作者: Richard E. Mewshaw , James A. Nelson , Uresh S. Shah , Xiaojie Shi , Hossein Mazandarani
DOI: 10.1016/S0960-894X(99)00434-5
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摘要: Abstract The synthesis of several-bioisosteric analogs based on the 3-OH-phenoxyethylamine dopamine D 2 agonist template (i.e., 3 ) is described. benzimidazol-2-ones and benzthioimidazol-2-ones ( 7–10 2-trifluoromethyl-benzimidazole 13 were observed to have excellent affinity for receptor.