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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1600556Generated: October 31, 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/1600556

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): δ 4.03 (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 numberUS05977028
Source datasetuspto-grants-1999_11
ORD IDord-56345f17caae496e95b917e6c27267ed
Source noteuspto-grants-1999_11