Synthesis of radioiodo-[4-(2-iodo-4-fluoro-benzoyl)piperidin-1-yl]-2′-acetonaphthone
✍ Scribed by J. Mertens; M. Thomas
- Book ID
- 102375743
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- French
- Weight
- 202 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Radioiodo‐[4‐(2‐1‐4‐fluorobenzoyl)piperidin‐1‐yl]‐2′‐acetonaphthone was synthesised as a potential in vivo tracer of the glutamate release inhibiting system. The labeling was performed by Cu^1+^ assisted non isotopic nucleophilic exchange on [4‐(2‐bromo‐4‐fluorobenzoyl)piperidin‐1‐yl]‐2′‐acetonaphthone.
The labeled compound is obtained after HPLC separation and mini‐column recovery. The brominated substrate is obtained by Kl catalyzed coupling of 2‐bromo‐acetonaphthone to the piperidinyl entity in ethanol at room temperature using triethylamine.
📜 SIMILAR VOLUMES
The molecule of the title compound, C 16 H 17 FN 4 OS 2 , is built up around a chiral C atom, and exists in a propeller-like arrangement. The structure is stablized by van der Waals interactions.