## Abstract Propiconazole was labelled with ^14^C in three different positions: in the benzene ring, in the position 5 of the dioxolane ring, and in the triazole ring. The synthesis of three new key intermediates [(m‐dichloro[U‐^14^C]benzene], 1,2,4‐[U‐^14^C]triazole, [1‐^14^C]‐pentane‐1,2‐diol) we
Synthesis of SCH 42427 labelled with 14C in two different positions
✍ Scribed by D. Hesk; C. Bowlen; T. Duelfer; D. Koharski; P. McNamara; S. Saluja
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- French
- Weight
- 484 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
[^14^C]‐Sch 42427 was synthesized by two different methods, resulting in incorporation of the label in different parts of the molecule. In the first synthesis [benzyl‐α‐^14^C]‐Sch 42427 was synthesized in overall 1.7% yield via a 6 step procedure, using [^14^C]‐trimethyl sulphoxonium iodide as the source of label. The second synthesis gave rise to [SO~2~‐^14^CH~3~]‐Sch 42427, which was prepared via a 2 step procedure from [^14^C]‐sodium thiomethoxide. Radiochemical purities were greater than 99% for both batches, and analysis by chiral hplc failed to detect any of the undesired S,S enantiomer.
📜 SIMILAR VOLUMES
Diuron and Linuron, two herbicides, with very similar structures were labelled in their aromatic ring with I4C. The yields of the synthesis (starting from BaI4C03) was 8.5% and 4.8%, respectively. Linuron was also labelled with 14C in its urea group with 3 3 % yield.
## Abstract A synthetic procedure for 2‐^14^C‐N‐nitrosohexamethyl‐eneimine 1‐aza‐l‐nitroso‐(2‐^14^C)‐cycloheptane is presented. The starting material was 1‐^14^ C‐cyclohexanone which underwent ring expansion, reduction, and finally nitrosation. The synthesis resulted in a product in good yield (68%
## Abstract Methylation under pressure of o‐allyloxyphenol with ^14^C‐metheyl iodide was successfully used for the synthesis of ^14^C‐eugenol and isoeugenol labeled in the methoxy position. Eugenol and isoeugenol are important compounds in the practice of dentistry.