HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetonitrile → 2-[4-cyanomethyl-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 | Chloroacetonitrile | HCID 7856 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 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 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-[4-cyanomethyl-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 14402883 | 70.8% |
Reaction Steps
A mixture composed of 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 (2.04 g), potassium carbonate (1.06 g), chloroacetonitrile (0.96 g) and acetonitrile (30 ml) is refluxed for 3 hours. The reaction mixture is made free from acetonitrile by evaporation in vacuo and mixed with water. The resultant solid is collected by filtration and washed with a small amount of ethanol to obtain an end product 2-[4-cyanomethyl-7-fluoro-2H-1,4-benzoxazin-3(4H)-on-6-yl]-hexahydro-1H-(1,2,4)-triazolo (1,2-a)-pyridazine-1,3-dione (1.62 g),
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04804394 |
| Source dataset | uspto-grants-1989_02 |
| ORD ID | ord-1817e246e0bf4aa1bf9addaf6b5208f4 |
| Source note | uspto-grants-1989_02 |