HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → Methyl 3-(2-bromophenethylamino)-2-phenylquinoxaline-6-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Bromophenethylamine | HCID 2734091 | — |
| Reactant | Methyl 3-chloro-2-phenylquinoxaline-6-carboxylate | HCID 77231183 | — |
| Solvent | Dimethylsulfoxide toluene | HCID 22340214 | — |
| Product | Methyl 3-(2-bromophenethylamino)-2-phenylquinoxaline-6-carboxylate | HCID 67042168 | — |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
Into a 10-mL sealed tube, was placed methyl 3-chloro-2-phenylquinoxaline-6-carboxylate (150 mg, 0.50 mmol, 1.00 equiv), 2-(2-bromophenyl)ethanamine (300.5 mg, 1.51 mmol, 3.00 equiv), potassium carbonate (347.3 mg, 2.52 mmol, 5.00 equiv), toluene/DMSO (5/1 mL). The resulting solution was stirred for overnight at 100° C. in an oil bath. The resulting mixture was concentrated under vacuum and applied onto a silica gel column with ethyl acetate/petroleum ether (1:50). This resulted in 110 mg (47%) of methyl 3-(2-bromophenethylamino)-2-phenylquinoxaline-6-carboxylate as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08916560B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-b705ce725f6f48f8b7a66033b616b8b6 |
| Source note | uspto-grants-2014_12 |