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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 224594Generated: October 25, 2026

4-(3-(Trifluoromethyl)phenyl)-1-piperazineethanol → Ethyl 2-(8-trifluoromethyl-4-quinolinylamino)-5-fluorobenzoate

https://huagongshe.com/reaction/224594

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(3-(Trifluoromethyl)phenyl)-1-piperazineethanolHCID 217994—
ReactantMethyl 2-(8-trifluoromethyl-4-quinolinylamino)-5-fluoro-benzoateHCID 23331699—
ProductEthyl 2-(8-trifluoromethyl-4-quinolinylamino)-5-fluorobenzoateHCID 86737324—

Reaction Steps

Using the procedure of Example 13, methyl 2-(8-trifluoromethyl-4-quinolinylamino)-5-fluoro-benzoate and 2-[-4-(3-trifluoromethylphenyl)-piperazin-1-yl]-ethanol were reacted to obtain 2-[4-3-trifluoromethylphenyl)-piperazin-1-yl]-ethyl 2-(8-trifluoromethyl-4-quinolinylamino)-5-fluorobenzoate. The said product was dissolved in absolute ethanol and an ethanolic solution of hydrogen chloride was added thereto followed by anhydrous ether. The mixture crystallized was vacuum filtered and the product was washed with anhydrous ether and was dried to form the desired hydrochloride salt melting at 230°-240° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04233305
Source datasetuspto-grants-1980_11
ORD IDord-6cb0733c43ea4c23ba30073be53b3ff7
Source noteuspto-grants-1980_11