HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1-(4-fluorophenyl)-1H-pyrazolo[4,3-c]pyridine-4-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Reactant | 1-(4-fluorophenyl)-1H-pyrazolo[4,3-c]pyridine 5-oxide | HCID 58084244 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-(4-fluorophenyl)-1H-pyrazolo[4,3-c]pyridine-4-carbonitrile | HCID 59278518 | — |
Reaction Steps
To a solution of 1-(4-fluorophenyl)-1H-pyrazolo[4,3-c]pyridine 5-oxide (0.300 g, 1.31 mmol) in acetonitrile (10 mL) was added trimethylsilyl cyanide (TMSCN) (931 μL, 6.99 mmol) followed by Et3N (0.930 mL, 6.69 mmol) and the mixture was warmed at reflux. After 3 hours, the mixture was diluted with water and the solid collected by filtration washing with water. The flakey solid was then dissolved in methanol and concentrated to afford 1-(4-fluorophenyl)-1H-pyrazolo[4,3-c]pyridine-4-carbonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07879873B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-20f9d24611e047cba3d40f097cca470c |
| Source note | uspto-grants-2011_02 |