反应 #82368

反应方程式

N2 [3(S)-amino-2(R)-hydroxy-4-phenylbutyl]-N1 -tert.butyl-L-prolinamide

N-(benzyloxycarbonyl)-S-methyl-L-cysteine

hydroxybenzotriazole

N-ethylmorpholine

dicyclohexylcarbodiimide

→

N1 -tert.butyl-L-prolinamide

溶剂

ethyl acetate

tetrahydrofuran

反应条件

后处理

1. 1
   过滤filtered
2. 2
   洗涤The filtrate was washed with aqueous sodium bicarbonate solution and sodium chloride solution
3. 3
   其他The solvent was removed by evaporation
4. 4
   其他the residue was chromatographed on silica gel using System G for the elution

实验过程

A solution of 650 mg of N2 -[3(S)-amino-2(R)-hydroxy-4-phenylbutyl]-N1 -tert.butyl-L-prolinamide and 538 mg of N-(benzyloxycarbonyl)-S-methyl-L-cysteine in 20 ml of dry tetrahydrofuran was cooled in an ice/salt mixture. 270 mg of hydroxybenzotriazole, 230 mg of N-ethylmorpholine and 412 mg of dicyclohexylcarbodiimide were added and the mixture was stirred for 16 hours. The mixture was diluted with ethyl acetate and filtered. The filtrate was washed with aqueous sodium bicarbonate solution and sodium chloride solution. The solvent was removed by evaporation and the residue was chromatographed on silica gel using System G for the elution to give 800 mg of N2 -[3(S)-[N-(benzyloxycarbonyl)-S-methyl-L-cysteinyl]amino]-2(R)-hydroxy-4-phenylbutyl]-N1 -tert.butyl-L-prolinamide; MS: m/e 585 [M+H]+.

来源