Synthesis and properties of 4-substituted-1-piperazinyl-propyl derivatives of 1-phenyl-7-methylpyrimido-[4,5-d]pyrimidin-4-one.

W Malinka, H E Zajac, A Dereń, T Zawisza, M Wilimowski, L Kedzierska-Goździk, J Barczyńska, M Rutkowska, W Wojewódzki, A Szelag
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引用次数: 0

Abstract

In reactions of 1-phenyl-7-methyl-4-oxo-2-thioxo-1,2,3,4-tetrahydropyrimido[ 4,5-d]pyrimidin e (1) with 1-(3-chloropropyl)-4-methyl(phenyl, 3-chlorophenyl, 2-pyrimidynyl, 2-thiazolyl)piperazines (5), mixtures of isomeric N- and S-substituted derivatives of compound 1 (3 and 4) were obtained. Isomers were separated by fractional crystallization. The structure of novel compounds 3 and 4 was confirmed by elemental and spectral analyses. In pharmacological screening compounds 3b and 4b displayed rather strong analgesic action, inhibited amphetamine hyperactivity and abolished apomorphine stereotypy. Compounds 3e,3d and 4e attenuated m-chlorophenylpiperazine-induced hypothermia.

1-苯基-7-甲基嘧啶-[4,5-d]嘧啶-4-酮的4-取代-1-哌嗪基-丙基衍生物的合成与性质
在1-苯基-7-甲基-4-氧-2-硫氧-1,2,3,4-四氢嘧啶[4,5-d]嘧啶e(1)与1-(3-氯丙基)-4-甲基(苯基,3 -氯苯基,2 -嘧啶基,2 -噻唑基)哌嗪(5)的反应中,得到了化合物1(3和4)的N-和s -取代异构体衍生物的混合物。用分式结晶法分离异构体。新化合物3和4的结构通过元素分析和光谱分析得到了证实。在药理筛选中,化合物3b和4b表现出较强的镇痛作用,抑制安非他明多动,消除阿啡啡刻板印象。化合物3e、3d和4e减弱间氯苯哌嗪引起的低温。
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