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Chemical Structure| 1356055-11-2 Chemical Structure| 1356055-11-2

Structure of 1356055-11-2

Chemical Structure| 1356055-11-2

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Product Details of [ 1356055-11-2 ]

CAS No. :1356055-11-2
Formula : C6H4F3IN2O
M.W : 304.01
SMILES Code : FC(F)(F)COC1=NC=NC=C1I
MDL No. :MFCD18909136

Safety of [ 1356055-11-2 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 1356055-11-2 ]

* 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 [ 1356055-11-2 ]

[ 1356055-11-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 75-89-8 ]
  • [ 63558-65-6 ]
  • [ 1356055-11-2 ]
YieldReaction ConditionsOperation in experiment
To a solution of 2,2,2-trifluoroethanol (0.672 mL, 9.36 mmol) in THF (18.08 mL), was added, portionwise, at 0C, NaH (0.424 g, 10.61 mmol). The reaction mixture was stirred at 0C for 30 min. Then <strong>[63558-65-6]4-chloro-5-iodopyrimidine</strong> (1.5 g, 6.24 mmol) was added and the reaction mixture was refluxed for about 1 h. The reaction mixture was allowed to cool to room temperature, then a saturated aqueous solution of NH4CI was added. The mixture was diluted with EtOAc and the layers were separated. The aqueous phase was extracted with EtOAc (2X). The combined organics were washed with brine (IX), dried over Na2S04, filtered, and concentrated in vacuo to afford Intermediate 106A as a yellow solid. MS (ESI) : m/z = 304.7 [M+H]+ HPLC Peak ret. T = 0.88 minutes was product. (HPLC conditions: Condition F).
Preparation 12A: 5-Iodo-4-(2,2,2-trifluoroethoxy)pyrimidine[00150] To a solution of 2,2,2-trifluoroethanol (0.672 mL, 9.36 mmol) in THF (18.08 mL) was added, portion wise, at 0 C, NaH (0.424 g, 10.61 mmol). The reaction mixture was stirred at 0 C for 30 min. Then <strong>[63558-65-6]4-chloro-5-iodopyrimidine</strong> (1.5 g, 6.24 mmol) was added and the reaction mixture was refluxed for about 1 hr. The reaction mixture was allowed to cool to room temperature, then a saturated aqueous solution of NH4C1 was added. The mixture was diluted with EtO Ac and the layers were separated. The aqueous phase was extracted with EtO Ac (2X). The combined organics were washed with brine (IX), dried over a2S04, filtered, and concentrated in vacuo to afford the title compound as a yellow solid. ESI MS (M+H)+ = 304.7.
 

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