HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 629934Erstellt: 25. Oktober 2026
Triethylamine → Ethyl (2,6-dibromo-3-nitropyridin-4-yl)(4-((diethoxyphosphoryl)methyl)benzyl)carbamate
https://huagongshe.com/reaction/629934
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Phosphonic acid, [[4-(bromomethyl)phenyl]methyl]-, diethyl ester | HCID 14750222 | — |
| Edukt | Ethyl (2,6-dibromo-3-nitropyridin-4-yl)carbamate | HCID 86614481 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | Ethyl (2,6-dibromo-3-nitropyridin-4-yl)(4-((diethoxyphosphoryl)methyl)benzyl)carbamate | HCID 86667761 | 38% |
Reaktionsschritte
To a solution of ethyl (2,6-dibromo-3-nitropyridin-4-yl)carbamate (1 equiv.) (described in ref. 18, Preparation 67) in acetonitrile (0.40 M) was added triethyl amine (1.5 equiv.) and diethyl 4-(bromomethyl)benzylphosphonate (1.3 equiv.) (described in ref. 88, Ex 25 Step 1). The reaction mixture was then heated to 60° C. for 18 h. At this point the reaction mixture was allowed to cool to room temperature and the volatiles were removed in vacuo. The resulting residue was purified by a COMBIFLASH™ system using a gradient of 0-5% MeOH/DCM to provide the title compound (38%) as a solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09315530B2 |
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| Quelldatensatz | uspto-grants-2016_04 |
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| ORD ID | ord-429a103333fe42548bbd9299f57f1e24 |
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| Quellennotiz | uspto-grants-2016_04 |
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