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Chemical Structure| 51549-54-3 Chemical Structure| 51549-54-3

Structure of 51549-54-3

Chemical Structure| 51549-54-3

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Product Details of [ 51549-54-3 ]

CAS No. :51549-54-3
Formula : C24H21N5O5
M.W : 459.45
SMILES Code : OC[C@@H]1[C@H](C[C@H](N2C=NC3=C2N=CN=C3NC(C4=CC=CC=C4)=O)O1)OC(C5=CC=CC=C5)=O
English Name :(2R,3S,5R)-5-(6-Benzamido-9H-purin-9-yl)-2-(hydroxymethyl)tetrahydrofuran-3-yl benzoate
MDL No. :MFCD00056180

Safety of [ 51549-54-3 ]

Application In Synthesis of [ 51549-54-3 ]

* 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 [ 51549-54-3 ]

[ 51549-54-3 ] Synthesis Path-Downstream   1~6

  • 1
  • [ 93966-66-6 ]
  • [ 51549-54-3 ]
YieldReaction ConditionsOperation in experiment
100% With trifluoroacetic acid In chloroform
With trifluoroacetic acid In chloroform at 0℃; for 0.0833333h;
With benzenesulfonic acid In methanol; chloroform
5 g With trifluoroacetic acid In methanol; dichloromethane at 0 - 20℃; for 1h; Inert atmosphere; 5.2 Step 2. Detritylation (A-OH) A-OBz (13.69 g, unpurified, 17 mmol) was dissolved in dichloromethane/methanol mixture (1:1, 300 ml) and cooled to 0° C. under nitrogen. Trifluoroacetic acid (2.75 ml, 36 mmol) was added via syringe. Reaction stirred while warming to room temperature for one hour. Monitored reaction progress by TLC. Reaction quenched at 0° C. by addition of solid NaHCO3 (3 g, 36 mmol). Removed solvent in vacuo at temperature<40° C. and the residue was diluted with AcOEt (800 mL), and washed five times with water (5×250 ml). Dried the organic layer over MgSO4, filtered and dried in vacuo to yield a white foam. Purification by column chromatography (gradient elution with 1:1 petroleum ether/ethyl acetate to ethyl acetate) afforded the target product as a white powder. (5.0 g, 60% yield (2 steps), Rf=0.35 in 100% ethyl acetate) 1H NMR (400 MHz, DMSO-d6) δ 11.25 (s, 1H), 8.78 (s, 1H), 8.75 (s, 1H), 8.07 (ddt, J=10.1, 7.0, 1.4 Hz, 4H), 7.75-7.68 (m, 1H), 7.68-7.62 (m, 1H), 7.62-7.51 (m, 4H), 6.64 (dd, J=8.6, 5.9 Hz, 1H), 5.68 (dt, J=6.1, 1.9 Hz, 1H), 5.28 (t, J=5.7 Hz, 1H), 4.31 (td, J=4.4, 1.8 Hz, 1H), 3.72 (tdd, J=11.8, 6.4, 4.7 Hz, 2H), 3.19 (ddd, J=14.4, 8.7, 6.1 Hz, 1H), 2.75 (ddd, J=14.1, 5.9, 1.8 Hz, 1H).
With dichloro-acetic acid In dichloromethane at 20 - 23℃; for 0.5h;

  • 2
  • [ 92611-10-4 ]
  • [ 51549-54-3 ]
  • [ 117854-36-1 ]
YieldReaction ConditionsOperation in experiment
83% With N,N-diisopropylamine tetrazolide In dichloromethane at 30℃; for 1h;
  • 3
  • [ 84416-85-3 ]
  • [ 51549-54-3 ]
  • [ CAS Unavailable ]
YieldReaction ConditionsOperation in experiment
With 1H-tetrazole In tetrahydrofuran at 20℃; for 5h;
  • 4
  • [ 84416-83-1 ]
  • [ 51549-54-3 ]
  • [ CAS Unavailable ]
YieldReaction ConditionsOperation in experiment
With 1H-tetrazole In tetrahydrofuran at 20℃; for 5h;
  • 5
  • [ 51549-54-3 ]
  • [ 143997-08-4 ]
YieldReaction ConditionsOperation in experiment
90% With pyridine; tris(2,4,6-tribromo-phenoxy)dichlorophosphorane for 0.0833333h; Ambient temperature;
90% With tris(2,4,6-tribromo-phenoxy)dichlorophosphorane In pyridine for 0.0833333h; Ambient temperature;
  • 6
  • [ 51549-54-3 ]
  • [ 999-97-3 ]
  • [ 174865-59-9 ]
YieldReaction ConditionsOperation in experiment
97% With pyridine; chloro-trimethyl-silane for 0.25h; Ambient temperature;
 

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