反应详情

Add N-(4-Fluoro-benzyl)-4-(3-iodo-indole-1-sulfonyl)-benzamide (268 mg, 0.0.50 mmol), 2-chlorophenylboronic acid (78.2 mg, 0.50 mmol), PdCl2(dppf).CH2Cl2 (41 mg, 0.05 mmol) and 2M Na2CO3 (0.55 mL, 1.1 mmol) respectively to DMF (15.0 mL) at ambient temperature under N2. Heat the reaction to 100° C. for 16 h. Cool the reaction to ambient temperature and pour into a H2O-EtOAc mixture (200 mL/100 mL). Separate the EtOAc, extract several times with H2O and wash with brine. Dry (MgSO4), filter and evaporate the filtrate. Purify the crude material on silica gel using a gradient hexane-EtOAc system to give 0.155 g (60% yield) of 4-[3-(2-chloro-phenyl)-indole-1-sulfonyl]-N-(4-fluoro-benzyl)-benzamide: Mass spectrum (m/e) M−1) 517.0787.

1. customat ambient temperature
2. temperatureHeat
3. customthe reaction to 100° C. for 16 h
4. temperatureCool
5. customthe reaction to ambient temperature
6. customSeparate the EtOAc
7. extractionextract several times with H2O
8. washwash with brine
9. dry with materialDry (MgSO4)
10. filtrationfilter
11. customevaporate the filtrate
12. customPurify the crude material on silica gel using a gradient hexane-EtOAc system