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Chemical Structure| 1280205-96-0 Chemical Structure| 1280205-96-0

Structure of 1280205-96-0

Chemical Structure| 1280205-96-0

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Product Details of [ 1280205-96-0 ]

CAS No. :1280205-96-0
Formula : C15H17BrN2O3
M.W : 353.21
SMILES Code : O=C(OC(C)(C)C)NC1=C(C2=CC=C(Br)C=C2)ON=C1C

Safety of [ 1280205-96-0 ]

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

Application In Synthesis of [ 1280205-96-0 ]

* 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 [ 1280205-96-0 ]

[ 1280205-96-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 91182-60-4 ]
  • [ 75-65-0 ]
  • [ 1280205-96-0 ]
YieldReaction ConditionsOperation in experiment
66% With diphenyl phosphoryl azide; triethylamine; In toluene; at 90℃; for 3h; Compound VII-1 (300 mg, 1.02 mmol) was dissolved in 15 mL of toluene. To the resulting solution was added DPPA (353 mg, 1.28 mmol), t-BuOH (95 mg, 1.28 mmol) and Et3N (216 mg, 2.14 mmol), and then the solution was stirred at 90 C for 3 hrs. After cooling to rt, the mixture was poured into water and extracted with EtOAc (30 mLx 3). The combined organic layer was washed with brine, dried over anhydrous sodium sulfate, concentrated in vacuo. The residue was purified by prep-TLC (Petroleum ether:EtOAc = 3: 1) to afford compound VII-2 (250 mg, yield 66%).
With diphenylphosphoranyl azide; triethylamine;Reflux; Step 5 : [5-(4-Bromo-phenyl)-3-methyl-isoxazol-4-yl[-carbamic acid tert-butyl ester : 5-(4-Bromo-phenyl)-3-methyl-isoxazole-4-carboxylic acid (1.6 g, 6.0 mmol), diphenylphosphoryl azide (1.6 g, 6.0 mmol), and triethylamine (1.3 mL, 9.3 mmol) were combined in t-BuOH and refluxed overnight. After cooling, the mixture was concentrated, and the residue was partitioned between EtOAc and H2O. The organic layer was separated and concentrated, and the residue was purified by silica gel chromatography (16-18% EtOAc in hexanes) to give the title compound.
With diphenyl phosphoryl azide; triethylamine;Reflux; Step 5: [5-(4-Bromo-phenyl)-3-methyl-isoxazol-4-yl]-carbamic acid tert-butyl ester 5-(4-Bromo-phenyl)-3-methyl-isoxazole-4-carboxylic acid (1.6 g, 6.0 mmol), diphenylphosphoryl azide (1.6 g, 6.0 mmol), and triethylamine (1.3 mL, 9.3 mmol) were combined in t-BuOH and refluxed overnight. After cooling, the mixture was concentrated, and the residue was partitioned between EtOAc and H2O. The organic layer was separated and concentrated, and the residue was purified by silica gel chromatography (16-18% EtOAc in hexanes) to give the title compound.
 

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