Convenient syntheses of 2,4-,a,a-and 5,B-deuterium labelled 6-hydroxydopamines have been developed. 2,4,5-Trimethoxybenzaldehyde (1) was reductively aminated to give 2,4,5-trimethoxybenzylamine (2). Quaternization of the amine with methyliodide followed by displacement with cyanide gave 2,4,5-trimet
Regioselective labelling of anilides with deuterium
β Scribed by W J S Lockley
- Publisher
- John Wiley and Sons
- Year
- 1985
- Tongue
- French
- Weight
- 298 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0022-2135
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β¦ Synopsis
N-Aryl amides may be deuterated by exchange with deuterium oxide in the presence of rhodium(fI1) chloride. Under such conditions deuterium is introduced into positions t o the anilide nitrogen atom with a high degree of regioselectivity.
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A method f o r t h e p r e p a r a t i o n o f deuterium l a b e l l e d unsymm e t r i c a l hydrazines was developed. This method was used t o prepare l-benzyl-2-methyl-\*H1-hydrazine hydrobromide and l-benzyl-zH~-2-methylhydrazine hydrobromide, analogs o f t h e cancer chemotheraputic agent proca
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