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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1581921Generated: October 26, 2026

Triethylamine → N-(1-[bis(4-chlorophenyl)methyl]azetidin-3-yl}-4-fluorophenylsulfonamide

https://huagongshe.com/reaction/1581921

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Fluorobenzenesulfonyl chlorideHCID 9588—
Reactant1-[Bis(4-chlorophenyl)methyl]azetidin-3-ylamineHCID 21896598—
SolventDichloromethaneHCID 6344—
ProductN-(1-[bis(4-chlorophenyl)methyl]azetidin-3-yl}-4-fluorophenylsulfonamideHCID 1029854238.7%

Reaction Steps

0.214 g of 4-fluorophenylsulfonyl chloride and 0.28 cm3 of triethylamine are added, at room temperature under an argon atmosphere, to a solution of 0.307 g of 1-[bis(4-chlorophenyl)methyl]azetidin-3-ylamine in 10 cm3 of dichloromethane. After stirring for 16 hours at room temperature, the reaction mixture is washed with 10 cm3 of distilled water, dried over magnesium sulfate, filtered and concentrated to dryness under reduced pressure (2.7 kPa). The residue obtained is purified by flash chromatography on silica gel [eluant: dichloromethane/ethyl acetate (100/0 to 95/5 by volume) gradient]. 0.18 g of N-{1-[bis(4-chlorophenyl)methyl]azetidin-3-yl}-4-fluorophenylsulfonamide is obtained in the form of a white foam [1H NMR spectrum (300 MHz, CDCl3, δ in ppm): 2.74 (broad t, J=7.5 Hz: 2H); 2.39 (broad t, J=7.5 Hz: 2H); 3.98 (mt: 1H); 4.20 (s: 1H); 4.79 (d, J=9 Hz: 1H); from 7.10 to 7.35 (mt: 10H); 7.86 (mt: 2H)].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06734176B2
Source datasetuspto-grants-2004_05
ORD IDord-142716878d094ef0b6a2a03e4d2f05b0
Source noteuspto-grants-2004_05