Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 864023Generated: October 30, 2026

Water → 1,3-bis[4-(4-pyridylthio)butyl]-quinazoline-2(1H)-thion-4(3H)-one dihydrochloride

https://huagongshe.com/reaction/864023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-(4-Chlorobutylthio)pyridineHCID 15816978—
Reactant3-[4-(4-pyridylthio)butyl]quinazoline-2(1H)-thion-4(3H)-oneHCID 131718180—
SolventDimethylformamideHCID 6228—
Product1,3-bis[4-(4-pyridylthio)butyl]-quinazoline-2(1H)-thion-4(3H)-one dihydrochlorideHCID 13171958897.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 515 mg (1.5 mmol) of 3-[4-(4-pyridylthio)butyl]quinazoline-2(1H)-thion-4(3H)-one and 332 mg (1.65 mmol) of 4-(4-chlorobutylthio)pyridine in 15 ml of dimethylformamide, 0.25 ml (1.65 mmol) of 1,8-diazabicyclo-[5.4.0]-7-undecene was added, and the mixture was stirred at 80° C. for 16 hours. After cooling, water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was dried and the solvent was distilled off. The residue was purified by flash column chromatography (eluent:ethyl acetate/ethanol=25:1 to 10:1) to give 0.694 mg of the desired product (97.1% yield; colorless oil).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05561147
Source datasetuspto-grants-1996_10
ORD IDord-43f3b7e8591547a3b4498cb7e3d86257
Source noteuspto-grants-1996_10