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HRID 1420002作成日:2026年10月25日

Triethylamine → N-[4-(4H-Furo[2,3-e]pyrrolo[1,2-a][1,4]-diazepin-10(9H)-ylcarbonyl)phenyl]-2-methyl benzamide

https://huagongshe.com/reaction/1420002

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物4-[(2-methylbenzoyl)amino]benzoyl ChlorideHCID 10707441—
反応物9,10-Dihydro-4H-furo[2,3-e]pyrrolo[1,2-a][1,4]diazepineHCID 21836966—
溶媒DichloromethaneHCID 6344—
生成物N-[4-(4H-Furo[2,3-e]pyrrolo[1,2-a][1,4]-diazepin-10(9H)-ylcarbonyl)phenyl]-2-methyl benzamideHCID 21837211—

反応条件

温度0 °C

反応手順

To a mixture of 1.1 mmol of 4-[(2-methylbenzoyl)amino]benzoyl chloride in 10 ml of methylene chloride, cooled to 0° C. is added 1.5 mmol of triethylamine. To the mixture is added 1 mmol of 9,10-dihydro-4H-furo[2,3-e]pyrrolo[1,2-a][1,4]diazepine and the mixture stirred at room temperature for 2 hours. The reaction mixture is concentrated in vacuo and the residue is dissolved in 100 ml of ethyl acetate and washed with water, 2N citric acid, aqueous NaHCO3 and brine. The solution is dried with Na2SO4 and the volatiles concentrated in vacuo to give a solid which is purified by flash chromatography to give the desired product.

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-c593577e214a4a958805a8689975652a
出典メモuspto-grants-1999_03