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| | Acetamide, N-(3-cyano-7-ethoxy-4-hydroxy-6-quinolinyl)- Basic information |
| Product Name: | Acetamide, N-(3-cyano-7-ethoxy-4-hydroxy-6-quinolinyl)- | | Synonyms: | Acetamide, N-(3-cyano-7-ethoxy-4-hydroxy-6-quinolinyl)-;N-(3-cyano-7-ethoxy-4-hydroxyquinolin-6-yl)acetaMide;3-Cyano-7-ethoxy-4-hydroxy-6-(acetylaMino)quinoline;Neratinib Intermediate4;N-(3-Cyano-7-ethoxy-4-hydroxyquinolin-6-yl);3-Cyano-7-ethoxy-4-hydroxy-6-(acetylaMino)quinolone;N-(3-cyano-7-ethoxy-4-oxo-1H-quinolin-6-yl)acetamide;Neratinib Impurity 18 | | CAS: | 848133-75-5 | | MF: | C14H13N3O3 | | MW: | 271.27 | | EINECS: | | | Product Categories: | | | Mol File: | 848133-75-5.mol |  |
| | Acetamide, N-(3-cyano-7-ethoxy-4-hydroxy-6-quinolinyl)- Chemical Properties |
| Melting point | >250℃ | | Boiling point | 552.1±50.0 °C(Predicted) | | density | 1.35±0.1 g/cm3(Predicted) | | storage temp. | Sealed in dry,Room Temperature | | pka | 0.84±0.50(Predicted) |
| | Acetamide, N-(3-cyano-7-ethoxy-4-hydroxy-6-quinolinyl)- Usage And Synthesis |
| Synthesis | Under ice bath conditions, 60% sodium hydride (82 mg, 2.05 mmol) was slowly added to dimethyl sulfoxide (2.5 mL) and stirred for 5 min at room temperature. Subsequently, N-(3-cyano-7-ethoxy-4-hydroxyquinolin-6-yl)acetamide (0.5 g, 1.37 mmol) was added in batches and stirring was continued for 2 h at room temperature. After confirming the complete consumption of raw materials by thin layer chromatography (TLC) monitoring, the reaction mixture was slowly poured into water (10 mL) and the pH was adjusted to 3-4 with 4 M hydrochloric acid solution.The precipitated light yellow solid was collected by filtration and dried to give N-(3-cyano-7-ethoxy-4-hydroxyquinolin-6-yl)acetamide (0.35 g, 94.3% yield). | | References | [1] Patent: US2011/263860, 2011, A1. Location in patent: Page/Page column 9-10 |
| | Acetamide, N-(3-cyano-7-ethoxy-4-hydroxy-6-quinolinyl)- Preparation Products And Raw materials |
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