4-Hydroxypyrrolidine → 1-(4-(4-(2-Methoxy-phenylsulfanyl)-3-trifluoromethyl-phenyl)-pyridin-2-yl)-4-propyl-piperazine

Beteiligte Stoffe

Reaktionsschritte

The title compound was prepared according to the procedures of Example 38E, substituting compound 76 with compound 96 (0.039 g, 0.0985 mmol) and 3-hydroxypyrrolidine with 1-propylpiperazine. A yellow solid 114 was obtained (0.033 g, 69%). 1H-NMR (CDCl3, 400 MHz) δ 1.03 (t, J=7.3 Hz, 3H), 1.83–1.92 (m, 2H), 2.65–3.10 (br, 8H), 2.98–3.04 (m, 2H), 3.83 (s, 3H), 6.89 (s, 1H), 6.99–7.06 (m, 3H), 7.09 (d, J=8.1 Hz, 1H), 7.43–7.52 (m, 3H), 7.85 (s, 1H), 8.26 (d, J=5.9 Hz, 1H); MS (APCI) m/z 488 (M+H)+.

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