HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → 2-(2,6-difluorophenyl)-5-ethoxy-N-phenyloxazole-4-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Carbodiimide | HCID 160435 | — |
| Reactant | 2-(2,6-Difluorophenyl)-5-ethoxyoxazole-4-carboxylic acid | HCID 59587518 | — |
| Reactant | HCID 178526939 | HCID 178526939 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(2,6-difluorophenyl)-5-ethoxy-N-phenyloxazole-4-carboxamide | HCID 59587484 | 102% |
Reaction Steps
To a solution of 2-(2,6-difluorophenyl)-5-ethoxyoxazole-4-carboxylic acid (0.10 g, 0.37 mmol) and hydroxybenzotriazole monohydrate (0.06 g, 0.39 mmol) in DCM (4 mL) was added PS-carbodiimide resin (0.36 g, 0.45 mmol, 1.25 mmol/g) followed by aniline (39 uL, 0.43 mmol). The resulting mixture was stirred at room temperature for 4 hours when a further portion of aniline (7 uL, 0.08 mmol) was added and the reaction stirred at room temperature overnight. The mixture was filtered through a silica-carbonate cartridge, followed by a MP-TsOH resin cartridge which was rinsed with DCM and MeOH to afford 2-(2,6-difluorophenyl)-5-ethoxy-N-phenyloxazole-4-carboxamide (0.13 g) which was used without further purification. LCMS (1) Rt: 2.30; m/z (ES+) 345.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09187465B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-7ec20af60f924b1194c594db48a62c90 |
| Source note | uspto-grants-2015_11 |