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Chemical Structure| 1190380-46-1 Chemical Structure| 1190380-46-1

Structure of 1190380-46-1

Chemical Structure| 1190380-46-1

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Product Details of [ 1190380-46-1 ]

CAS No. :1190380-46-1
Formula : C19H14N4
M.W : 298.34
SMILES Code : C12=NC=NN1C=C(N=C(C3=CC=CC=C3)C4=CC=CC=C4)C=C2

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Application In Synthesis of [ 1190380-46-1 ]

* 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 [ 1190380-46-1 ]

[ 1190380-46-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 356560-80-0 ]
  • [ 1013-88-3 ]
  • [ 1190380-46-1 ]
YieldReaction ConditionsOperation in experiment
95.8% With tris-(dibenzylideneacetone)dipalladium(0); 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; sodium t-butanolate; In toluene; at 100℃; for 4h; To a solution of 6-bromo-[l,2,4]triazolo[1,5-a]pyridine (700 mg, 3.5350 mmol), diphenylmethanimine (1.28 g, 7.06 mmol) and t-BuONa (680 mg, 7.076 mmol) in toluene (50 mL) were added BINAP (221 mg, 0.3549 mmol) and Pd2(dba)3 (167 mg, 0.1769 mmol). The mixture was degassed for 5 min and refilled with N2 and then stirred at 100 C for 4 h. The reaction was quenched with water (100 mL), and extracted with EtOAc (100 mLx 3). The combined organic layers were dried over anhydrous Na2S04, filtered, and concentrated in vacuo. The residue was purified by silica gel column chromatography (PE/EtOAc (v/v) = 5/1 to 1/1) to give the title compound as a yellow solid (1.01 g, 95.8%) .MS (ESI, pos. ion) m/z: 299.2 [M+H]+;1H NMR (400 MHz, CDCl3) d (ppm): 8.21 (s, 1H), 8.04 (d, 7 = 1.2 Hz, 1H), 7.79-7.73 (m, 2H), 7.50 (dd, J= 8.4, 2.9 Hz, 2H), 7.42 (t, J= 7.5 Hz, 2H), 7.31 (t, J= 6.2 Hz, 3H), 7.14 (dd, J= 7.7, 1.7 Hz, 2H), 7.03 (dd, J= 9.4, 2.0 Hz, 1H).
95.8% With tris-(dibenzylideneacetone)dipalladium(0); 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; sodium t-butanolate; In toluene; at 100℃; for 4h;Inert atmosphere; To <strong>[356560-80-0]6-bromo-[1,2,4]triazolo[1,5-a]pyridine</strong> (700 mg, 3.5350 mmol),Benzophenone imine (1.28g, 7.06mmol)And t-BuONa (680mg, 7.076mmol)Intoluene (50mL) solutionBINAP (221mg, 0.3549mmol)And Pd2(dba)3 (167 mg, 0.17690 mmol).The resulting mixture was degassed for 5 minutes.And charge N2,It was then stirred at 100 C for 4 hours.After the reaction,The reaction was quenched with water (100 mL).Extracted with EtOAc (100 mL×3).The combined organic phases were dried over anhydrous Na 2 SO 4 .Filter and concentrate under reduced pressure.The residue obtained was purified by silica gel column chromatography (EtOAc/EtOAc (v/v)The title compound was obtained as a yellow solid (1.01 g, 95.8%).
69% With sodium t-butanolate;tris-(dibenzylideneacetone)dipalladium(0); 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; In toluene; at 80℃; 6-Bromo-[l,2,4]triazolo[l,5-a]pyridine (300 mg, 1.5 mmol), bezophenone imine (326 mg, 1.8 mmol), Pd2(dba)3 (7 mg, 0.008 mmol), BINAP (14 mg, 0.02 mmol) and sodium terf-butoxide (202 mg, 2.1 mmol) were combined in toluene and heated at 80 0C overnight. The mixture was concentrated under reduced pressure and purified by Biotage SP4 (ethyl acetate / petroleum ether gradient) to give the desired product as a yellow crystalline solid (310 mg, 69 %). 1H NMR (400 MHz, DMSO-d6) delta ppm 7.21 (dd, J=9.39, 2.06 Hz, 1 H), 7.24 - 7.29 (m, 2 H), 7.32 - 7.40 (m, 3 H), 7.47 - 7.54 (m, 2 H), 7.55 - 7.62 (m, 1 H), 7.66 (d, J=8.70 Hz, 1 H), 7.68 - 7.74 (m, 2 H), 8.35 (s, 1 H), 8.41 (d, J=I.83 Hz, 1 H); m/z (ES+APCI)+ : 299 [M+H]+.
 

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