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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1740037Generated: November 1, 2026

Triethylamine → alpha-Chloro-N-[4-(5H-pyrrolo[2,1-c][1,4)benzodiazepin-10(11H)-ylcarbonyl)phenyl]benzeneacetamide

https://huagongshe.com/reaction/1740037

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantChloro(phenyl)acetyl chlorideHCID 102902—
Reactant1H-1,4-BenzodiazepineHCID 148431—
ReactantSodium BicarbonateHCID 516892—
SolventDichloromethaneHCID 6344—
Productalpha-Chloro-N-[4-(5H-pyrrolo[2,1-c][1,4)benzodiazepin-10(11H)-ylcarbonyl)phenyl]benzeneacetamideHCID 21837022—

Reaction Steps

To a solution of 0.61 g of 10,11-dihydro-10(4-aminobenzoyl)-5H-pyrrolo][2,1-c][1,4]benzodiazepine in 8 ml of methylene chloride is added 0.30 g of triethylamine followed by 0.47 g of (±)-2-chloro-2-phenylacetyl chloride in 2 ml of methylene chloride. The mixture is stirred at room temperature for 1 hour and then diluted with 10 ml of 50% NaHCO3. The methylene chloride is evaporated and the residue is extracted with ethyl acetate. The separated organic layer is washed with saturated NaHCO3 and brine and then dried with Na2SO4 followed by filtering through a pad of hydrous magnesium silicate. The filtrate is evaporated to a residue which is stirred with ether-hexane to give 0.98 g of pink solid. MS(CI): 456(M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05968930
Source datasetuspto-grants-1999_10
ORD IDord-9d05f96b86874db6be62f90be2669f62
Source noteuspto-grants-1999_10