HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-heptylthio-6-methoxy-5H-1,3,4-thiadiazolo[3,2-a]pyrimidin-5-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1,3,4-Thiadiazole, 2-amino-5-(heptylthio)- | HCID 534458 | — |
| Reactant | Propyl 3-hydroxy-2-methoxyprop-2-enoate | HCID 71336589 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-heptylthio-6-methoxy-5H-1,3,4-thiadiazolo[3,2-a]pyrimidin-5-one | HCID 15610795 | 64% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04971971 |
| Source dataset | uspto-grants-1990_11 |
| ORD ID | ord-3183bf8a420b4cbe81eb3c438a2e3056 |
| Source note | uspto-grants-1990_11 |