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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Carbon Dioxide | HCID 280 | — |
| 반응물 | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| 반응물 | Hexahydro-2,5-methanopentalene-3a(1H)-carboxylic acid | HCID 2733865 | — |
| 반응물 | 3-[1-(2-Pyrimidyl)-4-piperazinyl]propanol | HCID 14877868 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 생성물 | Hexahydro-2,5-methanopentalene-3a[1H]-carboxylic acid 3-[4-(2-pyrimidyl)-1-piperazinyl]propyl ester | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US04873331 |
|---|
| 출처 데이터셋 | uspto-grants-1989_10 |
|---|
| ORD ID | ord-e77e6fb2a7614f50947e60c25f65e231 |
|---|
| 출처 메모 | uspto-grants-1989_10 |
|---|