HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2363728Generated: October 29, 2026
Water → 6-formyl-N-phenylimidazo[1,2-a]pyridine-2-carboxamide
https://huagongshe.com/reaction/2363728
Participants
| Role | Name | HCID | Charge |
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| 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 | — |
| 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 for 20 hours at 20° C. and then for a further 48 hours while adding in four portions 100 μL of osmium tetroxide and 80 mg of sodium periodate. The reaction mixture is poured into 50 mL of water and the resulting mixture is extracted twice with 50 mL of ethyl acetate. The combined organic phases are washed with saturated aqueous sodium chloride solution, separated by settling, dried and concentrated to dryness under reduced pressure. The residue is chromatographed on silica, eluting 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 | US08691990B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-6c51fd4a29d743ff8003153a00759f1b |
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| Source note | uspto-grants-2014_04 |
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