反应详情

To a stirred solution of 2-fluoro-4-(7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl)benzoic acid (14, 1000 g, 2.12 mol) in acetonitrile (5 L) and CH2Cl2 (10 L) were charged HOBt (358 g, 2.65 mol, 1.25 equiv), and EDC hydrochloride (508.4 g, 2.65 mol, 1.25 equiv) at room temperature. Another portion of CH2Cl2 (10 L) was then added to the reaction mixture and the resulting reaction mixture was stirred at room temperature for 20 min. A 2.0 M solution of methylamine (MeNH2) in THF (3.44 L, 6.88 mol, 3.25 equiv) was added with stirring while maintaining the temperature at 15-30° C. The reaction mixture was stirred at room temperature for 2 h before an additional portion of 2.0 M solution of methylamine (MeNH2) in THF (1.06 L, 2.12 mol, 1 equiv) was added. The reaction mixture was stirred at room temperature for 1 h and a second portion of EDC hydrochloride (406 g, 2.12 mol, 1 equiv) was added and the stirring was continued for 6 h. When HPLC showed less than 1% of starting material (14) was remaining, the reaction mixture was concentrated under the reduced pressure at <50° C. During distillation acetonitrile (20 L) was added and distillation was continued until the remaining volume was about 20 L. The residue was treated with an aqueous solution of 2.5% sodium carbonate (Na2CO3, 40 L) and the resulting mixture was stirred at room temperature for 30 min. The solids were collected by filtration, washed with water (3×4.0 L), air dried by pulling vacuum on the filter to afford the crude desired product (15). The crude solids were treated with CH2Cl2 (17.6 L) and MeOH (5.2 L) at room temperature and resulting mixture was stirred until a clear solution was obtained. The solution was filtered to remove insoluble materials. With vigorous stirring a 2.5% aqueous solution of sodium carbonate (Na2CO3, 17.6 L) was added to the filtrate and the mixture was stirred at room temperature for 60 min to give a suspension. Heptane (20 L) was added and the mixture was stirred for an additional 60 min. The mixture was filtered and the solid was washed sequentially with water (3×4.0 L) and heptane (4.0 L), and dried in vacuum to afford 2-fluoro-N-methyl-4-(7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl)benzamide (15, 1095.3 g, 874.3 g theoretical) as a bright yellow solid, which was found to be not totally dry and to contain ˜25% residual solvents. This wet solid was used directly for the subsequent dihydrochloride salt (21) formation reaction without further drying. A small sample was dried completely for spectroscopic analyses and the data were consistent with those obtained by earlier method: For 15: 1H NMR (400 MHz, DMSO-d6) δ ppm 9.20 (s, 1H), 8.82 (dd, 1H, J=4.05, 1.56 Hz), 8.38 (br m, 1H), 8.27 (dd, 1H, J=8.50 Hz, 1.25 Hz), 8.06-7.93 (m, 5H), 7.81-7.74 (m, 2H), 7.49 (dd, 1H, J=8.40 Hz, 4.35 Hz), 4.62 (s, 2H), 2.78 (d, 3H, J=4.36 Hz); C23H17FN6O (MW 412.42), LCMS (EI) m/e 413.1 (M++H).

1. customthe resulting reaction mixture
2. stirringwith stirring
3. temperaturewhile maintaining the temperature at 15-30° C
4. additionwas added
5. stirringThe reaction mixture was stirred at room temperature for 1 h
6. waitthe stirring was continued for 6 h
7. concentrationthe reaction mixture was concentrated under the reduced pressure at <50° C
8. distillationDuring distillation acetonitrile (20 L)
9. additionwas added
10. distillationdistillation
11. additionThe residue was treated with an aqueous solution of 2.5% sodium carbonate (Na2CO3, 40 L)
12. stirringthe resulting mixture was stirred at room temperature for 30 min
13. filtrationThe solids were collected by filtration
14. washwashed with water (3×4.0 L), air
15. customdried
16. filtrationfilter
17. customto afford the crude desired product (15)
18. customresulting mixture
19. stirringwas stirred until a clear solution
20. customwas obtained
21. filtrationThe solution was filtered
22. customto remove insoluble materials
23. stirringWith vigorous stirring a 2.5% aqueous solution of sodium carbonate (Na2CO3, 17.6 L)
24. additionwas added to the filtrate
25. stirringthe mixture was stirred at room temperature for 60 min
26. customto give a suspension
27. stirringthe mixture was stirred for an additional 60 min
28. filtrationThe mixture was filtered
29. washthe solid was washed sequentially with water (3×4.0 L) and heptane (4.0 L)
30. customdried in vacuum