Sodium Methoxide → HCID 15603085, compound

Participants

Reaction Steps

To N-[3-(2-Chloro-pyridine-4-carbonyl)-5-(1-triisopropylsilanyl-1H-indol-4-yl)-phenyl]-acetamide (Example 83, 0.120 g, 0.22 mmol) in 25 mL of anhydrous methanol was added 0.036 g (0.66 mmol) NaOMe. The reaction mixture was refluxed overnight. The methanol was removed under vacuum and water added to the reaction mixture. The aqueous phase was extracted with ethyl acetate, washed with water and brine and dried over anhydrous sodium sulfate. The crude product was purifed on the preparative SFC to give 10 mg N-[3-(1H-indol-4-yl)-5-(2-methoxy-pyridine-4-carbonyl)-phenyl]-acetamide. 1H NMR (400 MHz, CD3COCD3): δ 10.46 (s, 1H), 9.50 (s, 1H), 8.41 (q, J=1.7 Hz, 1H), 8.37 (dd, J=5.1, 0.7 Hz, 1H), 8.11 (q, J=1.5 Hz, 1H), 7.82 (t, J=1.6 Hz, 1H), 7.49 (d, J=8.0 Hz, 1H), 7.45-7.42 (m, 1H), 7.28 (dd, J=5.1, 1.4 Hz, 1H), 7.20 (m, 2H), 7.08 (t, J=1.1 Hz, 1H), 6.75-6.73 (m, 1H), 3.96 (s, 3H), 2.14 (s, 3H).

Provenance & Evidence