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Synthesis and characterization of azanonaborane-containing purine derivatives for boron neutron capture therapy

机译:含氮杂硼烷的嘌呤衍生物的合成及表征,用于硼中子俘获治疗

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摘要

Derivatives of purine, adenine, guanine, and 2,6-diaminopurine linked to the azanonaborane (B8N cluster) have been prepared, for possible use as powerful agents for boron neutron capture therapy (BNCT). The synthesis was carried out via a ligand exchange reaction. The exo-NH2R group of the azanonaborane of the type [(RH2N)B8H_(11)NHR] can be exchanged by one hetero-nitrogen atom of the pyrimidine ring, and except for guanine, also by an N atom of the imidazole ring. The identity of the products was confirmed by NMR, elemental analysis, IR, and mass spectrometry. No reaction was found to occur with caffeine and theophylline under the same reaction conditions.
机译:已制备了与氮杂硼烷(B8N团簇)连接的嘌呤,腺嘌呤,鸟嘌呤和2,6-二氨基嘌呤的衍生物,可用作硼中子捕获疗法(BNCT)的有力药物。通过配体交换反应进行合成。 [[RH2N] B8H_(11)NHR]型的氮杂硼烷的exo-NH2R基团可以被嘧啶环的一个杂氮原子(鸟嘌呤除外)与咪唑环的一个N原子交换。通过NMR,元素分析,IR和质谱确认产物的身份。在相同的反应条件下,发现咖啡因和茶碱未发生反应。

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