𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Preparation and evaluation of [F-18]-labeled 5-HT1A Agonist: 1-[2-(4-[F-18]Fluorobenzamido)-1-Ethyl]-4-(1,2,3,4-Tetrahydronaphth-1-YL)-Piperidine (FBP)

✍ Scribed by D. R. Hwang; K. Ngo; L. Savenkova; Y. Huang; N. Guo; Z. Zhu; M. Laruelle

Book ID
112132870
Publisher
John Wiley and Sons
Year
2001
Tongue
French
Weight
166 KB
Volume
44
Category
Article
ISSN
0022-2135

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis of N-(piperidin-1-yl)-5-(4-met
Synthesis of N-(piperidin-1-yl)-5-(4-methoxyphenyl)-1-(2-chlorophenyl)-4-[18F]fluoro-1H-pyrazole-3-carboxamide by nucleophilic [18F] fluorination: a PET radiotracer for studying CB1 cannabinoid receptors
✍ Reeti Katoch-Rouse; Andrew G. Horti 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 French ⚖ 91 KB

## Abstract The feasibility of nucleophilic displacement of bromide in the 4‐bromopyrazole ring with [^18^F]fluoride has been demonstrated by the synthesis of two radiolabeled compounds: __N__‐(piperidin‐1‐yl)‐5‐(4‐methoxyphenyl)‐1‐(2‐chlorophenyl)‐4‐[^18^F]fluoro‐1__H__‐pyrazole‐3‐carboxamide, ([^

18F-labelling of a potent nonpeptide CCR
18F-labelling of a potent nonpeptide CCR1 antagonist: synthesis of 1-(5-chloro-2-{2-[(2R)-4-(4-[18F]fluorobenzyl)-2-methylpiperazin-1-yl]-2-oxoethoxy}phenyl)urea in an automated module
✍ P. Mäding; F. Füchtner; B. Johannsen; J. Steinbach; C. S. Hilger; M. Friebe; M. 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 French ⚖ 195 KB

## Abstract The synthesis of 1‐(5‐chloro‐2‐{2‐[(2R)‐4‐(4‐[^18^F]fluorobenzyl)‐2‐methylpiperazin‐1‐yl]‐2‐oxoethoxy}phenyl)urea (**[^18^F]4**), a potent nonpeptide CCR1 antagonist, is described as a module‐assisted two‐step one‐pot procedure. The final product was obtained utilizing the reductive ami