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使用胺类和烷基碘化物通过[(11)C]一氧化碳进行光引发羰基化反应。

Photoinitiated carbonylation with [(11)C]carbon monoxide using amines and alkyl iodides.

作者信息

Itsenko Oleksiy, Kihlberg Tor, Långström Bengt

机构信息

Department of Organic Chemistry, Institute of Chemistry, Uppsala University, Box 531, S-751 21 Uppsala, Sweden, and Uppsala Imanet AB, Box 967, S-751 09 Uppsala, Sweden.

出版信息

J Org Chem. 2004 Jun 25;69(13):4356-60. doi: 10.1021/jo049934m.

Abstract

Photoinitiated radical carbonylation with [(11)C]carbon monoxide at low concentration was employed in syntheses of carbonyl-(11)C-labeled amides using alkyl iodides and amines as precursors. Eleven (11)C-amides were synthesized in up to 74% decay-corrected radiochemical yields with reaction times of 400 s and with up to 95% conversion of carbon monoxide. Starting with 26.3 GBq of [(11)C]carbon monoxide, 10.6 GBq of 1-cyclohexane [(11)C]carbonyl-4-phenyl-piperazine (15) was obtained within 35 min from the end of bombardment (33 microA) and with a specific radioactivity of 192 GBq/micromol at the same time point. The influence of solvents was investigated. The described procedure extends the range of accessible labeling methods. The method may also be useful for preparation of (13)C- and (14)C-substituted compounds.

摘要

在以烷基碘化物和胺为前体合成羰基 - (11)C 标记的酰胺时,采用了低浓度 [(11)C]一氧化碳的光引发自由基羰基化反应。在 400 秒的反应时间内,以高达 95%的一氧化碳转化率,合成了 11 种 (11)C - 酰胺,衰变校正后的放射化学产率高达 74%。从 26.3 GBq 的 [(11)C]一氧化碳开始,在轰击结束(33 μA)后的 35 分钟内,获得了 10.6 GBq 的 1 - 环己烷 [(11)C]羰基 - 4 - 苯基 - 哌嗪(15),且在同一时间点的比活度为 192 GBq/μmol。研究了溶剂的影响。所描述的方法扩展了可获得的标记方法的范围。该方法也可能有助于制备 (13)C - 和 (14)C - 取代的化合物。

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