HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Methoxyethylamine → 3-bromo-N-(2-methoxyethyl)-5-nitropyridin-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Methoxyethylamine | HCID 8018 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Bromo-2-chloro-5-nitropyridine | HCID 230889 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-bromo-N-(2-methoxyethyl)-5-nitropyridin-2-amine | HCID 79535320 | 134% |
Reaction Steps
Triethylamine (53 μl) and 2-methoxyethylamine (23 mg) were added to a tetrahydrofuran (2 ml) solution containing 3-bromo-2-chloro-5-nitropyridine (60 mg), followed by stirring at room temperature for 1 hour. Water was added to the reaction solution, followed by extraction with ethyl acetate. The resultant was washed with saturated saline and dried over anhydrous sodium sulfate. Subsequently, the solvent was distilled away under reduced pressure, the obtained residue was purified by silica gel chromatography (n-hexane:ethyl acetate=6:1 to 3:1), and a light yellow solid of 3-bromo-N-(2-methoxyethyl)-5-nitropyridin-2-amine (93.5 mg) was thus obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08809371B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-ffb41d66bb6640fd904afee497974673 |
| Source note | uspto-grants-2014_08 |