Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Ethyl cysteinate hydrochloride | HCID 2723617 | — |
| Edukt | 2-{4-[(3,5-Dichloropyridin-2-yl)oxy]phenoxy}propanoyl chloride | HCID 13189478 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Produkt | HCID 86746864 | HCID 86746864 | — |
Reaktionsschritte
Triethylamine is added to a stirred mixture of L-cysteine ethyl ester hydrochloride (2.71 g, 14.66 mmol) in chloroform under nitrogen. After the reaction mixture is cooled to 0° C., a solution of 2-{p-[(3,5-dichloro-2-pyridyl)oxy]phenoxy}propionyl chloride (5.08 g, 1 4.66 mmol) in chloroform (30 mL) is added dropwise with stirring. The reaction mixture is then stirred overnight at room temperature, concentrated in vacuo and filtered to obtain a semi-solid. Chromatography of the semi-solid using silica gel and eluting with methylene chloride followed by 2% to 5% ethyl acetate in methylene chloride gives the title product as a white solid, mp 89°-91° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05213606 |
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| Quelldatensatz | uspto-grants-1993_05 |
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| ORD ID | ord-7a66a7d5a4a642e08eba198e56733654 |
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| Quellennotiz | uspto-grants-1993_05 |
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