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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 216673Generated: October 27, 2026

2-Amino-5-cyanopyridine → Ethyl 2-(6-cyanoimidazo[1,2-a]pyridin-3-yl)acetate

https://huagongshe.com/reaction/216673

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-cyanopyridineHCID 818260—
ReactantEthyl (2E)-4-oxo-2-butenoateHCID 7019541—
SolventAcetonitrileHCID 6342—
ProductEthyl 2-(6-cyanoimidazo[1,2-a]pyridin-3-yl)acetateHCID 5919204330.3%

Reaction Conditions

Temperature90 °C

Reaction Steps

2-Amino-5-cyanopyridine (5.0 g, 39.9 mmol) and ethyl-(E)-4-oxobutenoate (5.92 g, 43.9 mmol, 1.1 equiv) are dissolved in acetonitrile (25 ml). The solution is heated for 14 hours at 90° C. After cooling, volatiles are removed in vacuo, and the residue is purified by flash chromatography (gradient hexane/EtOAc 100:0 to 50:50) to afford the title compound (2.77 g, 29%). 1H NMR (400 MHz, d6-DMSO): δ=9.17-9.15 (m, 1H), 7.60 (dd, J=9.3/1.0 Hz, 1H), 7.54 (s, 1H), 7.37 (dd, J=9.3/1.7 Hz, 1H), 4.07 (s, 2H), 3.99 (q, J=7.4 Hz, 2H), 1.07 (t, J=7.1 Hz, 3H). MS (ES+): 230 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193236B2
Source datasetuspto-grants-2012_06
ORD IDord-cbeeafdecb1e44ed8914da769ca40fb7
Source noteuspto-grants-2012_06