反応式
[Cl:1][C:2]1[S:3][C:4]([CH:7]=[O:8])=[CH:5][N:6]=1.C(=O)([O-])[O-].[K+].[K+].[F:15][C:16]([Si](C)(C)C)([F:18])[F:17]>CN(C)C=O>[Cl:1][C:2]1[S:3][C:4]([CH:7]([OH:8])[C:16]([F:18])([F:17])[F:15])=[CH:5][N:6]=1参加物
5
実験手順
According to Reference Example 8-2, by use of 2-chlorothiazole-5-carbaldehyde (300 mg, 2.03 mmol) dissolved in N,N-dimethylformamide (4 mL), potassium carbonate (56 mg, 0.41 mmol) and (trifluoromethyl)trimethylsilane (0.360 mL, 2.44 mmol), the mixture was stirred and reacted at room temperature for 1.3 hours. Then, purification by preparative thin-layer chromatography (chloroform/methanol=15/1) was performed to give
後処理
- customreacted at room temperature for 1.3 hours
- customThen, purification by preparative thin-layer chromatography (chloroform/methanol=15/1)
- customto give
出典と根拠
- ORDレコード
- ord-9fb403dcf9c6448d8721f7ff0532fff1
- 出典データセット
- uspto-grants-2014_03
- 特許番号
- US08673908B2
関連ノート
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