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Chemical Structure| 1038408-35-3 Chemical Structure| 1038408-35-3

Structure of 1038408-35-3

Chemical Structure| 1038408-35-3

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Product Details of [ 1038408-35-3 ]

CAS No. :1038408-35-3
Formula : C9H13BrN2
M.W : 229.12
SMILES Code : NC1=CC=C(Br)C=C1NC(C)C
MDL No. :MFCD12923357

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Application In Synthesis of [ 1038408-35-3 ]

* 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 [ 1038408-35-3 ]

[ 1038408-35-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1038408-35-3 ]
  • [ 64-19-7 ]
  • [ 1038408-36-4 ]
YieldReaction ConditionsOperation in experiment
90% for 2.0h;Heating / reflux; Part D:A solution of compound 226 (0.56 g, 2.45 mmol) in acetic acid (20 mL) was stirred at reflux for 2 hours, at which time LC-MS analysis indicated that the reaction was complete. The reaction mixture was concentrated under vacuum. Purification by column chromatography (SiO2, 5% MeOH / DCM) afforded compound 227 as a red oil 0.55 g (90%). 1H NMR (400 MHz, DMSO-d6) delta 7.82 (d, 1 H), 7.44 (1 H), 7.24 (dd, 1 H), 4.75 (m, 1 H), 2.54 (s, 3H), 1.51 (d, 6H).
80.1% for 2.0h;Reflux; 5-bromo-N-isopropylbenzene-1,2-diamine (2.6 g, 11.40 mmol) was added into 117 glacial acetic acid (40 mL), and the reaction was refluxed for 2 hrs. After cooling to room temperature, acetic acid was removed under reduce pressure, the pH of the residue was adjusted to about 7 with saturated solution of 52 sodium bicarbonate, extracted with dichloromethane (50×3), the organic layer was combined, washed with brine, dried over anhydrous sodium sulfate, the filtrate was concentrated under reduced pressure, and the filtrate was separated on column chromatography (eluant:dichloromethane/methanol (v/v)=20:1) to afford 2.31 g a brown-yellow solid, yield was 80.10%, LC-MS(APCI): m/z=253.1 (M+1).
 

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