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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1825308Generated: November 1, 2026

3-Iodobenzene-1-sulfonamide → 3-(4-{[6-(benzyl{(2R)-2-[4-(benzyloxy)-3-(formylamino)phenyl]-2-hydroxyethyl}amino)hexyl]oxy}but-1-ynyl)benzenesulfonamide

https://huagongshe.com/reaction/1825308

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Iodobenzene-1-sulfonamideHCID 11219806—
Reactant5-((1R)-2-{Benzyl[6-(but-3-ynyloxy)hexyl]amino}-1-hydroxyethyl)-2-(benzyloxy)phenylformamideHCID 11443930—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventAcetonitrileHCID 6342—
SolventTriethylamineHCID 8471—
Product3-(4-{[6-(benzyl{(2R)-2-[4-(benzyloxy)-3-(formylamino)phenyl]-2-hydroxyethyl}amino)hexyl]oxy}but-1-ynyl)benzenesulfonamideHCID 4262566851%

Reaction Steps

A stirred solution of 5-((1R)-2-{benzyl[6-(but-3-ynyloxy)hexyl]amino}-1-hydroxyethyl)-2-(benzyloxy)phenylformamide (500 mg) and 3-iodobenzenesulfonamide (340 mg) in acetonitrile (10 ml) and triethylamine (10 ml) with cuprous iodide (50 mg) and bis(triphenylphosphine) palladium dichloride (100 mg) was stirred at ambient temperature under nitrogen for 2 h. The mixture was evaporated in vacuo and the residue was purified by chromatography on Biotage (40 g) cartridge eluting with light petroleum 40-600/ethyl acetate (9:1) to give the title compound (330 mg). LCMS RT=3.04 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07045658B2
Source datasetuspto-grants-2006_05
ORD IDord-8825e80b97cf4326870742731f622316
Source noteuspto-grants-2006_05