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Volumn 55, Issue 10, 2010, Pages 689-695

Synthesis of novel imidazo[1,5-a]pyridine derivates

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EID: 79952090170     PISSN: 00353930     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (6)

References (34)
  • 3
    • 67649852044 scopus 로고    scopus 로고
    • Chem Abstr. 2001, 134, 93136;
    • (2001) Chem Abstr. , vol.134 , pp. 93136
  • 5
    • 79954608467 scopus 로고    scopus 로고
    • Chem Abstr. 2005. 142, 440277.
    • (2005) Chem Abstr. , vol.142 , pp. 440277
  • 23
    • 67649841647 scopus 로고    scopus 로고
    • A one-pot synthesis of imidazo[1,5-a]pyridines
    • J.M. Crawforth, M. Paoletti, "A one-pot synthesis of imidazo[1,5-a]pyridines", Tetrahedron Lett. 2009, 50, 4916-4918 .
    • (2009) Tetrahedron Lett. , vol.50 , pp. 4916-4918
    • Crawforth, J.M.1    Paoletti, M.2
  • 31
    • 79952091626 scopus 로고    scopus 로고
    • The 2-aminomethyl-3-chloro-5-trifluoromethyl-pyrridine (1) is commercially available but is expensive even in small amounts. For example the supplier Amfinecom Inc. sell 1 g of the amine (1) at 622 $
    • The 2-aminomethyl-3-chloro-5-trifluoromethyl-pyrridine (1) is commercially available but is expensive even in small amounts. For example the supplier Amfinecom Inc. sell 1 g of the amine (1) at 622 $.
  • 32
    • 79952096466 scopus 로고    scopus 로고
    • (Bayer Cropscience SA Fr) EP 1422220 A1 20040526
    • M. Vanghelisti, M. Amin and R. W. Pannell (Bayer Cropscience SA, Fr), EP 1422220 A1 20040526, 2004, 11 pp.
    • (2004)
    • Vanghelisti, M.1    Amin, M.2    Pannell, R.W.3
  • 33
    • 79952074254 scopus 로고    scopus 로고
    • To a mixture of triphosgene in 100 ml of chlorbenzene cooled down to 00C was added dropwise the amine (1) dissolved in 150 mL chlorobenzene. When addition was finished the reaction mixture was allowed to warm up to room temperature. Reaction was monitored by disappearance of the amine (1) by TLC analysis. When reaction was finished the pyridine was added and the reaction mixture was filtered and excess of solvent was distilled off at a pressure of 1 mbar. The residue was concentrated under reduced pressure and purified on silica gel (ethyl acetate : hexane). The product (6) was obtained in 45% yield
    • To a mixture of triphosgene in 100 ml of chlorbenzene cooled down to 00C was added dropwise the amine (1) dissolved in 150 mL chlorobenzene. When addition was finished the reaction mixture was allowed to warm up to room temperature. Reaction was monitored by disappearance of the amine (1) by TLC analysis. When reaction was finished the pyridine was added and the reaction mixture was filtered and excess of solvent was distilled off at a pressure of 1 mbar. The residue was concentrated under reduced pressure and purified on silica gel (ethyl acetate : hexane). The product (6) was obtained in 45% yield.


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