Butler D E, Wise L D, DeWald H A
J Med Chem. 1984 Nov;27(11):1396-400. doi: 10.1021/jm00377a003.
A series of novel (1,3-dialkyl-5-amino-1H-pyrazol-4-yl)arylmethanones was synthesized. Pharmacological evaluation of these compounds demonstrated central nervous system depressant activity, potential anticonvulsant properties, and a low order of acute toxicity. In addition, selected compounds showed potential antipsychotic effects. This report focuses on the synthesis and structure-activity relationships of these compounds. (5-Amino-1-ethyl-3-methyl-1H-pyrazol-4-yl)(2-chlorophenyl) methanone (21) was the most active compound against pentylenetetrazole-induced convulsions. (5-Amino-1,3-dimethyl-1H-pyrazol-4-yl)(3-chlorophenyl)methanone (4) also has a favorable anticonvulsant depression ratio. (5-Amino-1,3-dimethyl-1H-pyrazol-4-yl)(3-trifluoromethylphenyl)methan one (8), (5-amino-1,3-dimethyl-1H-pyrazol-4-yl)(3-thienyl)methanone (13), and (5-amino-3-ethyl-1-methyl-1H-pyrazol-4-yl)phenylmethanone (14) are very potent depressants. (5-Amino-1,3-dimethyl-1H-pyrazol-4-yl)(2-thienyl)methanone (12) possessed marked central depressant activity without anticonvulsant activity and without impairment of motor functioning. (5-Amino-1,3-dimethyl-1H-pyrazol-4-yl) (2-fluorophenyl)methanone (2) has a behavioral profile suggestive of antipsychotic activity and gave a positive Ames test result.
合成了一系列新型的(1,3 - 二烷基 - 5 - 氨基 - 1H - 吡唑 - 4 - 基)芳基甲酮。对这些化合物的药理学评估表明它们具有中枢神经系统抑制活性、潜在的抗惊厥特性以及低急性毒性。此外,所选化合物显示出潜在的抗精神病作用。本报告重点关注这些化合物的合成及构效关系。(5 - 氨基 - 1 - 乙基 - 3 - 甲基 - 1H - 吡唑 - 4 - 基)(2 - 氯苯基)甲酮(21)是对抗戊四氮诱导惊厥活性最强的化合物。(5 - 氨基 - 1,3 - 二甲基 - 1H - 吡唑 - 4 - 基)(3 - 氯苯基)甲酮(4)也具有良好的抗惊厥抑制率。(5 - 氨基 - 1,3 - 二甲基 - 1H - 吡唑 - 4 - 基)(3 - 三氟甲基苯基)甲酮(8)、(5 - 氨基 - 1,3 - 二甲基 - 1H - 吡唑 - 4 - 基)(3 - 噻吩基)甲酮(13)和(5 - 氨基 - 3 - 乙基 - 1 - 甲基 - 1H - 吡唑 - 4 - 基)苯基甲酮(14)是非常有效的抑制剂。(5 - 氨基 - 1,3 - 二甲基 - 1H - 吡唑 - 4 - 基)(2 - 噻吩基)甲酮(12)具有显著的中枢抑制活性,但无抗惊厥活性且不损害运动功能。(5 - 氨基 - 1,3 - 二甲基 - 1H - 吡唑 - 4 - 基)(2 - 氟苯基)甲酮(2)具有提示抗精神病活性的行为特征,且Ames试验结果为阳性。