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HRID 1172697作成日:2026年10月27日

Water → 2,5-Difluoro-4-{1-[4-methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-yl]-propoxy}-benzonitrile

https://huagongshe.com/reaction/1172697

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物2,4,5-TrifluorobenzonitrileHCID 593813—
反応物1-[4-Methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-yl]-propan-1-olHCID 23549129—
反応物Potassium tert-butoxideHCID 23665647—
溶媒tert-ButanolHCID 6386—
溶媒TetrahydrofuranHCID 8028—
生成物2,5-Difluoro-4-{1-[4-methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-yl]-propoxy}-benzonitrileHCID 5955630995.5%

反応条件

温度5 °C

反応手順

To a solution of 900 mg of 1-[4-methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-yl]-propan-1-ol in 2 mL of tetrahydrofuran at 5° C. was slowly added 3.3 mL of a molar solution of potassium tert-butoxide in tert-butanol. After stirring at 5° C. for 30 minutes, the resulting solution was slowly added to a solution of 469 mg of 2,4,5-trifluoro-benzonitrile in 2 mL of tetrahydrofuran at −60° C. The resulting mixture was stirred for 1 h at −60° C. then stirred overnight allowing the temperature to warm up to room temperature. It was then poured into water and extracted with dichloromethane. The organic extracts were dried over magnesium sulfate, filtered and concentrated under reduced pressure. The crude product was purified by column chromatography on silica gel (gradient from heptane 100 to heptane 80/ethyl acetate 20) to give 1.25 g of 2,5-difluoro-4-{1-[4-methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-yl]-propoxy}-benzonitrile.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07834030B2
出典データセットuspto-grants-2010_11
ORD IDord-640d9a37120e4412a9ff258c71214264
出典メモuspto-grants-2010_11