HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Methyl 4-amino-6-bromo-3-methoxypicolinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Methyl 4-azido-6-bromo-3-methoxypyridine-2-carboxylate | HCID 21696596 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 4-amino-6-bromo-3-methoxypicolinate | HCID 21696668 | 66% |
Reaction Steps
To methyl 4-azido-6-bromo-3-methoxypyridine-2-carboxylate (0.500 g, 1.74 mmol) in 10 mL of methanol was added NaBH4 (0.046 g, 1.22 mmol). The reaction mixture was stirred at room temperature for 10 min. Ethyl acetate and water were added and the phases were separated. The organic phase was washed with H2O, dried (MgSO4) and concentrated to dryness in vacuo. The residue was purified by chromatography (silica gel). Elution with 100% ethyl acetate gave 0.300 g of a white solid. 1H NMR(CDCl3): δ 3.90 (s, 1H); 3.95 (s, 1H); 4.60 (s, 2H); 6.85 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06297197B1 |
| Source dataset | uspto-grants-2001_10 |
| ORD ID | ord-f67d112592824055bec8951e8c7feabc |
| Source note | uspto-grants-2001_10 |