Basic information Safety Supplier Related

5-Amino-6-chloro-3-pyridinecarboxylic acid methyl ester

Basic information Safety Supplier Related

5-Amino-6-chloro-3-pyridinecarboxylic acid methyl ester Basic information

Product Name:
5-Amino-6-chloro-3-pyridinecarboxylic acid methyl ester
Synonyms:
  • 5-Amino-6-chloro-3-pyridinecarboxylic acid methyl ester
  • 3-Pyridinecarboxylic acid, 5-aMino-6-chloro-, Methyl ester
  • 5-AMino-6-chloro-nicotinic acid Methyl ester
  • Methyl 5-aMino-6-chloropyridine-3-carboxylate
  • Methyl 5-amino-6-chloro-3-pyridinecarboxylate
  • Fampridine Impurity 231
CAS:
211915-96-7
MF:
C7H7ClN2O2
MW:
186.6
Product Categories:
  • pharmacetical
Mol File:
211915-96-7.mol
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5-Amino-6-chloro-3-pyridinecarboxylic acid methyl ester Chemical Properties

Boiling point:
328.2±37.0 °C(Predicted)
Density 
1.384±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
0.20±0.10(Predicted)
Appearance
Off-white to light yellow Solid
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Safety Information

HS Code 
2933399990
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5-Amino-6-chloro-3-pyridinecarboxylic acid methyl ester Usage And Synthesis

Synthesis

59237-53-5

211915-96-7

General procedure for the synthesis of 5-amino-6-chloronicotinic acid methyl ester from 6-chloro-5-nitronicotinic acid: a suspension of methyl 6-chloro-5-nitronicotinic acid (1 eq.), iron powder (5.2 eq.) and NH4Cl (5.3 eq.) in methanol was heated and reacted for 2 hr at 75 °C. Upon completion of the reaction, the mixture was filtered through a diatomaceous earth pad while hot and the filtrate was subsequently concentrated in vacuum to afford the target product methyl 5-amino-6-chloronicotinate in 56% yield.

References

[1] Patent: WO2010/71853, 2010, A1. Location in patent: Page/Page column 68
[2] Patent: WO2013/169704, 2013, A2. Location in patent: Paragraph 0290
[3] Patent: WO2015/95795, 2015, A1. Location in patent: Paragraph 0378

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