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HRID 2389作成日:2026年10月23日

Permanganate → (S)-2(isopropylsulfonyl)-amino-3-methyl-butyric acid-N-[2-(3,4-dimethoxyphenyl)-ethyl]-amide

https://huagongshe.com/ja/reaction/2389

反応式

関与物質

役割名称HCID仕込み量
反応物PermanganateHCID 24401—
反応物Potassium PermanganateHCID 516875—
反応物(S)-2-(isopropylsulfinyl)-amino-3-methyl-butyric acid N-[2-(3,4-dimethoxyphenyl)-ethyl]-amideHCID 67569267—
溶媒AcetoneHCID 180—
生成物(S)-2(isopropylsulfonyl)-amino-3-methyl-butyric acid-N-[2-(3,4-dimethoxyphenyl)-ethyl]-amideHCID 67569348—

反応手順

3.7 g of (S)-2-(isopropylsulfinyl)-amino-3-methyl-butyric acid N-[2-(3,4-dimethoxyphenyl)-ethyl]-amide (Example 3.90) are dissolved in 50 ml of acetone at room temperature. An acetone solution saturated with potassium permanganate is added dropwise to this stirred solution until the reaction mixture retains the violet colour of the permanganate; the reaction mixture is then stirred at room temperature for 45 minutes. The resulting manganese dioxide is removed by filtration over Celite. The filtrate is evaporated to dryness and the resulting residue is dissolved in 500 ml of methyl acetate. This organic phase is washed once with 200 ml of water, dried over sodium sulfate and concentrated. The resulting residue is chromatographed over silica gel with a mixture of one part of methyl acetate and one part of n-hexane. (S)-2-(isopropylsulfonyl)-amino-3-methyl-butyric acid N-[2-(3,4-dimethoxyphenyl)-ethyl]-amide, which can be further purified by recrystallization from methyl acetate/n-hexane, is obtained, melting point 86°-87° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05728875
出典データセットuspto-grants-1998_03
ORD IDord-4b5f4cb68ad14383914fad9f4aa70cd0
出典メモuspto-grants-1998_03