HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → N-(2-thienylcyanomethyl)-2-chloroisonicotinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2-Chloropyridine-4-carbonyl chloride | HCID 2800003 | — |
| Reactant | HCID 11344054 | HCID 11344054 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-(2-thienylcyanomethyl)-2-chloroisonicotinamide | HCID 14253457 | 31.8% |
Reaction Steps
3 g (0.017 mol) of 2-chloroisonicotinoyl chloride was added dropwise to a solution of 2.8 g (0.02 mol) of 2-amino-2-(2-thienyl)acetonitrile and 1.6 g (0.02 mol) of pyridine in 30 ml of toluene while the temperature was kept at 10° to 15° C. The mixture was stirred at room temperature for 1 h. A saturated aqueous common salt solution was added thereto. The organic layer was separated and dried over anhydrous sodium sulfate. The solvent was concentrated under reduced pressure and the crude product was purified according to silica gel column chromatography to obtain 1.5 g (yield: 31.8%) of light brown crystals having a melting point of 123° to 125° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04804762 |
| Source dataset | uspto-grants-1989_02 |
| ORD ID | ord-9c4cc4aa59bd4091b7b6673d734ef464 |
| Source note | uspto-grants-1989_02 |