戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2351545作成日:2026年10月27日

Carbon Dioxide → Hexahydro-2,5-methanopentalene-3a[1H]-carboxylic acid 3-[4-(2-pyrimidyl)-1-piperazinyl]propyl ester

https://huagongshe.com/reaction/2351545

反応式

関与物質

役割名称HCID仕込み量
反応物Carbon DioxideHCID 280—
反応物1,1'-CarbonyldiimidazoleHCID 68263—
反応物Hexahydro-2,5-methanopentalene-3a(1H)-carboxylic acidHCID 2733865—
反応物3-[1-(2-Pyrimidyl)-4-piperazinyl]propanolHCID 14877868—
溶媒ChloroformHCID 6212—
生成物Hexahydro-2,5-methanopentalene-3a[1H]-carboxylic acid 3-[4-(2-pyrimidyl)-1-piperazinyl]propyl esterHCID 14877869—

反応手順

To stirred solution of hexahydro-2,5-methanopentalene-3a[1H]-carboxylic acid (0.6 g, 3.6×10-3 mol) in 25 ml of chloroform under a dry nitrogen atmosphere was added carbonyldiimidazole (0.58 g, 3.6×10-3 mol). The resulting solution was stirred at ambient temperature for three hours, during which time a gas (CO2) was evolved. A solution of 3-[1-(2-pyrimidyl)-4-piperazinyl]propanol (0.80 g, 3.6×10-3 mol) in 25 ml of chloroform was then added, and the resulting reaction mixture was stirred under nitrogen at ambient temperature for two days. The mixture was diluted to 150 ml with chloroform, washed with three-one hundred ml portions of water, dried over anhydrous sodium sulfate, and concentrated on a rotary evaporator. The desired product (TLC on silica using a 30% methanol in ethyl acetate solvent system, Rf=0.48) was isolated by gravity chromatography on silica gel and converted to the hydrochloride salt with isopropanolic HCl (0.79 g, 51% yield), mp.=231°-232° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04873331
出典データセットuspto-grants-1989_10
ORD IDord-e77e6fb2a7614f50947e60c25f65e231
出典メモuspto-grants-1989_10