N-cyclopropyl-5-ethynylpyrimidin-2-amine → N-Cyclopropyl-5-(2-(2-methyl-5-(6-((4-methylpiperazin-1-yl)methyl)-1H-benzo[d]imidazol-2-yl)phenyl)ethynyl)pyrimidin-2-amine

Participants

Reaction Steps

The title compound was synthesized from N-cyclopropyl-5-ethynylpyrimidin-2-amine (as prepared above) and 2-(3-iodo-4-methylphenyl)-6-((4-methylpiperazin-1-yl)methyl)-1H-benzo[d]imidazole (as prepared in Example 1) in a manner similar to that described for in Example 1. The title compound was obtained as a brown solid. Mp: 136-137° C.; 1H NMR (300 MHz, CDCl3) δ: 8.40 (2H, s), 8.21 (1H, s), 7.96-7.99 (1H, d, J=9.0 Hz), 7.52-7.55 (1H, d, J=9.0 Hz), 7.49-7.52 (1H, d, J=9.0 Hz), 7.23-7.26 (1H, d, J=9.0 Hz), 7.15-7.18 (1H, d, J=9.0 Hz), 5.81 (1H, s), 5.28 (1H, s), 3.57 (2H, s), 2.78 (1H, s), 2.55 (8H, brs), 2.46 (3H, s), 2.32 (3H, s), 0.83-0.87 (2H, m), 0.56 (2H, brs). HRMS (ESI-TOF+): m/z [M+H]+ calcd for C29H32N7: 478.2714. found: 478.2718.

Provenance & Evidence