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[C-11]/(C-13)Carbon monoxide in palladium-mediated synthesis of imides

机译:[C-11] /(C-13)一氧化碳在钯介导的酰亚胺合成中的作用

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C-11]Carbon monoxide in low concentration with palladium(0) complexes (in the range of 5 mu mol) and aryl halides (about 10 mu mol) were used in the synthesis of the C-11-labelled imides, thalidomide, N-phthaloyl-L-glutamic acid, N-phthaloylhexane and aniracetam. The labellings were performed with ring closure reactions except in the case of aniracetam. These imides were obtained in nearly quantitative radiochemical yields, calculated from the [C-11]carbon monoxide, with specific radioactivities between 70-600 GBq mu mol(-1). The radiochemical purity of the LC-purified products exceeded 98%. N-(C-13)Phthaloyl-L-glutamic acid 2 was produced to verify the position of the label (delta 167.5 ppm) with C-13 NMR, and this also indicates that the discussed approach is valuable forlabelling with other carbon isotopes. In a typical experiment starting with 2.8 GBq of [C-11]carbon monoxide, 0.6 GBq of HPLC-purified [C-11]-N-phthaloyl-L-glutamic acid 2 was obtained within 40 minutes from the start of the carbonylation reaction (84% decay-corrected radiochemical yield). [References: 19
机译:C-11]低浓度的一氧化碳与钯(0)配合物(在5μmol范围内)和芳基卤化物(约10μmol)用于合成C-11-标记的酰亚胺,沙利度胺,N -邻苯二甲酰基-L-谷氨酸,N-邻苯二甲酰基己烷和阿拉西坦。除阿尼西坦的情况外,标记均通过闭环反应进行。这些酰亚胺是以[C-11]一氧化碳计算的,几乎是定量的放射化学收率,比活度在70-600 GBq mu mol(-1)之间。 LC纯化产品的放射化学纯度超过98%。生成了N-(C-13)邻苯二甲酰基-L-谷氨酸2以通过C-13 NMR验证标记的位置(δ167.5 ppm),这也表明所讨论的方法对于用其他碳同位素标记非常有价值。在从2.8 GBq的[C-11]一氧化碳开始的典型实验中,从羰基化反应开始的40分钟内获得了0.6 GBq的HPLC纯化的[C-11] -N-邻苯二甲酰基-L-谷氨酸2 (84%经衰变校正的放射化学产率)。 [参考:19

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