5-(4-Formylphenyl)pyrimidine → 3-{3-[(4-Pyrimidin-5-yl-benzylamino)-methyl]-phenyl}propionic acid methyl ester

Beteiligte Stoffe

Reaktionsschritte

The title compound of Step A was prepared from 3-(3-aminomethyl-phenyl)-propionic acid methyl ester hydrochloride salt, of Preparation 44, and 4-pyrimidin- 5-yl-benzaldehyde, of Preparation 26, using the method described in Example 1, Step A except the mine was formed in MeOH at reflux over 2 h. 1H NMR (400 MHz, CDCl3) δ 9.19 (s, 1H), 8.92 (s, 2H), 7.55 (m, 4H), 7.25 (m, 3H), 7.11 (d, 1H), 3.87 (s, 2H), 3.81 (s, 2H), 3.66 (s, 3H), 2.95 (t, 2H), 2.63 (t, 2H); MS 362 (M+1).

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