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Oxindole → 4-(2-Carboxyethyl)-3-methyl-5-(2-oxo-1,2-dihydroindol-3-ylidenemethyl)-1H-pyrrole-2-carboxylic Acid Ethyl Ester

HRID 1860872
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인쇄 미리보기

반응식

HRID 1860872 반응식
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][C:2]1=[O:10].[CH2:11]([O:13][C:14]([C:16]1[NH:17][C:18]([CH:27]=O)=[C:19]([CH2:22][CH2:23][C:24]([OH:26])=[O:25])[C:20]=1[CH3:21])=[O:15])[CH3:12]>>[CH2:11]([O:13][C:14]([C:16]1[NH:17][C:18]([CH:27]=[C:3]2[C:4]3[C:9](=[CH:8][CH:7]=[CH:6][CH:5]=3)[NH:1][C:2]2=[O:10])=[C:19]([CH2:22][CH2:23][C:24]([OH:26])=[O:25])[C:20]=1[CH3:21])=[O:15])[CH3:12]
참가 물질실험 절차출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 321710OxindoleHCID 152706233-[5-(Ethoxycarbonyl)-2-formyl-4-methyl-1H-pyrrol-3-yl]propanoic acid

생성물 1

HCID 542461354-(2-Carboxyethyl)-3-methyl-5-(2-oxo-1,2-dihydroindol-3-ylidenemethyl)-1H-pyrrole-2-carboxylic Acid Ethyl Ester수율 65%

실험 절차

Oxindole (0.25 g, 1.88 mmol) was condensed with 4-(2-carboxyethyl)-5-formyl-3-methyl-1H-pyrrole-2-carboxylic acid ethyl ester (0.5 g, 1.97 mmol) to give 0.45 g (65%) of the title compound.

출처 및 근거

ORD 기록
ord-af21bde1a9174b43a71593d780d84770
출처 데이터셋
uspto-grants-2003_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06531502B1

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