反应详情

(2S)-1-Amino-3-(3-pyridinyloxy)-2-propanol (0.21 g, 1.25 mmol) (which was obtained in Example 124) and 5-[4-(4-oxo-1-piperidinyl)benzyl]-1,3-thiazolidine-2,4-dione (which was obtained in Example 38) (0.413, 1.25 mmol) were mixed in N,N-dimethylformamide (12 mL) and then treated with sodium triacetoxyborohydride (0.56 g, 2.5 mmol) and acetic acid (0.26 mL). After stirring, at room temperature under a nitrogen atmosphere for one day, the mixture was purified by column chromatography (dichloromethane/methyl alcohol 85/5) to give the title compound as a yellow solid (0.25 g, 56% yield); mp; 130–132° C.; 1H NMR (400 MHz, DMSO-d6) δ 1.20–1.54 (m, 2 H), 1.90–2.02 (m, 2 H), 2.67 (t, 2 H), 2.78–2.97 (m, 4 H), 3.22–3.26 (m, 1 H), 3.35 (brs, 2 H), 3.64–3.70 (d, 2 H), 3.97–4.08 (m, 3 H), 4.60–4.63 (m, 1 H), 6.84–6.86 (m, 2 H), 7.03–7.05 (m, 2 H), 730–7.36 (m, 1 H), 7.38–7.40 (m, 1 H), 8.16–8.17 (m, 1 H), 8.8.29–8.30 (m, 1 H); MS (ES) m/z: 457 (MH+).

1. customthe mixture was purified by column chromatography (dichloromethane/methyl alcohol 85/5)