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6-(4-METHYLPIPERAZIN-1-YL)NICOTINONITRILE synthesis

1synthesis methods
109-01-3 Synthesis
1-Methylpiperazine

109-01-3
646 suppliers
$5.00/5G

33252-28-7 Synthesis
2-chloro-5-cyanopyridine

33252-28-7
432 suppliers
$6.00/1g

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Yield:54864-89-0 85%

Reaction Conditions:

with sodium carbonate in N,N-dimethyl-formamide at 90; for 5 h;Inert atmosphere;

Steps:

15.1 Step 1

To a solution of 6-chloro-3-cyanopyridine (200 mg, 1.45 mmol) in N, N-dimethylformamide (10 mL) under nitrogen was added N-methylpiperazine (150 mg, 1.45 mmol). , Sodium carbonate (310 mg, 2.9 mmol), and the reaction system was stirred at 90 ° C for 5 hours.The reaction system was diluted with water, extracted with ethyl acetate, and the organic phase was concentrated under reduced pressure to obtain 6- (4-methylpiperazin-1-yl) nicotinonitrile (250 mg, yield: 85%) as a yellow solid.

References:

CN110467629,2019,A Location in patent:Paragraph 0213-0216

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