反应详情

A mixture of (5-chloro-1H-pyrrolo[2,3-b]pyridin-4-yl)(cyclobutyl)methanone (0.2 g, 0.85 mmol), anhydrous hydrazine (0.13 mL, 4.26 mmol) and AcOH (0.008 mL, 0.142 mmol) in ethanol (10 mL) was heated at reflux for about 20 h. During this time, water was distilled from the reaction mixture via the use of a Dean-Stark trap. The volatiles were removed under reduced pressure and the residue was partitioned between water (10 mL) and EtOAc (20 mL). The organic phase was dried over anhydrous MgSO4, filtered, and the solvent evaporated under reduced pressure. The crude material was purified by chromatography over silica gel using a 10 to 50% gradient of EtOAc in heptane as the eluent to provide 5-chloro-4-(cyclobutyl(hydrazono)methyl)-1H-pyrrolo[2,3-b]pyridine as an off-white solid (0.10 g, 49%): LC/MS (Table 2, Method o) Rt=2.22 min; m/z: 249 and 251 (M+H)+.

1. temperaturewas heated
2. temperatureat reflux for about 20 h
3. distillationDuring this time, water was distilled from the reaction mixture via the use of a Dean-Stark trap
4. customThe volatiles were removed under reduced pressure
5. customthe residue was partitioned between water (10 mL) and EtOAc (20 mL)
6. dry with materialThe organic phase was dried over anhydrous MgSO4
7. filtrationfiltered
8. customthe solvent evaporated under reduced pressure
9. customThe crude material was purified by chromatography over silica gel using a 10 to 50% gradient of EtOAc in heptane as the eluent