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HRID 1646309생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1646309

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05179125
출처 데이터셋uspto-grants-1993_01
ORD IDord-13810f6da6f741fa8735a5e65e237175
출처 메모uspto-grants-1993_01