【结 构 式】 |
【分子编号】12663 【品名】1-Chloro-3-(2-fluoro[1,1'-biphenyl]-4-yl)-2-butanone 【CA登记号】 |
【 分 子 式 】C16H14ClFO 【 分 子 量 】276.7376632 【元素组成】C 69.44% H 5.1% Cl 12.81% F 6.87% O 5.78% |
与该中间体有关的原料药合成路线共 1 条
合成路线1
该中间体在本合成路线中的序号:(III)The reaction of 2-(2-fluorobiphenyl-4-yl)propionic acid (I) with thionyl chloride followed by treatment with tris (trimethylsilyloxy)ethylene gives 3-(2-fluorobiphenyl-4-yl)-1-hydroxy-2-butanone (II), which upon treatment with carbon tetrachloride and triphenylphosphine affords 1-chloro-3-(2-fluorobiphenyl-4-yl)-2-butanone (III). Finally, compound (III) is heated with N-methylthiourea in water.
【1】 Ozato, Y.; Tamura, N.; Masumori, H.; Yamamoto, M.; Kojima, A.; Nishikakau, F.; Kimura, Y. (Sumitomo Pharmaceuticals Co., Ltd.); Aminazole derivatives and their production and use. EP 0248399; JP 1988152368; JP 1993247014; US 4914112; US 5066666; US 5180731 . |
【2】 Prous, J.; Castaner, J.; Graul, A.; SM-8849. Drugs Fut 1994, 19, 4, 347. |
Extended Information