Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2283347Generated: October 31, 2026

Triethylamine → (E)-N,N-diallyl-4-(2-(4-bromophenyl)vinylsulfonamido)pyridine-3-sulfonamide

https://huagongshe.com/reaction/2283347

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant(E)-2-(4-bromophenyl)ethene-1-sulfonyl chlorideHCID 23084300—
ReactantN,N-diallyl-4-aminopyridine-3-sulfonamideHCID 57750998—
SolventPyridineHCID 1049—
Product(E)-N,N-diallyl-4-(2-(4-bromophenyl)vinylsulfonamido)pyridine-3-sulfonamideHCID 5775106360%

Reaction Steps

Triethylamine (0.440 mL, 3.16 mmol) added was to a solution of N,N-diallyl-4-aminopyridine-3-sulfonamide (0.40 g, 1.58 mmol) in pyridine (10 mL), the mixture was stirred for 5 min and (E)-2-(4-bromophenyl)ethenesulfonyl chloride (0.53 g, 1.89 mmol) was added. After stirring over night the pyridine was evaporated, diluted hydrochloric acid was added and the mixture was extracted with ethyl acetate. The organic phase was dried over magnesium sulfate and the solvent was evaporated. Purification by column chromatography, using chloroform/methanol (97:3) as the eluent, gave the title compound in 60% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145380B2
Source datasetuspto-grants-2015_09
ORD IDord-1f907b8c63574329bb167839e0a88764
Source noteuspto-grants-2015_09