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HRID 4922作成日:2026年10月24日

4-(2-Pyrimidinyl)-1-piperazinebutanamine → 3-(4-[4-(2-Pyrimidinyl)-1-piperazinyl]butyl)-3-azabicyclo[3.2.2]nonan-2,4-dione

https://huagongshe.com/ja/reaction/4922

反応式

関与物質

役割名称HCID仕込み量
反応物4-(2-Pyrimidinyl)-1-piperazinebutanamineHCID 12840705—
反応物3-Oxabicyclo[3.2.2]nonane-2,4-dioneHCID 14097169—
生成物3-(4-[4-(2-Pyrimidinyl)-1-piperazinyl]butyl)-3-azabicyclo[3.2.2]nonan-2,4-dioneHCID 197971978.7%

反応手順

An intimate mixture of 0.5 g (2.14 mmol) of 1-(4-aminobutyl)-4-(2-pyrimidinyl) piperazine and 0.22 g (1.42 mmol) of 3-oxabicyclo[3.2.2]nonan-2,4-dione was heated in an oil bath at 220°-230° C. for 15 minutes. An additional 0.22 g (1.42 mmol) of 3-oxabicyclo[3.2.2]nonan-2,4-dione was added. Heating in an oil bath at 220°-230° C. was continued for 15 minutes and then an additional 0.22 g (1.42 mmol) of 3-oxabicyclo[3.2.2]-nonan-2,4-dione was added. Heating was continued for 30 minutes at 220°-230° C. and then the reaction mixture was cooled. The resulting product was chromatographed on silica gel, eluting with dichloromethane/methanol (96:4 followed by 94:6), to give 46 mg of the title compound (6% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05242911
出典データセットuspto-grants-1993_09
ORD IDord-c7add3cb537741d8851d853240637af1
出典メモuspto-grants-1993_09