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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274722Generated: October 26, 2026

Water → 3-[3-(4-pyridylthio)propyl]quinazoline-2,4(1H,3H)-dione

https://huagongshe.com/reaction/274722

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantQuinazolinedioneHCID 64048—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant4-[(3-Chloropropyl)sulfanyl]pyridineHCID 15816984—
SolventDimethylformamideHCID 6228—
Product3-[3-(4-pyridylthio)propyl]quinazoline-2,4(1H,3H)-dioneHCID 1907909231.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 1.62 g (10 mmol) of benzoylene urea and 1.88 g (10 mmol) of 4-(3-chloropropylthio)pyridine in 50 ml of dimethylformamide, 1.65 ml (11 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 column chromatography (eluent: ethyl acetate/ethanol=25:1 to 10:1 to 2:1). First, 0.973 g of 3-[3-(4-pyridylthio)propyl]quinazoline-2,4-(1H,3H)-dione (31.1% yield, pale yellow crystals) was obtained, and then, 0.487 of the desired product was obtained (10.4% yield, yellow oil).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05389658
Source datasetuspto-grants-1995_02
ORD IDord-c1a66e78774b4757adf3b1f2bf316a4b
Source noteuspto-grants-1995_02