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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607546Generated: October 31, 2026

Chlorobenzene → 2-hexylthio-7-hydroxy-5H-1,3,4-thiadiazolo[3,2-a]pyrimidin-5-one

https://huagongshe.com/reaction/1607546

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorobenzeneHCID 7964—
ReactantSbb043676HCID 1579472—
ReactantBis(2,4,6-trichlorophenyl) propanedioateHCID 2783450—
SolventHexaneHCID 8058—
Product2-hexylthio-7-hydroxy-5H-1,3,4-thiadiazolo[3,2-a]pyrimidin-5-oneHCID 13596748787%

Reaction Steps

A mixture of 65.2 g of the thus obtained 2-amino-5-hexylthio-1,3,4-thiadiazole, 141.7 g of bis(2,4,6-trichlorophenyl) malonate and 240 ml of chlorobenzene was heated to 137°~140° C. and stirred for 1 hour. After cooling, hexane was added to the mixture, and the formed precipitate was separated by filtration, the residue was washed with hexane, and thus 74.7 g of 2-hexylthio-7-hydroxy-5H-1,3,4-thiadiazolo[3,2-a]pyrimidin-5-one was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04866064
Source datasetuspto-grants-1989_09
ORD IDord-a7c0aa6fb7ac444bbf7d29dbd6848f2b
Source noteuspto-grants-1989_09