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HRID 230676作成日:2026年10月26日

N,N-Dimethylglycine → {4-[3-(trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazol-1-yl]phenyl}methanol

https://huagongshe.com/reaction/230676

反応式

関与物質

役割名称HCID仕込み量
反応物N,N-DimethylglycineHCID 673—
反応物Potassium CarbonateHCID 11430—
反応物4-Iodobenzyl alcoholHCID 29012—
反応物3-(Trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazoleHCID 2802863—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒Dimethyl SulfoxideHCID 679—
生成物{4-[3-(trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazol-1-yl]phenyl}methanolHCID 2482581086%

反応条件

温度130 °C

反応手順

A mixture of 4-iodobenzylalcohol (1.23 g, 5.25 mmol), 3-(trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazole (950 mg, 5 mmol), copper (I) iodide (10 mol %, 95 mg, 0.5 mmol), N,N-dimethylglycine (20 mol %, 103 mg, 1 mmol) and potassium carbonate (1.45 g, 10.5 mmol) in dimethylsulfoxide (30 ml) was stirred at 130° C. in an oil bath for 23 h. The reaction mix was cooled and partitioned between dichloromethane (30 ml) and brine (150 ml). The organic layer was removed filtered and the solvent removed under reduced pressure. The resulting product was purified by flash column chromatography on a Biotage 40+M column eluting from 0-60% ethyl acetate in pentane to give the title compound as a yellow oil (1.27 g, 86%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07566735B2
出典データセットuspto-grants-2009_07
ORD IDord-71647b96e3d44e71b10c96f979a56248
出典メモuspto-grants-2009_07