Basic information Uses Safety Supplier Related
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3-AMINO-PYRIDINE-2-CARBOXYLIC ACID AMIDE

Basic information Uses Safety Supplier Related

3-AMINO-PYRIDINE-2-CARBOXYLIC ACID AMIDE Basic information

Product Name:
3-AMINO-PYRIDINE-2-CARBOXYLIC ACID AMIDE
Synonyms:
  • 3-AMINO-PYRIDINE-2-CARBOXYLIC ACID AMIDE
  • 3-AMINOPYRIDINE-2-CARBOXAMIDE
  • 2-Pyridinecarboxamide,3-amino-(9CI)
  • 2-Pyridinecarboxamide, 3-amino-
  • 3-AMinopicolinaMide
  • 3-aMino-2-PyridinecarboxaMide
  • H66691
  • 3-Amino-pyridine-2-carboxylic acid amide 98%
CAS:
50608-99-6
MF:
C6H7N3O
MW:
137.14
EINECS:
251-156-6
Product Categories:
  • AMIDE
  • pharmacetical
Mol File:
50608-99-6.mol
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3-AMINO-PYRIDINE-2-CARBOXYLIC ACID AMIDE Chemical Properties

storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
Appearance
Off-white to yellow Solid
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Safety Information

HS Code 
2933399990
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3-AMINO-PYRIDINE-2-CARBOXYLIC ACID AMIDE Usage And Synthesis

Uses

3-Aminopyridine-2-carboxamide is an amide derivative that can be used as a pharmaceutical intermediate.

Synthesis

51674-77-2

50608-99-6

171347-62-9

General procedure for the synthesis of 4-anilino-pyrido[3,2-d]pyrimidine methanesulfonate from 4-chloropyrido[3,2-d]pyrimidine: 4-chloropyrido[3,2-d]pyrimidine (84 mg, 0.5 mmol), aniline (56 mg, 0.6 mmol), and triethylamine (62 mg, 0.6 mmol) were dissolved in ethanol (2 mL) under nitrogen protection. reflux stirring for 2 hours. Upon completion of the reaction, the crude product was purified by preparative thin layer chromatography plate (silica gel) using chloroform solution containing 3% methanol as eluent. The major bands were collected, concentrated to dryness under reduced pressure, and the residual solids were dissolved in acetone (5 mL), filtered, and methanesulfonic acid (32 μL, 0.5 mmol) was added slowly. The precipitate was collected by filtration, washed with acetone and dried in a vacuum oven to afford 4-anilino-pyrido[3,2-d]pyrimidine methanesulfonate (91 mg, 57% yield) as dark yellow needle-like crystals.1H NMR (DMSO) δ 11.75 (1H, s, br), 9.11 (1H, dd, J = 1.5, 4.3 Hz), 8.97 (1H, s ), 8.32 (1H, dd, J = 1.5, 8.4 Hz), 8.12 (1H, dd, J = 4.3, 8.5 Hz), 7.88 (2H, d, J = 8.2 Hz), 7.49 (2H, t, J = 8.0 Hz), 7.32 (1H, t, J = 7.0 Hz), 2.34 (3H, s).

References

[1] Patent: US5654307, 1997, A

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