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HCID 70202469, 화합물 → rac-tert-butyl N-[(3R,4S)-4-methylpyrrolidin-3-yl]carbamate

HRID 580566
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인쇄 미리보기

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HRID 580566 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 70202469HCID 70202469, 화합물HCID 178418361HCID 178418361, 화합물

생성물 1

HCID 53686699rac-tert-butyl N-[(3R,4S)-4-methylpyrrolidin-3-yl]carbamate수율 93.3%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

A suspension of 1-benzyl-trans-3-t-butoxycarbonylamino-4-methylpyrrolidine (4.8 g) and 10% palladium-on-charcoal (1.8 g) in ethanol (40 ml) was shaken with hydrogen were absorbed under elevated pressure (100 kg/cm2) at 50°-70° C. for 6.5 hours. The catalyst was removed by filtration and the filtrate was evaporated to give the title compound (3.09 g) as brown oil. This oil was gradually solidified at room temperature.

후처리

  1. customwere absorbed under elevated pressure (100 kg/cm2) at 50°-70° C. for 6.5 hours
  2. customThe catalyst was removed by filtration
  3. customthe filtrate was evaporated

출처 및 근거

ORD 기록
ord-cba856acedb249e185beebb58b31f2d8
출처 데이터셋
uspto-grants-1988_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04753953

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