HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 628003Erstellt: 25. Oktober 2026
Dimethylformamide → 3-Methylcarboxy-6,7-dihydropyrido[3,2-b]thieno[2,3-d]oxepine
https://huagongshe.com/reaction/628003
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Triphenylphosphine | HCID 11776 | — |
| Edukt | Methyl 6-iodo-5-(2-(thiophen-3-yl)ethoxy)nicotinate | HCID 57900415 | — |
| Katalysator | palladium(II) acetate | HCID 167845 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | 3-Methylcarboxy-6,7-dihydropyrido[3,2-b]thieno[2,3-d]oxepine | HCID 66869300 | 52,8% |
Reaktionsschritte
To a solution of 6-Iodo-5-(2-thiophen-3-yl-ethoxy)-nicotinic acid methyl ester (4.40 g, 11.3 mmol) in N,N-Dimethylformamide (176 mL, 2270 mmol) was added potassium carbonate (9.37 g, 67.8 mmol), triphenylphosphine (1.19 g, 4.52 mmol) and palladium acetate (508 mg, 2.26 mmol). The reaction mixture was stirred at 90° C. 8 h. The reaction mixture was diluted with MeOH then filtered through celite. The filtrate was concentrated. The crude product was purified by flash chromatography EtOAc/Hex (0-100%) (product eluted at 30%) to give 3-methylcarboxy-6,7-dihydropyrido[3,2-b]thieno[2,3-d]oxepine (52.8%). MS: (ESI+) 262.0
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09309265B2 |
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| Quelldatensatz | uspto-grants-2016_04 |
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| ORD ID | ord-f67f708bc7094f0bbb33c86a7e42f08e |
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| Quellennotiz | uspto-grants-2016_04 |
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