HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1255201Erstellt: 25. Oktober 2026
Cesium carbonate → Di-tert-butyl 1-[6-(2-methoxy-5-methylphenyl)-4-nitropyridin-2-yl]hydrazine-1,2-dicarboxylate
https://huagongshe.com/reaction/1255201
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Cesium carbonate | HCID 10796 | — |
| Edukt | Di-tert-butyl bicarbamate | HCID 85431 | — |
| Edukt | 2-Chloro-6-(2-methoxy-5-methylphenyl)-4-nitropyridine | HCID 86633494 | — |
| Katalysator | Ferrocene-1,1'-bis-(diphenylphosphine) | HCID 635956 | — |
| Katalysator | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | Di-tert-butyl 1-[6-(2-methoxy-5-methylphenyl)-4-nitropyridin-2-yl]hydrazine-1,2-dicarboxylate | HCID 67158740 | — |
Reaktionsschritte
A mixture of the title compound from Example 19 Step A (1.5 g, 5.4 mmol), di-tert-butyl hydrazine-1,2-dicarboxylate (1.375 g, 5.92 mmol), DPPF (360 mg, 0.65 mmol), Pd2 dba3 (0.4 g, 0.43 mmol), Cs2CO3 (1.90 g, 5.83 mmol) and 12 mL toluene was stirred at 100° C. After 20 h, the mixture was allowed to cool to ambient temperature, then purification by flash chromatography on silica gel using hexane-EtOAc (20:1 to 4:1 v/v) as mobile phase provided the title compound: LCMS m/z 375.6 (observed [M+H]+ for the ion corresponding to loss of one Boc group); 1H NMR (400 MHz, acetone-d6) δ 7.86 (d, J=2.1 Hz, 1H), 7.26 (dd, J=8.4, 2.1 Hz, 1H), 7.07 (d, J=8.4, 2.1 Hz, 1H), 3.93 (s, 3H), 2.31 (s, 3H), 1.54 (s, 9H), 1.47 (s, 9H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08455638B2 |
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| Quelldatensatz | uspto-grants-2013_06 |
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| ORD ID | ord-6d9ca54d3ad94644a7ff75360075ce41 |
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| Quellennotiz | uspto-grants-2013_06 |
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