Trimethylsilyl chloride as a promoter for the groebke-blackburn reaction: Preparation of imidazo[2,1-b][1,3]benzothiazoles

Synthetic Communications

Volumn 40, Issue 1, 2010, Pages 111-119

  Tsirulnikov, Sergey ^a,b   Kysil, Volodymyr ^c   Ivachtchenko, Alexandre ^c   Krasavin, Mikhail ^a  

^a Chemical Diversity Research Institute   (Russian Federation)

^b TULA STATE LEV TOLSTOY PEDAGOGICAL UNIVERSITY   (Russian Federation)

^c CHEMDIV INC   (United States)

Author keywords

Groebke Blackburn reaction; Imidazo 1,2 x azoles; Isocyanide based multicomponent reactions; Trimethylsilyl chloride

Indexed keywords

2 [4 (DIMETHYLAMINO)PHENYL] N (2 METHOXYETHYL) 7 METHYLIMIDAZO[2,1 B][1,3]BENZOTHIAZOL 3 AMINE; 2 METHOXY 4 [3 [(3 METHOXYPROPYL)AMINO] 7 METHYLIMIDAZO[2,1 B][1,3]BENZOTHIAZOL 2 YL]PHENOL; 4 [3 (TERT BUTYLAMINO) 7 ETHOXYIMIDAZO[2,1 B][1,3]BENZOTHIAZOL 2 YL]PHENOL; 4 [3 (TERT BUTYLAMINO) 7 METHOXYIMIDAZO[2,1 B][1,3]BENZOTHIAZOL 2 YL] 2 METHOXYPHENOL; 4 [3 [(3 ISOPROPOXYPROPYL)AMINO] 7 METHYLIMIDAZO[2,1 B][1,3]BENZOTHIAZOL 2 YL]BENZONITRILE; 4 [3 [(3 ISOPROPOXYPROPYL)AMINO]IMIDAZO[2,1 B][1,3]BENZOTHIAZOL 2 YL] 2 METHOXYPHENOL; 4 [7 ETHOXY 3 [(3 ISOPROPOXYPROPYL)AMINO]IMIDAZO[2,1 B][1,3]BENZOTHIAZOL 2 YL]BENZONITRILE; 5 [3 (TERT BUTYLAMINO) 7 ETHOXYIMIDAZO[2,1 B][1,3]BENZOTHIAZOL 2 YL] 2 METHOXYPHENOL; 7 CHLORO 2 [4 (DIMETHYLAMINO)PHENYL] N (2 METHOXYETHYL)IMIDAZO[2,1 B][1,3]BENZOTHIAZOL 3 AMINE; 7 CHLORO 2 [4 (DIMETHYLAMINO)PHENYL] N (3 METHOXYPROPYL)IMIDAZO[2,1 B][1,3]BENZOTHIAZOL 3 AMINE; BENZOTHIAZOLE DERIVATIVE; CHLOROTRIMETHYLSILANE; IMIDAZO[2,1 B][1,3]BENZOTHIAZOLE DERIVATIVE; N (1H 1,2,3 BENZOTRIAZOL 5 YLMETHYL) N (3 METHOXYPROPYL)AMINE; N (1H 1,2,3 BENZOTRIAZOL 5 YLMETHYL) N PHENYLAMINE; N (TERT BUTYL) 2 (2 FLUOROPHENYL)IMIDAZO[2,1 B][1,3]BENZOTHIAZOL 3 AMINE; N (TERT BUTYL) 2 (4 FLUOROPHENYL) 7 METHOXYIMIDAZO[2,1 B][1,3]BENZOTHIAZOL 3 AMINE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; CRYSTALLIZATION; GROEBKE BLACKBURN REACTION; SYNTHESIS;

EID: 72049109139     PISSN: 00397911     EISSN: 15322432     Source Type: Journal    
DOI: 10.1080/00397910902953331     Document Type: Article

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