Suppr超能文献

4-(苯并[b]噻吩-2-基)-5-(3,4,5-三甲氧基苯基)-2H-1,2,3-三唑与4-(苯并[b]噻吩-2-基)-2-甲基-5-(3,4,5-三甲氧基苯基)-2H-1,2,3-三唑的晶体结构比较

Comparison of crystal structures of 4-(benzo[b]thio-phen-2-yl)-5-(3,4,5-tri-meth-oxy-phen-yl)-2H-1,2,3-triazole and 4-(benzo[b]thio-phen-2-yl)-2-methyl-5-(3,4,5-tri-meth-oxy-phen-yl)-2H-1,2,3-triazole.

作者信息

Penthala Narsimha Reddy, Madadi Nikhil Reddy, Bommagani Shobanbabu, Parkin Sean, Crooks Peter A

机构信息

Department of Pharmaceutical Sciences, College of Pharmacy, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.

Department of Chemistry, University of Kentucky, Lexington KY 40506, USA.

出版信息

Acta Crystallogr Sect E Struct Rep Online. 2014 Oct 24;70(Pt 11):392-5. doi: 10.1107/S1600536814023095. eCollection 2014 Nov 1.

Abstract

The title compound, C19H17N3O3S (I), was prepared by a [3 + 2]cyclo-addition azide condensation reaction using sodium azide and l-proline as a Lewis base catalyst. N-Methyl-ation of compound (I) using CH3I gave compound (II), C20H19N3O3S. The benzo-thio-phene ring systems in (I) and (II) are almost planar, with r.m.s deviations from the mean plane = 0.0205 (14) in (I) and 0.016 (2) Å in (II). In (I) and (II), the triazole rings make dihedral angles of 32.68 (5) and 10.43 (8)°, respectively, with the mean planes of the benzo-thio-phene ring systems. The trimeth-oxy phenyl rings make dihedral angles with the benzo-thio-phene rings of 38.48 (4) in (I) and 60.43 (5)° in (II). In the crystal of (I), the mol-ecules are linked into chains by N-H⋯O hydrogen bonds with R (2) 1(5) ring motifs. After the N-methyl-ation of structure (I), no hydrogen-bonding inter-actions were observed for structure (II). The crystal structure of (II) has a minor component of disorder that corresponds to a 180° flip of the benzo-thio-phene ring system [occupancy ratio 0.9363 (14):0.0637 (14)].

摘要

标题化合物C₁₉H₁₇N₃O₃S(I)通过使用叠氮化钠和L-脯氨酸作为路易斯碱催化剂的[3 + 2]环加成叠氮缩合反应制备。使用CH₃I对化合物(I)进行N-甲基化得到化合物(II),C₂₀H₁₉N₃O₃S。(I)和(II)中的苯并噻吩环系统几乎是平面的,(I)中与平均平面的均方根偏差为0.0205(14)Å,(II)中为0.016(2)Å。在(I)和(II)中,三唑环分别与苯并噻吩环系统的平均平面形成32.68(5)°和10.43(8)°的二面角。三甲氧基苯基环与(I)中苯并噻吩环的二面角为38.48(4)°,与(II)中苯并噻吩环的二面角为60.43(5)°。在(I)的晶体中,分子通过具有R(2)₁(5)环基序的N-H⋯O氢键连接成链。在结构(I)进行N-甲基化后,未观察到结构(II)的氢键相互作用。(II)的晶体结构有一个较小的无序成分,对应于苯并噻吩环系统180°翻转[占有率比0.9363(14):0.0637(14)]。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e2c/4257340/4ee349bfce16/e-70-00392-fig1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验