Reaction of 4-substituted thiosemicarbazides with (2,4,7-trinitro-9H-fluoren-9-ylidene)propanedinitrile
✍ Scribed by Alaa A. Hassan; Yusria R. Ibrahim; Ahmed M. Shawky; Dietrich Döpp
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2006
- Tongue
- English
- Weight
- 128 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0022-152X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
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4‐Substituted thiosemicarbazides 4a‐c reacted with (2,4,7‐trinitro‐9__H__‐fluoren‐9‐ylidene)‐propanedinitrile (2) in pyridine with admission of air to form spiro[fluorene‐9,3′‐(1,2,4‐triazole)]derivatives 5a‐c and (4‐substituted thiosemicarbazono)propanedinitriles 6a‐c in modest yields. 2,4,7‐Trinitro‐9‐fluorenone (8) as well as one reduction product thereof and of 2, namely compounds 9 and 10, respectively are also found. A rationale for the conversions observed is presented.
📜 SIMILAR VOLUMES
## Abstract Novel spiro[fluorene‐9,4′‐(1′,2′,3′,4′‐tetrahydropyridine)]‐5′‐carbonitriles 6a‐c have been obtained from the reaction of __N__^1^,__N__^2^‐diarylacetamidines 1a‐c with (2,4,7‐trinitro‐9__H__‐fluoren‐9‐ylidene)propanedinitrile (2) in ethyl acetate solutions at ambient temperature for 6a