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Chemical Structure| 1267028-34-1 Chemical Structure| 1267028-34-1

Structure of 1267028-34-1

Chemical Structure| 1267028-34-1

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Product Details of [ 1267028-34-1 ]

CAS No. :1267028-34-1
Formula : C12H18N2O3
M.W : 238.28
SMILES Code : O=C(OC(C)(C)C)NC1=CC=C(OC)C(N)=C1
MDL No. :MFCD09835451

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Application In Synthesis of [ 1267028-34-1 ]

* 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 [ 1267028-34-1 ]

[ 1267028-34-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1267028-34-1 ]
  • [ 1197953-49-3 ]
  • [ 1407519-99-6 ]
YieldReaction ConditionsOperation in experiment
62% With potassium phosphate;palladium diacetate; 4,5-bis(diphenylphos4,5-bis(diphenylphosphino)-9,9-dimethylxanthenephino)-9,9-dimethylxanthene; In N,N-dimethyl-formamide; at 120℃; Step 3 : Synthesis of 4:A suspension of 2( 1.27g, 4.0 mmol), 3-Boc-amino-5-methoxyaniline(965mg, 4.0mmol), palladium acetate( 133mg, 0.59mmol), XantPhos(352mg, 0.61 mmol) and potassium phosphate(l .4g, 6.6mmol) in anhydrous DMF(35 mL) was heated at 120 C overnight. After the reaction was cooling to room temperature, ethyl acetate was added to dilute the reaction and the content was filtered through celite. Solvent was removed under vacuum. The residue was purified by flash column chromatography on silica gel to give pure product 1.3g (yield 62%) as a tan solid.
62% With potassium phosphate; palladium diacetate; 4,5-bis(diphenylphos4,5-bis(diphenylphosphino)-9,9-dimethylxanthenephino)-9,9-dimethylxanthene; In N,N-dimethyl-formamide; at 120℃; A suspension of 2(1.27g, 4.0 mmol), 3-Boc-amino-5-methoxyaniline(965mg, 4.0mmol), palladium acetate(133mg, 0.59mmol), XantPhos(352mg, 0.61 mmol) and potassium phosphate(1.4g, 6.6mmol) in anhydrous DMF(35 mL) was heated at 120 C overnight. After the reaction was cooling to room temperature, ethyl acetate was added to dilute the reaction and the content was filtered through celite. Solvent was removed under vacuum. The residue was purified by flash column chromatography on silica gel to give pure product 1.3g (yield 62%) as a tan solid.
 

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