반응식
[CH3:1][NH2:2].[S:3]1[C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][C:6]=2[CH:5]=[C:4]1[C:12](Cl)=[O:13]>C1COCC1>[CH3:1][NH:2][C:12]([C:4]1[S:3][C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][C:6]=2[CH:5]=1)=[O:13]참가 물질
4
실험 절차
To a stirred solution of 2.0 M methylamine in THF (60 mL) and THF (60 mL) was added dropwise at 0° C. a solution of benzothiophene-2-carbonyl chloride (10.8 g, 55 mmole) in THF (50 mL) over 15 minutes. After the addition the reaction was allowed to warm to RT then was concentrated under vacuum. Trituration with a cold solution of 4:1 H2O/methanol (50 mL), filtration, and drying under vacuum gave the title compound (10.35 g, 98%) as a white solid: MS (ES) m/e 191.9 (M+H)+.
후처리
- additionAfter the addition the reaction
- concentrationthen was concentrated under vacuum
- filtrationTrituration with a cold solution of 4:1 H2O/methanol (50 mL), filtration
- customdrying under vacuum
출처 및 근거
- ORD 기록
- ord-47d206de047e4ee68e496aeaa0acb160
- 출처 데이터셋
- uspto-grants-2012_05
- 특허 번호
- US08173646B2
연결된 노트
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