Production Method 1

886365-43-1

794592-13-5

Reaction Conditions

1.1 Catalysts: Sulfuric acid Solvents: Ethanol ;  rt; 8 h, 80 °C

Reference

Design, synthesis and biological evaluation of pyridone-aminal derivatives as MNK1/2 inhibitors

Yuan, Xinrui; Wu, Hanshu; Bu, Hong; Zheng, Peiyuan; Zhou, Jinpei; et al, Bioorganic & Medicinal Chemistry, 2019, 27(7), 1211-1225

5-Bromo-3-Methylpyridine-2-Carboxylic Acid Ethyl Ester Raw materials

• 5-Bromo-3-methylpyridine-2-carboxylic acid

5-Bromo-3-Methylpyridine-2-Carboxylic Acid Ethyl Ester Preparation Products

• 5-Bromo-3-Methylpyridine-2-Carboxylic Acid Ethyl Ester (794592-13-5)

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• 4. Excess electrons in lithium–ethylamine solutions—density, electrical conductivity and EPR studies
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• 5. Enabling chloride salts for thermal energy storage: implications of salt purity?
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• 1048678-21-2(methyl 5-bromo-3-(bromomethyl)pyridine-2-carboxylate)
• 213771-32-5(methyl 5-bromo-3-methylpyridine-2-carboxylate)
• 77199-09-8(Ethyl 5-bromopicolinate)
• 89909-42-2(1H-Pyrrole-2-carboxylicacid, 4-bromo-3-methyl-, ethyl ester)
• 1303968-43-5(3-Bromo-7H-furo3,4-bpyridin-5-one)
• 886365-43-1(5-Bromo-3-methylpyridine-2-carboxylic acid)
• 1356037-30-3(tert-butyl 5-bromo-3-methylpyridine-2-carboxylate)
• 521980-82-5(Dimethyl 5-bromopyridine-2,3-dicarboxylate)
• 98278-78-5(3-bromo-5H,7H-furo[3,4-b]pyridine-5,7-dione)
• 110239-01-5