A reversed-phase high-performance liquid chromatographic assay using electrochemical detection in the reductive mode has been developed for the analysis of 4-bromo-2,7-dimethoxy-3H-phenothiazin-3-one (1) in plasma to determine drug absorption. Free drug in plasma in concentrations as little as 0.25
Synthesis of carbon-14 labeled 4-bromo-2,7-dimethoxy-3H-phenothiazin-3-one
✍ Scribed by S. R. Prakash; R. L. Ellsworth; H. E. Mertel
- Publisher
- John Wiley and Sons
- Year
- 1987
- Tongue
- French
- Weight
- 352 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Two different syntheses of (z), one labeled with carbon-14 in the quinonoid ring and the other in the phenyl ring are described. methoxy benzenethiol yielded ( I ) , which was methoxylated to provide a mixture of isomers (&) and (8). isomers followed by bromination of (2) gave (2). Thiocyanation of p-[U-14C]anisidine provided (x), which was hydrolysed to give labeled aminothiol (E); the latter was condensed with 2-bromo-6-methoxy-p-benzoquinone to afford (2).
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