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HRID 1419986作成日:2026年10月25日

2-Methylbenzoyl chloride → N-[4-(5H-Pyrrolo[2,1-c][1,4]benzodiazepin-10(11H)ylcarbonyl)-2-methylphenyl]-2-methylbenzamide

https://huagongshe.com/reaction/1419986

反応式

関与物質

役割名称HCID仕込み量
反応物2-Methylbenzoyl chlorideHCID 70276—
反応物DiisopropylethylamineHCID 81531—
反応物10,11-Dihydro-10-(4-amino-3-methylbenzoyl)-5H-Pyrrolo[2,1-c][1,4]benzodiazepineHCID 10686975—
溶媒DichloromethaneHCID 6344—
生成物N-[4-(5H-Pyrrolo[2,1-c][1,4]benzodiazepin-10(11H)ylcarbonyl)-2-methylphenyl]-2-methylbenzamideHCID 2183716665.9%

反応手順

A solution of 0.83 g of 10,11-dihydro-10-(4-amino-3-methylbenzoyl)-5H-pyrrolo[2,1-c][1,4]benzodiazepine, 0.5 g of N,N-diisopropylethylamine and 0.6 g of 2-methylbenzoyl chloride in 50 ml of methylene chloride is stirred at room temperature for 18 hours. The reaction mixture is washed with water, the organic layer dried with Na2SO4 and passed through a pad of hydrous magnesium silicate. Hexane is added at the boil to give 0.75 g of a solid which is crystallized from methylene chloride-hexane to give 0.61 g of the desired product, m.p. 125°-130° C.

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-cf15231f1bdc410d84338e2178f8879b
出典メモuspto-grants-1999_03