Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Azidotrimethylsilane | HCID 78378 | — |
| Reactant | Ethyl 6-ethynylimidazo[1,2-a]pyridine-2-carboxylate | HCID 44136342 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178469439 | HCID 178469439 | — |
Reaction Steps
To a solution of 220 mg of ethyl 6-ethynylimidazo[1,2-a]pyridine-2-carboxylate and 0.21 mL of azidotrimethylsilane in 4 mL of a mixture (9/1) of N,N-dimethylformamide and methanol are added 9.8 mg of cuprous iodide. The reaction mixture is stirred for 2 hours at 100° C. and then cooled, diluted with 4 mL of dichloromethane, filtered through alumina and concentrated to dryness. The residue is chromatographed on silica, eluting with a mixture of dichloromethane and ethanol (97/3). The fractions containing the expected product are combined and concentrated to dryness under reduced pressure to give 125 mg of ethyl 6-(1H-1,2,3-triazol-4-yl)imidazo[1,2-a]pyridine-2-carboxylate in the form of an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08691990B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-1269da8990be4d8faf31e35639320f66 |
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| Source note | uspto-grants-2014_04 |
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