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HRID 1253264作成日:2026年10月27日

Dichloromethane → 3-[4-[4-(3-Chlorophenyl)-1-piperazinyl]butyl]-3-azabicyclo[3.2.1]octane-2,4-dione

https://huagongshe.com/reaction/1253264

反応式

関与物質

役割名称HCID仕込み量
反応物DichloromethaneHCID 6344—
反応物O-XyleneHCID 7237—
反応物1,3-Cyclopentanedicarboxylic anhydrideHCID 239799—
反応物4-[4-(3-Chlorophenyl)piperazin-1-yl]butan-1-amineHCID 12840704—
溶媒WaterHCID 962—
生成物3-[4-[4-(3-Chlorophenyl)-1-piperazinyl]butyl]-3-azabicyclo[3.2.1]octane-2,4-dioneHCID 14156369—

反応手順

1,3-Cyclopentane dicarboxylic anhydride (2.2 g., 15 mmole) and 4.0 g. (15 mmole) of 1-(4-aminobutyl)-4-(3-chlorophenyl)piperazine were combined in 300 ml. of methylene chloride and stirred for 30 minutes at room temperature. The solvent was replaced with xylene and the mixture was refluxed for 48 hours with water removal via a Dean-Stark trap. The solvent was removed in vacuum and the residue filtered through 75 g. of silica gel with 2% ethanol/chloroform as eluent. The product was concentrated in vacuum and crystallized from 50 ml. of isopropanol with addition of 4N isopropanolic HCl. Recrystallization from ethanol gave 1.6 g. of the title compound as the hydrochloride, quarter hydrate; m.p. 199°-202° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04748240
出典データセットuspto-grants-1988_05
ORD IDord-0414f49d39d6428e8394f535d7f0ce73
出典メモuspto-grants-1988_05