反应详情

2-methyl-1-(tetrahydropyran-4-yl)benzimidazole-5-carboxylic acid HCl salt (see Working Example 4-3) (250 mg, 0.842 mmol), 2-amino-4-tert-butylphenol (139 mg, 0.842 mmol), DMF (2 mL), chloroform (5 mL) and WSC (178 mg, 0.926 mmol) were stirred for 22 hours. Water was added, and the solid obtained was filtered off, washed with water, and dried to give a solid that was taken up in dioxane (5 mL) to which was added methanesulfonic acid (140 mg, 1.46 mmol), and this was heated to reflux for 18 hours. After the reaction solution was cooled, water and saturated aqueous sodium hydrogen carbonate solution were added, and this was extracted with chloroform. After the organic layer obtained was dried over anhydrous sodium sulfate, it was filtered and concentrated. The residue obtained was purified by silica gel column chromatography to yield the title compound (160 mg, 49% yield) as white crystals.

1. customthe solid obtained
2. filtrationwas filtered off
3. washwashed with water
4. customdried
5. customto give a solid
6. temperaturethis was heated
7. temperatureto reflux for 18 hours
8. temperatureAfter the reaction solution was cooled
9. extractionthis was extracted with chloroform
10. customAfter the organic layer obtained
11. dry with materialwas dried over anhydrous sodium sulfate, it
12. filtrationwas filtered
13. concentrationconcentrated
14. customThe residue obtained
15. customwas purified by silica gel column chromatography