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Chemical Structure| 610794-16-6 Chemical Structure| 610794-16-6

Structure of 610794-16-6

Chemical Structure| 610794-16-6

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Product Details of [ 610794-16-6 ]

CAS No. :610794-16-6
Formula : C10H10BrN
M.W : 224.10
SMILES Code : CC1=C(Br)C2=C(N(C)C=C2)C=C1

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Application In Synthesis of [ 610794-16-6 ]

* 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 [ 610794-16-6 ]

[ 610794-16-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 610794-15-5 ]
  • [ 74-88-4 ]
  • [ 610794-16-6 ]
YieldReaction ConditionsOperation in experiment
92% NaH (60% in oil, 81.4 mg, 3.39 mmol) is added to a RT solution of 4-bromo-5-methyl-1 H-indole (500 mg,2.26 mmol) in DMF (5 mL). It is stirred at RT for 20 min and iodomethane (0.156 mL, 2.49 mmol) is added. The RM is stirred at RT for 3h. Water is added, and the mixture is extracted twice with EtOAc. Combined organic layers are washed with brine, dried (MgSCXi), filtered and concentrated under reduced pressure. The residue is purified by FC (heptane:EtOAc, 1 :0 to 7:3), affording the title compound as a beige solid (464 mg, 92%). LC-MS B: tR = 1.02 min; [M+H]+ = 226.2.
STEP B. PREPARATION OF 4-BROMO-1, 5-DIMETHYL-lH-INDOLE A solution of <strong>[610794-15-5]4-bromo-5-methylindole</strong> (3.55g, 16. 9mmol) (21) in 10 ml of anhydrous DMF is added to a suspension of sodium hydride (l. Olg, 60% in mineral oil, 25.3 mmol, 1.5 eq. ) in 10 ml of DMF under nitrogen at 0C. The resulting mixture is stirred at 0C for 30 minutes, and then warmed to room temperature. After stirring at room temperature for an additional 2 hours, the reaction mixture is cooled to 0C. Iodomethane (2.40g, 18.6mmol, 1.1 eq. ) is added dropwise, the mixture is stirred at 0C for 2 hours, and then is warmed to 50C and stirred for an additional 2 hours. The reaction mixture is poured into 100ml of ice-water, extracted with ethyl acetate (30 ml x 3), washed with water and brine dried over anhydrous sodium sulfate. The solvent is evaporated and the product (22) is taken to dryness under high vacuum to give 3.75g of pure compound.'H NMR (400 MHz, CDC13) 8 7.17 (1H, d, J = 8.4 Hz), 7.08 (1H, d, J = 8.4 Hz), 7.05 (1H, 4, J = 3.2 Hz), 650 (1H, dd, J = 0.4, 2.8 Hz), 3.77 (3H, 3), 2.51 (3H, s); MS (+VE) m/z 224 (M+).
 

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