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Chemical Structure| 273-21-2 Chemical Structure| 273-21-2

Structure of 273-21-2

Chemical Structure| 273-21-2

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Product Details of [ 273-21-2 ]

CAS No. :273-21-2
Formula : C6H5N3
M.W : 119.12
SMILES Code : C12=NC=NC1=CC=CN2
MDL No. :MFCD13176755
InChI Key :GAMYYCRTACQSBR-UHFFFAOYSA-N
Pubchem ID :67504

Safety of [ 273-21-2 ]

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

Application In Synthesis of [ 273-21-2 ]

* 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 [ 273-21-2 ]

[ 273-21-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 5409-39-2 ]
  • [ 273-21-2 ]
  • 2
  • [ 1798-06-7 ]
  • [ 273-21-2 ]
  • [ 913173-51-0 ]
YieldReaction ConditionsOperation in experiment
Procedure B; A mixture of 4-iodophenylacetic acid (400 mg, 1.53 mmol), 4-azabenzimidazole (273 mg, 2.29 mmol, 1.5 equiv), trans.trans-dibenzylideneacetone (17.9 mg, 0.0763 mmol, 0.05 equiv) 1,10-phenanthroline (303 mg, 1.53 mmol), copper (I) trifluoromethanesulfonate benzene complex (19.2 mg, 0.0763 mmol, 0.05 equiv), and Cs2CO3 (547 mg, 1.68 mmol) in xylene (1.5 mL) is stirred for 80 h at 125C. The reaction mixture is allowed to cool to rt and concentrated in vacuo. The residue is dissolved in a 1N NaOH aqueous solution and extracted with EtOAc. The aqueous layer is made acidic by addition of a 1 N HCI aqueous solution and extracted with CH2CI2. The organic phase is dried (Na2SO4), filtered and concentrated. The residue is purified by reversed phase MPLC (CH3CN/H2O/TFA) to provide the title compound.
A mixture of 400 mg of 4-ιodophenylacetιc acid, 273 rng of 4-azabenzιmιdazole, 17 9 mg of trans, trans-dibenzylideneacetone, 303 mg of 1 ,10-phenanthrolιne, 19 2 mg of copper (I) tϖfluoromethanesulfonate benzene complex and 547 mg of Cs2CO3 in 1 5 ml of xylene is stirred for 80 hours at 125C The mixture obtained is allowed to cool to rt and concentrated in vacuo The concentration residue obtained is dissolved in aqueous 1 N NaOH solution and extracted with EtOAc To the aqueous layer aqueousi N HCI is added in order to obtain an acidic pH and the mixture obtained is extracted with CH2CI2 The organic phase obtained is dried (Na2SO4), filtered and concentrated The concentration residue obtained is subjected to reversed phase MPLC (CH3CN/H2O/TFA) (4-lmιdazo[4,5-b]pyrιdιn-3-yl-phenyl)-acetιc acid is obtained
 

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