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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1084545Generated: October 31, 2026

Triethylamine → N-[5-(2-Fluoro-phenyl)-2-oxo-2,3-dihydro-1H-benzo[e][1,4]diazepin-3-yl]-4-trifluoromethyl-benzamide

https://huagongshe.com/reaction/1084545

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-(Trifluoromethyl)benzoyl chlorideHCID 67607—
Reactant1,3-dihydro-5-(2-fluorophenyl)-3-amino-2H-1,4-benzodiazepin-2-oneHCID 15637150—
SolventDichloromethaneHCID 6344—
ProductN-[5-(2-Fluoro-phenyl)-2-oxo-2,3-dihydro-1H-benzo[e][1,4]diazepin-3-yl]-4-trifluoromethyl-benzamideHCID 14208248—

Reaction Steps

1,3-Dihydro-3-(RS)-amino-5-(2-fluorophenyl)-2H-1,4-benzodiazepin-2-one (42 mg, 0.156 mmole) and p-trifluoromethylbenzoyl chloride (32.5 mg, 0.156 mmole) were combined in 3 ml of methylene chloride (CH2Cl2), treated with triethylamine (0.0157 g, 0.156 mmole) and stirred at room temperature 15 minutes. The mixture was diluted with CH2Cl2 (20 ml), washed with 10% citric acid (2×5 ml), dilute sodium bicarbonate (2×5 ml), and water (2×5 ml), dried over sodium sulfate, filtered, and evaporated to dryness in vacuo. The residue was crystallized from ethyl acetate (0.4 ml)/ether (1 ml) to give the title compound which was dried in vacuo at 90°: (m.p. 209°-211°).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05004741
Source datasetuspto-grants-1991_04
ORD IDord-63bbaf22f53a4bb79ff1bd8d589f5792
Source noteuspto-grants-1991_04