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HRID 28397作成日:2026年10月24日

4-Carboxyphenylboronic Acid → 4-({4-[(5-chloro-1H-indol-2-yl)sulphonyl]piperazin-1-yl}carbonyl)phenyl boronic acid

https://huagongshe.com/ja/reaction/28397

反応式

関与物質

役割名称HCID仕込み量
反応物4-Carboxyphenylboronic AcidHCID 312183—
反応物O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
反応物5-chloro-2-(piperazine-1-sulfonyl)-1H-indoleHCID 22710571—
溶媒DimethylformamideHCID 6228—
生成物4-({4-[(5-chloro-1H-indol-2-yl)sulphonyl]piperazin-1-yl}carbonyl)phenyl boronic acidHCID 6930738956%

反応手順

5-Chloro-2-(piperazin-1-ylsulphonyl)-1H-indole (5.42 g, 18.1 mmol) was added to a solution of 4-carboxyphenyl boronic acid (3.00 g, 18.1 mmol) N,N-diisopropylethylamine (2.34 g, 18.1 mmol) and O-(benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium tetrafluoroborate (5.81 g, 18.1 mmol) in 80 mL N,N-dimethylformamide, the mixture was stirred for 2 hours at room temperature. N,N-Dimethylformamide was removed in vacuo and the crude was purified by flash chromatography three times (dichloromethane/methanol, 100-98/2) to give 4-({4-[(5-chloro-1H-indol-2-yl)sulphonyl]piperazin-1-yl}carbonyl)phenyl boronic acid as a colourless solid (56% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07419979B2
出典データセットuspto-grants-2008_09
ORD IDord-4b86f7cb244e4996a5c483f75e27e621
出典メモuspto-grants-2008_09