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HRID 3521作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/3521

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 Na2 SO4 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US05733905
出典データセットuspto-grants-1998_03
ORD IDord-e07587b1de2c4d5a8150e75521845099
出典メモuspto-grants-1998_03