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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703829Generated: October 30, 2026

Phosphorus oxychloride → 2-benzylthio-7-chloro-6-methyl-5H-1,3,4-thiadiazolo[3,2-a]pyrimidin-5-one

https://huagongshe.com/reaction/703829

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantPhosphorus pentachlorideHCID 24819—
Reactant2-benzylthio-7-hydroxy-6-methyl-5H-1,3,4-thiadiazolo[3,2-a]pyrimidin-5-oneHCID 136087661—
Product2-benzylthio-7-chloro-6-methyl-5H-1,3,4-thiadiazolo[3,2-a]pyrimidin-5-oneHCID 1425442272%

Reaction Steps

A mixture of 18.3 g of the thus obtained 2-benzylthio-7-hydroxy-6-methyl-5H-1,3,4-thiadiazolo[3,2-a]pyrimidin-5-one, 13.1 g of phosphorus pentachloride and 36.8 g phosphorus oxychloride was stirred at 85°-95° C. for 1.5 hours. Thereafter, the reaction mixture was concentrated under reduced pressure, and the residue was dissolved in toluene. The organic layer was washed with an aqueous potassium carbonate solution and water respectively, and dried over anhydrous sodium sulfate. The solvent was distilled off and the residue was purified by silica gel column chromatography using an ethyl acetate/toluene (3:7) mixture as an eluent. Then the solvent was distilled off, and thus 14.0 g of 2-benzylthio-7chloro-6-methyl-5H-1,3,4-thiadiazolo[3,2-a]pyrimidin-5-one was obtained m.p. 102°-104° C. Yield 72%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04985432
Source datasetuspto-grants-1991_01
ORD IDord-352a7c52424345b4b34d54ac87522b3c
Source noteuspto-grants-1991_01