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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 978447Generated: October 29, 2026

Potassium Iodide → 3-[2-[4-[2-(4-fluorophenyl)-1,3-dioxolan-2-yl]-1-piperidinyl]ethyl]-6-nitro-2,4(1H,3H)-quinazolinedione

https://huagongshe.com/reaction/978447

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium BicarbonateHCID 516892—
Reactant2-(4-Fluorophenyl)-2-(4-piperidyl)1,3-dioxolaneHCID 13279099—
Reactant3-(2-chloroethyl)-6-nitro-2,4(1H,3H)-quinazolinedioneHCID 13851201—
SolventDimethylformamideHCID 6228—
Product3-[2-[4-[2-(4-fluorophenyl)-1,3-dioxolan-2-yl]-1-piperidinyl]ethyl]-6-nitro-2,4(1H,3H)-quinazolinedioneHCID 1385117664%

Reaction Steps

A mixture of 16.2 parts of 3-(2-chloroethyl)-6-nitro-2,4(1H,3H)-quinazolinedione, 15 parts of 4-[2-(4-fluorophenyl)-1,3-dioxolan-2-yl]piperidine, 10 parts of sodium hydrogen carbonate, 0.1 parts of potassium iodide and 135 parts of N,N-dimethylformamide was stirred and heated overnight at 100°-120° C. The reaction mixture was cooled and poured onto water. Stirring was continued till complete precipitation. The precipitate was filtered off and dissolved in trichloromethane. The thus formed emulsion was dried, filtered and evaporated. The residue was crystallized from acetonitrile, yielding 18.6 parts (64%) of 3-[2-[4-[2-(4-fluorophenyl)-1,3-dioxolan-2-yl]-1-piperidinyl]ethyl]-6-nitro-2,4(1H,3H)-quinazolinedione; mp. 250.9° C. (28).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04665075
Source datasetuspto-grants-1987_05
ORD IDord-43552f0949b54fb39d4a1931feba9fd7
Source noteuspto-grants-1987_05