ChemicalBook--->CAS DataBase List--->25391-59-7

25391-59-7

25391-59-7 Structure

25391-59-7 Structure
IdentificationBack Directory
[Name]

2-Hydroxy-5-iodo-3-nitropyridine
[CAS]

25391-59-7
[Synonyms]

5-IODO-3-NITROPYRIDIN-2-OL
5-Iodo-3-nitropyridin-2(1H)-one
2-Hydroxy-3-nitro-5-iodopyridine
2-Hydroxy-5-iodo-3-nitropyridine
2(1H)-Pyridinone, 5-iodo-3-nitro-
[Molecular Formula]

C5H3IN2O3
[MDL Number]

MFCD09743049
[MOL File]

25391-59-7.mol
[Molecular Weight]

265.99
Chemical PropertiesBack Directory
[Melting point ]

252-256°C
[Boiling point ]

314.0±42.0 °C(Predicted)
[density ]

2.27±0.1 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[pka]

6.50±0.10(Predicted)
[Appearance]

Light yellow to yellow Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[Hazard Codes ]

Xi,Xn
[Risk Statements ]

22-36/37/38
[Safety Statements ]

26-36/37
[WGK Germany ]

3
[HazardClass ]

IRRITANT
[HS Code ]

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

2-Hydroxy-5-iodo-3-nitropyridine(25391-59-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

3-Nitro-2-pyridinol

6332-56-5

2-Hydroxy-5-iodo-3-nitropyridine

25391-59-7

3-Nitropyridin-2(1H)-one (10.3 g, 73.4 mmol, 1 eq.) was used as a raw material and suspended in a mixed solution of 46 mL acetic acid, 20 mL water, 1.4 mL concentrated sulfuric acid and periodate (3.5 g, 18 mmol, 0.25 eq.). The reaction mixture was stirred at 90 °C for 15 min until completely dissolved. Subsequently, iodine crystals (7.7 g, 30.1 mmol, 0.4 eq.) were added in batches and formation of a dense yellow precipitate was observed after 20 min of reaction. The reaction mixture was cooled to room temperature and 50 mL of saturated sodium thiosulfate solution was added to quench the reaction. The solid product was collected by filtration and washed sequentially with 50 mL of saturated sodium thiosulfate solution and water. Finally, the solid was dried under vacuum to give 5-iodo-3-nitropyridin-2-ol (XIII-2, 14 g, 72% yield).

[References]

[1] Bioorganic and Medicinal Chemistry Letters, 2012, vol. 22, # 12, p. 3973 - 3977
[2] Journal of Medicinal Chemistry, 2009, vol. 52, # 19, p. 5785 - 5788
[3] Patent: US2014/94456, 2014, A1. Location in patent: Paragraph 0656-0657
[4] Patent: WO2015/153683, 2015, A1. Location in patent: Paragraph 0413
[5] Bioorganic & Medicinal Chemistry Letters, 2003, vol. 13, # 3, p. 525 - 528
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