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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1464154Generated: October 30, 2026

[(4-Iodophenyl)sulfonyl]-2-pyridylamine → Methyl 2-hydroxy-5-[[4-[(2-pyridinylamino)sulfonyl]phenyl]ethynyl]benzoate

https://huagongshe.com/reaction/1464154

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[(4-Iodophenyl)sulfonyl]-2-pyridylamineHCID 1143526—
ReactantMethyl 5-ethynyl-2-hydroxybenzoateHCID 14172485—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
ProductMethyl 2-hydroxy-5-[[4-[(2-pyridinylamino)sulfonyl]phenyl]ethynyl]benzoateHCID 19423375—

Reaction Conditions

Temperature60 °C

Reaction Steps

4-Iodo-N-(2-pyridinyl)benzenesulfonamide (35 g, 97 mmol) was dissolved in a mixture of triethylamine and tetrahydrofuran (750+750 ml). The mixture was deaerated with nitrogen and dichlorobis(triphenylphosphine)palladium (1.2 g, 1.7 mmol) and copper(I) iodide (0.6 g, 3.4 mmol) were added. Finally methyl 5-ethynyl-2-hydroxybenzoate (23 g, 130 mmol) was added. The mixture was heated to 60° C. for 4 h, evaporated to dryness. The residue was dissolved in chloroform (1000 ml) and washed with water (3×200 ml) and dried with MgSO4. The solvent was evaporated in vacuo. Yield 31 g (77%). The product can be purified by flash-chromatography on silica with chloroform as the eluent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05302718
Source datasetuspto-grants-1994_04
ORD IDord-19bc88cf39aa43dbaa5c813d617d99db
Source noteuspto-grants-1994_04