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HRID 606269作成日:2026年10月26日

Acetonitrile → 5-[4-(2-(2-Fluorophenyl)acetyl]piperidino]methyl-2,4-dihydro-[1,2,4]triazol-3-one

https://huagongshe.com/reaction/606269

反応式

関与物質

役割名称HCID仕込み量
反応物AcetonitrileHCID 6342—
反応物Potassium CarbonateHCID 11430—
反応物2-(2-Fluorophenyl)-1-(piperidin-4-yl)ethanone hydrochlorideHCID 22248124—
反応物3H-1,2,4-Triazol-3-one, 5-(chloromethyl)-1,2-dihydro-HCID 135546685—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物5-[4-(2-(2-Fluorophenyl)acetyl]piperidino]methyl-2,4-dihydro-[1,2,4]triazol-3-oneHCID 1355930127%

反応手順

After adding 150 mg of 5-chloromethyl-2,4-dihydro-[1,2,4]triazol-3-one, 335 mg of 2-(2-fluorophenyl)-1-(piperidin-4-yl)ethanone hydrochloride and 180 mg of anhydrous potassium carbonate to acetonitrile, the mixture was stirred overnight at room temperature. Water was added to the reaction mixture and extraction was performed with ethyl acetate. The organic layer was washed with water and saturated brine and dried over anhydrous magnesium sulfate, and then the solvent was distilled off under reduced pressure. Diethyl ether was added to the residue and the mixture was filtered to obtain the title compound (23 mg, 7% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07915274B2
出典データセットuspto-grants-2011_03
ORD IDord-5cb4b923a59642c3aff4bf2140455a60
出典メモuspto-grants-2011_03