돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1373559생성일: 2026년 10월 25일

1-(2-Chloro-3-piperazin-1-yl-phenyl)-ethanone trifluoroacetate → 7-{4-[4-(3-Acetyl-2-chloro-phenyl)-piperazin-1-yl]-butoxy}-1H-[1,8]naphthyridin-2-one

https://huagongshe.com/reaction/1373559

반응식

참여 물질

역할이름HCID투입량
반응물1-(2-Chloro-3-piperazin-1-yl-phenyl)-ethanone trifluoroacetateHCID 21073138—
반응물4-(7-Oxo-7,8-dihydro-1,8-naphthyridin-2-yloxy)butanalHCID 21073380—
생성물7-{4-[4-(3-Acetyl-2-chloro-phenyl)-piperazin-1-yl]-butoxy}-1H-[1,8]naphthyridin-2-oneHCID 21073648—

반응 단계

In a manner similar to that of other examples above, 1-(2-chloro-3-piperazin-1-yl-phenyl)-ethanone trifluoroacetate was coupled by reductive amination to 4-(7-oxo-7,8-dihydro-[1,8]naphthyridin-2-yloxy)-butyraldehyde followed by typical workup and purification to give the title compound, mp 108–110° C. MS: APCI: M+1: 455.2 (Exact Mass: 454.18).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07160888B2
출처 데이터셋uspto-grants-2007_01
ORD IDord-f27b2e2cea7f42c49310decc16ac5fe2
출처 메모uspto-grants-2007_01