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HRID 1253271作成日:2026年10月25日

O-Xylene → 3-[4-[4-(2-Pyrimidinyl)-1-piperazinyl]butyl]-8,8-dimethyl-3-azabicyclo[3.2.1]octane-2,4-dione

https://huagongshe.com/reaction/1253271

反応式

関与物質

役割名称HCID仕込み量
反応物O-XyleneHCID 7237—
反応物4-(2-Pyrimidinyl)-1-piperazinebutanamineHCID 12840705—
反応物8,8-Dimethyl-3-oxabicyclo(3.2.1)octane-2,4-dioneHCID 19797203—
溶媒WaterHCID 962—
生成物3-[4-[4-(2-Pyrimidinyl)-1-piperazinyl]butyl]-8,8-dimethyl-3-azabicyclo[3.2.1]octane-2,4-dioneHCID 14097164—

反応手順

2,2-Dimethylcyclopentane-1,3-dicarboxylic anhydride (1.68 g., 10 mmole) and 1-(4-aminobutyl)-4-(2-pyrimidinyl)piperazine (2.55 g., 11 mmole) were combined in 500 ml. of xylene and refluxed for 48 hours with water removal via a Dean-Stark trap. The solvent was removed in vacuo and the residue column chromatographed on 100 g. of silica gel using a gradient elution from straight chloroform to 5% ethanol/chloroform. Concentration of the product in vacuum and recrystallization from isopropanol with addition of 4N isopropanolic HCl and acetone gave 600 mg. of the title compound as the dihydrochloride, monohydrate; m.p. 227°-229° C. (d).

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-8ddbe2487e454406bb2cccb7cc2b861b
出典メモuspto-grants-1988_05