ChemicalBook--->CAS DataBase List--->171178-21-5

171178-21-5

171178-21-5 Structure

171178-21-5 Structure
IdentificationBack Directory
[Name]

6-CHLORO-3-NITROPYRIDINE-2-CARBOXAMIDE
[CAS]

171178-21-5
[Synonyms]

6-CHLORO-3-NITROPYRIDINE-2-CARBOXAMIDE
2-CARBOXAMIDE-6-CHLORO-3-NITROPYRIDINE
6-chloro-3-nitro-2-PyridinecarboxaMide
2-Pyridinecarboxamide, 6-chloro-3-nitro-
6-Chloro-3-nitro-pyridine-2-carboxylic acid amide
[Molecular Formula]

C6H4ClN3O3
[MDL Number]

MFCD07780776
[MOL File]

171178-21-5.mol
[Molecular Weight]

201.57
Chemical PropertiesBack Directory
[Boiling point ]

323.6±42.0 °C(Predicted)
[density ]

1.610±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[pka]

13.58±0.50(Predicted)
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P280-P305+P351+P338
[HS Code ]

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

6-CHLORO-3-NITROPYRIDINE-2-CARBOXAMIDE(171178-21-5)1HNMR
Hazard InformationBack Directory
[Synthesis]

6-CHLORO-2-CYANO-3-NITROPYRIDINE

93683-65-9

6-CHLORO-3-NITROPYRIDINE-2-CARBOXAMIDE

171178-21-5

Step 2) Preparation of 6-chloro-3-nitropyridinecarboxamide: A mixture of 6-chloro-3-nitropyridinecarbonitrile (12 g, 65.4 mmol) and tin(II) chloride dihydrate (59 g, 262 mmol) in ethanol (144 mL) was heated to 85°C and the reaction was carried out for 3 hours. Upon completion of the reaction, the solution was concentrated under reduced pressure, diluted with the addition of water, followed by the slow addition of saturated aqueous sodium bicarbonate to adjust the pH to 8. The mixture was extracted several times with ethyl acetate, and the organic layers were combined and dried over anhydrous sodium sulfate. Finally, the organic layer was concentrated under reduced pressure to give 6-chloro-3-nitropyridinecarboxamide in quantitative yield.

[References]

[1] Patent: EP2273992, 2016, B1. Location in patent: Paragraph 0334; 0336
[2] Patent: WO2011/131741, 2011, A1. Location in patent: Page/Page column 80
[3] Patent: US2012/94976, 2012, A1. Location in patent: Page/Page column 48-49
[4] Journal of Medicinal Chemistry, 1996, vol. 39, # 9, p. 1823 - 1835
[5] Patent: US5654307, 1997, A
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