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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 502893Generated: November 2, 2026

4-(Cyclopropylmethyl)-1-(ethylsulfonyl)piperidine-4-carbonitrile → 1-[4-(Cyclopropylmethyl)-1-(ethylsulfonyl)piperidin-4-yl]methanamine

https://huagongshe.com/reaction/502893

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Cyclopropylmethyl)-1-(ethylsulfonyl)piperidine-4-carbonitrileHCID 59428186—
CatalystNickelHCID 935—
SolventAmmonia methanolHCID 21705897—
Product1-[4-(Cyclopropylmethyl)-1-(ethylsulfonyl)piperidin-4-yl]methanamineHCID 68620156—

Reaction Steps

A solution of 4-(cyclopropylmethyl)-1-(ethylsulfonyl)piperidine-4-carbonitrile (I-4, 3.1 mg, 11.1 mmol) in 2 M NH3/MeOH (50 mL) was treated with excess Raney Ni and agitated under an atmosphere of H2 (40 psi) in a Parr apparatus. After 5 h, the reaction was filtered through Celite (MeOH wash) and concentrated under reduced pressure to afford 1-[4-(cyclopropylmethyl)-1-(ethylsulfonyl)-piperidin-4-yl]methanamine (I-5, M+H+=261.2) as a yellow oil. This material was used in subsequent reactions without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776886B2
Source datasetuspto-grants-2010_08
ORD IDord-09d675b5db4d4b7c8294c54422a51ea9
Source noteuspto-grants-2010_08