反应详情

The title compound was prepared using the procedure from Example 102 (Diethyl (4-{[4-{[4-fluoro-2-(methylcarbamoyl)phenyl]amino}-5-(trifluoromethyl)pyrimidin-2-yl]amino}-3-benzyl)phosphonate) with diethyl (4-{[4-chloro-5-(trifluoromethyl)pyrimidin-2-yl]amino}benzyl)phosphonate (10.0 mg, 0.0236 mmol) and 2-amino-5-cyano-N-methylbenzamide (Compound 150A, 8.3 mg, 0.0472 mmol). The crude mixture was purified by MDP to obtain the title compound as white solid (2.9 mg, 22% yield). 1H NMR (400 MHz, CD3OD) δ=1.28 (t, J=7.1 Hz, 6H), 2.92 (s, 3H), 3.26 (d, J=21.5 Hz, 2H), 4.07 (qd, J=7.3, 7.1 Hz, 4H), 7.28 (dd, J=8.8, 2.5 Hz, 2H), 7.56 (d, J=6.3 Hz, 2H), 7.76 (d, J=8.6 Hz, 1H), 8.04 (d, J=1.8 Hz, 1H), 8.42 (s, 1H), 8.88 (br. s., 1H). MS (ES+): m/z 563.17 (100) [MH+]; HPLC: tR=1.04 min (UPLC, purity).

1. customThe title compound was prepared
2. customThe crude mixture was purified by MDP