HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-[(4-Bromophenyl)amino]-6-nitro-3-quinolinecarbonitrile → 6-Amino-4-[(4-bromophenyl)amino]-3-quinolinecarbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-[(4-Bromophenyl)amino]-6-nitro-3-quinolinecarbonitrile | HCID 22466762 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 6-Amino-4-[(4-bromophenyl)amino]-3-quinolinecarbonitrile | HCID 22466597 | 79.5% |
Reaction Steps
A mixture of 3.10 g (8.40 mmol) 4-[(4-bromophenyl)amino]-6-nitro-3-quinolinecarbonitrile, 155 ml ethanol, and 9.47 g (42.0 mmol) SnCl2 dihydrate was heated to reflux under N2. After 4 hours, removed heat and added ice water. Made basic with sodium bicarbonate and stirred for 2 hours. With mixture still basic, extracted with chloroform, stirred organic layer with Darco and dried with sodium sulfate. Filtered, stripped solvent and dried in vacuo, giving 2.265 g of brown-yellow solid: mass spectrum (electrospray m/e): M+H=339.0, 341.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06002008 |
| Source dataset | uspto-grants-1999_12 |
| ORD ID | ord-8b6c547541b14b05919e8c384c60ef10 |
| Source note | uspto-grants-1999_12 |