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4,6-Dihydroxy-5-nitropyridine-3-carboxylic acid ethyl ester

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4,6-Dihydroxy-5-nitropyridine-3-carboxylic acid ethyl ester Basic information

Product Name:
4,6-Dihydroxy-5-nitropyridine-3-carboxylic acid ethyl ester
Synonyms:
  • 4,6-Dihydroxy-5-nitropyridine-3-carboxylic acid ethyl ester
  • 4,6-Dihydroxy-5-nitronicotinic acid ethyl ester
  • Ethyl 4,6-dihydroxy-5-nitronicotinate
  • Nsc25750
  • ethyl 4,6-dihydroxy-5-nitropyridine-3-carboxylate
  • 3-Pyridinecarboxylic acid, 1,6-dihydro-4-hydroxy-5-nitro-6-oxo-, ethyl ester
  • Ethyl4,6-dihydroxy-5-nitronicotinate,97%
  • 4,6-Dihydroxy-5-nitropyridine-3-carboxylic acid ethyl ester ISO 9001:2015 REACH
CAS:
6317-97-1
MF:
C8H8N2O6
MW:
228.16
EINECS:
604-604-1
Mol File:
6317-97-1.mol
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4,6-Dihydroxy-5-nitropyridine-3-carboxylic acid ethyl ester Chemical Properties

Melting point:
243-246°
Boiling point:
325.7±42.0 °C(Predicted)
Density 
1.55±0.1 g/cm3(Predicted)
storage temp. 
2-8°C
pka
4.50±1.00(Predicted)
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Safety Information

Hazard Codes 
Xi
HazardClass 
IRRITANT
HS Code 
2933399990
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4,6-Dihydroxy-5-nitropyridine-3-carboxylic acid ethyl ester Usage And Synthesis

Synthesis

6975-44-6

6317-97-1

Step 2: Preparation of ethyl 4,6-dichloro-5-nitronicotinate (15) To a solution of concentrated sulfuric acid (330 ml) of ethyl 4,6-dihydroxynicotinate (14) (40.0 g, 0.22 mol) cooled to 0°C, fuming nitric acid (12.7 ml) was added dropwise slowly. After the dropwise addition was completed, the reaction mixture was stirred at 0°C for 1 hour, then brought to room temperature and continued stirring for 1 hour. After completion of the reaction, the mixture was slowly poured into ice water and stirred vigorously for 10 minutes. The precipitate precipitated was collected by filtration, washed well with water and dried under vacuum to give a light yellow solid product 15 (38.7 g, 77.6% yield). The melting point of the product was 238-240 °C. 1H NMR (300 MHz, DMSO-d6) δ (ppm): 8.22 (s, 1H), 4.31 (q, J = 7.0 Hz, 2H), 1.29 (t, J = 7.0 Hz, 3H). MS (ESI (+) 70V) m/z: 227 [M-H]-.

References

[1] Bioorganic and Medicinal Chemistry, 2015, vol. 23, # 20, p. 6551 - 6559
[2] Patent: WO2008/17696, 2008, A1. Location in patent: Page/Page column 51
[3] Patent: WO2009/106419, 2009, A1. Location in patent: Page/Page column 79
[4] Patent: WO2008/17696, 2008, A1. Location in patent: Page/Page column 51
[5] Recueil des Travaux Chimiques des Pays-Bas, 1948, vol. 67, p. 29,37

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