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HRID 2389Erstellt: 23. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPermanganateHCID 24401—
EduktPotassium PermanganateHCID 516875—
Edukt(S)-2-(isopropylsulfinyl)-amino-3-methyl-butyric acid N-[2-(3,4-dimethoxyphenyl)-ethyl]-amideHCID 67569267—
LösungsmittelAcetoneHCID 180—
Produkt(S)-2(isopropylsulfonyl)-amino-3-methyl-butyric acid-N-[2-(3,4-dimethoxyphenyl)-ethyl]-amideHCID 67569348—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05728875
Quelldatensatzuspto-grants-1998_03
ORD IDord-4b5f4cb68ad14383914fad9f4aa70cd0
Quellennotizuspto-grants-1998_03