反应详情

To a solution of 2-pyrrolidin-1-yl-ethylamine in DCE was added trimethyl aluminum (1.03 mmol, 0.51 mL of 2N solution in DCM). After the reaction was stirred at ambient temperature for 30 minutes, a solution of 4-(3-tert-butyl-5-{3-[4-(pyridin-4-yloxy)phenyl]ureido}pyrazol-1-yl}benzoic acid methyl ester (100 mg, 0.21 mmol) in DCE was added, and the reaction mixture was stirred at 80° C. for 16 h. The reaction mixture was quenched with two drops of water, dried over MgSO4, filtered, and evaporated at reduced pressure. Purification using MPLC (eluting with 15% NH3 in MeOH (2N)/EtOAc) afforded 34 mg (29%) of the title compound. 1H-NMR (acetone-d6) δ 8.43 (d, J=9.0 Hz, 2H), 7.94 (d, J=9.0 Hz, 2H), 7.69 (d, J=9.0 Hz, 2H), 7.60 (d, J=9.0 Hz, 2H), 7.07 (d, J=9.0 Hz, 2H), 6.84 (d, J=4.0 Hz, 2H), 6.48 (s, 1H), 3.52 (t, J=7.5 Hz, 2H), 2.67 (t, J=3.0 Hz, 2H), 2.50 to 2.64 (m, 4H), 1.70 to 1.72 (m, 4H), 1.31 (s, 9H); MS LC-MS [M+H]+=568, RT=2.48 min.

1. stirringthe reaction mixture was stirred at 80° C. for 16 h
2. customThe reaction mixture was quenched with two drops of water
3. dry with materialdried over MgSO4
4. filtrationfiltered
5. customevaporated at reduced pressure
6. customPurification
7. washMPLC (eluting with 15% NH3 in MeOH (2N)/EtOAc)