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Chemical Structure| 51549-49-6 Chemical Structure| 51549-49-6

Structure of 51549-49-6

Chemical Structure| 51549-49-6

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Product Details of [ 51549-49-6 ]

CAS No. :51549-49-6
Formula : C23H21N3O6
M.W : 435.43
SMILES Code : O=C(O[C@@H]1[C@@H](CO)O[C@@H](N2C=CC(NC(C3=CC=CC=C3)=O)=NC2=O)C1)C4=CC=CC=C4
English Name :N4,3-o-dibenzoyl-2-deoxycytidine
MDL No. :MFCD00036252

Safety of [ 51549-49-6 ]

Application In Synthesis of [ 51549-49-6 ]

* 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 [ 51549-49-6 ]

[ 51549-49-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 40615-35-8 ]
  • [ 51549-49-6 ]
  • [ 93966-67-7 ]
YieldReaction ConditionsOperation in experiment
68% With ambelyst-15 In dichloromethane for 2h; Reflux; Molecular sieve; regioselective reaction; General experimental procedure for the 4,40-dimethoxytritylation and pixilationof diols 1a-1n General procedure: To a mixture of diol 1a-1n (1.0 mmol) and Dimethoxy triphenylmethonol1 (1.1 mmol) in dichloromethane (10 mL), (10% w/w) of Ambelyst-15 wasadded and the wine red heterogeneous reaction mixture refluxed for 3-6 h.After completion of the starting material 1a-1n, (monitored by TLC), thecatalyst was removed by fitration and the solvents were distilled out onrotary evaporator to get crude product. The crude compound was purifiedby column chromatography using 60-120 silica gel and (ethyl acetate inhexane) to afford 2a-2n
 

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