HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 13485Erstellt: 23. Oktober 2026
Dimethylformamide → N-methyl{4-[3-(methylamino)-4-nitro-phenoxy](2-pyridyl))carboxamide
https://huagongshe.com/de/reaction/13485
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 5-Fluoro-2-nitroaniline | HCID 75399 | — |
| Edukt | 3-hydroxy-N-methylbenzamide | HCID 353710 | — |
| Edukt | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| Produkt | N-methyl{4-[3-(methylamino)-4-nitro-phenoxy](2-pyridyl))carboxamide | HCID 131725842 | — |
Reaktionsschritte
The mixture containing 5-fluoro-2-nitrophenylamine (1 eq), Potassium bis(trimethylsilyl)amide (2 eq) was stirred in dimethylformamide for 2 hours at room temperature. To this mixture was added (3-hydroxyphenyl)-N-methylcarboxamide (1 eq) and Potassium carbonate (1.2 eq) and stirred at 90° C. for 16 h. The reaction mixture was then concentrated and partitioned between ethyl acetate and water. The organic layer was separated and washed with brine, dried, filtered and concentrated in vacuum to give brown solid. Purification on silica gel gave N-methyl{4-[3-(methylamino)-4-nitro-phenoxy](2-pyridyl))carboxamide. It was taken in methanol and hydrogenated with catalytic amount of 10% Pd/C to give {4-[4-amino-3-(methylamino)phenoxy](2-pyridyl)}-N-methylcarboxamide. MS: MH+=272.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07728010B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-6b6dff67f14a4b098baa503d8c3178a8 |
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| Quellennotiz | uspto-grants-2010_06 |
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