A rapid, one-pot synthesis of 2-deoxy-2-[18F] fluoroacetamido-D-glucopyranose (g-[ 18F] f luoroacetyl-D-glucosamine) (1) starting from [ 18F] fluoride and ethyl bromoacetate is described. The synthesis was accomplished by a combination of halogen exchange, alkaline hydrolysis, and condensation. [18
A rapid synthesis of [fluoroacetyl-18F]fluoromelatonin (Nω-[18F]fluoroacetyl-5-methoxytryptamine), a potential diagnostic imaging agent
✍ Scribed by Masao Tada; Ren Iwata; Hiroshi Sugiyama; Kazunori Sato; Claudio Pascali; Hiroshi Fukuda; Kazuo Kubota; Roko Kubota; Hiromu Takahashi; Akira Wakui; Yoshinao Abe; Takehiko Fujiwara; Tachio Sato; Tatsuo Ido
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- French
- Weight
- 334 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
An efficient synthesis of [fluoroacetyl‐^18^F]fluoromelatonin (__N__ω‐[^18^F]Fluoroacetyl‐5‐methoxytryptamine) starting from [^18^F]fluoride and ethyl p‐toluensulfonyloxyacetate is described. The total time required for its synthesis is ca. 90 min. The radiochemical yield, purity and specific activity (end of bombardment) of the desired compound are 14.2%,>98%, and 540 mCi/μmol, respectively.
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