Process for producing derivatives of substituted oxycyclohexahylacetic

专利摘要:
Novel substituted oxy-cyclohexylacetic acid derivatives as antihyperlipidemic agents are given. The compounds have the formula <IMAGE> (I) <IMAGE> (II) <IMAGE> (III) wherein n is 1 or 2; m is 0, 1 or 2; R1 represents a halogen atom, trifluoromethyl, a lower alkyl, a lower alkoxy, a lower alkylcarbonyl, dimethylphenylmethyl, cyclohexyl, phenyl, halogenophenyl, phenoxy or halogenophenoxy group, and two of R1 groups can be bonded to form an orthocondensed saturated alkylene ring; Hal represents a halogen atom; and R2 represents a hydrogen atom or a lower alkyl group.
公开号:SU978723A3
申请号:SU792847564
申请日:1979-11-30
公开日:1982-11-30
发明作者:Хамазаки Ясухико；Сери Кендзи；Исияма Нобуо；Ямамото Тосиюки；Сакасаи Масао；Сато Рейко
申请人:Какен Кемикал Ко. Лтд (Фирма)；
IPC主号:

专利说明:

39 and R2 are as above, where p, R are values with ot-halogencyclohexyl acetic acid ethyl ester in the presence of a base in an organic solvent medium, and if necessary, the product is hydrolyzed. Preferably, potassium carbonate, sodium carbonate, sodium methylate or sodium ethoxide is used as the base. Dimethylformamide, acetone or a mixture thereof is advisable as a solvent. The process is preferably carried out at 10Q-180 ° C for 1-10 hours, or at 20 ° C for 1-2 days. The hydrolysis of the esters obtained, if necessary, is carried out under alkaline conditions (aqueous solution or KOH with alcohol). The obtained new compounds show appreciable antihyperlipidemic activity and are effective in practice as anti-lipidemic agents for the treatment of hyperlipidemia, they have low toxicity and do not cause hepatic diseases (hepatitis), which, as it was found, show with the use of ethyl L- (p-chlorophenoxy) isobutyrate, which also has antihyperlipidemic activity. Example 1. Ethyl (p-ethylphenoxy) -o6-cyclohexyl acetate. 575 mg (0.025 mol) of metallic sodium are dissolved in 30 ml of anhydrous ethanol and then 3.05 g (0.025 mol) of p-ethylphenol is added. The mixture was stirred at 20 ° C. within 30 min. Ethanol is distilled off under reduced pressure and 10 ml of dimethylformamide is added to the residue, then dimethylformamide is distilled off under reduced pressure, after which 30 ml of dimethylformamide is added to the residue. 5.0 g (0.02 mol) of ethyl-c (gb | e-c6-cyclohexyl acetate) are poured into the solution, the mixture is heated under reflux for 6 n, then dimethylformamide is distilled off under reduced pressure. The residue is mixed with 50 ml water and extracted twice with an LLP with benzene ml. The benzene layer is combined, washed three times with 30 ml each of a 5% aqueous solution of sodium hydroxide, then with water, dried over sodium sulphate and distilled off in vacuo to give 3.1 g of ethyl-1- ( p-ethylphene 34 bc-y-cyclohexyl acetate, yield 50 of theory. Example 2. Ethyl-o - (p-cyclohex silphenoxy) -o1-cyclohexyl acetate 575 mg (0.025 mol) of metallic sodium was added to 30 ml of anhydrous ethanol and g (0.025 mol) of p-cyclohexylphenol was added. The mixture was stirred for 3 hours. Ethanol was distilled off under reduced pressure and 10 ml were added to the residue. dimethylformamide, then dimethylformamide is distilled off under reduced cpenpe Y (and then 30 ml of dimethylformamide is added to dissolve the residue. 5.0 g (0.02 mole of ethyl-o (gbromo-o-cyclohexyl acetate) is added to the solution, the mixture is boiled with reflux condenser for 8 h, then dimethylformamide is distilled off under reduced pressure ii. The residue is mixed with 50 ml of water, extracted twice with lOt) ml of benzene. The benzene layers were combined, washed three times with 30 ml of a 5% aqueous solution of sodium hydroxide, then with water, dried over sodium sulfate and distilled in vacuo to give 3.8 g of ethyl-o6- (p-cyclohexylphenoxy) -o6-cyclohexyl acetate. exit 57, from theory. Example 3. Ethyl-oC- (p-phenylphenoxy) -oL-cyclohexyl acetate. 575 mg (0.025 mol) of metallic sodium are dissolved in 30 ml of anhydrous ethanol and 25 g (0.025 mol) of p-phenylphenol is added. The mixture is stirred at 30 minutes. Ethanol was distilled off under reduced pressure and 10 ml of dimethylformamide was added to the residue, then dimethylformamide was distilled off under reduced pressure, after which 30 ml of dimethylformamide was added to dissolve the residue. 5.0 g (0.02 mol) of aegyl-c (-bromo-oC-cyclohexyl acetate) is added to the solution. The mixture is heated under reflux for 7, and then dimethylformamide is distilled off under reduced pressure. To a residue 50 ml of water are added to the mixture, 160 ml of benzene are extracted twice. The benzene layers are combined, washed three times with 30 ml of an aqueous solution of sodium hydroxide, then with water, dried over nati sulfate, distilled in vacuum, 2.55 g of ethyl o1g are obtained (n phenylphenoxy) -o1-cyclohexyl acetate, yield 37.7 from the theory.
Example 4. Ethyl-o6- (5,6,7 8-tetrahydro-2-naphthoxy) -oL-cyclohexyl acetate.
575 ml (0.025) of metallic sodium are dissolved in 30 ml of anhydrous ethanol and 3.7 g (0.025 mol) of 5,6,7,8-tetrahydro-2 naphthol are added; The mixture was stirred at 20 ° C for 30 minutes. Ethanol is distilled off under reduced pressure and 10 ml of dimethylformamide is added to the residue, and then dimethylformamide is distilled off under reduced pressure, after which 30 ml of dimethylformamide is added to dissolve the residue.
5.0 g (0.02 mol) of ethyl-cC-bromo-o6-cyclohexyl acetate are added to the solution. The mixture is boiled under reflux for 6 hours, then dimethylformamide is distilled off under increased pressure. The residue is mixed with 50 ml of water, extracted twice with 100 ml of benzene. The benzene layers were combined, washed three times with 30 ml of a 5% aqueous solution of sodium hydroxide, then water, dried over sodium sulfate, and distilled in vacuo to give 3.2 g of ethyl-6- (5,6,7,8гтет | : / agidro-2-naphthoxy) -o1-cyclohexyl acetate, yield 50.7 from theory.
Example 5. 205 mg (0.0089 mol) of metallic sodium was dissolved in anhydrous ethanol and then 1.8 g (0.0089 mol | p-phenoxyphenol) was added. The mixture was stirred at room temperature for 30 minutes. Ethanol was distilled off at 5 ml of dimethylformamide is added to the residue, then dimethylformamide is distilled off under reduced pressure, and then 15 ml of dimethylformamide is added to dissolve the residue. In solution (2.5 g (0.01 mol) ethyl-O-bromo oo-cyclohexyl acetate. The mixture is heated under reflux for 8 hours, then distilled. dimethylformamide under reduced pressure. The residue is mixed with 50 ml of water, extracted twice with benzene (50 ml). The benzene layers are combined, washed three times with 30 ml of an aqueous sodium hydroxide solution, then with water, dried over sodium sulfate, distilled in vacuo, get 1 , 4 g ethyl-ot- (l-phenylphenoxy) -ot-cyclohexyl acetate, yield 42, bt, from theory
Example 6 B15 ml of ethanol was dissolved with 430 mg of potassium hydroxide and then ethyl (l-cyclohexylphenoxy) - "A-cyclohexyl acetate) was added. The mixture is heated on a water bath at b5-70 ° C for 90 minutes, then ethanol is distilled off under reduced pressure. The NII, the residue is mixed with water, washed twice with benzene. The aqueous layer is acidified with a 10% aqueous hydrochloric acid solution to precipitate a precipitate. The precipitate is filtered off, washed with water and dried. The product is recrystallized from n-hexane, get 0.7 g sA- (cyclohexylphenoxy) - "(-cyclohexyl acetate, yield, 9 o
 theories.
In tab. I presents data on the physicochemical properties of the compounds of example 1-6 and other compounds obtained similarly;
In tab. 2 shows data on. the activity of the obtained new derivatives of substituted oxyc clohexyl acetic acid.
Table 1
dH
ABOUT
117-118 / 0.15
1755
133-135 / 0.275
1760
4 s170-172 / 1
/
dHa
fc HjUS-Ue / l dHi
CiHvO
C2 "5
4 JHV - C Hj19 -198 / Q, 055
8 Continued table.
978723
1755
1760 17t5
167-169 / 0.32
1760
1750
1765
210-212 / 0.1
1762
11 dH3 d
C, Hj
. five "
0
1760 1750 1690 ()
1755 1700 () 1, / L-o- / L
H 5
15
di
16Ci.Hs- /
H “5
17. (Jl - / y-O
V - /
H1.
18
TSN5
nineteen
12.1
ABOUT
.З
38.5
39.0
52.3
i.2,6
178-181 / 0.15
192-195 / 0.12
205-208 / 0.03
185-189 / 0,045
Melting point 99-100 ° C
table 2
2500 2500 3000 3000 3000 3000. 128-130 / 0.1 135-137 / 0.2i
eleven
978723
12 Continued table. 2

权利要求:
Claims (1)
[1]
Invention Formula
The method of obtaining derivatives of substituted hydroxycyclohexylacetic acid of the general formula
ri 1-2;
R is chlorine, trifluoromethyl, methyl, ethyl, 2-methylpropyl, methoxy, acetoxy, dimethylphenyl, phenoxy, halophenoxy, cyclohexyl;
two R2 together - ortho-condensed saturated alkylene ring; R is hydrogen, ethyl,
from l and tea, and with the fact that compounds containing a hydroxy group of the general formula
Hdo
he
or
he
where n, R and R have the indicated meanings,
expose the interaction with ethyl ester of oC-halogen and clohexylacetic
13978723
acids in the presence of a base in the sources of information
environment of an organic solvent and taken into account in the examination, if necessary, the product of hydrolysis 1. Buhler, C. Pearson, D. Organic Synthesis, including H, p. 326-327, 1973.

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法律状态:

优先权:

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申请号 | 申请日 | 专利标题

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JP14774678A|JPS5576840A|1978-12-01|1978-12-01|New oxyacetic acid derivative, its preparation and blood- lipid depressor containing it as active principle|

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