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HRID 19871作成日:2026年10月25日

4-Cyanophenylboronic acid → 4-[5-(1-Isopropyl-piperidin-4-yloxy)-2-(morpholine-4-carbonyl)-indol-1-yl]-benzonitrile

https://huagongshe.com/reaction/19871

反応式

関与物質

役割名称HCID仕込み量
反応物4-Cyanophenylboronic acidHCID 2734326—
反応物(5-(1-isopropylpiperidin-4-yloxy)-1H-indol-2-yl)(morpholino)methanoneHCID 11717680—
生成物4-[5-(1-Isopropyl-piperidin-4-yloxy)-2-(morpholine-4-carbonyl)-indol-1-yl]-benzonitrileHCID 16739591—

反応手順

In analogy to the procedure described for the synthesis of example 6, the title compound was synthesized from [5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-morpholin-4-yl-methanone (intermediate 2) and 4-cyanophenylboronic acid. The title compound was obtained in 31% yield as yellow foam. MS (m/e): 473.2 (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-80ac577fc94c432c9e5c0805a6d801e4
出典メモuspto-grants-2010_06