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Chemical Structure| 79491-48-8 Chemical Structure| 79491-48-8

Structure of 79491-48-8

Chemical Structure| 79491-48-8

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Product Details of [ 79491-48-8 ]

CAS No. :79491-48-8
Formula : C7H7BrN2O4
M.W : 263.05
SMILES Code : O=[N+]([O-])C1=CC(OC)=C(N=C1Br)OC
MDL No. :N/A

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Application In Synthesis of [ 79491-48-8 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 79491-48-8 ]

[ 79491-48-8 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 79491-46-6 ]
  • [ 79491-48-8 ]
  • 2
  • [ 124-41-4 ]
  • [ 79491-46-6 ]
  • [ 79491-48-8 ]
YieldReaction ConditionsOperation in experiment
89% In methanol; at 20℃; for 1.0h; To a solution of Compound 138 (200 mg, 0.64 mmol) in anhyd MeOH (6 mL) was added NaOMe (46 mg, 0.85 mmol). The reaction mixture was stirred at room temperature for 1 h and then concentrated under vacuum. The resulting residue was washed with water and filtered. The collected solids were washed with ice cold water and dried under vacuum to give Compound 139 (150 mg, 89% yield).
In methanol; at 20℃; for 1.0h; E4. 2-Bromo-5,6-dimethoxy-3-nitropyridine 20 g of <strong>[79491-46-6]2,6-dibromo-3-methoxy-5-nitropyridine</strong> (example E3) are dissolved in 550 ml of anhydrous methanol at 30-40 C. 4.6 g sodium methoxide dissolved in 30 ml anhydrous methanol is added to this solution. The reaction mixture is stirred for one hour at room temperature, poured into 700 ml of water and stored in the refrigerator overnight. The precipitate is filtered, washed with ice cold water and dried under vacuum to yield the title compound. 1H NMR (400 MHz, CDCl3): delta = 3.95 (s, 3H), 4.12 (s, 3H), 7.69 (s, 1 H). 13C NMR (100 MHz, CDCl3): delta = 55.68, 56.73, 115.33, 121.89, 143.18, 155.10.
  • 3
  • [ 67-56-1 ]
  • [ 79491-46-6 ]
  • [ 79491-48-8 ]
YieldReaction ConditionsOperation in experiment
83% With sodium methylate; at 20℃; for 16.0h; Sodium methoxide (0.5M in methanol; 11.4 mL, 5.71 mmol) was added to a slurry of <strong>[79491-46-6]2,6-dibromo-3-methoxy-5-nitropyridine</strong> (34b; 1.62 g, 5.19 mmol) in anhydrous MeOH (20 mL), and the resulting mixture was stirred at ambient temperature for 16 h, then cooled to 0 C and diluted with water (30 mL). The cold mixture was vacuum filtered and the collected solid was rinsed with ice-cold MeOH (10 mL). The collected solid was then dried in vacuo to give 2-bromo-5,6-dimethoxy-3-nitropyridine (1.14 g, 4.33 mmol, 83% yield) as a light-yellow solid.
 

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