Реакция #87081

ord-994c34d7db0c4a69bbdac155e930d8e8

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    КонцентрированиеThe mixture was concentrated
  2. 2
    Промывкаthe residue was washed with petroleum ether (100 mL)

Методика

A solution of (S)-benzyl 2-((S)-2-((tert-butoxycarbonyl)amino)propanamido)-3-(4-methoxyphenyl)propanoate (29.0 g, 63.6 mmol) in 3 N HCl-EtOAc (150 mL) was stirred for 1 h at ambient temperature. The mixture was concentrated and the residue was washed with petroleum ether (100 mL) to afford (S)-benzyl 2-((S)-2-aminopropanamido)-3-(4-methoxyphenyl)propanoate as an HCl salt (quant.), which was used directly in the next step without further purification.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US09434761B2uspto-grants-2016_09