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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 86689864, 화합물 → HCID 86689866, 화합물

HRID 2409056
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인쇄 미리보기

반응식

HRID 2409056 반응식
[CH3:1][Si:2]([CH3:19])([CH3:18])[CH2:3][CH2:4][O:5][CH2:6][N:7]1[C:11]2[CH:12]=[N:13][CH:14]=[C:15]([C:16]#[N:17])[C:10]=2[CH:9]=[CH:8]1>[Ni].N.CO>[CH3:1][Si:2]([CH3:19])([CH3:18])[CH2:3][CH2:4][O:5][CH2:6][N:7]1[C:11]2=[CH:12][N:13]=[CH:14][C:15]([CH2:16][NH2:17])=[C:10]2[CH:9]=[CH:8]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 86689864HCID 86689864, 화합물

생성물 1

HCID 86689866HCID 86689866, 화합물수율 97.1%

시약·촉매·용매 2

HCID 935Nickel촉매HCID 21705897Ammonia methanol용매

실험 절차

To a solution of 1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-c]pyridine-4-carbonitrile (683 mg, 2.5 mmol) in a solution of NH3/MeOH (7 N, 20 mL) was added Raney nickel (300 mg). The mixture was stirred under hydrogen for 3 h. The reaction mixture was filtered and the filtrate concentrated under reduced pressure to afford 673 mg (97.1%) of (1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-c]pyridin-4-yl)methanamine as a yellow oil. MS (ESI): m/z=278.1 [M+1]+.

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  1. filtrationThe reaction mixture was filtered
  2. concentrationthe filtrate concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-7aa97baf27e44d7195dfe5847c22c618
출처 데이터셋
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08815877B2

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