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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464667Generated: October 29, 2026

Potassium Iodide → HCID 15586425, compound

https://huagongshe.com/reaction/464667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium CarbonateHCID 10340—
Reactantp-Fluorophenyl 4-piperidyl ketone hydrochlorideHCID 3084438—
Reactant6-(2-Chloroethyl)-3,7-dimethyl-5H-[1,3]thiazolo[3,2-a]pyrimidin-5-oneHCID 13477811—
SolventWaterHCID 962—
SolventMethyl Isobutyl KetoneHCID 7909—
ProductHCID 15586425HCID 15586425—

Reaction Steps

A mixture of 3.75 parts of 6-(2-chloroethyl)-3,7-dimethyl-5H-thiazolo[3,2-a]pyrimidin-5-one, 3.6 parts of (4-fluorophenyl) (4-piperidinyl)methanone hydrochloride, 12 parts of sodium carbonate, 0.1 parts of potassium iodide and 200 parts of 4-methyl-2-pentanone was stirred and refluxed for 22 hours using a water-separator. The reaction mixture was filtered hot over Hyflo and the filtrate was evaporated. The residue was purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (90:10 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from a mixture of acetonitrile and 2,2'-oxybispropane, yielding 5 parts of 6-[2-[4-(4-fluorobenzoyl)-1-piperidinyl]ethyl]-3,7-dimethyl-5H-thiazolo[3,2-a]pyrimidin-5-one; mp. 199.7° C. (compound 4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04548938
Source datasetuspto-grants-1985_10
ORD IDord-28f6688896424f249ff4521bc5dfa5d6
Source noteuspto-grants-1985_10