HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1266962Erstellt: 25. Oktober 2026
Water → 1,1-Dimethylethyl 2-(4-(4-fluorophenyl)-1-piperazinyl)-2-oxo-1-(phenylmethyl)ethylcarbamate
https://huagongshe.com/reaction/1266962
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Boc-Phe-ONp | HCID 111308 | — |
| Edukt | 1-(4-Fluorophenyl)piperazine dihydrochloride | HCID 16211916 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 1,1-Dimethylethyl 2-(4-(4-fluorophenyl)-1-piperazinyl)-2-oxo-1-(phenylmethyl)ethylcarbamate | HCID 53804735 | 92,2% |
Reaktionsschritte
To a solution of 1-(4-fluorophenyl)piperazine dihydrochloride (2.53 g, 10 mmol) in N,N-dimethylformamide (40 ml) were added triethylamine (2.8 ml, 20 mmol) and N-tert butoxycarbonylphenylalanine p-nitrophenyl ester (2.65 g, 10 mmol) in the order mentioned, and the mixture was stirred at room temperature overnight. The reaction mixture was poured into cold water and extracted with ethyl acetate. The extract was washed with 1 w/v % aqueous ammonia, saturated brine, 0.1N hydrochloric acid, saturated brine, saturated aqueous sodium hydrogencarbonate solution, and saturated brine in the order mentioned, and the organic layer was dried over anhydrous magnesium sulfate and further concentrated under reduced pressure. The residue was purified by silica gel column chromatography using chloroform-methanol (50:1, v/v) to give 1,1-dimethylethyl 2-(4-(4-fluorophenyl)-1-piperazinyl)-2-oxo-1-(phenylmethyl)ethylcarbamate (2.7 g, 92.2%) as colorless oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06551999B1 |
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| Quelldatensatz | uspto-grants-2003_04 |
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| ORD ID | ord-2f8fa56f589e43c6b3b8e47658fbfe98 |
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| Quellennotiz | uspto-grants-2003_04 |
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