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HRID 1865955作成日:2026年10月25日

3-Fluorobenzoyl chloride → 5-Bromo-1'-{[6-chloro-1-(3-fluorobenzoyl)-1H-indol-3-yl]carbonyl}-3H-spiro[2-benzofuran-1,4'-piperidin]-3-one

https://huagongshe.com/reaction/1865955

反応式

関与物質

役割名称HCID仕込み量
反応物3-Fluorobenzoyl chlorideHCID 74376—
反応物5-bromo-1'-[(6-chloro-1H-indol-3-yl)carbonyl]-3H-spiro[2-benzofuran-1,4'-piperidin]-3-oneHCID 59657619—
生成物5-Bromo-1'-{[6-chloro-1-(3-fluorobenzoyl)-1H-indol-3-yl]carbonyl}-3H-spiro[2-benzofuran-1,4'-piperidin]-3-oneHCID 59657651—

反応手順

Following the general procedure VII as described above, the acylation of 5-bromo-1′-[(6-chloro-1H-indol-3-yl)carbonyl]-3H-spiro[2-benzofuran-1,4′-piperidin]-3-one with commercially available 3-fluorobenzoyl chloride gave the title compound. ES-MS m/e (%): 581.2 (M+H+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07629353B2
出典データセットuspto-grants-2009_12
ORD IDord-7389883b67ed4b269990ee85e7d8a492
出典メモuspto-grants-2009_12