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2-(1H-Pyrrolo[3,2-c]pyridin-3-yl)acetonitrile → 2-(1H-pyrrolo[3,2-c]pyridin-3-yl)ethanamine

HRID 1593506
노트
인쇄 미리보기

반응식

HRID 1593506 반응식
[NH:1]1[C:9]2[CH:8]=[CH:7][N:6]=[CH:5][C:4]=2[C:3]([CH2:10][C:11]#[N:12])=[CH:2]1.[H][H]>C(O)C.[NH4+].[OH-].[Rh]>[NH2:12][CH2:11][CH2:10][C:3]1[C:4]2[C:9](=[CH:8][CH:7]=[N:6][CH:5]=2)[NH:1][CH:2]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 2

HCID 226630522-(1H-Pyrrolo[3,2-c]pyridin-3-yl)acetonitrileHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 226629862-(1H-pyrrolo[3,2-c]pyridin-3-yl)ethanamine

시약·촉매·용매 3

HCID 23948Rhodium촉매HCID 702Ethanol용매HCID 14923Ammonium Hydroxide용매

실험 절차

A mixture of (1H-pyrrolo[3,2-c]pyridin-3-yl)-acetonitrile (0.260 g, 1.66 mmol) and 5% rhodium on alumina (0.26 g) in ethanol (10 mL) and concentrated NH4OH (5 mL) is placed under 55 psi hydrogen pressure on a Parr shaker. After 24 h at ambient temperature, the reaction mixture is filtered through Celite and concentrated in vacuo to afford the title amine, identified by NMR and mass spectral analyses.

후처리

  1. filtrationthe reaction mixture is filtered through Celite
  2. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-e4e89e60ac03425587cef80e3affc944
출처 데이터셋
uspto-grants-2007_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07297705B2

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