39184-83-3Relevant articles and documents
One-pot preparation of 2 (alkly)arylbenzothiazoles from the corresponding o-halobenzanilides
Bernardi, Dan,Ba, Lalla A?cha,Kirsch, Gilbert
, p. 2121 - 2123 (2008/02/09)
Thionation of o-halobenzanilides was carried out in the presence of Lawesson's reagent. Subsequently, the formed thioamides reacted with cesium carbonate to give the corresponding benzothiazole derivatives in the same pot. Georg Thieme Verlag Stuttgart.
Photochemical Synthesis of Benzothiazoles
Paramasivam, R.,Ramakrishnan, V. T.
, p. 930 - 934 (2007/10/02)
Irradiation of o-halothioacetanilides (1a-p) affords benzothiazoles (2a-p) in general.In methanol medium, polyhalogenated thioacetanilides yield benzothiazoles with the loss of bromine atom in the 4- or 6-position of the benzothiazole.Arylation of benzothiazoles occurs in benzene medium.