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Chemical Structure| 327990-62-5 Chemical Structure| 327990-62-5

Structure of 327990-62-5

Chemical Structure| 327990-62-5

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Product Details of [ 327990-62-5 ]

CAS No. :327990-62-5
Formula : C12H13BrN2
M.W : 265.15
SMILES Code : NC1C(NC2=C3C=C(Br)C=C2)=C3CCC1
MDL No. :MFCD00470092

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Application In Synthesis of [ 327990-62-5 ]

* 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 [ 327990-62-5 ]

[ 327990-62-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 59514-18-0 ]
  • [ 327990-62-5 ]
YieldReaction ConditionsOperation in experiment
50% With ammonium acetate; sodium cyanoborohydride; In methanol; at 60℃; 6-Bromo-2,3,4,9-tetrahydro-1H-carbazol-1-one (250 mg, 0.95 mmol), ammoniumacetate (732 mg, 9.5 mmol) and sodium cyanoborohydride (298 mg, 4.75 mmol) were dissolved in methanol (5 mL). The reaction mixture was stirred for overnight at 60 C. After removal of the solvent, the reaction mixture was diluted with ethyl acetate. The organic layer was washed with 10% NaOH and brine, and it was dried over Na2SO4. The organic layer was concentratedunder reduced pressure. The residue was purified on an ISCO chromatograph (0-10% methanol/dichloromethane + 0.1% NH4OH) to give the product as a white solid (127 mg, 50%);?H NIVIR (300 IVIHz) (CD3OD) 7.49 (s, 1H), 7.19 (d, J= 9Hz, 1H), 7.12 (dd, J 9Hz, J = 2Hz, 1H), 4.05 (t, J= 6Hz, 1H), 2.62 (t, J= 6Hz, 2H), 2.19-1.99 (m, 2H), 1.82-1.66 (m, 2H); LC/MS RT = 2.62 (M-H: 263/265).
General procedure: Solid NH4OAc (5.0 mmol) was added to a stirring solution of requisite ketone iii (0.5 mmol) dissolved in 20 mL solvent grade CH3OH, and this mixture was allowed to stir at room temperature (23 C) for 3-6 h. Upon complete consumption of iii, as determinedby thin layer chromatography, solid NaCNBH3 (2.5 mmol) was added andthe temperature was raised to 60 C. After stirring 12-16 h, the reaction was cooled to room temperature (23 C) and treated with an aqueous 1 M HCl solution. The mixture was extracted with ethyl acetate, and the combined organic layers were washed with brine and dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure to afford the crude product. The desired product was purified by flash column chromatography (SiO2) using CH2Cl2 and CH3OH as the eluent. NMR of products were compared to literature values to confirm structure.
 

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