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HRID 248702생성일: 2026년 10월 24일

Potassium Iodide → Diethylaminocarbonylmethyl 3-[(2-acetylthiomethyl-3-phenylpropionyl)amino]benzoate

https://huagongshe.com/ko/reaction/248702

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물TriethylamineHCID 8471—
반응물Chloro-N,N-diethylacetamideHCID 16844—
반응물Benzoic acid, 3-[[2-[(acetylthio)methyl]-1-oxo-3-phenylpropyl]amino]-HCID 10215552—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물Diethylaminocarbonylmethyl 3-[(2-acetylthiomethyl-3-phenylpropionyl)amino]benzoateHCID 1567024874.9%

반응 단계

3-[(2-Acetylthiomethyl-3-phenylpropionyl)amino]-benzoic acid (compound of Example 68-(b)-[1]) (0.72 g) and potassium iodide (0.37 g) are dissolved in DMF, and thereto are added triethylamine (0.2 g) and 2-chloro-N,N-diethylacetamide (0.33 g) with stirring at room temperature, and the mixture is reacted three nights. The reaction mixture is mixed with water and extracted with ethyl acetate. The extract is washed with water, dried over anhydrous magnesium sulfate, and ethyl acetate is distilled off under reduced pressure. The residue is purified by a medium pressure column chromatography using silica gel (eluant, chloroform). The fractions containing the desired compound are collected, and chloroform is distilled off under reduced pressure to give the title compound (0.71 g). m.p.: 143°-144° C. (amorphous) IR (KBr; cm-1): 1725, 1690, 1635

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05210266
출처 데이터셋uspto-grants-1993_05
ORD IDord-bd327e3a4f3a4b43ac7cc8bcd61a6a65
출처 메모uspto-grants-1993_05