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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 22352생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/22352

반응식

참여 물질

역할이름HCID투입량
반응물1-(4-Nitrophenyl)piperazineHCID 80447—
반응물FumarateHCID 5460307—
반응물8-(3-chloropropoxy)-2,3-dihydro-7-methoxycyclopenta[c][1]benzopyran-4(1H)-oneHCID 19927690—
용매AcetoneHCID 180—
생성물2,3-dihydro-7-methoxy-8-{3-[4-(4-nitrophenyl)-1-piperazinyl]propoxy}cyclopenta[c][1]benzopyran-4(1H)-oneHCID 1992766843%

반응 단계

Method B (60 h at 50° C.); starting materials: 8-(3-chloropropoxy)-2,3-dihydro-7-methoxy-cyclopenta[c][1]benzopyran-4(1H)-one (example 83) and 1-(4-nitrophenyl)piperazine; yield 43%; fusion point 226°-228° C. (decomposes; from acetone). Fumarate: method E; yield 92%; fusion point 216° C. (decomposes; from acetone).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05428038
출처 데이터셋uspto-grants-1995_06
ORD IDord-4fbeac3717a44a1b98fa1cdb5f7bd5dd
출처 메모uspto-grants-1995_06