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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1586715Generated: October 30, 2026

Proton sponge → 6-Methanesulfonamido-2-(4-piperidyl)indan-1-one hydrochloride

https://huagongshe.com/reaction/1586715

Reaction equation

Participants

RoleNameHCIDCharge
ReactantProton spongeHCID 88675—
Reactant1-Chloroethyl chloroformateHCID 521305—
Reactant6-Methanesulfonamido-2-(1-methyl-4-piperidyl)indan-1-oneHCID 14985994—
Solvent1,2-DichloroethaneHCID 11—
Product6-Methanesulfonamido-2-(4-piperidyl)indan-1-one hydrochlorideHCID 19759183—

Reaction Steps

To a solution of 1.35 g (0.00419 mol) of 6-methanesulfonamido-2-(1-methyl-4-piperidyl)indan-1-one in 46 mL of 1,2-dichloroethane was added 1.35 g (0.0063 mol) of 1,8-bis(dimethylamino)naphthalene. The solution was cooled in an ice bath and 1.80 g (0.0126 mol) of 1-chloroethylchloroformate was added dropwise over 5 minutes. The mixture was allowed to warm to room temperature and then was refluxed for 5 hours. The cooled mixture was filtered through a small column of silica gel using methylene chloride to wash the column. The eluate was evaporated in vacuo. The residual 1.35 g of thick oil was dissolved in 10 mL of methanol, and the solution was refluxed for 24 hours. Evaporation of the methanol and crystallization of the residue from methanol afforded 6-methanesulfonamido-2-(4-piperidyl)indan-1-one hydrochloride as a hemi methanol solvate salt: mp 254°-256° (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05215989
Source datasetuspto-grants-1993_06
ORD IDord-462c44f4396446cca36bfb16ef3909e6
Source noteuspto-grants-1993_06