HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorobenzene → 2-heptylthio-7-hydroxy-6-methyl-5H-1,3,4-thiadiazolo[3,2-a]pyrimidin-5-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorobenzene | HCID 7964 | — |
| Reactant | 1,3,4-Thiadiazole, 2-amino-5-(heptylthio)- | HCID 534458 | — |
| Reactant | Bis(2,4,6-trichlorophenyl) methylpropanedioate | HCID 12320374 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 2-heptylthio-7-hydroxy-6-methyl-5H-1,3,4-thiadiazolo[3,2-a]pyrimidin-5-one | HCID 136120198 | 78% |
Reaction Steps
A mixture of 19.7 g of the thus obtained 2-amino-5-heptylthio-1,3,4-thiadiazole, 40.9 g of bis (2,4,6-trichlorophenyl) 2-methyl-malonate and 55 ml of chlorobenzene was stirred at 140°~144° C. for 45 minutes. After cooling, n-hexane was added thereto, the precipitate was collected by filtration. Further n-hexane was added to the filtrate, and the precipitate was collected. The collected precipitates were combined. The combinedprecipitate was washed with n-hexane and thus 21.2 g of 2-heptylthio-7-hydroxy-6-methyl-5H-1,3,4-thiadiazolo-[3,2-a]pyrimidin-5-one was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04866064 |
| Source dataset | uspto-grants-1989_09 |
| ORD ID | ord-2ae8caf0855c42a392cf073a48a21c16 |
| Source note | uspto-grants-1989_09 |