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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1735004Generated: November 1, 2026

2,6-Lutidine → HCID 19436809, compound

https://huagongshe.com/reaction/1735004

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-LutidineHCID 7937—
ReactantEthyl AcetateHCID 8857—
Reactant3-Chloro-5-methoxypyridazineHCID 10975612—
ReactantHCID 178481858HCID 178481858—
SolventTolueneHCID 1140—
ProductHCID 19436809HCID 19436809—

Reaction Steps

1-Methyl-3-(pentafluoroethyl)-1H-pyrazol-5-ol (0.44 g, 0.002 mole), 3-chloro-5-methoxypyridazine (0.29 g, 0.002 mole), and 2,6-lutidine (0.27 g, 0.0024 mole) were refluxed under N2 in toluene (8 mL) for 15 h. This mixture was poured into ethyl acetate and washed with 7% HCl, water and then with saturated sodium bicarbonate. The organic layer was dried (MgSO4), filtered through silica gel with ethyl acetate, and evaporated in vacuo to give 5-methoxy-3-[[1-methyl-3-(pentafluoroethyl)-1H-pyrazol-5-yl]oxy]pyridazine as a light yellow solid. The compound was recrystallized to give (0.45 g, 69% yield) Compound 18, a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05536701
Source datasetuspto-grants-1996_07
ORD IDord-a16259c0ac4643e399bf3b455fc4feeb
Source noteuspto-grants-1996_07