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一种手性酶动力学拆分方法用于对映体纯 (R)-和 (S)-度洛西汀。

A chemoenzymatic dynamic kinetic resolution approach to enantiomerically pure (R)- and (S)-duloxetine.

机构信息

Department of Organic Chemistry, Arrhenius Laboratory, Stockholm University, SE-106 91 Stockholm, Sweden.

出版信息

J Org Chem. 2011 May 20;76(10):3917-21. doi: 10.1021/jo2003665. Epub 2011 Apr 18.

Abstract

The synthesis of (R)-duloxetine is described. Dynamic kinetic resolution of β-hydroxynitrile rac-1 using Candida antarctica lipase B (CALB, N435) and ruthenium catalyst 6 afforded β-cyano acetate (R)-2 in high yield and in excellent enantioselectivity (98% ee). The subsequent synthetic steps were straightforward and (R)-duloxetine was isolated in 37% overall yield over 6 steps. The synthetic route also constitute a formal total synthesis of (S)-duloxetine.

摘要

(R)-度洛西汀的合成描述。使用南极假丝酵母脂肪酶 B(CALB,N435)和钌催化剂 6,对β-羟基腈外消旋体 rac-1 进行动态动力学拆分,以高产率和优异的对映选择性(98%ee)得到β-氰基乙酸酯(R)-2。随后的合成步骤简单,(R)-度洛西汀经过 6 步反应,总收率为 37%。该合成路线也构成了(S)-度洛西汀的正式全合成。

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