HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylamine → 3-Bromo-4-(2-ethylaminopyridin-3-yl)thiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylamine | HCID 6341 | — |
| Reactant | 3-Bromo-4-(2-fluoropyridin-3-yl)thiophene | HCID 15408561 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-Bromo-4-(2-ethylaminopyridin-3-yl)thiophene | HCID 15408562 | 83.7% |
Reaction Steps
A solution of 3-bromo-4-(2-fluoropyridin-3-yl)thiophene (0.344 g) and ethylamine (0.2 g) in dioxane (1 mL), in a sealed tube, was heated at 100° C. for four days. The mixture was cooled, diluted with ethyl acetate, washed with water, dried, filtered, and evaporated. The residue was fractionated by chromatography to give 3-bromo-4-(2-ethylaminopyridin-3-yl)thiophene (0.316 g) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05919779 |
| Source dataset | uspto-grants-1999_07 |
| ORD ID | ord-67dba326e7f74299a9e4d9ef7e85b997 |
| Source note | uspto-grants-1999_07 |