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Novel 4,5-dihydroisoxazolylalkylpiperazine derivatives having selective biological activity at dopamine D3 and D4 receptors, and preparation thereof

机译:对多巴胺D3和D4受体具有选择性生物活性的新型4,5-二氢异恶唑基烷基哌嗪衍生物及其制备

摘要

The present invention relates to 4,5-dihydroisoxazolylalkylpiperazine derivatives having selective biological activity at dopamine D3 and D4 receptors represented by the following Formula (1), and its preparation method through reductive amination reaction in the presence of reducing agent,wherein R1, R2, X and n are the same as defined in the specification.
机译:本发明涉及对下式(1)所示的多巴胺D3和D4受体具有选择性生物活性的4,5-二氢异恶唑基烷基哌嗪衍生物及其在还原剂的存在下通过还原胺化反应的制备方法,其中R1,R2, X和n与规范中定义的相同。

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