HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 59515506, compound → 7-(4-chlorophenyl)-8-(pyridin-4-yl)-[1,2,4]triazolo[4,3-b]pyridazine-3,6(2H,5H)-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 59515506 | HCID 59515506 | — |
| Reactant | Potassium trimethylsilyloxide | HCID 86599933 | — |
| Reactant | HCID 178504318 | HCID 178504318 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-(4-chlorophenyl)-8-(pyridin-4-yl)-[1,2,4]triazolo[4,3-b]pyridazine-3,6(2H,5H)-dione | HCID 59515533 | 22% |
Reaction Steps
To the solution of 6-chloro-7-(4-chlorophenyl)-8-(pyridin-4-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3(2H)-one (28 mg, 0.078 mmol), prepared as described in Example 8B, in THF (3 ml) was added potassium trimethylsilyloxide, TMSOK, (36 mg, 0.28 mmol). The reaction mixture was refluxed for 1 hour. After this time, the solution was cooled to RT. The solution was concentrated under reduced pressure. The resulting crude product was purified by reverse phase HPLC to give the title compound, 7-(4-chlorophenyl)-8-(pyridin-4-yl)-[1,2,4]triazolo[4,3-b]pyridazine-3,6(2H,5H)-dione, (8 mg, 22%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07816357B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-5a4860bd1eb249498ee4be46114b0b12 |
| Source note | uspto-grants-2010_10 |