4-Aminophenethyl alcohol → 2-[4-{2-Amino-6-(2-benzyloxy-5-chloro-phenyl)-pyrimidin4-ylamino]-phenyl}-ethanol

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Following the method described in Example 72, 4-(2-benzyloxy-5-chloro-phenyl)-6-chloro-pyrimidin-2-ylamine and 2-(4-amino-phenyl)-ethanol provided the title compound (71% yield). 1H NMR (CD3OD) δ 2.85 (t, 2H, J=6.9 Hz, CH2), 3.78 (t, 2H, J=6.9 Hz, CH2), 5.27 (s, 2H, CH2), 6.42 (s, 1H, Ar), 7.28-7.30 (m, 2H, Ar), 7.32-7.36 (m, 2H, Ar), 7.39 (d, 4H, J=6.3 Hz, Ar), 7.58 (d, 2H, J=8.4 Hz, Ar), 7.68-7.70 (m, 2H, Ar).

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