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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1796201Generated: November 1, 2026

2-Bromopyridine → HCID 22181068, compound

https://huagongshe.com/reaction/1796201

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopyridineHCID 7973—
ReactantHCID 22181052HCID 22181052—
SolventPyridineHCID 1049—
SolventEthyl AcetateHCID 8857—
ProductHCID 22181068HCID 2218106820%

Reaction Conditions

Temperature150 °C

Reaction Steps

To a suspension of 3-chloro-4-(piperidin-4-yloxy)nitrobenzene (3.00 g) obtained in reference example 8 in pyridine (30 ml) was added 2-bromopyridine (1.25 ml) at room temperature, and the resulting mixture was stirred at 150° C. for 16 hours. After cooling to room temperature, the reaction mixture was diluted with ethyl acetate, and the organic layer was washed with a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate and evaporated in vacuo. The residue obtained was purified by chromatography on a silica gel column using a mixed solvent of ethyl acetate and hexane (1:2) as the eluent to afford the title compound (0.80 g, yield: 20%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07030138B2
Source datasetuspto-grants-2006_04
ORD IDord-fb136cea15524a588eec33bf8a0ece06
Source noteuspto-grants-2006_04