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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608827Generated: October 26, 2026

4-(Trifluoromethyl)benzoyl chloride → N-[2-(1H-Imidazol-2-yl)ethyl]-2-[[4-(trifluoromethyl)-benzoyl]amino]benzamide

https://huagongshe.com/reaction/1608827

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethyl)benzoyl chlorideHCID 67607—
Reactant2-Amino-N-[2-(1H-imidazol-2-yl)ethyl]benzamideHCID 20085578—
SolventEthyl AcetateHCID 8857—
ProductN-[2-(1H-Imidazol-2-yl)ethyl]-2-[[4-(trifluoromethyl)-benzoyl]amino]benzamideHCID 2008569285.8%

Reaction Steps

The titled compound was prepared substantially in accordance with the method detailed in Example 11 using 2.00 g (0.00869 mol) of 2-amino-N-[2-(1H-imidazol-2-yl)-ethyl]benzamide, prepared as in Example 6A, and 3.62 g (0.01738 mol) of p-trifluoromethylbenzoyl chloride with the exception that removal of ethyl acetate provided a solid. This solid was recrystallized from ethyl acetate containing a small amount of methanol to provide 3.00 g of the desired titled compound (m.p. 207°-215° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05397798
Source datasetuspto-grants-1995_03
ORD IDord-e4c2ab607abe45e18466599201fa5356
Source noteuspto-grants-1995_03