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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1865931생성일: 2026년 10월 27일

2-Chloro-1-(4-methylpiperazin-1-yl)ethanone → 1'-({6-Chloro-1-[2-(4-methylpiperazin-1-yl)-2-oxoethyl]-1H-indol-3-yl}carbonyl)-5-fluoro-3H-spiro[2-benzofuran-1,4'-piperidin]-3-one

https://huagongshe.com/reaction/1865931

반응식

참여 물질

역할이름HCID투입량
반응물2-Chloro-1-(4-methylpiperazin-1-yl)ethanoneHCID 818173—
반응물1'-[(6-chloro-1H-indol-3-yl)carbonyl]-5-fluoro-3H-spiro[2-benzofuran-1,4'-piperidin]-3-oneHCID 59657623—
생성물1'-({6-Chloro-1-[2-(4-methylpiperazin-1-yl)-2-oxoethyl]-1H-indol-3-yl}carbonyl)-5-fluoro-3H-spiro[2-benzofuran-1,4'-piperidin]-3-oneHCID 59657640—

반응 단계

Following the general procedure V as described hereinabove, the alkylation of 1′-[(6-chloro-1H-indol-3-yl)carbonyl]-5-fluoro-3H-spiro[2-benzofuran-1,4′-piperidin]-3-one (the preparation of which have been described in example 19) with commercially available 2-chloro-1-(4-methyl-piperazin-1-yl)-ethanone as electrophile, the title compound was obtained as a white solid. ES-MS m/e (%): 539.4 (M+H+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07629353B2
출처 데이터셋uspto-grants-2009_12
ORD IDord-97ee2c3eb90d4e7fbe7264697a4972ea
출처 메모uspto-grants-2009_12