HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzenamine, 3-(methylthio)- → 4-[(3-Methylsulfanylphenyl)amino]-6-nitro-3-quinolinecarbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzenamine, 3-(methylthio)- | HCID 15693 | — |
| Reactant | 4-Chloro-6-nitroquinoline-3-carbonitrile | HCID 11085690 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-[(3-Methylsulfanylphenyl)amino]-6-nitro-3-quinolinecarbonitrile | HCID 22466628 | 67% |
Reaction Steps
A mixture of 5.00 g (21.5 mmol) 4-chloro-6-nitro-3-quinolinecarbonitrile, 200 ml ethanol, and 3.18 ml (25.8 mmol) 3-methylsulfanylaniline was heated to reflux under N2. At 2 hours, removed heat and made basic with saturated sodium bicarbonate. Stripped solvents and air dried. Washed residue with hexane, collected solids and washed with water. Dissolved in ethyl acetate, stirred with Darco, stripped solvent and dried in vacuo, giving 4.848 g of yellow solid: mass spectrum (electrospray m/e): M+H=337.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06384051B1 |
| Source dataset | uspto-grants-2002_05 |
| ORD ID | ord-eb1d44a174914f05b50986a7668b4834 |
| Source note | uspto-grants-2002_05 |