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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1863010Generated: October 30, 2026

Triethylamine → HCID 13544850, compound

https://huagongshe.com/reaction/1863010

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Chloro-2-methylthiopyrimidineHCID 97113—
Reactant1-Piperazinyl(4-((7-(trifluoromethyl)-4-quinolinyl)amino)phenyl)methanoneHCID 3055243—
SolventEthanolHCID 702—
ProductHCID 13544850HCID 1354485026.8%

Reaction Steps

A mixture of 1.50 g (0.0037 mol) of 4-[4-[[7-(trifluoromethyl)-4-quinolinyl]amino]benzoyl]piperazine [U.S. Pat. No. 4,025,629], 0.44 ml (0.00375 mol) of 4-chloro-2-methylthiopyrimidine, 0.52 ml (0.00375 mol) of triethylamine, and 125 ml of ethanol is stirred at reflux for 3 hours. After cooling, the ethanol is removed in vacuo and the residue is stirred with methylene chloride and aqueous sodium bicarbonate. The resultant solid is collected and washed with water and ether. Crystallization from methanol-chloroform gives 0.52 g (26%) of 1-[2-(methylthio)-4-pyrimidinyl]-4-[4-[[7-(trifluoromethyl)-4-quinolinyl]amino]benzoyl]piperazine, of melting point 166°-267° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04167567
Source datasetuspto-grants-1979_09
ORD IDord-dedc21b8eed34e128e56795b9a8b0b05
Source noteuspto-grants-1979_09