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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353578Generated: October 30, 2026

4-Methoxybenzenesulfonyl chloride → Methyl 4-(4-but-2-ynyloxybenzenesulfonyl)-1-[(4-methoxyphenyl)sulfonyl]-4-piperidinecarboxylate

https://huagongshe.com/reaction/353578

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxybenzenesulfonyl chlorideHCID 7401—
ReactantTriethylamineHCID 8471—
Reactant2-DimethylaminopyridineHCID 21885—
Reactant4-(4-but-2-ynyloxy-benzenesulfonyl)-piperidine-4-carboxylic Acid Methyl EsterHCID 54136994—
SolventDichloromethaneHCID 6344—
ProductMethyl 4-(4-but-2-ynyloxybenzenesulfonyl)-1-[(4-methoxyphenyl)sulfonyl]-4-piperidinecarboxylateHCID 2351382388%

Reaction Steps

To a solution of 4-(4-but-2-ynyloxy-benzenesulfonyl)-piperidine-4-carboxylic acid methyl ester (500 mg, 1.29 mmol) in methylene chloride (10 ml) was added triethylamine (261 mg, 2.58 mmol), 4-methoxyphenylsulfonyl chloride (320 mg, 1.55 mmol) followed by a catalytic amount of dimethylaminopyridine. The resulting mixture was stirred for 15 hours at room temperature, quenched with water and extracted with methylene chloride. The organic layer was dried over anhydrous sodium sulfate and concentrated to give 590 mg (88%) of the product as a solid. HR-MS: m/z Calculated for C24H72N8O8S2 522.1251; Found 522.1252.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06753337B2
Source datasetuspto-grants-2004_06
ORD IDord-4a50ea01789043429e30a6f98c7b5336
Source noteuspto-grants-2004_06