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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1624572Generated: November 4, 2026

HCID 59436282, compound → HCID 59436279, compound

https://huagongshe.com/reaction/1624572

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59436282HCID 59436282—
ReactantHCID 178418573HCID 178418573—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59436279HCID 5943627998%

Reaction Steps

To a solution of N-methoxy-N,5-dimethyl-4-oxo-1-[3-(trifluoromethyl)phenyl]-1,4-dihydropyridazine-3-carboxamide (0.535 g, 1.6 mmol) in THF (10 mL) at −78° C. was added methylmagnesium bromide (1.1 mL, 3.2 mmol, 3 M in diethyl ether). The reaction was stirred at that temperature for 1 h then quenched with saturated ammonium chloride aqueous solution (5 mL) then water (2 mL) with slow warming to room temperature. The reaction mixture was diluted with ethyl acetate (20 mL) and the layers were separated. The aqueous layer was extracted with ethyl acetate (2×10 mL) and the combined organic extracts are washed with 1 N HCl aqueous solution (15 mL), brine (15 mL), dried (Na2SO4), filtered and concentrated to provide 3-acetyl-5-methyl-1-[3-(trifluoromethyl)phenyl]pyridazin-4(1H)-one (0.463 g, 98%) as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778944B2
Source datasetuspto-grants-2014_07
ORD IDord-26e5ea2e6f944462a7da5db86f32545b
Source noteuspto-grants-2014_07