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HRID 905746作成日:2026年10月25日

N-(2-Aminoethyl)piperidine → 4-methyl-2-[(2-piperidin-1-yl-ethyl carbamoyl)-methyl]-1H-pyrrole-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/905746

反応式

関与物質

役割名称HCID仕込み量
反応物N-(2-Aminoethyl)piperidineHCID 33944—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物2-carboxymethyl-4-methyl-1H-pyrrole-3-carboxylic acid ethyl esterHCID 49840328—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物4-methyl-2-[(2-piperidin-1-yl-ethyl carbamoyl)-methyl]-1H-pyrrole-3-carboxylic acid ethyl esterHCID 6661451585%

反応手順

A stirred solution of 2-carboxymethyl-4-methyl-1H-pyrrole-3-carboxylic acid ethyl ester (2.67 g, 12.67 mmol) in N,N-dimethylformamide (6.5 ml) and dichloromethane (65 ml) was added with 2-piperidin-1-yl-ethylamine (1.78 g, 13.9 mmol), N-ethyl-N′-(dimethylaminopropyl)-carbodiimide hydrochloride (4.84 g, 25.34 mmol) and 1-hydroxybenzotriazol (1.71 g, 12.67 mmol) in an ice/water-bath. Upon completion of the addition, the reaction mixture was stirred at room temperature overnight, then added with cold water (50 ml), and extracted with dichloromethane (50 ml×3). The combined organic extracts were washed with saturated sodium bicarbonate (50 ml), water (50 ml), brine (50 ml), dried with anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give 4-methyl-2-[(2-piperidin-1-yl-ethyl carbamoyl)-methyl]-1H-pyrrole-3-carboxylic acid ethyl ester (3.46 g, 85%) as a brown oil which was used as such.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08012966B2
出典データセットuspto-grants-2011_09
ORD IDord-7a886fb7eeda4224b377e749aead6f7f
出典メモuspto-grants-2011_09