HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,5-Dibromopyridine → 5-Bromo-N-(2,2-dimethoxyethyl)pyridin-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,5-Dibromopyridine | HCID 69353 | — |
| Reactant | Aminoacetaldehyde dimethyl acetal | HCID 89728 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Product | 5-Bromo-N-(2,2-dimethoxyethyl)pyridin-2-amine | HCID 16414251 | — |
Reaction Steps
After 50 g of 2,5-dibromopyridine and 50 mL aminoacetaldehyde dimethyl acetal were heated at 130° C. for 8 hours, an aqueous saturated sodium bicarbonate solution was added thereto, and the reaction mixture was extracted with ethyl acetate. The extract was washed with brine, the organic layer was dried over anhydrous sodium sulfate, the solvent was removed, and the resulting crude product was purified by silica gel column chromatography (ethyl acetate/hexane), to give 23.53 g of the title compound (pale yellow oil).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07074801B1 |
| Source dataset | uspto-grants-2006_07 |
| ORD ID | ord-7826fd182752414c9f1a1263d827f13b |
| Source note | uspto-grants-2006_07 |