反应详情

温度

0 °C

To a stirred solution of N-(4-bromo-3-methylphenyl)3-aminothiophene-2-carboxamide (1 equiv, prepared as described above for EXAMPLE 1, part 1, using 4-bromo-3-methylaniline instead of 4-trifluoromethoxyaniline) in THF at 0° C. in an open flask, was added 2-(N-methylcarbamoyl)pyridine-4-carboxaldehyde (prepared as described in International Patent Publication No. WO 01/23375) (1.1 equiv) in THF and 4M H2SO4 (0.1 equiv) and the mixture was stirred for 30 min at 0° C. Sodium borohydride (1 equiv) was added portionwise and the mixture was allowed to warm to RT and stirred for 2 h. Water was then added, the mixture was basified to pH 12 with 2M sodium hydroxide solution, and the resulting product was extracted into ethyl acetate. The combined extracts were washed with water followed by brine, dried (MgSO4), filtered and concentrated in vacuo to afford a yellow semisolid, which was purified by column chromatography eluting with a 95:5 mixture of hexane:ethyl acetate increasing gradually to a 50:50 mixture. MS (ES+): 459, 461 [MH+]

1. customat 0° C.
2. temperatureto warm to RT
3. stirringstirred for 2 h
4. extractionthe resulting product was extracted into ethyl acetate
5. washThe combined extracts were washed with water
6. dry with materialdried (MgSO4)
7. filtrationfiltered
8. concentrationconcentrated in vacuo
9. customto afford a yellow semisolid, which
10. customwas purified by column chromatography
11. washeluting with a 95:5 mixture of hexane