反応式
[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]参加物
4
実験手順
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 4:1H2Q/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)+.
後処理
- additionAfter the addition the reaction
- concentrationthen was concentrated under vacuum
- filtrationTrituration with a cold solution of 4:1H2Q/methanol (50 mL), filtration
- customdrying under vacuum
出典と根拠
- ORDレコード
- ord-cc351b4018cf441c9e96d3268c0f6bbe
- 出典データセット
- uspto-grants-2005_01
- 特許番号
- US06846819B1
関連ノート
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