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HRID 2055455作成日:2026年10月27日

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

反応式

関与物質

役割名称HCID仕込み量
反応物1-[2-(3,4-Dimethoxyphenyl)ethyl]-5-methoxy-2-methylindole-3-carboxylic acidHCID 1082708—
反応物3H-spiro(isobenzofuran-1,4'-piperidin)-3-oneHCID 9834255—
生成物1'-({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—

反応手順

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+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07332501B2
出典データセットuspto-grants-2008_02
ORD IDord-8663f155d2384bb2a3672d735a97f4e9
出典メモuspto-grants-2008_02