4-Chloroaniline → 6-[5-Bromo-2-(2-methoxy-ethoxy)-phenyl]-N*4*-(4-chloro-phenyl)-pyrimidine-2,4-diamine

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Following the method described in Example 4, 4-[5-bromo-2-(2-methoxy-ethoxy)-phenyl)-6-chloro-pyrimidin-2-ylamine and 4-chloro-phenylamine provided the title compound (79% yield). 1H NMR (DMSO-d6) δ 3.26 (s, 3H, CH3), 3.71 (t, 2H, J=4.7 Hz, CH2), 4.19 (t, 2H, J=4.4 Hz, CH2), 6.36 (s, 2H, NH2), 6.74 (s, 1H, Ar), 7.11 (d, 1H, J=8.8 Hz, Ar), 7.31 (d, 2H, J=8.8 Hz, Ar), 7.52 (dd, 1H, J=8.8 Hz, J=2.6 Hz, Ar), 7.76 (d, 2H, J=8.7 Hz, Ar), 8.01 (d, 1H, J=2.6 Hz, Ar), 9.27 (s, 1H, NH).

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