Abstract
A simple four-stage conversion of 2-methyl-4(5)-nitroimidazole to 2-methyl-4(5)-nitro[15N1(3)]imidazole is reported. The method consists in N-nitration of the initial compound to 2-methyl-1.4-dimtroimidazole, treating the latter with [15N]glycine and N-dealkylation of the obtained (2-methyl-4-nitro[15N1]imidazol-1-yl)acetic acid through its bromination in the presence of phosphorus trichloride, followed by the hydrolysis of the non-isolated intermediate.
| Original language | English |
|---|---|
| Pages (from-to) | 395-401 |
| Number of pages | 7 |
| Journal | Journal of Labelled Compounds and Radiopharmaceuticals |
| Volume | 38 |
| Issue number | 4 |
| DOIs | |
| Publication status | Published - 1996 |
Keywords
- N-dealkylation
- Synthesis
- [N]labelled nitroimidazoles
ASJC Scopus subject areas
- Analytical Chemistry
- Biochemistry
- Radiology, Nuclear Medicine and Imaging
- Drug Discovery
- Spectroscopy
- Organic Chemistry
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