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Ammonia → tert-Butyl (3R)-3-(aminomethyl)pyrrolidine-1-carboxylate

HRID 2228768
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HRID 2228768 반응식
[C:1]([C@@H:3]1[CH2:7][CH2:6][N:5]([C:8]([O:10][C:11]([CH3:14])([CH3:13])[CH3:12])=[O:9])[CH2:4]1)#[N:2].N>[Ni].C(O)C>[NH3:2].[NH2:2][CH2:1][C@H:3]1[CH2:7][CH2:6][N:5]([C:8]([O:10][C:11]([CH3:14])([CH3:13])[CH3:12])=[O:9])[CH2:4]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 2

HCID 222AmmoniaHCID 7018344(R)-1-Boc-3-cyanopyrrolidine

생성물 2

HCID 222AmmoniaHCID 1515152tert-Butyl (3R)-3-(aminomethyl)pyrrolidine-1-carboxylate수율 195.3%

시약·촉매·용매 2

HCID 935Nickel촉매HCID 702Ethanol용매

실험 절차

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

A mixture of tert-butyl (3R)-3-cyano-1-pyrrolidinecarboxylate (preparation 79) (1.60 g, 8.13 mmol) and Raney® Nickel (1 g) in 0.88 ammonia (20 ml) and ethanol (150 ml), was hydrogentaed at 60 psi and room temperature for 8 hrs. The mixture was filtered through Arbocel®, and the filtrate concentrated under reduced pressure. The crude product was purified by column chromatography on silica gel using an elution gradient of dichloromethane:methanol:0.88 ammonia (100:0:0 to 90:10:1) to yield the desired product as an oil, (1.59 g, 98%).

후처리

  1. filtrationThe mixture was filtered through Arbocel®
  2. concentrationthe filtrate concentrated under reduced pressure
  3. customThe crude product was purified by column chromatography on silica gel using an elution gradient of dichloromethane

출처 및 근거

ORD 기록
ord-df6a02490cab4c9da16355af19358bb6
출처 데이터셋
uspto-grants-2002_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06417203B1

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