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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 985503Generated: October 30, 2026

Water → HCID 11564945, compound

https://huagongshe.com/reaction/985503

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant(3-Methoxyphenyl)boronic acidHCID 2734370—
Reactant3-Bromo-7-methylimidazo[1,2-a]pyridineHCID 16740476—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventSodium CarbonateHCID 10340—
ProductHCID 11564945HCID 1156494593%

Reaction Steps

A mixture of 3-bromo-7-methylimidazo[1,2-α]pyridine (18.0 g, 86 mmol) and 3-methoxyphenylboronic acid (17.0 g, 112 mmol) in 1,2-dimethoxyethane (250 ml) and sodium carbonate (120 ml of a 2M aqueous solution) was degassed for 25 minutes. Tetrakis(triphenylphosphine)pallidum(0) (500 mg, 0.4 mmol) was then added and the mixture heated at reflux for 17 hours. After cooling to ambient temperature the reaction was poured into water (400 ml), extracted with ethyl acetate (3×400 ml) and the combined organics dried over anhydrous magnesium sulphate. Filtration and evaporation to dryness afforded 3-(3-methoxyphenyl)-7-methylimidazo[1,2-α]pyridine as a colourless oil (19 g, 93%). 1H NMR (360 MHz, CDC3) δH 2.40 (3H, s), 3.84 (3H, s), 6.63-6.65 (1H, m), 6.91-6.95 (1H, m), 7.05-7.07 (1H, m), 7.10-7.12 (1H, m), 7.30-7.38 (1H, m), 7.42 (1H, s), 7.66 (1H, s), 8.22 (1H, d, J 7); m/z (ES+) 239 (M++H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06872731B2
Source datasetuspto-grants-2005_03
ORD IDord-dc8fea058bcd46fbb4ef20aa47fb163b
Source noteuspto-grants-2005_03