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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 962695Erstellt: 24. Oktober 2026

Water → 17beta-[N-(Diphenylmethyl)carbamoyl]androsta-3,5-diene-3-carboxylic acid

https://huagongshe.com/de/reaction/962695

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktPotassium HydroxideHCID 14797—
EduktMethyl 17beta-[N-(diphenylmethyl)carbamoyl]androsta-3,5-diene-3-carboxylateHCID 15380280—
LösungsmittelMethanolHCID 887—
Produkt17beta-[N-(Diphenylmethyl)carbamoyl]androsta-3,5-diene-3-carboxylic acidHCID 15380256—

Reaktionsschritte

10 ml of water and 1 g of potassium hydroxide were added to a solution of 25 ml of methanol containing 214 mg of methyl 17β-(N-diphenylmethylcarbamoyl)-androsta-3,5-diene-3-carboxylate (prepared as described in Example 27). The reaction mixture was then heated under reflux for 4 hours. At the end of this time, methanol from the reaction mixture was removed by distillation under reduced pressure. The mixture was then made acidic by the addition of 1N aqueous hydrochloric acid and extracted with methylene chloride three times. The combined organic extracts were washed with water and with a saturated aqueous solution of sodium chloride, in that order, dried over anhydrous magnesium sulfate, and concentrated by evaporation under reduced pressure. The resulting residue was subjected to column chromatography using 20 g of silica gel and using a gradient elution method, with mixtures of acetone and methylene chloride in ratios ranging from 2:98 to 50:50 by volume as the eluent, to give 110 mg of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05760025
Quelldatensatzuspto-grants-1998_06
ORD IDord-ee28675541644a479b3b56df0fc959b7
Quellennotizuspto-grants-1998_06