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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 905746생성일: 2026년 10월 26일

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

반응식

참여 물질

역할이름HCID투입량
반응물N-(2-Aminoethyl)piperidineHCID 33944—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물2-carboxymethyl-4-methyl-1H-pyrrole-3-carboxylic acid ethyl esterHCID 49840328—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물4-methyl-2-[(2-piperidin-1-yl-ethyl carbamoyl)-methyl]-1H-pyrrole-3-carboxylic acid ethyl esterHCID 6661451585%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08012966B2
출처 데이터셋uspto-grants-2011_09
ORD IDord-7a886fb7eeda4224b377e749aead6f7f
출처 메모uspto-grants-2011_09