Multistep parallel synthesis of substituted 5-aminobenzimidazoles in solution phase

Journal of Combinatorial Chemistry

Volumn 6, Issue 5, 2004, Pages 811-821

  Li, Li ^a   Liu, Gang ^a   Wang, Zhanguo ^a   Yuan, Yunyun ^a   Zhang, Chunxu ^b   Tian, Hongyu ^b   Wu, Xianghong ^a   Zhang, Jing ^a  

^a INSTITUTE OF MATERIA MEDICA   (China)

^b BEIJING TECHNOLOGY AND BUSINESS UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

1 (1 METHYLHEXYL) 6 PHENOXY 2 (3,4,5 TRIMETHOXYPHENYL) 1H BENZOIMIDAZOL 5 YLAMINE; 1 (3 BUTOXYPROPYL) 2 (2 FURAN 2 YLVINYL) 6 (QUINOLIN 8 YLOXY) 1H BENZOIMIDAZOL 5 YLAMINE; 1 [1 [2 (3,4 DIMETHOXYPHENYL)ETHYL] 6 FLUORO 2 (3,4,5 TRIMETHOXYPHENYL) 1H BENZOIMIDAZOL 5 YL] 3 (4 TRIFLUOROMETHYLPHENYL)UREA; 1 [2 (3,4 DIMETHOXYPHENYL)ETHYL] 6 (4 ETHYLPHENOXY) 2 THIOPHEN 2 YL 1H BENZOIMIDAZOL 5 YLAMINE; 1 BENZYL 3 [1 [2 (3,4 DIMETHOXYPHENYL)ETHYL] 6 FLUORO 2 (3,4,5 TRIMETHOXYPHENYL) 1H BENZOIMIDAZOL 5 YL]UREA; 1,5 DIFLUORO 2,4 DINITROBENZENE; 2 (1 ETHYLPROPYL) 1 (1 METHYLHEPTYL) 6 PHENOXY 1H BENZOIMIDAZOL 5 YLAMINE; 2 (3,4 DIFLUOROPHENYL) 6 FLUORO 1 (3 ISOPROPOXYPROPYL) 1H BENZOIMIDAZOL 5 YLAMINE; 2 (4 METHOXYPHENYL) 6 MORPHOLIN 4 YL 1 PROPYL 1H BENZOIMIDAZOL 5 YLAMINE; 6 (3,5 DIMETHYLPHENOXY) 1 (1,1 DIMETHYLPROPYL) 2 PHENETHYL 1H BENZOIMIDAZOL 5 YLAMINE; 6 (3,5 DIMETHYLPHENOXY) 2 (2 FLUOROPHENYL) 1 (3 PHENYLPROPYL) 1H BENZOIMIDAZOL 5 YLAMINE; 6 FLUORO 1 PHENETHYL 2 (3,4,5 TRIMETHOXYPHENYL) 1H BENZOIMIDAZOL 5 YLAMINE; BENZENE DERIVATIVE; BENZIMIDAZOLE DERIVATIVE; FLUORINE; N [1 (3 METHOXYPROPYL) 6 PIPERIDIN 1 YL 2 THIOPHEN 2 YL 1H BENZOIMIDAZOL 5 YL]BENZENESULFONAMIDE; N [1 [2 (3,4 DIMETHOXYPHENYL)ETHYL] 6 (4 ETHYLPHENOXY) 2 PYRIDIN 3 YL 1H BENZOIMIDAZOL 5 YL] 4 METHYLBENZENESULFONAMIDE; N [1 [2 (3,4 DIMETHOXYPHENYL)ETHYL] 6 FLUORO 2 (3,4,5 TRIMETHOXYPHENYL) 1H BENZOIMIDAZOL 5 YL]ACETAMIDE; N [1 [2 (3,4 DIMETHOXYPHENYL)ETHYL] 6 FLUORO 2 THIOPHEN 2 YL 1H BENZOIMIDAZOL 5 YL] 4 METHYLBENZENESULFONAMIDE; N [2 (3,4 DIFLUOROPHENYL) 1 (3 METHOXYPROPYL) 6 (5,6,7,8 TETRAHYDRONAPHTHALEN 1 YLOXY) 1H BENZOIMIDAZOL 5 YL]BENZENESULFONAMIDE; N [2 (3,4 DIFLUOROPHENYL) 6 FLUORO 1 (3 ISOPROPOXYPROPYL) 1H BENZOIMIDAZOL 5 YL]ACETAMIDE; N [2 (3,5 DITRIFLUOROMETHYLPHENYL) 1 [2 (3,4 DIMETHOXYPHENYL)ETHYL] 6 ETHOXY 1H BENZOIMIDAZOL 5 YL]BENZENESULFONAMIDE; N [2 (4 BUTOXYPHENYL) 1 (3 METHOXYPROPYL) 6 PIPERIDIN 1 YL 1H BENZOIMIDAZOL 5 YL] 4 METHYLBENZENESULFONAMIDE; N [2 (4 METHOXYPHENYL) 6 MORPHOLIN 4 YL 1 PROPYL 1H BENZOIMIDAZOL 5 YL]BENZENESULFONAMIDE; N [6 (3,5 DIMETHYLPHENOXY) 1 (1,1 DIMETHYLPROPYL) 2 PHENETHYL 1H BENZOIMIDAZOL 5 YL]ACETAMIDE; N [6 (3,5 DIMETHYLPHENOXY) 1 (3 ISOPROPOXYPROPYL) 2 (5 NITROFURAN 2 YL) 1H BENZOIMIDAZOL 5 YL]BENZENESULFONAMIDE; N [6 (3,5 DIMETHYLPHENOXY) 1 (3 METHOXYPROPYL) 2 PHENETHYL 1H BENZOIMIDAZOL 5 YL]BENZENESULFONAMIDE; N [6 (3,5 DIMETHYLPHENOXY) 2 (2,5 DIMETHYLPHENYL) 1 (3 METHOXYPROPYL) 1H BENZOIMIDAZOL 5 YL] 4 METHYLBENZENESULFONAMIDE; N [6 ETHOXY 1 PENTYL 2 (3,4,5 TRIMETHOXYPHENYL) 1H BENZOIMIDAZOL 5 YL]BENZENE SULFONAMIDE; N [6 FLUORO 1 (3 ISOPROPOXYPROPYL) 2 (3,4,5 TRIMETHOXYPHENYL) 1H BENZOIMIDAZOL 5 YL]BENZENESULFONAMIDE; UNCLASSIFIED DRUG;

ARTICLE; ATOM; CHEMICAL MODIFICATION; DRUG SYNTHESIS; METHODOLOGY; OXIDATION; REACTION ANALYSIS; REDUCTION; ROOM TEMPERATURE;

EID: 4944265215     PISSN: 15204766     EISSN: None     Source Type: Journal    
DOI: 10.1021/cc049932f     Document Type: Article

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