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Chemical Structure| 122481-11-2 Chemical Structure| 122481-11-2

Structure of 122481-11-2

Chemical Structure| 122481-11-2

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Product Details of [ 122481-11-2 ]

CAS No. :122481-11-2
Formula : C3H4BrN3
M.W : 161.99
SMILES Code : NN1C=C(Br)C=N1
MDL No. :MFCD16620056

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Application In Synthesis of [ 122481-11-2 ]

* 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 [ 122481-11-2 ]

[ 122481-11-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 122481-11-2 ]
  • [ 114078-88-5 ]
YieldReaction ConditionsOperation in experiment
8.8 g With sodium periodate; In dichloromethane; water; at 0℃; for 12.0h; One step up the crude was added methylene chloride (200 mL) and water (76 mL), cooled to 0 , sodium periodate (29.4g, 137mmol) with stirring. After the addition was complete the reaction was stirred for 12 hours 0 . Warmed to 25 , liquid separation, the aqueous phase was extracted with dichloromethane (100mL × 3), the organic phases were combined, saturated brine (250mL), dried over anhydrous sodium sulfate, filtered, and the filtrate was concentrated and the crude product was purified by silica gel column chromatography (petroleum ether: ethyl acetate = 10: 1) gave the title compound as a white solid (8.8g, yield 73.5% in two steps).
710 mg With sodium periodate; In dichloromethane; water; at 20℃; for 16.0h; To a solution of compound S2 (1 g, crude) in DCM (15 mL) and water (5 mL) was added NaIO4(2 g, 9.3 mmol). The reaction was stirred at room temperature for 16 hrs. The mixture was diluted with DCM and washed with water, brine, dried over anhydrous Na2SO4, filtered, and concentrated. The residue was purified by silica gel column (eluted with EtOAc/PE=1/5) to give the title compound (710 mg, 65.2% yield) as a purple solid.
With sodium periodate; In dichloromethane; water; at 0℃; for 4.0h; A solution of crude 4-bromopyrazol-l-amine (20.0 g, crude) in DCM (500 mL) and water (200 mL) was cooled to 0 C. To the solution was added NaI04 (52.8 g, 246.93 mmol). The resulting mixture was stirred at 0 C for 4 hrs and extracted with DCM (100 mL) for three times. The combined organic layer was washed with brine (100 mL), dried over anhydrous Na2S04 and concentrated in vacuo to give 5-bromotriazine (20.0 g) as brown solid, which was used in next step directly without any further purification
 

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