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Chemical Structure| 1140917-39-0 Chemical Structure| 1140917-39-0

Structure of 1140917-39-0

Chemical Structure| 1140917-39-0

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Product Details of [ 1140917-39-0 ]

CAS No. :1140917-39-0
Formula : C12H21N3O
M.W : 223.31
SMILES Code : NC1=CC(C(C)(C)C)=NN1C[C@H]2OCCC2

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Application In Synthesis of [ 1140917-39-0 ]

* 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 [ 1140917-39-0 ]

[ 1140917-39-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 207981-46-2 ]
  • [ 1140917-39-0 ]
  • [ 1140917-50-5 ]
YieldReaction ConditionsOperation in experiment
With triethylamine; In tetrahydrofuran; at 20℃; for 3.16667h; To a solution of the product of Example 1C (7.8 g) and triethylamine (14.6 mL, 105 mmol) in THF (60 mL) at ambient temperature was added <strong>[207981-46-2]2-fluoro-5-(trifluoromethyl)benzoyl chloride</strong> (5.3 mL, 35.0 mmol) dropwise over 10 min. The mixture was stirred at ambient temperature for 3 h. The mixture was quenched with saturated, aqueous NaHCO3 (20 mL) and diluted with EtOAc (20 mL). The layers were separated and the aqueous layer was extracted with EtOAc (3×10 mL). The combined organics were dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure. Purification by column chromatography (SiO2, 40% hexanes/EtOAc) gave the title compound (11.0 g, 26.6 mmol). MS (DCI/NH3) m/z 414 (M+H)+
With triethylamine; In tetrahydrofuran; at 20℃; for 3.16667h; To a solution of the product of Example 1C (7.8 g) and triethylamine (14.6 mL, 105 mmol) in THF (60 mL) at ambient temperature was added <strong>[207981-46-2]2-fluoro-5-(trifluoromethyl)benzoyl chloride</strong> (5.3 mL, 35.0 mmol) dropwise over 10 min. The mixture was stirred at ambient temperature for 3 h. The mixture was quenched with saturated, aqueous NaHCO3 (20 mL) and diluted with EtOAc (20 mL). The layers were separated and the aqueous layer was extracted with EtOAc (3×10 mL). The combined organics were dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure. Purification by column chromatography (SiO2, 40% hexanes/EtOAc) gave the title compound (11.0 g, 26.6 mmol). MS (DCI/NH3) m/z 414 (M+H)+
 

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