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ChemicalBook CAS DataBase List 4-ethoxy-1-(4-fluorophenyl)-2-oxo-1,2-dihydropyridine-3-carboxylicacid

4-ethoxy-1-(4-fluorophenyl)-2-oxo-1,2-dihydropyridine-3-carboxylicacid synthesis

8synthesis methods
ethyl 4-ethoxy-1-(4-fluorophenyl)-2-oxo-1,2-dihydropyridine-3-carboxylate

1174046-87-7
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4-ethoxy-1-(4-fluorophenyl)-2-oxo-1,2-dihydropyridine-3-carboxylicacid

1174046-90-2
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Yield: 84%

Reaction Conditions:

with lithium hydroxide monohydrate in ethanol;water at 70;

Steps:

1.3 Step 3: Synthesis of 4-ethoxy-1-(4-fluorophenyl)-2-oxo-1,2-dihydropyridine-3-carboxylic acid
The compound obtained in step 2 (1.5 g, 4.91 mmol) was dissolved in 15 mL of ethanol and 10 mL of water, and then lithium hydroxide monohydrate (0.82 g, 19.6 mmol) was added at room temperature and stirred at 70 ° C for 3 hours or more. It was. After cooling to room temperature, the solvent was concentrated under reduced pressure, and 1N hydrochloric acid aqueous solution was slowly added dropwise at 0 ° C. to maintain a pH of 2.0. The resulting solid was filtered, washed with water and dried to give the title compound (1.1 g, yield: 84%, white solid).

References:

Welmakeo Bio Co., Ltd.;Lee Hyeon-ho;Park Jun-ho;Huh Seon-cheol;Moon Jae-hui;Shin Jae-sik;Hong Seung-u;Park Yun-seon;Kim Yo-sep;Lee So-hui;Kim Hyo-jin;Park Hye-bin KR2019/106802, 2019, A Location in patent:Paragraph 0171; 0180-0183

1174046-84-4 Synthesis
Ethyl 4-Ethoxy-2-oxo-1,2-dihydropyridine-3-carboxylate

1174046-84-4
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4-ethoxy-1-(4-fluorophenyl)-2-oxo-1,2-dihydropyridine-3-carboxylicacid

1174046-90-2
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35260-93-6 Synthesis
ethyl 2-cyano-3-ethoxycrotonate

35260-93-6
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4-ethoxy-1-(4-fluorophenyl)-2-oxo-1,2-dihydropyridine-3-carboxylicacid

1174046-90-2
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1345855-03-9 Synthesis
ethyl 2-cyano-5-(dimethylamino)-3-ethoxypenta-2,4-die

1345855-03-9
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4-ethoxy-1-(4-fluorophenyl)-2-oxo-1,2-dihydropyridine-3-carboxylicacid

1174046-90-2
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