4H-3,1-benzoxazin-4-ones and related compounds, pharmaceutical compositions containing them, and processes for their preparation
    8.
    发明公开
    4H-3,1-benzoxazin-4-ones and related compounds, pharmaceutical compositions containing them, and processes for their preparation 失效
    4H-3,1-苯并恶嗪-4-酮及相关化合物,含有它们的进程的药物组合物及其制造。

    公开(公告)号:EP0147211A2

    公开(公告)日:1985-07-03

    申请号:EP84309013.5

    申请日:1984-12-21

    摘要: Novel 2-amino-4H-3,1-benzoxazin-4-ones represented by the formula
    and the pharmaceutically acceptable esters and salts thereof wherein R' is hydrogen or lower alkyl;

    R 2 and R 3 are each independently hydrogen, halo, lower alkyl, hydroxy, lower alkoxy, lower thioalkyl, -N0 2 , -N(R') 2 , -NR'COR', -NHCON(R') 2 or -NHCOOR',
    with the proviso that at least one of R 1 , R 2 and R 3 is not hydrogen when X is NHR or NR'COR"; and
    X is a radical chosen trom
    in which:
    R is lower alkyl, lower alkenyl, lower alkynyl, optionally substituted lower cycloalkyl or optionally substituted phenyl lower alkyl;
    each R' is independently hydrogen or lower alkyl, or lower alkenyl or lower alkynyl where the unsaturated bond is at least one carbon removed from the O or N atom;
    each R" is independently R, lower alkoxy, NHR' or AOR'; and
    A is an amino acid residue, or a peptide of 2 to 3 amino acid residues, are useful as enzyme inhibitors in animals.

    摘要翻译: 新颖的2-氨基-4H-3,1-苯并恶嗪-4-酮由式表示,并且其药学上可接受的盐和酯worin - [R <1>是氢或低级烷基; [R <2>和R <3>各自独立地是氢,卤素,低级烷基,羟基,低级烷氧基,低级硫代烷基,-NO 2,-N(R“)2,-NR COR分钟分钟,-NHCON(R分钟) 2或--NHCOOR分钟,条件做的R的至少一个<1>,R <2>和R <3>不为氢时,X是NHR或NR COR分秒; 并且X是一个基团,从在其中选择的:R是低级烷基,低级烯基,低级炔基,低级环烷基或任选substituiertem OPTIONALLY substituiertem苯基低级烷基; 每个R min是独立地为氢或低级烷基,或低级链烯基或低级炔基,其中不饱和键的至少一个碳从O或N原子除去 每个R独立地秒R,低级烷氧基,NHR min或AOR分钟; 而A是一个氨基酸残基,或2至3个氨基酸残基的肽,如在动物酶抑制剂是有用的。