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Chemical Structure| 879014-17-2 Chemical Structure| 879014-17-2

Structure of 879014-17-2

Chemical Structure| 879014-17-2

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Product Details of [ 879014-17-2 ]

CAS No. :879014-17-2
Formula : C10H9BrN2O2
M.W : 269.10
SMILES Code : COC1=CC2=NN=CC(Br)=C2C=C1OC
MDL No. :MFCD21364503

Safety of [ 879014-17-2 ]

Application In Synthesis of [ 879014-17-2 ]

* 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 [ 879014-17-2 ]

[ 879014-17-2 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 879014-17-2 ]
  • [ 23972-42-1 ]
  • 6,7-dimethoxy-4-(2-phenylmorpholin-4-yl)cinnoline [ No CAS ]
YieldReaction ConditionsOperation in experiment
37.0% With sodium t-butanolate;tris-(dibenzylideneacetone)dipalladium(0); 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; In toluene; at 50.0℃;sealed microwave tube; [00202] Into a 10 ml sealed microwave tube was added 4-bromo-6,7- dimethoxycinnoline (99.9 mg, 0.371 mmol), 2-phenylmorpholine hydrochloride (89.6 mg, 0.449 mmol), tris(dibenzylideneacetone)dipalladium(0) (20.4 mg, 0.0223 mmol), 9,9- dimethyl-4,5-bis(diphenylphosphino)xanthane (22.8 mg, 0.0394 mmol), sodium tert-butoxide (93.8 mg, 0.976 mmol) and toluene (3 mL). The resulting red-brown suspension was stirred at 50 0C overnight, and then filtered through celite, which was washed with ethyl acetate (20 mL). The combined organics were concentrated, and the crude product was purified by column chromatography (using a gradient elution of 20-80% acetonitrile: water with 0.1% formic acid and a flow rate of 45 mL/min). The organic layer was loaded onto an SCX column (1.0 g). The SCX column was rinsed once with two column volumes of methanol and the product was eluted using 7.0 M ammonia in methanol (8 mL). Volatiles were removed in vacuo to afford 48.3 mg of 6,7-dimethoxy-4-(2-phenylmorpholin-4-yl)cinnoline (37.0 % yield). 1H NMR (CDCl3) d 8.81 (s, 1 H), 7.71 (s, 1 H), 7.40 (m, 5 H), 7.17 (s, 1 H), 4.88 (d, J = 9.0 Hz, 1 H), 4.28 (d, J = 12.0 Hz, 1 H), 4.17 (d, J = 12.0 Hz, 1 H), 4.09 (s, 6 H), 3.64 (d, J = 12.0 Hz, 1 H), 3.52 (d, J = 12.0 Hz, 1 H), 3.29 (t, J = 10.5 Hz, 1 H), 3.07 (t, J = 12.0 Hz, 1 H). LC/MS (EI) tR 4.2 min (Method B), m/z 352.1 (M++.).
  • 2
  • [ 879014-17-2 ]
  • [ 904326-92-7 ]
  • [ 1119718-08-9 ]
YieldReaction ConditionsOperation in experiment
With sodium carbonate;trans-bis(triphenylphosphine)palladium dichloride; In 1,2-dimethoxyethane; water; at 80℃; To 100 mL round-bottomed flask was added 4-bromo-6,7-dimethoxycinnoline (15.4 g, 57 mmol), <strong>[904326-92-7]6-fluoro-5-methylpyridin-3-ylboronic acid</strong> (10.1 g, 71 mmol), and trans-dichlorobis(triphenyl-phosphine)palladium (II) (3.4 g, 4.6 mmol) in 1,2-dimethoxyethane. An aqueous solution of sodium carbonate (27 g, 257 mmol) was added and the temperature was brought to 80 C. stir overnight. Upon completion, the reaction mixture was diluted with water (10 mL) and extracted with ethyl acetate. The organic extract was washed with water, saturated sodium chloride solution, dried with magnesium sulfate, filtered, and concentrated. The crude product was adsorbed onto a plug of silica gel and chromatographed through a Biotage pre-packed silica gel column eluding with a gradient of 1% to 5% methanol in dichloromethane, to provide 4-(6-fluoro-5-methylpyridin-3-yl)-6,7-dimethoxycinnoline.
With sodium carbonate;trans-bis(triphenylphosphine)palladium dichloride; In 1,2-dimethoxyethane; water; at 80℃; To 100 mL round-bottomed flask was added 4-bromo-6,7-dimethoxycinnoline (15.3809 g, 57 mmol), <strong>[904326-92-7]6-fluoro-5-methylpyridin-3-ylboronic acid</strong> (10.9899 g, 71 mmol), and trans-dichlorobis(triphenyl-phosphine)palladium (II) (3.3834 g, 4.6 mmol) in 1,2-dimethoxyethane. An aqueous solution of sodium carbonate (27 g, 257 mmol) was added and the temperature was brought to 80 C. stir overnight. Upon completion, the reaction mixture was diluted with water (10 mL) and extracted with ethyl acetate. The organic extract was washed with water, saturated sodium chloride solution, dried with magnesium sulfate, filtered, and concentrated. The crude product was adsorbed onto a plug of silica gel and chromatographed through a Biotage pre-packed silica gel column eluting with a gradient of 1% to 5% methanol in dichloromethane, to provide 4-(6-fluoro-5-methylpyridin-3-yl)-6,7-dimethoxycinnoline.
  • 3
  • [ 879014-17-2 ]
  • [ 1366482-32-7 ]
  • [ 1366482-55-4 ]
  • 4
  • [ 879014-17-2 ]
  • [ 1366482-40-7 ]
  • [ 1366482-63-4 ]
 

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