A short and efficient synthesis of zamifenacin a muscarinic M-3 receptor antagonist

被引:28
作者
Cossy, J
Dumas, C
Pardo, DG
机构
[1] Laboratoire de Chimie Organique, Associé au CNRS, ESPCI, 75231 Paris Cedex
关键词
D O I
10.1016/S0960-894X(97)00221-7
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A short synthesis of zamifenacin is described by using a ring enlargement of a L-prolinol derivative. (C) 1997 Elsevier Science Ltd.
引用
收藏
页码:1343 / 1344
页数:2
相关论文
共 8 条
[1]  
ALKER D, 1990, Patent No. 350309
[2]   Pharmacokinetics and metabolism of zamifenacin in mouse, rat, dog and man [J].
Beaumont, KC ;
Causey, AG ;
Coates, PE ;
Smith, DA .
XENOBIOTICA, 1996, 26 (04) :459-471
[3]   FORMATION OF OPTICALLY-ACTIVE 3-HYDROXYPIPERIDINES [J].
COSSY, J ;
DUMAS, C ;
MICHEL, P ;
PARDO, DG .
TETRAHEDRON LETTERS, 1995, 36 (04) :549-552
[4]  
MCRITCHIE B, 1993, BRIT J PHARMACOL, V109, pP38
[5]  
QUINN P, 1993, BRIT J PHARMACOL, V109, pP37
[7]   PRECLINICAL AND CLINICAL-PHARMACOLOGY OF SELECTIVE MUSCARINIC M(3) RECEPTOR ANTAGONISTS [J].
WALLIS, RM .
LIFE SCIENCES, 1995, 56 (11-12) :861-868
[8]  
WALLIS RM, 1993, BRIT J PHARMACOL, V109, pP36