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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 580517Generated: November 2, 2026

3-(Trifluoromethyl)benzoic acid → HCID 14232986, compound

https://huagongshe.com/reaction/580517

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)benzoic acidHCID 9963—
ReactantThionyl ChlorideHCID 24386—
Reactant3,4-DiaminoquinolineHCID 1514289—
SolventAcetonitrileHCID 6342—
SolventHexamethylphosphoramideHCID 12679—
SolventSodium BicarbonateHCID 516892—
ProductHCID 14232986HCID 1423298698.6%

Reaction Steps

To a solution of 500 mg of 3-trifluoromethylbenzoic acid in 6 ml of anhydrous hexamethylphosphoramide (HMPA) and 0.6 ml of anhydrous acetonitrile is added dropwise 305 mg of thionyl chloride at -5°-0° C. under nitrogen. After stirring at the same temperature for 30 minutes, 380 mg of 3,4-diaminoquinoline is added and stirred at 0°-5° C. for 3 hours. The mixture is diluted with ice-water and neutralized with saturated aqueous sodium bicarbonate. The resulting crystals are filtered, washed with water, and dried to give 780 mg of 4-amino-3-(3-trifluoromethylbenzoylamino)quinoline B1 as a crude product. It is suspended in 15 g of polyphosphoric acid and heated at 120° C. for 4 hours with stirring. The mixture is poured into ice-water and neutralized with 1N sodium hydroxide. The resulting solid is filtered, washed with water and dried. It is chromatographed on silica gel with chloroform-methanol (10:1 v/v) as eluent, yielding 350 mg (47%) of C1 as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04753951
Source datasetuspto-grants-1988_06
ORD IDord-8b117dd8b5d44f5fb8586032ee787adf
Source noteuspto-grants-1988_06