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HCID 22570321, 화합물 → Methyl 3-(5-hydoxylindolyl)-2-benzylpropanoate

HRID 1295114
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HRID 1295114 반응식
C([O:8][C:9]1[CH:10]=[C:11]2[C:15](=[CH:16][CH:17]=1)[NH:14][C:13]([CH2:18][CH:19]([CH2:24][C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1)[C:20]([O:22][CH3:23])=[O:21])=[CH:12]2)C1C=CC=CC=1>C(O)C.[Pd]>[OH:8][C:9]1[CH:10]=[C:11]2[C:15](=[CH:16][CH:17]=1)[NH:14][C:13]([CH2:18][CH:19]([CH2:24][C:25]1[CH:26]=[CH:27][CH:28]=[CH:29][CH:30]=1)[C:20]([O:22][CH3:23])=[O:21])=[CH:12]2
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참가 물질

4

반응물 1

HCID 22570321HCID 22570321, 화합물

생성물 1

HCID 69512901Methyl 3-(5-hydoxylindolyl)-2-benzylpropanoate수율 100%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

A mixture of methyl 3-(5-benzyloxyindolyl)-2-benzylpropanoate (0.16, 0.39 mmol), as prepared in the preceding step, 10% palladium(0) on carbon (0.02 g) in ethanol (10 mL) was stirred at ambient temperature under hydrogen (balloon) overnight (16 h). The catalyst was removed by filtration through Celite. The filtrate was concentrated to give the title compound as a light brown oil (0.12 g, 100%) which was used directly in next reaction.

후처리

  1. customThe catalyst was removed by filtration through Celite
  2. concentrationThe filtrate was concentrated

출처 및 근거

ORD 기록
ord-0e4d86a40cf24a069bb9d3952b34a314
출처 데이터셋
uspto-grants-2007_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07241789B2

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