HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → 2-(Bromomethyl)-3-(2-chlorophenyl)-5-nitroquinoxaline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 3-Nitro-1,2-phenylenediamine | HCID 4359525 | — |
| Reactant | 3-Bromo-1-(2-chlorophenyl)propane-1,2-dione | HCID 57556170 | — |
| Product | 2-(Bromomethyl)-3-(2-chlorophenyl)-5-nitroquinoxaline | HCID 57707807 | — |
Reaction Steps
To a solution of 3-bromo-1-(2-chlorophenyl)propane-1,2-dione (Prepared in Example 81, 4.2971 g, 16.4325 mmol) in ethyl acetate (109.55 mL, 16.433 mmol) was added 3-nitro-1,2-phenylenediamine (2.5165 g, 16.433 mmol) at room temperature and the resulting red mixture was stirred at room temperature. After 26 h of stirring at room temperature, the mixture was concentrated under reduced pressure to give 2-(bromomethyl)-3-(2-chlorophenyl)-5-nitroquinoxaline including its regioisomer as a red syrup: LC-MS (ESI) m/z 378.0 and 379.9 [M+H]+. The crude product as a red syrup was carried on crude without purification for the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08586739B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-38ae53c62c2b40e48d0a3a5590d77bc1 |
| Source note | uspto-grants-2013_11 |