Acetic Anhydride → N-(3-Bromopyridin-2-yl)acetamide
Reaction equation
[Br:1][C:2]1[C:3]([NH2:8])=[N:4][CH:5]=[CH:6][CH:7]=1.[C:9](OC(=O)C)(=[O:11])[CH3:10]>>[Br:1][C:2]1[C:3]([NH:8][C:9](=[O:11])[CH3:10])=[N:4][CH:5]=[CH:6][CH:7]=1Participants
3
Conditions
- Temperature
- 100 °C
Procedure
3-Bromo-pyridin-2-ylamine (1.00 g, 5.78 mmol) was dissolved in acetic anhydride (12.4 mL). This solution was heated at 100° C. for 16 h and cooled to room temperature. The mixture was concentrated in vacuo, diluted with EtOAc (100 mL) and poured into a mixture of ice and saturated NaHCO3 solution (150 mL). This mixture was then saturated with solid NaHCO3 and extracted with EtOAc (3×150 mL). The combined EtOAc extracts were dried (MgSO4), filtered and concentrated in vacuo to give 1.49 g of N-(3-Bromo-pyridin-2-yl)-acetamide in a quantitative yield. HPLC Rt=1.79 min (YMC S5 ODS column 4.6×50 mm, 10-90% aqueous methanol over 4 minutes containing 0.2% phosphoric acid, 4 mL/min, monitoring at 220 nm) LC/MS: M+H+=215.
Workup
- temperaturecooled to room temperature
- concentrationThe mixture was concentrated in vacuo
- additiondiluted with EtOAc (100 mL)
- additionpoured into a mixture of ice and saturated NaHCO3 solution (150 mL)
- extractionsaturated with solid NaHCO3 and extracted with EtOAc (3×150 mL)
- dry with materialThe combined EtOAc extracts were dried (MgSO4)
- filtrationfiltered
- concentrationconcentrated in vacuo
Sources & evidence
- ORD record
- ord-fdc3ca9954a94343980105c8b29d97a9
- Source dataset
- uspto-grants-2008_05
- Patent number
- US07378426B2
Reaction notes
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