Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Pharmaceutical intermediates >  Heterocyclic compound >  Pyridine compound >  Pyridine derivatives >  2-METHYL HYDROGEN PYRIDINE-2,5-DICARBOXYLATE

2-METHYL HYDROGEN PYRIDINE-2,5-DICARBOXYLATE

Basic information Safety Supplier Related

2-METHYL HYDROGEN PYRIDINE-2,5-DICARBOXYLATE Basic information

Product Name:
2-METHYL HYDROGEN PYRIDINE-2,5-DICARBOXYLATE
Synonyms:
  • 2-METHYL HYDROGEN PYRIDINE-2,5-DICARBOXYLATE
  • 6-(METHOXYCARBONYL)NICOTINIC ACID
  • (Methoxycarbonyl)pyridine-3-carboxylic acid
  • 5-Carboxy-2-(methoxycarbonyl)pyridine, 6-(Methoxycarbonyl)pyridine-3-carboxylic acid
  • 6-(Methoxycarbonyl)pyridine-3-carboxylic acid
  • 2,5-Pyridinedicarboxylic acid, 2-methyl ester
  • 6-Methoxycarbonylpyridine-3-carboxylicaci
  • 2-Methylhydrogenpyridin-2,5-dicarboxylic acid
CAS:
17874-76-9
MF:
C8H7NO4
MW:
181.15
Product Categories:
  • Esters
  • Pyridines
Mol File:
17874-76-9.mol
More
Less

2-METHYL HYDROGEN PYRIDINE-2,5-DICARBOXYLATE Chemical Properties

Melting point:
161.5 °C(Solv: methanol (67-56-1))
Boiling point:
383.8±27.0 °C(Predicted)
Density 
1.361±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
form 
Solid
pka
3.04±0.10(Predicted)
Appearance
White to off-white Solid
More
Less

Safety Information

HS Code 
2933399990
More
Less

2-METHYL HYDROGEN PYRIDINE-2,5-DICARBOXYLATE Usage And Synthesis

Synthesis

67-56-1

100-26-5

17874-76-9

The general procedure for the synthesis of 6-(methoxycarbonyl)nicotinic acid from methanol and 2,5-dipyridinecarboxylic acid is as follows: with reference to the literature method 66, a selective esterification reaction was first carried out on 2,5-pyridinedicarboxylic acid (58). 58 was dissolved in methanol, a catalytic amount of sulfuric acid was added and the reaction was refluxed for 2 hours. Upon completion of the reaction, the monomethyl ester product (59) was purified by recrystallization from water in 42% yield. Subsequently, the monomethyl ester 59 was converted to the corresponding acyl chloride (60) by reflux reaction with an excess of thionyl chloride. Finally, the acylation of compound 35 was completed using the reflux reaction of the chloride 60 with an excess of aluminum trichloride in dichloromethane (DCM) (Scheme 10).

References

[1] Patent: WO2011/103321, 2011, A1. Location in patent: Page/Page column 23
[2] Patent: US2006/293319, 2006, A1. Location in patent: Page/Page column 47
[3] Patent: WO2007/70173, 2007, A2. Location in patent: Page/Page column 145-146
[4] European Journal of Inorganic Chemistry, 2010, # 13, p. 1913 - 1928
[5] Patent: WO2012/121973, 2012, A1. Location in patent: Page/Page column 89

2-METHYL HYDROGEN PYRIDINE-2,5-DICARBOXYLATESupplier

Beijing HwrkChemical Technology Co., Ltd
Tel
18515581800 18501085097
Email
sales.bj@hwrkchemical.com
Beijing Ouhe Technology Co., Ltd
Tel
010-010-82967028 13522913783
Email
2355560935@qq.com
ChemCell Biomedicine Co.,Ltd.
Tel
020-13556033878 2965585218 13556033878
Email
chemcell@hotmail.com
Syntechem Co.,Ltd
Tel
Email
info@syntechem.com
Shanghai Sunway Pharmaceutical Technology Co., Ltd
Tel
18270980682
Email
mlcheng@sunwaypharm.cn