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作为新型选择性正电子发射断层显像(PET)σ1受体探针的N-[ω-(6-甲氧基萘-1-基)烷基]衍生物的碳-11标记哌啶环的合成

Synthesis of carbon-11-labeled piperidine ring of N-[omega-(6-methoxynaphthalen-1-yl)alkyl] derivatives as new selective PET sigma1 receptor probes.

作者信息

Gao Mingzhang, Wang Min, Hutchins Gary D, Zheng Qi-Huang

机构信息

Department of Radiology, Indiana University School of Medicine, Indianapolis, IN 46202-2111, USA.

出版信息

Appl Radiat Isot. 2010 Mar;68(3):459-65. doi: 10.1016/j.apradiso.2009.12.035. Epub 2009 Dec 22.

Abstract

Carbon-11-labeled piperidine ring of N-[omega-(6-methoxynaphthalen-1-yl)alkyl] derivatives were first designed and synthesized as new selective PET sigma(1) receptor probes. The target tracers were prepared by O-[(11)C]methylation of their corresponding phenolic hydroxyl precursors using [(11)C]CH(3)OTf under basic conditions and isolated by a simplified SPE method in 40-50% radiochemical yields based on [(11)C]CO(2) and decay corrected to EOB. The overall synthesis time from EOB was 15-20 min, the radiochemical purity was >99%, and the specific activity at EOS was 111-185 GBq/micromol.

摘要

N- [ω-(6-甲氧基萘-1-基)烷基]衍生物的碳-11标记哌啶环首先被设计并合成为新型选择性PET σ(1)受体探针。通过在碱性条件下使用[(11)C] CH(3)OTf对其相应的酚羟基前体进行O- [(11)C]甲基化来制备目标示踪剂,并通过简化的固相萃取方法以基于[(11)C] CO(2)的40-50%放射化学产率进行分离,并衰减校正至EOB。从EOB开始的总合成时间为15-20分钟,放射化学纯度> 99%,EOS时的比活为111-185 GBq /微摩尔。

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