HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-bromo-N-pyridin-2-yl-acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Aminopyridine | HCID 10439 | — |
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-bromo-N-pyridin-2-yl-acetamide | HCID 3415837 | — |
Reaction Steps
To a solution of 2-aminopyridine (48.8 mmol) in anhydrous THF (98 mL) at room temperature was added Et3N (58.6 mmol) and bromoacetyl bromide (58.6 mmol) dropwise The mixture was stirred overnight and quenched with sat. NaHCO3 (aq). EtOAc was added to the mixture and the layers separated. The aqueous phase was extracted with EtOAc and the combined organics dried (MgSO4) and concentrated in vacuo to a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08329729B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-6549214e493a46aa947896b6d4871768 |
| Source note | uspto-grants-2012_12 |