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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 869153Generated: October 30, 2026

Potassium Carbonate → HCID 67453616, compound

https://huagongshe.com/reaction/869153

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1,4-DioxaneHCID 31275—
Reactant(2-Methoxypyridin-3-yl)boronic acidHCID 2762709—
ReactantHCID 86686129HCID 86686129—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 67453616HCID 6745361677%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a 20 dram vial was added 6-chloro-N-((1-(3-fluoropyridin-2-yl)cyclobutyl)methyl)pyridazin-3-amine (1.8 g, 6.23 mmol, 1.0 equiv), 2-methoxypyridin-3-ylboronic acid (1.0 g, 6.54 mmol, 1.1 equiv), Cl2Pd(dppf) (350 mg, 0.43 mmol, 0.07 equiv), 2M potassium carbonate (8 mL, 15.5 mmol, 2.5 equiv), and dioxane (21 mL). The reaction was stirred and heated to 90° C. for 2 h and then diluted with water (20 mL) and ethyl acetate (50 mL). After transferring to a separatory funnel and shaking, the organic layer was separated from the aqueous layer and then washed with lithium chloride (1×20 mL). The organic layer was then dried over Na2SO4, filtered, and concentrated to give a crude solid that was purified by silica gel column chromatography to give N-((1-(3-fluoropyridin-2-yl)cyclobutyl)methyl)-6-(2-methoxypyridin-3-yl)pyridazin-3-amine (1.7 g, 77%) as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969346B2
Source datasetuspto-grants-2015_03
ORD IDord-227de07533e547b6962c3cd99a5d750b
Source noteuspto-grants-2015_03