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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2302259Generated: November 3, 2026

4-(Trifluoromethyl)benzoyl chloride → HCID 22057983, compound

https://huagongshe.com/reaction/2302259

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethyl)benzoyl chlorideHCID 67607—
ReactantHCID 22057974HCID 22057974—
SolventTriethylamineHCID 8471—
ProductHCID 22057983HCID 2205798352%

Reaction Steps

Using an analogous procedure to that described in Example 4, 4-trifluoromethylbenzoyl chloride was reacted with N-(5-amino-2methylphenyl)-quinoline-6-carboxamide in the presence of triethylamine. The reaction mixture was stirred at ambient temperature for 18 hours and then evaporated. The residue was purified by column chromatography on silica using increasingly polar mixtures of methylene chloride and methanol as eluent. There was thus obtained the title compound in 52% yield; Mass Spectrum: M+H+ 450.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06432949B1
Source datasetuspto-grants-2002_08
ORD IDord-c86fb135c71f45c886efa84ebd057889
Source noteuspto-grants-2002_08