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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1752796Generated: October 28, 2026

3,5-Heptanedione → 5,7-Diethyl-2-(methylsulfanyl)-[1,2,4]triazolo[1,5-a]pyrimidine

https://huagongshe.com/reaction/1752796

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-HeptanedioneHCID 81923—
ReactantHCID 178503514HCID 178503514—
SolventAcetic AcidHCID 176—
Product5,7-Diethyl-2-(methylsulfanyl)-[1,2,4]triazolo[1,5-a]pyrimidineHCID 8671931988%

Reaction Conditions

Temperature135 °C

Reaction Steps

A mixture of 3,5-heptanedione (9.85 g, 76.8 mmol), 3-amino-5-methylthio-1H-1,2,4-triazole (10.0 g, 76.8 mmol), and glacial acetic acid (60 mL) was added to a 200 mL RBF with a magnetic stirring bar. The flask was fitted with a condenser, and warmed in an oil bath to a gentle reflux at 135° C. The mixture was heated for 24 hours. Progress of the reaction was monitored by analytical HPLC with UV detection at 215 and 254 nm. The starting material 3-amino-5-methylthio-1H-1,2,4-triazole eluted rapidly with retention time of 0.7 min, and the product eluted with retention time of 4.7 min. The mixture was cooled to room temperature, then slowly poured into stirring ice/water (800 mL) to precipitate product and stirred ˜20 minutes. Solids were isolated by filtration, rinsed with water (200 mL), and then dried under reduced pressure to afford the title compound as a powder (15.0 g, 88% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09163027B2
Source datasetuspto-grants-2015_10
ORD IDord-0731c6b706e34c9b8bfd0845c401823c
Source noteuspto-grants-2015_10