Preparation of Heteroaryloxetanes and Heteroarylazetidines by Use of a Minisci Reaction

被引:82
作者
Duncton, Matthew A. J. [1 ]
Estiarte, M. Angels [1 ]
Johnson, Russell J. [1 ]
Cox, Matthew [1 ]
O'Mahony, Donogh J. R. [1 ]
Edwards, William T. [1 ]
Kelly, Michael G. [1 ]
机构
[1] Evotec USA, San Francisco, CA 94080 USA
关键词
FREE-RADICAL REACTIONS; PROTONATED HETEROAROMATIC BASES; TRIVALENT IODINE COMPOUNDS; HORMONE TRH ANALOGS; O-SULFONIC ACID; HOMOLYTIC ACYLATION; NUCLEOPHILIC CHARACTER; ANTITUMOR-ACTIVITY; CARBOXYLIC-ACIDS; ACYL RADICALS;
D O I
10.1021/jo9010624
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Introduction of oxetan-3-yl and azetidin-3-yl groups into heteroaromatic bases was achieved by using a radical addition method (Minisci reaction). To demonstrate utility. the process was used to introduce an oxetane Or azetidine into heteroaromatic systems that have found important uses in the drug discovery industry, such as the marketed EGFR inhibitor geftinib, a quinolinecarbonitrile Src tyrosine kinase inhibitor, and the antimalarial hydroquinine.
引用
收藏
页码:6354 / 6357
页数:4
相关论文
共 81 条
  • [1] Enthalpic and polar effects in the reactions of perfluoroalkyl radicals - New selective synthetic developments with alkenes and heteroaromatic bases
    Antonietti, F
    Mele, A
    Minisci, F
    Punta, C
    Recupero, F
    Fontana, F
    [J]. JOURNAL OF FLUORINE CHEMISTRY, 2004, 125 (02) : 205 - 211
  • [2] ARNONE A, 1973, GAZZ CHIM ITAL, V103, P13
  • [3] HETEROGENEOUS BIMOLECULAR REDUCTION .1. GENERAL CONSIDERATIONS OF MECHANISM - THE EMMERT REACTION
    BACHMAN, GB
    HAMER, M
    DUNNING, E
    SCHISLA, RM
    [J]. JOURNAL OF ORGANIC CHEMISTRY, 1957, 22 (11) : 1296 - 1302
  • [4] Studies leading to the identification of ZD1839 (Iressa™):: An orally active, selective epidermal growth factor receptor tyrosine kinase inhibitor targeted to the treatment of cancer
    Barker, AJ
    Gibson, KH
    Grundy, W
    Godfrey, AA
    Barlow, JJ
    Healy, MP
    Woodburn, JR
    Ashton, SE
    Curry, BJ
    Scarlett, L
    Henthorn, L
    Richards, L
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2001, 11 (14) : 1911 - 1914
  • [5] Synthesis and Src kinase inhibitory activity of a series of 4-phenylamino-3-quinolinecarbonitriles
    Boschelli, DH
    Wang, YD
    Ye, F
    Wu, BQ
    Zhang, N
    Dutia, M
    Powell, DW
    Wissner, A
    Arndt, K
    Weber, JM
    Boschelli, F
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 2001, 44 (05) : 822 - 833
  • [6] Synthesis using aromatic homolytic substitution - recent advances
    Bowman, W. Russell
    Storey, John M. D.
    [J]. CHEMICAL SOCIETY REVIEWS, 2007, 36 (11) : 1803 - 1822
  • [7] NUCLEOPHILIC CHARACTER OF ACYL RADICALS - SUBSTITUENT EFFECTS ON HOMOLYTIC ACYLATION OF PROTONATED HETEROAROMATIC BASES
    CARONNA, T
    GARDINI, GP
    FRONZA, G
    PORTA, O
    MINISCI, F
    [J]. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2, 1972, (10): : 1477 - &
  • [8] NUCLEOPHILIC CHARACTER OF ACYL RADICALS - A NEW SELECTIVE TYPE OF AROMATIC ACYLATION
    CARONNA, T
    GARDINI, GP
    MINISCI, F
    [J]. JOURNAL OF THE CHEMICAL SOCIETY D-CHEMICAL COMMUNICATIONS, 1969, (05): : 201 - &
  • [9] HOMOLYTIC ACYLATION OF PROTONATED PYRIDINE AND PYRAZINE DERIVATIVES
    CARONNA, T
    MINISCI, F
    PORTA, O
    FRONZA, G
    [J]. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2, 1972, (14): : 2035 - &
  • [10] Castro B., 1973, TETRAHEDRON LETT, V14, P4459, DOI [10.1016/S0040-4039(01)87248-8, DOI 10.1016/S0040-4039(01)87248-8]