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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 838948Generated: October 31, 2026

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

https://huagongshe.com/reaction/838948

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2-[4-(4-Chlorophenyl)piperazin-1-yl]ethanolHCID 258211—
ReactantMethyl 3-(8-trifluoromethyl-4-quinolylamino)-2-thiophene-carboxylateHCID 15916787—
SolventTolueneHCID 1140—
Product2-[4-(4-Chlorophenyl)-1-piperazinyl]-ethyl 3-(8-trifluoromethyl 4-quinolylamino)-2-thiophene-carboxylateHCID 2032546676.7%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 7.04 g of methyl 3-(8-trifluoromethyl-4-quinolylamino)-2-thiophene-carboxylate, 5.5 g of 4-(4-chlorophenyl)-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 after cooling the mixture to 60° C, 150 ml of sodium hydride were added. The mixture was refluxed with stirring for 16 hours and the toluene was distilled. The residue was extracted with methylene chloride, was washed and dried. The product was crystallized from 95% ethanol, iced and vacuum filtered. The precipitate was washed with ethanol and dried to obtain 8.6 g of 2-[4-(4-chlorophenyl)-1-piperazinyl]-ethyl 3-(8-trifluoromethyl 4-quinolylamino)-2-thiophene-carboxylate melting at 155° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04093724
Source datasetuspto-grants-1978_06
ORD IDord-cdb6d4f942434e97a4b5e05c05f13702
Source noteuspto-grants-1978_06