HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-6-Chloropyrazine → 3-Bromo-6-chloropyrazin-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-6-Chloropyrazine | HCID 118458 | — |
| Reactant | N-Bromosuccinamide | HCID 9834204 | — |
| Reactant | 5-Bromo-6-chloropyrazin-2-amine | HCID 18180207 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3-Bromo-6-chloropyrazin-2-amine | HCID 17955991 | — |
Reaction Steps
N-bromosuccinamide (6.9 g) was added portionwise over 0.5 h to a stirred solution of 6-chloro-2-pyrazinamine (5.0 g) in chloroform (200 mL) heated under reflux. After the addition was complete the reaction mixture was allowed to cool, washed with water and evaporated to give a 3:1 mixture of 5-bromo-6-chloro-2-pyrazinamine and the subtitle compound which were separated by silica gel chromatography eluting with dichloromethane. Yield 2.0 g. Used directly.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07662825B2 |
| Source dataset | uspto-grants-2010_02 |
| ORD ID | ord-ba26584da5664429a6a77c885fde4624 |
| Source note | uspto-grants-2010_02 |