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Chemical Structure| 446284-14-6 Chemical Structure| 446284-14-6

Structure of 446284-14-6

Chemical Structure| 446284-14-6

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Product Details of [ 446284-14-6 ]

CAS No. :446284-14-6
Formula : C6H6BrNO2
M.W : 204.02
SMILES Code : COC1=CC=C(Br)C=[N+]1[O-]

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Application In Synthesis of [ 446284-14-6 ]

* 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 [ 446284-14-6 ]

[ 446284-14-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 446284-14-6 ]
  • [ 7677-24-9 ]
  • [ 1186637-43-3 ]
YieldReaction ConditionsOperation in experiment
82.7% With triethylamine; In acetonitrile; at 80.0℃; for 15.0h;Inert atmosphere; Step 2: preparation of 3-Bromo-6-methoxypicolinonitrile (3D): To a stirred solution of 2D (28 g, 137.9 mmol) in MeCN (60 ml) was added TMSCN (54.6 g, 551.6mmol) and TEA (41.8 g, 413.7). The mixture was stirred at 80C for 15 h under N2. After the reaction mixture was concentrated and water (60 mL) was added, it was extracted with EtOAc (80 mL X 2), dried over Na2S04, concentrated and purified by column (PE:EtOAc = 3:1) to give the product as white solid (24.4 g, 82.7%). NMR (400MHz, CDC13) delta 8.16 (d, J= 9.2 Hz, 1H), 7.15 (d, J= 8.8 Hz, 1H), 3.86 (s, 3H).
With triethylamine; In acetonitrile; at 100.0℃; for 14.0h; To a solution of 5-bromo-2-methoxypyridine 1-oxide (1eq) in CH3CN was added TEA (3eq) followed by TMSCN (4eq). The reaction was warmed to 100 C for 14h, and then cooled and quenched with saturated aqueous NaHCO3 and diluted with EtOAc. The layers were separated, and the organic layer was washed with sat. aq. NaHCO3, brine, dried (MgSO4) and concentrated in vacuo to give the title compound which was purified by chromatography on SiO2 (0793) (EtOAc/hex) to give the title compound. ESI-MS (m/z): 213.19 [M+1]+.
 

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