to 8.55 (1H, d), 7.65 to 7.74 (7H, m), 7.11 to 6.91 (4H, m), 2.46 (3H, s)
IR (KBr) 3057, 1589, 1504, 1339, 1215, 800 cm ^-1
Example 48 3- (4-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-fluorophenyl) -2- (4 instead of 2- (4-fluorophenyl) -6-fluoro-3- (4- (methylthio) phenyl) -4H-1-benzopyran-4-one -(Methylthio) phenyl) -4H-1-benzothiopyran-4-one (0.155 g, 0.41 mmol) was carried out in the same manner as in Example 5, except that the title compound was obtained. It was.
mp 189-190 ° C
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.60 to 8.57 (1H, d), 7.87 to 7.84 (2H, m), 7.70 to 7.61 (3H, m), 7.46 to 7.44 (2H, m), 7.09 to 7.04 (2H, m), 6.97-6.71 (2H, m) 3.05 (3H, s)
IR (KBr) 3068, 2927, 1617, 1590, 1505, 1314, 1159, 772 cm ^-1
Example 49 3- (4-Fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one-1,1-dioxide
3- (4-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one (0.055 g, 0.013 mmol) was dissolved in dichloromethane (5 mL). , MCPBA (0.07 g, 0.40 mmol) was added and stirred at room temperature for 24 hours. The solution was diluted with dichloromethane, washed with sodium bicarbonate and dried over anhydrous magnesium sulfate. The solution was filtered and concentrated under reduced pressure to give 0.051 g (86%) of the title compound.
mp 268-270 ° C
¹ H NMR (CDCl ₃ , 300 MHz); 8.32 to 8.29 (1H, m), 8.17 to 8.14 (1H, m), 7.98 to 7.83 (4H, m), 7.64 to 7.61 (2H, m), 7.07 to 6.63 (4H, m), 3.05 (3H , s)
IR (KBr) 3091, 2939, 1666, 1509, 1304, 1150 cm ^-1
Example 50 2- (4- (Bromophenyl) -3- (4-fluorophenyl) -4H-1-benzothiopyran-4-thione
2- (4- (bromophenyl) -3- (4- instead of 3- (4-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one The title compound was obtained in the same manner as in Example 28, except for using fluorophenyl) -4H-1-benzothiopyran-4-one (0.13 g, 0.32 mmol).
mp 195-196 ℃
¹ H NMR (CDCl ₃ , 300 MHz) δ 9.02 to 9.00 (1H, d), 7.67 to 7.74 (2H, m), 7.61 to 7.58 (1H, m), 7.39 to 7.36 (2H, m), 7.08 to 7.05 (2H, m), 6.98-6.91 (4H, m)
IR (KBr) 1599, 1552, 1515, 1477, 1218, 1152, 783 cm ^-1
Example 51 3- (4-Fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-thione
3- (4-fluorophenyl) -2- (4- (methyl instead of 3- (4-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one The title compound was obtained in the same manner as in Example 28, except that sulfonyl) phenyl) -4H-1-benzothiopyran-4-one (0.04 g, 0.097 mmol) was used.
mp 212-213 ° C
¹ H NMR (CDCl ₃ , 300 MHz): δ 9.01-8.98 (1H, d), 7.84-7.81 (2H, m), 7.69-7.61 (3H, m), 7.43-7.40 (2H, m), 6.97- 6.87 (4 H, m)
IR (KBr) 3054, 2928, 1595, 1516, 1478, 1312, 1222, 1152, 771 cm ^-1
Example 52 3- (4-Fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran
3- (4-Fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one (0.095 g, 0.24 mmol) was dissolved in acetic acid (10 mL), and zinc ( 0.23 g, 3.61 mmol) was added and heated to reflux for about 1 day. The solution was diluted with dichloromethane and water and washed with saturated sodium bicarbonate solution. The organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure, and then separated by column chromatography (hexane: ethyl acetate = 4: 1) to obtain 0.015 g (17%) of the title compound.
mp 130 ~ 132 ℃
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.03-8.00 (1H, m), 7.87-7.84 (2H, d), 7.62-7.57 (1H, m), 7.42-7.39 (2H, d), 7.18- 7.09 (2H, m), 6.98-6.72 (4H, m), 5.64-5.60 (1H, d), 4.14-4.10 (1H, d), 3.03 (3H, s)
IR (KBr) 2901, 1503, 1455, 1325, 1289, 1132, 780 cm ^-1
Example 53 3- (4-Fluorophenyl) -N-methyl-2- (4- (methylsulfonyl) phenyl) -quinolin-4-one
Stage 1; N-methyl-2- (4-bromophenyl) -quinolin-4-one
Anhydrous THF (50 mL) was added to the reaction vessel, LDA (35.21 mmol) was added at 0 ° C, and 4-bromoacetophenone (7.01 g, 35.21 mmol) dissolved in anhydrous THF (30 mL) was slowly added dropwise. After stirring for 80 minutes. N-methylisatoic anhydride (4.04 g, 22.58 mmol) was added to another reaction vessel, dissolved in anhydrous THF (15 mL), and the temperature of the reaction vessel was lowered to 78 ° C., followed by 4-bromoa. Anion of cetophenone was added dropwise. The reaction mixture was stirred at 78 ° C. for 12 hours, gradually raised to room temperature, and then saturated ammonium chloride solution was added to separate the organic layer. Then, the water layer was extracted twice with dichloromethane, the organic layers were collected, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The concentrate was separated by tube chromatography (dichloromethane: methanol = 98: 2) to give 4.84 g (68%) of the title compound.
mp 173-175 ℃
¹ H NMR (CDCl ₃ ) d 8.50 (dd, J = 8.4 Hz, 1.6 Hz, 1H) 7.74 (m, 1H), 7.65 (d, J = 7.2 Hz, 2H), 7.54 (d, J = 8.7 Hz, 1H), 7.45 (t, J = 7.2 Hz, 1H), 7.30 (d, J = 8.4 Hz, 2H), 6.23 (s, 1H), 3.60 (s, 3H)
IR (KBr) 1621, 1571, 1468, 842 cm ^-1
Two steps; N-methyl-2- (4- (methylthio) phenyl) -quinolin-4-one
N-methyl-2- (4-bromophenyl) -quinolin-4-one (4.04 g, 12.86 mmol) prepared in step 1 was dissolved in anhydrous THF (40 mL) and HMPA (10 mL), followed by sodium Thiomethoxide (0.99 g, 14.12 mmol) was added thereto, and the mixture was refluxed for 18 hours. The reaction mixture was diluted with dichloromethane and water and washed with saturated sodium chloride solution. The organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure, and the residue was separated by column chromatography (dichloromethane: ethyl acetate = 1: 1) to obtain 2.88 g (80%) of the title compound.
mp 144-145 ° C
¹ H NMR (CDCl ₃ , 300 MHz) δ 8.51 (1H, dd, J = 8.1, 1.8 Hz), 7.76-77.7 (1H, m), 7.55 (1H, d, J = 8.7 Hz), 7.44 (1H, t , 8.1 Hz), 7.39 to 7.32 (4H, m), 3.63 (3H, s), 2.56 (3H, s)
IR (KBr) 1623, 1598, 1408 cm ^-1
Three steps; N-methyl-2- (4- (methylsulfonyl) phenyl) -quinolin-4-one
N-methyl-2- (4-methylthio) phenyl) -quinolin-4-one (2.88 g, 10.24 mmol) prepared in step 2 was dissolved in dichloromethane (30 mL), and then methanol (30 mL), THF (30 mL), water (30 mL) were added thereto, oxone (6.96 g, 11.32 mmol) was added thereto, followed by stirring at room temperature for 12 hours. The reaction mixture was concentrated under reduced pressure, dissolved in dichloromethane (400 mL), and washed with water and saturated sodium chloride solution. The organic layer was dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, and separated by column chromatography (dichloromethane: ethyl acetate = 1: 1) to give 2.61 g (82%) of the title compound.
mp 220-221 ° C
¹ H NMR (CDCl ₃ , 300 MHz) δ 8.51 (1H, d, J = 8.4 Hz), 8.14 to 8.11 (2H, m), 7.79 to 7.73 (1H, m), 7.69 to 7.62 (2H, m), 7.57 (1H, d, J = 8.2 Hz), 7.47 (1H, t, 7.5 Hz), 6.26 (1H, s), 3.60 (3H, s), 3.16 (3H, s)
IR (KBr) 1621, 1468, 1311, 1151 cm ^-1
4 steps; 3-iodine-N-methyl-2- (4- (methylsulfonyl) phenyl) -quinolin-4-one
N-methyl-2- (4- (methylsulfonyl) phenyl) -quinolin-4-one (1.74 g, 5.55 mmol) prepared in step 3 was dissolved in acetonitrile (70 mL), followed by iodine (1.76 g). , 6.93 mmol) and CAN (3.35 g, 6.11 mmol) were added and stirred at 30 ° C. for 5 hours. Saturated sodium thiosulfate aqueous solution was added to the reaction mixture, and the mixture was stirred to remove brown color, extracted with ethyl acetate, and washed with water again. The water layer was extracted with dichloromethane, and the organic layers were collected, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to obtain 2.36 g (97%) of the title compound.
mp 235-238 ° C
¹ H NMR (CDCl ₃ , 300 MHz) δ 8.53 (1H, dd, J = 8.3, 1.7 Hz), 8.19-8.16 (2H, m), 7.79-7.77 (1H, m), 7.59-7.72 (2H, m) , 7.55 (1H, d, J = 8.4 Hz), 7.49 (1H, t, 7.4 Hz), 3.58 (3H, s), 3.19 (3H, s)
IR (KBr) 1591, 1310, 1147, 759 cm ^-1
5 steps; 3- (4-Fluorophenyl) -N-methyl-2- (4- (methylsulfonyl) phenyl) -quinolin-4-one
4-Fluorobenzeneboronic acid (0.15 g, to 3-iodine-N-methyl-2- (4- (methylsulfonyl) phenyl) -quinolin-4-one (0.44 g, 1.0 mmol) prepared in step 4 was prepared. 1.07mmol) and tetrakis (triphenylphosphine) palladium (0.03g, 0.026mmol) were added, and toluene, 2M sodium carbonate and ethanol mixed solution (10ml, 2: 2: 1) were added and refluxed for 18 hours. After lowering the temperature of the reaction solution to room temperature, it was diluted with ethyl acetate and washed with water and saturated sodium chloride solution. The organic layer was dried over anhydrous magnesium sulfate, and the solution was concentrated under reduced pressure, and then separated by column chromatography (dichloromethane: ethyl acetate = 1: 1) to obtain 0.30 g (74%) of the title compound.
mp 270-273 ℃
¹ H NMR (CDCl ₃ , 300 MHz) δ 8.56 (1H, dd, J = 7.5, 1.7 Hz), 7.92 to 9.90 (2H, m), 7.80 to 7.74 (1H, m), 7.58 (1H, d, J = 8.7 Hz), 7.48 (1H, t, 7.2 Hz), 7.43-7.40 (2H, m), 6.95-6.70 (4H, m), 3.53 (3H, s), 3.04 (3H, s)
IR (KBr) 1590, 1506, 1314, 1155 cm ^-1
Example 54 3- (2-Fluorophenyl) -N-methyl-2- (4- (methylsulfonyl) phenyl) -quinolin-4-one
The title compound was obtained in the same manner as step 5 of Example 53, except that 2-fluorobenzeneboronic acid was used instead of 4-fluorobenzeneboronic acid.
mp 270-280 ℃
¹ H NMR (CDCl ₃ , 300 MHz): δ 8.57 (1H, dd, J = 8.1, 1.4 Hz), 7.91-7.80 (2H, m), 7.79-7.77 (1H, m), 7.60-7.40 (4H, m ), 7.14 to 7.07 (1H, m), 7.03 to 6.81 (3H, m), 3.54 (3H, s), 3.01 (3H, s)
IR (KBr) 2970,1743, 1412, 1235, 1085 cm ^-1
Example 55 3- (4-Fluorophenyl) -N-methyl-2- (4- (methylsulfonyl) phenyl) -quinolin-4-thione
3- (4-fluorophenyl) -N-methyl-2- (4- (methylsulfonyl) phenyl) -quinolin-4-one (0.15 g, 0.37 mmol) was dissolved in toluene (10 mL), followed by Lawson reagent. (0.07 g, 0.17 mmol) was added and refluxed for 12 hours. After lowering the temperature of the reaction vessel to room temperature, it was diluted with dichloromethane and washed with water and saturated sodium chloride solution. The organic layer was dried over anhydrous sodium sulfate, and the solution was concentrated under reduced pressure, and then separated by column chromatography (dichloromethane: ethyl acetate: hexane = 2: 2: 1) to obtain 0.10 g (64%) of the title compound.
mp 253-254 ° C
¹ H NMR (CDCl ₃ , 300 MHz) δ 9.22 (1H, dd, J = 8.1, 1.2 Hz), 7.91-7.89 (2H, m), 7.85-7.79 (1H, m), 7.68 (1H, d, J = 8.7 Hz), 7.57 (1H, t, J = 8.4 Hz), 7.39 to 7.36 (2H, m), 6.98 to 6.94 (2H, m), 6.88 to 6.63 (2H, m), 3.61 (3H, s), 3.03 (3H, s)
IR (KBr) 2970,1743, 1412, 1236, 1086 cm ^-1
Example 56 3- (2-Fluorophenyl) -N-methyl-2- (4- (methylsulfonyl) phenyl) -quinolin-4-thione
3- (2-fluorophenyl) -N-methyl-2- (4 instead of 3- (4-fluorophenyl) -N-methyl-2- (4- (methylsulfonyl) phenyl) -quinolin-4-one The title compound was obtained in the same manner as in Example 55 except for using-(methylsulfonyl) phenyl) -quinolin-4-one.
mp 225-227 ° C
¹ H NMR (CDCl ₃ , 300 MHz): δ 9.21 (1H, dd, J = 8.1, 1.2 Hz), 7.91-7.79 (3H, m), 7.67 (1H, d, J = 8.1 Hz), 7.59-7.7.5 (2H, m), 7.41-7.37 (1H, m), 7.16-7.07 (1H, m), 7.01-6.95 (2H, m), 6.88-6.82 (1H, m), 3.62 (3H, s), 3.00 (3H, s)
IR (KBr) 2970, 1743, 1412, 1246, 1085 cm ^-1
Example 57 3- (4-Fluorophenyl) -N-methyl-2- (4- (methylsulfinyl) phenyl) -quinolin-4-one
Stage 1; N-methyl-2- (4- (methylsulfinyl) phenyl) -quinolin-4-one
N-methyl-2- (4- (methylthio) phenyl) -quinolin-4-one (0.60 g, 2.13 mmol) was dissolved in dichloromethane (20 mL), followed by MCPBA (0.45 g, 2.09 mmol). Stir at room temperature. After the starting material disappeared, the reaction mixture was washed in the order of saturated sodium bicarbonate, water and saturated sodium chloride solution. The organic layer was dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure, and then separated by column chromatography (dichloromethane: ethyl acetate: MeOH = 10: 10: 1) to obtain 0.53 g (84%) of the title compound.
mp 199-200 ℃
¹ H NMR (CDCl ₃ , 300 MHz) δ 8.52 (1H, d, J = 8.4 Hz), 7.84-7.81 (2H, m), 7.78-7.73 (1H, m), 7.64-7.72 (3H, m), 7.46 (1H, t, J = 7.4 Hz), 6.30 (1H, s), 3.62 (3H, s), 2.83 (3H, s)
IR (KBr) 1732, 1395, 1213, 1052 cm ^-1
Two steps; 3-iodine-N-methyl-2- (4- (methylsulfinyl) phenyl) -quinolin-4-one
N-methyl-2- (4- (methylsulfinyl) phenyl) -quinoline-4 prepared in step 1 instead of N-methyl-2- (4- (methylsulfonyl) phenyl) -quinolin-4-one The title compound was obtained in the same manner as the Step 4 of Example 53, except that -one (0.85 g, 2.86 mmol) was used.
mp 208-210 ° C
¹ H NMR (CDCl ₃ , 300 MHz) δ 8.55 (1H, dd, J = 8.3, 1.7 Hz), 7.97-7.73 (1H, m), 7.84-7.81 (1H, m), 7.79-7.77 (1H, m) , 7.59 to 7.46 (4H, m), 3.60 (3H, s), 2.86 (3H, s)
IR (KBr) 1614, 1521, 1398, 1264, 1080, 759 cm ^-1
Three steps; 3- (4-Fluorophenyl) -N-methyl-2- (4- (methylsulfinyl) phenyl) -quinolin-4-one
3-iodine-N-methyl-2- (4- (methylsulfonate) prepared in step 2 instead of 3-iodine-N-methyl-2- (4- (methylsulfonyl) phenyl) -quinolin-4-one The title compound was obtained in the same manner as Step 5 of Example 53, except that Finyl) phenyl) -quinolin-4-one (0.42 g, 1.0 mmol) was used.
mp 223-225 ° C
¹ H NMR (CDCl ₃ , 300 MHz) δ 8.57 (1H, d, J = 8.1 Hz), 7.80 to 7.74 (1H, m), 7.67 to 7.74 (1H, m), 7.60 to 7.55 (2H, m), 7.47 (1H, t, 7.7 Hz), 7.38-7.32 (2H, m), 7.00-6.95 (2H, m), 6.84-6.97 (2H, m), 3.56 (3H, s), 2.70 (3H, s)
IR (KBr) 2970, 1743, 1412, 1235, 1085 cm ^-1
Example 58 3- (4-fluorophenyl) -N-methyl-2-phenylquinolin-4-one
Stage 1; N-methyl-2-phenylquinolin-4-one
The title compound was obtained in the same manner as step 1 of Example 53, except that acetophenone (0.84 g, 7.2 mmol) was used instead of 4-bromoacetophenone.
mp 142-145 ° C
¹ H NMR (CDCl ₃ , 300 MHz) δ 8.51 (1H, d, J = 7.8 Hz), 7.75-7.70 (1H, m), 7.57-7.41 (7H, m), 6.30 (3H, s), 3.61 (3H , s)
IR (KBr) 1621, 1411, 1302, 1155 cm ^-1
Two steps; 3-iodine-N-methyl-2-phenylquinolin-4-one
N-methyl-2-phenylquinolin-4-one (0.09 g, 0.38 mmol) prepared in step 1 was used instead of N-methyl-2- (4- (methylsulfonyl) phenyl) -quinolin-4-one. The title compound was obtained in the same manner as in Example 4, except that it was used.
mp 218-220 ° C
¹ H NMR (CDCl ₃ , 300 MHz) δ 8.57 (1H, dd, J = 8.4, 1.7 Hz), 7.77 to 7.71 (1H, m), 7.62 to 7.54 (3H, m), 7.49 to 7.44 (1H, m) , 7.32-7.26 (2H, m), 3.60 (3H, s)
IR (KBr) 1614, 1591, 1482, 1392, 751 cm ^-1
Three steps; 3- (4-fluorophenyl) -N-methyl-2-phenylquinolin-4-one
3-iodine-N-methyl-2-phenylquinolin-4-one prepared in step 2 instead of 3-iodine-N-methyl-2- (4- (methylsulfonyl) phenyl) -quinolin-4-one Except for using (0.47g, 1.30mmol) in the same manner as in step 5 of Example 53 to obtain the title compound.
mp 235-236 ° C
¹ H NMR (CDCl ₃ , 300 MHz) δ 8.58 (1H, dd, J = 8.4, 1.8 Hz), 7.77 to 7.71 (1H, m), 7.58 (1H, d, 8.7 Hz), 7.48 to 7.43 (1H, m ), 7.32-7.27 (2H, m), 7.18-7.13 (2H, m), 7.03-6.98 (2H, m), 6.84-6.81 (2H, m), 3.56 (3H, s)
IR (KBr) 3038, 1594, 1502, 1208 cm ^-1
Example 59 N-methyl-3- (4-methylsulfonylphenyl) -2-phenylquinolin-4-one
Stage 1; N-methyl-3- (4- (methylthio) phenyl) -2-phenylquinolin-4-one
3-iodine-N-methyl-2-phenylquinoline-4-instead of 3-iodine-N-methyl-2- (4- (methylsulfonyl) phenyl) -quinolin-4-one and 4-fluorobenzeneboronic acid The title compound was obtained in the same manner as the Step 5 of Example 53, except that ON (0.96 g, 2.66 mmol) and 4-methylthiobenzeneboronic acid (0.49 g, 2.92 mmol) were used.
¹ H NMR (CDCl ₃ , 300 MHz) δ 8.57 (1H, dd, J = 8.2, 1.8 Hz), 7.75-7.69 (1H, m), 7.56 (1H, d, 8.1 Hz), 7.43 (1H, t, 7.9 Hz), 7.30-7.27 (3H, m), 7.17-7.13 (2H, m), 7.03-6.94 (4H, dd, J = 18.8, 8.3 Hz), 3.53 (3H, s), 2.38 (3H, s)
Two steps; N-methyl-3- (4-methylsulfonylphenyl) -2-phenylquinolin-4-one
N-methyl-3- (4- (methylthio) phenyl) -2-phenylquinoline-prepared in step 1 instead of N-methyl-2- (4- (methylthio) phenyl) -quinolin-4-one The title compound was obtained in the same manner as the Step 3 of Example 53, except that 4-one (0.43 g, 1.21 mmol) was used.
mp 240-241 ℃
¹ H NMR (CDCl ₃ , 300 MHz) δ 8.57 (1H, dd, J = 8.3, 1.8 Hz), 7.80 to 7.75 (1H, m), 7.70 to 7.62 (2H, m), 7.62 (1H, d, 8.4 Hz ), 7.49 (1H, t, 7.8 Hz), 7.34 to 7.25 (5H, m), 7.17 to 7.13 (2H, m), 3.59 (3H, s), 2.97 (3H, s)
IR (KBr) 3050, 1615, 1469, 1301, 1151 cm ^-1
Example 60 3- (4-Fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -quinolin-4-one
Stage 1; 2-amino-4- (methylthio) chalcon
2-aminoacetophenone (8.0 g, 59.2 mmol), 4- (methylthio) benzaldehyde (8.97 g, 58.93 mmol) and catalytic amount of sodium hydroxide were added to ethanol (50 mL) and stirred at room temperature for 40 hours. After confirming that the reaction was completed, the reaction mixture was concentrated under reduced pressure, which was dissolved in dichloromethane. The mixture was then washed with water and saturated sodium chloride solution and then dried over anhydrous magnesium sulfate. The solution was filtered, concentrated under reduced pressure, and separated by column chromatography (dichloromethane) to give 15.68 g (98%) of the title compound.
¹ H NMR (CDCl ₃ , 300 MHz) δ 7.86 (1H, dd, J = 8.7, 1.8 Hz), 7.68 (1H, s), 7.60 (1H, s), 7.57 to 7.54 (2H, m), 7.30 to 7.25 (3H, m), 6.73-6.68 (2H, m), 6.32 (2H, s), 2.52 (3H, s)
IR (KBr) 3300, 1632, 1230 cm ^-1
Two steps; 2- (4- (methylthio) phenyl) -1,2,3,4-tetrahydroquinolin-4-one
2-amino-4- (methylthio) chalcone (3.14 g, 11.7 mmol) prepared in step 1 was dissolved in acetic acid (15 mL) and 80% phosphoric acid (7.0 mL) was slowly added dropwise while refluxing. After refluxing for 4 hours, the reaction mixture was added dropwise to ice water, extracted with ethyl acetate, and washed with aqueous sodium bicarbonate solution and water. The organic layer was dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, and separated by column chromatography (dichloromethane) to give 2.52 g (80%) of the title compound.
mp 129-131 ℃
¹ H NMR (CDCl ₃ , 300 MHz) δ 7.88 (1H, dd, J = 8.1, 1.5 Hz), 7.40-7.27 (5H, m), 6.80 (1H, t, J = 7.7 Hz), 6.71 (1H, d , J = 8.1 Hz), 4.72 (1H, dd, J = 13.2, 4.2 Hz), 4.46 (1H, s), 2.88-2.68 (2H, m), 2.78 (3H, s)
IR (KBr) 3323, 1663, 1493, 1306 cm ^-1
Three steps; 2- (4- (methylthio) phenyl) -quinolin-4-one
2- (4- (methylthio) phenyl-1,2,3,4-tetrahydroquinolin-4-one (0.28 g, 1.04 mmol) prepared in step 2 was prepared by 1,2-dimethoxyethane (1, After dissolving in 2-dimethoxyethane (DME); 10 ml), Tl (OTs) ₃ was added and refluxed for 4 hours The reaction mixture was concentrated under reduced pressure, dissolved in THF, and then purified by column chromatography (dichloromethane: methanol = 10: 1). ) Yielded 0.16 g (58%) of the title compound.
mp 255-256 ℃
¹ H NMR (DMSO-d ₆ , 300 MHz) δ 11.65 (1H, s), 8.09 (1H, d, J = 8.1 Hz), 7.81-7.76 (3H, m), 7.70-7.7.6 (1H, m), 7.47 ~ 7.44 (2H, m), 7.36-7.31 (1H, m), 6.37 (1H, s), 2.56 (3H, s)
IR (KBr) 3261, 2970, 1633, 1569, 1440, 1098 cm ^-1
4 steps; 2- (4- (methylsulfonyl) phenyl) -quinolin-4-one
2- (4- (methylthio) phenyl) -quinolin-4-one (1.00 g, 3.74 mmol) prepared in step 3 was dissolved in THF (60 mL), and methanol (60 mL) and water (60 mL). ) Was added. Oxon (2.53 g, 4.11 mmol) was added to the solution, stirred at room temperature for 12 hours, the reaction mixture was concentrated under reduced pressure, dissolved in dichloromethane (300 mL), and washed with water and saturated sodium chloride solution. The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to yield 1.12 g (100%) of the title compound.
mp 246∼248 ℃
¹ H NMR (DMSO-d ₆ , 300 MHz) δ 11.87 (1H, s), 8.12 (5H, s), 7.78 to 7.68 (2H, m), 7.39 to 7.74 (1H, m), 6.42 (1H, s) , 3.33 (3H, s)
IR (KBr) 3211, 1635, 1196 cm ^-1
5 steps; 3-iodine-2- (4- (methylsulfonyl) phenyl) -quinolin-4-one
2- (4- (methylsulfonyl) phenyl) -quinolin-4-one (1.12 g, 3.74 mmol) prepared in step 4 was dissolved in acetonitrile (250 mL), followed by iodine (1.41 g, 4.49 mmol), CAN (2.26 g, 4.12 mmol) was added and refluxed for 16 hours. An aqueous sodium thiosulfate solution was added to remove brown at room temperature, and then extracted with a mixture of dichloromethane and acetonitrile. The organic layer was dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure and separated by tube chromatography (dichloromethane: acetonitrile = 2: 1) to give 1.25 g (79%) of the title compound.
mp ＞ 270 ° C
¹ H NMR (DMSO-d ₆ , 300 MHz) δ 8.25 (1H, d, J = 8.4 Hz), 8.17-8.15 (2H, m), 7.96-7.73 (2H, m), 7.88-7.82 (1H, m) , 7.75 (1H, d, J = 7.5 Hz), 7.57 to 7.52 (1H, m), 3.34 (3H, s)
IR (KBr) 3454, 2928, 1544, 1492 cm ^-1
6 steps; 3- (4-fluorophenol) -2- (4- (methylsulfonyl) phenyl) -quinolin-4-one
3-iodine-2- (4- (methylsulfonyl) phenyl) prepared in step 5 instead of 3-iodine-N-methyl-2- (4- (methylsulfonyl) phenyl) -quinolin-4-one Except for using -quinolin-4-one (0.42g, 1.0mmol) in the same manner as in step 5 of Example 53 to obtain the title compound.
mp> 300 ° C
¹ H NMR (DMSO-d ₆ , 300 MHz) δ 12.00 (1H, s), 8.17 (1H, d, J = 8.1 Hz), 7.93-7.90 (2H, m), 7.74-7.52 (4H, m), 7.42 ~ 7.36 (1H, m), 7.13-6.99 (4H, m), 3.23 (3H, s)
IR (KBr) 3431, 2970, 1707, 1412, 1238, 1086 cm ^-1
Example 61 3- (4-Fluorophenyl) -2- (4- (aminosulfonyl) phenyl) -4H-1-benzopyran-4-one
Stage 1; 1,3-dioxo-1- (2-hydroxyphenol) -3- (4-nitrophenyl) propane
2-hydroxyacetophenone (28.74 g, 0.211 mol) and 4-benzoyl chloride (39.21 g, 0.211 mol) were dissolved in pyridine (25 mL) and chloroform (50 mL), and then refluxed for 2 hours, and then 12 hours. Stir at room temperature. The reaction mixture was diluted with dichloromethane and washed with water and saturated ammonium chloride solution. Then, the organic layer was dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, dissolved in pyridine (250 ml), heated to 50 ° C. with potassium hydroxide and heated until an orange solid was formed, and then the temperature was maintained at room temperature. Lower and acetic acid (200 mL) was added. The resulting solid was isolated, washed with water and taken up in dichloromethane. The organic layer was washed with water, dried over anhydrous sodium sulfate, concentrated under reduced pressure, and recrystallized from dichloromethane and petroleum ether to give 24.6 g (43%) of the title compound.
¹ H NMR (CDCl ₃ , 300 MHz) δ 11.93 (1H, s), 8.37 to 8.32 (2H, m), 8.13 to 8.09 (2H, m), 7.80 (1H, dd, J = 8.1, 1.5 Hz), 7.55 ~ 7.49 (1H, m), 7.06-6.61 (3H, m)
IR (KBr) 3210, 1740, 1675, 1550, 1327 cm ^-1
Two steps; 2- (4-nitrophenyl) -4H-1-benzopyran-4-one
1,3-dioxo-1- (2-hydroxyphenol) -3- (4-nitrophenyl) propane (24.59 g, 90.64 mmol) prepared in step 1 was dissolved in 150 ml of acetic acid, followed by concentrated sulfuric acid. (3 ml) was added and refluxed for 4 hours. The reaction temperature was lowered to room temperature and ice water (400 mL) was added thereto. The resulting solid was washed with water and then dissolved in dichloromethane. The organic layer was washed with sodium bicarbonate solution, water and sodium chloride solution, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. Recrystallization from dichloromethane and petroleum ether afforded 22.5 g (93%) of the title compound.
mp 236-237 ℃
¹ H NMR (CDCl ₃ , 300 MHz) δ 7.46 to 7.38 (2H, m), 8.25 (1H, dd, J = 7.8, 1.5 Hz), 8.15 to 8.11 (2H, m), 7.80 to 7.74 (1H, m) , 7.62 (1H, dd, J = 8.4, 1.2 Hz), 7.51-7.46 (1H, m), 6.92 (1H, s)
IR (KBr) 1661, 1520, 1467, 1346, 856 cm ^-1
Three steps; 3-bromo-2- (4-nitrophenyl) -4H-1-benzopyran-4-one
2- (4-nitrophenyl) -4H-1-benzopyran-4-one (21.81 g, 81.0 mmol) prepared in step 2 was dissolved in dichloromethane (400 mL) and pyridine (50 mL) was added thereto. Bromine (20 mL, 0.39 mol) was slowly added dropwise. After refluxing for 8 hours, the mixture was stirred at room temperature for 12 hours. The reaction mixture was diluted with dichloromethane and the remaining bromine was removed with an aqueous sodium thiosulfate solution. The organic layer was washed with sodium bicarbonate solution, water and sodium chloride solution, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. Recrystallization from dichloromethane and petroleum ether gave 22.5 g (97%) of the title compound.
mp 214-217 ° C
¹ H NMR (CDCl ₃ , 300 MHz) δ 8.42 to 8.38 (2H, m), 8.34 to 8.31 (1H, m), 8.09 to 8.05 (2H, m), 7.81 to 7.75 (1H, m), 7.55 to 7.49 ( 2H, m)
IR (KBr) 1660, 1559, 1485, 1349 cm ^-1
4 steps; 3- (4-fluorophenyl) -2- (4-nitrophenyl) -4H-1-benzopyran-4-one
3-Bromo-2- (4-nitrophenyl) -4H- prepared in step 3 instead of 3-iodine-N-methyl-2- (4- (methylsulfonyl) phenyl) -quinolin-4-one The title compound was obtained in the same manner as the Step 5 of Example 53, except that 1-benzopyran-4-one (1.47 g, 4.22 mmol) was used.
mp 154-155 ℃
¹ H NMR (CDCl ₃ , 300 MHz) δ 8.30 (1H, dd, J = 8.1, 1.2 Hz), 8.18 to 8.15 (2H, m), 7.80 to 7.74 (1H, m), 7.61 to 7.57 (3H, m) , 7.55 to 7.46 (1H, m), 7.27 to 7.17 (2H, m), 7.06 to 7.04 (2H, m)
IR (KBr) 2929, 1641, 1510, 1347, 1229 cm ^-1
5 steps; 2- (4-aminophenyl) -3- (4-fluorophenyl) -4H-1-benzopyran-4-one
3- (4-Fluorophenyl) -2- (4-nitrophenyl) -4H-1-benzopyran-4-one (1.43 g, 3.94 mmol) prepared in step 4 was dissolved in ethyl acetate (60 mL). Tin chloride (II) hydrate (5.31 g, 23.5 mmol) was added thereto, and the mixture was refluxed for 4 hours. The reaction solution was cooled to room temperature, diluted with ethyl acetate, and washed with water and sodium bicarbonate solution. The solution was dried over anhydrous sodium sulfate, concentrated under reduced pressure, and recrystallized from dichloromethane and petroleum ether to give 1.23 g (90%) of the title compound.
mp 229-231 ° C
¹ H NMR (CDCl ₃ , 300 MHz) δ 8.28 to 8.25 (1H, m), 7.71 to 7.62 (1H, m), 7.54 to 7.51 (1H, m), 7.43 to 7.38 (1H, m), 7.26 to 7.18 ( 4H, m), 7.05-6.99 (2H, m), 6.55-6.51 (2H, m), 3.98 (2H, s)
IR (KBr) 3343, 2929, 1598, 1377, 1224 cm ^-1
6 steps; 3- (4-fluorophenyl) -2- (4-mercaptophenyl) -4H-1-benzopyran-4-one
Concentrated hydrochloric acid (0.25 mL) and water (1 mL) were added to the reaction vessel, and the 5-step 2- (4-aminophenyl) -3- (4-fluorophenyl) -4H-1 dissolved in DMF (10 mL) was added. -Benzopyran-4-one (0.50 g, 1.48 mmol) was slowly added dropwise. Water (3 mL) and DMF (6 mL) were added to the reaction mixture, which was dissolved completely. Sodium nitrite (0.12 g, 1.74 mmol) was added thereto, followed by stirring at room temperature for 30 minutes. The reaction mixture was slowly added dropwise to an ethyl xanthate (0.28 g, 1.75 mmol) solution dissolved in water (6 mL) at 40 to 50 ° C. The mixture was stirred at room temperature for 2 hours, concentrated under reduced pressure, dissolved in ethanol (20 ml), potassium carbonate (1.04 g, 7.52 mmol), and stirred at room temperature for 12 hours. The reaction mixture was concentrated under reduced pressure and then dissolved in dichloromethane. The organic layer was washed with water and sodium chloride solution, dried over anhydrous sodium sulfate, concentrated under reduced pressure and separated by tube chromatography (dichloromethane) to obtain 0.18 g (35%) of the title compound.
mp 99-100 ℃
¹ H NMR (CDCl ₃ , 300 MHz) δ 8.29 (1H, dd, J = 8.1, 1.5 Hz), 7.75-7.69 (1H, m), 7.54 (1H, d, J = 7.8 Hz), 7.47-7.26 (5H m), 7.22 to 7.18 (2H, m), 7.03 to 6.97 (2H, m)
IR (KBr) 2935, 2540, 1582, 1350, 1210 cm ^-1
7 steps; 2- (4- (aminosulfonyl) phenyl) -3- (4-fluorophenyl) -4H-1-benzopyran-4-one
3- (4-fluorophenyl) -2- (4-mercaptophenyl) -4H-1-benzopyran-4-one (0.18 g, 0.52 mmol) prepared in step 6 was added to acetonitrile (10 mL). After melting, sulfuryl chloride (0.12 ml, 1.49 mmol) and potassium nitrate (0.13 g, 1.29 mmol) were added at 0 ° C. and stirred for 1 hour. Excess ammonia water was added to the reaction mixture, which was stirred at room temperature for 30 minutes, and then diluted with dichloromethane. The organic layer was washed with water and sodium chloride solution, dried over anhydrous sodium sulfate, concentrated under reduced pressure and separated by column chromatography (dichloromethane: ethyl acetate = 1: 1) to obtain 0.03 g (15%) of the title compound.
mp 84 ~ 85 ℃
¹ H NMR (CDCl ₃ , 300 MHz) δ 8.31 to 8.28 (1H, m), 7.87 to 7.84 (1H, m), 7.78 to 7.69 (1H, m), 7.57 to 7.27 (5H, m), 7.22 to 7.16 (2H, m), 7.06-6.70 (2H, m), 5.03 (NH, s)
IR (KBr) 3325, 1609, 1467, 1337, 1151, 833 cm ^-1
[Test Example 1]
Inhibitory effect of COX-2 and COX-1 on the indomethacin as an example compound and a reference substance, the edema inhibitory effect of rat ears and the paw edema inhibition effect of carrageenin induced rats by the following experimental method It measured and the result is shown in Table 1.
1. Evaluation of COX-2 Inhibitory Effect
After disinfecting the abdomen of C57BL / 6 mice with 70% ethanol, remove the abdominal skin, taking care not to damage the peritoneum, add 5 ml of cold phosphate buffer (PBS) into the abdominal cavity, and let the macrophage out after a certain period of time. The prepared abdominal fluid was collected using a syringe. The collected solution was dispersed by centrifugation at 1500 rpm for 5 minutes by adding RPMI-1640 medium containing 100 units / ml penicillin and 100 mg / ml streptomycin. At this time, 500 μM of aspirin was treated to inactivate COX-1 present in the cells. Cell number 1 × 10 ⁶ cells / ㎖ is a cell suspension, a 24-well microtiter was added to each well of the plate by 1㎖ macrophages were cultured for 2 hours under conditions of _{37 ℃, 5% CO 2/} 95% O 2 to be Was attached to the bottom of the plate. Other non-attached cells were removed by washing twice with PBS. The purity of macrophages obtained through this procedure was confirmed by differential counting. RPMI-1640 medium containing 3% fetal bovine serum was added to the macrophages (usually 5 × 10 ⁵ cells / ml) and LPS (lipopolysaccharide) was treated to give a final concentration of 10µg / ml at 37 ° C and 5% CO _2. Incubated for 16 hours under the conditions of. After inducing COX-2 with LPS, the cell culture was removed and the macrophages were washed twice with PBS. Again, 1 ml of RRPI-1640 medium was added to each well, the sample was treated with an appropriate concentration, and incubated at 37 ° C. for 10 minutes. The whole amount was taken. The amount of PGE ₂ produced in the reaction supernatant was quantified by PGE ₂ radio immunoassay. The activity of 100% COX-2 was based on the difference in the amount of PGE ₂ produced in the supernatant of the 10 μM arachidonic acid treated group and the untreated group.
2. Evaluation of COX-1 Inhibitory Effect
Except for the aspirin pretreatment and LPS treatment when macrophages are attached, the evaluation was performed in the same manner as in the evaluation of COX-2 inhibition efficacy.
3. Measurement of Mouse Ear Edema Inhibition
A proper volume of sample was dissolved in a 20 μl DMSO: acetone 1: 9 solution in a left ear of an ICR mouse weighing 20 g, and then applied, and 30 μg of TPA (tetradecanoylphorbol acetate) was applied to both ears after 30 minutes. . Inhibition of inflammation inhibition was based on the number of neutral granulocytes that collect in the ear 5 hours after TPA inflammation. The number of neutral granulocytes was calculated by measuring the activity of myeloperoxidase.
4. Determination of plantar edema suppression induced by carrageenan
One hour after oral administration of a solution in which an appropriate amount of a sample is suspended in 0.5% carboxymethyl cellulose and 0.2% TWEN solution in a male Sprague-Dawley rat weighing 150-200 g, 1% carrageenin- Edema was induced by injection of 0.1 ml of carrageenan-saline solution. Edema rate was calculated by measuring the volume of the rats with Displacement Plethysmometer (Ugo Basile, Italy) immediately after and 3 hours after inflammation caused by carrageenan. The drug was administered 1 hour before the carrageenan injection. Edema inhibition rate is calculated by the following equation 1, the results are shown in Table 1.
% Edema inhibition rate = (1-ΔV _{treated group} / ΔV _control ) × 100
ΔV: change in volume
COX-2 (IC ₅₀ : μM)COX-1 (IC ₅₀ : μM)Ear edema inhibition rate (ED ₅₀ ,% inhibition)Inhibition of edema caused by carrageenin (oral administration) (ED ₅₀ ,% inhibition) Indomethacin0.050.010.4 mg / ear, ED ₅₀ 4.3 mg / kg, ED ₅₀ po Example 10.11> 100.4 mg / ear, ED ₅₀ 50 mg / kg, 43% inhibition Example 20.59--- Example 50.16> 101.2 mg / ear, ED ₅₀ 50 mg / kg, 52% inhibition Example 70.16> 10-- Example 80.15> 10-50 mg / kg, 37% inhibition Example 120.08> 100.6 mg / ear, ED ₅₀ - Example 130.03> 10-30 mg / kg, 17% inhibition Example 140.03> 100.4 mg / ear, ED ₅₀ - Example 160.7--- Example 210.2-0.6 mg / ear, ED ₅₀ 50 mg / kg, 23% inhibition Example 230.14> 10-- Example 240.19> 100.8 mg / ear, ED ₅₀ - Example 260.88--- Example 430.43--50 mg / kg, 17% inhibition Example 440.26---
As can be seen in Table 1, the diarylbenzopyran derivative of the general formula (I) according to the present invention has a 300 times higher selectivity to COX-2 and selectively inhibits the action of COX-2. You can.
The present invention relates to cyclooxygenase-2 inhibitors containing a therapeutically effective amount of a compound of formula (I) together with one or more non-toxic, pharmaceutically acceptable carriers, adjuvants or diluents, or other active ingredients. (cyclooxygenase-2 inhibitor) composition, wherein the composition of the present invention is in the form of a solution, suspension or emulsion in an oil or an aqueous medium, or a dry powder that is dissolved in sterile, pyrogen-free water before use. Oral formulations, subcutaneous injections, intravenous injections, intramuscular injections, intramuscular injections, parenteral formulations such as suppositories, topical formulations such as creams, gels, ointments or suspensions, mouthwashes and the like.
In the case of oral dosage forms, the compositions of the present invention may be used in a known manner using pharmaceutically acceptable carriers and excipients, for example tablets, troches, sugar-containing tablets, aqueous or oily suspensions, dispersible flours or particles. It is formulated in the form of emulsions, soft or hard capsules, syrups, elixirs, which are contained in unit dosage forms and in multidose containers.
In oral formulations, tablets may be inert diluents such as calcium carbonate, sodium carbonate, lactose, calcium phosphate, sodium phosphate; Granulating agents such as corn, starch and alginic acid; Disintegrants; Binders such as starch, gelatin and acacia; The compound of the present invention is mixed with an excipient which can be used for the preparation of tablets, such as lubricants such as magnesium stearate, stearic acid and talc. Tablets may be used uncoated or coated to inhibit absorption of the gastrointestinal tract and disintegration of the tablets. For example, you may apply time inhibiting substances, such as glyceryl monostearate and glyceryl distearate. Hard capsule is a compound of the present invention is mixed with an inert solid diluent such as calcium carbonate, calcium phosphate, kaolin, etc., soft capsule is a solvent such as water and mixed with propylene glycol, PEGs, ethanol and peanut oil, liquid paraffin, olive It is a mixture of active ingredients mixed with oil solvents such as oil.
The water-soluble suspending agent is a mixture of excipients and active ingredients suitable for the preparation of water-soluble suspending agents. Excipients include, for example, sodium carboxymethyl cellulose, methyl cellulose, hydroxy-propyl methyl cellulose, sodium alginate, polyvinyl-pi Suspending agents such as ralidone, gum tragacanth, gum acacia and the like; Condensed fatty acids and alkylene oxides such as polyoxyethylene stearate; Compounds in which alkylene oxides are condensed to long fatty acids such as heptadecaethyleneoxycetanol; Compounds condensed with ethylene oxide with partial esters derived from anhydrous hexitol anhydride and fatty acids such as polyoxyethylene sorbitol monooleate; Wetting agents; Or dispersing agents. Water-soluble suspensions contain preservatives, colorants, spices, sweeteners and the like.
The oily suspension is a suspension of an active ingredient in a vegetable oil such as olive oil, sesami oil, or a mineral oil such as liquid paraffin. For example, a thickening agent such as beeswax, hardened paraffin, cetyl alcohol, etc. may be used. It contains. It also contains preservatives, colorants, spices, sweeteners and the like, which can be preserved by adding antioxidants such as vitamin C.
Dispersible powders and particles have an active ingredient in a state in which a dispersing agent, a wetting agent, a suspending agent, a preservative and the like are mixed together. Suitable dispersing, wetting or suspending agents can be mentioned by way of example already mentioned above. Additional excipients are, for example, sweeteners, spices, colorants and the like.
Water-in-oil emulsions are derived from vegetable oils such as olive oil or mineral oils such as liquid paraffin, and are derived from natural phospholipids such as soy bean lecithin, and esters of anhydrous hecitol or fatty acids such as sorbitan monooleate. The active ingredient is emulsified using compounds obtained by condensation of ethylene oxide with partial esters derived from anhydrous hexitol anhydride and fatty acids, such as lyoxyethylene sorbitol monooleate.
Syrups and elixirs are a mixture of active ingredients with sweeteners such as glycerol, propylene glycol, sorbitol and sucrose.
Parenteral formulations are injected by injection into a sterile injectable solution or a suspension in which the active ingredient is suspended in a non-toxic usable diluent or solvent such as 1,3-butanediol. Among the excipients or solvents that may be employed are water, Ringer's solution and isotonic saline solution. Cosolvents such as ethanol, polyethylene glycol, and polypropylene glycol can also be used. In addition, sterile, nonvolatile oils can be customarily used as solvents or suspending solvents. Mixed, non-stimulating, bland fixed oils for this purpose include synthetic mono- and diglycerides. In addition, fatty acids such as oleic acid can be used for the preparation of injectables. The suppository form is formulated by mixing the drug with a suitable non-irritating excipient such as cocoa butter or polyethylene glycol, which is solid at room temperature but liquid at the rectal temperature and will melt in the rectum to release the drug. Administration.
Topical formulations generally consist of pharmaceutical carriers, cosolvents, emulsifiers, penetration enhancers, preservatives, emollients.
When treating a disease using the composition of the present invention, the dose of the active compound (I) is determined by the age, body weight, general state of health, sex, meal, time of administration, rate of excretion, combination of drugs, during treatment. Depending on the severity of the disease, depending on the disease can be used up to 0.01 ~ 140mg / kg body weight daily, 0.5mg ~ 7g per patient can be used. For example, inflammation can be effectively treated by administering the compositions of the present invention to 0.01-50 mg / kg body weight, or up to 0.5 mg-3.5 g per patient per day.
On the other hand, the amount of the compound of the present invention mixed with the carrier material to determine one formulation depends on the mode of administration and the patient being treated. For example, a formulation intended for oral administration to humans will contain from 5 to 95% of the carrier substance and 0.5 mg to 5 g of active ingredient, and a formulation intended for parenteral administration to humans Carrier materials account for 5 to 99% of the total composition and 0.1 mg to 2.5 g of active ingredient.
As described above, the compound (I) of the present invention has high selectivity to cyclooxygenase-2 (COX-2), so that the biosynthetic action of the prostaglandin of COX-2 is effectively It can be suppressed and is effective in the treatment of diseases involving COX-2.

权利要求:
Claims (3)
[1" claim-type="Currently amended] Diarylbenzopyran derivatives represented by the following general formula (I) and pharmaceutically acceptable salts thereof:
(Ⅰ)
In the above formula,
X is O, NR ⁵ or S (O) n,
Wherein n is 0, 1 or 2,
R ⁵ is hydrogen, lower alkyl having 1 to 6 carbon atoms or NR ⁶ R ⁷ group,
Wherein R ⁶ and R ⁷ are the same as or different from each other and are hydrogen or a lower alkyl group having 1 to 6 carbon atoms.
Y is O, S, H ₂ or N (OR ⁶ ),
Wherein R ⁶ is the same as defined in X above.
R ¹ and R ² are the same as or different from each other, and are hydrogen, halogen, lower alkyl having 1 to 6 carbon atoms, trifluoromethyl, alkoxy, hydroxy, nitro, nitrile or carboxyl group,
R ³ is hydrogen, halogen, lower alkyl, trifluoromethyl, alkoxy, hydroxy, nitro, nitrile, carboxyl, S (O) nR ⁵ or NR ⁸ R ⁹ ,
Wherein n and R ⁵ are the same as defined above in X,
R ⁸ and R ⁹ are the same as or different from each other and are hydrogen, a lower alkyl or methylsulfonyl group having 1 to 6 carbon atoms.
R ⁴ is oxazolyl, benzo [b] thienyl, benzodioxyl, naphthyl, tetrahydronaphthyl, thiazolyl, indanyl, indolyl, pyrroyl, oxocyclopentenyl, oxohydrofuryl, benzofuranyl , Dihydrobenzofuranyl, pyrazinyl, phenylethynyl, phenylethenyl, dihydrobenzopyranyl, dihydrobenzothiopyranyl or a substituent having the following structures.

Wherein R ¹⁰ to ¹⁴ are the same as or different from each other, and are hydrogen, halogen, lower alkyl having 1 to 6 carbon atoms, phenyl, trifluoromethyl, alkoxy, hydroxy, hydroxyalkyl, nitro, S (O) nR ⁵ , NR ⁶ R ⁷ , trifluoromethoxy, nitrile, carboxyl, acetyl, morpholino and formyl groups.
Wherein n, R⁵, R⁶or R⁷Is X and R³As defined in.

Wherein R ¹⁵ is hydrogen, halogen, lower alkyl having 1 to 6 carbon atoms, phenyl, trifluoromethyl, alkoxy, hydroxy, nitro, S (O) nR ⁵ , NR ⁶ R ⁷ , trifluoromethoxy, nitrile, Carboxyl, acetyl, morpholino, and formyl groups.
Wherein n, R⁵, R⁶or R⁷Is X and R³As defined in.
or
Wherein R ^16-18 are the same as or different from each other, hydrogen, halogen, lower alkyl having 1 to 6 carbon atoms, phenyl, trifluoromethyl, alkoxy, hydroxy, nitro, S (O) nR ⁵ , NR ⁶ R ⁷ , Trifluoromethoxy, nitrile, carboxyl, acetyl, morpholino, and formyl groups.
Wherein n, R⁵, R⁶or R⁷Is X and R³As defined in.
, or
Wherein R ¹⁹ is the same as or different from each other, hydrogen, halogen, lower alkyl having 1 to 6 carbon atoms, phenyl, trifluoromethyl, alkoxy, hydroxy, nitro, S (O) nR ⁵ , NR ⁶ R ⁷ , tri Fluoromethoxy, nitrile, carboxyl, acetyl, morpholino and formyl groups.
Wherein n, R⁵, R⁶or R⁷Is X and R³As defined in.
or
Wherein R ²⁰ is hydrogen, halogen, lower alkyl of 1 to 6 carbon atoms, phenyl, trifluoromethyl, alkoxy, hydroxy, nitro, NR ⁶ R ⁷ , trifluoromethoxy, nitrile, carboxyl, acetyl, morpholy Furnace, formyl, S (O) nR ⁵ .
Wherein n, R⁵, R⁶or R⁷Is X and R³As defined in.
or
Wherein R ²¹ to ²³ silver hydrogen, halogen, lower alkyl of 1 to 6 carbon atoms, phenyl, trifluoromethyl, alkoxy, hydroxy, nitro, NR ⁶ R ⁷ , trifluoromethoxy, nitrile, carboxyl, acetyl, Morpholino, formyl, S (O) nR ⁵ .
Wherein n, R⁵, R⁶or R⁷Is X and R³As defined in.
[2" claim-type="Currently amended] The diarylbenzopyran derivative and pharmaceutically acceptable salt thereof according to claim 1, wherein the compound represented by the general formula (I) is a compound described below.
2- (4- (methylsulfonyl) phenyl) -3-phenyl-4H-1-benzopyran-4-one
3- (4-aminophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (4- (methylthio) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (4-nitrophenyl) -4H-1-benzopyran-4-one
3- (4-ethoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (2-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (2-chlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-cyanophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4- (N, N-dimethylamino) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4- (N-methylamino) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2- (methylthio) phenyl) -4H-1-benzopyran-4-one
3- (2,5-dichlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (3- (methylthio) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (4-trifluoromethoxyphenyl) -4H-1-benzopyran-4-one
3- (3-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-isopropylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (2,6-dichlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-t-butylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-ethylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-hydroxymethylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-isobutylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-n-butoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (4-morpholinophenyl) -4H-1-benzopyran-4-one
3- (2- (methylsulfinyl) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (4-trifluoromethylphenyl) -4H-1-benzopyran-4-one
3- (3- (methylsulfinyl) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-hydroxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (2,3-difluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-chloro-3-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3,5-difluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-hydroxy-3-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3,4-dihydroxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4- (methylsulfinyl) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-hydroxy-3-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (2,6-difluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,5,6-trifluorophenyl) -4H-1-benzopyran-4-one
3- (2-hydroxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (2,4-dimethoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (2,4-difluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (2,4-dichlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-acetylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-chloro-2-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (2,4-dimethylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-formylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (pentafluorophenyl) -4H-1-benzopyran-4-one
3- (4-chloro-3-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3,4-dimethoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,4,6-trichlorophenyl) -4H-1-benzopyran-4-one
3- (4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3,4-dichlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,4,5-trichlorophenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,3,4,5-tetrafluorophenyl) -4H-1-benzopyran-4-one
3- (2-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3,5-dichlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,3,4-trifluorophenyl) -4H-1-benzopyran-4-one
3- (4-chlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,4,5-trifluorophenyl) -4H-1-benzopyran-4-one
3- (4-chloro-3-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
6-chloro-3- (4-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (3-nitrophenyl) -4H-1-benzopyran-4-one
3- (3,4-difluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (1-naphthyl) -4H-1-benzopyran-4-one
3- (3-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3,4-dimethylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (2-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3-chloro-4-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,3,5,6-tetrafluorophenyl) -4H-1-benzopyran-4-one
3- (4-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3-fluoro-4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-bromophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (2,3-dichlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-Fluoro-3-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3-chlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-Fluoro-3- (methylthio) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (5-methyl-2-thienyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3-fluoro-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-Fluoro-3-hydroxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylthio) phenyl) -3- (4-trifluoromethylphenyl) -4H-1-benzopyran-4-one
3- (4-Fluoro-3-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (2,5-difluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3-bromo-4- (methylthio) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,5,6-trichlorophenyl) -4H-1-benzopyran-4-one
3- (3-chloro-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
6,8-dichloro-3- (4-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3-ethyl-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,3,4-trichlorophenyl) -4H-1-benzopyran-4-one
3- (3-fluoro-4- (methylthio) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3-chloro-4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3-methyl-4- (methylthio) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-methyl-3-nitrophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-fluoro-2-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3-chloro-4- (methylthio) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (3,4,5-trichlorophenyl) -4H-1-benzopyran-4-one
3- (2,4-dimethyl-3-thienyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-chloro-3- (methylthio) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3-hydroxy-3-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2-oxazolyl) -4H-1-benzopyran-4-one
3- (4-methoxy-3-propylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (2-fluoro-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,3,4,5-tetrachlorophenyl) -4H-1-benzopyran-4-one
3- (4-methoxy-3-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (2-chloro-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-Fluoro-2-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3-hydroxy-4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (5-chloro-2-thienyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3-amino-4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3-methoxy-4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
6-Fluoro-2- (4-fluorophenyl) -3- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (2-fluoro-4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3-bromo-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-chloro-2-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (2,5-dichloro-3-thienyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3,5-dimethyl-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3-fluoro-4-hydroxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (2-chloro-4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (5-bromo-2-furyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (3,4,5-trifluorophenyl) -4H-1-benzopyran-4-one
3- (3,5-dichloro-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-chloro-3-hydroxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3-chloro-4-methoxy-5-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (5-chloro-2-furyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3,5-difluoro-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2-naphthyl) -4H-1-benzopyran-4-one
3- (4-methyl-1,3-benzodioxol-5-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,4,6-trifluorophenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,3,4,6-tetrafluorophenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (pentachlorophenyl) -4H-1-benzopyran-4-one
3- (2-benzothienyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3-biphenyl-2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (1,2,3,4-tetrahydronaphth-6-6yl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,3,4,6-tetrachlorophenyl) -4H-1-benzopyran-4-one
3- (6-methoxy-2-naphthyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2-pyridyl) -4H-1-benzopyran-4-one
3- (1,4-benzodioxan-6-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,3,5,6-tetrachlorophenyl) -4H-1-benzopyran-4-one
3- (1,3-benzodioxol-5-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (4-methyl-1,3-benzodioxol-6-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2-thiazolyl) -4H-1-benzopyran-4-one
3- (5-bromo-2-thienyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (5-benzothienyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (benzofuran-2-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2-thienyl) -4H-1-benzopyran-4-one
3- (benzofuran-5-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (2,3-dihydrobenzofuran-5-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3,4-dihydro-2H-1-benzopyran-6-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3,4-dihydro-2H-1-benzothiopyran-6-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2-pyrazinyl) -4H-1-benzopyran-4-one
3- (6-methyl-3-pyridyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (4-pyridyl) -4H-1-benzopyran-4-one
3- (2,5-dimethyl-3-furyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (5-methyl-2-furyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (2-furyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (5-Indanyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4-methylphenyl) -3- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4-fluorophenyl) -6-methyl-3- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4-fluorophenyl) -6-methoxy-3- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3-phenylethynyl-4H-1-benzopyran-4-one
8-Fluoro-3- (3-fluorophenyl) -5-hydroxy-2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2-phenylethenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (3-oxocyclopent-1 (5) -enyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2-oxocyclopent-1 (5) -enyl) -4H-1-benzopyran-4-one
3- (4-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran
3- (3-fluorophenyl) -5-hydroxy-2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
3- (3-fluorophenyl) -5-methoxy-2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (5-oxo-4-hydro-2-furyl) -4H-1-benzopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (5-oxo-4-hydro-3-furyl) -4H-1-benzopyran-4-one
3- (4-aminophenyl) -2- (4-aminosulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-methylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,5-dichlorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-bromophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,4-dihydroxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-fluoro-2-methoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3-phenyl-4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,4-difluorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-chloro-3-fluorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,5-dichlorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-t-butylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-chloro-4-fluorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,4-dichlorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-chlorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,6-difluorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-chlorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-chlorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-hydroxy-4-methylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4- (N, N-dimethylamino) phenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-ethylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-ethoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,3-difluorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-fluorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-chloro-4-methylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-fluorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,5-difluorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-hydroxymethylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-isobutylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,4-difluorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-fluoro-4-methoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-methylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4- (methylthio) phenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-methoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4- (N-methylamino) phenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2- (methylthio) phenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2- (methylsulfinyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-chloro-4-hydroxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3- (methylsulfinyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4- (methylsulfinyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-methylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-chloro-4-methoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-methoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,5,6-trifluorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,3,4,5-tetrafluorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-methoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-morpholinophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-hydroxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-nitrophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-trifluoromethylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-trifluoromethoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-hydroxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-isopropylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (1,3-benzodioxol-5-yl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-n-butoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,4-dichlorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,6-dichlorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-fluorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,3-dichlorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,5-difluorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,4-dimethoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,4-dimethoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,4,5-trifluorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,4-dimethylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,4-dimethylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-bromo-4- (methylthio) phenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-cyanophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-chloro-3-methylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,3,4,6-tetrafluorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-chloro-4-methoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-fluoro-3-methoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-ethyl-4-methoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-hydroxy-3-methoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,3,4-trifluorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-fluoro-4-methylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-fluoro-2-methylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-fluoro-4-hydroxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,5,6-trichlorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-fluoro-4- (methylthio) phenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-methyl-1,3-benzodioxol-5-yl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-fluoro-3-hydroxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-chloro-3- (methylthio) phenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-methyl-4- (methylthio) phenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-fluoro-3- (methylthio) phenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-chloro-4- (methylthio) phenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-methyl-3-nitrophenyl) -4H-1-benzopyran-4-one
3- (3-amino-4-methylphenyl) -2- (4- (aminosulfonyl) phenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-hydroxy-3-methylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-methoxy-3-methylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-methoxy-3-propylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-fluoro-4-methoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-chloro-2-methoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,4,6-trichlorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-fluoro-4-methylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-thiazolyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-fluoro-3-methylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (pentafluorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-chloro-4-methylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-chloro-2-methylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-bromo-4-methoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,5-dimethyl-4-methoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-chloro-4-methoxy-5-methylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,5-dichloro-4-methoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,5-difluoro-4-methoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,4,6-trifluorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-methoxy-4-methylphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,4,5-trifluorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-pyridyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-chloro-3-hydroxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (benzofuran-5-yl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,3,5,6-tetrafluorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,4,5-trichlorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,4,5-trichlorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,3,4,5-tetrachlorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (5-chloro-2-furyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-hydroxy-4-methoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,3,4,6-tetrachlorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-chloro-3-methoxyphenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,3,5,6-tetrachlorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (pentachlorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3-biphenyl-4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (1,2,3,4-tetrahydronaphth-6-6yl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-naphthyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (6-methoxy-2-naphthyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-phenylethenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (1,4-benzodioxan-6-yl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-methyl-1,3-benzodioxol-6-yl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-oxazolyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-thienyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (5-bromo-2-thienyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (5-chloro-2-thienyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,4-dimethyl-3-thienyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,5-dichloro-3-thienyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (5-methyl-2-thienyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (5-benzothienyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,3,4-trichlorophenyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-benzothienyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (benzofuran-2-yl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,3-dihydrobenzofuran-5-yl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,4-dihydro-2H-1-benzopyran-6-yl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,4-dihydro-2H-1-benzothiopyran-6-yl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-pyrazinyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (6-methyl-3-pyridyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-pyridyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,5-dimethyl-3-furyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (5-methyl-2-furyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (5-bromo-2-furyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-furyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (5-indanyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -8-fluoro-3- (3-fluorophenyl) -5-hydroxy-4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-oxocyclopent-1- (5) enyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-oxocyclopent-1- (5) enyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-fluorophenyl) -5-hydroxy-4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-fluorophenyl) -5-methoxy-4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (5-oxo-4-hydro-2-furyl) -4H-1-benzopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (5-oxo-4-hydro-3-furyl) -4H-1-benzopyran-4-one
3- (4-ethoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3-phenyl-4H-1-benzopyran-4-thione
3- (4- (methylsulfinyl) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-aminophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-methoxy-3-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3,4-dimethoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4- (N-methylamino) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-cyanophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4- (N, N-dimethylamino) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (4- (methylthio) phenyl) -4H-1-benzopyran-4-thione
3- (3- (methylsulfinyl) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (4-nitrophenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (4-trifluoromethylphenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (4-trifluoromethoxyphenyl) -4H-1-benzopyran-4-thione
3- (2-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-isopropylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (2,6-dichlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-t-butylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-ethylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-hydroxymethylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-isobutylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (4-morpholinophenyl) -4H-1-benzopyran-4-thione
3- (4-hydroxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2,4,6-trichlorophenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2,3,5,6-tetrafluorophenyl) -4H-1-benzopyran-4-thione
3- (4-n-butoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (2-hydroxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (2,5-dichlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (2,3-difluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-chloro-3-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (3,4,5-trifluorophenyl) -4H-1-benzopyran-4-thione
3- (4-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3,5-difluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3,4-dihydroxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2,3,4,5-tetrafluorophenyl) -4H-1-benzopyran-4-thione
3- (2-chlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (2,6-difluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2,3,4-trifluorophenyl) -4H-1-benzopyran-4-thione
3- (2,4-dimethoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3-fluoro-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (2,4-dimethylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2,4,5-trifluorophenyl) -4H-1-benzopyran-4-thione
3- (3,4-difluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3,4-dimethylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2,3,5,6-tetrachlorophenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (pentafluorophenyl) -4H-1-benzopyran-4-thione
3- (2,4-dichlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (2-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (3-nitrophenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (1-naphthyl) -4H-1-benzopyran-4-thione
3- (2-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3-chloro-4-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-chloro-2-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -6-nitro-4H-1-benzopyran-4-thione
3- (4-chlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-bromophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (2,3-dichlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
6-chloro-3- (4-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2-oxazolyl) -4H-1-benzopyran-4-thione
3- (3-chlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylthio) phenyl) -3- (4-trifluoromethylphenyl) -4H-1-benzopyran-4-thione
3- (2,5-difluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3-bromo-4- (methylthio) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (pentachlorophenyl) -4H-1-benzopyran-4-thione
3- (3-chloro-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2,5,6-trifluorophenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2,3,4,6-tetrafluorophenyl) -4H-1-benzopyran-4-thione
3- (3-ethyl-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3-fluoro-4- (methylthio) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3-chloro-4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3-methyl-4- (methylthio) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-methyl-3-nitrophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-Fluoro-2-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3-chloro-4- (methylthio) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
6,8-dichloro-3- (4-fluoromethyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-methoxy-3-propylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (2-Fluoro-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2- (methylthio) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2- (methylthio) phenyl) -4H-1-benzopyran-4-thione
3- (4-hydroxy-3-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (2-chloro-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (2- (methylsulfinyl) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-Fluoro-2-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3-amino-4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
6-Fluoro-2- (4-fluorophenyl) -3- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (2-fluoro-4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (2,5-dichloro-3-thienyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-Fluoro-3-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3-bromo-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-chloro-2-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3,5-dimethyl-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (2-chloro-4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3,5-dichloro-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (5-bromo-2-furyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3-chloro-4-methoxy-5-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3,5-difluoro-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2,4,6-trifluorophenyl) -4H-1-benzopyran-4-thione
3- (2,4-difluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (3,4,5-trichlorophenyl) -4H-1-benzopyran-4-thione
3- (3,5-dichlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3,4-dichlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2,5,6-trichlorophenyl) -4H-1-benzopyran-4-thione
3- (3-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2,3,4,5-tetrachlorophenyl) -4H-1-benzopyran-4-thione
3- (2-benzothienyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3-biphenyl-2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (1,2,3,4-tetrahydronaphth-6-6yl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2-naphthyl) -4H-1-benzopyran-4-thione
3- (6-methoxy-2-naphthyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (1,4-benzodioxan-6-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (1,3-benzodioxol-5-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-methyl-1,3-benzodioxol-6-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-methyl-1,3-benzodioxol-5-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2-thiazolyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2,4,5-trichlorophenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2-thienyl) -4H-1-benzopyran-4-thione
3- (5-bromo-2-thienyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2,3,4,6-tetrachlorophenyl) -4H-1-benzopyran-4-thione
3- (5-chloro-2-thienyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (2,4-dimethyl-2-thienyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (5-methyl-2-thienyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (5-benzothienyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (benzofuran-2-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (benzofuran-5-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (2,3-dihydrobenzofuran-5-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3,4-dihydro-2H-1-benzopyran-6-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3,4-dihydro-2H-1-benzothiopyran-6-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2-pyrazinyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2-pyridyl) -4H-1-benzopyran-4-thione
3- (6-methyl-3-pyridyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (4-pyridyl) -4H-1-benzopyran-4-thione
3- (2,5-dimethyl-3-furyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (5-methyl-2-furyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (5-chloro-2-furyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2,3,4-trichlorophenyl) -4H-1-benzopyran-4-thione
3- (2-furyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (5-Indanyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4-methylphenyl) -3- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4-fluorophenyl) -6-methyl-3- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4-fluorophenyl) -6-methoxy-3- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3-phenylethynyl-4H-1-benzopyran-4-thione
8-Fluoro-3- (3-fluorophenyl) -5-hydroxy-2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (methylsulfonyl) phenyl) -3- (2-phenylethenyl) -4H-1-benzopyran-4-thione
3- (3-fluorophenyl) -5-hydroxy-2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (3-fluorophenyl) -5-methoxy-2- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
3- (4-aminophenyl) -2- (4-aminosulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-bromophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-t-butylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2-chlorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-cyanophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-chloro-4-hydroxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-chlorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4- (N, N-dimethylamino) phenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-fluorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2-fluoro-4-methoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-ethylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2-chloro-4-methylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-ethoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,5-dichlorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-fluorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2-fluorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-hydroxymethylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-isobutylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-methylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4- (methylthio) phenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2-methoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2- (methylthio) phenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4- (N-methylamino) phenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3- (methylsulfinyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-methylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4- (methylsulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2-methylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-hydroxy-4-methylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-methoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-methoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-morpholinophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2-hydroxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-nitrophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-trifluoromethylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,3,5,6-tetrafluorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3,4,5-trifluorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-trifluoromethoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-hydroxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-isopropylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3,5-dichlorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,3,5,6-tetrachlorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3,4,5-trichlorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-n-butoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3,4-dichlorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,3,4-trifluorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,3,4,5-tetrafluorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,6-dichlorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,3-difluorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,5-difluorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2- (methylsulfinyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,4-difluorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,6-difluorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3,5-difluorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3,4-dihydroxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,4-dimethoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3,4-dimethoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,4-dimethylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3,4-dimethylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-bromo-4- (methylthio) phenyl) -4H-1-benzopyran-4
2- (4- (aminosulfonyl) phenyl) -3- (3-methoxy-4-methylphenyl) -4H-1-benzopyran-4-thione-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-chloro-4-fluorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-chloro-3-methylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,4-dimethyl-3-thienyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4- (methylsulfinyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-chloro-4-methoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-ethyl-4-methoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,3,4-trichlorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,3,4,5-tetrachlorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-fluoro-2-methoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (5-chloro-2-thienyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,5-dichloro-3-thienyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-fluoro-3-methylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2-oxazolyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2-thienyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-fluoro-4-methoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-fluoro-4- (methylthio) phenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-methyl-4- (methylthio) phenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-fluoro-4-hydroxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-fluoro-4-methylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3-phenyl-4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-fluoro-3-methoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-chloro-3-fluorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-chloro-3-methoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-chloro-4- (methylthio) phenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-fluoro-3-hydroxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-chloro-3- (methylthio) phenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-fluoro-3- (methylthio) phenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-chloro-3-hydroxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,3-dichlorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-hydroxy-4-methylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-methyl-3-nitrophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-hydroxy-4-methoxyphenyl) -4H-1-benzopyran-4-thione
3- (3-amino-4-methylphenyl) -2- (4- (aminosulfonyl) phenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-hydroxy-3-methoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (5-methyl-2-furyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2-fluoro-4-methoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-chlorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-chloro-3-methoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-fluoro-3-methylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (1,3-benzodioxol-5-yl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-chloro-4-methylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2-chloro-4-methylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-chloro-2-methylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-bromo-4-methoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3,5-dimethyl-4-methoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-chloro-4-methoxy-5-methylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3,5-dichloro-4-methoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3,5-difluoro-4-methoxyphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,4,6-trifluorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3-biphenyl-4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (1,2,3,4-tetrahydronatthi-6-yl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,4,6-trichlorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,3,4,6-tetrafluorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,4,5-trifluorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,5,6-trifluorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,4-dichlorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,3,4,6-tetrachlorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,4,5-trichlorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,5,6-trichlorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (pentachlorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (5-chloro-2-furyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (pentafluorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2-naphthyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3,4-difluorophenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (6-methoxy-2-naphthyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2-phenylethenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (1,4-benzodioxan-6-yl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-methyl-1,3-benzodioxol-6-yl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-methyl-1,3-benzodioxol-5-yl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2-thiazolyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (5-bromo-2-thienyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (5-methyl-2-thienyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (5-benzothienyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-methoxy-3-methylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-methoxy-3-propylphenyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (benzofuran-2-yl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (benzofuran-5-yl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,3-dihydrobenzofuran-5-yl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3,4-dihydro-2H-1-benzopyran-6-yl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3,4-dihydro-2H-1-benzothiopyran-6-yl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2-pyrazinyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2-pyridyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (6-methyl-3-pyridyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (4-pyridyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2,5-dimethyl-3-furyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (5-bromo-2-furyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2-benzothienyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (2-furyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (5-indanyl) -4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -8-fluoro-3- (3-fluorophenyl) -5-hydroxy-4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-fluorophenyl) -5-hydroxy-4H-1-benzopyran-4-thione
2- (4- (aminosulfonyl) phenyl) -3- (3-fluorophenyl) -5-methoxy-4H-1-benzopyran-4-thione
3- (4- (methylsulfonyl) phenyl) -2-phenyl-4H-1-benzothiopyran-4-one
2- (4-bromophenyl) -3- (4-fluorophenyl) -4H-1-benzothiopyran-4-one
3- (4-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one-1,1-dioxide
2- (4-bromophenyl) -3- (4-fluorophenyl) -4H-1-benzothiopyran-4-thione
3- (3,5-difluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-thione
3- (4-aminophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-bromophenyl) -2- (4-fluorophenyl) -4H-1-benzothiopyran-4-one
3- (4-t-butylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (2-chlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3-chlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-cyanophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-chlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4- (N, N-dimethylamino) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-ethylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-ethoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-isobutylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (4- (methylthio) phenyl) -4H-1-benzothiopyran-4-one
3- (2-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4- (N-methylamino) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2- (methylthio) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (3- (methylthio) phenyl) -4H-1-benzothiopyran-4-one
3- (2- (methylsulfinyl) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3- (methylsulfinyl) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4- (methylsulfinyl) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (2-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (4-morpholinophenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (4-nitrophenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (4-trifluoromethylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (4-trifluoromethoxyphenyl) -4H-1-benzothiopyran-4-one
3- (4-hydroxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-isobutylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-n-butoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3,4-dichlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (2,4-dichlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (2,6-dichlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (2,5-dichlorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (2,3-difluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (2,5-difluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-fluorophenyl) -2- (4- (methylthio) phenyl) -4H-1-benzothiopyran-4-one
3- (2,4-difluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (2,6-difluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3,4-dihydroxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (2,4-dimethoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3,4-dimethoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (2,4-dimethylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3,4-dimethylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3-bromo-4- (methylthio) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-Fluoro-3-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-chloro-3-hydroxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-chloro-3-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3-chloro-4-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-chloro-3-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-chloro-2-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (2-Fluoro-4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (3,4,5-trifluorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,4,5-trifluorophenyl) -4H-1-benzothiopyran-4-one
3- (3-chloro-4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3-chloro-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3-ethyl-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-Fluoro-2-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-Fluoro-2-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3-fluoro-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3-fluoro-4- (methylthio) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3-Fluoro-4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-Fluoro-3- (methylthio) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-Fluoro-3-hydroxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-chloro-3-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3-chloro-4-hydroxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3-methyl-4- (methylthio) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3-chloro-4- (methylthio) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-chloro-3- (methylthio) phenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3-hydroxy-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-hydroxy-3-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3-hydroxy-4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-methyl-3-nitrophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (2-fluorophenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-hydroxymethylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3-amino-4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (2-benzothienyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (benzofuran-2-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-hydroxy-3-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-methoxy-3-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (2-chloro-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,5,6-trifluorophenyl) -4H-1-benzothiopyran-4-one
3- (4-Fluoro-3-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (2-chloro-4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-chloro-2-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3-bromo-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3,5-dimethyl-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3-methoxy-4-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3-chloro-4-methoxy-5-methylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3,5-dichloro-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3,5-difluoro-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,4,6-trifluorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,3,4-trichlorophenyl) -4H-1-benzothiopyran-4-one
3- (3-fluoro-4-hydroxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (3,4,5-trichlorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,4,5-trichlorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (pentafluorophenyl) -4H-1-benzothiopyran-4-one
3-biphenyl-2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (1,2,3,4-tetrahydronaphth-6-yl) -4H-1-benzothiopyran-4-one
3- (5-bromo-2-furyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2-naphthyl) -4H-1-benzothiopyran-4-one
3- (6-methoxy-2-naphthyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2-phenylethenyl) -4H-1-benzothiopyran-4-one
3- (1,4-benzodioxan-6-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-methoxy-3-propylphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (2-Fluoro-4-methoxyphenyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (1,3-benzodioxol-5-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-methyl-1,3-benzodioxol-6-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-methyl-1,3-benzodioxol-5-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2-thiazolyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2-oxazolyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2-thienyl) -4H-1-benzothiopyran-4-one
3- (5-bromo-2-thienyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (5-chloro-2-thienyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (2,4-dimethyl-3-thienyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (2,5-dimethyl-3-thienyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (5-methyl-2-thienyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (5-benzothienyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (benzofuran-5-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (2,3-dihydrobenzofuran-5-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3,4-dihydro-2H-1-benzopyran-6-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (3,4-dihydro-2H-1-benzothiopyran-6-yl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,5,6-trichlorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (pentachlorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2-pyrazinyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2-pyridyl) -4H-1-benzothiopyran-4-one
3- (6-methyl-3-pyridyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (4-pyridyl) -4H-1-benzothiopyran-4-one
3- (2,5-dimethyl-3-furyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (5-methyl-2-furyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,4,6-trichlorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (methylsulfonyl) phenyl) -3- (2,3,4-trifluorophenyl) -4H-1-benzothiopyran-4-one
3- (5-chloro-2-furyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (2-furyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (2-indanyl) -2- (4- (methylsulfonyl) phenyl) -4H-1-benzothiopyran-4-one
3- (4-aminophenyl) -2- (4-aminosulfonyl) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,6-difluorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-bromophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-t-butylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-chlorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,5-dichlorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-cyanophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-chlorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4- (N, N-dimethylamino) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-ethylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-ethoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-fluorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-hydroxymethylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-isobutylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-methylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4- (methylthio) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-methoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4- (N-methylamino) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2- (methylsulfinyl) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3- (methylsulfinyl) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4- (methylsulfinyl) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-methylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-methylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,5-difluorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-methoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-methoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-morpholinophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-nitrophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-trifluoromethylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-methoxy-4-methylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-fluoro-3-hydroxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-trifluoromethoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-hydroxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-isopropylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-n-butoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,4-dichlorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-chloro-4-methoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,4-dichlorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,3-difluorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-chlorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,4-difluorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,5-difluorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,4-dihydroxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,4-dimethoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,4-dimethoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,4-dimethylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,4-dimethylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-bromo-4- (methylthio) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-chloro-3-fluorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-chloro-3-hydroxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-chloro-4-fluorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-chloro-3-methylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-chloro-4-methylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3-phenyl-4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-chloro-4-methoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,4,5-trifluorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-chloro-4-hydroxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-ethyl-4-methoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-fluoro-2-methoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-fluoro-2-methylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-benzothienyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (benzofuran-2-yl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-fluoro-4-methoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-fluoro-4- (methylthio) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (6-methyl-3-pyridyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-pyridyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-chloro-3-methoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,4,5-trichlorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,5-dichloro-3-thienyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-methyl-4- (methylthio) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-chloro-4- (methylthio) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,6-dichlorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,5,6-trichlorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-chloro-3- (methylthio) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-hydroxy-4-methylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (5-chloro-2-furyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-fluoro-3-methoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-methyl-3-nitrophenyl) -4H-1-benzothiopyran-4-one
3- (3-amino-4-methylphenyl) -2- (4- (aminosulfonyl) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-hydroxy-3-methylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,3,4-trichlorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-methoxy-3-methylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-fluoro-3- (methylthio) phenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-hydroxy-4-methoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-fluoro-4-hydroxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-methoxy-3-propylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-hydroxy-3-methoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-fluorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (5-bromo-2-furyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-fluorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-fluoro-4-methoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-chloro-2-methoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-chloro-4-methoxy-5-methylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-fluoro-4-methylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-fluoro-3-methylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-chloro-4-methylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-chloro-2-methylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-fluoro-4-methylphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3-biphenyl-4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3-bromo-4-methoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,5-dimethyl-4-methoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,5-dichloro-4-methoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,5-difluoro-4-methoxyphenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,4,6-trifluorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,4-dihydro-2H-1-benzopyran-6-yl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,4,6-trichlorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,3,4-trifluorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,4,5-trichlorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (pentafluorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (1,2,3,4-tetrahydronaphth-6-6yl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-naphthyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (6-methoxy-2-naphthyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-phenylethenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (1,4-benzodioxan-6-yl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (1,3-benzodioxol-5-yl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-methyl-1,3-benzodioxol-6-yl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-thiazolyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,5,6-trifluorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-oxazolyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-thienyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,4,5-trichlorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (pentachlorophenyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (5-bromo-2-thienyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (4-methyl-1,3-benzodioxol-5-yl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (5-chloro-2-thienyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,4-dimethyl-3-thienyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (5-methyl-2-thienyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (5-benzothienyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (benzofuran-5-yl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,3-dihydrobenzofuran-5-yl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (3,4-dihydro-2H-1-benzothiopyran-6-yl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-pyrazinyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-pyridyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2,5-dimethyl-3-furyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (5-methyl-2-furyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (2-furyl) -4H-1-benzothiopyran-4-one
2- (4- (aminosulfonyl) phenyl) -3- (5-indanyl) -4H-1-benzothiopyran-4-one
3- (4-Fluorophenyl) -N-methyl-2- (4- (methylsulfonyl) phenyl) -quinolin-4-one
3- (2-Fluorophenyl) -N-methyl-2- (4- (methylsulfonyl) phenyl) -quinolin-4-one
3- (4-Fluorophenyl) -N-methyl-2- (4- (methylsulfonyl) phenyl) -quinolin-4-thione
3- (2-Fluorophenyl) -N-methyl-2- (4- (methylsulfonyl) phenyl) -quinolin-4-thione
3- (4-Fluorophenyl) -N-methyl-2- (4- (methylsulfinyl) phenyl) -quinolin-4-one
3- (4-Fluorophenyl) -N-methyl-2-phenyl-quinolin-4-one
N-methyl-3- (4- (methylsulfonyl) phenyl) -2-phenylquinolin-4-one
3- (4-Fluorophenyl) -2- (4- (methylsulfonyl) phenyl-quinolin-4-one
[3" claim-type="Currently amended] A cyclooxygenase-2 inhibitor composition comprising the diarylbenzopyran derivative according to claim 1 and a pharmaceutically acceptable salt thereof in an effective amount.

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引用文献:

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公开号 | 申请日 | 公开日 | 申请人 | 专利标题

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法律状态:
1998-08-22|Application filed by 서경배, 주식회사 태평양

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1998-08-22|Priority to KR1019980034131A

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1998-08-22|Priority claimed from KR1019980034131A

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2000-03-15|Publication of KR20000014628A

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2001-07-12|Application granted

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2001-07-12|Publication of KR100295206B1

优先权:

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申请号 | 申请日 | 专利标题

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KR1019980034131A|KR100295206B1|1998-08-22|Diarylbenzopyran derivatives and cyclooxygenase-2 inhibitor composition containing the same|