Synlett 2018; 29(04): 410-414
DOI: 10.1055/s-0036-1591734
cluster
© Georg Thieme Verlag Stuttgart · New York

A Novel 18F-Labeling Method for the Synthesis of [18F]-Piperidine-Containing Ligands as Potential PET Radiotracers for σ Receptors

Gerardo X. Ortiz Jr.
a   Department of Chemistry, Duke University, Durham, NC 27708, USA   eMail: qiu.wang@duke.edu
,
Kantapat Chansaenpak
b   Department of Radiology, University of North Carolina-Chapel Hill, Chapel Hill, NC 27599, USA   eMail: zibo_li@med.unc.edu
c   National Nanotechnology Center (NANOTEC), National Science and Technology Development Agency (NSTDA), 111 Thailand Science Park, Pathum Thani, 12120, Thailand
,
Mengzhe Wang
b   Department of Radiology, University of North Carolina-Chapel Hill, Chapel Hill, NC 27599, USA   eMail: zibo_li@med.unc.edu
,
Xiaofen Ma
b   Department of Radiology, University of North Carolina-Chapel Hill, Chapel Hill, NC 27599, USA   eMail: zibo_li@med.unc.edu
d   Department of Medical Imaging, Guangdong No. 2 Provincial People’s Hospital, Guangzhou City, Guangdong Province, P. R. of China
,
Hui Wang
b   Department of Radiology, University of North Carolina-Chapel Hill, Chapel Hill, NC 27599, USA   eMail: zibo_li@med.unc.edu
,
Zibo Li*
b   Department of Radiology, University of North Carolina-Chapel Hill, Chapel Hill, NC 27599, USA   eMail: zibo_li@med.unc.edu
,
Qiu Wang  *
a   Department of Chemistry, Duke University, Durham, NC 27708, USA   eMail: qiu.wang@duke.edu
› Institutsangaben
We acknowledge financial support to this project from Duke University, the Camille and Henry Dreyfus Foundation (QW), and the Department of Radiology and BRIC at UNC Chapel Hill.
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Publikationsverlauf

Received: 22. September 2017

Accepted after revision: 08. November 2017

Publikationsdatum:
19. Dezember 2017 (online)


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Published as part of the Cluster Alkene Halofunctionalization

# These authors contributed equally to this work.

Abstract

We report a novel 18F-labeling method for the preparation of 18F-containing piperidine derivatives. This method is demonstrated on the design and synthesis of 18F-labeled potential PET radiotracers of σ receptors for initial biological evaluations.

1 Introduction

2 Design and Synthesis of Novel [19F]-3 and [ 19F]-3′

3 Radiosynthesis of Novel [18F]-3 and [18F]-3′

4 In vivo Uptake and Pharmacokinetics of [18F]-3 and [18F]-3′

5 Conclusion

Supporting Information