ChemicalBook CAS DataBase List 7-Methoxy-3,4-dihydro-1H-quinolin-2-one

7-Methoxy-3,4-dihydro-1H-quinolin-2-one synthesis

12synthesis methods

Product Name:7-Methoxy-3,4-dihydro-1H-quinolin-2-one
CAS Number:22246-17-9
Molecular formula:C10H11NO2
Molecular Weight:177.2

22246-18-0 Synthesis

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74-88-4
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22246-17-9
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Yield: 90%

Reaction Conditions:

Stage #1:7-hydroxy-3,4-dihydro-2-(1H)-quinolinone with potassium carbonate in isopropyl alcohol at 20; for 0.5 h;Inert atmosphere;
Stage #2:methyl iodide in isopropyl alcohol for 60 h;Reflux;

Steps:

4.A
A. Synthesis of a Compound of Formula (4) To a solution of 7-hydroxy-3,4-dihydroquinolin-2(1H)-one (3) (16.317 g, 100 mmol) in anhydrous isopropanol (200 mL) was added potassium carbonate (16.585 g, 120.0 mmol) with stirring under an atmosphere of dry N₂. The reaction mixture was stirred at room temperature for 30 minutes, then iodomethane (10.0 mL, 161.3 mmol) was added slowly. The reaction was heated to reflux with stirring for 60 hours, cooled, and the solvent evaporated under reduced pressure. To this residue water (200 mL) was added, and the mixture stirred and sonicated, filtered, and the pale yellow solid was washed with water (1000 mL), and dried under resuced pressure. To the crude dry solid was added 15% ethyl acetate in n-hexane (150 mL), and the mixture sonicated, filtered, washed with n-hexane (50 mL), and dried under reduced pressure, to afford 7-methoxy-3,4-dihydroquinolin-2(1H)-one (15.865 g, 89.5 mmol, 90%), the compound of formula (4). LCMS mz 178.0 (M+H), 200.0 (M+Na), anal HPLC>95% in purity, ¹H NMR (400 MHz; dorso-D6) δ 7.09 (d, J=8.2 Hz, 1H); 6.57 (dd, J=8.2 and 2.7 Hz, 1H); 6.48 (d, J=2.7 Hz, 1H); 3.78 (s, 2H); 2.90 (t, J=7.0 Hz, 2H); 2.57 (t, J=7.0 Hz, 2H).

References:

Gilead Palo Alto, Inc. US2010/113514, 2010, A1 Location in patent:Page/Page column 18; 19

22246-18-0 Synthesis

22246-18-0
612 suppliers
$5.00/5g