메뉴 건너뛰기




Volumn 67, Issue 29, 2011, Pages 5293-5303

3-Acylindoles as versatile starting materials for pyridine ring annulation: Synthesis of 1-deazapurine isosteres

Author keywords

1 Deazapurine isosteres; 3 Acylindoles; Cyclocondensation; Pyridine ring annulation; Regioselectivity

Indexed keywords

1 DEAZAPURINE DERIVATIVE; 1 METHYL 6 (N METHYL 2 AMINOPHENYL)PYRIDO[2,3 D]PYRIMIDINE 2,4(1H,3H) DIONE; 1 METHYL 6 (N PHENYL 2 AMINOPHENYL)PYRIDO[2,3 D]PYRIMIDINE 2,4(1H,3H) DIONE; 1 TERT BUTYL 3 CYANO 4 METHYL 5 (N METHYL 2 AMINOPHENYL)PYRROLO[2,3 B]PYRIDINE; 1 TERT BUTYL 3 CYANO 5 (N METHYL 2 AMINOPHENYL)PYRROLO[2,3 B]PYRIDINE; 1 TERT BUTYL 3 CYANO 5 (N PHENYL 2 AMINOPHENYL)PYRROLO[2,3 B]PYRIDINE; 10 CYANO 8 CYCLOHEXYL 5H 6,8 DIHYDRO 6 OXO BENZO[F]PYRROLO[2,3 B][1,7]NAPHTHYRIDINE; 3 ACYLINDOLE DERIVATIVE; 3 AMINO 4 [(1 METHYL 1H INDOL 3 YL)METHYLENE] 1 PHENYL 1H PYRAZOL 5(4H) ONE; 3 CYANO 1 (4 METHOXYBENZYL) 4 METHYL 5 (N METHYL 2 AMINOPHENYL)PYRROLO[2,3 B]PYRIDINE; 3 CYANO 1 (4 METHOXYBENZYL) 5 (N METHYL 2 AMINOPHENYL)PYRROLO[2,3 B]PYRIDINE; 3 CYANO 1 CYCLOHEXYL 5 (N METHYL 2 AMINOPHENYL)PYRROLO[2,3 B]PYRIDINE; 3 CYANO 1 CYCLOHEXYL 5 (N PHENYL 2 AMINOPHENYL)PYRROLO[2,3 B]PYRIDINE; 3 CYANO1 CYCLOHEXYL 4 METHYL 5 (N METHYL 2 AMINOPHENYL)PYRROLO[2,3 B]PYRIDINE; 3 METHYL (N METHYL 2 AMINOPHENYL) 1 PHENYLPYRAZOLO[3,4 B]PYRIDINE; 3 METHYL 5 (N PHENYL AMINOPHENYL) 1 PHENYLPYRAZOLO[3,4 B]PYRIDINE; 5 (2 AMINOPHENYL) 1 TERT BUTYL 3 CYANO 4 METHYLPYRROLO[2,3 B]PYRIDINE; 5 (2 AMINOPHENYL) 3 CYANO 1 (4 METHOXYBENZYL) 4 METHYLPYRROLO[2,3 B]PYRIDINE; 5 (2 AMINOPHENYL) 3 CYANO 1 CYCLOHEXYL 4 METHYLPYRROLO[2,3 B]PYRIDINE; 5 (2 AMINOPHENYL) 3 CYANO 1 TERT BUTYLPYRROLO[2,3 B]PYRIDINE; 5 (2 AMINOPHENYL) 3 METHYL 1 PHENYLPYRAZOLO[3,4 B]PYRIDINE; 5 [(1H INDOL 3 YL)METHYLENE] 2 (PIPERIDIN 1 YL)THIAZOL 4(5H) IMINIUM CHLORIDE; 6 (2 AMINOPHENYL) 1 METHYLPYRIDO[2,3 D]PYRIMIDINE 2,4(1H,3H) DIONE; 8 TERT BUTYL 10 CYANO 5H 6,8 DIHYDRO 6 OXO BENZO[F]PYRROLO[2,3 B][1,7]NAPHTHYRIDINE; INDOLE DERIVATIVE; PURINE DERIVATIVE; PYRIDINE; UNCLASSIFIED DRUG;

EID: 79958770938     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2011.05.037     Document Type: Article
Times cited : (14)

References (49)
  • 15
    • 78149427966 scopus 로고
    • Chem. Abstr. 1995, 122, 314537.
    • (1995) Chem. Abstr. , vol.122 , pp. 314537
  • 16
    • 78149450799 scopus 로고
    • EP 0605836, 1994
    • (a) Tsushima, M.; Kano, I. EP 0605836, 1994; Chem. Abstr. 1995, 122, 31198;
    • (1995) Chem. Abstr. , vol.122 , pp. 31198
    • Tsushima, M.1    Kano, I.2
  • 18
    • 32944459567 scopus 로고    scopus 로고
    • Chem. Abstr. 1999, 131, 336878;
    • (1999) Chem. Abstr. , vol.131 , pp. 336878
  • 20
    • 78149462961 scopus 로고
    • Chem. Abstr. 1991, 114, 228904;
    • (1991) Chem. Abstr. , vol.114 , pp. 228904
  • 49
    • 79958769320 scopus 로고    scopus 로고
    • CCDC 801766-801770 contain the crystallographic data (excluding structure factors) for the structures of 13e, 13l, 13h, 14 and 16b reported in this paper. These data have been deposited with the Cambridge Crystallographic Data Centre as Supplementary data and can be obtained free of charge on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK; fax: +44 1223 336033; e-mail: deposit@ccdc.cam.ac.uk, or via
    • CCDC 801766-801770 contain the crystallographic data (excluding structure factors) for the structures of 13e, 13l, 13h, 14 and 16b reported in this paper. These data have been deposited with the Cambridge Crystallographic Data Centre as Supplementary data and can be obtained free of charge on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK; fax: +44 1223 336033; e-mail: deposit@ccdc.cam.ac.uk, or via www.ccdc.cam.ac.uk/data-request/cif.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.