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Chemical Structure| 1062292-60-7 Chemical Structure| 1062292-60-7

Structure of 1062292-60-7

Chemical Structure| 1062292-60-7

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Product Details of [ 1062292-60-7 ]

CAS No. :1062292-60-7
Formula : C15H10BrFN2O
M.W : 333.16
SMILES Code : O=C1NN=C(CC2=CC=C(F)C(Br)=C2)C3=C1C=CC=C3
MDL No. :MFCD22683267

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Application In Synthesis of [ 1062292-60-7 ]

* 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 [ 1062292-60-7 ]

[ 1062292-60-7 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 1062292-60-7 ]
  • [ 59878-57-8 ]
  • <SUP>14</SUP>carbon monoxide [ No CAS ]
  • [ 1422374-59-1 ]
  • 2
  • [ 1062292-60-7 ]
  • [ 201230-82-2 ]
  • [ 59878-57-8 ]
  • olaparib [ No CAS ]
YieldReaction ConditionsOperation in experiment
97% With dmap; tetrakis(triphenylphosphine) palladium(0); potassium bromide; In N,N-dimethyl-formamide; at 120℃; c. In the round bottom flask, the compound V29.14g was sequentially added.1-cyclopropionylpiperazine 13.34g, pd(PPh3)4 4.99g,0.173 mol of 4-dimethylaminopyridine, 10.29 g of potassium bromide, 500 ml of N,N-dimethylformamide, and then placed on a condenser, which was evacuated and flushed into CO.Repeatedly, then a balloon filled with carbon monoxide is placed on the upper end of the condenser.The temperature was controlled at 120 C, the reaction was continuously stirred, and the reaction was monitored by TLC.After the reaction is over, the temperature is lowered to room temperature and mixed.The extract was extracted with ethyl acetate, washed with purified water and dried over anhydrous sodium sulfate.Vacuum drying to obtain Olaparib (I) 36.48g, yield 97%The purity is 99.93%.
96% With dmap; tetrakis(triphenylphosphine) palladium(0); potassium bromide; In N,N-dimethyl-formamide; at 120℃; The round bottom flask is sequentially added in the compound V 26.99 g, 1 - cyclopropanecarboxylic formyl piperazine 12.49 g, 4.7 gpd (PPh3)4, 4 - Dimethylamino pyridine (0.162 muM), potassium bromide 9.64 g, N, N - dimethyl formamide 500 ml, then covering with the condenser tube, will be its evacuation and into the CO, repeatedly, in the condenser and then the upper end of the sleeve is a balloon filled with carbon monoxide. The temperature control in the 120 C, continuously stirring reaction, for monitoring the reaction TLC, to be after the reaction temperature to the room temperature, the mixture of ethyl acetate extraction, purified water washing, anhydrous sodium sulfate drying, vacuum drying to obtain aurar handkerchief nepal (I) 33.81 g, yield 96%, purity 99.93%.
  • 3
  • [ 1062292-60-7 ]
  • [ 1641-69-6 ]
  • [ 59878-57-8 ]
  • [ 1622398-78-0 ]
 

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