Cl.[CH:2]1([O:7][C:8]2[C:13]([O:14][CH3:15])=[CH:12][CH:11]=[CH:10][C:9]=2[CH2:16][CH2:17][NH2:18])[CH2:6][CH2:5][CH2:4][CH2:3]1.C([N:21]([CH2:24][CH3:25])[CH2:22][CH3:23])C.Cl.[C:27](O)(=[O:34])[C:28]1C=CN=C[CH:29]=1>[Cl-]>[CH:2]1([O:7][C:8]2[C:13]([O:14][CH3:15])=[CH:12][CH:11]=[CH:10][C:9]=2[CH2:16][CH2:17][NH:18][C:27](=[O:34])[CH2:28][C:29]2[CH:23]=[CH:22][N:21]=[CH:24][CH:25]=2)[CH2:3][CH2:4][CH2:5][CH2:6]1Operating analogously to example 46 using 2-(2-cyclopentyloxy-3-methoxy-phenyl)-ethylamine hydrochloride (1 g, 3.68 mmoles), obtained as described in example 3, in methliene chloride (20 ml), triethylamine (1.69 ml, 1.23 g, 12.14 mmoles) and isonicotinic acid hydrochloride (0.72 g, 4.05 mmoles), 1.42 g of the title product were obtained (yield: 99.9%).
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