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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2089278생성일: 2026년 10월 27일

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → N-[3-Amino-2-hydroxy-3-oxo-1-(phenylmethyl)propyl]-2-(4-phenyl-1H-imidazol-1-yl)pyridine-3-carboxamide

https://huagongshe.com/reaction/2089278

반응식

참여 물질

역할이름HCID투입량
반응물1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
반응물Sodium BicarbonateHCID 516892—
반응물3-Amino-2-hydroxy-4-phenylbutanamide hydrochlorideHCID 22593883—
반응물2-(4-phenyl-1H-imidazol-1-yl)pyridine-3-carboxylic acidHCID 66720089—
반응물HCID 178418300HCID 178418300—
용매DichloromethaneHCID 6344—
용매TriethylamineHCID 8471—
생성물N-[3-Amino-2-hydroxy-3-oxo-1-(phenylmethyl)propyl]-2-(4-phenyl-1H-imidazol-1-yl)pyridine-3-carboxamideHCID 6672008237.3%

반응 조건

온도2 °C

반응 단계

0.75 g of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC), 0.51 g of hydroxylbenzotriazole (HOBt) and 0.55 ml of triethylamine (Et3N) were successively added to a solution of 1.0 g of 2-(4-phenyl-1H-imidazol-1-yl)pyridine-3-carboxylic acid (3.77 mmol) in 50 ml of dichloromethane at 0-4° C., and the mixture was stirred at 0-4° C. for 1 hour. 0.9 g of 3-amino-2-hydroxy-4-phenylbutanamide hydrochloride (3.9 mmol) and 0.55 ml of Et3N were then added and, after about 5 minutes, a pH of 8-9 was adjusted by adding 0.5 ml of Et3N. The mixture was stirred at 0-4° C. for 1 hour and then at room temperature overnight. 50 ml of saturated NaHCO3 solution were then added to the mixture, and the organic phase was separated off. Drying and evaporating the solvent resulted in 620 mg of a reddish oil, which was reacted further immediately without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08436034B2
출처 데이터셋uspto-grants-2013_05
ORD IDord-949239e502294078944066e64d5ff91f
출처 메모uspto-grants-2013_05