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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1592728Generated: October 31, 2026

Pyridine → HCID 12673494, compound

https://huagongshe.com/reaction/1592728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDichloromethaneHCID 6344—
Reactant2-BromophenolHCID 7244—
Reactant3-Pyridinylboronic acidHCID 2734378—
CatalystCupric acetateHCID 8895—
SolventWaterHCID 962—
ProductHCID 12673494HCID 126734946%

Reaction Steps

2-Bromophenol (355 mg, 2.05 mmol), 3-pyridyl-boronic acid (500 mg, 4.1 mmol), copper acetate (745 mg, 4.1 mmol) and pyridine (3.3 mL, 41 mmol) were added to dichloromethane (41 mL) and stirred for about 48 hours under air. The reaction was diluted with water (50 mL) and the layers separated. The organic layer was washed with 5N NaOH. The organic layer was concentrated, and chromatographed on silica gel (MeOH/dichloromethane) to yield 3-(2-bromo-phenoxy)-pyridine (30 mg, 6%) as a yellow oil. MS found 249.1 M+1. 3-(2-Bromo-phenoxy)-pyridine was coupled to piperazine using the Buchwald chemistry described in preparation 1A to afford the title compound. LRMS (ESI+): 256.1 (M+1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07291619B2
Source datasetuspto-grants-2007_11
ORD IDord-15780cdd69714f9aa79fd742f6eee012
Source noteuspto-grants-2007_11