反应详情

To a solution of compound 145-C (23.41 g, 169.0 mmol) in acetonitrile (170 mL) was added methyl thioglycolate (16.2 mL, 178 mmol) and K2CO3 (46.72 g, 338 mmol). The mixture was heated under reflux for 3 h then filtered hot and the filter cake rinsed with acetonitrile. The filter cake was suspended in refluxing acetonitrile, filtered hot, and rinsed with additional acetonitrile. The combined filtrates were evaporated in vacuo, the residue triturated with warm water (250 mL), filtered, and rinsed with water. The solid was dissolved in warm methanol (500 mL), treated with charcoal, filtered, and evaporated in vacuo. The residue was triturated with ethanol (25 mL), filtered, washed with ethanol (25 mL), and dried in vacuo to afford compound 145-D as a brown powder (21.65 g, 62%). 1H-NMR (DMSO-d6): δ 3.83 (s, 3H), 6.91 (s, 2H), 7.52-7.59 (m, 1H), 8.40 (dd, 1H), 8.69 (dd, 1H); MS: m/z 209.1 (MH+).

1. temperatureThe mixture was heated
2. temperatureunder reflux for 3 h
3. filtrationthen filtered hot
4. washthe filter cake rinsed with acetonitrile
5. temperaturein refluxing acetonitrile
6. filtrationfiltered hot
7. washrinsed with additional acetonitrile
8. customThe combined filtrates were evaporated in vacuo
9. customthe residue triturated with warm water (250 mL)
10. filtrationfiltered
11. washrinsed with water
12. dissolutionThe solid was dissolved in warm methanol (500 mL)
13. additiontreated with charcoal
14. filtrationfiltered
15. customevaporated in vacuo
16. customThe residue was triturated with ethanol (25 mL)
17. filtrationfiltered
18. washwashed with ethanol (25 mL)
19. customdried in vacuo
20. customto afford compound 145-D as a brown powder (21.65 g, 62%)