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HRID 248702作成日:2026年10月26日

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

https://huagongshe.com/reaction/248702

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium IodideHCID 4875—
反応物TriethylamineHCID 8471—
反応物Chloro-N,N-diethylacetamideHCID 16844—
反応物Benzoic acid, 3-[[2-[(acetylthio)methyl]-1-oxo-3-phenylpropyl]amino]-HCID 10215552—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物Diethylaminocarbonylmethyl 3-[(2-acetylthiomethyl-3-phenylpropionyl)amino]benzoateHCID 1567024874.9%

反応手順

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

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05210266
出典データセットuspto-grants-1993_05
ORD IDord-bd327e3a4f3a4b43ac7cc8bcd61a6a65
出典メモuspto-grants-1993_05