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Chemical Structure| 825618-95-9 Chemical Structure| 825618-95-9

Structure of 825618-95-9

Chemical Structure| 825618-95-9

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Product Details of [ 825618-95-9 ]

CAS No. :825618-95-9
Formula : C11H7F2N3O3
M.W : 267.19
SMILES Code : O=C(C1=NNC=C1NC(C2=C(F)C=CC=C2F)=O)O

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Application In Synthesis of [ 825618-95-9 ]

* 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 [ 825618-95-9 ]

[ 825618-95-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 825618-95-9 ]
  • [ 51498-33-0 ]
  • 4-[4-(2,6-difluoro-benzoylamino)-1H-pyrazole-3-carbonyl]-amino}-cyclohexanecarboxylic acid ethyl ester [ No CAS ]
YieldReaction ConditionsOperation in experiment
Thionyl chloride (0.32 ml, 4.40 mmol) was slowly added to a mixture of 4-aminocyclohexanecarboxylic acid (572 mg, 4.00 mmol) in EtOH (10 ml) and stirred at ambient temperature for 16 hours. The mixture was reduced in vacuo, azeotroping with toluene, to give the corresponding ethyl ester (650 mg) as a pale solid.A mixture of the ethyl ester (103 mg, 0.60 mmol), 4-(2,6-difluoro-benzoylamino)-1H-pyrazole-3-carboxylic acid (134 mg, 0.50 mmol), EDC (115 mg, 0.60 mmol) and HOBt (81 mg, 0.60 mmol) in DMF (5 ml) was stirred at ambient temperature for 16 hours. The mixture was reduced in vacuo, the residue taken up in EtOAc and washed successively with saturated aqueous sodium bicarbonate, water and brine. The organic portion was dried (MgSO^ and reduced in vacuo to give 4-[4-(2,6-difluoro-benzoylamino)-1H-pyrazole-3-carbonyl]-amino}- cyclohexanecarboxylic acid ethyl ester (112 mg).
Thionyl chloride (0.32 ml, 4.40 mmol) was slowly added to a mixture of 4-aminocyclohexanecarboxylic acid (572 mg, 4.00 mmol) in EtOH (10 ml) and stirred at ambient temperature for 16 hours. The mixture was reduced in vacuo, azeotroping with toluene, to give the corresponding ethyl ester (650 mg) as a pale solid.A mixture of the ethyl ester (103 mg, 0.60 mmol), 4-(2,6-difluoro-benzoylamino)-1H-pyrazole-3-carboxylic acid (134 mg, 0.50 mmol), EDC (115 mg, 0.60 mmol) and HOBt (81 mg, 0.60 mmol) in DMF (5 ml) was stirred at ambient temperature for 16 hours. The mixture was reduced in vacuo, the residue taken up in EtOAc and washed successively with saturated aqueous sodium bicarbonate, water and brine. The organic portion was dried (MgSO^ and reduced in vacuo to give 4-[4-(2,6-difluoro-benzoylamino)-1H-pyrazole-3-carbonyl]-amino}- cyclohexanecarboxylic acid ethyl ester (112 mg).
With benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; In DMF (N,N-dimethyl-formamide); at 20℃; for 16h; Thionyl chloride (0.32 ml, 4.40 mmol) was slowly added to a mixture of 4- aminocyclohexanecarboxylic acid (572 mg, 4.00 mmol) in EtOH (10 ml) and stirred at ambient temperature for 16 hours. The mixture was reduced in vacuo, azeotroping with toluene, to give the corresponding ethyl ester (650 mg) as a pale solid. A mixture of the ethyl ester (103 mg, 0.60 mmol), 4- (2, 6-difluoro-benzoylamino)-1H-pyrazole-3-carboxylic acid (134 mg, 0.50 mmol), EDC (115 mg, 0.60 mmol) and HOBt (81 mg, 0.60 mmol) in DMF (5 ml) was stirred at ambient temperature for 16 hours. The mixture was reduced in vacuo, the residue taken up in EtOAc and washed successively with saturated aqueous sodium bicarbonate, water and brine. The organic portion was dried (MgS04) and reduced in vacuo to give 4-[4-(2,6-difluoro-benzoylamino)-1H-pyrazole-3-carbonyl]0amino}-cyclohexanecarboxylic acid ethyl ester (112 mg).
 

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