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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1354034Generated: November 1, 2026

1,3-Propanediol → HCID 131726459, compound

https://huagongshe.com/reaction/1354034

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-PropanediolHCID 10442—
ReactantPotassium CarbonateHCID 11430—
Reactant1,4-DioxaneHCID 31275—
Reactant3-(Diethylboryl)pyridineHCID 642851—
Reactant4-(6-Bromopyridazin-3-yl)-1,4-diazabicyclo[3.2.2]nonaneHCID 17984760—
ProductHCID 131726459HCID 131726459—

Reaction Steps

A mixture of 4-(6-bromo-pyridazin-3-yl)-1,4-diazabicyclo[3.2.2]nonane (0.49 g, 1.7 mmol), diethyl-3-pyridylborane (0.38 g, 2.6 mmol), aqueous potassium carbonate (2.6 ml, 2M), palladium(0)tetrakistriphenylphosphine (59 mg, 0.051 mmol), 1,3-propandiol (0.37 ml, 5.1 mmol) and dioxane (5 ml) was stirred at reflux for 15 hours. The mixture was evaporated. Aqueous sodium hydroxide (10 ml, 4M) was added. The mixture was extracted with dichloromethane (3×20 ml). Chromatography on silica gel with dichloromethane, 10% methanol and 1% aqueous ammonia as solvent gave the title compound as an oil. Yield 0.10 g, 21%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07223753B2
Source datasetuspto-grants-2007_05
ORD IDord-3bd49ec799fb4f47a2141b83a4087a24
Source noteuspto-grants-2007_05