HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 733357Generated: October 31, 2026
Triethylamine → Ethyl[2-[2-(5-cyano-2-methoxybenzenesulfonylamino)ethyl]-5-isopropylphenoxy]acetate
https://huagongshe.com/reaction/733357
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-Cyano-2-methoxybenzene-1-sulfonyl chloride | HCID 11528751 | — |
| Reactant | Ethyl[2-(2-aminoethyl)-5-isopropylphenoxy]acetate | HCID 18456985 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl[2-[2-(5-cyano-2-methoxybenzenesulfonylamino)ethyl]-5-isopropylphenoxy]acetate | HCID 17856206 | 72.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07589126B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-d7a94cbe79894849a397198aad5d2ef8 |
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| Source note | uspto-grants-2009_09 |
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