Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2428195Generated: November 2, 2026

2,5-Dibromopyridine → 5-Bromo-2-(3-(2-chloro-3,6-difluorophenyl)isoxazol-5-ylmethoxy)pyridine

https://huagongshe.com/reaction/2428195

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-DibromopyridineHCID 69353—
ReactantSodium t-butoxideHCID 23676156—
ReactantHCID 67148834HCID 67148834—
Catalyst1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
Product5-Bromo-2-(3-(2-chloro-3,6-difluorophenyl)isoxazol-5-ylmethoxy)pyridineHCID 6714857765%

Reaction Steps

2,5-Dibromopyridine (12.6 g, 53.0 mmol) and [3-(2-chloro-3,6-difluoro-phenyl)-isoxazol-5-yl]-methanol (10.0 g, 40.7 mmol) were dissolved in toluene (400 mL). tBuONa (5.87 g, 61.1 mmol), xantphos (1.42 g, 2.45 mmol) and Pd2(dba)3 (732 mg, 0.800 mmol) were added to the sol. The resulting mixture was refluxed overnight, and was allowed to cool down to rt. The mixture was filtered through Celite (washed with EtOAc), and was washed with aq. sat. NaHCO3 (1×) and brine (2×). The org. layer was dried over MgSO4, filtered, and concentrated under reduced pressure. Purification of the crude by FC (EtOAc/heptane 10:90) yielded the title compound (10.6 g, 65%). LC-MS: tR=1.10 min; ES+: 400.66.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968720B2
Source datasetuspto-grants-2011_06
ORD IDord-36ba01bb74b544d8a00c62a100345932
Source noteuspto-grants-2011_06