HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 1-(7-Benzyloxy-3-nitroquinolin-4-ylamino)-2-methylpropan-2-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-(2-methylpropyl)hydroxylamine | HCID 9543329 | — |
| Reactant | 7-(Benzyloxy)-4-chloro-3-nitroquinoline | HCID 21075751 | — |
| Product | 1-(7-Benzyloxy-3-nitroquinolin-4-ylamino)-2-methylpropan-2-ol | HCID 67051017 | — |
Reaction Steps
Triethylamine (81.3 g, 0.803 mol) was added to a solution of 230.0 g (0.731 mol) of 7-benzyloxy-4-chloro-3-nitroquinoline (230.0 g, 0.731 mmol), prepared in Parts A-D of Example 1, in methanol (1.84 L). Hydroxyisobutylamine (71.6 g, 0.803 mol) was then added over a period of five minutes; the temperature rose from 30° C. to 39° C. during the addition. The reaction mixture was heated at reflux for four hours and then allowed to cool to room temperature. The solid product was isolated by filtration, washed with ethanol (1 L), and dried under vacuum at 55° C. to provide 261.2 g of 1-[(7-benzyloxy-3-nitroquinolin-4-yl)amino]-2-methylpropan-2-ol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07897597B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-4fe4e0a93777480c9fd2c26b7b619fea |
| Source note | uspto-grants-2011_03 |