Electrogenerated base-promoted synthesis and antimicrobial activity of 2-(1,3-dithian-2-ylidene)-2-arylacetonitrile and 2-(1,3-dithiolan-2-ylidene)-2-arylacetonitrile

被引:7
|
作者
Hamrouni, Kaouthar [1 ]
Saied, Taieb [1 ,2 ]
El Abed, Nariman [3 ]
Ahmed, Sami Ben Hadj [3 ]
Boujlel, Khaled [1 ]
Ben Khoud, Mohamed Lamine [1 ]
机构
[1] Univ Tunis El Manar, Fac Sci Tunis, Lab Chim Analyt & Electrochim, Tunis, Tunisia
[2] Inst Natl Sci Appl & Technol, Dept Chim & Biol Appl, Tunis, Tunisia
[3] Univ Carthage, Inst Natl Sci Appl & Technol, Lab Prot & Mol Bioact Ingn, Ctr Urbain Nord, Tunis, Tunisia
关键词
antimicrobial activity; carbone disulfur; 2-(1,3-dithian-2-ylidene)-2-arylacetonitrile; 2-(1,3-dithiol-2-ylidene)-2-arylacetonitrile; anion EGBs; CYANOMETHYL ANION; DERIVATIVES; OXAZOLIDIN-2-ONES; ESTERS; AMINES;
D O I
10.1080/17415993.2015.1005620
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The new preparation of 2-(1,3-dithian-2-ylidene)-2-arylacetonitrile and 2-(1,3-dithiol-2-ylidene)-2-arylacetonitrile is described. The electrogenerated cyanomethyl base/anion obtained from the electroreduction of acetonitrile promotes reactions between arylacetonitrile, carbon disulfide and 1-bromo-3-chloropropane or 1,2-dibromoethane. Obtained products have been identified according to their spectroscopic data (IR and H-1 NMR and C-13 NMR) and elemental analysis. The possible antibacterial activities of some of these compounds were investigated. Promising results were found against few types of bacteria.
引用
收藏
页码:196 / 206
页数:11
相关论文
共 50 条
  • [1] 2-(1,3-Dithian-2-ylidene)-1-phenylbutane-1,3-dione
    Zhang, Lan-Cui
    Li, Na
    Li, Xiao-Hui
    Huang, Cui-Ying
    Zhou, Guang-Hua
    ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE, 2008, 64 : O534 - U3127
  • [2] ALTERNATIVE METHOD FOR SYNTHESIS AND MECHANISM OF 2-(1,3-DITHIAN-2-YLIDENE)-ACETONITRILE
    Ferreira, Marcelle S.
    Figueroa-Villar, Jose D.
    QUIMICA NOVA, 2015, 38 (02): : 233 - 236
  • [3] 'SEMI-INDUSTRIAL TECHNOLOGY FOR SYNTHESIS OF 2-(1,3-DITHIOLAN-2-YLIDENE) MALONONITRILE
    Lipin, K., V
    IZVESTIYA VYSSHIKH UCHEBNYKH ZAVEDENII KHIMIYA I KHIMICHESKAYA TEKHNOLOGIYA, 2020, 63 (04): : 68 - 73
  • [4] Diisopropyl (1,3-dithiolan-2-ylidene)malonate
    Chopra, D
    Mohan, TP
    Rao, KS
    Row, TNG
    ACTA CRYSTALLOGRAPHICA SECTION E-CRYSTALLOGRAPHIC COMMUNICATIONS, 2005, 61 : O3 - O5
  • [5] (Z)-2-[4-(2-chlorophenyl)-1,3-dithiolan-2-ylidene]-2-(imidazol-1-yl)acetonitrile
    Lin, Yuan
    Xiao, Tao
    Wang, Jin-Tang
    ACTA CRYSTALLOGRAPHICA SECTION E-CRYSTALLOGRAPHIC COMMUNICATIONS, 2006, 62 : O3159 - O3160
  • [6] (E)-2-[4-(2-Chlorophenyl)-1,3-dithiolan-2-ylidene]-2-(imidazol-1-yl)acetonitrile
    Xiao, Tao
    Lin, Yuan
    Zhang, Xiao-Qing
    Chen, Jing
    Wang, Jin-Tang
    ACTA CRYSTALLOGRAPHICA SECTION E-CRYSTALLOGRAPHIC COMMUNICATIONS, 2006, 62 : O5052 - O5053
  • [7] 2-(1,3-Dithiolan-2-ylidene)-1-phenyl-2-(1,2,4-triazol-1-yl)ethanone
    Jian, FF
    Xu, LZ
    Shi, JG
    Xiao, HL
    ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE, 2004, 60 : O1204 - O1205
  • [8] (Z)-methyl 2-(1,3-dithian-2-ylidene)-4-(triphenylstannyl) but-3-enoate
    Zhu, Chao-Guang
    Zhu, Dong-Sheng
    Wu, Xiao-Yan
    Wang, Yan-Hua
    Du, Da-Feng
    ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE, 2007, 63 : M2346 - U916
  • [9] Odorless and practical thioacetalization reagent: Methyl 2-(1,3-dithian-2-ylidene)-3-oxobutanoate
    Sun, R
    Liu, Q
    Yu, HF
    Zhao, YL
    Liu, J
    Ouyang, Y
    Dong, DW
    CHINESE JOURNAL OF CHEMISTRY, 2005, 23 (08) : 1060 - 1064
  • [10] SYNTHESIS OF NEW THIOETHER TRANSITION-METAL COMPLEXES OF 2-(1,3-DITHIOLAN-2-YLIDENE)-1,3-DITHIEPIN AND 2-[BIS(ETHYLTHIO)METHYLENE]-1,3-DITHIEPIN
    LONG, CJ
    BEREMAN, RD
    TUCKER, C
    BORDNER, J
    INORGANICA CHIMICA ACTA, 1988, 149 (02) : 295 - 300