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(2S,3'S)-2-Methyl-1'-(6-nitro-pyridin-3-yl)-[1,3']bipyrrolidinyl → HCID 68211102, 화합물

HRID 536307
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인쇄 미리보기

반응식

HRID 536307 반응식
[CH3:1][C@H:2]1[CH2:6][CH2:5][CH2:4][N:3]1[C@H:7]1[CH2:11][CH2:10][N:9]([C:12]2[CH:13]=[N:14][C:15]([N+:18]([O-])=O)=[CH:16][CH:17]=2)[CH2:8]1>CO.[Pd]>[CH3:1][C@H:2]1[CH2:6][CH2:5][CH2:4][N:3]1[C@H:7]1[CH2:11][CH2:10][N:9]([C:12]2[CH:17]=[CH:16][C:15]([NH2:18])=[N:14][CH:13]=2)[CH2:8]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 68213028(2S,3'S)-2-Methyl-1'-(6-nitro-pyridin-3-yl)-[1,3']bipyrrolidinyl

생성물 1

HCID 68211102HCID 68211102, 화합물수율 93%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

To a solution of (2S,3′S)-2-methyl-1′-(6-nitro-pyridin-3-yl)-[1,3′]bipyrrolidinyl (0.110 g, 0.398 mmol) in methanol (30 mL) in a 250 mL parr bottle was added 5% Pd/C (0.030 g). The reaction mixture was allowed to shake under a hydrogen atmosphere (55 psi) at room temperature for 3 hours. The reaction mixture was filtered through a pad of Celite and the filtrate was concentrated under vacuum to afford 0.091 g (93%) of title compound.

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후처리

  1. customat room temperature
  2. customfor 3 hours
  3. filtrationThe reaction mixture was filtered through a pad of Celite
  4. concentrationthe filtrate was concentrated under vacuum

출처 및 근거

ORD 기록
ord-fdadc9bdb31b4218925d99d1758fab60
출처 데이터셋
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08859588B2

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