Andreani A, Rambaldi M, Locatelli A, Bossa R, Fraccari A, Galatulas I
Università di Bologna, Dipartimento di Scienze Farmaceutiche, Via Belmeloro 6, Italy.
J Pharm Belg. 1993 Sep-Oct;48(5):378-82.
A series of imidazo[2,1-b]thiazole adamantylthioureas (3a-f) was synthesized by reaction of the methylsulfanylethylamines 2a-f (prepared in turn from the hydroxymethylimidazo[2,1-b]thiazoles 1a-f and cysteamine) with 1-adamantylisothiocyanate. 1-Adamant-1-yl-3-[2-(6-chloro-2,3- dihydroimidazo[2,1-b]thiazol-5-ylmethylsulfanyl)ethyl] thiourea (3d) was significantly active.
通过甲硫烷基乙胺2a - f(依次由羟甲基咪唑并[2,1 - b]噻唑1a - f和半胱胺制备)与1 - 金刚烷基异硫氰酸酯反应,合成了一系列咪唑并[2,1 - b]噻唑金刚烷基硫脲(3a - f)。1 - 金刚烷 - 1 - 基 - 3 - [2 - (6 - 氯 - 2,3 - 二氢咪唑并[2,1 - b]噻唑 - 5 - 基甲基硫烷基)乙基]硫脲(3d)具有显著活性。