HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitrogen → 5-Phenyl-oxazole-4-carboxylic acid [1-(2-acetyl-oxazol-5-ylmethyl)-1H-pyrazol-3-yl]-amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | 5-Phenyl-oxazole-4-carboxylic acid {1-[2-(1-hydroxy-ethyl)-oxazol-5-ylmethyl]-1H-pyrazol-3-yl}-amide | HCID 66929386 | — |
| Catalyst | Manganese dioxide | HCID 14801 | — |
| Solvent | 2-Oxopropiononitrile | HCID 69430 | — |
| Product | 5-Phenyl-oxazole-4-carboxylic acid [1-(2-acetyl-oxazol-5-ylmethyl)-1H-pyrazol-3-yl]-amide | HCID 66929161 | — |
Reaction Steps
In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of 5-phenyl-oxazole-4-carboxylic acid {1-[2-(1-hydroxy-ethyl)-oxazol-5-ylmethyl]-1H-pyrazol-3-yl}-amide (140 mg, 0.37 mmol) in AcCN (4.0 mL) was treated at rt with MnO2 (267 mg, 2.77 mmol) and the reaction mixture was stirred at rt overnight before being filtered through Celite. Purification of the residue by FC (3:7 hept-EA) gave the title compound as a white foam. TLC: rf (3:7 hept-EA)=0.28. LC-MS-conditions 02: tR=0.95 min; [M+H]+=378.21.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08288419B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-ae5563a4825c4d4a8a816e654ef7f8ac |
| Source note | uspto-grants-2012_10 |