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Chemical Structure| 1019780-48-3 Chemical Structure| 1019780-48-3

Structure of 1019780-48-3

Chemical Structure| 1019780-48-3

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Product Details of [ 1019780-48-3 ]

CAS No. :1019780-48-3
Formula : C9H8BrN3
M.W : 238.08
SMILES Code : BrC1=NC=C(CN2C=CN=C2)C=C1
MDL No. :MFCD25954275

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Application In Synthesis of [ 1019780-48-3 ]

* 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 [ 1019780-48-3 ]

[ 1019780-48-3 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 288-32-4 ]
  • [ 101990-45-8 ]
  • [ 1019780-48-3 ]
YieldReaction ConditionsOperation in experiment
71% With potassium carbonate; In N,N-dimethyl-formamide; Step 1: Synthesis of 5- ((1H-imidazol- 1-yl)methyl)-2-bromopyridine. The starting material 2-bromo-5-(bromomethyl)pyridine was synthesized according to a published protocol (Tetr. Lett. 2002, 43, 1697). To a stirring solution ofthis compound (2 g, 8 mmol) in 20 mL of DMF was added imidazole (537 mg, 8 mmol, 1 eq) and K2C03 (3.32 g, 24 mmol, 3 eq) and stirred overnight. The reaction was concentrated in vacuo. The crude mixture was disolved in EtOAc and 10 mL of 10% citric acid and extracted. The organic layer was washed with H20 then brine, dried with Mg504, concentrated in vacuo, and purified byautomated chromatography to yield 1.35 g of an off-white solid (71% yield, R 0.30 in 10% MeOH in DCM). 1H NMR (400 MHz, CDCN) d 8.26 (d, J 2.4 Hz,111), 7.61 (s, 1H), 7.51 (d, J- 8.2 Hz, 1H), 7.45 (dd, J= 8.3, 2.5 Hz, 1H), 7.04 (s,1H), 6.97 (s, 1H), 5.15 (s, 2H).
60% With 18-crown-6 ether; potassium carbonate; In acetonitrile;Reflux; Synthesized using 1 b (1.32 g, 5.26 mmol), imidazole (0.75 g, 1 1.00 mmol), K2C03 (1.13 g, 8.16 mmol) and 18-crown-6 according to Method B. Yellow solid. Yield: 0.75 g, 60 %. 1 H NMR (CDCI3, 500 MHz): δΗ (ppm) = 5.12 (s, 2H), 6.88 (t, J = 1.2 Hz, 1 H), 7.13 (s, 1 H), 7.28 (d, J = 2.5 Hz, 1 H), 7.48 (d, J = 8.5 Hz, 1 H),7.56 (s, 1 H), 8.28 (d, J = 2.5 Hz, 1 H); MS (ESI): m/z = 239.08 [M+H]+.The cr-brominated compounds, imidazole (2 eq), a catalytic amount of 18-crown-6 and anhydrous K2C03 (1.5 eq) in dry acetonitrile were heated under reflux overnight. After cooling, water (50 ml_) was added, and the aqueous layer was extracted with ethyl acetate (3 x 30 ml_). The combined organic layers were washed with brine (25 ml_), dried over Na2S04 and evaporated in vacuo. The crude product was purified by column chromatography on silica-gel, using 5% methanol in ethyl acetate.
  • 2
  • [ 1019780-48-3 ]
  • [ 22237-12-3 ]
  • [ 1311148-75-0 ]
 

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