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(S)-3-(5-(1-methylpyrrolidin-2-yl)pyridin-3-yl)acrylonitrile → (S)-3-(5-(1-methylpyrrolidin-2-yl)pyridin-3-yl)propanenitrile

HRID 874070
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인쇄 미리보기

반응식

HRID 874070 반응식
[CH3:1][N:2]1[CH2:6][CH2:5][CH2:4][C@H:3]1[C:7]1[CH:8]=[C:9]([CH:13]=[CH:14][C:15]#[N:16])[CH:10]=[N:11][CH:12]=1>CO.[Pd]>[CH3:1][N:2]1[CH2:6][CH2:5][CH2:4][C@H:3]1[C:7]1[CH:8]=[C:9]([CH2:13][CH2:14][C:15]#[N:16])[CH:10]=[N:11][CH:12]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 86659932(S)-3-(5-(1-methylpyrrolidin-2-yl)pyridin-3-yl)acrylonitrile

생성물 1

HCID 86659933(S)-3-(5-(1-methylpyrrolidin-2-yl)pyridin-3-yl)propanenitrile수율 75.3%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

(S)-3-(5-(1-Methylpyrrolidin-2-yl)pyridin-3-yl)acrylonitrile (preparation 2) (185 mg, 0.87 mmol) and 5% Pd/C (50 mg) in MeOH (5 mL) were stirred under an atmosphere of hydrogen for 72 hours. The reaction mixture was filtered through Celite then the solvent evaporated. The crude product was purified by flash chromatography (5% [20% ammonia in MeOH] in DCM) to give the title compound as a pale yellow oil (141 mg, 75%).

후처리

  1. filtrationThe reaction mixture was filtered through Celite
  2. customthe solvent evaporated
  3. customThe crude product was purified by flash chromatography (5% [20% ammonia in MeOH] in DCM)

출처 및 근거

ORD 기록
ord-1eb61d0a62c54ee99e5831e557af821f
출처 데이터셋
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08980276B2

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