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HRID 19852作成日:2026年10月25日

2-Methoxyphenylboronic acid → (4,4-Difluoro-piperidin-1-yl)-[5-(1-isopropyl-piperidin-4-yloxy)-1-(2-methoxy-phenyl)-1H-indol-2-yl]-methanone

https://huagongshe.com/reaction/19852

反応式

関与物質

役割名称HCID仕込み量
反応物2-Methoxyphenylboronic acidHCID 2733958—
反応物(4,4-Difluoropiperidin-1-yl)[5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]methanoneHCID 11603838—
生成物(4,4-Difluoro-piperidin-1-yl)-[5-(1-isopropyl-piperidin-4-yloxy)-1-(2-methoxy-phenyl)-1H-indol-2-yl]-methanoneHCID 16739442—

反応手順

In analogy to the procedure described for the synthesis of example 6, the title compound was synthesized from (4,4-difluoro-piperidin-1-yl)-[5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-methanone (intermediate 1) and 2-methoxyphenylboronic acid. The title compound was obtained in 7% yield as yellow oil. MS (m/e): 512.3 (MH+, 100%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07745479B2
出典データセットuspto-grants-2010_06
ORD IDord-cff77b2c6d6e4f489cad09671e734fa1
出典メモuspto-grants-2010_06