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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 277137Generated: October 30, 2026

HCID 178418361, compound → HCID 178527242, compound

https://huagongshe.com/reaction/277137

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178418361HCID 178418361—
ReactantHCID 178527243HCID 178527243—
CatalystPalladium hydroxideHCID 9942167—
SolventAcetic AcidHCID 176—
SolventHydrochloric AcidHCID 313—
ProductHCID 178527242HCID 178527242102.9%

Reaction Steps

N-Azetidin-3-yl-N-(3,5-difluorophenyl)methylsulfonamide hydrochloride is obtained in the following manner: in a 500-cm3 hydrogenator, a solution of 1 g of N-(1-benzhydrylazetidin-3-yl)-N-(3,5-difluorophenyl)methylsulfonamide in a mixture of 2.5 cm3 of 1M hydrochloric acid and 0.41 cm3 of acetic acid is hydrogenated in the presence of 0.161 g of palladium hydroxide at a hydrogen pressure of 30 bar for 4 hours. The catalyst is removed by filtration on a celite bed and then the filtrate is concentrated to dryness at 40° C. under 2.7 kPa to give 630 mg of N-azetidin-3-yl-N-(3,5-difluorophenyl)methylsulfonamide, melting at 216° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06355631B1
Source datasetuspto-grants-2002_03
ORD IDord-9a13a606fcdf45f3826491d3aac7394f
Source noteuspto-grants-2002_03