Cyclopentylamine → 1-[3-Chloro-6-(2-cyclopentylamino-ethoxy)-4-methoxy-2-methyl-5-(3-phenyl-propoxy)-phenyl]-ethanone

Beteiligte Stoffe

Reaktionsbedingungen

Reaktionsschritte

Example 34b (217 mg, 0.48 mmol) was reacted with cyclopentylamine as described under General Procedure B (except heated to 65° C.) and the crude was purified by flash chromatography (silica-gel, MeOH/DCM 5:95) yielding the title compound (151 mg, 68%) as an oil. 1H NMR (300 MHz, CDCl3) δ 7.32-7.19 (m, 5H), 4.14 (t, J=5.1 Hz, 2H), 4.07 (t, J=6.3 Hz, 2H), 3.88 (s, 3H), 3.24-3.04 (m, 1H), 2.87-2.79 (m, 4H), 2.49 (s, 3H), 2.19 (s, 3H), 2.10-2.04 (m, 2H), 1.85-1.78 (m, 3H), 1.69-1.66 (m, 2H), 1.56-1.51 (m, 2H), 1.35-1.31 (m, 2H). MS (ES+) m/z 460 (M+H+).

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