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HRID 1419990作成日:2026年10月25日

Triethylamine → N-[4-(5H-Imidazo[2,1-c][1,4]benzodiazepin-10(11H)ylcarbonyl)phenyl]-2-methylbenzamide

https://huagongshe.com/reaction/1419990

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物5H-Imidazo(2,1-c)(1,4)benzodiazepine, 10,11-dihydro-HCID 3060399—
反応物4-[(2-methylbenzoyl)amino]benzoyl ChlorideHCID 10707441—
溶媒DichloromethaneHCID 6344—
生成物N-[4-(5H-Imidazo[2,1-c][1,4]benzodiazepin-10(11H)ylcarbonyl)phenyl]-2-methylbenzamideHCID 21837073—

反応条件

温度0 °C

反応手順

To a mixture of 1.37 g (5 mmol) of 4-[(2-methylbenzoyl)amino]benzoyl chloride in 15 ml of methylene chloride, cooled to 0° C. is added 1.5 ml of triethylamine. After-stirring for 3 minutes, 5 mmol of 10,11-dihydro-5H-imidazo[2,1-c][1,4]benzodiazepine in 5 ml of methylene chloride is added. The cooling bath is removed and after about 30 minutes a complete solution is obtained. The reaction mixture is allowed to stir at room temperature for 1 hour and the volatiles are concentrated in vacuo. The residue is dissolved in 100 ml of ethyl acetate and washed with water, 2N citric acid, and brine. The solution is dried with Na2SO4 and the volatiles concentrated in vacuo to give the desired product as a solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05889001
出典データセットuspto-grants-1999_03
ORD IDord-eb9e00df672341779902c3c20c286054
出典メモuspto-grants-1999_03