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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 22354생성일: 2026년 10월 25일

Potassium Bicarbonate → 2,3-dihydro-7-methoxy-8-{3-[4-(2-pyrimidinyl)-1-piperazinyl]propoxy}cyclopenta[c][1]benzopyran-4(1H)-one

https://huagongshe.com/reaction/22354

반응식

참여 물질

역할이름HCID투입량
반응물Potassium BicarbonateHCID 516893—
반응물FumarateHCID 5460307—
반응물2-Piperazinylpyrimidine dihydrochlorideHCID 11680272—
반응물8-(3-chloropropoxy)-2,3-dihydro-7-methoxycyclopenta[c][1]benzopyran-4(1H)-oneHCID 19927690—
용매AcetoneHCID 180—
용매EthanolHCID 702—
용매ChloroformHCID 6212—
생성물2,3-dihydro-7-methoxy-8-{3-[4-(2-pyrimidinyl)-1-piperazinyl]propoxy}cyclopenta[c][1]benzopyran-4(1H)-oneHCID 1992772954%

반응 단계

Method B (60 h at 50° C.; 4 equivalents of potassium hydrogencarbonate); starting materials: 8-(3-chloropropoxy)-2,3-dihydro-7-methoxy-cyclopenta[c][1]benzopyran-4(1H)-one (example 83) and 1-(2-pyrimidinyl)piperazine dihydrochloride; yield 54%; fusion point 184°-186° C. (from chloroform and ethanol). Fumarate: method E; yield 77%; fusion point 226°-228° C. (from acetone).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05428038
출처 데이터셋uspto-grants-1995_06
ORD IDord-29ae1e67f57a4e9cbf6cce38fbf412f8
출처 메모uspto-grants-1995_06