HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → RS 14203
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(Chloromethyl)pyridine | HCID 74571 | — |
| Reactant | 8-(3-Nitrophenyl) pyrido[2,3-d]pyridazin-5-one | HCID 19700720 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | RS 14203 | HCID 9808563 | 26.9% |
Reaction Steps
To a solution of 8-(3-nitrophenyl)-pyrido[2,3-d]pyridazin-5-one (0.16 g, 0.6 moles) in tetrahydrofuran (50 ml) was added potassium carbonate (0.19 g, 7.1 moles), potassium iodide (1.0 g, 6.0 moles) and 4-picolyl chloride (0.98 g, 6.0 mmoles). The mixture was stirred and refluxed under an inert atmosphere for 18 hours. The solvent was removed under vacuum. The residue was partitioned in methanol/ethyl acetate (1:1), chromatographed in 100% hexane followed by 100% ethyl acetate. The remaining solvent was removed yielding 0.58 g of crude 6-(4-pyridylmethyl)-8-(3-nitrophenyl)pyrido[2,3-d]pyridazin-5-one, which was recrystallized from methanol yielding 0.08 g of the pure compound (37.1%), mp. 167°-168° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05716954 |
| Source dataset | uspto-grants-1998_02 |
| ORD ID | ord-19a752b1b84f440dbad589e4b7fefe06 |
| Source note | uspto-grants-1998_02 |