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HRID 585065作成日:2026年10月25日

Diisopropylethylamine → 3-(4-{[3-(3-Fluorophenyl)(1,2,4-oxadiazol-5-yl)]methyl}piperazinyl)-1-(2-methylbenzothiazol-5-yloxy)propan-2-ol

https://huagongshe.com/reaction/585065

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物5-(Chloromethyl)-3-(3-fluorophenyl)-1,2,4-oxadiazoleHCID 16736248—
反応物1-(2-Methylbenzothiazol-5-yloxy)-3-piperazin-1-ylpropan-2-olHCID 21911691—
溶媒EthanolHCID 702—
生成物3-(4-{[3-(3-Fluorophenyl)(1,2,4-oxadiazol-5-yl)]methyl}piperazinyl)-1-(2-methylbenzothiazol-5-yloxy)propan-2-olHCID 22064207—

反応条件

温度90 °C

反応手順

To 5-(chloromethyl)-3-(3-fluorophenyl)-1,2,4-oxadiazole (300 mg, 1.41 mmol) and 1-(2-methylbenzothiazol-5-yloxy)-3-piperazine-1-yl-propan-2-ol, a compound of formula (6) (291 mg, 0.94 mmol) in EtOH (20 mL, anhydrous) was added diisopropylethylamine (0.329 m, 1.89 mmol), and the reaction was shaken on a J-Kem™ block overnight at 90° C. Upon cooling to room temperature, the solution was concentrated to an oil and purified on an Isco™ Combi Flash Si 10X, using Redi Sep columns (10 g), eluting with ethyl acetate, then gradient to 4:1 ethyl acetate/methanol, to yield 3-(4-{[3-(3-fluorophenyl)(1,2,4-oxadiazol-5-yl)]methyl}piperazinyl)-1-(2-methylbenzothiazol-5-yloxy)propan-2-ol, a compound of Formula I, (136 mg, 30%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06930111B2
出典データセットuspto-grants-2005_08
ORD IDord-107f667267564e1cad1bdc3f4907e1ef
出典メモuspto-grants-2005_08