HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → HCID 66880495, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2-(4-Aminophenyl)-2-methylpropanenitrile | HCID 10057801 | — |
| Reactant | Quinoline, 4,6-dichloro-3-nitro- | HCID 10681670 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 66880495 | HCID 66880495 | — |
Reaction Steps
A solution of 4,6-dichloro-3-nitroquinoline (Compound of Preparation E, 4.0 g, 16.46 mmol) and 2-(4-aminophenyl)-2-methylpropanenitrile (2.63 g, 16.46 mmol) in acetic acid (350 ml) was stirred for 2 hours. Water was added and the yellow precipitate was filtered off, washed with water and saturated aqueous NaHCO3. The yellow solid was dried to obtain the title compound. Yield: 5 g (83%); 1H NMR (DMSO-d6, 300 MHz): δ 10.074 (s, 1H), 9.062 (s, 1H,), 8.552-8.558 (d, 1H, J=1.8 Hz), 7.995-8.025 (d, 1H, J=9 Hz), 7.875-7.912 (t, 1H), 7.437-7.466 (d, 2H, J=8.4 Hz), 7.100-7.128 (d, 2H, J=8.4 Hz), 1.664 (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08637670B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-bc56c849829c446ea468e4d262fb47fd |
| Source note | uspto-grants-2014_01 |