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1-Benzyl-cis-3-t-butoxycarbonylamino-4-methylpyrrolidine → (3S,4S)-3-(Boc-amino)-4-methylpyrrolidine

HRID 580563
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인쇄 미리보기

반응식

HRID 580563 반응식
C([N:8]1[CH2:12][C@H:11]([CH3:13])[C@H:10]([NH:14][C:15]([O:17][C:18]([CH3:21])([CH3:20])[CH3:19])=[O:16])[CH2:9]1)C1C=CC=CC=1.[H][H]>C(O)C.[Pd]>[C:18]([O:17][C:15]([NH:14][C@H:10]1[C@@H:11]([CH3:13])[CH2:12][NH:8][CH2:9]1)=[O:16])([CH3:21])([CH3:19])[CH3:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 108808031-Benzyl-cis-3-t-butoxycarbonylamino-4-methylpyrrolidineHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 11138119(3S,4S)-3-(Boc-amino)-4-methylpyrrolidine수율 87.8%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

A suspension of 1-benzyl-cis-3-t-butoxycarbonylamino-4-methylpyrrolidine (5.37 g) and 10% palladium-on-charcoal (2.70 g) in ethanol (50 ml) was shaken with hydrogen were absorbed under elevated pressure (100 kg/cm2) at room temperature for 22 hours. The catalyst was removed by filtration and the filtrate was evaporated to give the title compound (3.25 g). The compound was gradually solidified at room temperature.

후처리

  1. customwere absorbed under elevated pressure (100 kg/cm2) at room temperature for 22 hours
  2. customThe catalyst was removed by filtration
  3. customthe filtrate was evaporated

출처 및 근거

ORD 기록
ord-6fa11b429bad4daea129c07ad2314b43
출처 데이터셋
uspto-grants-1988_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04753953

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