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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 750312Generated: November 1, 2026

Ammonia → 1-(4-Aminomethylbenzenesulfonyl)piperidine-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/750312

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant1-(4-Cyanobenzenesulfonyl)piperidine-4-carboxylic acid ethyl esterHCID 3854242—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Aminomethylbenzenesulfonyl)piperidine-4-carboxylic acid ethyl esterHCID 6915773377%

Reaction Steps

[Step 2] To a mixture of 1-(4-cyanobenzenesulfonyl)piperidine-4-carboxylic acid ethyl ester (1.36 g) in ethanol (84 ml) and tetrahydrofuran (14 ml) was added 28% aqueous ammonia (3 ml) and then Raney nickel (500 mg) was added. Under a hydrogen pressure (0.5 Mpa), the mixture was stirred at room temperature for 2 hrs., and undesired substances were removed by filtration. The filtrate was concentrated under reduced pressure to give 1-(4-aminomethylbenzenesulfonyl)piperidine-4-carboxylic acid ethyl ester (1.05 g, 77%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07402595B2
Source datasetuspto-grants-2008_07
ORD IDord-e56ebbc421664cd19e0d9cbb2970ebae
Source noteuspto-grants-2008_07