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
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