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Volumn 66, Issue 24, 2010, Pages 4383-4389

New heteroaromatic aminations on 5-aryl-1,2,4-triazines and 1,2,4,5-tetrazines by palladium catalysis

Author keywords

[No Author keywords available]

Indexed keywords

1,2,4 TRIAZINE DERIVATIVE; AMINE; HETEROCYCLIC COMPOUND; METHYLSULFUR ACID; PALLADIUM; SULFUR ACID DERIVATIVE; TETRAZINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 77953122472     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2010.03.099     Document Type: Article
Times cited : (17)

References (33)
  • 8
    • 77953123037 scopus 로고    scopus 로고
    • For examples of activities of functionalized 3-amino-1,2,4-triazines, see
    • For examples of activities of functionalized 3-amino-1,2,4-triazines, see:
  • 9
    • 77953121712 scopus 로고    scopus 로고
    • Compounds useful as kinase inhibitors for the treatment of hyperproliferative diseases
    • WO 076984
    • Bondinell, W.E.; Holt, D.A.; Lago, M.A.; Neeb, M.J. Semones, M.A. Compounds useful as kinase inhibitors for the treatment of hyperproliferative diseases. WO 076984, 2002;
    • (2002)
    • Bondinell, W.E.1    Holt, D.A.2    Lago, M.A.3    Neeb, M.J.4    Semones, M.A.5
  • 10
    • 77953122659 scopus 로고    scopus 로고
    • Inhibitors of C-JUN
    • N-Terminal kinases (JNK) and others protein kinases. WO 083667, 2002;
    • Cao, J.; Green, J.; Moon, Y.C.; Wang, J.; Ledeboer, M.; Gao, H. Harrington, E. Inhibitors of C-JUN N-Terminal kinases (JNK) and others protein kinases. WO 083667, 2002;
    • Cao, J.1    Green, J.2    Moon, Y.C.3    Wang, J.4    Ledeboer, M.5    Gao, H.6    Harrington, E.7
  • 13
    • 77954626646 scopus 로고    scopus 로고
    • Pharmaceuticals Compounds
    • WO 059259
    • Boyle, R.G.; Travers, S. Pharmaceuticals Compounds. WO 059259, 2008.
    • (2008)
    • Boyle, R.G.1    Travers, S.2
  • 15
    • 77953121291 scopus 로고    scopus 로고
    • For other Pd-catalyzed C-3 functionalizations, see:
    • For other Pd-catalyzed C-3 functionalizations, see:
  • 19
    • 77953121392 scopus 로고    scopus 로고
    • For others desulfuratives cross-coupling reactions reported by our group, see
    • For others desulfuratives cross-coupling reactions reported by our group, see:
  • 29
    • 77953124030 scopus 로고    scopus 로고
    • note
    • More than 20 h were needed to get full completion when the reaction was run under reflux conditions. See Ref. 5.
  • 30
    • 77953122750 scopus 로고    scopus 로고
    • note
    • CCDC 755055 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge at www.ccdc.cam.uk/cont/retrieving.html (or from Cambridge Crystallographic Data Centre, University Chemical Lab, 12, Union Road, Cambridge, CB2 1EZ, U.K.; E-mail: deposit@ccdc.cam.ac.uk).
  • 31
    • 77953122680 scopus 로고    scopus 로고
    • Fields and Boger described that N-substituted 6-(methylthio)-1,2,4,5-tetrazin-3-amines could be obtained through the direct displacement of the SMe moiety by amines, without the use of palladium catalysis. However the reported yields were poor. See:
    • Fields and Boger described that N-substituted 6-(methylthio)-1,2,4,5-tetrazin-3-amines could be obtained through the direct displacement of the SMe moiety by amines, without the use of palladium catalysis. However the reported yields were poor. See:
  • 33


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.