HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 3-[4-(2-Cyano-benzyloxy)-phenyl]-isoxazole-5-carboxylic acid amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(Bromomethyl)benzonitrile | HCID 89599 | — |
| Reactant | 3-(4-Hydroxy-phenyl)-isoxazole-5-carboxylic acid amide | HCID 136491250 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-[4-(2-Cyano-benzyloxy)-phenyl]-isoxazole-5-carboxylic acid amide | HCID 76284358 | 27% |
Reaction Steps
3-(4-Hydroxy-phenyl)-isoxazole-5-carboxylic acid amide (which may be prepared as described in Preparation of Intermediate 2; 50 mg, 0.24 mmol), K2CO3 (37 mg, 0.27 mmol) and tetrabutylammonium iodide (9 mg, 0.024 mmol) were taken up in DMF (2.4 mL). 2-Cyanobenzyl bromide (53 mg, 0.27 mmol) was added and the reaction mixture was stirred at room temperature overnight. The solvent was evaporated and the residue was purified by high-throughput purification to give 3-[4-(2-cyano-benzyloxy)-phenyl]-isoxazole-5-carboxylic acid amide (20.7 mg, 27%). LRMS (ESI+): m/z [M+CH3CN+H]+ 361.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09296711B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-1160c5f5f61c410a902e468c3458ffa0 |
| Source note | uspto-grants-2016_03 |