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Chemical Structure| 1446007-99-3 Chemical Structure| 1446007-99-3

Structure of 1446007-99-3

Chemical Structure| 1446007-99-3

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Product Details of [ 1446007-99-3 ]

CAS No. :1446007-99-3
Formula : C12H12BrN3O
M.W : 294.15
SMILES Code : O=C(C1=CNN=C1)N[C@H](C2=CC=C(Br)C=C2)C
MDL No. :MFCD27999760

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Application In Synthesis of [ 1446007-99-3 ]

* 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 [ 1446007-99-3 ]

[ 1446007-99-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 37718-11-9 ]
  • [ 27298-97-1 ]
  • [ 1446007-99-3 ]
YieldReaction ConditionsOperation in experiment
(S)-<strong>[37718-11-9]1H-Pyrazole-4-carboxylic acid</strong> [1 -(4-bromo-phenyl)-ethyl]-amide D To 5.0 g (44.6 mmol) <strong>[37718-11-9]4-pyrazolecarboxylic acid</strong> in 100 mL DMF 15.2 mL (89.2 mmol) DIPEA and 15.7 g (49.1 mmol) TBTU are added and the mixture is stirred for 10 min at rt. Subsequently 8.9 g (44.6 mmol) (S)-1 -(4-bromophenyl)ethylamine are added and stirring is continued over night. The mixture is poured on water and is extracted with ethyl acetate. The combined organic layers are dried over sodium sulphate and the solvent is removed in vacuo. The residue is triturated with DCM to yield the desired product. Ci2Hi2BrN3O (M = 294.1 g/mol), ESI-MS: 294 [M+H]+ Rt (HPLC): 1 .23 min (method E1 )
To 5.0 g (44.6 mmol) <strong>[37718-11-9]4-pyrazolecarboxylic acid</strong> in 100 mL DMF 15.2 mL (89.2 mmol) DIPEA and 15.7 g (49.1 mmol) TBTU are added and the mixture is stirred for 10 min at rt. Subsequently 8.9 g (44.6 mmol) (S)-1-(4-bromophenyl)ethylamine are added and stirring is continued over night. The mixture is poured on water and is extracted with ethyl acetate. The combined organic layers are dried over sodium sulphate and the solvent is removed in vacuo. The residue is triturated with DCM to yield the desired product. C12H12BrN3O (M=294.1 g/mol), ESI-MS: 294 [M+H]+ Rt (HPLC): 1.23 min (method E1)
 

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