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Sodium trimethylsilanolate → 6-Chloro-1-methylcarbamoylmethyl-1H-indole-3-carboxylic acid

HRID 505073
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인쇄 미리보기

반응식

HRID 505073 반응식
[Cl:1][C:2]1[CH:10]=[C:9]2[C:5]([C:6]([C:16](=[O:21])C(F)(F)F)=[CH:7][N:8]2[CH2:11][C:12]([NH:14][CH3:15])=[O:13])=[CH:4][CH:3]=1.C[Si](C)(C)[O-:24].[Na+]>ClCCCl>[Cl:1][C:2]1[CH:10]=[C:9]2[C:5]([C:6]([C:16]([OH:21])=[O:24])=[CH:7][N:8]2[CH2:11][C:12](=[O:13])[NH:14][CH3:15])=[CH:4][CH:3]=1
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참가 물질

4

반응물 2

HCID 23672319Sodium trimethylsilanolateHCID 667442882-[6-Chloro-3-(2,2,2-trifluoro-acetyl)-indol-1-yl]-N-methyl-acetamide

생성물 1

HCID 597567026-Chloro-1-methylcarbamoylmethyl-1H-indole-3-carboxylic acid수율 27%

시약·촉매·용매 1

HCID 111,2-Dichloroethane용매

실험 절차

2-[6-Chloro-3-(2,2,2-trifluoro-acetyl)-indol-1-yl]-N-methyl-acetamide was suspensed in DCE and treated with (2.2 eq.) of sodium trimethylsilanolate. After shaking at room temperature for 20 min, the mixture was concentrated in vacuo and purified by prep. HPLC to give the title compound in 27% yield.

후처리

  1. concentrationthe mixture was concentrated in vacuo
  2. custompurified by prep

출처 및 근거

ORD 기록
ord-e290cce8ef914ea8a3ff203da847e888
출처 데이터셋
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07781436B2

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