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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1407153Generated: October 31, 2026

N,N,N-trimethyl-1,1-bis(1-methylethoxy)amine → Methyl 1-[2-fluoro-4-(trifluoromethoxy)phenyl]-5-methoxy-4-oxo-1,4-dihydropyridazine-3-carboxylate

https://huagongshe.com/reaction/1407153

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N-trimethyl-1,1-bis(1-methylethoxy)amineHCID 87682—
ReactantHCID 178496283HCID 178496283—
SolventTolueneHCID 1140—
ProductMethyl 1-[2-fluoro-4-(trifluoromethoxy)phenyl]-5-methoxy-4-oxo-1,4-dihydropyridazine-3-carboxylateHCID 5943618486%

Reaction Steps

A solution of methyl 2-{[2-fluoro-4-(trifluoromethoxy)phenyl]hydrazono}-4-methoxy-3-oxobutanoate (3.8 g, 11 mmol) and N,N-dimethylformamide diisopropyl acetal (9.5 mL, 54 mmol) in toluene (60 mL) was refluxed for 5 h. The mixture was concentrated under reduced pressure. The residue was diluted with AcOEt, washed with water and brine. The organic layer was dried over MgSO4, filtered and concentrated under reduced pressure. The residue was chromatographed on silica gel (10/90-100/0 AcOEt/hexane) to give the title compound (3.4 g, 86% yield) as pale yellow crystals: 1H NMR (300 MHz, CDCl3): δ ppm 3.91 (3H, s), 3.97 (3H, s), 7.17-7.25 (2H, m), 7.68-7.76 (2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916566B2
Source datasetuspto-grants-2014_12
ORD IDord-05f750729e744f818c47572ca8c2a534
Source noteuspto-grants-2014_12