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14628-57-0

4-CHLORO-5-METHOXY-2-METHYL-2,3-DIHYDROPYRIDAZIN-3-ONE synthesis

14synthesis methods
-

Yield:14628-57-0 432mg

Reaction Conditions:

in methanol at 0 - 20; for 3 h;

Steps:

5.3 Synthesis of 4-chloro-5-methoxy-2-methyl-pyridazin-3-one

4,5-dichloro-2-methyl-3 (2H)-pyridazinone (500 mg, 2.70 mmol) was dissolved in methanol, 0 ° C. at 28% sodium methoxide - methanol solution (587 μL, 3.35 mmol) was added and the mixture was stirred at room temperature for 3 hours. To this suspension resulting residue was concentrated under reduced pressure was diluted with ethyl acetate, and washed with water. The organic phase was dried over anhydrous sodium sulfate to give the title compound (432 mg) by vacuum concentration.

References:

JP2016/37467,2016,A Location in patent:Paragraph 0063

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