Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | HCID 10685112 | HCID 10685112 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 19040023 | HCID 19040023 | 27% |
Reaction Steps
A mixture of 11.9 g of semicarbazide from Example 17 Part C, 8.10 g of carbonyldiimidazole, 0.5 mL of triethylamine and 400 mL of anhydrous DMF was stirred at 25° C. for 4 days, diluted with 1 L of H2O and filtered. The filtrate was evaporated. The residue was treated with 100 mL of MeOH and the solid was filtered and dried to give 3.43 g of 1-[(4-(2-(2-phenyl-4-oxazolyl)ethoxy)phenyl)methyl]1,2,4-triazolidin-3,5-dione (27%. mp 223.5°-230° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05641796 |
|---|
| Source dataset | uspto-grants-1997_06 |
|---|
| ORD ID | ord-f3ed5f6705ab487e8499cca500e83f2a |
|---|
| Source note | uspto-grants-1997_06 |
|---|