HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 645367Generated: October 28, 2026
Water → 6-formyl-N-phenylimidazo[1,2-a]pyridine-2-carboxamide
https://huagongshe.com/reaction/645367
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Sodium periodate | HCID 23667635 | — |
| Reactant | N-phenyl-6-vinylimidazo[1,2-a]pyridine-2-carboxamide | HCID 24771613 | — |
| Catalyst | Osmium Tetroxide | HCID 30318 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 6-formyl-N-phenylimidazo[1,2-a]pyridine-2-carboxamide | HCID 24771615 | 66.2% |
Reaction Steps
A suspension of 150 mg of N-phenyl-6-vinylimidazo[1,2-a]pyridine-2-carboxamide, 232 μl of osmium tetroxide and 167.5 mg of sodium periodate in a mixture of 6 ml of THF, 3 ml of t-butanol and 3 ml of water is stirred at 20° C. for 20 hours and then for a further 48 hours while adding, on 4 occasions, an additional 100 μl of osmium tetroxide and 80 mg of sodium periodate. The reaction mixture is poured into 50 ml of water and extraction is carried out twice with 50 ml of ethyl acetate. The combined organic phases are washed with a saturated aqueous sodium chloride solution, separated by settling, dried and concentrated to dryness under reduced pressure. The residue is chromatographed on silica, elution being carried out with a mixture of cyclohexane and ethyl acetate (gradient from 0 to 50%), to give 100 mg of 6-formyl-N-phenylimidazo[1,2-a]pyridine-2-carboxamide in the form of a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07704989B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-67c43a094a8645c2803ac8df31853735 |
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| Source note | uspto-grants-2010_04 |
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