[CH2:1]([O:3][C:4]([CH:6]=P(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)=[O:5])[CH3:2].[N:26]1[CH:27]=[C:28]([CH:35]=O)[N:29]2[CH:34]=[CH:33][CH:32]=[CH:31][C:30]=12>O1CCCC1.C(OCC)(=O)C>[N:26]1[CH:27]=[C:28](/[CH:35]=[CH:6]/[C:4]([O:3][CH2:1][CH3:2])=[O:5])[N:29]2[CH:34]=[CH:33][CH:32]=[CH:31][C:30]=12(Ethoxycarbonylmethylene)triphenylphosphorane (0.72 g, 2.05 mmol) was added to a solution of imidazo[1,2-a]pyridine-3-carbaldehyde (0.25 g, 1.71 mmol) in anhydrous tetrahydrofuran (THF) (20 mL) at room temperature. The reaction mixture was heated overnight at 65° C. After completion of the reaction as indicated by HPLC, the reaction mixture was diluted with ethyl acetate (EtOAc) (20 mL) and quenched with a saturated solution of ammonium chloride (10 mL). The organic layer was washed with water (3×20 mL) and brine (15 mL). It was dried over anhydrous Na2SO4, filtered and evaporated to get the crude product. This crude was purified by silica gel column chromatography using 50-80% EtOAc in Hexanes to provide pure (E)-ethyl 3-(imidazo[1,2-a]pyridin-3-yl)acrylate (0.19 g) as a white solid. ES+(M+H)+217.
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