Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thymine | HCID 1135 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1H-1,2,4-Triazole | HCID 9257 | — |
| Reactant | Diphenyl chlorophosphate | HCID 75654 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178430897 | HCID 178430897 | 32.3% |
Reaction Steps
69 g (1 mol) of 1,2,4-triazole are suspended in 800 ml of dry acetonitrile under a protecting gas (argon). 251 g (0.95 mol) of diphenyl chlorophosphate are added to the suspension at 0°-10° C. Subsequently, in the course of 1 hour, 151.79 g (1.5 mol) of triethylamine are added dropwise before 63 g (0.5 mol) of thymine are added. The resulting suspension is stirred for 12 hours at room temperature. Finally, the mixture is heated for 5 hours at 60°-80° C. 40 ml of methanol are added to the cooled suspension and the mixture is stirred for 2 hours at room temperature. The suspension is filtered; the residue is stirred with one liter of diisopropyl ether, filtered off again by suction and stirred with 800 ml of water. The aqueous suspension is filtered and the solid residue is recrystallized from 1300 ml of dimethylformamide. 28.6 g of 5-methyl-4-(1,2,4 -triazol-1-yl)pyrimdin-2(1H)-one are obtained with melting point 275°-280° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05359067 |
|---|
| Source dataset | uspto-grants-1994_10 |
|---|
| ORD ID | ord-96ec81c771054dfe92db7d8e28b63041 |
|---|
| Source note | uspto-grants-1994_10 |
|---|