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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2089786Generated: October 26, 2026

N,4-dimethoxy-N-methyl-6-oxo-[3-(trifluoromethyl)phenyl]-1,6-dihydropyridazine-3-carboxamide → 6-Acetyl-5-methoxy-2-[3-(trifluoromethyl)phenyl]pyridazin-3(2H)-one

https://huagongshe.com/reaction/2089786

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,4-dimethoxy-N-methyl-6-oxo-[3-(trifluoromethyl)phenyl]-1,6-dihydropyridazine-3-carboxamideHCID 86643932—
ReactantHCID 178418689HCID 178418689—
SolventTetrahydrofuranHCID 8028—
Product6-Acetyl-5-methoxy-2-[3-(trifluoromethyl)phenyl]pyridazin-3(2H)-oneHCID 5943614645.3%

Reaction Steps

MeMgBr (1 M solution in THF, 4 mL, 12 mmol) was added dropwise at −78° C. to a solution of N,4-dimethoxy-N-methyl-6-oxo-1-[3-(trifluoromethyl)phenyl]-1,6-dihydropyridazine-3-carboxamide (1.43 g, 4 mmol) in THF (15 mL). After stirring for 1 h, the reaction mixture was quenched with saturated NH4Cl aqueous solution and extracted with AcOEt. The extract was washed with brine, dried over MgSO4, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography eluting with hexane/AcOEt (1/1) and recrystallized from hexane/AcOEt to give the title compound (566 mg, 45% yield) as a white solid: mp 136-138° C.; NMR (300 MHz, CDCl3): δ ppm 2.57 (3H, s), 3.93 (3H, s), 6.31 (1H, s), 7.63 (1H, t, J=7.9 Hz), 7.69 (1H, d, J=7.9 Hz), 7.84-7.88 (1H, m), 7.91 (1H, s). Anal. Calcd for C14H11F3N2O3: C, 53.85; H, 3.55; N, 8.97. Found: C, 53.96; H, 3.57; N, 8.96.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08435995B2
Source datasetuspto-grants-2013_05
ORD IDord-80324d3a62e24d85861608b6bbe6a7fb
Source noteuspto-grants-2013_05