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Chemical Structure| 106791-93-9 Chemical Structure| 106791-93-9

Structure of 106791-93-9

Chemical Structure| 106791-93-9

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Product Details of [ 106791-93-9 ]

CAS No. :106791-93-9
Formula : C10H7BrClN3
M.W : 284.54
SMILES Code : NC1=NC(C2=CC=CC=C2)=C(Br)C(Cl)=N1
MDL No. :MFCD16653252

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Application In Synthesis of [ 106791-93-9 ]

* 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 [ 106791-93-9 ]

[ 106791-93-9 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 56741-95-8 ]
  • [ 106791-93-9 ]
  • 2
  • [ 36314-97-3 ]
  • [ 106791-93-9 ]
YieldReaction ConditionsOperation in experiment
With bromine; In acetic acid; Example 6 Synthesis of 5-bromo-<strong>[36314-97-3]4-chloro-6-phenyl-2-pyrimidinamine</strong>; 2-amino-5-bromo-4-chloro-6-phenylpyrimidine To 1.5 g (7.3 mM) of <strong>[36314-97-3]4-chloro-6-phenyl-2-pyrimidinamine</strong> is added 75 ml of glacial acetic acid. This mixture is stirred to dissolve and 0.44 ml of bromine is added. The reaction is stirred at ambient temperature for 24 hours. The solution is evaporated to dryness under vacuum to yield 1.75 g of 5-bromo-<strong>[36314-97-3]4-chloro-6-phenyl-2-pyrimidinamine</strong>. Calculated for C10 H7 BrClN3: C, 42.20; H, 2.48; N, 14.77; Br, 28.10; Cl, 12.46. Found: C, 42.09; H, 2.59; N, 14.68; Br, 29.90; Cl, 11.05. NMR H'-7.53.
With N-Bromosuccinimide; In N,N-dimethyl-formamide; for 1h; Compound 1e (13 g, 7.34 mmol) was dissolved in 300 mL of N,N-dimethylformamide and N-bromosuccinimide (12.38 g, 69.54 mmol) was added, and the reaction was stirred for 1 hour. The reaction was stopped, the reaction solution was poured into 1 L of water, stirred for 20 minutes, filtered, and the filter cake was dried.The crude title compound 2a (18 g) was obtained, which was used for the next step without purification.
With N-Bromosuccinimide; In N,N-dimethyl-formamide; for 1h; Compound 1a (500 mg, 2.431 mmol) and N-bromosuccinimide (519 mg, 2.918 mmol) were dissolved in 16 mL of N,N-dimethylformamide. After completion of the addition, the reaction solution was stirred for 1 hour. The reaction solution was added with 50 mL of water, and extracted with ethyl acetate (50 mL*3). The organic phases were combined, washed with water (100 mL*3) and saturated sodium chloride solution (200 mL) successively, dried over anhydrous sodium sulfate, and filtrated to collect the filtrate. The filtrate was concentrated under reduced pressure to obtain the crude title compound 2a (698 mg), which was used directly in the next step without purification.
 

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