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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703835Generated: October 30, 2026

Phosphorus oxychloride → 2-benzylthio-7-chloro-5H-1,3,4-thiadiazolo[3,2-a]pyrimidin-5-one

https://huagongshe.com/reaction/703835

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantPhosphorus pentachlorideHCID 24819—
Reactant2-(Benzylthio)-7-hydroxy-5H-1,3,4-thiadiazolo(3,2-a)pyrimidin-5-oneHCID 135594371—
Product2-benzylthio-7-chloro-5H-1,3,4-thiadiazolo[3,2-a]pyrimidin-5-oneHCID 1425442425%

Reaction Steps

A mixture of 31.7 g of the thus obtained 2-benzylthio-7-hydroxy-5H-1,3,4-thiadiazolo[3,2-a]-pyrimidin-5-one, 24.0 g of phosphorus pentachloride and 117 g of phosphorus oxychloride was heated to 70°-80° C. and stirred for 25 minutes. After cooling, the reaction mixture was concentrated under reduced pressure and chloroform and water were added to the residue. The organic layer was washed with an aqueous sodium hydrogen carbonate solution and water, and dried over anhydrous sodium sulfate. The solvent was distilled off and the residue was separated by silica gel column chromatography using an ethyl acetate/hexane mixture as an eluent, and thus 8.5 g of 2-benzylthio-7-chloro-5H-1,3,4-thiadiazolo[3,2-a]pyrimidin-5-one was obtained. m.p. 138°-140° C. Yield 25%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04985432
Source datasetuspto-grants-1991_01
ORD IDord-184e950f863a4ecca58f75b2a2f93a6a
Source noteuspto-grants-1991_01