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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1661112Generated: October 30, 2026

Hydrogen Peroxide → Di-tert-butyl (8-(4-chlorophenyl)-7-(4-cyanophenyl)-5-((2-methyl-6-(trifluoromethyl)pyridin-3-yl)methyl)-6-oxo-5,6-dihydro-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl phosphate

https://huagongshe.com/reaction/1661112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
Reactant1H-1,2,4-TriazoleHCID 9257—
ReactantSodium SulfiteHCID 24437—
ReactantDi-tert-butyl diethylphosphoramiditeHCID 4251849—
ReactantBenzonitrile, 4-[8-(4-chlorophenyl)-5,6-dihydro-3-(hydroxyMethyl)-5-[[2-Methyl-6-(trifluoroMethyl)-3-pyridinyl]Methyl]-6-oxo-1,2,4-triazolo[4,3-b]pyridazin-7-yl]-HCID 25026694—
Solvent1,2-DichloroethaneHCID 11—
ProductDi-tert-butyl (8-(4-chlorophenyl)-7-(4-cyanophenyl)-5-((2-methyl-6-(trifluoromethyl)pyridin-3-yl)methyl)-6-oxo-5,6-dihydro-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl phosphateHCID 86638628—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a round bottom flask was added 4-(8-(4-chlorophenyl)-3-(hydroxymethyl)-5-((2-methyl-6-(trifluoromethyl)pyridin-3-yl)methyl)-6-oxo-5,6-dihydro-[1,2,4]triazolo[4,3-b]pyridazin-7-yl)benzonitrile (25 mg, 0.0454 mmol), di-tert-butyl diethylphosphoramidite (34 mg, 0.136 mmol), 1,2,4-triazole (9.5 mg, 0.136 mmol) and 1,2-dichloroethane (3 ml). The reaction was stirred at 60° C. for 24 hr. After this time the reaction was cooled to rt. H2O2(7 N, 0.5 ml) was then added and the reaction was stirred at rt for 60 min. Na2SO3 (10%, 1 ml) was added and the reaction was stirred at rt for an additional 30 min. After this time, the reaction mixture was concentrated. The residue was diluted with EtOAc (50 ml) and the resulting solution was washed with water (25 ml) and saturated NaCl (25 ml). The organic layer was dried over MgSO4, filtered and concentrated. The crude intermediate was purified by silica gel column chromatography (4 g silica gel) eluting with a gradient of 0-50% EtOAc/Hex to give di-tert-butyl (8-(4-chlorophenyl)-7-(4-cyanophenyl)-5-((2-methyl-6-(trifluoromethyl)pyridin-3-yl)methyl)-6-oxo-5,6-dihydro-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl phosphate as clear oil. To this purified intermediate was added CH2Cl2(2 ml) and TFA (0.5 ml). The reaction was stirred at rt for 10 min. After this time the solution was concentrated. The crude product was purified by preparative HPLC eluting with water/MeOH to give the product (28 mg). The product was then dissolved in water (1 ml) and 1N NaOH (1N, 0.0445 mmol) was added. The resulting solution was concentrated on a lyophilizer to give the title compound, sodium (8-(4-chlorophenyl)-7-(4-cyanophenyl)-5-((2-methyl-6-(trifluoromethyl)pyridin-3-yl)methyl)-6-oxo-5,6-dihydro-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl hydrogenphosphate, as a white solid (29 mg, 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030306B2
Source datasetuspto-grants-2011_10
ORD IDord-9f85856d37684d7b923fb5efc98dff46
Source noteuspto-grants-2011_10