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Volumn 5, Issue 7, 2002, Pages 565-570

Alkylaminopropenones and alkylamino-propenoates as efficient and versatile synthons in microwave-assisted combinatorial synthesis

Author keywords

[No Author keywords available]

Indexed keywords

ACRYLIC ACID; AMINOPROPENOATE; AMINOPROPENONE; CHROMONE DERIVATIVE; HETEROCYCLIC AMINE; ISOXAZOLE; PYRAZOLE; PYRIDINE; PYRIMIDINONE DERIVATIVE; UNCLASSIFIED DRUG; AMINE; HETEROCYCLIC COMPOUND;

EID: 0036828671     PISSN: 13862073     EISSN: None     Source Type: Journal    
DOI: 10.2174/1386207023330048     Document Type: Article
Times cited : (22)

References (20)
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    • Cotterill, I. C.; Usyatinsky, A. Y.; Arnold, J. M.; Clark, D. S.; Dordick, J. S. Tetrahedron Lett., 1998, 39, 1117; Hsieh, H.-P.; Chen, S.-T.; Wang, K.-T. J. Chin. Chem. Soc., (Taipei) 1997, 44, 597; Stadler, A.; Kappe, C. O. J. Comb. Chem., 2001, 3, 624-630; Öhberg, L.; Westman, J. Synlett., 2001, 1296.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 1117
    • Cotterill, I.C.1    Usyatinsky, A.Y.2    Arnold, J.M.3    Clark, D.S.4    Dordick, J.S.5
  • 6
    • 0000784247 scopus 로고    scopus 로고
    • Cotterill, I. C.; Usyatinsky, A. Y.; Arnold, J. M.; Clark, D. S.; Dordick, J. S. Tetrahedron Lett., 1998, 39, 1117; Hsieh, H.-P.; Chen, S.-T.; Wang, K.-T. J. Chin. Chem. Soc., (Taipei) 1997, 44, 597; Stadler, A.; Kappe, C. O. J. Comb. Chem., 2001, 3, 624-630; Öhberg, L.; Westman, J. Synlett., 2001, 1296.
    • (1997) J. Chin. Chem. Soc., (Taipei) , vol.44 , pp. 597
    • Hsieh, H.-P.1    Chen, S.-T.2    Wang, K.-T.3
  • 7
    • 0001260317 scopus 로고    scopus 로고
    • Cotterill, I. C.; Usyatinsky, A. Y.; Arnold, J. M.; Clark, D. S.; Dordick, J. S. Tetrahedron Lett., 1998, 39, 1117; Hsieh, H.-P.; Chen, S.-T.; Wang, K.-T. J. Chin. Chem. Soc., (Taipei) 1997, 44, 597; Stadler, A.; Kappe, C. O. J. Comb. Chem., 2001, 3, 624-630; Öhberg, L.; Westman, J. Synlett., 2001, 1296.
    • (2001) J. Comb. Chem. , vol.3 , pp. 624-630
    • Stadler, A.1    Kappe, C.O.2
  • 8
    • 0034904876 scopus 로고    scopus 로고
    • Cotterill, I. C.; Usyatinsky, A. Y.; Arnold, J. M.; Clark, D. S.; Dordick, J. S. Tetrahedron Lett., 1998, 39, 1117; Hsieh, H.-P.; Chen, S.-T.; Wang, K.-T. J. Chin. Chem. Soc., (Taipei) 1997, 44, 597; Stadler, A.; Kappe, C. O. J. Comb. Chem., 2001, 3, 624-630; Öhberg, L.; Westman, J. Synlett., 2001, 1296.
    • (2001) Synlett. , pp. 1296
    • Öhberg, L.1    Westman, J.2
  • 9
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    • and references cited therein
    • Stanovnik, B.; Svete, J. Synlett 2000, 8, 1077, and references cited therein.
    • (2000) Synlett , vol.8 , pp. 1077
    • Stanovnik, B.1    Svete, J.2
  • 10
    • 0035148326 scopus 로고    scopus 로고
    • Pleier, A-K.; Glas, H.; Grosche, M.; Sirsch, P.; Thiel, W. R. Synthesis, 2001, 55, Dahmani, Z.; Rahmouni, M.; Brugidou, R.; Bazureau, J. P.; Hamelin, J. Tetrahedron Lett., 1998, 39, 8453, Meziane, M. A. A.; Rahmouni, M.; Bazureau, J. P.; Hamelin, J. Synthesis, 1998, 967.
    • (2001) Synthesis , pp. 55
    • Pleier, A.-K.1    Glas, H.2    Grosche, M.3    Sirsch, P.4    Thiel, W.R.5
  • 11
    • 0032511926 scopus 로고    scopus 로고
    • Pleier, A-K.; Glas, H.; Grosche, M.; Sirsch, P.; Thiel, W. R. Synthesis, 2001, 55, Dahmani, Z.; Rahmouni, M.; Brugidou, R.; Bazureau, J. P.; Hamelin, J. Tetrahedron Lett., 1998, 39, 8453, Meziane, M. A. A.; Rahmouni, M.; Bazureau, J. P.; Hamelin, J. Synthesis, 1998, 967.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 8453
    • Dahmani, Z.1    Rahmouni, M.2    Brugidou, R.3    Bazureau, J.P.4    Hamelin, J.5
  • 12
    • 0031851335 scopus 로고    scopus 로고
    • Pleier, A-K.; Glas, H.; Grosche, M.; Sirsch, P.; Thiel, W. R. Synthesis, 2001, 55, Dahmani, Z.; Rahmouni, M.; Brugidou, R.; Bazureau, J. P.; Hamelin, J. Tetrahedron Lett., 1998, 39, 8453, Meziane, M. A. A.; Rahmouni, M.; Bazureau, J. P.; Hamelin, J. Synthesis, 1998, 967.
    • (1998) Synthesis , pp. 967
    • Meziane, M.A.A.1    Rahmouni, M.2    Bazureau, J.P.3    Hamelin, J.4
  • 14
    • 0005139972 scopus 로고    scopus 로고
    • note
    • In this project SmithSynthesizer™ available from Personal Chemistry AB was used. This instrument is fully automated, equipped with temperature and pressure control and can run up to 120 unattended reactions sequentially. The process vial is cooled actively by pressurized air after the irradiation.
  • 15
    • 0005134884 scopus 로고    scopus 로고
    • note
    • General procedure for the formation on 1a-13a: 2 mmol of 1-13 was mixed with 1.5-2.5 eq. of DMFDEA. DMF was added to a total volume of 5 ml. The reaction mixtures were exposed to microwaves at 180 °C for 5 min and then cooled to room temperature. The residue was split into ten portions for further synthesis without work-up.
  • 16
    • 0005185353 scopus 로고    scopus 로고
    • note
    • 2), 6.82 (dd, 1H, ArH), 6.99 (dt, 1H, ArH), 7. 15 (dt, 1H, ArH), 7.28 (dd, 1H, ArH), 7.47 (m, 5H, ArH), 7.56 (s, 1H, ArH, pyrazole).
  • 19
    • 0005143915 scopus 로고    scopus 로고
    • note
    • 3), 7.53 (m, 3H, phenyl), 7.70 (m, 2H, phenyl), 8.38 (dd, 2H, pyridyl), 8.80 (dd, 2H, pyridyl), 9.16 (s, 1H, pyrimidine).
  • 20
    • 0005134384 scopus 로고    scopus 로고
    • note
    • 2), 7.18 (dd, 1H, ArH), 7.46 (m, 2H, ArH), 7.93 (dd, 1H, ArH), 8.13 (s, 1H, NH), 8.80 (s, 1H, CH).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.