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Volumn 56, Issue 20, 2000, Pages 3245-3253

Pd(0) amination of benzimidazoles as an efficient method towards new (benzimidazolyl)piperazines with high affinity for the 5-HT(1A) receptor

Author keywords

5 HT(1A) receptor; Arylpiperazines; Pd(0) amination

Indexed keywords

[BENZIMIDAZOL 4(7) YL]PIPERAZINE DERIVATIVE; BENZIMIDAZOLE DERIVATIVE; PALLADIUM; PIPERAZINE DERIVATIVE; SEROTONIN 1A RECEPTOR; UNCLASSIFIED DRUG;

EID: 2942615843     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(00)00225-8     Document Type: Article
Times cited : (29)

References (58)
  • 19
    • 0004273844 scopus 로고    scopus 로고
    • For a recent review of the synthetic methods to obtain benzimidazoles, see: (a) Meth-Cohn, O., Ed.; Academic: New York
    • For a recent review of the synthetic methods to obtain benzimidazoles, see: (a) Grimmett, M. R. In Imidazole and Benzimidazole Synthesis; Meth-Cohn, O., Ed.; Academic: New York, 1997.
    • (1997) Imidazole and Benzimidazole Synthesis
    • Grimmett, M.R.1
  • 20
    • 0032580502 scopus 로고    scopus 로고
    • For recent papers on the synthesis of functionalized benzimidazole rings, see: (b)
    • For recent papers on the synthesis of functionalized benzimidazole rings, see: (b) Edlin, C. D.; Parker, D. Tetrahedron Lett. 1998, 39, 2797.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 2797
    • Edlin, C.D.1    Parker, D.2
  • 27
    • 4243429498 scopus 로고
    • (b) Parke, Davis & Co.
    • (b) Parke, Davis & Co. Chem. Abstr. 1961, 55, 8444h.
    • (1961) Chem. Abstr. , vol.55
  • 35
    • 0032541260 scopus 로고    scopus 로고
    • For recent reviews in this area, see: (g)
    • For recent reviews in this area, see: (g) Hartwig, J. F. Angew. Chem., Int. Ed. Engl. 1998, 37, 2046.
    • (1998) Angew. Chem., Int. Ed. Engl. , vol.37 , pp. 2046
    • Hartwig, J.F.1
  • 49
    • 0000344058 scopus 로고
    • 5-(6)-Bromobenzimidazole was obtained in a single step
    • 5-(6)-Bromobenzimidazole was obtained in a single step: Mistry, A. G.; Smith, K.; Bye, M. R. Tetrahedron Lett. 1986, 27, 1051.
    • (1986) Tetrahedron Lett. , vol.27 , pp. 1051
    • Mistry, A.G.1    Smith, K.2    Bye, M.R.3
  • 51
    • 0342950122 scopus 로고    scopus 로고
    • 2 (1.1%) and phenyl (2.0%), and no effect on any other benzimidazole proton was observed
    • 2 (1.1%) and phenyl (2.0%), and no effect on any other benzimidazole proton was observed.
  • 57
    • 0342950120 scopus 로고    scopus 로고
    • 6-Iodo-1-tritylbenzimidazole (8b) was partially characterized but not isolated from the crude mixture because it was not necessary to obtain the target benzimidazolylpiperazines
    • 6-Iodo-1-tritylbenzimidazole (8b) was partially characterized but not isolated from the crude mixture because it was not necessary to obtain the target benzimidazolylpiperazines.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.