反应详情

温度

85 °C

To a stirred solution of 2-(2-methoxyphenyl)-1,3-thiazole-4-carboxylic acid (0.22 g, 0.94 mmol) in toluene (10 mL) at RT and under N2 was added TEA (0.3 mL). After 5 min, (PhO)2PON3 (0.32 mL) was added and the reaction mixture was heated at 85° C. for 20 min followed by the addition of 6-(piperidylmethyl)-2-pyridylamine (0.27 g, 1.41 mmol). The resulting mixture was heated at reflux for 4 h using a Dean-Stark trap. The mixture was cooled to RT, concentrated by rotary evaporation and purified on silica gel (5:95 MeOH/CH2Cl2). The yellow solid obtained was dissolved in EtOAc (15 mL) and washed with saturated NH4Cl (10 mL). The organic phase was separated, dried over MgSO4, filtered and concentrated by rotary evaporation to afford the title compound as a pale-yellow solid. EI-MS m/z 424 (M+H). Calc'd for C22H25N5O2S: 423.17.

1. temperatureThe resulting mixture was heated
2. temperatureat reflux for 4 h
3. temperatureThe mixture was cooled to RT
4. concentrationconcentrated by rotary evaporation
5. custompurified on silica gel (5:95 MeOH/CH2Cl2)
6. customThe yellow solid obtained
7. washwashed with saturated NH4Cl (10 mL)
8. customThe organic phase was separated
9. dry with materialdried over MgSO4
10. filtrationfiltered
11. concentrationconcentrated by rotary evaporation