A preparative route to fused 4-hydroxy-3-phenylindeno(benzothieno)pyridin-2-ones

被引:0
|
作者
Genevois-Borella, A [1 ]
Vuilhorgne, M [1 ]
Mignani, S [1 ]
机构
[1] Aventis Pharma SA, Ctr Rech Paris, F-94403 Vitry Sur Seine, France
关键词
D O I
暂无
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Syntheses of fused 4-hydroxy-3-phenylindeno(benzothieno)-pyridin-2-one derivatives (1a,b) are described.
引用
收藏
页码:317 / 322
页数:6
相关论文
共 50 条
  • [31] Design, synthesis, and thrombin-inhibitory activity of pyridin-2-ones as P2/P3 core motifs
    Hanessian, Stephen
    Simard, Daniel
    Bayrakdarian, Malken
    Therrien, Eric
    Nilsson, Ingemar
    Fjellstrom, Ola
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2008, 18 (06) : 1972 - 1976
  • [32] Condensation of amino derivatives of benzimidazol-2-ones and imidazo[4,5-b]pyridin-2-ones with 2,6-dimethyl-γ-pyrone in acetic acid
    O. Yu. Pankina
    T. S. Koval’
    N. I. Korotkikh
    N. N. Smolyar
    Russian Journal of Organic Chemistry, 2013, 49 : 779 - 781
  • [33] Erratum to: A Domino Reaction for the Synthesis of 2H-Pyrano-[4'',3'',2'':4',5']chromeno [2',3':4,5]thieno-[2,3-b]pyridin-2-ones
    Svitlana P. Bondarenko
    Igor V. Zhytnetskyi
    Serhii V. Semenov
    Mykhaylo S. Frasinyuk
    Chemistry of Heterocyclic Compounds, 2016, 52 : 352 - 352
  • [34] Condensation of amino derivatives of benzimidazol-2-ones and imidazo[4,5-b]pyridin-2-ones with 2,6-dimethyl-γ-pyrone in acetic acid
    Pankina, O. Yu.
    Koval', T. S.
    Korotkikh, N. I.
    Smolyar, N. N.
    RUSSIAN JOURNAL OF ORGANIC CHEMISTRY, 2013, 49 (05) : 779 - 781
  • [35] Fluorescent 2-Hydroxy-3-(pyridin-2-yl)-4H-quinolizin-4-ones through Dimerization of Pyridineacetic Acids
    Sokolov, Anatolii, I
    Sycheva, Maria A.
    Farkhutdinova, Dilara A.
    Myasnyanko, Ivan N.
    Mikhaylov, Andrey A.
    Baleeva, Nadezhda S.
    Bochenkova, Anastasia, V
    Baranov, Mikhail S.
    EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2022, 2022 (30)
  • [36] ONE-STEP SYNTHESIS OF 3-CYANO-4-(5-NITROBENZOTHIENYL)PYRIDINES AND 3-CYANO-4-(5-NITROBENZOTHIENYL)PYRIDIN-2-ONES FOR BIOLOGICAL EVALUATION
    ZAYED, SMAD
    ATTIA, A
    JOURNAL OF HETEROCYCLIC CHEMISTRY, 1983, 20 (01) : 129 - 131
  • [37] Electrospray ionisation and ion-trap fragmentation of substituted 3,4-dihydro-2(1H)-pyridin-2-ones
    Suárez, M
    Martínez-Alvarez, R
    Martín, N
    Verdecia, Y
    Ochoa, E
    Alba, L
    Seoane, C
    Kayali, N
    RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2002, 16 (08) : 749 - 754
  • [38] Synthesis and Biological Activity Evaluation of Novel 5-Methyl-7-phenyl-3H-thiazolo[4,5-b]pyridin-2-ones
    Lozynskyi, Andrii
    Konechnyi, Yulian
    Senkiv, Julia
    Yushyn, Ihor
    Khyluk, Dmytro
    Karpenko, Olexandr
    Shepeta, Yulia
    Lesyk, Roman
    SCIENTIA PHARMACEUTICA, 2021, 89 (04)
  • [39] Eschenmoser reaction: An unexpected route to tetrahydrothieno[2,3-b]pyridin-3-ones and azepan-3-ones
    Marchand, P
    Bellec, C
    FargeauBellassoued, MC
    Nezry, C
    Lhommet, G
    HETEROCYCLES, 1996, 43 (01) : 63 - 70
  • [40] Dioxomolybdenum(VI) complexes containing 1-alkyl-2-ethyl-3-hydroxy-4-pyridin-4(1H)-ones
    Tam, NC
    Fletcher, SP
    Vogels, CM
    Westcott, SA
    Decken, A
    TRANSITION METAL CHEMISTRY, 2003, 28 (01) : 103 - 109