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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073794Generated: October 25, 2026

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

https://huagongshe.com/reaction/1073794

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1,3,4-Thiadiazole, 2-amino-5-(heptylthio)-HCID 534458—
ReactantPropyl 3-hydroxy-2-methoxyprop-2-enoateHCID 71336589—
SolventChloroformHCID 6212—
Product2-heptylthio-6-methoxy-5H-1,3,4-thiadiazolo[3,2-a]pyrimidin-5-oneHCID 1561079564%

Reaction Steps

A mixture of 4.7 g of 2-amino-5-heptylthio-1,3,4-thiadiazole, 3.3 g of propyl 3-hydroxy-2-methoxy-2-propenoate and 12 g of polyphosphoric acid was heated to 130°~135° C. and stirred for 30 minutes. After cooling, water and chloroform were added to the mixture and extraction was carried out. The organic layer was washed with a sodium hydrogen carbonate aqueous solution and water respectively, 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/toluene mixture as an eluent. Thus 4.0 g of 2-heptylthio-6-methoxy-5H-1,3,4-thiadiazolo[3,2-a]pyrimidin-5-one was obtained. m.p. 68°~71° C. Yield 64%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04971971
Source datasetuspto-grants-1990_11
ORD IDord-3183bf8a420b4cbe81eb3c438a2e3056
Source noteuspto-grants-1990_11