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4-Chloro-1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylic acid synthesis

3synthesis methods
821791-58-6 Synthesis
4-CHLORO-1-METHYL-6-OXO-1,6-DIHYDRO-PYRIDINE-3-CARBOXYLIC ACID ETHYL ESTER

821791-58-6
48 suppliers
$53.00/250mg

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Yield:821791-59-7 60%

Reaction Conditions:

with water;sodium hydroxide in tetrahydrofuran;methanol at 20; for 3 h;

Steps:

35.1 (Step 1) Preparation of 4-chloro- 1 -methyl-6-oxo- 1 ,6-dihydropyridine-3-carboxylic acid

Ethyl 4-chloro- 1 -methyl-6-oxo- 1 ,6-dthydropyridine-3-carboxylate (300 mg, 1.0 eq) dissolved in a mixed solvent of tetrahydrofuran/methanol (7 mL/ 7 mL) was added with 2 N sodium hydroxide (4 mL), and stirred at room temperature for 3 hours. Upon completion of the reaction, the resultant was diluted with ethyl acetate and water to separate the aqueous layer. The resulting aqueous layer was acidified with 2 N HC1 to form crystals. The resulting crystals were filtered to obtain a title compound (yield;60%).

References:

WO2015/60613,2015,A1 Location in patent:Paragraph 353; 354