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2-Hydroxy-3-iodo-5-nitropyridine 97

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2-Hydroxy-3-iodo-5-nitropyridine 97 Basic information
Product Name:2-Hydroxy-3-iodo-5-nitropyridine 97
Synonyms:2(1H)-Pyridinone, 3-iodo-5-nitro-;2-Hydroxy-3-iodo-5-nitropyridine≥ 99% (HPLC);3-iodo-5-nitropyridin-2(1H)-one;3-iodo-5-nitro-1,2-dihydropyridin-2-one;2-HYDROXY-3-IODO-5-NITROPYRIDINE 97 ISO 9001:2015 REACH;3-Iodine-2-hydroxy-5-nitropyridine;2-Hydroxy-3-iodo-5-nitropyridine;3-IODO-5-NITROPYRIDIN-2-OL
CAS:25391-58-6
MF:C5H3IN2O3
MW:265.99
EINECS:
Product Categories:Pyridines;C5Heterocyclic Building Blocks;Halogenated Heterocycles;Heterocyclic Building Blocks;alcohol|alkyl Iodine|nitro-compound
Mol File:25391-58-6.mol
2-Hydroxy-3-iodo-5-nitropyridine 97 Structure
2-Hydroxy-3-iodo-5-nitropyridine 97 Chemical Properties
Melting point 203-207 °C(lit.)
Boiling point 317.9±42.0 °C(Predicted)
density 2.27±0.1 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
form solid
pka6.62±0.10(Predicted)
AppearanceLight yellow to yellow Solid
InChI1S/C5H3IN2O3/c6-4-1-3(8(10)11)2-7-5(4)9/h1-2H,(H,7,9)
InChIKeyDPHDSYLWPVMRTM-UHFFFAOYSA-N
SMILESOc1ncc(cc1I)[N+]([O-])=O
Safety Information
Hazard Codes Xn
Risk Statements 22-41
Safety Statements 26-39
WGK Germany 3
HS Code 2933399990
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
Eye Dam. 1
MSDS Information
2-Hydroxy-3-iodo-5-nitropyridine 97 Usage And Synthesis
Chemical PropertiesBrick red to brown powder
Synthesis
2-Hydroxy-5-nitropyridine

5418-51-9

2-HYDROXY-3-IODO-5-NITROPYRIDINE  97

25391-58-6

Synthesis of 3-iodo-5-nitropyridin-2-ol (CXXI): a mixture of 2-hydroxy-5-nitropyridine (14 g, 99.9 mmol) and potassium carbonate (13.8 g, 99.9 mmol) was dissolved in N,N-dimethylformamide (100 mL). Iodine (25.3 g, 99.7 mmol) was added in batches at room temperature. The reaction mixture was heated at 85 °C for 15 h and subsequently cooled to room temperature. The reaction process was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the mixture was diluted with water (150 mL) and extracted with ethyl acetate (75 mL x 3). The organic phases were combined, washed with brine (150 mL × 3), dried over anhydrous sodium sulfate, and subsequently concentrated in vacuum. The residual solid was washed with hexane (50 mL × 2) and dried under a stream of air to afford the brown solid CXXI (14 g, 53% yield), which could be used in subsequent reactions without further purification.

References[1] Australian Journal of Chemistry, 2008, vol. 61, # 6, p. 438 - 445
[2] Patent: WO2015/73528, 2015, A1. Location in patent: Page/Page column 191
[3] Journal of Medicinal Chemistry, 2002, vol. 45, # 13, p. 2841 - 2849
[4] Fortschr. Teerfarbenfabr. Verw. Industriezweige, 1930, vol. 17, p. 2439
[5] Patent: US1753170, 1926,
2-Hydroxy-3-iodo-5-nitropyridine 97 Preparation Products And Raw materials
Raw materials2-Hydroxy-5-nitropyridine-->iodine-->Potassium carbonate-->N,N-Dimethylformamide
Preparation Products2-Chloro-5-nitro-3-(trifluoromethyl)pyridine-->6-Bromo-5-iodopyridin-3-amine-->2-Chloro-3-iodo-5-nitropyridine
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