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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1852953Generated: October 30, 2026

Hydrochloric Acid → 7-Chloroimidazo[1,2-c]pyrimidin-5-ol

https://huagongshe.com/reaction/1852953

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanethiolHCID 878—
ReactantPotassium HydroxideHCID 14797—
Reactant7-Chloro-5-(methylthio)imidazo[1,2-c]pyrimidine hydrochlorideHCID 86685296—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product7-Chloroimidazo[1,2-c]pyrimidin-5-olHCID 2132010287.5%

Reaction Steps

7-Chloro-5-(methylthio)imidazo[1,2-c]pyrimidine hydrochloride (10.5 g, 44.5 mmol) was partially dissolved in MeOH (40 mL) and then a solution of potassium hydroxide (11.2 g, 200 mmol) in water (100 mL) was slowly added and the reaction was heated to reflux. The reaction generates methane thiol, so caution was taken to contain this noxious gas in the hood. After 2 hours the reaction was cooled and then neutralized with a solution of 1N HCl to reach a pH of between 6 and 7. The reaction was filtered and the solid was washed with MeOH. The solids were dried on the filter cake and then dried on a high vacuum pump to provide 7-chloroimidazo[1,2-c]pyrimidin-5(6H)-one (6.6 g, 87% yield) as a white solid. MS (apci) m/z=170.1 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962596B2
Source datasetuspto-grants-2015_02
ORD IDord-6842477620a14f49a15ce5f184133153
Source noteuspto-grants-2015_02