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HRID 53066Erstellt: 25. Oktober 2026

Trifluoroacetic acid → (2S)-2-amino-3-methyl-butyric acid [11beta,17,21-trihydroxy-3,20-dioxo-pregn-4-en-21-yl] ester trifluoroacetate

https://huagongshe.com/reaction/53066

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrifluoroacetic acidHCID 6422—
Edukt(2S)-2-((1,1-dimethylethoxycarbonyl)-amino)-3-methylbutyric acid [11beta,17,21-trihydroxy-3,20-dioxo-pregn-4-en-21-yl] esterHCID 86750657—
Produkt(2S)-2-amino-3-methyl-butyric acid [11beta,17,21-trihydroxy-3,20-dioxo-pregn-4-en-21-yl] ester trifluoroacetateHCID 8675065876%

Reaktionsschritte

500 mg (0.89 mmol) of (2S)-2-((1,1-dimethylethoxycarbonyl) -amino)-3-methyl-butyric acid [11β,17,21-trihydroxy-3,20-dioxo -pregn-4-en-21-yl] ester (Example 27) is mixed with 1 ml of trifluoroacetic acid and stirred for 10 minutes at room temperature. Then, the trifluoroacetic acid is evaporated in a vacuum. The residue is mixed with stirring with a little diethyl ether, the white precipitate that is produced is suctioned off and dried. 385 mg (76%) of (2S)-2-amino-3-methyl-butyric acid [11β,17,21-trihydroxy-3,20-dioxo-pregn-4-en-21-yl] ester trifluoroacetate is obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05616573
Quelldatensatzuspto-grants-1997_04
ORD IDord-47a2d8e4b8b645a482a9b6f8488878c1
Quellennotizuspto-grants-1997_04