发明名称 Synthesis of intermediates for the preparation of pramipexol
摘要 A process for the preparation of an acid of formula (I), as the individual (R) enantiomer or (S), or a salt thereof wherein R is a protected amino group; and the asterisk * denotes the stereogenic carbon atom, comprising contacting an ester of formula (II), as mixture of (R,S) enantiomers, or a salt thereof, wherein R 1 is straight or branched C 1 -C 6 alkyl, optionally substituted with phenyl; and the asterisk * and R have the meanings defined above, with a lipase from Candida antarctica, under conditions effective to obtain a mixture comprising an acid of formula (I), as the individual (R) enantiomer, and an ester of formula (II), as the individual (S) enantiomer; the subsequent hydrolysis of the latter to obtain an acid of formula (I), as the individual (S) enantiomer; and, if desired, the conversion of an acid of formula (I), either as the (R) or (S) enantiomer, to a salt thereof.
申请公布号 EP1808492(A1) 申请公布日期 2007.07.18
申请号 EP20070000277 申请日期 2007.01.08
申请人 DIPHARMA FRANCIS S.R.L. 发明人 RIVA, SERGIO;FASSI, PAOLA;SCARPELLINI, MICHELE;ALLEGRINI, PIETRO;RAZZETTI, GABRIELE
分类号 C07D277/82;C12P17/14;C12P41/00 主分类号 C07D277/82
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