Japanese Patent JPS63435

B2

Aminoalcohol derivatives corresponding to the formula (I) in which Q is a group and the other substituents have the meaning shown in Claim 1 are prepared by reaction with a compound of formula I, in which Q represents a group or , with an amine of type R3R4NH, Z being a halogen. The alcohol can then be esterified by reaction with an acid or an anhydride as defined in Claim 1. The compounds obtained have activities on the cardiovascular system, for example antihypertensive and/or antispasmodic activities, peripheral vasodilative activity, protective activity against myocardial anoxia, hypolipidemiating activity, antithrombotic activity, beta -lytic activity or platelet aggregation inhibiting activity, and/or activity on the central nervous system, for example a tranquillising activity.

JORUJU RANBERIN
YOZEFU ROOBA
KUROODO GIRE
ROMEO RONKUSHI

JP13785976A

January 07, 1988

November 18, 1976

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CONTINENTAL PHARMA

A61K31/135; A61K31/195; A61K31/215; A61K31/22; A61K31/335; A61K31/38; A61K31/381; A61K31/382; A61K31/395; A61K31/435; A61K31/495; A61K31/13; A61K31/535; A61K31/54; A61P3/06; A61P9/00; A61P9/08; A61P9/12; A61P25/26; B01J23/00; B01J25/00; B01J27/00; B01J31/00; C07B61/00; C07C67/00; C07C213/00; C07C215/38; C07C217/56; C07C219/22; C07C225/16; C07C233/43; C07C233/73; C07C233/78; C07C255/24; C07C255/30; C07C255/58; C07C271/16; C07C311/01; C07C313/00; C07C323/25; C07C323/27; C07C323/32; C07C323/33; C07C323/41; C07C323/49; C07C323/62; C07D209/08; C07D211/14; C07D215/06; C07D223/16; C07D265/30; C07D265/36; C07D277/60; C07D279/08; C07D281/10; C07D307/79; C07D311/04; C07D313/08; C07D327/00; C07D327/06; C07D333/54; C07D335/06; C07D337/06; C07D337/08; C07D339/00; C07D339/06; C07D339/08; C07D401/10; C07D401/12; C07D403/10; C07D405/06; C07D409/06; C07D409/12; (IPC1-7): C07D333/54; C07D335/06; C07D337/06; C07D405/06; C07D409/06; C07D409/12

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