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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380257Generated: October 26, 2026

Potassium Iodide → Ritanserin

https://huagongshe.com/reaction/1380257

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium CarbonateHCID 10340—
Reactant6-(2-chloroethyl)-7-methyl-5H-(1,3)thiazolo(3,2-a)pyrimidin-5-oneHCID 817872—
Reactant4-(Bis(4-fluorophenyl)methylene)piperidineHCID 2724436—
SolventWaterHCID 962—
SolventMethyl Isobutyl KetoneHCID 7909—
ProductRitanserinHCID 5074—

Reaction Steps

A mixture of 3.8 parts of 6-(2-chloroethyl)-7-methyl-5H-thiazolo[3,2-a]pyrimidin-5-one, 3.5 parts of 4-[bis(4-fluorophenyl)methylene]piperidine, 10 parts of sodium carbonate, 0.1 parts of potassium iodide and 240 parts of 4-methyl-2-pentanone was stirred and refluxed for 20 hours using a water-separator. The reaction mixture was filtered hot and the filtrate was evaporated. The residue was purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from acetonitrile, yielding 2.8 parts of 6-[2-[4-[bis(4-fluorophenyl)methylene]-1-piperidinyl]ethyl]-7-methyl-5H-thiazolo[3,2-a]pyrimidin-5-one; mp. 145.5° C. (compound 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04581171
Source datasetuspto-grants-1986_04
ORD IDord-fb0720c6e4f94a26a3ce0f2dc8593ae2
Source noteuspto-grants-1986_04