1-Methylpiperidin-3-amine dihydrochloride → (+/-) 9-fluoro-10-(3-hydroxy-3-methyl-but-1-ynyl)-N3-(1-methyl-3-piperidyl)-5,6-dihydroimidazo[1,2-d][1,4]benzoxazepine-2,3-dicarboxamide

Beteiligte Stoffe

Reaktionsschritte

2-Carbamoyl-9-fluoro-10-(3-hydroxy-3-methyl-but-1-ynyl)-5,6-dihydroimidazo[1,2-d][1,4]benzoxazepine-3-carboxylic acid (0.06 g) was reacted with 1-methylpiperidin-3-amine dihydrochloride similar to as described in Example 2 to afford 22.3 mg of (±) 9-fluoro-10-(3-hydroxy-3-methyl-but-1-ynyl)-N3-(1-methyl-3-piperidyl)-5,6-dihydroimidazo[1,2-d][1,4]benzoxazepine-2,3-dicarboxamide following reverse phase hplc purification. MS (Q1) 470 (M)+. 1H NMR (400 MHz, DMSO) δ 11.28 (d, J=7.4 Hz, 1H), 8.59 (d, J=8.4 Hz, 1H), 8.34 (s, 1H), 7.83 (s, 1H), 7.01 (d, J=10.6 Hz, 1H), 5.48 (s, 1H), 5.08-4.88 (m, 2H), 4.63-4.46 (m, 2H), 3.99-3.83 (m, 1H), 2.74-2.64 (m, 1H), 2.48-2.42 (m, 1H), 2.06 (t, J=8.0 Hz, 1H), 1.97 (t, J=10.6 Hz, 1H), 1.75 (m, J=13.8 Hz, 2H), 1.59-1.51 (m, 1H), 1.49 (s, 6H), 1.36-1.19 (m, 1H).

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