Page 2890 in ref. [1] : In the experimental procedures reported for the synthesis of 2,6-Bis(4-iodopyrazol-1-yl)pyridine ( 4) the iodinating agents HIO 3 and I 2 must be dissolved in acetic acid (CH 3 COOH), not in water (H 2 O), by using the same proportions as described in the text for both the sm
One-Step Synthesis of Symmetrically Substituted 2,6-Bis(pyrazol-1-yl)pyridine Systems
✍ Scribed by Giorgio Zoppellaro; Martin Baumgarten
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 106 KB
- Volume
- 2005
- Category
- Article
- ISSN
- 1434-193X
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✦ Synopsis
Abstract
A one‐pot synthetic route that allows functionalization of the 2,6‐bis(pyrazol‐1‐yl)pyridine backbone in the 4‐ and 4″‐pyrazole positions by direct H(4)‐pyrazole halogen exchange is described. The diiodo derivative in particular provides easy access to additional functionalities through both Sonogashira and Grignard exchange reactions. These synthons represent optimal building blocks for the extension of the chelating core and for the assembly of rigid organic and metalloorganic nanostructures. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2005)
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The synthesis of three novel pyrazole-containing complexing acids, N,N,N',N'-{ 2,6-bis[3-(aminomethyl)pyrdzol-l-yl]-4-methoxypyridine}tetrakis(acetic acid) (l), N,N,N',N'-{2,6-bis[3-(aininomethyl)pyrdzoI-1-yl]pyrazine}tetrakis(acetic acid) (2), and N,N,N',N'-{6,6'-bis[3-(aminomethyl)pyrazol-l-yl]-2,
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
## Abstract The 3,5‐bis(5‐carboxy‐6‐azauracil‐1‐yl)aniline (**7**) and 1,3,5‐tris(5‐carboxy‐6‐azauracil‐1‐yl)benzene (**10**) were prepared from 3‐amino‐5‐nitroacetanilide (**1**) __via__ intermediates **2–6**. A series of other substituted 6‐azauracil derivatives **9, 11‐14** were also prepared.
## Abstract For Abstract see ChemInform Abstract in Full Text.