## Abstract The MMPI [^14^C]ABT‐770 **(1)**, __N‐__[__(1S)__‐1‐[(4,4‐Dimethyl‐2,5‐dioxo‐1‐imi‐dazolidinyl)methyl]]‐2‐[[4′‐(trifluoromethoxy)[1,1′‐biphenyl]‐4‐yl]oxy]ethyl]‐__N__‐hydroxyformamide was synthesized in 8 steps using 4‐bromophenol‐UL‐^14^C **(10)** as a starting material. The Carbon‐14 l
Synthesis of [3H]ABT-518, a matrix metalloproteinase inhibitor (MMPI) labeled in the phenyl rings
✍ Scribed by Shirish N. Raja; Bruce W. Surber; Jia Du; Jeffrey L. Cross
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- French
- Weight
- 131 KB
- Volume
- 52
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
A novel matrix metalloproteinase inhibitor, ABT‐518, [S‐(R^*^, R^*^)]‐N‐[1‐(2, 2‐dimethyl‐1,3‐dioxol‐4‐yl)‐2‐[[4‐[4‐(trifluoromethoxy)‐phenoxy]phenyl]sulfonyl]ethyl]‐N‐hydroxyformamide, was labeled with tritium in two phenyl rings in a seven‐step synthesis. The overall radiochemical yield of [^3^H]ABT‐518 in seven steps starting from 1‐(methylsulfonyl)‐4‐[4‐(trifluoromethoxy)phenoxy]benzene was 6.2% with the radiochemical purity of 99.4%. Copyright © 2009 John Wiley & Sons, Ltd.
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