HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 40324Erstellt: 23. Oktober 2026
Oxalyl chloride → N-Methoxy-N-methylquinoline-6-carboxamide
https://huagongshe.com/de/reaction/40324
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Oxalyl chloride | HCID 65578 | — |
| Edukt | Methanamine, N-methoxy-, hydrochloride (1:1) | HCID 81138 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | 6-Quinolinecarboxylic acid | HCID 82571 | — |
| Katalysator | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | N-Methoxy-N-methylquinoline-6-carboxamide | HCID 55211172 | 95,2% |
Reaktionsschritte
A 250 mL RB flask was charged with quinoline-6-carboxylic acid (5.00 g, 28.9 mmol), DCM (100 ml, 1554 mmol), oxalyl chloride (3.79 ml, 43.3 mmol), and a few drops of DMF and stirred at RT for 2 hours, then concentrated. The residue was taken up in DCM (100 ml, 1554 mmol), cooled to 0° C., then Hunig's Base (17.7 ml, 101 mmol) and N-methoxymethanamine hydrochloride (2.96 g, 30.3 mmol) were added slowly. The mixture was stirred at room temperature for 16 hours (91463-3-1). The mixture was diluted with DCM (200 mL), then washed with water (250 mL), sat. NaHCO3 (250 mL), and brine (250 mL). The organic layer was dried with MgSO4, filtered, and concentrated to give a brown oil, which was purified by MPLC eluting with 2-6% MeOH/DCM to give N-methoxy-N-methylquinoline-6-carboxamide (5.943 g, 95.2% yield) as a brown oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08524900B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-1c22e723dddd4c25b16eeb5f4c0677ad |
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| Quellennotiz | uspto-grants-2013_09 |
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