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 and efficient synthesis of 2-deoxy-2-[18F]fluoroacetamido-D-mannopyranose and -D-galactopyranose
✍ Scribed by Masao Tada; Atsushi Oikawa; Ren Iwata; Kazunori Sato; Kazuo Kubota; Takehiko Fujiwara; Hiroshi Sugiyama; Yoshinao Abe; Tachio Sato; Taiju Matsuzawa; Hiromu Takahashi; Akira Wakui; Tatsuo Ido
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- French
- Weight
- 252 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
Rapid and efficient syntheses of 2‐deoxy‐2‐[^18^F]fluoroacetamido‐D‐mannopyranose (1) and ‐D‐galactopyranose (2), respectively, starting from [^18^F]fluoride and ethyl bromoacetate are described. [^18^F]Fluoride was produced by the ^18^O (p, n) ^18^F nuclear reaction using the cyclotron. The total times required for synthesis of (1) and (2) are ca. 80 min. The radiochemical yield and purity of (1) are an 18% and ≥98%, respectively. Compound (2) is also synthesized with the same radiochemical yield and purity.
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