Method for producing 6-substituted 6h-dibenzo (b,d) pyran derivatives or pharmaceutically or veterin

专利摘要:
The present invention relates to new 6-substituted 6H-dibenzo [b,d]pyran derivatives, to a process for their preparation and pharmaceutical and veterinary compositions containing them.
公开号:SU1318163A3
申请号:SU813346602
申请日:1981-10-19
公开日:1987-06-15
发明作者:Меллони Пьеро；Сальвадори Паоло；Паоло Ловисоло Пьер
申请人:Фармиталия Карло Эрба С.П.А. (Фирма)；
IPC主号:

专利说明:

required salt. Tests of PD show that they demonstrate an antisecretory effect and exhibit anti-ulcer activity better than the known methiamide and carbenoxolone, and do not possess anticholinergic activity.
t
This invention relates to a process for the preparation of novel 6-substituted 6H-dibenzo derivatives (b, d) pyran or their pharmaceutically or veterinarily acceptable salts, which possess anti-spinal activity.
The aim of the invention is to obtain New compounds that have new valuable biologically active properties in the range of dibenzo- (b, e) pyran.
The method is illustrated by the following examples.
Example 1. 6H, 6-Hydroxy-di-benzo (b, d) pyran (10 g, 0.05 mol) is treated with OCl. (50 ml) for 20 hours at room temperature. Thionyl chloride is evaporated, the organic residue is extracted with toluene and then the mixture is evaporated to dryness, yielding 6H, 6-hlordibenzo (b, d) pyran. The crude residue is taken up in anhydrous dimethylformamide (50 ml), then the saturated aqueous potassium cyanide solution (0.05 mol) is added at 0 ° C. The temperature is raised to room temperature and the mixture is maintained at this temperature for 20 hours. The reaction mixture is diluted with water and extracted with ethyl acetate. The organic phase is washed with water, dried over sodium sulfate and evaporated to dryness to obtain a clear oil that solidifies. Crystallization from methyl alcohol results in 6H, 6-cyano-dibenzo (b, d) pyrene as a white solid (4.2 g, -0.021 mole, 40% yield), mp 98-100 ° s By a similar procedure, the following compounds were obtained:
6H, 6-cyano-6-methyl-dibenzo (b, d) pi, wounds, m.p. 114-116 ° C;
6H, H-cyano-6-methyl-dibenzo (b, d) - pyran, so pl. 75-77 ° C;
In addition, PD show better antiviral activity than virazole can be used to treat sclerosis, transplantation and infectious diseases. 8 tab.
6H, H-cyano-6-phenyldibenzo (b, d) pyran, mp, 120-123 ° C,
6H, 6-cyano-2-chloro-dibenzo (b, d) pyran, m.p. 128-131 ° C
6H, 6-cyano-2-fluoro-dibenzo (b, d) pyran, m.p. 118-121 C,
6H, 6-cyano-6-methyl-2-chloro-dibenzo (b, d) nnpaH, m.p. III-IIG C,
6H, 6-cyano-6-methyl-2-fluoro-dibenzo (b, d) pyrane, m.p. 67-71 C.
Example 2. 6H, 6-Hydroxy-di-benzo (b, d) pyrene (4 g, 0.02 mol) is dissolved in anhydrous benzene (50 ml). Trimethylsilyl cyanide (1.98 g, 0.02 mol) and a catalytic amount of zinc chloride are added to the solution, then the reaction mixture is stirred for 20 minutes at room temperature. The solvent and excess trimethylsilyl cyanide are evaporated to an organic precipitate and extracted twice with toluene. The toluene is evaporated off and the residue is separated by chromatography on a column of raffia using silica gel as a carrier and chloroform as the mobile phase to give 6H, 6-cyano-dibenzo (b, d) - pyran as a white solid. (2.5 g, 0.012 mol), t.pcs.98-.
By a similar procedure, the following compounds were obtained:
bN, 6-cyano-6-methyl-dibenzo (b, d) ii H wounds, so pl. P4-116 C;
6H, 6-cyano-6-ethyl-dibenzo (b, d) pyran, m.p. 75-77 ° C
6H, 6-cyano-6-phenyl-dibenzo (b, d) - pyran, so pl. 75-77 ° C;
6.H, 6-cyano-6-phenyl-dibenzo (b, d) - pyran, t. Pl. 120-123 ° C; .
6H, 6-cyano-2-chloro-dibenzo (b, d) pyran, m.p. 128-131 s,
6H, 6-cyano-2-fluoropibenzo (b, d) pyran, m.p. 118-1 21 s;
313
6H, 6-cyano-6-methyl-2-chloro-diben-3o (b, d) nHpaH, m.p. 11-116 ° C;
6H, 6-cyano-6-methyl-2-fluoro-dibenzo (b, c1) pyran, m.p. 67-71 ° C
Example 3. 6H, 6-Hydroxy-di- 6enzo (B, e,) pyran, (4 g, 0.02 mol) was dissolved in anhydrous benzene and piperazine (35 g, 0.4 mol) was added at a time, dissolved in 100 ml of anhydrous dimethylformamide. The mixture is refluxed at. for 3 days and then poured into ice water. The organic layer is separated and the aqueous phase is extracted with ethyl acetate. The solvent is evaporated to dryness in vacuo and the residue is separated on a column of silica gel (mobile phase chloroform: MEON: 32% ammonium hydroxide 190: 10: 1) to give 6H, 6- (1-pi-pepsinsI) dibenzo (b , d) oil in the form of an oily substance, which is converted to hydrochloride in diethyl ether with a stoichiometric amount of a 14% ethanol solution
hydrochloric acid (3 g, 50%), mp. 240 243 C.
The following compounds are prepared analogously:
6H, 6- (1- (4-Methyl-piperazinyl)) - di-benzo (b, a) pyran, m.p. 118-121 C;
6H, 6- (1-piperazinyl) -2-chloro-di- 6eH3o (b, d) nnpaH, m.p. 178-181 Cj
6H, 6- (1-piperazinyl) -8,9,10-trime c-dibenzo (b, d) pyran, mp. 131-134 C.
EXAMPLE 4 6H, 6-Cyano-6-methyl -2-chloro-dibenzo (b, d) pyrane (6.3 g, 0.025 mol) and sodium hydroxide (6.3 g, 0.15 mol) is dissolved in 80% ethanol (100 ml) and the solution refluxed for 16 hours. After extracting the solvent, the residue is dissolved in water and the solution is washed with diethyl ether. The aqueous solution is then acidified with 3% hydrochloric acid and extracted with ethyl acetate. bN, 6-carboxy-6-methyl--2-chloro-dibenzo (b, d) pyrene is obtained by evaporation of the solution to dryness (5.4 g, 80%) so pl. 174-177 seconds
The following compounds are prepared analogously:
6H, 6-carboxy-dibenzo (b, d) nHpaH, m.p. 184-186 ° C



bN, 6-carboxy-6-methyl-dibenzo (b, d

piran, so pl. 147-151 C;
6H, 6-carboxy-6-ethyl-dibenzo (b, d) | piran, so pl. 157-158 ° Ci
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6H, 6-carboxy-6-phenyl-dibenzo (b, d) pyran, m.p. 161-163 Cj
6H, 6-carbox-2-chloro-dibenzo (b, d) pyran, t. Pl. 1b4-167 C;
6H, 6-carbox-2-fluoropibenzo (b, d) piran, t. Pl. 148-152 Cj
6H, 6-carboxy-6-methyl-2-fluoro-di-6eH3o (b, d) nnpaH, m.p. 142-145 ° C;
6H, 6-carboxy-6-methyl-2-methoxy-dibenzo (b, d) pyran, m.p. ..
EXAMPLE 5 6H, 6-Carboxy-6-methyl-2-chloro-dibenzo (b, d) Pyran (4.1 g, 0.015 mol) is dissolved in 100 ml of absolute ethanol and the solution is refluxed for 16 h, gaseous hydrogen chloride passes through it. The solvent is evaporated to dryness, the residue is redissolved in diethyl ether, and the organic solvent is washed with N / 10 NaOH and water to neutrality. bN, 6-ethoxycarbonyl-6-methyl-2-chloro-dibene (b, d) pyran is obtained as a thick oil, after evaporation of the ether and cured by pentane to obtain 4.3 g (95%) of the product in the form of white crystals, so pl. 62-65 ° C.
The following compounds are prepared analogously:
6H, b-ztoxycarbonyl-cibenzo (b, d) - pyran, t.pcs. 43-45 ° C;
6H, 6-ztoxycarbonylmethyl-dibenzo- (b, d) nHpaH, t. Pl. 45-47 C;
6H, 6-ethoxycarbonyl-6-methyl-diben-3o (b, d) pyran
NMR (CC1c): / 1.03 (triplet, 3N, CHjCHj), 1.9 (singlet, 3N, CHj), 3.95 (quartet, 2H, CH), 6.75-7.7 (multiplet 8H) ,
6H, 6-ethoxycarbonylmethyl-6-methyl-dibenzo (b, d) pyran, m.p. 56-59 Cj
6H, 6- (2dimethylaminoethoxy-carbonyl) -dibenzo (b, d) pyran, HCl, m.p. 158-160 ° C;
6H, 6- (2-dimethylaminoethoxy-carbonyl) -6-methyl-dkbenzo (b, d) pyran, HC1, t. Sh1.165-167 C,
6H, H- (2-dimethylaminostoxy-carbonyl) -6-ethyl-dibenzo (b, d) pyran, HCl, t. Pl. 147-150 ° Ci
6H, 6- (2-dimethylaminoethoxy-carbonyl) -2-chloro-dibenzo (B, d) pyran, HC1,
t
square 183-186 seconds;
6H, 6- (2-dimethylaminoethoxy-carbonyl) -2-fluoro-dibenzo (b, d) pyran, HC1, t. Pl. TBZ-TBB,
6H, 6- (2-AH3THnaNraHO3TOKCH-Kap6p-nyl) -dibenzo (b, y) pyran, oil nD - 1.5841;
6H, 6- (2-dimethylaminoethoxy-carbOHHnMeTHn) -flH6eH3o (b, d) nHpaH, HCl, t. Pl. 136-139 ° C;
6H, 6-ethoxycarbonyl-2-chloro-diben-3o (b, d) nHpaH, mp. 49-52 ° C;
6H, 6-ethoxycarbonyl-2-fluoro-dibenzo (b, Yupiran, mp 43-4b C;
6H, 6-ztoxycarbonylmethyl-2-chloro-dibenzo (b, e) pyran; melting point 61-64 ° C;
, 6H, 6-ethoxycarbonylmethyl-2-fluoro-dibenzo (b, d) pyran melting point 49-52 0; 6H, 6-ethoxycarbonyl-methyl-6-phenesh1-dibenzo (b, e) pyran, m.p.71-73 ° C
6H, 6-ethoxycarbonylmethyl-6-methyl--2-chloro-dibenzo (b, d) pyrene, mp. 67-
6H, 6-ethoxycarbonylmethyl-6-methyl--2-ftor-dibenzo (b, d) pyran, mp 56-59 C.
EXAMPLE 6 6H, 6-Carboxy-dibenzo (b, d) pyrene (4 g, 0.018 mol) is suspended in thionyl chloride (40 ml, 0.55 mol) and maintained at room temperature for 24 The clean solution is extracted with toluene and the solvent is evaporated to dryness (Vacuum. The crude residue is dissolved in 100 ml of diethyl ether and the resulting solution is added dropwise at room temperature to a solution of 2-dimethylaminoethanol (53 ml, 0.053 mol) in 100 ml diethyl ether. After 30 min, the solution is washed with water and dried over sodium sulfate. The resulting 6H, 6- (2 dimethyl-aminoethoxy Bonil) -dibenzo (b, d) py wounds are precipitated as hydrochloride with 14% alcohol, hydrochloric acid solution (4.4 g, 75% yield), mp 158-160 C. The following procedure is obtained using a similar procedure. compounds:
6H, 6-ethoxycarbonyl-6-methyl-2- -hlop-dibenzo (b, d) pyran, m.p. 62-.
6H, 6-Ethoxycarbonyl-dibenzo (b, d) - pyrHp t. Pl, 43-45 Cj
bN, 6-ethoxycarbonylmethyl-dibenzo- (b, d) pyran, t.pcs. 45-47 С
6H, 6-ethoxycarbonyl-6-methyl-dibenzo (b, d) pyran;
NMR (CCl) .03 (triplet, 3N, CH, CHjCH3) i 1.9 (singlet, 3N, CHj);


0
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3.95 Tkvartet, 2H, CH), L.75-7.7 (multiplet, 3N)}
6H, 6-ethoxycarbonylmethyl-6-methyl-dibenzo (b, d) pyrene, m.p. 56-59 C;
6H, 6- (2-dimethylamino-ethoxy-carbonyl) -6-methyl-dibenzo (b, d) pyran HC1, t. Pl. 165-1b7 C;
6H, 6- (2-dimethylaminoxytoxy-carbonyl) -6-ethyl-dibenzo (b, d) pyran, HC1, m.p. 147-150 Ci
6H, 6- (2-dimethylaminosotopecarbonyl) -2-chloro-dibenzo (b, d) pyran, HC1, t. Pl. l83-186 cj
bN, 6- (2-dimethylaminostoxy-carbonyl) -2-fluoropenoxy (b, d) pyran, HC1, t. pl. 163-166 With,
6H, 6- (2-diethylaminoethoxy-carbonyl) -dibenzo (b, d) pyran, oil p 1.5841;
6H, 6- (2-dimethylaminoethoxy-carbonylmethyl) -dibenzo (B, d) pyran-, HC1, t. Pl. 136-139 ° C;
6H, 6-ethoxycarbonyl-2-chloro-dibenzo (b, d) pyrene, mp. 49-52 ° C;
bN, 6-ethoxycarbonyl-2-fluoro-dibenzo (b, d) pyrene, mp. 43-46 ° Cj
6H, 6-ethoxycarbonylmethyl-2-chloro-dibenzo (b, d) pyran, mp 61-64 ° C;
6H, 6-ztoxycarbonylmethyl-2-fluoro-dibenzo (b, d) pyran, m.p. 49-52 s.
PRI me R 7, Solution 6H, 6 ethoxycarbonyl-dibenzo (b, d) pyrene (5 g, 0.02 mol) in 100 ml of 32% ammonium hydroxide and 50 ml of methanol are stirred in a hermetically sealed flask at room temperature for 10 hours. Solid 6H, 6-aminocarbonyl-di- 6eH3o (b, d) pyran is filtered off j (2.9 g, yield 64%), mp 193-194 0.
The following compounds are prepared analogously:
6H, 6-aminocarbonyl-6-methyl-2- - hoop-dibenzo (b, d) pyran, mp 167-70 ° C;
6H, 6-aminocarbonyl-methyl-dibenzo- (b, d) pyrane, m.p. 148-150 C-,
6H, 6-methylaminocarbonyl-methyl-di 6eH3o (b, d) pyran, m.p. 130-131 C;
6H, 6-dimethylaminocarbonyl-methyl-dibenzo (b, d) pyran, m.p. 87-89 0.
Example8. To a 30% solution, 20 ml is added at 6H, 6-chloroparbonyl-dibenzo (b, d) pyran (7.2 g, -28 mol) in tetrahydrofuran 50 ml. After stirring for 8 hours, the mixture is washed with water, extracted with diethyl ether and the organic solution is evaporated to dryness. Residue twice
fO
treated with diisopropyl ether to obtain (yield 62.0%) of 6H, 6-aminocarbonyl-methyl-dibene (B, I) pyran, t. pl. 148-150 C.
Similarly, the following compounds are obtained: 5
6H, 6-aminocarbonyl-6-methyl-2-chloro-dibenzo (b, d) pyrene, m.p. 167-170 ° C;
6H, 6-methylaminocarbonyl-methyl-dibenzo (b, d) pyran, m.p. 130-131 ° C;
6H, 6-dimethylaminocarbonyl-methyl-dibenzo (b, g) pyran, m.p. 87-89 Cj
PRI me R 9. A solution of 6H, 6-ethoxycarbonylmethyl-dibenzo (L, d) pyran (3 g, 0.011 mol) in 23% hydrochloric acid (30 ml) and dioxane (15 ml) bale t t under reflux for 10 h.
After dilution with water, the mixture is extracted with ethyl acetate and the organic solvent is evaporated to dryness. The residue is cured with isopropyl ether to obtain 2 g (47%) of 6H, 6-carbox of boxymethyl-dibenzo (b, d) pyran, t. Pl. 110-111 S.
The following compounds are prepared analogously:
6H, 6-carboxymethyl-2-chloro-diben-3o (b, d) nHpaH, m.p. 140-144 C,
Follow
6H (b, d) n
Pr-cyano Pirana
f5
20
25
bN, 6-carboxymethyl-2-fluoro-dibenzo-0 t. PL,
slow motions of fumes and 1 mixture for 2 hours. R balms are cooked. 3 sodium and 6H are added to the water, 6-pyran is 14% in alcohol
By
6H,
(b, d) piran, so pl. 128-13GS.
Example 10. A solution of 6H, 6-cyano-dibenzo (b, d) pyran (4 g, 0902 mol in 100 ml of anhydrous diethyl ether) is slowly added with stirring to LiAlH (15 g, 0.04 mol) in 70 ml anhydrous diethyl ether. After 20 h, excess LiAlH4 is decomposed with water and sodium hydroxide. The suspension is filtered, the solid is washed thoroughly with diethyl ether and the solvent is evaporated to dryness. The residue is extracted with 8% hydrochloric acid. The resulting solution is washed with diethyl ether and then
alkalinized with 35% atri hydroxide. The mixture is extracted with diethyl ether.
. The organic solution is washed with a saturated sodium chloride aqueous solution and dried over sodium sulfate. 6H, 6-aminomethyl-diben-3o (b, d) Pyran is precipitated as hydroloride with 14% hydrochloric acid in an alcohol solution and crystallized from ethanol: (3.5 g, yield 73%), mp. 250 C.
6H, (b, d) p
Pr -amino 35 (4.2 g of water-added BHj per tonne of 40 h 2
6H, 6-a ray improving 65%),
45 Ana Connect
6H, (b, d) p
6H, 50 (b, d) n
Etc
(11 ml
55
lm to 3o (b, d. anhydrous d with k tari
-,
e- 5
R- ;
13181638
The following compounds were prepared by this procedure:
6H, 6-aminomethyl-2-fluoro-dibenz o- (b, d) nnpaH HCl, t.sh1.212-217 C.
Example 11. To a solution of 6H, 6-α-cyano-8,9,10-trimethoxy-dibenzo (L pyran in 100 ml of tetrahydrofuran
m pl
1.00 ml of a molar solution of BH in tetrahydrofuran is added slowly at 10 ° C. The reaction mixture is maintained at room temperature overnight, then 10 ml of water and 1 ml of 37% hydrochloric acid are added and the mixture is heated at room temperature for 2 hours. The solvent is evaporated to dryness, the residue is extracted with 2N. hydrochloric acid and the resulting solution was extracted several times with diethyl ether. The aqueous solution is then basified with a 35% sodium hydroxide solution, extracted with diethyl ether, and the ether solution is dried. 6H, 6-aminomethyl-2-chloro-dibenzo (b, d) - pyran is precipitated as hydrochloride with a 14% solution of hydrochloric acid in alcohol: (75% yield), mp.248-251 ° С
By this method: the following compounds are obtained;
6H, 6-aminomethyl-dibenzo (b, c1) pyran,
250 Ci
6H, 6-aminomethyl-2-fluoro-dibenzo- (b, d) pyranHCl, m.p. 212-217 C.
Example 12. To a solution of 6H, 6-α-aminocarbonyl-dibenzo (b, d) pyran (4.2 g, 0.0186 mol) in 100 ml of anhydrous tetrahydrofuran is added dropwise 100 ml of a molar solution of BHj in tetrahydrofuran, Mixture boil under reflux for 2 hours. After the heat
6H, 6-aminomethyl-dibenzo (b, d) pyran is obtained in the form of hydrochloride, which is improved by rubbing in acetone (3.0 g 65%), mp, 250 C.
The following compounds are prepared analogously:
6H, 6-aminomethyl-2-chloro-dibenzo- (b, d) pyran "HCl, t. Pl. 248-251 ° C;
6H, 6-aminomethyl-2-fluoro-dibenzo- (b, d) pyran.HC1, so pl. 212-217 C.
Example 13. Oxalyl chloride
(11 ml, 0.125 mol) is added by drop
lm to a solution of bN, 6-carboxy-diben-3o (b, d) nHpaHa (0.06 mol) in 300 ml of anhydrous benzene and 0.5 ml of anhydrous dimethylformamide. After 24 hours at room temperature, the solution is evaporated to dryness and the residue is dissolved.
200 MP diethyl ether. This solution is added to an ether solution of diazomethane (11 g) and the reaction mixture is maintained at room temperature for 16 hours. Thereafter, nitrogen is passed through for 2 hours at 40 ° C to remove excess diazomethane and the solution is evaporated to dryness. The residue is dissolved in 80 ml of dioxane and a mixture consisting of: (4.4 g, 0.019 mol), NajSjOj-SHjO (10.5 g, 0.042 mol) and (14 g, 0.049 mol) is added to the resulting solution. in 300 ml of distilled water. The temperature is increased to and maintained at this temperature for 24 hours. Then the reaction mixture is poured into water. ice is filtered off and the aqueous solution is extracted several times with diethyl ether. After acidifying with 8% hydrochloric acid solution, the precipitate is extracted with ethyl acetate and the organic solution is evaporated to dryness. The oily residue is extracted with diisopropyl ether to give 6H, 6-carboxymethyl-dibenzo- (b, e) pyran (yield 48%), mp 110-W C.
The following compounds were obtained by this procedure:
6H, 6-carboxymethyl-2-chloro-dibenzo (b, e) pyran, m.p. 140-144 ° C;
6H, 6-carboxymethyl-2-fluoro-dibenzo (b, a) pyran, m.p. 128-13l c.
Example 14. To a stirred solution of 6H, 6-cyano-dibenzo (b, b) - pyran (4.2 g, 0.02 mol) and methyl iodide (28.4 g, 0.2 mol) in 100 ml of dimethylformamide, 50% NaH (1.5 g, 0.03 mol) is added portionwise. After 16 h at room temperature, the mixture is poured into water and extracted with diethyl ether. The organic phase is washed with water and dried over sodium sulfate. Evaporation of the solvent results in 6H, 6-cyano-6- -methyl-dibenzo (b, e) pyran in the form of a white solid (3.1 g, 0.014 mol) yield of 70%, mp.114-116 ° C
By a similar procedure, the following compounds were obtained:
6H, 6-cyano-6-metsh1-2-chloro-dibenzo (b, d) pyran, so pl. 112-115 ° C;
6H, 6-cyano-6-methyl-2-fluoro-diben-: h2o (b, a) pyran, m.p. 98-102 ° C-,
310
6H, 6-cyano-6-methyl-dibenzo (b, d) pyran, m.p. 75-77 ° C.
Example 15. A solution of 6H, 6-cyano-6-methyl-dibenzo (B, g) pyran (11.3 g, 0.05 mol) and sulfuryl chloride (25 ml, 0.3 mol) in chloroform ( 120 ml) remain for 4 days at room temperature. After thoroughly washing the N / 10 solution with sodium hydroxide and water to neutrality, the solvent is evaporated under reduced pressure and the residue is treated with isopropyl ether. The solid is filtered off to give 7.5 g (60%) of 6H, 6-cyano-6-methyl-2-chloro-dibenzo (b, d) pyran, t. Pl. 110-112 C.
Example 16. A solution of sodium hydroxide (0.8 g, 0.02 mol) in methyl alcohol (10 ml) is added to a solution of 6H, 6-carboxy-6-methyl-2-chloro-dibenzo (b, e ) pyran (5.5 g, 0.02 mol) in methyl alcohol (100 ml). The solvent is evaporated, the residue is extracted with 99% ethyl alcohol and the solvent is again evaporated, thus obtaining 6H, 6-carboxy-6-methyl-2-chloro-diben-30 (b, d) pyran sodium salt (5.9 g, 0.02 mol, yield 100%), so pl. 250 ° C.
Example 17. In a dehydrated reaction apparatus, under an atmosphere of nitrogen, 6H-dibenzo (H, g) pyran-6-one (30 g, 0.15 mol) was dissolved in anhydrous toluene. The mixture is cooled to -60 ° C and a 1.2 M solution of diisobutyl aluminum hydride (D1 VAN) in toluene (150 ml) is added. The temperature is maintained at -60 ° C for 2 hours and then water (150 ml) and decalite are added.
(3 g), the mixture is filtered and the residue is washed with toluene. The organic layer is separated, washed with water, dried over anhydrous sodium sulfate.
ri and evaporate to dryness to give
semi-solid product, which is crystallized from n-hexane, 6H, 6-hydroxy-dibenzo (H5d) pyran (21 g, 0.106 mol, 70% yield) is obtained in the form of white
solids, mp 89-91 ° C.
Example 18. To a solution of bN-di-benzo (b, d) pyran-6-one (30 g, 0.153 mol) in a mixture of 250 ml of anhydrous diethyl ether and 250 ml
anhydrous benzene, an ethanol solution of Grignard reagent prepared from bromobenzene (23 ml, 0.23 mol) is added dropwise at 0 ° C. The
eleven
The perature is increased to room temperature and the solution is stirred for 2 hours. After a flush of 1N. with a solution of hydrochloric acid and water until neutrality, the solvent is distilled off in vacuo to obtain 6H, 6-hydroxy-6-phenyl-dibenyl; 3o (b, g) pyran (39.3 g, yield 94%) in the form of light yellow oil.
The compounds of formula I actively affect the gastroenteric system, in particular, they have anti-ulcer, gastritic antisecretory and very little anti-cholinergic activity and are useful in therapy, for example in the prevention and treatment of preodenal, gastritic and exophageal ulcers and in the inhibition of gastritic acid secretion.
The compounds of the formula I are also useful in reducing the undesirable gastrointestinal side effects that occur with the systematic use of anti-inflammatory prostaglandin systhetase inhibitors and may be useful for these purposes with them.
The anti-linking activity of these compounds is supported by the fact that they are active in inhibition tests of isolated ulcers in rats. According to this method, the test compounds were applied per os (p. O) one hour before immobilization. Six male Spragus Dawly rats (100-120 g), euthanized for 24 hours, were used for experiments, square flexible, finely meshed wire mesh was used for immobilization and 4 hours after immobilization, the rats were euthanized, their stomachs were removed and organ damage evaluated under a microscope.
In tab. Figure 1 shows the EDG values of the anti-ulcer activity in rats obtained for the four compounds according to the invention after dental use.
Table 1
Compound
Anti-linking activity of P.O., mg / kg
FCE 20524 FCE 20618
4.8 7.0
FCE 20493
20.0
12
Continued table.
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The extremely high anti-inflammatory activity of the compounds of the formula I in comparison with the known compounds methiamide and carbenoxolone is shown in Table. one.
The compounds of formula I have been found to possess gastritic antisecretory activity; they provide activity after intraduodenal use in inhibiting gastritic secretion in rats.
According to this method, the test compound is administered intraduodenally (i.d.) during the ligature. I Six male rats Shragus Danly (110-130 g) were used for each group. 24 hours before the test, the rats were deprived of food, but were supplied with drinking water. On the day of surgery, the pylorus was transferred with Light ether anesthesia. Four hours after the ligature, the rats were euthanized. Gastric secretion was collected and centrifuged at 3500 rpm for 10 minutes, and the volume where sedimentation was observed was the least. The amount of hydrochloric acid in gastritic basis was determined by titration with 0.01 N sodium hydroxide solution to pH 7.
Tab. 2 represents, for example, the EDU values of antisecretory activity in rats obtained for the compounds listed in Table. one.
table 2
Compound
Antisecretory activity EDD i .d.Mr / kg
FCE 20524
FCE 20618
FCE 20493
1.5 20.0
FCE 20679
1.0
13
Continuation of table 2
Combination Antisecretory activity mg / kg
 - ---.-. -. "... m .... (J -
Metiamid60,0
Carbenoxolone
100.0.
Tab. 2 indicates the extremely high anti-ulcer activity of the compounds of formula I as compared with the known compounds, methiamide and carbenoxolone.
It is noted that many anti-ulcer agents exhibit, as well as atropine, a significant anticholinergic activity, which is undesirable, the compounds are evaluated for their antagonism against the syndrome induced by oxotremorine in mice. According to this method, 5 male males, 20–25 g of live weight, were used in each group.
Tab. 3 shows, for example, approximate values of AU. anticholinergic activity. The data table. 3 shows that the compounds proposed do not have undesirable antifichinergic activity.
Table 3
Compound
Anticholinergic activity, o., Mg / kg
he

100 100 100
7100 7100
710G
LD mg / kg - 7400 g 800 800 400 800
2
1A
. Continuation of table. 3
Compound
Anticholinergic actively, Edud R.,
mg / kg

FCE 20519 FCE 20562 FCE 20513 FCE 20561 FCE 20881 FCE 20521 FCE 20524 FCE 20618 FCE 20696 FCE 21849
800 400: 800
800
800 400 800
800
400 800 400 800 7400 800 400 800
0
five
0
five
0
five
Methiamide 1-methyl-3- 2- (5-methyl-imidazol-4-yl-methylthio) -ethylZ-thiomerchevine.
Carbenoxolone 3 / J-hydroxy-11-oxo-20 / i-olean-12-ene 29-oic acid hydrogen butanedioate,
These codes refer to the following compounds:
FCE 20770 6H, 6-carboxy-6-methyl--2-chloro-dibenzo (b, d) pyrene;
FCE 20493 6H, 6-cyano-dibenzo (b, a) pyran-,
FCE 20519 6H, H-cyano-6-methyl-dibenzo (b, d) pyran;
FCE 20562 bN, H-carboxy-6-methyl-dibenzo (b, d) pyran,
FCE 20518 6H, 6-cyano-6-hydroxymethyl-dibenzo (b, d) pyran;
FCE 20561, 6H, 6-carboxy-6-hydroxymethyl-dibenzo (b, d) pyran;
FCE 20881 6H, H-carboxymethyl-di-- 6eH3o (b, d) nHpaHi
FCE 20521 6H, 6-ethoxycarbonyl-dibenzo (b, d) nHpaH-,
FCE 20524 bN, 6-aminomethyl-diben-3o (b, d) nHpaH-,
FCE 20618 6H, 6- (1-piperazanyl) - -dibenzo (b, d) pyran-,
FCE 20696 6H, 6- (2-dimethylamino-ethoxycarbonyl) -dibenzo (b, d) pyranj
FCE 21849 6H, H- (2-diethylamino-ethoxycarbonyl) -dibenzo (b, d) pyran;
FCE 20523 6H, 6-carboxy-diben-3o (b, d) nHpaH-,
FCE 20679 6H, 6- (1- (4-methyl-piperazinyl)) - dibenzo (b, d) pyran;
FCE 21312 6H, 6-ethoxycarbonyl-6-methyl-dibenzo (b, d) pyran.
As anti-ulcer and antisecretory agents, the compounds are administered in the usual way, for example orally, parenterally or as a suppository. The amount is 50-200 mg per dose, 1 to 5 times daily for oral administration in humans. Compound FCE 20618, for example, is preferably administered orally to humans at doses of 100-150 mg per dose, 1 to 5 times daily. The compounds also possess immunomodulatory activity and, in particular, activial activity. Their immunomodulatory activity is manifested in their ability to modify antibodies introduced into the organism by suboptimal dose of sheep red blood balls (SPBC), administered intraperitoneally. Groups of 10 male CD-1 mice have been administered i.p, 2x10 SPBC as antigen. Test compounds were entered by i.p. at two dose levels: 50 and 5 mg / kg of live weight for 2 hours before applying the antigen. A control group of mice received SPBC and saline instead of a compound. After 6 days, mice were euthanized and antibody titers against SPBC in their serum were determined. An increase in the production of hemolytic antibodies has been shown, for example, using the compound FCE 20696 and FCE 21849. These two compounds
O
five
0
five
0
five
0
increased antibody titers several times compared with the control group.
The anti-viral activity of the compound was evaluated, for example, by influenza virus and herpes, experimentally introduced in the mouse.
The groups of DM-1 mice were infected by an intra-osseal method with an influenza virus strain, APR 8, and another group of mice were infected with an intraperitoneal method of a depressive IPC strain. The test compounds were applied by various methods, for example by an intraperitoneal, subcutaneous, or dental method. The effect of the tested compounds against the influenza virus was evaluated on the basis of the number of lung injuries and against the infection of the litus, considered as a parameter for the protection against mortality, since it is known that the depriving infection is lethal. Noah for mice. Test compounds have been shown to be effective in protecting children against both viral infections. For example, the compound FCE 20696, when applied in the form of a single dose for one or two days after infection, showed significant pharmacological activity in the form of a significant decrease in the number of lung injuries infected with influenza infection and protection of up to 45% of animals from death after being infected with the infection .
The results of the determination of the antiviral activity of the compound FCE 20696 in comparison with virazole, isoprinozinbm and the copolymer are shown in Table. four.
n)
 a s h
YU
flj
H
191
The compounds of formula (1) are therefore useful in the treatment of transplant reactions, such as kidney, heart, bone marrow, skin, and indocrine gland transplants. Other areas of pathology in which the immunomodulating properties of these compounds are therapeutically successful, consists of the following: therapy of neoplastic diseases, acute and chronic infections, both bacterial and viral onset, and diseases characterized by immunological imbalance, like primary or congenital immune deficiency and av oimmunnym to damage This last category includes rheumatoid arthritis, systemic tuberculosis erythema, nephritis, vascular diseases and blood. The therapeutic regimen for various clinical syndromes must be adapted to the type of pathology,
In transplant and infectious diseases, the time of onset and the clinical course is usually known, on the other hand, the onset of immunological diseases is unknown and their clinical course is usually long and complicated. Therefore, the therapeutic dose should be determined for each specific clinical case, with the fact that this effect also depends on the method of application. Oral administration is commonly used for all conditions requiring such compounds. Preference is given to parenteral administration, for example, intravenous injection or infusion for protection against abnormalities and treatment of acute infections. In the latter case, typical applications can also be used. For maintenance of oral sludge parenteral regimens, for example, intramuscular or subcutaneous injections are preferred. For these purposes, compounds of the invention, for example, FCE 20696 can be administered orally at doses ranging, for example, from 5 to 100 mg / kg of live weight per day, the total amount being from 0.35 to 7 g of active compound for one patient with with a live weight of 70 kg over a period of 24 hours. Doses of active compounds in the range, for example, 5-100 mg / kg of live weight, can also be used for parente 6320
Raline use. Of course, these dose regimens can be adjusted to provide the optimum therapeutic effect. The proposed compounds also have the ability to prevent lowering of lipids and anti-atherosclerosis activity, in particular, they are active in lowering the total hopsile and triglycerides of surem, in increasing the total hBH of cholesterol surem.
Drugs that increase HDL-cholesterol in blood and / or the ratio between oL and cholesterol lipoproteins are known to be useful in treating atherosclerosis
The activity of the compounds was assessed)) in the group of male rats (SPF Sap) CER, which was put on a hypocholesterol diet, or 2) in the group of male rats (SFC) Iva-SIV, put on the standard MS / K diet Altromin R, experiment 2 MS / K Alti o min means trademark. Test compounds were suspended in Methocel (methylcellulose, 0.5% solution in water) and applied using a gastric tube at a dose of 50 mg / kg for 4 days in both experiments. Control groups of animals were treated only with a suspending agent. Total Suresma cholesterol was determined by the method of Allian, Clin. Chem. Serum trigly cerides were determined by the method of Menelez. I., Clin Chem. Total HDL serum cholesterol was determined according to Demacker P.N.H. Clin Chem.
Total cholesterol / 5 lipoprotein was determined by the difference between total serum cholesterol and HDL - cholesterol. Statistical analysis in Experiments 1 and 2 was carried out by testing Student st for independent samples or by testing Sochran s when the differences were not uniform when testing the F ratio. The data table. 5 show that in animals set on a hypercholesterol diet (experiment 1), test compounds, for example, FCE 20881, reduce total serum cholesterol and increase total HDL - cholesterol. The data in Table. 6 show that in animals fed on the NS / K Altromin diet (experiment 2), the test compounds (for example, FCE 20881) reduce the total serum cholesterol, in particular lipoprotein B, serum triglycerides
s

and and
l
u p
And s
h
about
n) H
ten
15
20
2313181
The results in the table. 7 show that when applied to animals containing a high cholesterol diet (Experiment 1) of the proposed compound, said compound 5 has a higher serum cholesterol lowering activity than the known compound clofibrate.
The results table. 8 shows that when applied to animals containing a high cholesterol diet (Experiment 1), the compounds of formula I have a much higher antiatheroscopic activity than the known compound Clofibrate. From the point of view of high lipid-lowering activity, new compounds are useful in the treatment of hyperlipidemia. They can be applied in various pharmaceutical forms, for example, orally in the form of tablets, capsules, sugar or film-coated tablets, liquid solutions or suspensions, rectally, 25 in the form of a suppository, parenterally, for example, subcutaneously, intravenously or intramuscularly. injections or infusions.
The dosage of these compounds depends on the age, weight, condition
the patient and the method of administration, for example, the compound FCE 20881 is dosed for an oral administration method for an adult patient of 50-200 mg / dose, 1-2 times per day, preferably 100-200 mg / dose once a day. The toxicity of the compounds is insignificant. Mice that were deprived of food for 9 hours were treated stoically at a dose of increased doses at a time, then they were put on a normal diet. On the seventh day after treatment, approximate acute toxicity (LDjp) was estimated and, for example, the following data were obtained:
thirty
35
45
20770 20493
LDyg mg / kg
7400 800 400 800
Table 7 (experiment 1)
Compound
Serum cholesterol processed./controlled
FCE 20770
0.43
63
24 Continuation of table 7
Compound
Cholesterol levels processed / control
FCE 21312 Klofibr.
0.43 0.59
P 0.01; values of 1 indicate serum cholesterol-reducing activity.
Table B (experiment 1)
 ..
40
35
p 0.01 j values of 1 mean anti-atherosclerotic activity.
0
five
0
five
Codes: FCE 20519 FCE 20562 FCE 20513 FCE 20561 FCE 20881 FCE 20521 FCE 20524 FCE 20618 FCE 20696 FCE 21849
LDjo mg / kg
7 800 400 800
7800
7800 400 800
800
7400 800 7400 800 7400 800 7400 800
refer to the following compounds:
FCE 20770 6H, 6-carboxy-6-methyl- -2-chloro-dibenzo (b, d) pi y
FCE 20493 6H, 6-cyano-dibenzo (b, and pyran
FCE 20519 6H, 6-cyano-6-methyl-dibenzo (b, d) n HpaH;
FCE 20562 6H, 6-carboxy-6-methyl-dibenzo (b, d) pyran,
FCE 20518 bN, 6-cyano-6-hydroxymethyl -dibenzr (b, d) pyrani
FCE 20561 6H, b-carboxy-6-hydroxy-oximethyl-dibenzo (b, d) pyran;
FCE 20881 6H, 6-carboxymethyl-di-benzo (b, d) pyrene
FCE 20521 bN, 6-ethoxycarbonyl- -dibenzo (b, d) pyrene
; FCE 20524 6H, 6-aminomethyl-diben-30 (b, d) pyran j
FCE 20618 6H, 6- (1-piperazanyl) -dibenzo (b, d) pyran;
FCE 20696 bN, 6- (2-dimethylamino-ethoxycarbonyl) -dibenzo (b, d) nHpaHi
FCE 21849 6H, 6- (2-diethylamino-ethoxycarbonyl) -dibenzo (b, d) pyran;
FCE 20523 6H, 6-carboxy-diben-3o (b, d) nHpaHi
FCE 20679 6H, 6 - / (4-methyl-piperazinyl) / dibenzo (b, d) pyranium
FCE 21312 6H, 6-ethoxycarbonyl-6-methyl-dibenzo (b, d) pyran,
FCE.21459 6H, 6-carboxymethyl-2-chloro-dibenzo (b, d) pyrene,
FCE 21533 6H, 6-carboxy-6-phenyl-dibenzo (b, d) pyran.
The invention includes pharmaceutical compositions containing the compound along with pharmaceutically acceptable excipients (which are
can be carriers or dilute
tel mi).
Pharmaceutical compositions are usually prepared according to standard methods and used in a pharmaceutically suitable form. For example, solid oral forms may contain, along with the active compound, diluents, for example, lactose, dextrose, sucrose, cellulose, wheat starch and potato starch; lubricants, for example silica, talcum stearic acid, calcium or magnesium stearate and / or polyethylene glycols; binding agents, for example starch: gum arabic, gelatin, methylcellulose, carboxymethylcellulose, polyvinylpyrrolidone; anti-aggregating agents, for example starch, alginic acid, alginates, sodium starch glycol
c

R
five
0
lt; gas-forming mixtures, dyes, sweet ingredients, wetting agents, such as lekitin, polysorbates, lauryl sulfates, non-toxic and pharmaceutically inactive substances used in pharmacology. These pharmaceutical preparations can be obtained in a known manner, for example by mixing, granulating, tableting, sugar coating or coating. Liquid dispersions for dental use may be, for example, syrups, emulsions and suspensions.
Syrups may contain as carriers, for example, sucrose with glycerol and / or mannitol and / or sorbitol, in particular a syrup that is administered to diabetic patients, may contain as carriers only substances that do not metabolize glucose, or are metabolized in a very small amount such as sorbitol. Suspensions and emulsions may contain as carriers, for example, natural gum, agar, sodium alginate, pectin, methylcellulose, carboxylmethylcellulose, or polyvinyl alcohol.
Suspensions or solutions for intramuscular injections may contain, together with the active compound, pharmaceutically acceptable carriers, for example, sterile water, olive oil, ethyl acetate, glycols, for example, propylene glycol and, if necessary, an appropriate amount of lidocaine hydrochloride.
Solutions for intravenous injection or infusion may contain, for example, sterile water as a carrier, or preferably they may be in the form of sterile aqueous isotonic saline solutions.
Suppositories may contain, together with the active compound, a pharmaceutically acceptable carrier, for example coconut oil, polyethylene glycol, polyoxyethylene sorbitan, fatty acid ester surfactants or lecithin.
For typical applications, other pharmaceutical, for example, creams, lotions or pastes for dermatological treatments can be used. For these compositions, the active ingredient can be mixed with
27
standard masloobrazuyuschimi or emulsifying excipients. Below are examples of compositions.
Composition 1. Tablet (50 mg).
Tablets weighing 150 mg, containing 50 mg of active substance are obtained as follows:
Ingredients (for 10,000 tablets) g: 6H, 6-carboxy-6-α-methyl-2-chloro-dibenzo (b, y) pyran 500 Lactose 710
Wheat starch 237.5 Talcum powder37,5
Magnesium stearate. 15 Mixed 6H, 6-carboxy-6-methyl-2- -chloropibenzo (b, d) pyran, lactose and half wheat starch, then the mixture is sifted through a sieve with 0.5 mm cells. Wheat starch (18 g) was suspended in warm water (180 m. The resulting paste was used to granulate the powder. The granules were dried, sorted on a sieve with 1.4 cells, then the rest of the starch, talc and magnesium stearate were added, mixed thoroughly. using a stamping press with a hole diameter of 8 mm. Composition 2. Intramuscular injection.
The pharmaceutical composition of dp injection was obtained by dissolving 150,500 mg of 6H, 6-carboxy-6-methyl-2-chloro-dibenzo (L, 6) pyran sodium salt in sterile water or sterile normal saline (1-2 ml). Similarly, pharmacological injectable compositions containing the compounds described in the preceding examples were prepared.
Compositions Z. Capsules (50 mg).
Composition, mg:
6H, 6-ethoxycarbonyl-6-methyl-2-chloro-dibenzo (b, d) pyran 50 Lactose 298
Wheat Starch 50 Magnesium Stearate 2
Capsulated into biphasic hard gelatin capsules.
Compositions A. Suppositories (50 mg). Composition, g / g: 6H, 6-carboxy-6
 ).
.
15
1816328
-methyl-2-chloro-dibenzo (b, d) pyran lecithin cocoa butter
5 Composition Composition, mg / g: 6H, 6-carboxy-6- -methyl-2-chloro-dibenzo (b, d) pyran
 O White Vaseline
Cetyl stearyl alcohol
Mineral oil Polypropylene glycol
4-Chloro-m-cresol Purified water Composition Composition, mg / g: bN, 6-carboxy-6-α-methyl-2-chloro-dibenzo (b, d) pyrane Mineral oil Propylene glycol Vaseline
Composition Composition, g: 6H, 6-carboxy-6-β-methyl-2-chloro di 30 benzo (b, d) pyran Sodium salt Tragacanth resin Me tyl-p-hydr acybenzoate
35 Propyl p-hydroxybenzoate Polyoxymethylene sorbitan monolaurate Glycerin 30 Her Sucrose
Natural fragrances Purified water
20
25
40
five,
6,
7,
0.05
0.07
0.88
Cream.
50.0 100.0
.72.0 60.0
2.0
1.0 1.0 Ointment.
50.0
50.0
50.0
1.0
Syrup.
45
0.5 1.0 0.135 0.015
five
five
50
Required quantity
100 ml

权利要求:
Claims (1)
[1]
Invention Formula
The method of obtaining derivatives of 6-substituted 6H-dibenzo (b, d) pyran of the general formula I
3 R, (CH, lnRi
2913
where R is a cyano group, a carboxy group - COORj, tfle Rg - C —C-alkyl unsubstituted or substituted by the group —NRjRjj, where Rp and R are independently C —C-alkyl, a group -, where
t each of R d and RI, is a hydrogen atom
or taken together with the nitrogen atom to which they are bound form a pi-perazine ring unsubstituted or substituted by C-C-alkyl, or groups
pa - where Rj and Rj independently, a hydrogen atom or C -C-alkyl, n - an integer equal to O or 1, R - a hydrogen atom, C -C-alkyl or phenyl; f5 Rj, R and Rj - a hydrogen atom ; each of R ,, R and Rg is the same or different, a hydrogen and halogen atom, or their pharmaceutically or veterinarily acceptable salts, about tl and - 20 in that the compound of formula II
thirty
Rg is C -C-alkyl, unsubstituted or substituted by the group -NRj, Rj, where R and RJ have the indicated meanings, or, if necessary, restore the compound of formula I, where R, is the group -CN, an is an integer equal to O, and compounds of the formula I, where R is an amino group, an is an integer equal to 1, or, if necessary, a compound of formula I, with R is a carboxy group or a group - COORg, where
Rg has the indicated meanings, is reacted with an amine of form- R.
ly hn r or its derivative and
The compounds of formula I are isolated, wherein
Re
R, - CON:
where R and Rf atom
hydrogen or C-Cg-alkyl, or, if necessary, hydrolyzing a compound of formula 1, where R is a group
l
COyGy, or where R is a COORg group, where RJ has the indicated meanings and isolates compounds of formula I,
where R, is a carboxy group, or, if necessary, reduce the compound of formula I, where R is a group - CONHj, n is an integer equal to O, and a compound of formula I, where
where R is a halogen atom or a hydroxy group Rj, Rj, R + i Rff, Rfc, RT and Rg have the indicated meanings, is reacted with an alkali metal cyanide in an aqueous organic medium at from to room temperature or with C-C-alkylsilyl cyanide in an organic solvent at room temperature in the presence of Znl, or
RO
with an amine of the formula HN, where R., and
RB
RJ have the indicated meanings, in an organic solvent medium, at a reflux temperature, and give the desired product of formula I, where
.and is equal to O, R is the group-CN or -N,
where R, Rg, R, Rj, R, R, R ,, R, and Rg have the indicated meanings, or, if necessary, convert compounds of formula I, where (-CN) to a compound of formula I, where R is carboxy, alkaline hydrolysis with by subsequent acidification, or, if necessary, esterifying a compound of formula I, where R is a carboxy group, and to obtain compounds of formula I, where R-, is a group - COORg, where
R group -N.
where R and R are a hydrogen atom, an is an integer equal to 1, or, if necessary, is converted into a compound of formula I,
where Rg is a hydrogen atom, p- is an integer equal to O, and R is a cyano or carboxy group, or is a COORg group, where Rg has the indicated values, to a compound of formula I, where C is C-alkyl, or if necessary, translate the compound of formula I, where n is an integer equal to O and R is a carboxy group, to a compound of formula I, where n is an integer equal to 1,
and R, is a carboxy group or a group - COOR, where Rg has the indicated meanings, -or, if necessary, halides a compound of formula I, where Rg, R and Rg is a hydrogen atom, and compounds of formula I, where one or more of Rg is a halogen atom, and / or, if necessary, a compound of formula I is converted to a pharmaceutically or veterinarily acceptable salt.
Priority featured:
2П.10.8О with cyano group, carboxy group COORg, where Rg - C -Ctj31
-alkyl, or the group SOMIR, where the group is N; Pp and Rp- independently, the atom is hydrogen. , a or C is Cf-alkyl, p is a whole number equal to O or 1, Rj is a hydrogen atom or Cj is alkyl, R ,, RJ ,, 5 is a hydrogen atom, R, (, and Kg is a hydrogen or halogen atom , and (d - halogen atom or oxy group - a,
09/14/81 with R - cyano group, carboxy group or group - COOR, where RP is a C-C-alkyl ,. unsubstituted or deputy, still by the group NR (, R, where RC and Rf are independently C1-C4-alkyl, / 5
fO
hydrogen sludge with which about single to
substituted
group where
the hydrogen atom is a natue number, and Rf is a and R g is the same hydrogen or halogen or il
18163
group - N; . ,
/five
32 where R
and RI, is an atom
fO
 s
hydrogen or, together with the nitrogen atom to which they are bound, form a pipa ring, unsubstituted or
substituted with.-alkyl, -CONC
f group, where R and R - independently,
hydrogen or C-C-alkyl, p is an integer of O or 1, R is a hydrogen atom, C -C alkyl or phenyl, R, R4 and Rf is a hydrogen atom, Rg, - and R g are the same or different, atom hydrogen or halogen; and a halogen atom or hydroxy group.

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同族专利:

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公开号 | 公开日

---

DE3141387C2|1991-05-02|

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FI84824C|1992-01-27|

---

DK461381A|1982-04-21|

---

CA1235703A|1988-04-26|

---

NL8104749A|1982-05-17|

---

NL191562B|1995-05-16|

---

FR2492378B1|1985-06-28|

---

ATA448781A|1985-09-15|

---

US4463001A|1984-07-31|

---

AT380245B|1986-04-25|

---

SE8106167L|1982-06-02|

---

FI84824B|1991-10-15|

---

SE452009B|1987-11-09|

---

NL191562C|1995-09-19|

---

DE3141387A1|1982-08-12|

---

DK154974C|1989-06-12|

---

IL64008D0|1982-01-31|

---

IL64008A|1986-07-31|

---

AU7616181A|1982-09-09|

---

FR2492378A1|1982-04-23|

---

FI813144L|1982-04-21|

---

HK9186A|1986-02-14|

---

IT1168040B|1987-05-20|

---

CH651302A5|1985-09-13|

---

IT8124552D0|1981-10-19|

---

DK154974B|1989-01-16|

---

AU542121B2|1985-02-07|

---

MY8600398A|1986-12-31|

引用文献:

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GB1464695A|1974-06-24|1977-02-16|Smithkline Corp|Dibenzo-b,c-pyrans and pharmaceutical compositions thereof|FR2512024B1|1981-08-27|1984-01-06|Adir|

---

GB8505756D0|1985-03-06|1985-04-11|Erba Farmitalia|Tricyclic dibenzo condensed derivatives|

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US5180736A|1989-03-23|1993-01-19|Warner-Lambert Company|Polycyclic amines useful as cerebrovascular agents|

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US5202446A|1990-05-23|1993-04-13|E. I. Du Pont De Nemours And Company|Fluoridated monomers based on 9-phenyl-9-perfluoroalkylxanthene|

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WO1995029163A1|1994-04-27|1995-11-02|Nippon Soda Co., Ltd.|Imidazole derivative and process for producing the same|

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ES2131020B1|1997-10-13|2000-03-01|Lacer Sa|DERIVATIVES OF BENZOFURANO, DIHIDROBENZOFUNARO, DIHIDROBENZOPIRANO AND BENZOPIRANO AS ANTIDEPRESSIVE AGENTS.|

法律状态:

优先权:

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申请号 | 申请日 | 专利标题

---

GB8033774|1980-10-20|

---

GB8127718|1981-09-14|

---