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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1581920Generated: November 1, 2026

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

https://huagongshe.com/reaction/1581920

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPyridine-3-sulfonyl chlorideHCID 3164136—
Reactant1-[Bis(4-chlorophenyl)methyl]azetidin-3-ylamineHCID 21896598—
SolventDichloromethaneHCID 6344—
ProductN-{1-[bis(4-chlorophenyl)methyl]azetidin-3-yl}pyrid-3-ylsulfonamideHCID 1029751368.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

0.79 cm3 of triethylamine is added, at room temperature under an argon atmosphere, to a solution of 0.7 g of 1-[bis(4-chlorophenyl)methyl]azetidin-3-ylamine in 25 cm3 of dichloromethane. The mixture is cooled to around 0° C. before adding thereto a solution of 1.2 g of pyrid-3-ylsulfonyl chloride in 25 cm3 of dichloromethane, and then it is stirred at room temperature for 16 hours. The reaction mixture is diluted with 50 cm3 of dichloromethane and is then washed with twice 25 cm3 of distilled water. The organic phase is 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/methanol (97.5/2.5 by volume)]. 0.7 g of N-{1-[bis(4-chlorophenyl)methyl]azetidin-3-yl}pyrid-3-ylsulfonamide is obtained in the form of a cream-colored foam which solidifies in the presence of isopropanol into a cream-colored powder melting at 164° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06734176B2
Source datasetuspto-grants-2004_05
ORD IDord-45e7c703d4884c3995c668a893429b68
Source noteuspto-grants-2004_05