HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(2-Nitrophenyl)oxazolo[5,4-b]pyridine → 2-(2-Aminophenyl)oxazolo[5,4-b]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(2-Nitrophenyl)oxazolo[5,4-b]pyridine | HCID 12461420 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(2-Aminophenyl)oxazolo[5,4-b]pyridine | HCID 12461421 | — |
Reaction Steps
A mixture of 700 mg. of 2-(2-nitrophenyl)oxazolo[5,4-b]pyridine in 50 ml. of ethanol was hydrogenated over 150 mg. of 5% palladium on carbon catalyst. The catalyst was removed by filtration and the solvent was concentrated to dryness. The residue was recrystallized from chloroformpetroleum ether to give 2-(2-aminophenyl)oxazolo[5,4-b]pyridine, m.p. 142°-144° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04131677 |
| Source dataset | uspto-grants-1978_12 |
| ORD ID | ord-215ef813ee5d4fd49f9edfa1b6bcc4f1 |
| Source note | uspto-grants-1978_12 |