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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1160229Generated: November 1, 2026

HCID 59515506, compound → 7-(4-chlorophenyl)-8-(pyridin-4-yl)-[1,2,4]triazolo[4,3-b]pyridazine-3,6(2H,5H)-dione

https://huagongshe.com/reaction/1160229

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59515506HCID 59515506—
ReactantPotassium trimethylsilyloxideHCID 86599933—
ReactantHCID 178504318HCID 178504318—
SolventTetrahydrofuranHCID 8028—
Product7-(4-chlorophenyl)-8-(pyridin-4-yl)-[1,2,4]triazolo[4,3-b]pyridazine-3,6(2H,5H)-dioneHCID 5951553322%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07816357B2
Source datasetuspto-grants-2010_10
ORD IDord-5a4860bd1eb249498ee4be46114b0b12
Source noteuspto-grants-2010_10