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Chemical Structure| 58004-79-8 Chemical Structure| 58004-79-8

Structure of 58004-79-8

Chemical Structure| 58004-79-8

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Product Details of [ 58004-79-8 ]

CAS No. :58004-79-8
Formula : C6H5BrN2O
M.W : 201.02
SMILES Code : BrCC(=O)C1=CN=CN=C1
MDL No. :MFCD13172978

Safety of [ 58004-79-8 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 58004-79-8 ]

* 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 [ 58004-79-8 ]

[ 58004-79-8 ] Synthesis Path-Downstream   1~5

YieldReaction ConditionsOperation in experiment
2.60 g (94%) Step 1. 5-Bromoacetylpyrimidine A mixture of 5-bromopyrimidine (2.20 g, 13.85 mmol), (1-ethoxyvinyl)tributyltin (5.00 g, 13.85 mmol), and tetrakis(triphenylphosphine)palladium (1.60 g, 1.38 mmol) in toluene (20 ml) was refluxed for 29 h, and then cooled to room temperature. The mixture was filtered through a pad of Celite and the filtrate was concentrated to give an oily residue. The residue was diluted with THF (30 ml) and water (8 ml). N-Bromosuccinimide (2.96 g, 16.61 mmol) was added at 0 C. The resulting mixture was stirred at 0 C. for 0.5 h and concentrated to ca. 10 ml. The residue was diluted with ethyl acetate (200 ml) and washed with water (100 ml*2), then dried (MgSO4). Removal of solvent gave an oily residue, which was purified by flash column chromatography eluding with ethyl acetate-hexane (1:3) to afford 2.60 g (94%) of the title compound as an oil. 1H-NMR (CDCl3) delta: 9.41 (1 H, s), 9.29 (2 H, s), 4.40 (2 H, s).
130 mg With bromine; acetic acid; at 100.0℃; for 3.0h;Cooling with ice; General procedure: The 1 - [6-trifluoromethyl-imidazole [1,2-a] pyridin-3-yl] ethanone (0.4 g, 1 . 75 mmol) is dissolved in 10 ml of glacial acetic acid. Under cooling in ice water bath, the bromine (1.92 mmol) are added to a reaction system. In 100 C heating and stirring under 3 hours. Cooling to room temperature, adding ether to, filtering the obtained precipitate with ethyl ether washing 3 times, drying to obtain the crude product. In the product is dissolved in methylene chloride, washed with saturated aqueous solution of sodium carbonate, the organic phase dried, concentrated to obtain the title compound 0.52 g. 1 H-NMR (CDCl 3) delta 8.94 (1H, s), 8.11 (1H, d, J=8Hz), 7.98 (1H, d, J=8Hz), 4.85 (2H, s).
  • 2
  • [ 220269-23-8 ]
  • [ 58004-79-8 ]
  • 3-amino-6-chloro-1-ethoxycarbonyl-2-(5-pyrimidinylcarbonyl)indole [ No CAS ]
YieldReaction ConditionsOperation in experiment
Step 2. 3-Amino-6-chloro-1-ethoxycarbonyl-2-(5-pyrimidinylcarbonyl)indole The title compound was prepared according to the procedure described in step 2 of Example 1 from 4-chloro-2-(ethoxycarbonylamino)benzonitrile (Example 1, step 1) and <strong>[58004-79-8]5-bromoacetylpyrimidine</strong> (step 1). 1H-NMR (CDCl3) delta: 9.29 (1 H, s), 9.03 (2 H, s), 8.02 (1 H, d, J=1.6 Hz), 7.57 (1 H, d, J=8.4 Hz), 7.35 (1 H, dd, J=1.6, 8.4 Hz), 6.13 (2 H, br s), 4.01 (2 H, q, J=7.1 Hz), 1.02 (3 H, t, J=7.1 Hz).
  • 4
  • [ 14222-60-7 ]
  • [ 58004-79-8 ]
  • 2-(2-propylpyridin-4-yl)-4-(pyrimidin-5-yl)thiazole [ No CAS ]
  • 5
  • 4-((4-(4-chloro-3-(trifluoromethyl)phenoxy)benzyl)oxy)pyrimidin-2-amine [ No CAS ]
  • [ 58004-79-8 ]
  • 7-((4-(4-chloro-3-(trifluoromethyl)phenoxy)benzyl)oxy)-2-(pyrimidin-5-yl)imidazo[1,2-a]pyrimidine [ No CAS ]
 

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