3288-02-6Relevant academic research and scientific papers
Synthesis of ethyl 2-arylaminoimidazo[2,1-b]benzothiazole-3-carboxylates
Khalafy, Jabbar,Ebrahimlo, Ali Reza Molla,Dilmaghani, Karim Akbari
, p. 1347 - 1352 (2004)
3-Arylamino-4-ethoxycarbonylisoxazol-5(2H)-ones, substituted on nitrogen with a benzothiazole group, reacts with triethylamine in ethanol under reflux conditions to provide a convenient synthesis of ethyl 2-arylaminoimidazo[2,1-b] benzothiazole-3-carboxyl
Rearrangements of 2-pyridyl-3-arylaminoisoxazol-5(2H)-ones to imidazo[1,2-a]pyridines under flash-vacuum-pyrolysis
Setamdideh, Davood,Khanahmadzadeh, Salah,Khorshidi, Nasrin
experimental part, p. 2884 - 2890 (2012/07/17)
2-Pyridyl-3-arylaminoisoxazol-5(2H)-ones, rearranged under flash-vacuum-pyrolysis (FVP) conditions accompanied by elimination of carbon dioxide to give imidazo[1,2-a]pyridines in high to excellent yields (85-95 %).
