反应详情

A mixture of 6-(5-phenyl-1H-pyrrol-2-yl)-2-naphthol (200 mg, 0.701 mmol), prepared in step 5 of Example 1, dimethyl 4-(bromomethyl)isophthalate (241 mg, 0.841 mmol) and cesium carbonate (1.14 g, 3.50 mmol) in 50 mL of acetone was stirred at room temperature for 1.5 h. The reaction was concentrated under reduced pressure to remove the acetone. The residue was partitioned between methylene chloride and water. The aqueous layer was separated and extracted two times with methylene chloride. The combined extracts were dried (MgSO4), filtered and the solvent removed under reduced pressure to give a yellow solid. Purification of the solid on a Biotage Horizon™ system with a KP-SIL Flash 40+M column using a gradient of 85% methylene chloride in hexane to 100% methylene chloride as the eluent gave dimethyl 4-({[6-(5-phenyl-1H-pyrrol-2-yl)-2-naphthyl]oxy}methyl)isophthalate (280 mg, 81%) as a yellow solid, mp 203–205° C. Elemental Analysis for C31H25NO5.0.10 CH2Cl2 Calc'd: C, 74.70; H, 5.08; N, 2.80. Found: C, 74.24; H, 4.80; N, 2.76.

1. concentrationThe reaction was concentrated under reduced pressure
2. customto remove the acetone
3. customThe residue was partitioned between methylene chloride and water
4. customThe aqueous layer was separated
5. extractionextracted two times with methylene chloride
6. dry with materialThe combined extracts were dried (MgSO4)
7. filtrationfiltered
8. customthe solvent removed under reduced pressure
9. customto give a yellow solid
10. customPurification of the solid on a Biotage Horizon™ system with a KP-SIL Flash 40+M column