A thorough study on the reaction of DMAD with 1-arylaminoimidazole-2-thiones. Expeditious synthesis of imidazo[2,1-b][1,3]thiazoles through a novel arylamino rearrangement

Upon reaction of 1-arylamino-imidazole-2-thiones 1 with dimethyl acetylenedicarboxylate (DMAD) in the presence of 2.2 equiv of sodium hydride, imidazothiazoles 4 were exclusively formed (71–82% yield). However, from the reaction of 1 with DMAD in the absence of base, only the S-substituted products 5 were formed as an E/Z mixture (53–55%), which could also be converted to 4 with 2.0 equiv of sodium hydride (65–68%). Furthermore, 5a-E/Z was converted to arylamino-substituted derivatives 8a upon reaction with 1.1 equiv of sodium hydride in 78% yield. Formation of 8a (75% yield) was also possible by reaction of thione 1a with DMAD in the presence of sodium methoxide in methanol. Substitution on the imidazole 3-NH of thione 1a leading to 6a-Z was observed either by heating 1a with DMAD (91%) or by heating the 5a-E/Z mixture in benzene (90% yield). Finally, when 5a-E reacted with acetic anhydride the acetylated derivative 7a-Z was the only isolated product (58%). Full assignment of all 1H and 13C NMR chemical shifts has been unambiguously achieved.