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HRID 53065Erstellt: 26. Oktober 2026

Cortisol → (2S)-2-((1,1-dimethylethoxycarbonyl)-amino)-3-methylbutyric acid [11beta,17,21-trihydroxy-3,20-dioxo-pregn-4-en-21-yl] ester

https://huagongshe.com/reaction/53065

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCortisolHCID 5754—
EduktDicyclohexylcarbodiimideHCID 10868—
EduktBoc-L-ValineHCID 83693—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDichloromethaneHCID 6344—
Produkt(2S)-2-((1,1-dimethylethoxycarbonyl)-amino)-3-methylbutyric acid [11beta,17,21-trihydroxy-3,20-dioxo-pregn-4-en-21-yl] esterHCID 8675065751%

Reaktionsschritte

A solution of 3.63 g (10 mmol) of hydrocortisone in 150 ml of dichloromethane is mixed with 2.34 g (10.8 mmol) of N-(tert -butoxycarbonyl)-valine, 500 mg (4.1 mmol) of 4-dimethylaminopyridine and 3.1 g (15 mmol) of dicyclohexylcarbodiimide. The solution is stirred for 3 hours at room temperature, the precipitate that is produced is suctioned off and washed with dichloromethane. The filtrate is concentrated by evaporation in a vacuum. The chromatography on silica gel (hexane→hexane/ethyl acetate 1:1) provides 2.87 g (51%) of (2S)-2-((1,1-dimethylethoxycarbonyl)-amino)-3-methylbutyric acid [11β,17,21-trihydroxy-3,20-dioxo-pregn-4-en-21-yl] ester. Crystallization from dichloromethane/diisopropyl ether.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05616573
Quelldatensatzuspto-grants-1997_04
ORD IDord-a60f758833af4ae5911eeed9ebfd2328
Quellennotizuspto-grants-1997_04