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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2100308Generated: November 1, 2026

1-(Propylsulfonyl)-3-pyridin-2-ylazetidine-3-carbonitrile → 1-[1-(Propylsulfonyl)-3-pyridin-2-ylazetidin-3-yl]methanamine

https://huagongshe.com/reaction/2100308

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Propylsulfonyl)-3-pyridin-2-ylazetidine-3-carbonitrileHCID 57798311—
CatalystNickelHCID 935—
SolventAmmonia methanolHCID 21705897—
Product1-[1-(Propylsulfonyl)-3-pyridin-2-ylazetidin-3-yl]methanamineHCID 57798319—

Reaction Steps

A solution of 1-(propylsulfonyl)-3-pyridin-2-ylazetidine-3-carbonitrile (II-1, 379 mg, 1.43 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-[1-(propylsulfonyl)-3-pyridin-2-ylazetidin-3-yl]methanamine (II-2) as a yellow oil. Analytical LCMS: single peak (214 nm), 1.791 min. This material was used in subsequent reactions without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572792B2
Source datasetuspto-grants-2009_08
ORD IDord-327c8255fdd34c21be39caec9098d427
Source noteuspto-grants-2009_08