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Volumn 39, Issue 40, 1998, Pages 7235-7238

A practical solid phase synthesis of quinazoline-2, 4-diones

Author keywords

[No Author keywords available]

Indexed keywords

QUINAZOLINE DERIVATIVE;

EID: 0032191551     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(98)01595-0     Document Type: Article
Times cited : (71)

References (22)
  • 3
    • 0010304544 scopus 로고    scopus 로고
    • (c) Special issue, Acc. Chem. Res. 1996, 29.
    • (1996) Acc. Chem. Res. , vol.29
  • 4
    • 0025856972 scopus 로고
    • 2. For recent examples, see: (a) Russo, J. Med. Chem. 1991, 34, 1850.
    • (1991) J. Med. Chem. , vol.34 , pp. 1850
    • Russo1
  • 7
    • 0031058373 scopus 로고    scopus 로고
    • (d) Kotani, T.; Nagaki, Y.; Ishii, A.; Konishi, Y. J. Med. Chem. 1997, 40, 684. Recently, 3,6-substituted quinazolinediones were described as fibrinogen receptor antagonists, see: Liverton, N. J.; Armstrong, D. J.; Claremon, D. A.; Remy, D. C.; Baldwin, J. J.; Lynch, R. J.; Zhang, G.; Gould, R. J. Bioorg. & Med. Chem. Lett. 1998, 8, 483.
    • (1997) J. Med. Chem. , vol.40 , pp. 684
    • Kotani, T.1    Nagaki, Y.2    Ishii, A.3    Konishi, Y.4
  • 16
    • 0026029284 scopus 로고
    • As far as we can ascertain, this resin has not been exploited for solid phase organic synthesis
    • Bayer, E. Angew. Chem. Int. Ed. Engl. 1991, 30, 113. As far as we can ascertain, this resin has not been exploited for solid phase organic synthesis.
    • (1991) Angew. Chem. Int. Ed. Engl. , vol.30 , pp. 113
    • Bayer, E.1
  • 17
    • 85038543466 scopus 로고    scopus 로고
    • note
    • 2O, 2 X MeOH, 3 X DCM, and dried over high vacuum overnight. The substitution on the resin was over 96% determined by element analysis of chlorine composition, and the loading capacity is as high as 1.8mmol/g based on the weight increase of polymer.
  • 18
    • 85038542103 scopus 로고    scopus 로고
    • note
    • 4
  • 19
    • 85038550767 scopus 로고    scopus 로고
    • note
    • -1) was observed.
  • 20
    • 85038540726 scopus 로고    scopus 로고
    • note
    • 1H-NMR (200MHz), δ 7.05 (m, 1H), 7.25 (m, 1H), 7.50 (m, 6H), 7.70 (s, 1H), 7.90 (m, 1H), 8.15 (m, 1H); LC-MS, [M+H]=322.40, purity is 94% based on LC trace.
  • 21
    • 0030876296 scopus 로고    scopus 로고
    • 3 cyclocleavage conditions to build an hydantoin library at room temperature, see also: (a) Matthews, J.; Rivero, R. A. J. Org. Chem. 1997, 62, 6090.
    • (1997) J. Org. Chem. , vol.62 , pp. 6090
    • Matthews, J.1    Rivero, R.A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.