反应详情

Under a nitrogen atmosphere, 5.90 g (14.30 mmol) of 2-(4-benzyloxy-5-ethyl-2-methoxy-phenyl)-6-(2,5-dimethyl-pyrrol-1-yl)-pyridine (6) and 27.06 g (429.1 mmol) of ammonium formate were combined in 125 mL of methanol and 500 mg of 20% Pd(OH)2 on carbon. The resultant slurry was allowed to reflux for 45 minutes. 500 mg of 20% Pd(OH)2 on carbon was added twice more, and the resultant slurry was allowed to reflux for 45 minutes. The reaction mixture was then allowed to cool to ambient temperature and passed through a pad of celite to remove the catalyst. The filtrate was concentrated in vacuo and the resultant yellow residue was partitioned between ethyl acetate (200 mL) and water (200 mL). The aqueous layer was extracted again with ethyl acetate (200 mL). The combined organic extracts were washed with brine (1×200 mL), dried over sodium sulfate, filtered and concentrated in vacuo to yield 4.52 g (98%) of 4-[6-(2,5-Dimethyl-pyrrol-1-yl)-pyridin-2-yl]-6-ethyl-3-methoxyphenol (7) as a tan solid.

1. temperatureto reflux for 45 minutes
2. temperatureto reflux for 45 minutes
3. customto remove the catalyst
4. concentrationThe filtrate was concentrated in vacuo
5. customthe resultant yellow residue was partitioned between ethyl acetate (200 mL) and water (200 mL)
6. extractionThe aqueous layer was extracted again with ethyl acetate (200 mL)
7. washThe combined organic extracts were washed with brine (1×200 mL)
8. dry with materialdried over sodium sulfate
9. filtrationfiltered
10. concentrationconcentrated in vacuo