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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2198487Generated: October 27, 2026

Dimethylformamide → N-(1-Ethyl-3-piperidyl)-4-(8-trifluoromethyl-4-quinolylamino)benzamide

https://huagongshe.com/reaction/2198487

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium CarbonateHCID 10340—
Reactant3-amino-N-ethylpiperidineHCID 98094—
Reactant4-(8-Trifluoromethyl-4-quinolylamino)benzoic acid hydrochloride monohydrateHCID 70545502—
CatalystThionyl ChlorideHCID 24386—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
ProductN-(1-Ethyl-3-piperidyl)-4-(8-trifluoromethyl-4-quinolylamino)benzamideHCID 2052013937%

Reaction Steps

11.6 Grams (0.03 mole) of 4-(8-trifluoromethyl-4-quinolylamino)benzoic acid hydrochloride monohydrate were refluxed in thionyl chloride containing a few drops of dimethyl formamide for one hour. The thionyl chloride was evaporated and 50 milliliters of benzene were added and evaporated. The resulting acid chloride hydrochloride was added in portions with stirring to a cooled mixture of 3.84 grams (0.03 mole) of 3-amino-1-ethylpiperidine in 80 milliliters of chloroform and 31.8 grams (0.3 mole) of sodium carbonate in 100 milliliters of water. The product began to precipitate almost at once, and the mixture was stirred vigorously for two hours, and allowed to stand overnight. Filtration gave a solid which was stirred in water, collected and dried. The resulting solid was dissolved in an ethanol:chloroform mixture and chromatographed on an alumine column made up in chloroform. Elution with chloroform gave 4.9 grams (37%) of title compound as a pale yellow solid, melting point 177°-178° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04357333
Source datasetuspto-grants-1982_11
ORD IDord-3328dc48c13a419da6dfce9ddbcfcab7
Source noteuspto-grants-1982_11