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2-(2,6-dichloro-phenyl)-1H-indole-5-carboxylic acid methyl ester → 2-(2,6-dichloro-phenyl)-1H-indole-5-carboxylic acid

HRID 1514926
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반응식

HRID 1514926 반응식
C[O:2][C:3]([C:5]1[CH:6]=[C:7]2[C:11](=[CH:12][CH:13]=1)[NH:10][C:9]([C:14]1[C:19]([Cl:20])=[CH:18][CH:17]=[CH:16][C:15]=1[Cl:21])=[CH:8]2)=[O:4]>[Li+].[OH-].C1COCC1>[Cl:21][C:15]1[CH:16]=[CH:17][CH:18]=[C:19]([Cl:20])[C:14]=1[C:9]1[NH:10][C:11]2[C:7]([CH:8]=1)=[CH:6][C:5]([C:3]([OH:4])=[O:2])=[CH:13][CH:12]=2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 669659532-(2,6-dichloro-phenyl)-1H-indole-5-carboxylic acid methyl ester

생성물 1

HCID 669657142-(2,6-dichloro-phenyl)-1H-indole-5-carboxylic acid

시약·촉매·용매 2

HCID 3939Lithium Hydroxide용매HCID 8028Tetrahydrofuran용매

실험 절차

A solution of 2-(2,6-dichloro-phenyl)-1H-indole-5-carboxylic acid methyl ester in 2N LiOH aqueous solution (1 mL) and THF (1 mL) was stirred at room temperature for 16 h. The mixture was washed with Et2O. The aqueous layer was acidified with 1N HCl aqueous solution, extracted with Et2O. The organic extracts were dried over Na2SO4, filtered and concentrated under reduced pressure to give 2-(2,6-dichloro-phenyl)-1H-indole-5-carboxylic acid as a white solid: MS (m/z) 306.1 (M+1).

후처리

  1. washThe mixture was washed with Et2O
  2. extractionextracted with Et2O
  3. dry with materialThe organic extracts were dried over Na2SO4
  4. filtrationfiltered
  5. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-3ebba98f0d4f4e34b5a27452e3ac2736
출처 데이터셋
uspto-grants-2012_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08222248B2

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