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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1735242Generated: October 25, 2026

Triethylamine → N-[5-(5H-Pyrrolo[2,1-c][1,4]benzodiazepin-10(11H)ylcarbonyl)-2-pyridinyl]-2-methylbenzeneacetamide

https://huagongshe.com/reaction/1735242

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanto-Tolyl-acetyl chlorideHCID 2760632—
Reactant10, 11-dihydro-10-(6-amino-3-pyridinylcarbonyl)-5H-pyrrolo[2,1-c][1,4]benzodiazepineHCID 18917501—
SolventDichloromethaneHCID 6344—
ProductN-[5-(5H-Pyrrolo[2,1-c][1,4]benzodiazepin-10(11H)ylcarbonyl)-2-pyridinyl]-2-methylbenzeneacetamideHCID 18917528—

Reaction Steps

A mixture of 2.0 mmol of 10, 11-dihydro-10-(6-amino-3-pyridinylcarbonyl)-5H-pyrrolo[2,1-c][1,4]benzodiazepine, 2.1 mmol of 2-methylbenzeneacetyl chloride and 5 mmol of triethylamine in 10 ml of dichloromethane is stirred under argon at room temperature for 16 hours. The solvent is removed under vacuum and the residue partitioned between 50 ml of ethyl acetate and 25 ml of water. The organic layer is separated, washed with H2O, 1N NaHCO3, brine and dried (Na2SO4). The solvent is removed and the residue chromatographed on silica gel with ethyl acetate-hexane as solvent to give the product as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05536718
Source datasetuspto-grants-1996_07
ORD IDord-fa9ad543ba63442b81d2d3bbf3850ef4
Source noteuspto-grants-1996_07