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HRID 1456154作成日:2026年10月25日

2,4-Dichlorobenzoyl chloride → Ethyl10-[4-[(2,4-dichlorobenzoyl)amino]-3-methylbenzoyl]-10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepine-3-carboxylate

https://huagongshe.com/reaction/1456154

反応式

関与物質

役割名称HCID仕込み量
反応物2,4-Dichlorobenzoyl chlorideHCID 66645—
反応物DiisopropylethylamineHCID 81531—
反応物ethyl 10,11-di-hydro-10-(4-amino-3-methylbenzoyl)-5H-pyrrolo[2,1-c][1,4]benzodiazepine-3-carboxylateHCID 21836996—
溶媒DichloromethaneHCID 6344—
生成物Ethyl10-[4-[(2,4-dichlorobenzoyl)amino]-3-methylbenzoyl]-10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepine-3-carboxylateHCID 2183701355.4%

反応手順

To a solution of 0.30 g of ethyl 10,11-dihydro-10-(4-amino-3-methylbenzoyl)-5H-pyrrolo[2,1-c][1,4]benzodiazepine-3-carboxylate in 20 ml of methylene chloride is added 0.15 g of N,N-diisopropylethylamine and 0.24 g of 2,4-dichlorobenzoyl chloride. The reaction mixture is stirred at room temperature for 18 hours and washed with water, saturated NaHCO3 and dried with Na2SO4. The organic layer is passed through a pad of hydrous magnesium silicate. Hexane is added to the filtrate at the boil to give 0.24 g of solid, m.p. 174°-184° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05843944
出典データセットuspto-grants-1998_12
ORD IDord-2229b6168d2c46a28302b7a1a7395b36
出典メモuspto-grants-1998_12