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HCID 57567342, 화합물 → HCID 57567410, 화합물

HRID 401348
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반응식

HRID 401348 반응식
[CH3:1][O:2][CH2:3][CH2:4][O:5][CH2:6][C:7]([C:10]1[CH:15]=[CH:14][C:13]([NH:16][C:17](=[O:19])[CH3:18])=[CH:12][C:11]=1[N+:20]([O-])=O)([CH3:9])[CH3:8]>CO.[Ni]>[NH2:20][C:11]1[CH:12]=[C:13]([NH:16][C:17](=[O:19])[CH3:18])[CH:14]=[CH:15][C:10]=1[C:7]([CH3:9])([CH3:8])[CH2:6][O:5][CH2:4][CH2:3][O:2][CH3:1]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 57567342HCID 57567342, 화합물

생성물 1

HCID 57567410HCID 57567410, 화합물수율 35.7%

시약·촉매·용매 2

HCID 935Nickel촉매HCID 887Methanol용매

실험 절차

A mixture of N-{4-[2-(2-methoxy-ethoxy)-1,1-dimethyl-ethyl]-3-nitro-phenyl}-acetamide (5 g, 16 mmol) and Raney Ni (1 g) in MeOH (50 mL) was stirred under H2 (1 atm) at room temperature 1 h. The catalyst was filtered off and the filtrate was concentrated. The residue was purified by column chromatography (petroleum ether-EtOAc, 100:1) to give N-{3-amino-4-[2-(2-methoxy-ethoxy)-1,1-dimethyl-ethyl]-phenyl}-acetamide (1.6 g, 35%).

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
filtration
The catalyst was filtered off
  • concentrationthe filtrate was concentrated
  • customThe residue was purified by column chromatography (petroleum ether-EtOAc, 100:1)
  • 출처 및 근거

    ORD 기록
    ord-380c50e495174fb4a7539cd48d5b5e17
    출처 데이터셋
    uspto-grants-2014_06
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US08741925B2

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