发明名称 PROCESS FOR PREPARING 1-(4-ARYL-CYCLOHEXYL)PIPERIDINE DERIVATIVES
摘要 The title compds. (I; Ar1 = aryl or 1,3-benzodioxolyl; R = H or lower alkyl; R1 = H, cyano, carboxyl, lower alkyloxycarbonyl, aminocarbonyl, mono- and di(lower alkyl) aminocarbonyl, hydroxy, lower alkyloxy, lower alkylcarbonyl, or aryl carbonyl; A = II or III; Ar2 = aryl or halogen-substituted aryl; R4 = H, lower alkyl, arylloweralkyl) were prepd. Thus, methyl 3-methyl-4-oxo-1- piperidinecarboxylate was reacted with 4-fluorobenzeneamine and mixed with sodium cyanide to give Me 4-cyano-4-((4-fluorophenyl)amino)3- methyl-1-piperidinecarboxylate, which was crystallized with trichloromethane, to give B-methyl 4-(aminocarbonyl(-4-((4- fluorophenyl)amino)-3-methyl-1-piperidine carboxylate.
申请公布号 KR850000026(B1) 申请公布日期 1985.02.11
申请号 KR19810000729 申请日期 1981.03.06
申请人 JANSSEN PHARMACEUTICA N.V. 发明人 STOKBROEKX, RAYMOND A.;WILLEMS, JOANNES J.M.;LUYCKX, MARCEL G.M.
分类号 C07D317/72;A61K;A61K31/435;A61K31/4402;A61K31/4418;A61K31/4427;A61K31/443;A61K31/4433;A61K31/445;A61K31/4468;A61P1/08;A61P25/20;A61P25/26;C07C45/59;C07C62/38;C07C67/00;C07C69/757;C07C253/00;C07C255/46;C07D;C07D211/66;C07D213/57;C07D317/54;C07D333/16;C07D333/24;C07D401/00;C07D401/04;C07D401/06;C07D405/14;C07D409/14;C07D471/10 主分类号 C07D317/72
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