Diisopropylethylamine → HCID 178520722, compound

Participants

Reaction Steps

(S)-2-(1,4-Dibromo-8-oxo-9-(2,2,2-trifluoroethyl)-3,6,7,8,9,10-hexahydroazepino[3,4-e]indazol-7-yl)acetic acid (49 mg, 0.098 mmol) was dissolved in N,N-dimethylformamide (1.5 mL). N,N-Diisopropylethylamine (70 μl, 0.402 mmol) was added to the mixture followed by TBTU (34.5 mg, 0.107 mmol). 8-Fluoro-3-(piperidin-4-yl)quinolin-2(1H)-one hydrochloride (33.0 mg, 0.117 mmol) was added to the mixture. Reaction stirred at room temperature for 3.5 hours. Reaction was quenched with 50% acetonitrile-water. Material was purified by reverse phase prep HPLC (acetonitrile-water-trifluoroacetic acid). Acetonitrile was removed from the fractions by roto-vap. Remaining aqueous was made basic with aqueous sodium bicarbonate. Material was extracted twice with ethyl acetate and the aqueous phase was discarded. Organics were dried MgSO4, filtered and then concentrated to dryness. Title compound was obtained as white solid in 59% yield. 1H NMR (500 MHz, DMSO-D6) δ ppm 13.91 (s, 1H) 11.81 (s, 1H) 7.77 (s, 1H) 7.48 (s, 2H) 7.26-7.41 (m, 1H) 7.06-7.18 (m, 1H) 5.58 (d, J=16.79 Hz, 1H) 5.40 (d, J=17.09 Hz, 1H) 4.55 (d, J=12.51 Hz, 1H) 4.28-4.44 (m, 1H) 4.06-4.22 (m, 2H) 3.86-4.07 (m, 1H) 3.13-3.24 (m, 2H) 3.06 (t, J=10.83 Hz, 1H) 2.98 (dd, J=16.48, 8.24 Hz, 1H) 2.84-2.95 (m, 1H) 2.65 (t, J=12.05 Hz, 1H) 2.33-2.48 (m, 1H) 1.93 (d, J=10.07 Hz, 1H) 1.78-1.89 (m, 1H) 1.47-1.62 (m, 1H) 1.32-1.46 (m, 1H). High resolution MS m/e (M+H)+=726.0337.

Provenance & Evidence