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13675-93-9

6-nitroquinoline-2-carbonitrile synthesis

3synthesis methods
Quinoline, 6-nitro-, 1-oxide

13675-92-8
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7677-24-9 Synthesis
Trimethylsilyl cyanide

7677-24-9
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$19.00/5g

6-nitroquinoline-2-carbonitrile

13675-93-9
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Yield:13675-93-9 93%

Reaction Conditions:

with tetrachloromethane;phosphonic acid diethyl ester;potassium hydroxide in 1,4-dioxane at 20; for 4 h;

Steps:

7 A method for synthesizing 6-nitro-2-cyanoquinoline includes the following steps:

6-nitro-quinoline-N-oxide (0.190 g, 1 mmol), trimethylcyanosilane (0.119 g, 1.2 mmol), diethyl H-phosphite (0.276 g, 2 mmol), carbon tetrachloride (0.308 g, 2 mmol), KOH (0.112 g, 2 mmol), 10 mL of dioxane in a 50 mL three-necked flask, and reacted at room temperature for 4 h. After the reaction was completed, the solvent was removed under reduced pressure and separated by column chromatography (petroleum Ether / ethyl acetate, V / V = 5: 1) to obtain the target compound as a yellow powder with a yield of 93% and the structural formula is as follows:

References:

CN110256342,2019,A Location in patent:Paragraph 0054-0058