반응식
[NH:1]1[C:9]2[C:4](=[N:5][CH:6]=[CH:7][CH:8]=2)[N:3]=[C:2]1[SH:10].CI.[C:13]([O-])([O-])=O.[K+].[K+]>CC(C)=O>[CH3:13][S:10][C:2]1[NH:3][C:4]2=[N:5][CH:6]=[CH:7][CH:8]=[C:9]2[N:1]=1참가 물질
5
실험 절차
To a solution of 1H-imidazo[4,5-b]pyridine-2-thiol (2 g) in acetone (30 mL) were added MeI (0.910 mL) and K2CO3 (5.48 g) at room temperature. After stirring for 10 h, the mixture was concentrated under reduced pressure. The residue was purified by column chromatography (NH-silica gel, eluted with 10%-100% EtOAc in hexane) to give 2-(methylsulfanyl)-3H-imidazo[4,5-b]pyridine (1.0 g) as a white solid.
후처리
- concentrationthe mixture was concentrated under reduced pressure
- customThe residue was purified by column chromatography (NH-silica gel, eluted with 10%-100% EtOAc in hexane)
출처 및 근거
- ORD 기록
- ord-92fa7ad1de724315966070998af52654
- 출처 데이터셋
- uspto-grants-2016_01
- 특허 번호
- US09226921B2
연결된 노트
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