HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitrogen → 2-Methyl-5-m-tolyl-oxazole-4-carboxylic acid [2-(2-acetyl-oxazol-5-ylmethyl)-2H-[1,2,3]triazol-4-yl]-amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | 2-Methyl-5-m-tolyl-oxazole-4-carboxylic acid {2-[2-(1-hydroxy-ethyl)-oxazol-5-ylmethyl]-2H-[1,2,3]triazol-4-yl}-amide | HCID 67365733 | — |
| Catalyst | Manganese dioxide | HCID 14801 | — |
| Solvent | 2-Oxopropiononitrile | HCID 69430 | — |
| Product | 2-Methyl-5-m-tolyl-oxazole-4-carboxylic acid [2-(2-acetyl-oxazol-5-ylmethyl)-2H-[1,2,3]triazol-4-yl]-amide | HCID 67365219 | — |
Reaction Steps
In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of 2-methyl-5-m-tolyl-oxazole-4-carboxylic acid {2-[2-(1-hydroxy-ethyl)-oxazol-5-ylmethyl]-2H-[1,2,3]triazol-4-yl}-amide (60 mg, 0.15 mmol) in AcCN (2.0 mL) was treated at rt with MnO2 (107 mg, 1.11 mmol) and the reaction mixture was stirred at rt overnight before being filtered through Celite. The solvent was removed under reduced pressure and the residue was dissolved in EA (10 mL), washed with water (10 mL), and brine. The org. layer was dried over MgSO4, filtered, and the solvents were removed under reduced pressure to give the title compound as a yellow solid. LC-MS-conditions 02: tR=1.04 min; [M+H]+=407.07.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08536209B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-169f19913d9c4333b163d5509b02e746 |
| Source note | uspto-grants-2013_09 |