HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 52110Erstellt: 26. Oktober 2026
Water → N-[4-(4-piperidinomethyl-2-pyridyloxy)-cis-2-butenyl]-2-(3-hydroxypropylthio)acetamide
https://huagongshe.com/reaction/52110
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | 3-Chloro-1-propanol | HCID 12313 | — |
| Edukt | Sodium Methoxide | HCID 10942334 | — |
| Edukt | N-[4-(4-Piperidinomethyl-2-pyridyloxy)-cis-2-butenyl]-2-(acetylthio)acetamide | HCID 86750622 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | N-[4-(4-piperidinomethyl-2-pyridyloxy)-cis-2-butenyl]-2-(3-hydroxypropylthio)acetamide | HCID 67726286 | 81% |
Reaktionsschritte
5 ml of a methanolic solution containing 0.26 g of a 28% w/v sodium methoxide solution were added, whilst ice-cooling, to a solution of 0.50 g of N-[4-(4-piperidinomethyl-2-pyridyloxy)-cis-2-butenyl]-2-(acetylthio)acetamide [prepared as described in step (b) above] in 5 ml of methanol, and the resulting solution was stirred for 20 minutes. At the end of this time, a solution of 0.11 ml of 3-chloro-1-propanol in 5 ml of methanol, was added, and the reaction mixture was heated under reflux for 5 hours. The solvent was then removed by distillation under reduced pressure. The residue thus obtained was mixed with water, and the aqueous mixture was extracted with ethyl acetate. The extract was concentrated by evaporation under reduced pressure, and the residue was purified by column chromatography through silica gel, using a 1:9 by volume mixture of methanol and methylene chloride as the eluent, to give 0.42 g (yield 81%) of the title compound as an oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05616579 |
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| Quelldatensatz | uspto-grants-1997_04 |
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| ORD ID | ord-75936c190cbc4c32ab18f956ab1df720 |
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| Quellennotiz | uspto-grants-1997_04 |
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