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Chemical Structure| 231950-42-8 Chemical Structure| 231950-42-8

Structure of 231950-42-8

Chemical Structure| 231950-42-8

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Product Details of [ 231950-42-8 ]

CAS No. :231950-42-8
Formula : C5H6BrN3O2
M.W : 220.02
SMILES Code : CN1C(CBr)=CN=C1N(=O)=O

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Application In Synthesis of [ 231950-42-8 ]

* 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 [ 231950-42-8 ]

[ 231950-42-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 403-01-0 ]
  • [ 231950-42-8 ]
  • [ 774233-67-9 ]
YieldReaction ConditionsOperation in experiment
With potassium carbonate; In acetone; for 4h;Heating / reflux; Into a 100 mL round-bottomed flask was added a mixture of A (100 mg), B (100 mg), K2CO3 (200 mg), and acetone (anhydrous, 1 mL). The mixture was heated to reflux for 4 hr. After the reaction was complete, the reaction mixture was poured into water (10 mL) and extracted with EtOAc (3×15 mL). The combined organic solution was washed with 5% K2CO3 (aq., 3×10 mL) to remove excess compound A and dried over Na2SO4. The dried organic solution was concentrated to yield compound C (130 mg) as a light yellow solid.
130 mg With potassium carbonate; In acetone; for 4h;Reflux; Into a 100 mL round-bottomed flask was added a mixture of A, R1 is fluoro, R2 is hydrogen (100 mg), B (100 mg), K2CO3 (200 mg) and Acetone (anhydrous, 1 mL). The mixture was heated to reflux for 4 hr. After the reaction was finished, the reaction mixture was poured into water (10 mL) and extracted with EtOAc (3x15 mL). The combined organic solution was then washed with 5% K2CO3 (aq., 3x10 mL) to remove the excess A and then dried over Na2SO4. Evaporation gave C, R1 is fluoro, R2 is hydrogen (130 mg) as a light yellow solid.
 

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