HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 401561Erstellt: 24. Oktober 2026
Potassium Carbonate → 1-Benzo[1,3]dioxol-5-yl-cyclopropanecarboxylic Acid[5-(2,4-dimethoxy-phenyl)-pyridin-2-yl]-amide
https://huagongshe.com/de/reaction/401561
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 2,4-Dimethoxybenzeneboronic acid | HCID 2734341 | — |
| Edukt | 1-(benzo[d][1,3]dioxol-5-yl)-N-(5-bromopyridin-2-yl)cyclopropanecarboxamide | HCID 59166163 | — |
| Katalysator | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 1-Benzo[1,3]dioxol-5-yl-cyclopropanecarboxylic Acid[5-(2,4-dimethoxy-phenyl)-pyridin-2-yl]-amide | HCID 16679709 | — |
Reaktionsschritte
1-Benzo[1,3]dioxol-5-yl-cyclopropanecarboxylic acid (5-bromo-pyridin-2-yl)-amide (36.1 mg, 0.10 mmol) was dissolved in 1 mL of N,N-dimethylformamide in a reaction tube. 2,4-Dimethoxybenzeneboronic acid (24 mg, 0.13 mmol), 0.1 mL of an aqueous 2 M potassium carbonate solution, and a catalytic amount of Pd(dppf)Cl2 (6.6 mg, 0.0090 mmol) were added and the reaction mixture was heated at 80° C. for three hours. The resulting material was cooled to room temperature, filtered, and purified by reverse-phase preparative liquid chromatography to yield the pure product as a trifluoroacetic acid salt. ESI-MS m/z calc. 418.2. found 419.0 (M+1)+. Retention time 3.18 minutes. 1H NMR (400 MHz, CD3CN) δ 1.25-1.29 (m, 2H), 1.63-1.67 (m, 2H), 3.83 (s, 3H), 3.86 (s, 3H), 6.04 (s, 2H), 6.64-6.68 (m, 2H), 6.92 (d, J=8.4 Hz, 1H), 7.03-7.06 (m, 2H), 7.30 (d, J=8.3 Hz, 1H), 7.96 (d, J=8.9 Hz, 1H), 8.14 (dd, J=8.9, 2.3 Hz, 1H), 8.38 (d, J=2.2 Hz, 1H), 8.65 (s, 1H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08741933B2 |
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| Quelldatensatz | uspto-grants-2014_06 |
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| ORD ID | ord-539ca337065a4419a8d4b528c58411be |
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| Quellennotiz | uspto-grants-2014_06 |
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