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HRID 504640作成日:2026年10月25日

1-Hydroxybenzotriazole → N-[(1-benzyl-4-hydroxypiperidin-4-yl)methyl]-7-[methyl(2-thienylsulfonyl)amino]-1H-indole-2-carboxamide

https://huagongshe.com/reaction/504640

反応式

関与物質

役割名称HCID仕込み量
反応物1-HydroxybenzotriazoleHCID 75771—
反応物Sodium BicarbonateHCID 516892—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物4-(Aminomethyl)-1-benzylpiperidin-4-olHCID 10421026—
反応物7-[methyl(2-thienylsulfonyl)amino]-1H-indole-2-carboxylic acidHCID 57475951—
溶媒DimethylformamideHCID 6228—
生成物N-[(1-benzyl-4-hydroxypiperidin-4-yl)methyl]-7-[methyl(2-thienylsulfonyl)amino]-1H-indole-2-carboxamideHCID 5913600476%

反応手順

To a solution of 7-[methyl(2-thienylsulfonyl)amino]-1H-indole-2-carboxylic acid in N,N-dimethylformamide (30 ml) were added 1H-1,2,3-benzotriazol-1-ol (0.738 g), N-[3-(dimethylamino)propyl]-N′-ethylcarbodiimide hydrochloride (0.520 g) and 4-(aminomethyl)-1-benzylpiperidin-4-ol (1.06 g), and the mixture was stirred at room temperature for 24 hr. Saturated aqueous sodium hydrogencarbonate solution was added to the reaction solution, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:methanol=100:0-95:5) to give the title compound (1.32 g, yield 76%) as a colorless amorphous solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07777047B2
出典データセットuspto-grants-2010_08
ORD IDord-cdf9c2263ae24249a935248ee59ee951
出典メモuspto-grants-2010_08