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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073786Generated: October 25, 2026

Water → 2-heptanesulfonyl-6-methoxy-5H-1,3,4-thiadiazolo[3,2-a]pyrimidin-5-one

https://huagongshe.com/reaction/1073786

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-heptylthio-6-methoxy-5H-1,3,4-thiadiazolo[3,2-a]pyrimidin-5-oneHCID 15610795—
ReactantPotassium hydroxy sulfiteHCID 23707502—
SolventMethanolHCID 887—
Product2-heptanesulfonyl-6-methoxy-5H-1,3,4-thiadiazolo[3,2-a]pyrimidin-5-oneHCID 1561092751%

Reaction Conditions

Temperature65 °C

Reaction Steps

In 55 ml of methanol, 3.3 g of 2-heptylthio-6-methoxy-5H-1,3,4-thiadiazolo[3,2-a]pyrimidin-5-one was dissolved. A dispersion of 19.4 g of OXONE® suspended in 0 ml of water was added to the methanol solution, and the resulting mixture was warmed to 65° C. and stirred for 1 hour. The residue obtained by the same procedure as in Preparation Example 7 was recrystallized from ethanol and thus 2.7 g of 2-heptanesulfonyl-6-methoxy-5H-1,3,4-thiadiazolo[3,2-a]pyrimidin-5-one was obtained. m.p. 106°~109° C. Yield 51%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04971971
Source datasetuspto-grants-1990_11
ORD IDord-7f2ec57f5e2643bfaeeb66ec72aed87a
Source noteuspto-grants-1990_11