5-(1-methyl-1H-benzo[d]imidazol-6-yl)-1H-pyrazol-3-amine 、
5-(1-methyl-1H-benzo[d]imidazol-5-yl)-1H-pyrazol-3-amine 、
2-(oxiran-2-ylmethyl)-1,2,3,4-tetrahydroisoquinoline 、
N,N-二异丙基乙胺 以
乙醇 为溶剂,
反应 16.0h,
以to give the desired 1-(3,4-dihydroisoquinolin-2(1H)-yl)-3-((5-(1-methyl-1H-benzo[d]imidazol-6-yl)-1H-pyrazol-3-yl)amino)propan-2-ol (4.5 mg, Yield 4.1%) 1H NMR (400 MHz, MeOD) 8.21-8.16 (m, 1H), 7.86 (s, 1H), 7.71-7.64 (m, 2H), 7.20-7.06 (m, 4H), 5.96 (s, 1H), 4.50-4.39 (m, 1H), 4.29-4.00 (m, 4H), 3.97-3.89 (m, 3H), 3.30-3.11 (m, 2H), 3.08-2.92 (m, 4H)的产率得到1-(3,4-dihydroisoquinolin-2(1H)-yl)-3-((5-(1-methyl-1H-benzo[d]imidazol-6-yl)-1H-pyrazol-3-yl)amino)propan-2-ol