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噻吩开环反应VI. 尝试向包含硫醇盐阴离子和位置合适的亲电碳的[稠合]三环体系进行环化反应。

Thiophene ring-opening reactions VI. Attempted cyclization towards [fused]-tricyclic system involving a thiolate anion and suitably located electrophilic carbon.

作者信息

Abdullah Ahmad H, Zahra Jalal A, Sabri Salim S, Awwadi Firas F, Hussein Ahmad Q, El-Abadelah Mustafa M

机构信息

Chemistry Department, Faculty of Science, The University of Jordan, Amman 11942, Jordan.

Faculty of Pharmacy, Zarqa University, Zarqa 13132, Jordan.

出版信息

Z Naturforsch C J Biosci. 2022 Aug 8;78(3-4):133-140. doi: 10.1515/znc-2022-0080. Print 2023 Mar 28.

DOI:10.1515/znc-2022-0080
PMID:35934877
Abstract

Model -chloro--nitrothieno[2,3-]pyridazines incorporating 1-(aryl) entity appended with -methoxycarbonyl or trifluoromethyl group were prepared intramolecular cyclization of their respective -arylhydrazone precursors. Interaction of these substrates with '-(-fluorophenyl)benzothiohydrazide, in the presence of NEt, furnished the respective 1,3,4-thiadiazoline-pyridazine thiolate hybrids that were -methylated to produce the corresponding "sulfanyl" derivatives. Their structures were deduced from spectral data, and confirmed by single-crystal X-ray diffraction.

摘要

通过各自的芳基腙前体的分子内环化反应制备了含有连接有甲氧基羰基或三氟甲基的1-(芳基)实体的模型 - 氯 - 硝基噻吩并[2,3 - ]哒嗪。在三乙胺存在下,这些底物与' - ( - 氟苯基)苯硫代酰肼相互作用,得到各自的1,3,4 - 噻二唑啉 - 哒嗪硫醇盐杂化物,将其甲基化以产生相应的“硫烷基”衍生物。它们的结构由光谱数据推导得出,并通过单晶X射线衍射得到证实。

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