Ultrasonic irradiation of the Ullmann condensation: Application to the preparation of dioxolo, dioxino, cyclopent, and imidazolo anthranilic acid derivatives

被引:21
作者
Robin, M [1 ]
Pique, V [1 ]
Faure, R [1 ]
Galy, JP [1 ]
机构
[1] Univ Aix Marseille 3, Fac Sci & Tech St Jerome, Lab Valorisat Chim Fine, F-13397 Marseille 20, France
关键词
D O I
10.1002/jhet.5570390537
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The synthesis of N-aryl anthranilic acid derivatives bearing dioxolo, dioxino, cyclopent, and imidazolo supplementary ring systems is reported. The Ullmann-Goldberg condensation of the N-aryl anthranilic acid is improved in yield and reaction time, compared to conventional heating; by ultrasonic irradiation.
引用
收藏
页码:1083 / 1085
页数:3
相关论文
共 17 条
  • [1] ACHESON RM, 1956, ACRIDINES, P160
  • [2] ALBERT A, 1985, SELECTIVE TOXICITY
  • [3] DENNY WA, 1994, MOL ASPECTS ANTICANC, P270
  • [4] Pyridinium betaines derived from thiazolo and imidazoacridinones
    Galy, JP
    Hanoun, JP
    Pique, V
    Jagerovic, N
    Elguero, J
    [J]. JOURNAL OF HETEROCYCLIC CHEMISTRY, 1997, 34 (06) : 1781 - 1787
  • [5] A CONVENIENT SYNTHESIS OF N-ARYLANTHRANILIC ACIDS USING ULTRASONICS IN THE ULLMANN-GOLDBERG CONDENSATION
    HANOUN, JP
    GALY, JP
    TENAGLIA, A
    [J]. SYNTHETIC COMMUNICATIONS, 1995, 25 (16) : 2443 - 2448
  • [6] ACRIDINE-DERIVATIVES .5. SYNTHESIS AND P388 ANTITUMOR-ACTIVITY OF THE NOVEL 9-ANILINO-2,3-ETHYLENEDIOXYACRIDINES
    KIMURA, M
    OKABAYASHI, I
    KATO, A
    [J]. JOURNAL OF HETEROCYCLIC CHEMISTRY, 1993, 30 (04) : 1101 - 1104
  • [7] ACRIDINE-DERIVATIVES .4. SYNTHESIS, MOLECULAR-STRUCTURE, AND ANTITUMOR-ACTIVITY OF THE NOVEL 9-ANILINO-2,3-METHYLENEDIOXYACRIDINES
    KIMURA, M
    KATO, A
    OKABAYASHI, I
    [J]. JOURNAL OF HETEROCYCLIC CHEMISTRY, 1992, 29 (01) : 73 - 80
  • [8] Acridine and phenothiazine derivatives as pharmacotherapeutics for prion disease
    Korth, C
    May, BCH
    Cohen, FE
    Prusiner, SB
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (17) : 9836 - 9841
  • [9] March J., 1992, ADV ORG CHEM
  • [10] Morel S, 1997, MAGN RESON CHEM, V35, P556, DOI 10.1002/(SICI)1097-458X(199708)35:8<556::AID-OMR135>3.0.CO