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HRID 1358498作成日:2026年10月25日

Water → 1-[(2S,3R)-2-benzyloxy-5-(2-oxobenzothiazol-3-yl)-3-pentyl]imidazole-4-carboxamide

https://huagongshe.com/reaction/1358498

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物BenzothiazoloneHCID 13625—
反応物Sodium hydrideHCID 24758—
反応物HCID 11164927HCID 11164927—
溶媒DimethylformamideHCID 6228—
生成物1-[(2S,3R)-2-benzyloxy-5-(2-oxobenzothiazol-3-yl)-3-pentyl]imidazole-4-carboxamideHCID 5701534752.7%

反応条件

温度65 °C

反応手順

To a stirred solution of 2-oxobenzothiazole (83 mg, 0.549 mmol) in DMF (3 ml) was added NaH (60% in mineral oil, 22 mg, 0.549 mmol) at room temperature. After 10 minutes, 1-[(2S,3R)-2-benzyloxy-5-methanesulfonyloxy-3-pentyl]imidazole-4-carboxamide in DMF (3 ml) was added and the resulting mixture was stirred for 6 hours at 60 to 70° C. The reaction mixture was poured into water (30 ml) and extracted with ethyl acetate. The organic layer was washed with brine, dried (sodium sulfate), and concentrated in vacuo. The residue was purified by silica gel (8 g) column chromatography eluting with chloroform/methanol (100:1 to 30:1) to give 1-[(2S,3R)-2-benzyloxy-5-(2-oxobenzothiazol-3-yl)-3-pentyl]imidazole-4-carboxamide (63 mg, 52.7%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06596738B1
出典データセットuspto-grants-2003_07
ORD IDord-7d5460f6e3734611b331b2cca7655c92
出典メモuspto-grants-2003_07