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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1625572Generated: November 5, 2026

Ethanol → HCID 58755934, compound

https://huagongshe.com/reaction/1625572

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPotassium CarbonateHCID 11430—
Reactant(2,4-Dimethylphenyl)boronic acidHCID 4198739—
ReactantHCID 58075191HCID 58075191—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 58755934HCID 5875593458%

Reaction Steps

3-Chloro-6-(pyridin-2-ylmethoxy)pyridazine (Example 15a) (221 mg, 1 mmol) was dissolved in toluene (10 mL), EtOH (2 mL), and water (1.5 mL). Then 2,4-dimethylphenylboronic acid (150 mg, 1 mmol) was added, followed by K2CO3 (276 mg, 2 mmol) and the mixture was degassed using argon stream. Tetrakis(triphenylphosphine)palladium (232 mg, 0.2 mmol) was added under argon and the mixture was refluxed overnight. The solvents were removed under vacuum and a residual solid was extracted with EtOAc, and successively washed with water and brine dried over MgSO4 filtered and evaporated. The crude material was purified on silica gel (Eluent: 50% EtOAc in hexanes) to give 3-(2,4-Dimethylphenyl)-6-(pyridin-2-ylmethoxy)pyridazine (169 mg, 58%) as a white solid. 1H NMR (300 MHz, dMSO): δ 2.26 (s, 3H), 2.32 (s, 3H), 5.62 (s, 2H), 7.13-7.15 (m, 2H), 7.28-7.40 (m, 2H), 7.55-7.56 (d, 1H), 7.78-7.84 (m, 2H), 8.58-8.60 (d, 1H); MS (M+H, 292).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08784782B2
Source datasetuspto-grants-2014_07
ORD IDord-0db18503de774fa9be0645fafaa28cd4
Source noteuspto-grants-2014_07