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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 838947Generated: October 26, 2026

Sodium hydride → 2-[4-(3-Trifluoromethylphenyl)-1-piperazinyl]-ethyl 3-(8-trifluoromethyl-4-quinolylamino)-2-thiophene-carboxylate

https://huagongshe.com/reaction/838947

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant4-(3-(Trifluoromethyl)phenyl)-1-piperazineethanolHCID 217994—
ReactantMethyl 3-(8-trifluoromethyl-4-quinolylamino)-2-thiophene-carboxylateHCID 15916787—
SolventTolueneHCID 1140—
Product2-[4-(3-Trifluoromethylphenyl)-1-piperazinyl]-ethyl 3-(8-trifluoromethyl-4-quinolylamino)-2-thiophene-carboxylateHCID 2032547292.3%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 7 g of methyl 3-(8-trifluoromethyl-4-quinolylamino)-2-thiophene-carboxylate, 6.17 g of 4-(3-trifluoromethylphenyl)-1-piperazine-ethanol and 50 ml of anhydrous toluene was refluxed for an hour while passing condensed toluene through a column filled with siliporite and the mixture was cooled to 60° C. 150 mg of sodium hydride were added and the mixture was refluxed with stirring for 10 hours. The toluene was distilled and the residue was extracted with ether, washed with water and dried. The product was crystallized from methylene chloride to obtain 10.9 g of 2-[4-(3-trifluoromethylphenyl)-1-piperazinyl]-ethyl 3-(8-trifluoromethyl-4-quinolylamino)-2-thiophene-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04093724
Source datasetuspto-grants-1978_06
ORD IDord-205c3ad1d60c43f0b14cf8a091ab813a
Source noteuspto-grants-1978_06