HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Pyridinecarboxamide → 4-(6-Bromopyridin-3-yl)-2-(pyridin-2-yl)oxazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Pyridinecarboxamide | HCID 15070 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-bromo-1-(6-bromopyridin-3-yl)ethanone | HCID 10850267 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-(6-Bromopyridin-3-yl)-2-(pyridin-2-yl)oxazole | HCID 53402021 | 10% |
Reaction Steps
A mixture of 2-bromo-1-(6-bromopyridin-3-yl)ethanone from Step A (2.3 g, 8.25 mmol) and pyridine-2-carboxamide (1 g, 8.25 mmol) was melted at 85°. Heating was continued until the mixture reached 140° at which point the product solidified. Ice, EtOAc and sat aq NaHCO3 were added. The aqueous layer was then back extracted with EtOAc/THF (3:1). Pooled organics were dried over MgSO4, filtered, concentrated, and purified on silica gel to afford 250 mg (10% yield) of 2-bromo-5-(2-pyridin-2-yl-1,3-oxazole-4-yl)pyridine. LC/MS: m/e 302.0 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08673941B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-a530822333cf46f7b0623500ec3cd92f |
| Source note | uspto-grants-2014_03 |