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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1432272Generated: October 31, 2026

Hydrochloric Acid → 2-(2-Ethoxycarbonylfuran-5-yl-methyl)-5-methanesulfonylindole

https://huagongshe.com/reaction/1432272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
Reactant1-Benzenesulfonyl-2-(2-ethoxycarbonylfuran-5-yl-methyl)-5-methanesulfonylindoleHCID 22504442—
SolventEthanolHCID 702—
Product2-(2-Ethoxycarbonylfuran-5-yl-methyl)-5-methanesulfonylindoleHCID 22504450—

Reaction Conditions

Temperature22.5 °C

Reaction Steps

To a solution of the compound obtained in Example 30 (4) (0.1722 g) in ethanol (14 ml), potassium hydroxide (0.047 g) was added and the mixture was stirred at 15 to 30° C. for 30 minutes. To the mixture was added 10% aqueous hydrochloric acid solution, and the mixture was extracted with ethyl acetate, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The resulting residue was separated using silica gel column chromatography (hexane:ethyl acetate=0.1:1) to obtain 0.07.48 g of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612070B2
Source datasetuspto-grants-2009_11
ORD IDord-645d93fef46149709b17645d0aa43247
Source noteuspto-grants-2009_11