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Chemical Structure| 64197-01-9 Chemical Structure| 64197-01-9

Structure of 64197-01-9

Chemical Structure| 64197-01-9

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Product Details of [ 64197-01-9 ]

CAS No. :64197-01-9
Formula : C6H3BrClNO
M.W : 220.45
SMILES Code : O=C(Cl)C1=NC=CC(Br)=C1
MDL No. :MFCD25965711

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Application In Synthesis of [ 64197-01-9 ]

* 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 [ 64197-01-9 ]

[ 64197-01-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 74-89-5 ]
  • [ 64197-01-9 ]
  • [ 1209459-88-0 ]
YieldReaction ConditionsOperation in experiment
52% In tetrahydrofuran; at 20℃; for 2h;Cooling with ice; 4.1.14 4-Bromo-N-methylpyridine-2-carboxamide (18) Compound (17) dissolved in anhydrous tetrahydrofuran was added dropwise to methylamine solution (8 mL), after the action was complete, the ice-bath was removed and the reaction was reacted at room temperature for 2 h. The product was extracted with AcOEt (30 mL * 3), washed twice with water and brine, and dried over Na2SO4. After filtration and concentration in vacuo, the residues was purified by silica gel flash chromatography (PE/AcOEt = 3:1) gave (18) (0.87 g, 52%) as white solid.
1.5 g In tetrahydrofuran; at 0 - 20℃; To a stirred solution of 5-1 (2.0 g, 9.09 mmol) in THF (20 mL) was added methylamine (2 M in THF) solution at 0C. After being stirred at rt overnight, the mixture was concentrated under reduced pressure. The resulting residue was dissolved in EtOAc and washed with water. The organic layer was dried over Na2SO4 and concentrated under reduced pressure to afford 5-2 (1.5 g, 70% over 2 steps) which was used in the next step without further purification.
 

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