New polyfunctional spiropyran of 1,3-benzoxazin-4-one series with carbonyl-containing substituents in the [2H]-chromene moiety

被引:1
|
作者
Ozhogin, I. V. [1 ]
Tkachev, V. V. [2 ]
Lukyanov, B. S. [1 ,3 ]
Shilov, G. V. [2 ]
Mukhanov, E. L. [1 ]
Vasilyuk, G. T. [4 ]
Aldoshin, S. M. [2 ]
Minkin, V. I. [1 ]
机构
[1] Southern Fed Univ, Res Inst Phys & Organ Chem, Rostov Na Donu 344090, Russia
[2] Russian Acad Sci, Inst Problems Chem Phys, Chernogolovka 142432, Moscow Oblast, Russia
[3] Don State Tech Univ, Rostov Na Donu 344000, Russia
[4] Yanka Kupala State Univ, Grodno 230023, BELARUS
基金
俄罗斯基础研究基金会;
关键词
D O I
10.1134/S0012500817110040
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A polyfunctional spiropyran of 1,3-benzoxazin-4-one series containing one hydroxy and two carbonyl substituents in the [2H]-chromene moiety was synthesized on the basis of a new analogue of 2,4-dihydroxyisophthalic aldehyde, methyl 3,5-diformyl-2,4-dihydroxybenzoate. The structure of resulting 6'-carbomethoxy-3,7-dimethyl-8'-formyl-5'-hydroxy-4-oxo-spiro-(1,3-benzoxazine-2,2'-[2H]-chromene) was unambiguously established by single crystal X-ray diffraction analysis. These data allowed us to reveal the route for the reaction of the new polyfunctional aldehyde with 1,3-benzoxazin-4-onium perchlorate.
引用
收藏
页码:244 / 247
页数:4
相关论文
共 50 条
  • [1] New polyfunctional spiropyran of 1,3-benzoxazin-4-one series with carbonyl-containing substituents in the [2H]-chromene moiety
    I. V. Ozhogin
    V. V. Tkachev
    B. S. Lukyanov
    G. V. Shilov
    E. L. Mukhanov
    G. T. Vasilyuk
    S. M. Aldoshin
    V. I. Minkin
    Doklady Chemistry, 2017, 477 : 244 - 247
  • [2] Synthesis, structure and photochromic properties of novel highly functionalized spiropyrans of 1,3-benzoxazin-4-one series
    Ozhogin, Ilya V.
    Tkachev, Valery V.
    Lukyanov, Boris S.
    Mukhanov, Eugene L.
    Rostovtseva, Irina A.
    Lukyanova, Maria B.
    Shilov, Gennady V.
    Strekal, Natalya D.
    Aldoshin, Sergey M.
    Minkin, Vladimir I.
    JOURNAL OF MOLECULAR STRUCTURE, 2018, 1161 : 18 - 25
  • [3] NEW SYNTHESIS OF 2-METHYL-3-(4-VINYLOXYPHENYL)-2,3-DIHYDRO-4H-1,3-BENZOXAZIN-4-ONE
    SKVORTSOVA, GG
    STEPANOVA, ZV
    ANDRIYANKOVA, LV
    KHIMIYA GETEROTSIKLICHESKIKH SOEDINENII, 1979, (09): : 1278 - 1279
  • [4] REACTIONS OF 2-ETHOXY-2,3-DIHYDRO-4H-1,3-BENZOXAZIN-4-ONE WITH CONJUGATED DIENES
    BENISHAI, D
    WARSHAWS.A
    JOURNAL OF HETEROCYCLIC CHEMISTRY, 1971, 8 (05) : 865 - &
  • [5] THIO DERIVATIVES OF 2,3,-DIHYDRO-4H-1,3-BENZOXAZIN-4-ONE - SYNTHESIS AND PHARMACOLOGICAL PROPERTIES
    TEOTINO, UM
    FRIZ, LP
    GANDINI, A
    BELLA, DD
    JOURNAL OF MEDICINAL CHEMISTRY, 1963, 6 (03) : 248 - &
  • [6] NEW HETEROCYCLES FROM CYANATES - 2-ARYLAMINO AND 2-ARYLAMINO-4H-1,3-BENZOXAZIN-4-ONE, THEIR TAUTOMERISM AND ANALYSIS OF THEIR REGIOSELECTIVE ALKYLATION
    HEDAYATULLAH, M
    LION, C
    PAILLER, J
    JOURNAL OF HETEROCYCLIC CHEMISTRY, 1991, 28 (01) : 133 - 137
  • [7] CONDENSATION-REACTIONS BETWEEN O-PHENYLENEDIAMINE AND 2-SUBSTITUTED 1,3-BENZOXAZIN-4-ONE
    RABILLOUD, G
    SILLION, B
    BULLETIN DE LA SOCIETE CHIMIQUE DE FRANCE PARTIE II-CHIMIE MOLECULAIRE ORGANIQUE ET BIOLOGIQUE, 1975, (11-1): : 2682 - 2686
  • [8] SOME REACTIONS OF 2-(PARA-CHLOROPHENYL)-4H-1,3-BENZOTHIAZIN-4-THIONE AND 2-(PARA-CHLOROPHENYL)-4H-1,3-BENZOXAZIN-4-ONE
    SALEH, RM
    PHOSPHORUS SULFUR AND SILICON AND THE RELATED ELEMENTS, 1989, 45 (3-4): : 269 - 274
  • [9] Synthesis and antimicrobial evaluation of fatty chain substituted 2,5-dimethyl pyrrole and 1,3-benzoxazin-4-one derivatives
    Varshney, Himani
    Ahmad, Aiman
    Rauf, Abdul
    Husain, Fohad M.
    Ahmad, Iqbal
    JOURNAL OF SAUDI CHEMICAL SOCIETY, 2017, 21 : S394 - S402
  • [10] Synthesis of 2H-1,3-benzoxazin-4(3H)-one derivatives containing indole moiety: Their in vitro evaluation against PDE4B
    Rao, Raja Mohan
    Luther, Bethala Jawahar
    Rani, Chekuri Sharmila
    Suresh, Namburi
    Kapavarapu, Ravikumar
    Parsa, Kishore V. L.
    Rao, Mandava V. Basaveswara
    Pal, Manojit
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2014, 24 (04) : 1166 - 1171