HRID652343

反应详情

EQUATION

反应方程式

HRID 652343 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A solution of N-[N-[(3S)-3-[[(t-butyloxy)carbonyl]amino]-2-hydroxybutyl]-L-phenylalanyl-L-leucine, t-butyl ester (slower isomer) (0.27 g, 0.52 mmol) in 20 ml of 1.3N hydrogen chloride in acetic acid was allowed to stir for 2 hours at room temperature, during which time a white precipitate separated. The mixture was concentrated under reduced pressure to approximately one third of the original volume, then diluted with ether and filtered yielding 185 mg of the title compound as a white solid, melting point 236°-239° C. (with slow decomposition >210° C.). Analysis by 400 MHz 1H-NMR revealed the presence of a small amount (<5%) of the faster isomer.

WORKUP

后处理

  1. customseparated
  2. concentrationThe mixture was concentrated under reduced pressure to approximately one third of the original volume
  3. additiondiluted with ether
  4. filtrationfiltered