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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351781Generated: November 4, 2026

Triethylamine → Ethyl[2-[2-(5-cyano-2-methoxybenzenesulfonylamino)ethyl]-5-isopropylphenoxy]acetate

https://huagongshe.com/reaction/1351781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant5-Cyano-2-methoxybenzene-1-sulfonyl chlorideHCID 11528751—
ReactantEthyl[2-(2-aminoethyl)-5-isopropylphenoxy]acetateHCID 18456985—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductEthyl[2-[2-(5-cyano-2-methoxybenzenesulfonylamino)ethyl]-5-isopropylphenoxy]acetateHCID 1785620672.5%

Reaction Steps

To a stirred solution of 326 mg of ethyl[2-(2-amino-ethyl)-5-isopropylphenoxy]acetate hydorochloride and 0.452 mL of triethylamine in a mixture of 10 mL of tetrahydrofuran and 5 mL of water was added 238 mg of 5-cyano-2-methoxybenzene-sulfonyl chloride under ice-cooling, and the mixture was stirred at room temperature for 6 hours. To the reaction mixture was added 30 mL of water, and the mixture was extracted with 120 mL of ethyl acetate. The organic layer was washed with 100 mL of water, and 100 mL of brine, and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure, and the residue was purified by column chromatography on silica gel (eluent: ethyl acetate-hexane) to give 343 mg of ethyl[2-[2-(5-cyano-2-methoxybenzenesulfonylamino)ethyl]-5-isopropylphenoxy]acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07217832B2
Source datasetuspto-grants-2007_05
ORD IDord-2b1966dd699b42839d332f6decbef902
Source noteuspto-grants-2007_05