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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1160231Generated: November 2, 2026

Potassium Carbonate → HCID 59515539, compound

https://huagongshe.com/reaction/1160231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-(Bromomethyl)benzonitrileHCID 86996—
ReactantHCID 68688231HCID 68688231—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 59515539HCID 5951553949.5%

Reaction Steps

The solution of 7-(4-chlorophenyl)-2-methyl-8-(pyridin-4-yl)-[1,2,4]triazolo[4,3-b]pyridazine-3,6(2H,5H)-dione (10 mg, 0.028 mmol), 4-(bromomethyl)benzonitrile (7 mg, 0.036 mmol), K2CO3(12 mg, 0.084 mmol) in DMF (0.5 ml), was heated at 80° C. for 20 min. After this time, the reaction mixture was cooled to RT and diluted with ethyl acetate. The resulting solution was then washed with water. The organic layer was dried over Na2SO4, filtered and concentrated under reduced pressure. The crude product was purified by reverse phase HPLC to give the title compound, 4-((7-(4-chlorophenyl)-2-methyl-3,6-dioxo-8-(pyridin-4-yl)-2,3-dihydro-[1,2,4]triazolo[4,3-b]pyridazin-5(6H)-yl)methyl)benzonitrile (6.5 mg, 40%) as the mono trifluoro acetate salt as a yellow solid. Rt=2.78, M+H=469; 1H NMR (CD3OD) δ 8.81(2H), 7.71-7.60(6H), 7.32(2H), 7.07(2H), 5.96(2H), 3.57(3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07816357B2
Source datasetuspto-grants-2010_10
ORD IDord-837a4ae8cada4a9ca010756bcace51c6
Source noteuspto-grants-2010_10