HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 7-(4-Fluoro-3-nitrophenyl)-2-(morpholin-4-yl)quinoxalin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Fluoro-3-nitrophenylboronic acid | HCID 24901765 | — |
| Reactant | 4-(7-Bromoquinoxalin-2-yl)morpholine | HCID 53363526 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-(4-Fluoro-3-nitrophenyl)-2-(morpholin-4-yl)quinoxalin | HCID 67034997 | 92% |
Reaction Steps
To a suspension of 7-bromo-2-morpholin-4-yl-quinoxaline (1 g, 3.4 mmol), potassium carbonate (0.56 g, 4.1 mmol) and [1,1,-Bis(diphenlyphosphino)ferrocene]palladium(II)chloride (0.83 g, 1.0 mmol) in THF (38 mL) and water (3.8 mL) was added (4-fluoro-3-nitrophenyl)boronic acid (1.26 g, 6.8 mmol). The reaction mixture was allowed to reflux for 6 h. After cooling to room temperature, the solvent was removed and the residue was purified by chromatography (silica gel, Hexane/EtOAc: 20%->100% EtOAc) giving rise to 1.1 g (92%) of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09340528B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-8c0181296ba3465ebd822e1ce588b7cf |
| Source note | uspto-grants-2016_05 |