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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 277665Generated: October 30, 2026

(4-Chloro-2-fluoro-5-methoxyphenyl)boronic acid → 2-(4-Chloro-2-fluoro-5-methoxyphenyl)imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/277665

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Chloro-2-fluoro-5-methoxyphenyl)boronic acidHCID 10932600—
Reactant2-Bromoimidazo[1,2-a]pyridineHCID 12428957—
CatalystHCID 178418476HCID 178418476—
Solvent1,2-DimethoxyethaneHCID 8071—
Product2-(4-Chloro-2-fluoro-5-methoxyphenyl)imidazo[1,2-a]pyridineHCID 2262560561.7%

Reaction Steps

A mixture of 0.8 g (4.1 mmol) of 2-bromoimidazo[1,2-a]pyridine, 0.8 g (4.2 mmol) of 4-chloro-2-fluoro-5-methoxyphenylboronic acid, and 0.2 g (0.28 mmol) of bis(triphenylphosphine)palladium(II) chloride were heated in 30 ml of glyme at reflux for 2 h. The reaction mixture was partitioned between 250 ml of ethyl acetate and 100 ml of water and the separated organic layer washed with brine and dried over magnesium sulfate. On evaporating in vacuo, the remaining residue was flash chromatographed on silice gel (1:1 hexane/ethyl acetate) to afford 0.7 g of the title compound (m.p. 139-141° C.). NMR (CDCl3, 400 MHz); δ4.03 (s, 3H), 6.81 (t, 1H), 7.21 (m, 2H), 8.63 (d, 1H), 7.92 (d, 1H), 8.04 (s, 1H), 8.14 (d, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06358885B1
Source datasetuspto-grants-2002_03
ORD IDord-79a7882507e94d84b93367b7e35c3798
Source noteuspto-grants-2002_03