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Chemical Structure| 1057682-52-6 Chemical Structure| 1057682-52-6

Structure of 1057682-52-6

Chemical Structure| 1057682-52-6

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Product Details of [ 1057682-52-6 ]

CAS No. :1057682-52-6
Formula : C6H4Br2Cl2N2
M.W : 334.82
SMILES Code : ClC1=NN=C(Cl)C(CBr)=C1CBr

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Application In Synthesis of [ 1057682-52-6 ]

* 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 [ 1057682-52-6 ]

[ 1057682-52-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 34584-69-5 ]
  • [ 1057682-52-6 ]
YieldReaction ConditionsOperation in experiment
53% With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); In tetrachloromethane; for 16h;Irradiation; Heating / reflux; To a stirred solution of <strong>[34584-69-5]3,6-dichloro-4,5-dimethylpyridazine</strong> (3 g, 16.9 mmol) in 56 mL carbon tetrachloride was added with N-bromosuccinimide (9.1 g, 50.8 mmol), and AIBN (27.8 mg, 0.17 mmol) in a round bottom flask equipped with a condenser. The reaction was continuously irradiated with a 300 W light and refluxed for 16 h. The formed succimide was filtered and the filtrate was concentrated to afford the crude material. The mixture was purified by flash chromatography on silica gel, eluting with 10 - 30percent EtOAc: heptane to afford a light yellow solid (3 g, yield: 53percent). <n="108"/>1H NMR (400MHz, CDCl3): 4.61 (s, 4 H) MS (m/z, MH+): meas. 335.0 calc. 334.8
11 g With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); In tetrachloromethane; at 80℃; for 16h; Step a. To a solution of <strong>[34584-69-5]3,6-dichloro-4,5-dimethylpyridazine</strong> (CAS Number 34584-69-5, available from Accela chembio) (6 g, 33.9 mmol) in CC14 (150 ml) were added NBS (18.08 g, 101.6 mmol) and AIBN (0.055 g, 0.33 mmol) at rt. The reaction mixture was heated at 80°C for 16 h. The resulting reaction mixture was filtered and evaporated to yield 4,5-bis(bromomethyl)-3,6-dichloropyridazine (11 g, 32.8 mmol), LCMS: Method A, 2.102 min, MS: ES+ 335.18.
 

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