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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603570Generated: October 31, 2026

4-(2-Bromo-6-pyrrolidin-1-ylpyridine-4-sulfonyl)phenylamine → 4-(2-Cyclohex-1-enyl-6-pyrrolidine-1-yl-pyridine-4-sulfonyl)-phenylamine

https://huagongshe.com/reaction/1603570

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(2-Bromo-6-pyrrolidin-1-ylpyridine-4-sulfonyl)phenylamineHCID 6918689—
ReactantStannane, tributyl-1-cyclohexen-1-yl-HCID 11783615—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventDimethylformamideHCID 6228—
Product4-(2-Cyclohex-1-enyl-6-pyrrolidine-1-yl-pyridine-4-sulfonyl)-phenylamineHCID 1960546550%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 382 mg (1 mmole) 4-(2-bromo-6-pyrrolidine-1-yl-pyridine-4-sulfonyl)-phenylamine, 371 mg (1 mmole) tributyl-cyclohex-1-enyl stannane, and 70 mg bis(triphenylphosphine)-palladium(II)-chloride in 20 ml dimethylformamide is stirred for 3 hours at 80° C. The solvent is removed and the residue is diluted with dichloromethane. The dichloromethane solution is washed twice with saturated aqueous potassium fluoride, dried over magnesiumsulfate and concentrated in vacuo. Flash chromatography of the residue (silicagel, hexane/AcOEt 3/1) yields 191 mg (50%) pure 4-(2-cyclohex-1-enyl-6-pyrrolidine-1-yl-pyridine-4-sulfonyl)-phenylamine as a white solid. mp 237-238° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05990105
Source datasetuspto-grants-1999_11
ORD IDord-d2253be82abb4962b5795b4eda388938
Source noteuspto-grants-1999_11