HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-[(3-Chloro-4-fluorophenyl)amino]-6-nitro-3-quinolinecarbonitrile → 6-Amino-4-[(3-chloro-4-fluorophenyl)amino]-3-quinolinecarbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-[(3-Chloro-4-fluorophenyl)amino]-6-nitro-3-quinolinecarbonitrile | HCID 11013311 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 6-Amino-4-[(3-chloro-4-fluorophenyl)amino]-3-quinolinecarbonitrile | HCID 11012433 | 91.4% |
Reaction Steps
A mixture of 5.360 g (15.6 mmol) 4-[(3-chloro-4-fluorophenyl)amino]-6-nitro-quinoline-3-carbonitrile, 250 ml ethanol, and 17.67 g (78.2 mmol) SnCl2 dihydrate was heated to reflux under N2. Removed heat at 1½ hours and added ice water. Made basic with sodium bicarbonate. Stirred for 2 hours extracted with chloroform. Added brine to the separatory funnel to help separate layers. Stirred organic layer with Darco and dried with sodium sulfate. Filtered, stripped solvent and dried in vacuo, giving 4.460 g of yellow-brown solid: mass spectrum (electrospray m/e): M+H=312.9, 315.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | USRE042376E1 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-4166f67997d74a30981bd05fc67a7bf2 |
| Source note | uspto-grants-2011_05 |