HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 660572Erstellt: 25. Oktober 2026
Potassium Acetate → 7-Oxo-6,7-dihydro-5H-dibenzo[c,e]azepine-5-carboxylic Acid Methyl Ester
https://huagongshe.com/reaction/660572
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Acetate | HCID 517044 | — |
| Edukt | (2-Iodobenzoylamino)-(2-iodophenyl)-acetic Acid Methyl Ester | HCID 68839341 | — |
| Katalysator | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 7-Oxo-6,7-dihydro-5H-dibenzo[c,e]azepine-5-carboxylic Acid Methyl Ester | HCID 68838469 | — |
Reaktionsschritte
To a solution of (2-iodobenzoylamino)-(2-iodophenyl)-acetic acid methyl ester (3.4 g, 6.53 mmol) in DMF (300 mL) under argon is added PdCl2(dppf) (269 mg, 0.33 mmol) and KOAc (1.28 g, 13.06 mmol) and the mixture is heated at 110° C. for 18 h. Additional PdCl2(dppf) is added and heating is continued until all starting material is consumed. The solvent is removed under reduced pressure and the residue purified by flash chromatography using a gradient of 0-50% MeOH/methylene chloride as eluent to give the title compound as a yellow oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08084448B2 |
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| Quelldatensatz | uspto-grants-2011_12 |
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| ORD ID | ord-f5e80b2965294fee9b2c92aaa0c2d7ed |
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| Quellennotiz | uspto-grants-2011_12 |
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