HuagongsheHuagongshe Chemistry Print Report · For research reference only
1(2H)-Pyridazinecarboxylic acid, tetrahydro-, ethyl ester → 2-[7-fluoro-2H-1,4-benzoxazin-3(4H)-on-6-yl]-hexahydro-1H-(1,2,4)-triazolo (1,2-a) pyridazine-1,3-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1(2H)-Pyridazinecarboxylic acid, tetrahydro-, ethyl ester | HCID 3014377 | — |
| Reactant | 6-isocyanato-7-fluoro-2H-1,4-benzoxazin-3(4H)-one | HCID 14402873 | — |
| Catalyst | Triethylamine | HCID 8471 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-[7-fluoro-2H-1,4-benzoxazin-3(4H)-on-6-yl]-hexahydro-1H-(1,2,4)-triazolo (1,2-a) pyridazine-1,3-dione | HCID 14402874 | 74.7% |
Reaction Steps
A mixture composed of 6-isocyanato-7-fluoro-2H-1,4-benzoxazin-3(4H)-one (2.14 g), 1-ethoxycarbonylhexahydropyridazine (1.62 g) and dioxane (30 ml) is treated with a few drops of triethylamine, stirred at an ambient temperature for 2 hours, and left overnight. The reaction mixture is made free from dioxane by evaporation in vacuo, mixed with methanol (30 ml) containing a catalytic amount of sodium, and refluxed for 2 hours. After removal of methanol by evaporation in vacuo, the resultant solid is collected, and washed with water to obtain an end product 2-[7-fluoro-2H-1,4-benzoxazin-3(4H)-on-6-yl]-hexahydro-1H-(1,2,4)-triazolo (1,2-a) pyridazine-1,3-dione (2.45 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04804394 |
| Source dataset | uspto-grants-1989_02 |
| ORD ID | ord-40b3fb53dace4500809f03c4b7c06459 |
| Source note | uspto-grants-1989_02 |