HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 79712Erstellt: 24. Oktober 2026
4-Methylmorpholine → ({[2-(4-Bromo-phenyl)-2-oxo-ethylcarbamoyl]-methyl}-tert-butoxycarbonyl-amino)-acetic acid
https://huagongshe.com/de/reaction/79712
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-Methylmorpholine | HCID 7972 | — |
| Edukt | 2-Amino-1-(4-bromophenyl)ethan-1-one hydrochloride | HCID 2798216 | — |
| Edukt | Tert-butyl 2,6-dioxomorpholine-4-carboxylate | HCID 11830836 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | ({[2-(4-Bromo-phenyl)-2-oxo-ethylcarbamoyl]-methyl}-tert-butoxycarbonyl-amino)-acetic acid | HCID 59611182 | 80,2% |
Reaktionsschritte
2,6-Dioxo-morpholine-4-carboxylic acid tert-butyl ester (2.5 g, 11.6 mmol) was added to a solution of 2-amino-1-(4-bromo-phenyl)-ethanone hydrochloride (3.05 g, 12.2 mmol) and 4-methylmorpholine (1.92 mL, 17.4 mmol) in dimethylformamide (15 mL). After 30 min the solvent was removed under reduced pressure. The residue was taken up in ethyl acetate (100 mL) and washed with water (50 mL), aqueous hydrogen chloride (0.5 N, 2×50 mL), and saturated sodium bicarbonate (2×50 mL). The basic extracts were neutralized and extracted with ethyl acetate (2×75 mL). The combined organic phases from the second extraction were dried over sodium sulfate, and filtered. The solvent was removed under reduced pressure to provide ({[2-(4-bromo-phenyl)-2-oxo-ethylcarbamoyl]-methyl}-tert-butoxycarbonyl-amino)-acetic acid (4 g, 9.3 mmol, 80%). C17H21BrN2O6 calculated 428.0 observed [M+1]+ 431.1; rt=2.36 min.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08841278B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-9d840e0cf03446569270480f17560e27 |
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| Quellennotiz | uspto-grants-2014_09 |
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