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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354874Generated: October 30, 2026

Hexane → 4H-pyrimido[1,2-c]quinazoline-4-one

https://huagongshe.com/reaction/354874

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantEthyl AcetateHCID 8857—
Reactant2,2-Dimethyl-5-[(4-quinazolinyl)amino]methylene-1,3-dioxane-4,6-dioneHCID 13060518—
SolventDiphenyl EtherHCID 7583—
Product4H-pyrimido[1,2-c]quinazoline-4-oneHCID 1306057069.4%

Reaction Steps

A mixture of 2,2-dimethyl-5-[(4-quinazolinyl)amino]methylene-1,3-dioxane-4,6-dione (3.5 g) in diphenylether (15 ml) was stirred for 10 minutes at 250°-260° C. and then cooled to ambient temperature. To the reaction mixture was added hexane and allowed to to stand at ambient temperature to give crystals, which were separated by filtration and washed with hexane to give crude crystals (3 g). The crude crystals were subjected to a column chromatography using silica gel (developing solvent: a mixture of ethyl acetate and hexane (3:7)). The eluate was concentrated under reduced pressure to give crystals, which were recrystallized from chloroform and hexane to give 4H-pyrimido[1,2-c]quinazoline-4-one (1.6 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04377580
Source datasetuspto-grants-1983_03
ORD IDord-da56535d6c40405bb8c1363e0f6181e7
Source noteuspto-grants-1983_03