## Abstract magnified image Pyrolysis of 1,7‐di‐[(__E__)‐1‐morpholinomethylidene]‐ and 1,7‐di‐[(__E__)‐1‐piperidino‐methylidene]‐4,6,10,12‐tetramethylamino‐2,8‐dioxo‐1,7‐diaza‐3,5,9,11‐cyclododecatetraene‐3,9‐dicarbonitrile **6a**, **6b** afforded pyridone **10** in addition to cyanamides **11a**,
Gas-phase pyrolysis in organic synthesis: New route for synthesis of functionally substituted imidazoles
✍ Scribed by Osman M. E. El-Dusouqui; Nouria A. Al-Awadi; Mohamed H. Elnagdi; Mervat M. Abdelkhalik
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2008
- Tongue
- English
- Weight
- 136 KB
- Volume
- 45
- Category
- Article
- ISSN
- 0022-152X
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✦ Synopsis
Abstract
magnified image
1,2,3‐Triazolylpropanone was prepared and coupled with aryldiazonium salts yielding the corresponding arylhydrazones. Gas‐phase pyrolysis of the hydrazono derivative produced N‐arylamino‐2‐acetylimidazole as well as 2‐acetylimidazole. The latter is the product of further pyrolysis of the former.
📜 SIMILAR VOLUMES
Gas-phase pyrolyses of ethyl N-(5-cyanomethyl-1,3,4thiadiazol-3-yl)carbamate ( ), 1-benzoyl-3-(3-methylpyrazol-5-yl)thiourea ( ), 1-benzoyl-3-(5-methylisoxazol-3-yl)thiourea ( ), and 1-acetyl-3-(3-phenylpyrazol-5-yl)thiourea ( ) have been studied. These reactions were homogeneous and unimolecular. T
## Abstract 3‐oxo‐3‐aryl‐2‐arylhydrazonopropanals **(1)** have been converted under thermal gas‐phase conditions cleanly into cinnolines **(2)**. A plausible mechanism is suggested to account for this transformation based on the kinetics and products of reaction. © 2001 John Wiley & Sons, Inc. Int