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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 862297Generated: October 25, 2026

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

https://huagongshe.com/reaction/862297

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium HydroxideHCID 14797—
ReactantMethyl 17beta-[N-(diphenylmethyl)carbamoyl]androsta-3,5-diene-3-carboxylateHCID 15380280—
SolventMethanolHCID 887—
Product17beta-[N-(Diphenylmethyl)carbamoyl]androsta-3,5-diene-3-carboxylic acidHCID 15380256—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05717088
Source datasetuspto-grants-1998_02
ORD IDord-4bf1da4d090a4f56b810c8f72ae5ca9e
Source noteuspto-grants-1998_02