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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598145Generated: October 30, 2026

Sodium hydride → 1-Mesityl-6-methyl-4-[[4-(trifluoromethyl)benzyl]oxy]-1,6-dihydro-7H-pyrrolo[2,3-d]pyridazin-7-one

https://huagongshe.com/reaction/598145

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant4-(Trifluoromethyl)benzenemethanolHCID 67684—
Reactant4-Chloro-1-mesityl-6-methyl-1,6-dihydro-7H-pyrrolo[2,3-d]pyridazin-7-oneHCID 67267127—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1-Mesityl-6-methyl-4-[[4-(trifluoromethyl)benzyl]oxy]-1,6-dihydro-7H-pyrrolo[2,3-d]pyridazin-7-oneHCID 5893854024.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 4-(trifluoromethyl)benzyl alcohol (0.062 ml, 0.45 mmol) in DMF (1 ml) was added sodium hydride (60% in oil, 18 mg, 0.45 mmol). The mixture was stirred for 10 min before addition of 4-chloro-1-mesityl-6-methyl-1,6-dihydro-7H-pyrrolo[2,3-d]pyridazin-7-one (45.3 mg, 0.15 mmol). The mixture was stirred at 60° C. for 1 hour, then diluted with water (30 ml) and extracted with ethyl acetate (50 ml). The extract was washed with water, dried over magnesium sulfate and concentrated in vacuo. The residue was purified by silica gel chromatography eluting with hexane/ethyl acetate (5:1) to give 16 mg (24%) of the title compound as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897607B2
Source datasetuspto-grants-2011_03
ORD IDord-b642894b1ad943d8902f3a00dc4ab04a
Source noteuspto-grants-2011_03