Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 2-Chloropyridine | HCID 7977 | — |
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | HCID 23433735 | HCID 23433735 | — |
| Product | HCID 23433766 | HCID 23433766 | — |
Reaction Steps
A mixture of 120 mg of 2-chloro-5-(2-methyl-4-phenyl-oxazol-5-yl)-pyridine in 1 mL of hydrazine (98%) was heated at 70° C. for 45 min before adding 0.5 mL of dichloromethane to get better mixing of the hydrazine and the chloro-pyridine. When the dichloromethane had evaporated 0.5 mL of ethanol was added and the mixture was heated for 11 hours. The layers were separated. The ethanol layer was diluted with ethyl acetate and washed with aqueous sodium carbonate (2×), dried (magnesium sulfate), filtered, and the filtrate was evaporated to give 110 mg of crude 5-(2-Methyl-4-phenyl-oxazol-5-yl)-pyridin-2-yl-hydrazine as an orange solid. This material was used with out purification in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06696464B2 |
|---|
| Source dataset | uspto-grants-2004_02 |
|---|
| ORD ID | ord-1646950dd12b45649f33122c227fbaa9 |
|---|
| Source note | uspto-grants-2004_02 |
|---|