1-(4-Methoxyphenyl)imidazolidine-2,4-dione

被引:3
|
作者
Sun, Su-Xia [1 ]
Zhang, Hao [1 ]
Cheng, Xian-Chao [1 ]
Wang, Run-Ling [1 ]
Dong, Wei-Li [1 ]
机构
[1] Tianjin Med Univ, Sch Pharm, Tianjin 300070, Peoples R China
基金
中国国家自然科学基金;
关键词
D O I
10.1107/S1600536810016478
中图分类号
O7 [晶体学];
学科分类号
0702 ; 070205 ; 0703 ; 080501 ;
摘要
In the title compound, C(10)H(10)N(2)O(3), the dihedral angle between the benzene and imidazolidine rings is 6.0 (4)degrees, consistent with an essentially planar molecule. In the crystal, intermolecular N-H center dot center dot center dot O hydrogen bonding between centro-symmetrically related molecules leads to loosely associated dimeric aggregates. These are connected into a three-dimensional network by C-H center dot center dot center dot O interactions, as well as pi-pi interactions [centroid-centroid distances = 3.705 (3) and 3.622 (3) angstrom] between the imidazolidine and benzene rings.
引用
收藏
页码:O1308 / U540
页数:8
相关论文
共 50 条
  • [21] EVALUATION OF ANTIARRYTHMIC ACTIVITY OF NOVEL IMIDAZO[2,1-F]PURINE-2,4-DIONE AND IMIDAZOLIDINE-2,4-DIONE DERIVATIVES WITH AMINOALKYL MOIETIES
    Zagorska, Agnieszka
    Czopek, Anna
    Chlon-Rzepa, Grazyna
    Pawlowski, Maciej
    Siwek, Agata
    Bednarski, Marek
    Zygmunt, Malgorzata
    Sapa, Jacek
    ACTA POLONIAE PHARMACEUTICA, 2017, 74 (06): : 1729 - 1738
  • [22] Serotonin transporter activity of imidazolidine-2,4-dione and imidazo[2,1-f]purine-2,4-dione derivatives in aspect of their acid–base properties
    Agnieszka Zagórska
    Anna Czopek
    Maciej Pawłowski
    Małgorzata Dybała
    Agata Siwek
    Gabriel Nowak
    Medicinal Chemistry Research, 2012, 21 : 3455 - 3459
  • [23] Synthesis and crystal structure of new imidazolidine-2,4-dione and imidazolidin-2-one derivatives
    Shtamburg, Vasilliy G.
    Anishchenko, Andrey A.
    Shtamburg, Victor V.
    Shishkin, Olleg V.
    Zubatyuk, Roman I.
    Mazepa, Alexander V.
    Rakipov, Dar M.
    Kostyanovsky, Remir G.
    MENDELEEV COMMUNICATIONS, 2008, 18 (02) : 102 - 104
  • [24] Synthesis and Crystal Structure of 3-Amino-1-(5-Chloro-2-Hydroxyphenyl)Imidazolidine-2,4-Dione
    Aydin, Abdullah
    Onkol, Tijen
    Akkurt, Mehmet
    Buyukgungor, Orhan
    Sahin, M. Fethi
    MOLECULAR CRYSTALS AND LIQUID CRYSTALS, 2013, 570 (01) : 119 - 127
  • [25] Serotonin transporter activity of imidazolidine-2,4-dione and imidazo[2,1-f]purine-2,4-dione derivatives in aspect of their acid-base properties
    Zagorska, Agnieszka
    Czopek, Anna
    Pawlowski, Maciej
    Dybala, Malgorzata
    Siwek, Agata
    Nowak, Gabriel
    MEDICINAL CHEMISTRY RESEARCH, 2012, 21 (11) : 3455 - 3459
  • [26] Crystal structure of (E)-1-(2-hydroxybenzylideneamino)imidazolidine-2,4-dione, C10H9N3O3
    Hu, Lei
    Liu, Xue-Xue
    Xu, Hua-Jie
    Sheng, Liang-Quan
    Liu, Zhao-Di
    ZEITSCHRIFT FUR KRISTALLOGRAPHIE-NEW CRYSTAL STRUCTURES, 2015, 230 (02): : 111 - 112
  • [27] Antinociceptive and Anti-inflammatory Effects of 3-Phenyl-5-(4-methylphenyl)-imidazolidine-2,4-dione in Mice
    Salgado, Paula R. R.
    Fonseca, Diogo V.
    Maia, Ana Karina H. L.
    Leite, Fagner C.
    Souza, Severino A.
    Athayde-Filho, Petronio F.
    Sousa Luis, Jose A.
    Piuvezam, Marcia R.
    Pordeus, Liana C. M.
    Almeida, Reinaldo N.
    LATIN AMERICAN JOURNAL OF PHARMACY, 2017, 36 (05): : 931 - 938
  • [28] 3-(4-Bromophenyl)-1-butyl-5-[1-(2chloro-6-methylphenyl)-1H-tetrazol-5yl]imidazolidine-2,4-dione
    Hall, Gabriel B.
    Medda, Federico
    Roberts, Sue A.
    Hulme, Christopher
    ACTA CRYSTALLOGRAPHICA SECTION E-CRYSTALLOGRAPHIC COMMUNICATIONS, 2013, 69 : O1102 - +
  • [29] SYNTHESIS AND ANTIARRHYTHMIC PROPERTIES OF BASIC AMIDE DERIVATIVES OF IMIDAZOLIDINE-2,4-DIONE AND PYRROLIDINE-2,5-DIONE .2.
    KIECKONONOWICZ, K
    BYRTUS, H
    ZEJC, A
    FILIPEK, B
    CHEVALLET, P
    FARMACO, 1995, 50 (05): : 355 - 360
  • [30] Design, synthesis and preliminary bioactivity studies of imidazolidine-2,4-dione derivatives as Bcl-2 inhibitors
    Wang, Gang
    Wang, Yutao
    Wang, Lei
    Han, Leiqiang
    Hou, Xuben
    Fu, Huansheng
    Fang, Hao
    BIOORGANIC & MEDICINAL CHEMISTRY, 2015, 23 (23) : 7359 - 7365