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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 229585Generated: October 25, 2026

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

https://huagongshe.com/reaction/229585

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant5-Cyano-2-methoxybenzene-1-sulfonyl chlorideHCID 11528751—
ReactantHCID 18456984HCID 18456984—
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-aminoethyl)-5-isopropylphenoxy]acetate hydrochloride 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-methoxybenzenesulfonyl 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 numberUS07563822B2
Source datasetuspto-grants-2009_07
ORD IDord-c4342bf9b9cb47d89015383cf1866a71
Source noteuspto-grants-2009_07