HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Sulfide → 7-Methoxy-4-(5-nitrothiophen-2-ylsulfanyl)quinoline-6-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Sulfide | HCID 14804 | — |
| Reactant | 2-Bromo-5-nitrothiophene | HCID 83222 | — |
| Reactant | 4-Chloro-7-methoxyquinoline-6-carboxamide | HCID 22936418 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 7-Methoxy-4-(5-nitrothiophen-2-ylsulfanyl)quinoline-6-carboxamide | HCID 22936624 | 39% |
Reaction Steps
4-Chloro-7-methoxyquinoline-6-carboxamide (1.18 g, 5.00 mmol) and sodium sulfide (1.20 g, 5.50 mmol) were heated and stirred in dimethylformamide (10 ml) at 60° C. for 3 hours. After cooling the reaction solution to room temperature, 2-bromo-5-nitrothiophene (1.25 g, 6.00 mmol) was added and the mixture was further heated and stirred at 60° C. for 1 hour. The reaction solution was returned to room temperature and then poured into ice water (50 ml), and the precipitated crystals were filtered out, washed with water and methanol and then blow-dried to obtain the title compound (700 mg, 1.94 mmol, 39%) as yellowish-brown crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08372981B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-012fea1c2dd441b8acf2f1e449f0c021 |
| Source note | uspto-grants-2013_02 |