Neuroleptic activity in 5-aryltetrahydro-.gamma.-carbolines
摘要:
A series of 5-aryltetrahydro-gamma-carbolines was prepared by a novel N-arylation procedure and tested for neuroleptic activity in a rat antiamphetamine model. The systematic exploration of structural parameters leading to 8-fluoro-5-(4-fluorophenyl)-2-[4-hydroxy-4-(4-fluorophenyl)butyl]-2,3,5-tetrahydro-1H-pyrido[4,3-b]indole (CP-36,584, flutroline), a potent and long-acting neuroleptic compound, is described. These semirigid compounds provide a new, structurally distinct series with which to probe the conformational requirements for potent activity at the dopamine receptor.
Neuroleptic activity in 5-aryltetrahydro-.gamma.-carbolines
作者:Charles A. Harbert、Jacob J. Plattner、Willard M. Welch、Albert Weissman、B. Kenneth Koe
DOI:10.1021/jm00180a011
日期:1980.6
A series of 5-aryltetrahydro-gamma-carbolines was prepared by a novel N-arylation procedure and tested for neuroleptic activity in a rat antiamphetamine model. The systematic exploration of structural parameters leading to 8-fluoro-5-(4-fluorophenyl)-2-[4-hydroxy-4-(4-fluorophenyl)butyl]-2,3,5-tetrahydro-1H-pyrido[4,3-b]indole (CP-36,584, flutroline), a potent and long-acting neuroleptic compound, is described. These semirigid compounds provide a new, structurally distinct series with which to probe the conformational requirements for potent activity at the dopamine receptor.
Chemoselective Oxyfunctionalization of Functionalized Benzylic Compounds with a Manganese Catalyst
A new bipiperidine-based manganese catalyst is introduced, which catalyzes the chemoselective benzylic oxidation of a wide range of diverse functionalized alkyl arenes with H2O2, affording various functionalized aryl ketones, cyclic imines, and bioactive molecules under mild conditions in a short time.