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ChemicalBook >  Product Catalog >  Pharmaceutical intermediates >  Heterocyclic compound >  Pyridine compound >  Aminopyridine >  5-TERT-BUTOXYCARBONYLAMINO-PYRIDINE-3-CARBOXYLIC ACID

5-TERT-BUTOXYCARBONYLAMINO-PYRIDINE-3-CARBOXYLIC ACID

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5-TERT-BUTOXYCARBONYLAMINO-PYRIDINE-3-CARBOXYLIC ACID Basic information

Product Name:
5-TERT-BUTOXYCARBONYLAMINO-PYRIDINE-3-CARBOXYLIC ACID
Synonyms:
  • 5-[(TERT-BUTOXYCARBONYL)AMINO]NICOTINIC ACID
  • 5-TERT-BUTOXYCARBONYLAMINO-PYRIDINE-3-CARBOXYLIC ACID
  • 5-TERT-BUTOXYCARBONYLAMINO-PYRIDINE-3-CARBOXYLIC A
  • 5-((tert-Butoxycarbonyl)
  • 5-(BOC-AMINO)NICOTINIC ACID
  • N-BOC-3-AMINO-PYRIDINE-5-CABOXYLIC ACID
  • 5-tert-Butoxycarbonylamino-pyridine-3-carboxylic acid ,97%
  • 5-[(2-methylpropan-2-yl)oxycarbonylamino]pyridine-3-carboxylicaci
CAS:
337904-92-4
MF:
C11H14N2O4
MW:
238.24
Mol File:
337904-92-4.mol
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5-TERT-BUTOXYCARBONYLAMINO-PYRIDINE-3-CARBOXYLIC ACID Chemical Properties

Boiling point:
360.4±27.0 °C(Predicted)
Density 
1.293±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
2.15±0.10(Predicted)
Appearance
White to light yellow Solid
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Safety Information

HS Code 
29333990
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5-TERT-BUTOXYCARBONYLAMINO-PYRIDINE-3-CARBOXYLIC ACID Usage And Synthesis

Chemical Properties

Off-white powder

Synthesis

100-26-5

337904-92-4

General procedure for the synthesis of 5-BOC-aminonicotinic acid from 2,5-pyridinedicarboxylic acid: (A) Preparation of 5-[(tert-butoxycarbonyl)amino]nicotinic acid: 2,5-pyridinedicarboxylic acid (5.00 g, 29.9 mmol) was suspended in tert-butanol (35 mL), and triethylamine (8.34 mL, 59.8 mmol) and diphenylphosphate azide ( 7.10 mL, 32.9 mmol), followed by heating the reaction mixture under reflux conditions for 3 hours. Upon completion of the reaction, it was cooled by an ice bath and the pH of the reaction mixture was adjusted to less than 10 by addition of 1N aqueous sodium hydroxide solution, followed by washing with ether. The reaction mixture was again cooled in an ice bath and the pH was adjusted with 1N aqueous sodium hydroxide solution to about 4. The precipitated solid was collected by filtration and washed sequentially with water and ether to give 5-BOC-aminonicotinic acid as a white powder (3.27 g, 45.9% yield).1H-NMR (DMSO-d6) δ: 1.49 (9H, s), 8.45 (1H, s ), 8.66 (1H, s), 8.75 (1H, s), 9.83 (1H, br).

References

[1] Patent: EP1227084, 2002, A1

5-TERT-BUTOXYCARBONYLAMINO-PYRIDINE-3-CARBOXYLIC ACID Preparation Products And Raw materials

Raw materials

5-TERT-BUTOXYCARBONYLAMINO-PYRIDINE-3-CARBOXYLIC ACIDSupplier

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