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HRID 915384作成日:2026年10月27日

Potassium Iodide → [6-[5-(4-Trifluoromethyl-phenyl)-1H-pyrazol-3-ylmethoxy]-indol-1-yl]-acetic acid tert-butyl ester

https://huagongshe.com/reaction/915384

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium IodideHCID 4875—
反応物Cesium carbonateHCID 10796—
反応物tert-Butyl (6-hydroxy-1H-indol-1-yl)acetateHCID 69283069—
反応物3-Chloromethyl-5-(4-trifluoromethyl-phenyl)-1H-pyrazoleHCID 178506111—
溶媒DimethylformamideHCID 6228—
生成物[6-[5-(4-Trifluoromethyl-phenyl)-1H-pyrazol-3-ylmethoxy]-indol-1-yl]-acetic acid tert-butyl esterHCID 1784512037%

反応条件

温度80 °C

反応手順

A mixture of (6-hydroxy-indol-1-yl)-acetic acid tert-butyl ester (37 mg, 0.15 mmol), 3-chloromethyl-5-(4-trifluoromethyl-phenyl)-1H-pyrazole (43 mg, 0.16 mmol), cesium carbonate (54 mg, 0.16 mmol) and a trace of potassium iodide were suspended in N,N-dimethylformamide (4 ml). The suspension was stirred at ambient temperature for 14 h and for 4 h at 80° C. The solvent was evaporated under reduced pressure and the residue dissolved in 1 N HCl/ice water 1/1 and ethyl acetate. The layers were separated and the aqueous layer was extracted two times with ethyl acetate. The combined organic layers were washed two times with brine and dried over sodium sulfate. The solvent was removed under reduced pressure and the residue purified by column chromatography (silica gel, heptane/AcOEt) to give 5 mg (10 μmol, 7%) of the title compound as orange oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07265149B2
出典データセットuspto-grants-2007_09
ORD IDord-9ed5a382e2e74487b457e32e74dee025
出典メモuspto-grants-2007_09