HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-Bromo-4-nitropyridine-2-carboxamide → 6-Bromo-4-(4-nitrophenylsulphanyl)-pyridine-2-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-Bromo-4-nitropyridine-2-carboxamide | HCID 19605533 | — |
| Reactant | 4Nitrothiophenol potassium salt | HCID 70002681 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-Bromo-4-(4-nitrophenylsulphanyl)-pyridine-2-carboxamide | HCID 19605494 | 87.5% |
Reaction Steps
0.25 g (0.001 mol) of 6-bromo-4-nitropyridine-2-carboxamide was dissolved in 5 ml of dimethylformamide, treated with 0.19 g (0.001 mol) of 4-nitrothiophenol potassium salt and stirred at room temperature for 18 hrs. The reaction mixture was partitioned in water and ethyl acetate and the organic phase was washed with water and sat. sodium chloride solution, dried over MgSO4 and concentrated in a vaccum. The residue was chromatographed on silica gel with ethyl acetate/hexane 1:1. There was obtained 0.31 g (86%) of 6-bromo-4-(4-nitrophenylsulphanyl)-pyridine-2-carboxamide as yellowish crystals; m.p.: 192-194° C. (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05990105 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-76fa1f9c95374dc0bcaa645581d33804 |
| Source note | uspto-grants-1999_11 |