HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 86630635, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | HCID 57556154 | HCID 57556154 | — |
| Reactant | HCID 57556186 | HCID 57556186 | — |
| Product | HCID 86630635 | HCID 86630635 | — |
Reaction Steps
To a stirring solution of a mixture of 3-(bromomethyl)-5-chloro-2-(2-chlorophenyl)quinoxaline and 2-(bromomethyl)-5-chloro-3-(2-chlorophenyl)-quinoxaline (8.5418 g, 23.21 mmol) in DMF (100.0 mL, 23.21 mmol) was added sodium azide (3.017 g, 46.42 mmol) at room temperature and the mixture was stirred at room temperature. After 40 min, the mixture was partitioned between EtOAc (200 mL) and H2O (100 mL). The organic layer was washed with brine (100 mL×1), dried over Na2SO4, filtered, and concentrated under reduced pressure to give 2-(azidomethyl)-5-chloro-3-(2-chlorophenyl)quinoxaline as a brown liquid: LC-MS (ESD major peak of m/z 330.1 [M+H]+. The crude product was carried on crude without purification for the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08901135B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-a04f87bc7ada48ec9b9767d8b3b89f48 |
| Source note | uspto-grants-2014_12 |