Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754119Generated: October 28, 2026

Hydrochloric Acid → HCID 86690341, compound

https://huagongshe.com/reaction/1754119

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-(3-(Trifluoromethyl)phenyl)piperazineHCID 4296—
ReactantSodium IodideHCID 5238—
ReactantSodium CarbonateHCID 10340—
Reactant3-(2-Chloroethyl)quinazolin-4(3H)-oneHCID 4518743—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
SolventIsopropanolHCID 3776—
ProductHCID 86690341HCID 8669034169%

Reaction Steps

The following were added to a 250 mL reactor: 3-(2-chloroethyl) quinazoline-4(3H)-one (1 g, 4.79 mmol), 1-(3-(trifluoromethyl)phenyl)piperazine (1,103 g, 4.79 mmol), sodium carbonate (0.762 g, 7.19 mmol), sodium iodide (0.072 g, 0.479 mmol), ethanol (50 ml) and toluene (150 ml). The reaction medium was kept under agitation and reflux for a period of twenty hours, during which 150 ml of the solvent were removed slowly with the assistance of a Dean-Stark. To the resulting mixture, 100 mL of an aqueous solution of acetic acid were added at 10% and 150 mL of ethyl acetate. The mixture was agitated, the organic phase separated, washed with 2 portions of 50 mL of a 5% sodium bicarbonate solution, dry with MgSO4, filtered and evaporated to dryness, yielding the raw product as a slightly yellowish oil. This oil was dissolved in isopropanol, adding 2 mL of concentrated HCl under agitation to the resulting solution. This agitation was maintained for two hours in order to complete the precipitation of the hydrochloride. The resulting solid was filtered and vacuum dried, yielding 1.45 g of 3-(2-(4-(3-(trifluoromethyl)phenyl)piperazine-1-yl)ethyl)quinazoline-4(3H)-one hydrochloride (3.3 mmol, yield=69%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169218B2
Source datasetuspto-grants-2015_10
ORD IDord-e86d929a616748c5bb7242cf38c87025
Source noteuspto-grants-2015_10