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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464668Generated: October 30, 2026

Potassium Iodide → 6-(2-(4-(1H-Indol-3-yl)piperidin-1-yl)ethyl)-3,7-dimethyl-5H-thiazolo(3,2-a)pyrimidin-5-one

https://huagongshe.com/reaction/464668

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium CarbonateHCID 10340—
Reactant3-(4-Piperidinyl)-1H-indoleHCID 702235—
Reactant6-(2-Chloroethyl)-3,7-dimethyl-5H-[1,3]thiazolo[3,2-a]pyrimidin-5-oneHCID 13477811—
SolventWaterHCID 962—
SolventMethyl Isobutyl KetoneHCID 7909—
Product6-(2-(4-(1H-Indol-3-yl)piperidin-1-yl)ethyl)-3,7-dimethyl-5H-thiazolo(3,2-a)pyrimidin-5-oneHCID 3086107—

Reaction Steps

A mixture of 3.75 parts of 6-(2-chloroethyl)-3,7-dimethyl-5H-thiazolo[3,2-a]pyrimidin-5-one, 3 parts of 3- (4-piperidinyl)-1H-indole, 10 parts of sodium carbonate, 0.1 parts of potassium iodide and 200 parts of 4-methyl-2-pentanone was stirred and refluxed for 20 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 ethanol, yielding 3.25 parts of 6-[2-[4-(1H-indol-3-yl)-1-piperidinyl]ethyl]-3,7-dimethyl-5H-thiazolo[3,2-a]pyrimidin-5-one; mp. 274.7° C. (compound 11).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04548938
Source datasetuspto-grants-1985_10
ORD IDord-345ab0ed5b5e448381b797ec8ce872ed
Source noteuspto-grants-1985_10