METHOD FOR THE PREPARATION OF MEU SUBSTITUTED IN POSITION-II,5,II-DIHYDRO-6H-PYRIDO(2,3-6)(1,4)BENZODIAZEPIN-6-ONES,申请号GR19167801563-传众专利搜索

METHOD FOR THE PREPARATION OF MEU SUBSTITUTED IN POSITION-II,5,II-DIHYDRO-6H-PYRIDO(2,3-6)(1,4)BENZODIAZEPIN-6-ONES

申请公布号：GR64535(B)

申请号：GR19167801563

申请日期：1978.05.24

申请公布日期：1980.04.10

申请人：

THOMAE GMBH K

分类号：A61K31/55;A61K31/5513;A61P1/04;A61P25/02;C07D471/04;C07D519/00;(IPC1-7):07D471/04

主分类号：A61K31/55

摘要：<p>Compounds of the formula <IMAGE> (I) wherein A is alkylene of 1 to 5 carbon atoms; R1 is amino, tert.butylamino, N-cyclohexyl-N-methyl-amino, dibenzylamino, benzylamino, trimethoxybenzyl-amino, 1-ethyl-2-pyrrolidinylmethylamino, 1-ethyl-3-piperidinyl-amino, 9-methyl-3,9-diazabicyclo[3.3.1]nonan-3-yl, 1,2,5,6-tetra-hydro-1-pyridyl, 4-benzyl-piperidino, 1,2,3,6,7,8,9,9a-octahydro-4H-pyrazino[1,2-a]-pyrimidine-1(or-8)yl, 3- or 4-hydroxypiperidino, 3-or 4-methoxypiperidino, 1,2,3,4-tetrahydro-2-isoquinolyl, 3-azaspiro[5.5]undecan-3-yl, 4-oxo-piperidino or the ethyleneketal thereof, hexahydro-3-methyl-1-pyrimidinyl, thiomorpholino, 1-oxido-thiomorpholino, hexahydro-4-methyl-1H-1,4-diazepin-1-yl, 2,6-dimethyl-morpholino,1,4-diazabicyclo [4.3.0]nonan-4-yl, 1,2,5,6-tetrahydro-pyrid-1-yl, (1-methylpyrrolindin-2-yl)-ethylamino, (1-methylpyrrolidin-2-yl)-methylamino, (1-n-propylpyrrolidin-2-yl)-methylamino, (1-allyl-pyrrolidin-2-yl)-methylamino, (1-n-butyl-pyrrolidin-2-yl)-methylamino, (1-benzyl-pyrrolidin-2-yl)-methylamino, (furan-2-yl)-methylamino, (tetrahydrofuran-2-yl)-methylamino, N-[(1-ethyl-pyrrolidin-2-yl)-methyl]-methylamino, (1-ethyl-pyrrolidin-3-yl)-methylamino or (1-allylpyrrolidin-3-yl)-methylamino; or, when A is alkylene of 2 to 5 carbon atoms, also dimethylamino, diethylamino, dipropylamino, diisopropylamino, di-n-butylamino, diisobutylamino, pyrrolidino, piperidino, methyl-piperidino, ethyl-piperidino or morpholino; and R2 is hydrogen, methyl or ethyl; and non-toxic, pharmacologically acceptable acid addition salts thereof. The compounds as well as the salts are useful as anti-ulcerogenics and secretion inhibitors.</p>