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HRID 867713生成日期:2026年10月23日

聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯] → 3-(1-Methyl-4-piperidinyl)-1-[3-(trifluoromethyl)phenyl]-1H-indazole

https://huagongshe.com/zh-CN/reaction/867713

反应方程式

参与物

角色名称HCID投料
反应物聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯]HCID 962—
反应物氢化钠HCID 24758—
反应物3-氟三氟甲苯HCID 67867—
反应物HCID 178480237HCID 178480237—
溶剂N,N-二甲基甲酰胺HCID 6228—
产物3-(1-Methyl-4-piperidinyl)-1-[3-(trifluoromethyl)phenyl]-1H-indazoleHCID 1403258318%

反应条件

温度90 °C

反应步骤

To a stirred suspension of 4.9 g of a 50% oil dispersion of sodium hydride in 60 ml of dimethylformamide was added dropwise a solution a 10.0 g of 3-(1-methyl-4-piperidinyl)-1H-indazole in 80 ml of hot dimethylformamide. The reaction mixture was stirred for 1 hr and then 15.2 g of 3-fluorobenzotrifluoride was added. The reaction was heated at 90° C. for 22 hrs, cooled and poured into water. The aqueous mixture was extracted with ether. The ethereal extracts were dried over anhydrous magnesium sulfate and concentrated to give an oil. The oil was flash chromatographed (silica gel, diethylamine-ethyl acetate (1:9)). Evaporation of the appropriate fractions followed by recrystallization twice from hexane yielded 2.96 g (18%) of product, mp 103°-105° C.

来源与证据

DOI10.6084/m9.figshare.5104873.v1
专利号US04775761
来源数据集uspto-grants-1988_10
ORD IDord-fd13768195974e9cbd4fe79b1f53cd19
来源说明uspto-grants-1988_10