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The synthesis of o- and p-[18F]fluorobenzyl bromides and their application to the prepatation of labeled neuroleptics

✍ Scribed by Kentaro Hatano; Tatsuo Ido; Ren Iwata


Publisher
John Wiley and Sons
Year
1991
Tongue
French
Weight
412 KB
Volume
29
Category
Article
ISSN
0022-2135

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✦ Synopsis


Abstract

The syntheses of o‐ and p‐ [^18^F]fluorobenzyl bromides as labeled synthons were described. They were obtained from nitrobenzaldehyde via a three step synthesis that exhibited good yield. The preparation of [^18^F]fluororinated analog of a benzamide neuroleptic, cis‐N‐[(2RS, 3RS)‐1‐[^18^F]fluorobenzyl‐2‐methylpyrrolidin‐3‐yl] ‐5‐chloro‐2‐methoxy‐4‐methylaminobenzamide, via N‐benzylation with the synthons was also mentioned.


📜 SIMILAR VOLUMES


Synthetic studies with [18F]p-fluorobenz
✍ Anthony L. Feliu 📂 Article 📅 1988 🏛 John Wiley and Sons 🌐 French ⚖ 405 KB

A route was devised to synthesize no-carrier-added or carrier-added C\*uFlp-fluorophenylhydratine from aqueous C'OFlfluoride. Key reaction in this three-step sequence is the reduction o f C1nFlp-fluorobenzenediazonium chloride with sodium cyanoborohydride. The utility of this method is demonstrated