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Chemical Structure| 474706-36-0 Chemical Structure| 474706-36-0

Structure of 474706-36-0

Chemical Structure| 474706-36-0

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Product Details of [ 474706-36-0 ]

CAS No. :474706-36-0
Formula : C9H6BrFN2
M.W : 241.06
SMILES Code : FC1=CC=C(C2=C(Br)C=NN2)C=C1
MDL No. :MFCD11855880

Safety of [ 474706-36-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 474706-36-0 ]

* 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 [ 474706-36-0 ]

[ 474706-36-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 154258-82-9 ]
  • [ 474706-36-0 ]
YieldReaction ConditionsOperation in experiment
99% With N-Bromosuccinimide; In N,N-dimethyl-formamide; at 20℃; for 1h; To a solution of 3-(4-fluorophenyl)-lH-pyrazole (10 g, 61.7 mmol) in DMF (50 ml) was added NBS (11 g, 61.7 mmol). The reaction mixture was stirred at rt for lh, quenched with water, extracted with EtOAc. The organic layer was washed with brine, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to give the crude product Intermediate 2A (14.47 g, 99%) as a white solid. MS(ES): m/z= 240.89/242.89 [M+H]+. HPLC Ret time (Method B): 3.56 min. NMR (400MHz, chloroform-d) delta 7.86 - 7.74 (m, 2H), 7.66 (s, 1H), 7.20 - 7.1 1 (m, 2H).
Production Example 8 4-Bromo-<strong>[154258-82-9]3-(4-fluorophenyl)-1H-pyrazole</strong> 24 g <strong>[154258-82-9]3-(4-fluorophenyl)pyrazole</strong> was dissolved in 150 ML N,N-dimethylformamide, then 28 g N-bromosuccinimide was added thereto little by little, and the mixture was stirred for 2 hours.. An aqueous sodium thiosulfate solution and an aqueous sodium dicarbonate solution were added thereto and stirred for 1 hour, and the formed solid was collected by filtration.. The product was dissolved in ethyl acetate, dried over magnesium sulfate, and then purified by silica gel column chromatography (ethyl acetate).. The resulting solid was crystallized from diethyl ether/hexane, to give 33.6 g colorless crystals.1H-NMR (CDCl3) delta: 7.10-7.17(m, 2H), 7.62(d, J=2.4Hz, 1H), 7.73-7.79(m, 2H)
 

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