Syntheses of some new 1H-pyrazole, pyridazin-3(2H)-one, and oxazin-4-one derivatives
✍ Scribed by Esvet Akbaş; Furgan Aslanoǧlu
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 82 KB
- Volume
- 17
- Category
- Article
- ISSN
- 1042-7163
- DOI
- 10.1002/hc.20170
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✦ Synopsis
Abstract
The new 1H‐pyrazole‐3‐carboxylic acid 2, pyridazin‐3(2H)‐one 3, and their various derivatives were prepared by the reactions of the 4‐benzoyl‐5‐phenyl‐2,3‐dihydro‐2,3‐furandione 1 and 2,5‐dichlorophenylhydrazine. Pyrazolo[3,4‐d]pyridazine 7 was obtained from cyclization of the pyrazole‐3‐carboxylic acid 2 with 2,5‐dichlorophenylhydrazine. The reaction of 1 and pyrazole‐3‐carbonitriles 6 gave the new oxazin‐4‐one 9 derivatives. The structures of compounds were characterized on the basis of elemental analyses, mass, IR, ^1^H, and ^13^C NMR spectra. © 2006 Wiley Periodicals, Inc. Heteroatom Chem 17:8–12, 2006; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20170
📜 SIMILAR VOLUMES
## Abstract Facile and convenient methods for the preparation of a variety of 2,6‐disubstituted 4__H__‐1,3‐oxazin‐4‐ones 3 by three complementary methods are described. Treatment of the branched aliphatic imidate 2c,d with diketene 1 in the presence of a catalytic amount of acetic acid affords 2‐su