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2-PHENYL-ISONICOTINIC ACID

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2-PHENYL-ISONICOTINIC ACID Basic information

Product Name:
2-PHENYL-ISONICOTINIC ACID
Synonyms:
  • 2-PHENYLPYRIDINE-4-CARBOXYLIC ACID
  • 2-PHENYL-ISONICOTINIC ACID
  • 2-Phenyl-4-pyridinecarboxylic acid
  • 2-Phenylpyridine-4-carboxylic acid, 4-Carboxy-2-phenylpyridine
  • 4-Pyridinecarboxylic acid, 2-phenyl-
  • 2-Phenylisonicotinicaci
CAS:
55240-51-2
MF:
C12H9NO2
MW:
199.21
EINECS:
200-258-5
Product Categories:
  • Carboxylic Acids
  • Pyridines
  • API intermediates
  • Carboxylic Acids
Mol File:
55240-51-2.mol
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2-PHENYL-ISONICOTINIC ACID Chemical Properties

Melting point:
270-271 °C
Boiling point:
478.8±33.0 °C(Predicted)
Density 
1.241±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
powder to crystal
pka
1.89±0.10(Predicted)
color 
White to Orange to Green
CAS DataBase Reference
55240-51-2
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
22
HS Code 
2933399990
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2-PHENYL-ISONICOTINIC ACID Usage And Synthesis

Synthesis

66572-56-3

98-80-6

55240-51-2

Under nitrogen protection, 2-bromo-4-pyridinecarboxylic acid (0.210 g, 1.040 mmol) was dissolved in degassed 1,2-dimethoxyethane (DME, 8 mL). Tetrakis(triphenylphosphine)palladium(0) (0.060 g, 0.052 mmol) was added to the solution and the reaction mixture was stirred for 15 minutes. Subsequently, aqueous potassium carbonate (4.16 mL, 8.32 mmol) and phenylboronic acid (0.171 g, 1.403 mmol) were added. The reaction mixture was refluxed at 95 °C for 18 h, after which it was cooled to room temperature. The reaction mixture was filtered through diatomaceous earth and the pH was adjusted to 3-4 with acid to precipitate a white precipitate, which was filtered and washed with water. The white powdery product 2-phenyl-pyridine-4-carboxylic acid was obtained by recrystallization from 2-methoxyethanol. Yield: 0.106 g, 57% yield. The product was characterized by 1H NMR (400 MHz, DMSO-d6): δ 7.44-7.60 (m, 3H), 7.71-7.86 (dd, J = 4.9, 1.5 Hz, 1H), 8.05-8.19 (m, 2H), 8.23-8.35 (t, J = 1.2 Hz, 1H), 8.79-8.93 (dd, J = 5.1, 0.8 Hz, 1H), 13.56-13.97 (s, 1H).UPLC-ESI analysis: retention time 1.37 min, m/z 200.5 [M + H]+ (purity 92%).

References

[1] Organic Letters, 2016, vol. 18, # 23, p. 6094 - 6097
[2] Patent: US2014/357650, 2014, A1. Location in patent: Paragraph 0456; 0457; 0458; 0459
[3] Journal of Medicinal Chemistry, 2014, vol. 57, # 7, p. 3053 - 3074
[4] Patent: WO2011/32269, 2011, A1. Location in patent: Page/Page column 34
[5] Patent: US2005/54627, 2005, A1. Location in patent: Page/Page column 44

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