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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1459499Generated: October 25, 2026

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

https://huagongshe.com/reaction/1459499

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methylbenzoyl chlorideHCID 70276—
ReactantDiisopropylethylamineHCID 81531—
Reactant10,11-Dihydro-10-(4-amino-3-methylbenzoyl)-5H-Pyrrolo[2,1-c][1,4]benzodiazepineHCID 10686975—
SolventDichloromethaneHCID 6344—
ProductN-[4-(5H-Pyrrolo[2,1-c][1,4]benzodiazepin-10(11H)ylcarbonyl)-2-methylphenyl]-2-methylbenzamideHCID 2183716665.9%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05854237
Source datasetuspto-grants-1998_12
ORD IDord-1094e52d93dd4211bec731b16b037a5a
Source noteuspto-grants-1998_12