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HRID 344382作成日:2026年10月27日

Potassium Carbonate → 4-amino-5-chloro-N-(1-(6-(2,3-dihydro-1,3-dioxo-1H-isoindol-2-yl)hexyl)-piperidin-4-ylmethyl)-2-methoxybenzamide

https://huagongshe.com/reaction/344382

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物6-BromohexylphthalimideHCID 21930853—
反応物4-Amino-5-chloro-2-methoxy-N-(piperidin-4-ylmethyl)benzamide hydrochlorideHCID 66780941—
溶媒DimethylformamideHCID 6228—
生成物4-amino-5-chloro-N-(1-(6-(2,3-dihydro-1,3-dioxo-1H-isoindol-2-yl)hexyl)-piperidin-4-ylmethyl)-2-methoxybenzamideHCID 5452067662.7%

反応条件

温度70 °C

反応手順

4-Amino-5-chloro-2-methoxy-N-(piperidin-4-ylmethyl)benzamide hydrochloride (8.5 g) was dissolved in dimethylformamide (100 ml). Potassium carbonate (10.5 g) and 6-bromohexylphthalimide (7.2 g) were added, and the mixture was stirred at 70° C. for 16 hr. The reaction mixture was concentrated under reduced pressure and the residue was extracted with ethyl acetate. The extract was dried over magnesium sulfate and concentrated under reduced pressure. The obtained residue was purified by silica gel chromatography to give 4.2 g of 4-amino-5-chloro-N-(1-(6-(2,3-dihydro-1,3-dioxo-1H-isoindol-2-yl)hexyl)-piperidin-4-ylmethyl)-2-methoxybenzamide.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05864039
出典データセットuspto-grants-1999_01
ORD IDord-b0302d1f48d04f79a5fc161d508661df
出典メモuspto-grants-1999_01