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Volumn 16, Issue 14, 2006, Pages 3755-3760

Preparation of 1-(4-methoxyphenyl)-1H-pyrazolo[4,3-d]pyrimidin-7(6H)-ones as potent, selective and bioavailable inhibitors of coagulation factor Xa

Author keywords

Anticoagulants; Antithrombotic agents; Bicyclic core; Factor Xa inhibitors; Pyrazole; Pyrazolo 4,3 d pyrimidin 7(6H) ones

Indexed keywords

BLOOD CLOTTING FACTOR 10A; PYRAZOLE DERIVATIVE; PYRIMIDINE DERIVATIVE;

EID: 33745154028     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2006.04.044     Document Type: Article
Times cited : (58)

References (22)
  • 17
    • 33746472931 scopus 로고    scopus 로고
    • note
    • For a preliminary account of part of this work, see: Fevig, J. M.; Cacciola, J.; Buriak, J., Jr.; Li, Y.-L.; Pinto, D. J.; Orwat, M. J.; Galemmo, R. A., Jr.; Wells, B.; Li, R.; Rossi, K. A.; Knabb, R. M.; Luettgen, J. M.; Wong, P. C.; Bai, S.; Wexler, R. R.; Lam, P. Y. S. Abstracts of Papers, 230th National Meeting of the American Chemical Society, Washington, DC, Aug 28-Sept 1, 2005; American Chemical Society: Washington, DC, 2005; MEDI 279.
  • 20
    • 33746575626 scopus 로고    scopus 로고
    • note
    • Compound 44 was prepared in 50% yield from 14 (Y = H) with tin(II) chloride hydrate in warm isopropanol, which prevented the concomitant conversion of the nitrile to an ester.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.