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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1252094Generated: November 3, 2026

Water → HCID 14100783, compound

https://huagongshe.com/reaction/1252094

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHCID 14208916HCID 14208916—
ReactantPotassium hydroxy sulfiteHCID 23707502—
SolventMethanolHCID 887—
ProductHCID 14100783HCID 1410078349%

Reaction Conditions

Temperature60 °C

Reaction Steps

In 240 ml of methanol, 6.3 g of 2-benzylthio-6-ethoxycarbonyl-5H-1,3,4-thiadiazolo[3,2-a]pyrimidin-5-one was dissolved. A suspension of 27.7 g of OXONE® dispersed in 110 ml of water was added to the methanol solution. The mixture was stirred at 60° C. for 2 hours, and was extracted with chloroform after cooling. The organic layer was washed with a sodium thiosulfate solution and water respectively and dried over anhydrous sodium sulfate. The solvent was distilled off. The residue was recrystallized from an acetonitrile/isopropylether (2:1) mixture and 3.3 g of 2-benzylsulfonyl-6-ethoxycarbonyl-5H-1,3,4-thiadiazolo[3,2-a]pyrimidin-5-one was obtained. m.p. 200°-203° C. Yield 49%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04742063
Source datasetuspto-grants-1988_05
ORD IDord-4e010cde2b5244c8ab5f0db36b0a9d0d
Source noteuspto-grants-1988_05