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Chemical Structure| 879488-53-6 Chemical Structure| 879488-53-6

Structure of 879488-53-6

Chemical Structure| 879488-53-6

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Product Details of [ 879488-53-6 ]

CAS No. :879488-53-6
Formula : C10H14BrN3
M.W : 256.14
SMILES Code : CN1CCN(C2=CC=C(Br)N=C2)CC1
MDL No. :MFCD14702603
InChI Key :VCDWKCPGKQANIF-UHFFFAOYSA-N
Pubchem ID :66521395

Safety of [ 879488-53-6 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H320-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 879488-53-6 ]

* 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 [ 879488-53-6 ]

[ 879488-53-6 ] Synthesis Path-Downstream   1~7

  • 2
  • [ 879488-53-6 ]
  • 6-(1H-benzo[d]imidazol-1-yl)pyrimidin-4-amine [ No CAS ]
  • 6-(1H-benzo[d]imidazol-1-yl)-N-(5-(4-methylpiperazin-1-yl)pyridin-2-yl)pyrimidin-4-amine [ No CAS ]
  • 3
  • [ 109-01-3 ]
  • [ 73290-22-9 ]
  • [ 879488-53-6 ]
YieldReaction ConditionsOperation in experiment
79.3% With tris-(dibenzylideneacetone)dipalladium(0); 4,5-bis(diphenylphos4,5-bis(diphenylphosphino)-9,9-dimethylxanthenephino)-9,9-dimethylxanthene; sodium t-butanolate; In toluene; at 60℃; for 24.0h;Inert atmosphere; Pd2(dba)3 (229 mg, 0.25 mmol), Xantphos (290 mg, 0.5 mmol) and sodium tert-butoxide (2.88 g, 30 mmol) were added to 2-bromo-5-iodopyridine (3.41 g, 12 mmol)And a solution of 1-methylpiperazine (1.0 g, 10 mmol) in toluene (50 ml), heated to 60 degrees Celsius under the protection of argon, and stirred for 24 hours.After the reaction solution was cooled to room temperature, the solid was filtered off, the filter cake was washed with ethyl acetate, and the filtrate was concentrated under reduced pressure to obtain a crude product, which was purified by Combi-flash column chromatography [DCM: MeOH = 100: 0 to 90:10] The compound 1-(6-bromopyridin-3-yl)-4-methylpiperazine was obtained (2.68 g, 79.3%).
  • 4
  • [ 879488-53-6 ]
  • C17H19BrN6 [ No CAS ]
  • 5
  • [ 879488-53-6 ]
  • C37H41N9O3 [ No CAS ]
  • 6
  • [ 879488-53-6 ]
  • 2-(4-(3-amino-7-(5-(4-methylpiperazin-1-yl)pyridin-2-yl)-1H-indazol-5-yl)-3-(hydroxymethyl)pyridin-2-yl)-7,7-dimethyl-2,3,4,6,7,8-hexahydro-1H-cyclopentadieno[4,5]pyrrolo[1,2-a]pyrazin-1-one [ No CAS ]
  • 7
  • [ 879488-53-6 ]
  • [ 1461-22-9 ]
  • C22H41N3Sn [ No CAS ]
YieldReaction ConditionsOperation in experiment
45% Under argon protection, a solution of compound B (1.3 g, 5.08 mmol) in tetrahydrofuran (20 ml) was cooled to -78 degrees Celsius, and n-butyllithium (2.5 M, 3 ml, 7.62 mmol) was slowly added dropwise. After the dropwise addition was completed, stirring was continued for 10 minutes, and tributyltin chloride (2.48 g, 7.62 mmol) was added.The reaction solution was slowly warmed to room temperature, quenched by adding potassium fluoride, and concentrated under reduced pressure. The crude product was purified by Combi-flash column chromatography [DCM: MeOH = 100: 0 to 95: 5] to obtain compound Z-1-1. (1.03 g, 45%).
 

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