Dimethylformamide → 4-amino-N-(2-(dimethylamino)ethyl)-3-(3-methoxy-4-(1-methyl-1H-indole-2-carboxamido)phenyl)thieno[3,2-c]pyridine-7-carboxamide

関与物質

反応条件

反応手順

In a 3-necked round bottom flask were combined 4-amino-3-(3-methoxy-4-{[(1-methyl-1H-indol-2-yl)carbonyl]amino}phenyl)thieno[3,2-c]pyridine-7-carboxylic acid (0.100 g, 0.180 mmol) and trans-dichloro[bis(triphenylphosphine)]palladium (II) (0.012 g, 0.018 mmol). The flask was filled and evacuated with nitrogen gas 4 times, followed by the addition of N,N-dimethylformamide (2.5 mL), triethylamine (0.050 mL, 0.361 mmol), and the appropriate amine (0.032 mg, 0.361 mmol). The flask was then filled and evacuated with carbon monoxide gas 3 times and the reaction mixture heated to 90° C. under an atmosphere of carbon monoxide for 4 hours. The reaction was cooled to room temperature, diluted with methylene chloride (50 mL), and washed with water and brine (50 mL each). The organic layer was separated and dried over magnesium sulfate, filtered, and the solvents removed. The crude product was purified by trituration with ethanol to give the title compound (0.034 mg, 36%) as a tan powder. LCMS (Conditions a): Rt 3.00 minutes, 543.3 (MH+); 1H NMR DMSO-d6 δ 9.50 (s, 1 H), 8.54 (s, 1 H), 8.43 (t, J=5.9 Hz, 1 H), 8.00 (d, J=8.2 Hz, 1 H), 7.70 (d, J=7.8 Hz, 1 H), 7.59 (d, J=8.6 Hz, 1 H), 7.58 (s, 1 H), 7.35 (s, 1 H), 7.32 (d, J=8.6 Hz, 1 H), 7.19 (s, 1 H), 7.15 (t, J=7.0 Hz, 1 H), 7.06 (d, J=7.0 Hz, 1 H), 4.04 (s, 3 H), 3.91 (s, 3 H), 3.40 (m, 2 H), 2.43 (m, 2 H), 2.20 (s, 6 H).

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