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ChemicalBook--->CAS DataBase List--->89694-10-0

89694-10-0

89694-10-0 Structure

89694-10-0 Structure
IdentificationMore
[Name]

2-Methoxy-5-nitro-3-picoline
[CAS]

89694-10-0
[Synonyms]

2-METHOXY-5-NITRO-3-PICOLINE
[Molecular Formula]

C7H8N2O3
[MDL Number]

MFCD04972416
[Molecular Weight]

168.15
[MOL File]

89694-10-0.mol
Chemical PropertiesBack Directory
[Appearance]

Off-white solid
[Boiling point ]

279.7±35.0 °C(Predicted)
[density ]

1.247±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

-0.34±0.20(Predicted)
[InChI]

InChI=1S/C7H8N2O3/c1-5-3-6(9(10)11)4-8-7(5)12-2/h3-4H,1-2H3
[InChIKey]

HEDKXDCXKNQWEX-UHFFFAOYSA-N
[SMILES]

C1(OC)=NC=C([N+]([O-])=O)C=C1C
[CAS DataBase Reference]

89694-10-0(CAS DataBase Reference)
Safety DataBack Directory
[HS Code ]

2933399990
Hazard InformationBack Directory
[Chemical Properties]

Off-white solid
[Uses]

2-Methoxy-3-methyl-5-nitropyridine is used in the preparation of heteroaromatic cyanoindoline derivative for use as NIK inhibitors.
[Synthesis]

2-Chloro-3-methyl-5-nitropyridine

22280-56-4

Sodium Methoxide

124-41-4

2-Methoxy-5-nitro-3-picoline

89694-10-0

1. 3-Methyl-5-nitropyridin-2-ol (134 g, 0.872 mol) was divided equally into three equal portions and placed in three 1L round bottom flasks. Phosphorus oxychloride (POCl3, 200mL) was added to each flask and the mixture was heated to reflux for 2 hours. Upon completion of the reaction, the solution was cooled and the excess POCl3 was removed under vacuum. the residue was slowly poured into ice water (1 L) under stirring, the precipitate was collected by filtration, and air-dried for 20 minutes. The products were combined and recrystallized using a hexane solution of 10% ethyl acetate (300 mL) and air dried to give 2-chloro-3-methyl-5-nitropyridine (139 g, 92% yield) as a white solid, which could be used in the next reaction without further purification. Product characterization data: 1H NMR (300MHz, CDCl3) δ 9.04 (d, J=2.5Hz, 1H), 8.33 (d, J=2.2Hz, 1H), 2.50 (s, 3H). 2. 2-Chloro-3-methyl-5-nitropyridine (139 g, 0.806 mol) prepared in the above steps was divided into two equal portions and placed in two 2L round-bottomed flasks and methanol (500 mL) was added. The solution was cooled in a dry ice/isopropanol bath and solid sodium methanol (26.5 g, 0.467 mol) was added in batches, controlling the reaction temperature below 20 °C. After the addition was completed, the mixture was heated to reflux for 1 hour. At the end of the reaction, the mixture was cooled and diluted with ice water (500 mL) to produce a white precipitate, which was collected by filtration. The combined filter cake was washed with water and air dried to give 2-methoxy-3-methyl-5-nitropyridine (127 g, 97% yield) as a white solid. Product characterization data: 1H NMR (400 MHz, CDCl3) δ 8.91 (d, J=2.0 Hz, 1H), 8.16 (s, 1H), 4.06 (s, 3H), 2.25 (s, 3H); 13C NMR (100 MHz, CDCl3) δ 165.83,141.91,139.37,132.92, 121.77,54.83,15.84. The analyzed sample was recrystallized from hexane to obtain white needle-like crystals with the melting point of 95-96.5 ℃. Elemental analysis results (C7H8N2O3): calculated value C 50.00, H 4.79, N 16.66; measured value C 49.73, H 5.02, N 16.48.

[References]

[1] Patent: US2010/29684, 2010, A1. Location in patent: Page/Page column 5; 14
[2] Journal of Medicinal Chemistry, 2009, vol. 52, # 23, p. 7653 - 7668
[3] Bioorganic and Medicinal Chemistry Letters, 2012, vol. 22, # 9, p. 3056 - 3062
Spectrum DetailBack Directory
[Spectrum Detail]

2-Methoxy-5-nitro-3-picoline(89694-10-0)1HNMR
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