HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorosuccinimide → Methyl 6-amino-5-bromo-3-chloropyridine-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | Methyl 6-amino-5-bromopicolinate | HCID 10704661 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Methyl 6-amino-5-bromo-3-chloropyridine-2-carboxylate | HCID 21873807 | 95.5% |
Reaction Steps
To a solution of methyl 6-amino-5-bromopyridine-2-carboxylate (20.04 g) in acetic acid (900 mL) was added N-chlorosuccinimide (13.96 g) and the resultant solution was heated to 120° C. for 1 hour. The solution was then evaporated and treated with excess aqueous sodium bicarbonate and extracted with dichloromethane. The organic fraction was dried and evaporated to give the product (21.98 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07312212B2 |
| Source dataset | uspto-grants-2007_12 |
| ORD ID | ord-843bb1eecd8a453a8afee779bc9d9cff |
| Source note | uspto-grants-2007_12 |