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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1632742Generated: October 26, 2026

Triethylamine → 4-[(2-Sulfamoyl-5-thienyl)sulfonyl]phenyl 1-acetylpiperidine-4-carboxylate

https://huagongshe.com/reaction/1632742

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant5-(4-Hydroxyphenyl)sulfonylthiophene-2-sulfonamideHCID 12736892—
Reactant1-Acetylpiperidine-4-carbonyl chloride hydrochlorideHCID 53430810—
SolventAcetoneHCID 180—
Product4-[(2-Sulfamoyl-5-thienyl)sulfonyl]phenyl 1-acetylpiperidine-4-carboxylateHCID 20442367—

Reaction Steps

A solution of 5-[(4-hydroxyphenyl)sulfonyl]thiophene-2-sulfonamide (3.19 g; 0.01 mole) in acetone (60 ml) at -15° was treated with triethylamine (1.11 g; 0.011 mole). Then 1-acetylpiperidine-4-carbonyl chloride hydrochloride (2.41 g; 0.011 mole) was added, portionwise, during 15 minutes at -15°. The cooling bath was removed and stirring was continued. After 20 hours at room temperature, the reaction mixture was treated with triethylamine (1.11 g; 0.011 mole). Then after stirring one hour longer, the reaction mixture was treated with 1-acetylpiperidine-4-carbonyl chloride hydrochloride (2.41 g; 0.011 mole) and triethylamine (2.22 g; 0.022 mole) and stirred at room temperature.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04477466
Source datasetuspto-grants-1984_10
ORD IDord-d259bbaad2a743b2b218fca536653630
Source noteuspto-grants-1984_10