HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → N-(3-quinolinyl)quinoxaline-2-carboxamide Hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Quinoxaline-2-carbonyl chloride | HCID 2734681 | — |
| Reactant | HCID 178461307 | HCID 178461307 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Hydrochloric Acid | HCID 313 | — |
| Product | N-(3-quinolinyl)quinoxaline-2-carboxamide Hydrochloride | HCID 22136337 | 98% |
Reaction Steps
A solution of 2-quinoxaloyl chloride (193 mg, 1 mmol) in dichloromethane (20 mL) was treated with trans-4-methylcyclohexylamine hydrochloride (150 mg, 1 mmol), and pyridine (0.2 mL) and stirred at ambient temperature for 60 min. After this time the reaction mixture was diluted with diethyl ether (50 mL). The organic solution was washed with 1 N NaOH (2×10 mL), brine (20 mL), dried over anhydrous MgSO4. Treatment with excess 1 M HCl in diethyl ether afforded 331 mg (98%) of 407:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07053104B2 |
| Source dataset | uspto-grants-2006_05 |
| ORD ID | ord-b80a9b23ab354b16a79069278e8a9fee |
| Source note | uspto-grants-2006_05 |