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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1739738Generated: October 26, 2026

1-(Diphenylmethyl)azetidin-3-yl methanesulfonate → HCID 21836533, compound

https://huagongshe.com/reaction/1739738

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Diphenylmethyl)azetidin-3-yl methanesulfonateHCID 2758716—
Reactant1-PiperazinesulfonamideHCID 11252198—
SolventAcetonitrileHCID 6342—
ProductHCID 21836533HCID 218365338.1%

Reaction Steps

A solution of 1-diphenylmethyl-3-methanesulphonyloxyazetidine (see Preparation 54) (4.8 g, 15.1 mmol) and 1-aminosulphonylpiperazine (see Example 123(f)) (5 g) in acetonitrile (50 ml) was heated under reflux for 4 hours. The reaction was cooled and the solid filtered off and washed with acetonitrile (50 ml). The filtrate was concentrated under reduced pressure and the residue slurried in hot toluene (50 ml), cooled, the solid filtered off and washed with toluene (50 ml). The product was then further purified by slurrying in hot ethyl acetate (3 ml), cooling and filtering to give the title compound (0.47 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05968923
Source datasetuspto-grants-1999_10
ORD IDord-911af1a100ac4763a5494b3269ad23cf
Source noteuspto-grants-1999_10