反应详情

EDC (0.70 g, 3.7 mmole) was added to a solution of (E)3-(6-aminopyridin-3-yl)acrylic acid (0.61 g, 3.7 mmole), 1-methyl-2-(methylaminomethyl)-1H-indole (0.65 g, 3.7 mmole), HOBt.H2O (0.50 g, 3.7 mmole), and triethylamine (0.52 mL, 3.7 mmole) in DMF (30 mL) at RT. The reaction was stirred overnight, then was concentrated in vacuo. The residue was diluted with 5% NaHCO3 and extracted with CH2Cl2. The combined organic extracts were washed with brine and dried over MgSO4. Flash chromatography on silica gel (3% MeOH/CH2Cl2) gave a colorless semisolid which was triturated with Et2O and dried. The title compound (1.0 g, 83%) was obtained as a white solid: 1H NMR (300 MHz, CDCl3) δ 8.20 (br s, 1 H), 7.45-7.70 (m, 3 H), 7.00-7.30 (m, 3 H), 6.69 (d, J=15.4 Hz, 1 H), 6.30-6.50 (m, 2 H), 4.89 (s, 2 H), 4.67 (br s, 2 H), 3.68 (s, 3 H), 3.01 (s, 3 H); MS (ES) m/e 321 (M+H)+. Anal. Calcd for C19H20N4O.0.40 H2O: C, 69.66; H, 6.40; N, 17.10. Found: C, 69.99; H, 6.27; N, 16.84.

1. customat RT
2. concentrationwas concentrated in vacuo
3. additionThe residue was diluted with 5% NaHCO3
4. extractionextracted with CH2Cl2
5. washThe combined organic extracts were washed with brine
6. dry with materialdried over MgSO4
7. customFlash chromatography on silica gel (3% MeOH/CH2Cl2) gave a colorless semisolid which
8. customwas triturated with Et2O
9. customdried