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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2197562Generated: November 2, 2026

Ethyl Acetate → Methyl 2-(6-bromo-8-phenylimidazo[1,2-a]pyridin-2-yl)acetate

https://huagongshe.com/reaction/2197562

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantPhenylboronic AcidHCID 66827—
ReactantMethyl 2-(6,8-dibromoimidazo[1,2-a]pyridin-2-yl)acetate hydrochlorideHCID 67008341—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
ProductMethyl 2-(6-bromo-8-phenylimidazo[1,2-a]pyridin-2-yl)acetateHCID 5820794073%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of methyl 2-(6,8-dibromoimidazo[1,2-a]pyridin-2-yl)acetate hydrochloride (0.26 g, 0.68 mmol) and phenylboronic acid (0.083 g, 0.68 mmol) in toluene (9 mL) and ethanol (0.5 mL) was bubbled nitrogen for 20 mins. The mixture was then treated with Pd(PPh3)4 (26 mg, 0.022 mmol) and K3PO4 (2 M, 1 mL, 2.0 mmol) and heated at 80° C. overnight. The reaction was cooled, poured into ethyl acetate (200 mL), washed with brine, separated, and concentrated. The residue was purified by column chromatography on silica gel using ethyl acetate in hexanes (10-25%) as eluent. The product containing fractions were concentrated to give 170 mg (73% yield) of methyl 2-(6-bromo-8-phenylimidazo[1,2-a]pyridin-2-yl)acetate as a white solid. LCMS B: 2.11 min (RT); (M+H)+=347.21 (100%), 345.21 (100%). 1H NMR, 400 MHz, CDCl3: δ 8.20 (d, J=1.6 Hz, 1 H), 7.96 (m, 2 H), 7.65 (s, 1H), 7.50-7.40 (m, 3 H), 7.33 (d, J=1.6 Hz, 1 H), 3.92 (s, 2 H), 3.75 (s, 3 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338604B2
Source datasetuspto-grants-2012_12
ORD IDord-e675716eb1364719b390804d959fd2e2
Source noteuspto-grants-2012_12