반응 #82355

ord-474762cbe1a646e4b0ee944d16f7042c

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The catalyst was removed by filtration
  2. 2
    기타the filtrate was evaporated

실험 절차

294 mg of N2 -[3(S)-[[N-[6-(benzyloxycarbonyl)-2-naphthoyl]-L-asparaginyl]amino]-2(R)-hydroxy-4-phenylbutyl]-N1 -tert.butyl-L-prolinamide in 100 ml of isopropanol was hydrogenated over 10% palladium-on-carbon at 20° C. and under atmospheric pressure for 16 hours. The catalyst was removed by filtration and the filtrate was evaporated to give 145 mg of N2 -[3(S)-[[N-(6-carboxy-2-naphthoyl)-L-asparaginyl]amino]-2(R)-hydroxy-4-phenylbutyl]-N1 -tert.butyl-L-prolinamide as a white solid from methanol/ethyl acetate; MS: m/e 646 [M+H]+.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05620987uspto-grants-1997_04