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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1821664Generated: November 1, 2026

3,6-dichloro-4-methoxypyridazine → HCID 23013667, compound

https://huagongshe.com/reaction/1821664

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,6-dichloro-4-methoxypyridazineHCID 6401343—
ReactantHCID 22940066HCID 22940066—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethyl SulfoxideHCID 679—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 22940173HCID 2294017330.8%
ProductHCID 23013667HCID 2301366739.1%

Reaction Steps

In a mixed solvent of 1,4-dioxane (2.5 mL) and dimethylsulfoxide (2.5 mL) was dissolved 190 mg (1.16 mmol) of 2-cyclopropyl-3-methoxyphenol, 146 mg (1.30 mmol) of potassium tert-butoxide was added to the solution and the resulting mixture was stirred for 10 minutes. To the mixture was added 170 mg (0.950 mmol) of 3,6-dichloro-4-methoxypyridazine and the resulting mixture was stirred overnight. The reaction mixture was poured into ice water and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The solvent was removed, and the obtained residue was purified by silica gel chromatography (Wakogel C-100, hexane-ethyl acetate, gradient) to obtain 90.1 mg (0.293 mmol, Yield: 30.8%) of 6-chloro-3-(2-cyclopropyl-3-methoxyphenoxy)-4-methoxypyridazine and 114 mg (0.371 mmol, Yield: 39.1%) of 3-chloro-6-(2-cyclopropyl-3-methoxyphenoxy)-4-methoxypyridazine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07608563B2
Source datasetuspto-grants-2009_10
ORD IDord-270c8b3d989b446b80c434d1f9918f05
Source noteuspto-grants-2009_10