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HRID 1166012作成日:2026年10月25日

2-Fluoroethyl p-Toluenesulfonate → 1-Tert-butoxycarbonyl-4-(2-fluoroethyl)-3-oxopiperazine

https://huagongshe.com/reaction/1166012

反応式

関与物質

役割名称HCID仕込み量
反応物2-Fluoroethyl p-ToluenesulfonateHCID 256019—
反応物Tert-butyl 3-oxopiperazine-1-carboxylateHCID 3157178—
反応物Potassium tert-butoxideHCID 23665647—
溶媒DimethylformamideHCID 6228—
生成物1-Tert-butoxycarbonyl-4-(2-fluoroethyl)-3-oxopiperazineHCID 22716468—

反応手順

1-t-Butoxycarbonyl-3-oxopiperazine (21.6 g) is dissolved in dry DMF (500 ml) and potassium t-butoxide (24.2 g) is added. The mixture is stirred at 20-25° for 30 minutes, then 1-(4-methylphenylsulfonyloxy)-2-fluoroethane (J. Med. Chem., 23(9), 985-90 (1980), 25.9 g) is added and stirring continued at the same temperature for 24 hours. The solvent is removed and the residue partitioned between ethyl acetate and water. The organic phase is washed with water and concentrated. The residue is dissolved in isopropanol and diluted with iso-hexane forming a precipitate which is removed by filtration. The mixture is chromatographed (silica; eluting with a gradient increasing in polarity from 0 to 50% isopropanol in iso-hexane) to give 1-t-butoxycarbonyl-4-(2-fluoroethyl)-3-oxopiperazine.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06613349B2
出典データセットuspto-grants-2003_09
ORD IDord-621c5abe763045aeaa6ef457cf15fbb7
出典メモuspto-grants-2003_09