发明名称 BASIC ETHERS, PHARMACEUTICAL PREPARATIONS CONTAINING THESE AND PROCESS FOR THEIR PREPARATION
摘要 For the Contracting States : BE, CH, DE, FR, GB, IT, NL, SE 1. Basic ethers of the general formula I see diagramm : EP0009683,P12,F1 wherein G is an unsubstituted phenyl oder benzyl group or a phenyl or benzyl group which is monosubstituted or disubstituted by halogen or is alkyl with 1-6 C atoms, Z is 1-imidazolyl or 2-methyl-1-imidazolyl, A is -CH=CR**1-, -CO-CHR**1-, -CHOH-CHR**1- or -CH2 -CHR**2-, n is 1, 2 or 3, R**1 is H or alkyl with 1-4 C atoms and R**2 is alkyl with 1-4 C atoms, and their physiologically acceptable acid addition salts. For the Contracting State : AT 1. Process for the preparation of basic ethers of the general formula I see diagramm : EP0009683,P13,F1 dans laquelle A is -CH=CR**1-, -CO-CHR**1, -CHOH-CHR**1- or -CH2 -CHR**2-. n is 1, 2 or 3, R**1 is H or alkyl with 1-4 C atoms and R**2 is alkyl with 1-4 C atoms, and their physiologically acceptable acid addition salts, characterized in that a compound of the general formula II R-Q wherein R is the group C-O- see diagramm : EP0009683,P13,F2 and Q is a radical which can be reduced to a group -A-(CH2 )n -Z, and G, Z, A and n have the meaning indicated above, is treated with a reducing agent, or in that a compound which corresponds to the general formula I but in which the hydroxyl group is present in a functionally modified form is treated with a solvolyzing agent with liberation of the hydroxyl group, or in that a compound of the general formula III R-A-(CH2 )n -X wherein X is Cl, Br, I, OH or reactively functionally modified OH and R, A and n have the meaning indicated above, is reacted with a compound of the general H-Z and in that, optionally, a resulting hydroxy compound of the formula I wherein A is -CHOH-CHR**1- is treated with a dehydrating agent and/or a resulting compound of the formula I wherein A is -CH=CR**1-, CO-CHR**1- or -CHOH-CHR**1 is treated with a reducing agent and/or a resulting base of the formula is converted to one of its physiologically acceptable acid addition salts by treatment with an acid.
申请公布号 ZA7905181(B) 申请公布日期 1980.12.31
申请号 ZA19790005181 申请日期 1979.09.28
申请人 MERCK PATENT GMBH 发明人 ORTH D;GANTE J;VOLKMAR RUDOLPH;KURMEIER H;PRUECHER H;WAHLIG H
分类号 A61K31/135;A61K31/415;A61P3/06;A61P7/02;A61P25/04;A61P29/00;A61P31/00;C07C67/00;C07C213/00;C07C217/56;C07C217/62;C07C217/64;C07C225/16;C07D233/60;C07D249/08;C07D521/00 主分类号 A61K31/135
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