Reaction Steps
To a solution of tert-butyl 3-(1-cyano-2-(pyridin-3-yl)vinyl)-5-hydroxy-1H-indole-1-carboxylate (see example 22) (110 mg, 0.30 mmol, 1.0 eq.) and isopropyl iodide (40 μL, 0.40 mmol, 1.3 eq.) in DMSO (8 mL) was added potassium carbonate (100 mg, 0.73 mmol, 2.4 eq.). The reaction apparatus was protected from light and the mixture was stirred at room temperature for 24 hours before sodium methanolate (41 mg, 0.75 mmol, 2.5 eq.) was added. The reaction was pursued at room temperature for 1 hour, and then quenched with a saturated aqueous ammonium chloride solution. The mixture was extracted with ethyl acetate and the organic layer was washed with brine, and then dried over MgSO4. The solvent was removed under reduced pressure, and the residue purified by silica gel flash-column chromatography (eluent: heptane/EtOAc, 60:40 to 40:60) to afford, after trituration with diethyl ether, the compound (23) as a yellow powder (50 mg, 55%). TLC: Rf=0.25 (heptane 40/EtOAc 60); mp: 211° C.; IR νmax (cm-1): 2218 (νCN); 1H NMR (DMSO, 300 MHz): δ (ppm): 1.29 (6H, d, J9′-8′=J9′-8′=6.1 Hz, 3H9′ and 3H10′), 4.65 (1H, h, J8′-9′=J8′-9′=6.1 Hz, H8′), 6.90 (1H, dd, J6′-7′=8.9 Hz, J6′-4′=2.1 Hz, H6′), 7.39 (1H, d, J7′-6′=8.9 Hz, H7′), 7.51 (1H, d, J4′-6′=2.1 Hz, H4′), 7.54 (1H, dd, J5″-4″=7.9 Hz, J5″-6″=4.9 Hz, H5″), 7.73 (1H, s, H3), 7.79 (1H, s, H2′), 8.32 (1H, d, J4″-5″=7.9 Hz, H4″), 8.59 (1H, dd, J6″-5″=4.9 Hz, J6″-4″=1.2 Hz, H6″), 8.98 (1H, d, J2″-4″=1.6 Hz, H2″), 11.64 (1H, s, indolic H); 13C NMR (DMSO, 75.5 MHz): δ (ppm): 22.5 (C9′ and C10′), 70.7 (C8′), 105.9 (C4′), 108.7 (C2), 110.6 (C3′), 113.6 (C6′), 114.6 (C7′), 118.6 (C1), 124.1 (C5″), 124.6 (C3a′), 128.1 (C2′), 131.4 (C3″), 132.7 (C3), 132.9 (C7a′), 135.1 (C4″), 150.0 (C6″), 150.4 (C2″), 152.9 (C5′); ESI-MS: m/z 304.1 ([M+H]+), 326.1 ([M+Na]+); HRESI-MS: m/z 304.1448 (calcd for C19H18N3O, 304.1450).
