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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2055455생성일: 2026년 10월 26일

1-[2-(3,4-Dimethoxyphenyl)ethyl]-5-methoxy-2-methylindole-3-carboxylic acid → 1'-({1-[2-(3,4-Dimethoxyphenyl)ethyl]-5-methoxy-2-methyl-1H-indol-3-yl}carbonyl)-3H-spiro[2-benzofuran-1,4'-piperidin]-3-one

https://huagongshe.com/reaction/2055455

반응식

참여 물질

역할이름HCID투입량
반응물1-[2-(3,4-Dimethoxyphenyl)ethyl]-5-methoxy-2-methylindole-3-carboxylic acidHCID 1082708—
반응물3H-spiro(isobenzofuran-1,4'-piperidin)-3-oneHCID 9834255—
생성물1'-({1-[2-(3,4-Dimethoxyphenyl)ethyl]-5-methoxy-2-methyl-1H-indol-3-yl}carbonyl)-3H-spiro[2-benzofuran-1,4'-piperidin]-3-oneHCID 59657585—

반응 단계

Following the general procedure I as described above, the acylation of 3H-spiro[2-benzofuran-1,4′-piperidin]-3-one prepared as described in example 16 above, with commercially available 1-[2-(3,4-dimethoxy-phenyl)-ethyl]-5-methoxy-2-methyl-1H-indole-3-carboxylic acid, gave the title compound. ES-MS m/e (%): 555.3 (M+H+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07332501B2
출처 데이터셋uspto-grants-2008_02
ORD IDord-8663f155d2384bb2a3672d735a97f4e9
출처 메모uspto-grants-2008_02