Synthesis of some new pyrazole-containing chelating agents
✍ Scribed by Willem L. Driessen
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 277 KB
- Volume
- 101
- Category
- Article
- ISSN
- 0165-0513
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✦ Synopsis
Abstract
Procedures are described involving the condensation of l‐(hydroxymethyl)pyrazole (1a) and l‐(hydroxymethyl)‐3,5‐dimethylpyrazole (1b) with the following amines (products given in parentheses): ethylamine (2a and 2b), aniline (3a and 3b), N,N′‐dimethyl‐ l,2‐ethanediamine (4a and 4b), 1,2‐ethanediamine (6a and 6b), diethylenetriamine (7a and 7b), triethylenetetramine (8a and 8b) and ammonia (9a and 9b). All amine hydrogens are completely substituted by pyrazol‐1‐ylmethyl groups (compounds 2a‐9a) or (3,5‐dimethylpyrazol‐1‐yl)methyl groups (compounds 2b‐9b with yields being better than 90%.
📜 SIMILAR VOLUMES
A new synthesis of bis(aminoethanethiols) containing a long-chain fatty acid moiety is described. The procedure described offers an advantage over literature methods since the use of strong reducing agents such as lithium aluminum hydride is avoided.
## Abstract Procedures are given for the preparation of new linear bidentate, tetradentate and tripodal heptadentate ligands incorporating benzimidazole, benzothiazole and pyridyl groups. The compounds were characterized by their nmr, uv and mass spectra. The crystal and molecular structure is repo
## Abstract magnified image A series of pyrazolo [3,4‐d] pyrimidine, pyrazolo [1,5‐a] pyrimidine, and pyrazolyl triazoles have been prepared __via__ reaction of ethyl 5‐amino‐3‐phenylpyrazole‐4‐carboxylate with isothiocyanic esters, α,β‐unsaturated nitriles, and some active methylene reagents. J. H