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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 722185Generated: October 27, 2026

Sodium Carbonate → 2-(1-Azabicyclo[2.2.2]oct-3-yl)-N-[4'-(hydroxymethyl)-1,1'-biphenyl-3-yl]acetamide Hydrochloride

https://huagongshe.com/reaction/722185

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantSodium HydroxideHCID 14798—
Reactant4-(Hydroxymethyl)benzeneboronic acidHCID 2734706—
Reactant2-(1-Azabicyclo[2.2.2]oct-3-yl)-N-(3-bromophenyl)acetamide HydrochlorideHCID 21883458—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventDimethylformamideHCID 6228—
Product2-(1-Azabicyclo[2.2.2]oct-3-yl)-N-[4'-(hydroxymethyl)-1,1'-biphenyl-3-yl]acetamide HydrochlorideHCID 21883461—

Reaction Conditions

Temperature80 °C

Reaction Steps

24.0 mg (0.16 mmol) of 4-(hydroxymethyl)phenylboronic acid, 0.17 ml (0.34 mmol) of 2M aqueous sodium carbonate solution and 5.8 mg (0.01 mmol) of 1,1′-bis(diphenylphosphino)ferrocenepalladium(II) chloride are added to a solution of 75 mg (0.16 mmol) of 2-(1-azabicyclo[2.2.2]oct-3-yl)-N-(3-bromophenyl)acetamide hydrochloride in 1 ml of DMF. The reaction mixture is stirred at 80° C. for 14 h. A further 24.0 mg (0.16 mmol) of 4-(hydroxymethyl)phenylboronic acid, 23.2 mg (0.03 mmol) of 1,1′-bis(diphenylphosphino)ferrocenepalladium(II) chloride and 0.48 ml (0.48 mmol) of 1M sodium hydroxide solution are added. The mixture is then heated at 80° C. for a further 12 h. After the reaction is complete, the mixture is cooled, filtered through silica gel and then purified by preparative HPLC. The product fractions are concentrated, taken up in methanol, mixed with 4M HCl in dioxane and again concentrated. Drying under high vacuum results in 25.9 mg (39.8% of theory) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07138410B2
Source datasetuspto-grants-2006_11
ORD IDord-aabb0758d6d342f6bce84c4ff86b97f1
Source noteuspto-grants-2006_11