HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 6-Bromo-2-methoxypyridin-3-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 6-Methoxy-3-pyridinylamine | HCID 81121 | — |
| Reactant | Benzyltrimethylammoniumtribromide | HCID 53442637 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-Bromo-2-methoxypyridin-3-amine | HCID 10536137 | — |
Reaction Steps
Part A: To 3.18 grams (25.6 mmol) of commercially available 5-amino-2-methoxypyridine in a solution of methylene chloride (50 ml) and methanol (20 ml) was added benzyltrimethylammonium tribromide (10 g, 25.6 mmol) and the mixture was stirred at room temperature for 24 hours. The solvent was then stripped and the resulting residue was taken up in water and extracted (3×100 mL) with ethyl acetate. The organic extracts were dried with magnesium sulfate, filtered, and concentrated in vacuo. The crude material was chromatographed on silica using 30% ethyl acetate in hexanes as solvent to afford 5-amino-2-bromo-6-methoxypyridine. C6H7N2OBr MS 203 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06342503B1 |
| Source dataset | uspto-grants-2002_01 |
| ORD ID | ord-3a170b9c823f40688c32e8fda4e8639f |
| Source note | uspto-grants-2002_01 |