HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 2,6-Difluoro-N-(1-{[2-(phenylmethyl)phenyl]methyl}-1H-pyrazol-3-yl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Benzyl benzylbromide | HCID 12422098 | — |
| Reactant | HCID 178522346 | HCID 178522346 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2,6-Difluoro-N-(1-{[2-(phenylmethyl)phenyl]methyl}-1H-pyrazol-3-yl)benzamide | HCID 59547906 | — |
Reaction Steps
2,6-Difluoro-N-1H-pyrazol-3-ylbenzamide (for a preparation see Intermediate 9)(45 mg, 0.202 mmol), potassium carbonate (42 mg, 0.304 mmol) and 1-(bromomethyl)-2-(phenylmethyl)benzene (for a preparation see Intermediate 3)(64 mg, 0.245 mmol) were weighed into a vial with a stirrer. DMF (1 ml) was added, the vial was capped and the mixture was stirred at room temperature for 17 h. The reaction mixture was filtered, washing with MeOH to give a total volume of 2 ml. This solution was purified by MDAP (Sunfire column, formic acid buffer) (Method B). The solvent was removed to give the title compound as a colourless solid (10 mg); LCMS: (System 4) MH+=404, tRET=3.23 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08399436B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-16b6b332a7db4ae081f7f80f6b6a7fce |
| Source note | uspto-grants-2013_03 |