反应 #1340611

ord-44bfbc1a0cf8406ea5ff3dac7cae99f3

反应方程式

[H][H]
hydrogen
C=CC1CN(C(=O)OCc2ccccc2)C[C@H]1NC(=O)OC(C)(C)C
(3S)-1-benzyloxycarbonyl-3-(tert-butoxycarbonyl)amino-4-vinylpyrrolidine
CCC1CNC[C@H]1NC(=O)OC(C)(C)C
title compound
CCC1CNC[C@H]1NC(=O)OC(C)(C)C
(3S)-3-(tert-Butoxycarbonyl)amino-4-ethylpyrrolidine

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    过滤After filtration
  2. 2
    浓缩the filtrate was concentrated under reduced pressure

实验过程

A 10% palladium carbon catalyst (15 mg) was added to a solution of (3S)-1-benzyloxycarbonyl-3-(tert-butoxycarbonyl)amino-4-vinylpyrrolidine [an isomer mixture of (4S)-form:(4R)-form (1:4)] (230 mg, 0.66 mmol) in ethanol (8 mL), followed by stirring in a hydrogen atmosphere under an ordinary pressure at room temperature for 12 hours. After filtration, the filtrate was concentrated under reduced pressure, to thereby yield the title compound (an isomer mixture of (4S)-form and (4R)-form (1:4)) as a colorless oily substance (148 mg, 100%).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08455482B2uspto-grants-2013_06