HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → (7-Bromo-3-nitroquinolin-4-yl)isobutylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Isobutylamine | HCID 6558 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 7-Bromo-4-chloro-3-nitroquinoline | HCID 21984361 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (7-Bromo-3-nitroquinolin-4-yl)isobutylamine | HCID 21984282 | 92.5% |
Reaction Steps
To a suspension of 7-bromo-4-chloro-3-nitroquinoline (25.0 g, 87.0 mmol) in DMF (70 mL) was added triethylamine (18.2 mL, 130 mmol). A solution of iso-butylamine (9.50 mL, 95.7 mmol) in DMF (20 mL) was added dropwise. The viscous reaction mixture was stirred overnight at ambient temperature. Water (200 mL) was added and the mixture was stirred for 1 hour. A solid was isolated by filtration, washed with water, and dried in a vacuum oven overnight to yield 26.1 g of 7-bromo-N-(2-methylpropyl)-3-nitroquinolin-4-amine as a yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08598192B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-887bd905b4874b6ab5f5c7402cf1bbfb |
| Source note | uspto-grants-2013_12 |