化学合成。
化学合成
路线1:以3-溴-1,1,1-三氟丙-2-酮和硫脲为原料
- 步骤: 将硫脲(4.0g,52.3mmol)和3-溴-1,1,1-三氟丙-2-酮(5.5mL,10g,52.3mmol)加入乙醇(100mL)中,于50℃加热反应2小时;冷却至室温,浓缩至干;残余物溶于水,用2M NaOH调pH>12,乙醚(4×)萃取;合并有机相,硫酸钠干燥,过滤,真空浓缩;硅胶色谱(CH₂Cl₂)纯化,得标题化合物(6.9g,79%)。
- 参考文献: [1] Patent: WO2008/36579, 2008, A1. Location in patent: Page/Page column 43;[2] Journal of Heterocyclic Chemistry, 1991, vol. 28, #4, p. 907-911;[3] Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, 1988, vol. 27, #1-12, p. 1051-1053;[4] Journal of Organic Chemistry, 1955, vol. 20, p. 499,505;[5] Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1981, p. 2335-2339;[6] Patent: US2009/286811, 2009, A1. Location in patent: Page/Page column 20;[7] Patent: US2003/236287, 2003, A1. Location in patent: Page 35;[8] Patent: WO2012/89607, 2012, A1. Location in patent: Page/Page column 38-39。
路线2:以2-(苯基磺酰基)-3-(三氟甲基)环氧乙烷和硫脲为原料
- 步骤: 将2-(苯基磺酰基)-3-(三氟甲基)环氧乙烷(1.0g)和2当量硫脲在4mL N,N-二甲基甲酰胺中,于90℃加热过夜;冷却后加入40mL CH₂Cl₂,依次用水和盐水洗涤;加入木炭,过滤,蒸发溶剂;残余物经硅胶色谱分离,得4-(三氟甲基)噻唑-2-胺(200mg,收率30%)。
- 条件: With thiourea In N,N-dimethyl-formamide at 90℃;
- 参考文献: [1] Patent: WO2010/30811, 2010, A2. Location in patent: Page/Page column 92。