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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1245488Generated: October 30, 2026

Potassium Carbonate → 3-(1,3-Oxazol-5-yl)-7-phenylimidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1245488

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTosylmethyl isocyanideHCID 161915—
Reactant7-phenyl-Imidazo[1,2-a]pyridine-3-carboxaldehydeHCID 21912839—
SolventMethanolHCID 887—
Product3-(1,3-Oxazol-5-yl)-7-phenylimidazo[1,2-a]pyridineHCID 10015507—

Reaction Steps

7-Phenylimidazo[1,2-a]pyridine-3-carbaldehyde (7-1, 0.030 g, 0.14 mmol), tosylmethyl isocyanide (0.032 g, 0.16 mmol) and K2CO3 (0.022 g, 0.16 mmol) were dissolved in 1 ml MeOH and the resulting solution was heated to reflux. After 4 h the reaction was quenched by the addition of water. The resulting mixture was extracted 3× with EtOAc, and the combined extracts were dried over Na2SO4, filtered and concentrated. The residue was purified by flash column chromatography, eluting with a gradient of DCM to 95:5 DCM/MeOH. The product was further purified by reverse phase preparative HPLC to afford the title compound. 1H NMR (CDCl3) δ 8.63 (d, 1H, J=7.1 Hz), 8.52 (s, 1H), 8.27 (s, 1H), 8.25 (s, 1H), 7.78 (m, 2H), 7.74 (dd, 1H, J=1.4, 7.3 Hz), 7.67 (s, 1H), 7.58 (m, 3H). LCMS m/z (M+1) Calc: 262.1, found 262.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07125888B2
Source datasetuspto-grants-2006_10
ORD IDord-fe29ea500a5d41ec992645db1baf28c2
Source noteuspto-grants-2006_10