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Structure of 909397-79-1

Chemical Structure| 909397-79-1

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Product Details of [ 909397-79-1 ]

CAS No. :909397-79-1
Formula : C13H12BrNO4
M.W : 326.14
SMILES Code : O=C(C(Br)=C1)N(CC2=CC=C(OC)C(OC)=C2)C1=O
MDL No. :MFCD31725180

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Application In Synthesis of [ 909397-79-1 ]

* 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 [ 909397-79-1 ]

[ 909397-79-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 5926-51-2 ]
  • [ 5763-61-1 ]
  • [ 909397-79-1 ]
YieldReaction ConditionsOperation in experiment
79% With acetic acid; at 80℃; for 3h; General procedure: 3-Bromomaleic anhydride (1.0 equiv, 5.65 mmol, 1.0 g) wasdissolved in AcOH (20 mL). Methylamine hydrochloride(1.0 equiv, 5.65 mmol, 0.37 g) was then added, and thereaction was heated at 80 °C for 3 h. Solvent was removed invacuo, and the crude mixture was purified by columnchromatography over silica gel (EtOAc?hexane 0?30percent)using an ISCOTM purification system to afford 0.97 g of awhite solid (90percent yield).
67% Example XI Preparation of l-Aryl-3-aza-bicyclo[3.1.0]hexane hydrochlorides Using Reaction Scheme 17 A. Synthesis of 3-Bromo-l-(3.4-dimethoxybenzyl)maleimide A solution of <strong>[5926-51-2]bromomaleic anhydride</strong> (Aldrich, 20.0 g, 0.113 mole) in anhydrous tetrahydrofuran (100 mL) under nitrogen was treated dropwise with a solution of 3,4-dimethoxybenzylamine (20.0 g, 0.1196 mole) in anhydrous THF (40 mL) over 30 min, and the stirred mixture was then refluxed for 3 h and maintained at room temperature for 20 h. The mixture was concentrated in vacuo, suspended in acetic anhydride (135 mL), treated with anhydrous sodium acetate (6.15 g, 75 mmol), and heated to 5O0C with stirring under nitrogen for 4 h (solids dissolved after a few minutes). The mixture was concentrated in vacuo and dissolved in methylene chloride (300 mL). The solution was washed with saturated aqueous sodium bicarbonate (150 mL), then with water (150 mL), dried (Na2SO4), and concentrated in vacuo to a brown residue. This was dissolved in methylene chloride and passed through a column of silica gel (~400 mL EPO <DP n="124"/>volume) and eluted with methylene chloride to afford a tan solid, which was recrystallized from ethyl acetate/heptane (2 crops) to afford 3-bromo-l-(3,4- dimethoxybenzyl)maleimide (24.75 g, 67percent) as a pale tan solid. NO MS (M+l) peak. 1H NMR (CDCl3) delta 6.89-6.94 (m, 2H), 6.84 (s, IH), 6.78 (d, IH, J=8Hz), 4.63 (s, 2H), 3.86 (s, 3H), 3.84 (s, 3H).
67% Example XII Preparation of l-(4-Trifluoromethoxyphenyl)-3-azabicvclo[3.1 ,0]hexane, hydrochlorideUsinfi Reaction Scheme 17A. Synthesis of 3-Bromo-l-(3,4-dimethoxybenzyl)maIeimide EPO <DP n="104"/>A solution of <strong>[5926-51-2]bromomaleic anhydride</strong> (Aldrich, 20.0 g, 0.113 mole) in anhydrous tetrahydrofuran (100 mL) under nitrogen was treated dropwise with a solution of 3,4-dimethoxybenzylamine (20.0 g, 0.1196 mole) in anhydrous THF (40 mL) over 30 min, then the stirred mixture was refluxed for 3 h and maintained at room temperature for 20 h. The mixture was concentrated in vacuo, suspended in acetic anhydride (135 mL), treated with anhydrous sodium acetate (6.15 g, 75 mmol), and heated to 5O0C with stirring under nitrogen for 4 h (solids dissolved after a few minutes). The mixture was concentrated in vacuo and dissolved in methylene chloride (300 mL). The solution was washed with saturated aqueous sodium bicarbonate (150 mL), then with water (150 mL), dried (Na2SO4), and concentrated in vacuo to a brown residue. This was dissolved in methylene chloride and passed through a column of silica gel (-400 mL volume) and eluted with methylene chloride to afford a tan solid, which was recrystallized from ethyl acetate/heptane (2 crops) to afford 3-bromo-l-(3,4-dimethoxybenzyl)maleimide (24.75 g, 67percent) as a pale tan solid. NO MS (M+l) peak. 1H NMR (CDCl3) delta 6.89-6.94 (m, 2H), 6.84 (s, IH), 6.78 (d, IH, J=8Hz), 4.63 (s, 2H), 3.86 (s, 3H), 3.84 (s, 3H).
 

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