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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3,5-Heptanedione | HCID 81923 | — |
| Reactant | HCID 178503514 | HCID 178503514 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 5,7-Diethyl-2-(methylsulfanyl)-[1,2,4]triazolo[1,5-a]pyrimidine | HCID 86719319 | 88% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09163027B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-0731c6b706e34c9b8bfd0845c401823c |
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| Source note | uspto-grants-2015_10 |
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