戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 19873作成日:2026年10月25日

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

https://huagongshe.com/reaction/19873

反応式

関与物質

役割名称HCID仕込み量
反応物2-Methoxypyrimidine-5-boronic acidHCID 2736778—
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-pyrimidin-5-yl)-1H-indol-2-yl]-methanoneHCID 16739593—

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-methoxy-5-pyrimidineboronic acid. The title compound was obtained in 9% yield as yellow oil. MS (m/e): 514.3 (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-e154e83fd07f47c2b0a97803028e276e
出典メモuspto-grants-2010_06