Aluminium lithium hydride → (1H-Pyrrolo[2,3-b]pyridin-5-yl)methanol
반응식
C[O:2][C:3]([C:5]1[CH:6]=[C:7]2[CH:13]=[CH:12][NH:11][C:8]2=[N:9][CH:10]=1)=O.[H-].[Al+3].[Li+].[H-].[H-].[H-]>C1COCC1>[NH:11]1[C:8]2=[N:9][CH:10]=[C:5]([CH2:3][OH:2])[CH:6]=[C:7]2[CH:13]=[CH:12]1참가 물질
4
실험 절차
To 1H-Pyrrolo[2,3-b]pyridine-5-carboxylic acid methyl ester (75 mg, 0.394 mmol) in THF at 0 C was added lithium aluminum hydride (45 mg, 1.18 mmol) and the reaction mixture was slowly allowed to warm to ambient temperature. The reaction was refluxed for 12 hr, allowed to cool and quenched with water. Extraction with ethyl acetate, washed with brine, dried (Na2SO4) to afford (1H-Pyrrolo[2,3-b]pyridin-5-yl)-methanol (57 mg, 98% yield).
후처리
- temperatureThe reaction was refluxed for 12 hr
- temperatureto cool
- customquenched with water
- extractionExtraction with ethyl acetate
- washwashed with brine
- dry with materialdried (Na2SO4)
출처 및 근거
- ORD 기록
- ord-970f12e663a64fd8a5d51b42c818c26c
- 출처 데이터셋
- uspto-grants-2008_11
- 특허 번호
- US07446199B2
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