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HCID 54245016, 화합물 → HCID 10870990, 화합물

HRID 356578
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HRID 356578 반응식
[C:1]([O:5][C:6]([NH:8][CH2:9][CH2:10][CH2:11][O:12][C:13]1[CH:14]=[CH:15][C:16]([N+:23]([O-])=O)=[C:17]([C:19](=[O:22])[CH:20]=[CH2:21])[CH:18]=1)=[O:7])([CH3:4])([CH3:3])[CH3:2]>C(O)C.[C].[Pd]>[C:1]([O:5][C:6]([NH:8][CH2:9][CH2:10][CH2:11][O:12][C:13]1[CH:14]=[CH:15][C:16]([NH2:23])=[C:17]([C:19](=[O:22])[CH2:20][CH3:21])[CH:18]=1)=[O:7])([CH3:2])([CH3:3])[CH3:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 54245016HCID 54245016, 화합물

생성물 1

HCID 10870990HCID 10870990, 화합물수율 83%

시약·촉매·용매 2

HCID 178418390HCID 178418390, 화합물촉매HCID 702Ethanol용매

실험 절차

1-[5'-(3"-t-Butoxycarbonylaminopropyloxy)-2'-nitrophenyl]-2-propen-1-one (325 mg) is dissolved in ethanol (15 ml), and thereto is added 10% palladium-carbon (40 mg), and the mixture is stirred for 1.5 hour under hydrogen atmosphere. The catalyst is removed by filtration, and the filtrate is concentrated, and the residue is purified by silica gel column chromatography to give 1-[5'-(3"-t-butoxycarbonylaminopropyloxy)-2'-aminophenyl]-propan-1-one (248 mg) as a yellow powder.

후처리

  1. customThe catalyst is removed by filtration
  2. concentrationthe filtrate is concentrated
  3. customthe residue is purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-fad2c1e312ac467ca10d5db148028337
출처 데이터셋
uspto-grants-1998_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05837673

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