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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2179596Generated: October 29, 2026

Sodium Hydroxide → HCID 58485533, compound

https://huagongshe.com/reaction/2179596

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant(3-Methoxyphenyl)boronic acidHCID 2734370—
ReactantN-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-6-bromo-1-benzofuran-2-carboxamideHCID 59341401—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventDimethylformamideHCID 6228—
ProductHCID 58485533HCID 58485533—

Reaction Steps

A mixture of 130 mg (0.86 mmol) of 3-methoxyphenylboronic acid, 200 mg. (0.57 mmol) of N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-6-bromo-1-benzofuran-2-carboxamide (Example 2A), 1.72 ml (1.72 mmol) of 1N sodium hydroxide solution, 40 mg (0.06 mmol) of 1,1′-bis(diphenylphosphino)ferrocenepalladium(II) chloride and 2 ml of DMF is heated at 80-85° C. for 18 h. The solvent is removed under reduced pressure. The crude product is purified on silica gel 60 (Merck, Darmstadt; eluent: dichloromethane, dichloromethane/methanol 20:1, dichloromethane/methanol-/ammonia 80:20:2). The solvent is removed under reduced pressure. Finally, the last residues of solvent are removed under high vacuum. 151 mg (64% of theory) of the title compound are isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067931B2
Source datasetuspto-grants-2015_06
ORD IDord-8e6064e40a284ed1b87d74b4edde726d
Source noteuspto-grants-2015_06