반응 #1606621
ord-e6b61af8cd3e4164b8cca0a9a44cb43c
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용매
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후처리
- 1온도The reaction mixture was cooled to room temperature
- 2기타partitioned between water and EtOAc (25 mL)
- 3추출The aqueous phase was extracted with EtOAc (2×25 mL)
- 4건조dried over sodium sulfate
- 5여과filtered
- 6기타the solvent was removed under reduced pressure
- 7기타The product was purified by crystallization (EtOAc)
실험 절차
A mixture of 6-bromopicolinaldehyde (2.8 g, 15 mmol), 2-amino-4,6-difluorobenzamide (2.5 g, 10 mmol), p-toluenesulfonic acid (4.2 g, 22 mmol), NaHSO3 (2.6 g, 25 mmol) and DMA (40 mL) was heated at 110° C. for 48 h in a sealed tube. The reaction mixture was cooled to room temperature and partitioned between water and EtOAc (25 mL). The aqueous phase was extracted with EtOAc (2×25 mL). The organic layers were combined, dried over sodium sulfate, filtered and the solvent was removed under reduced pressure. The product was purified by crystallization (EtOAc) to provide the title compound (500 mg, 15%): 1H NMR (500 MHz, DMSO-d6) δ 11.97 (s, 1H), 8.32 (d, J=7.7, 0.7 Hz, 1H), 8.05-7.96 (m, 1H), 7.91 (dd, J=7.7, 0.7 Hz, 1H), 7.46-7.29 (m, 2H).