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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2351545생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/2351545

반응식

참여 물질

역할이름HCID투입량
반응물Carbon DioxideHCID 280—
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물Hexahydro-2,5-methanopentalene-3a(1H)-carboxylic acidHCID 2733865—
반응물3-[1-(2-Pyrimidyl)-4-piperazinyl]propanolHCID 14877868—
용매ChloroformHCID 6212—
생성물Hexahydro-2,5-methanopentalene-3a[1H]-carboxylic acid 3-[4-(2-pyrimidyl)-1-piperazinyl]propyl esterHCID 14877869—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04873331
출처 데이터셋uspto-grants-1989_10
ORD IDord-e77e6fb2a7614f50947e60c25f65e231
출처 메모uspto-grants-1989_10