Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | HCID 68873567 | HCID 68873567 | — |
| Catalyst | 1,1'-Diethyl-4,4'-bipyridinium dibromide | HCID 11474262 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 68874499 | HCID 68874499 | — |
Reaction Steps
Ethyl N-(3-nitroquinolin-4-yl)-β-alaninate (62.0 g, 214 mmol, prepared as described in Part A of Example 15) was treated with sodium hydrosulfite (130.6 g, 750.1 mmol), potassium carbonate (117 g, 847 mmol), and ethyl viologen dibromide (0.802 g, 2.14 mmol) according to a modification of the method described in Part A of Example 8. After the reaction was stirred overnight, additional water (100 mL), dichloromethane, and sodium hydrosulfite (20.0 g, 115 mmol) were added, and the reaction was stirred for three additional hours. The organic layer was separated; washed with water (6×), saturated aqueous sodium bicarbonate, and brine; dried over magnesium sulfate; filtered; and concentrated under reduced pressure to provide 40.2 g of ethyl N-(3-aminoquinolin-4-yl)-β-alaninate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08697873B2 |
|---|
| Source dataset | uspto-grants-2014_04 |
|---|
| ORD ID | ord-9dc6ce1a239343ca94f922e8563efc6a |
|---|
| Source note | uspto-grants-2014_04 |
|---|