反应详情

2-(dimethylamino)acetic acid (16.0 mg, 1.25 eq), triethylamine (34.6 mL, 2.0 eq) and HATU (59.0 mg, 1.25 eq) were dissolved in 3 mL of dichloromethane and stirred at room temperature for 10 minutes. At this time N-(4-(2-aminoethoxy)-3-(1-methyl-1H-pyrazol-5-yl)phenyl)-3-methoxybenzamide hydrochloride (50.0 mg, 124 μmol) dissolved in 2.0 mL of dichloromethane was added and the reaction was stirred at room temperature for 3 hr. The solvents were evaporated under a stream of nitrogen and it was purified by HPLC. The proper fractions were collected and lyophilized. It was then stirred overnight in 2.0M hydrochloric acid in ether (310.3 μl, 5 eq). The solvents were evaporated under a stream of nitrogen and lyophilized to afford the title compound as a white solid in 43.0% yield. LCMS m/z (%)=452 (M+H, 100). 1H NMR (400 MHz, CDCl3) δ ppm 2.83 (s, 3H), 2.90 (s, 3H), 3.61-3.67 (m, 2H), 3.82 (s, 2H), 3.87 (s, 3H), 3.88 (s, 3H), 4.07 (t, J=4.55 Hz, 2H), 6.42 (d, J=2.53 Hz, 1H), 6.99 (d, J=8.59 Hz, 1H), 7.10 (dt, J=4.55, 2.53 Hz, 1H), 7.40 (d, J=5.05 Hz, 2H), 7.44 (s, 1H), 7.57 (dd, J=9.09, 2.53 Hz, 1H), 7.70 (d, J=2.53 Hz, 1H), 7.82 (d, J=2.53 Hz, 1H)

1. additionwas added
2. stirringthe reaction was stirred at room temperature for 3 hr
3. customThe solvents were evaporated under a stream of nitrogen and it
4. customwas purified by HPLC
5. customThe proper fractions were collected
6. customThe solvents were evaporated under a stream of nitrogen