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Chemical Structure| 77758-50-0 Chemical Structure| 77758-50-0

Structure of 77758-50-0

Chemical Structure| 77758-50-0

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Product Details of [ 77758-50-0 ]

CAS No. :77758-50-0
Formula : C12H14O3S
M.W : 238.30
SMILES Code : O=S(OCCCC#C)(C1=CC=C(C)C=C1)=O

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Application In Synthesis of [ 77758-50-0 ]

* 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 [ 77758-50-0 ]

[ 77758-50-0 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 77758-50-0 ]
  • [ 802919-90-0 ]
  • [ 1109183-36-9 ]
  • (Z)-6,6-difluoro-4-iodo-6-(phenylsulfonyl)hex-4-enyl 4-methylbenzenesulfonate [ No CAS ]
  • 2
  • [ 42726-73-8 ]
  • [ 77758-50-0 ]
  • [ 1219806-77-5 ]
  • 3
  • [ 2439-54-5 ]
  • [ 77758-50-0 ]
  • [ 1228425-61-3 ]
  • 4
  • [ 77758-50-0 ]
  • [ 10357-07-0 ]
  • C16H14FN3O2 [ No CAS ]
YieldReaction ConditionsOperation in experiment
DMF (7 ml) was added through a septum to an argon-purgedflask containing 4-<strong>[10357-07-0]N-benzoyl-5-fluorocytosine</strong> (200 mg, 0.9 mmol)and K2CO3 (142 mg, 1 mmol) and the resulting suspension wasstirred at rt for 20 min. Then pent-4-yn-1-yl tosylate (245 mg,1 mmol) was added to the solution. The mixture was stirred at rtand subsequently heated to 50 C for 8 h. DMF was co-evaporatedwith toluene under reduced pressure. The crude reaction mixturewas separated using flash column chromatography on silica gelwith gradient HEX to EA in 16 CV. Dried product was directly usedin the following reaction with methanolic ammonia (10 ml) atambient temperature. After 16 h NH3 and MeOH were evaporatedunder reduced pressure and the product was isolated by flash columnchromatography on silica gel with gradient from CH2Cl2 to 7%MeOH in 16 CV to give the product 2c as white solid in 20% yield(35 mg, 0.18 mmol).
 

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