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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 247028Generated: October 31, 2026

Hydrochloric Acid → 1-[3-{4-(diphenylmethyl)piperazin-1-yl}propyl]-3-methyl-2,4(1H,3H)quinazolinedione

https://huagongshe.com/reaction/247028

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
ReactantBenzhydrylpiperazineHCID 70048—
Reactant1-(3-bromopropyl)-3-methyl-2,4(1H)-quinazolinedioneHCID 13687208—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1-[3-{4-(diphenylmethyl)piperazin-1-yl}propyl]-3-methyl-2,4(1H,3H)quinazolinedioneHCID 13488385—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 1-(3-bromopropyl)-3-methyl-2,4(1H, 3H)-quinazolinedione (1.68 g), 1-diphenylmethylpiperazine (1.56 g), anhydrous potassium carbonate (2.33 g) and N,N-dimethylformamide (8 ml) was stirred for 3 hours at 60° C. After cooling, water was added to the reaction mixture and then the mixture was extracted twice with chloroform. The chloroform layer was washed with water and with saturated sodium chloride aqueous solution respectively, dried over anhydrous magnesium sulfate and evaporated in vacuo to give an oily residue. This oily residue was dissolved in methanol and then conc.hydrochloric acid solution was dropwise added to the solution to give a crystal, which was collected by filtration, washed with water and dried. This crude crystal was recrystallized from a mixture of methanol and water to give 1-[3-{4-(diphenylmethyl)-piperazin-1-yl}propyl]-3-methyl-2,4(1H, 3H)-quinazolinedione.2HCl.0.5H20 (2.4 g). m.p. 250°-253° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04705787
Source datasetuspto-grants-1987_11
ORD IDord-cd848dfa8db84ac59852d49f3a23ae31
Source noteuspto-grants-1987_11