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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 511088Generated: November 3, 2026

Hydrochloric Acid → Hydrochloric Acid

https://huagongshe.com/reaction/511088

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-[4-(4-Fluoro-benzenesulfonyl)-phenylamino]-piperidine-1-carboxylic acid tert-butyl esterHCID 58576272—
SolventDichloromethaneHCID 6344—
SolventTrifluoroacetic acidHCID 6422—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductHydrochloric AcidHCID 313—
Product[4-(4-Fluoro-benzenesulfonyl)-phenyl]-piperidin-4-yl-amine hydrochlorideHCID 66671912—

Reaction Steps

4-[4-(4-Fluoro-benzenesulfonyl)-phenylamino]-piperidine-1-carboxylic acid tert-butyl ester (640 mg; 1.47 mmol, prepared in accordance with Example 31) is dissolved in a 1 to 1 mixture of dichloromethane and trifluoroacetic acid (2 mL) and the resulting solution is stirred at room temperature until complete conversion is observed (about 90 minutes). After concentration under reduced pressure, the residue obtained is co-evaporated with dichloromethane (2×10 mL). The crude residue is then diluted in ethylacetate (2 mL) and a 4N solution of hydrochloric acid in dioxane (3 mL) is added under stiffing. The solid formed is filtered and dried under high vacuum to afford the desired product as hydrochloride (546 mg; 1.47 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096524B2
Source datasetuspto-grants-2015_08
ORD IDord-671b98c69c2a4a3cb7672fefe6574c42
Source noteuspto-grants-2015_08