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Volumn 70, Issue 35, 2014, Pages 5532-5540

Microwave-assisted synthesis of novel N-(4-phenylthiazol-2-yl)-benzo[d]thiazole-, thiazolo[4,5-b]pyridine-, thiazolo[5,4-b]pyridine- and benzo[d]oxazole-2-carboximidamides inspired by marine topsentines and nortopsentines

Author keywords

Benzo d oxazoles; Benzo d thiazoles; Copper mediated cyclisation; Microwave assisted chemistry; Thiazolopyridines

Indexed keywords

2 (4 CHLORO 5H 1,2,3 DITHIAZOL 5 YLIDENEAMINO)PHENOL; 2 BROMO N (4 CHLORO 5H 1,2,3 DITHIAZOL 5 YLIDENE)ANILINE; 2 CHLORO N (4 CHLORO 5H 1,2,3 DITHIAZOL 5 YLIDENE)PYRIDIN 3 AMINE; 2,4 DIBROMO N (4 CHLORO 5H 1,2,3 DITHIAZOL 5 YLIDENE)ANILINE; 3 BROMO N (4 CHLORO 5H 1,2,3 DITHIAZOL 5 YLIDENE)PYRIDIN 3 AMINE; 4 (2,4 DICHLOROPHENYL)THIAZOL 2 AMINE; 4 (4 CHLOROPHENYL)THIAZOL 2 AMINE; 4 (4 METHOXYPHENYL)THIAZOL 2 AMINE; 4 PHENYLTHIAZOL 2 AMINE; 6 BROMO N (4 PHENYLTHIAZOL 2 YL)BENZO[D]THIAZOLE 2 CARBOXIMIDAMIDE; 6 BROMO N (4 TOLYLTHIAZOL 2 YL)BENZO[D]THIAZOLE 2 CARBOXIMIDAMIDE; 6 BROMOBENZO[D]OXAZOLE 2 CARBONITRILE; 6 BROMOBENZO[D]THIAZOLE 2 CARBONITRILE; AMIDE; ANILINE DERIVATIVE; BENZOTHIAZOLE DERIVATIVE; BENZO[D]OXAZOLE 2 CARBONITRILE; BENZO[D]THIAZOLE 2 CARBONITRILE; CYANIDE; N (4 PHENYLTHIAZOL 2 YL)BENZO[D]THIAZOLE 2 CARBOXIMIDAMIDE; N (4 TOLYLTHIAZOL 2 YL)BENZO[D]THIAZOLE 2 CARBOXIMIDAMIDE; N [4 (2,4 DICHLOROPHENYL)THIAZOL 2 YL]BENZO[D]THIAZOLE 2 CARBOXIMIDAMIDE; N [4 (4 CHLOROPHENYL)THIAZOL 2 YL]BENZO[D]THIAZOLE 2 CARBOXIMIDAMIDE; N [4 (4 METHOXYPHENYL)THIAZOL 2 YL]BENZO[D]THIAZOLE 2 CARBOXIMIDAMIDE; OXAZOLE DERIVATIVE; PYRIDINE DERIVATIVE; THIAZOLO[4,5 B]PYRIDINE 2 CARBONITRILE; THIAZOLO[5,4 B]PYRIDINE 2 CARBONITRILE; TOPSENTIN; UNCLASSIFIED DRUG; UNINDEXED DRUG;

EID: 84949114998     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2014.06.102     Document Type: Article
Times cited : (12)

References (45)
  • 9
    • 84949147383 scopus 로고    scopus 로고
    • The first synthesis of 4,5-dichloro-1,2,3-dithiazolium chloride was described in 1985 by R. Appel. It was improved by C.W. Rees and co-workers who described the use of a phase transfer catalyst, Adogen®, used here as a source of chloride. Its addition improves the quality, but not the yield of the salt. For recent review see
    • ®, used here as a source of chloride. Its addition improves the quality, but not the yield of the salt. For recent review see
  • 16
    • 34248551722 scopus 로고
    • Chem. Abstr. 1994, 120, 236178m.
    • (1994) Chem. Abstr. , vol.120 , pp. 236178m
  • 18
    • 4243831539 scopus 로고
    • Chem. Abstr. 1991, 115, 35701z.
    • (1991) Chem. Abstr. , vol.115 , pp. 35701z
  • 20
    • 5744247980 scopus 로고
    • Chem. Abstr. 1990, 112, 185775d.
    • (1990) Chem. Abstr. , vol.112 , pp. 185775d
  • 22
    • 5744235741 scopus 로고
    • Chem. Abstr. 1989, 111, 160196g.
    • (1989) Chem. Abstr. , vol.111 , pp. 160196g
  • 24
    • 85057636509 scopus 로고
    • Chem. Abstr. 1988, 109, 129417q.
    • (1988) Chem. Abstr. , vol.109 , pp. 129417q
  • 28
    • 5744247694 scopus 로고    scopus 로고
    • Curr. Org. Chem. 8 2004 1691 1720
    • (2004) Curr. Org. Chem. , vol.8 , pp. 16911720
  • 41
    • 0015417053 scopus 로고
    • In this paper, proposals are presented for the stepwise selection for synthesis of analogues of an active compound. The diagrams are based on a fundamental assumption of the Hansch method that a particular substituent may modify activity relative to the parent compound by virtue of resulting changes in hydrophobic, electronic and steric effects. Using the Topliss scheme allowed to choose certain reagents to check the interest of a methodology, while starting to build a list of molecules with potential biological interest
    • J.G. Topliss J. Med. Chem. 15 1972 1006 1011 In this paper, proposals are presented for the stepwise selection for synthesis of analogues of an active compound. The diagrams are based on a fundamental assumption of the Hansch method that a particular substituent may modify activity relative to the parent compound by virtue of resulting changes in hydrophobic, electronic and steric effects. Using the Topliss scheme allowed to choose certain reagents to check the interest of a methodology, while starting to build a list of molecules with potential biological interest
    • (1972) J. Med. Chem. , vol.15 , pp. 1006-1011
    • Topliss, J.G.1
  • 42
    • 84949147392 scopus 로고    scopus 로고
    • Kinase screening experiments were performed by the Kinase Inhibitory Specialized Screening facility (KISSf) platform based in Station Biologique de Roscoff.
    • Kinase screening experiments were performed by the Kinase Inhibitory Specialized Screening facility (KISSf) platform based in Station Biologique de Roscoff.
  • 43
    • 0032330265 scopus 로고    scopus 로고
    • Dielectric properties are correlated with lost dissipation factor (tan δ), which expresses the capacity of a molecule or a material to transform electromagnetic energy into thermal energy. A very high susceptibility to microwaves is characterized by a high value (>0.5) of tan δ. For more details see
    • Dielectric properties are correlated with lost dissipation factor (tan δ), which expresses the capacity of a molecule or a material to transform electromagnetic energy into thermal energy. A very high susceptibility to microwaves is characterized by a high value (>0.5) of tan δ. For more details see: C. Gabriel, S. Gabriel, E.H. Grant, B.S.J. Halstead, and D.M.P. Mingos Chem. Soc. Rev. 27 1998 213 224
    • (1998) Chem. Soc. Rev. , vol.27 , pp. 213-224
    • Gabriel, C.1    Gabriel, S.2    Grant, E.H.3    Halstead, B.S.J.4    Mingos, D.M.P.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.