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HRID 1667749作成日:2026年10月25日

Dimethylformamide → 2-[6-(3-Chloro-propoxy)-benzoimidazol-1-yl]-4-(3-chloro-phenyl)-thiazole-5-carboxylic acid amide

https://huagongshe.com/reaction/1667749

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物1-Bromo-3-chloropropaneHCID 8006—
反応物Cesium carbonateHCID 10796—
反応物4-(3-Chloro-phenyl)-2-(6-hydroxy-benzoimidazol-1-yl)-thiazole-5-carboxylic acid amideHCID 67445498—
溶媒WaterHCID 962—
生成物2-[6-(3-Chloro-propoxy)-benzoimidazol-1-yl]-4-(3-chloro-phenyl)-thiazole-5-carboxylic acid amideHCID 6742729679.4%

反応手順

A mixture of 0.370 g (1 mmole) of 4-(3-chloro-phenyl)-2-(6-hydroxy-benzoimidazol-1-yl)-thiazole-5-carboxylic acid amide (I.25d), 3 mL of dimethylformamide, 1.6 g (5 mmole) of cesium carbonate and 0.297 mL (3 mmole) of 1-bromo-3-chloro-propane was heated at 100 degrees for 1 hour. The cooled mixture was diluted with 20 mL of water and the resulting precipitate collected by filtration. The solid was triturated with diethyl ether to give 0.355 g of 2-[6-(3-chloro-propoxy)-benzoimidazol-1-yl]-4-(3-chloro-phenyl)-thiazole-5-carboxylic acid amide (I.34a) as a brown solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08044213B2
出典データセットuspto-grants-2011_10
ORD IDord-5e83fa7949c64d4680ad219aa76b3619
出典メモuspto-grants-2011_10