HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanogen Bromide → HCID 86626276, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | 1-((3-Amino-2-chloroquinolin-4-yl)amino)-2-methylpropan-2-ol | HCID 22672654 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86626276 | HCID 86626276 | — |
Reaction Steps
Cyanogen bromide (4.78 g, 45.2 mmol) was added to a solution of 1-[(3-amino-2-chloro-4-quinolinyl)amino]-2-methyl-2-propanol (André et al, U.S. Pat. No. 4,988,815, Example 13, 10.0 g, 37.6 mmol) in ethanol (200 mL), and the solution was heated overnight at 90° C. and allowed to cool to ambient temperature. A precipitate formed and was isolated by filtration, washed once with diethyl ether, and then washed several times with dichloromethane to provide 9.28 g of 1-(4-chloro-2-amino-1H-imidazo[4,5-c]quinolin-1-yl)-2-methylpropan-2-ol hydrobromide as a gray powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08143270B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-8fd84e7ba845442ba836dcfddb499c11 |
| Source note | uspto-grants-2012_03 |