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Structure of 414910-03-5

Chemical Structure| 414910-03-5

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Product Details of [ 414910-03-5 ]

CAS No. :414910-03-5
Formula : C24H23F7N2O2
M.W : 504.44
SMILES Code : O=C(N1[C@@H](C2=CC=C(F)C=C2C)CC(CC1)=O)N([C@@H](C3=CC(C(F)(F)F)=CC(C(F)(F)F)=C3)C)C

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Application In Synthesis of [ 414910-03-5 ]

* 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 [ 414910-03-5 ]

[ 414910-03-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 414910-03-5 ]
  • [ 59878-57-8 ]
  • 4-(R)-(4-cyclopropanoyl-piperazin-1-yl)-2-(R)-(4-fluoro-2-methyl-phenyl)-piperidine-1-carboxylic acid [1-(R)-(3,5-bis-trifluoromethyl-phenyl)-ethyl]-methylamide [ No CAS ]
  • 4-(S)-(4-cyclopropanoyl-piperazin-1-yl)-2-(R)-(4-fluoro-2-methyl-phenyl)-piperidine-1-carboxylic acid [1-(R)-(3,5-bis-trifluoromethyl-phenyl)-ethyl]-methylamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
A solution of intermediate 4a (100 mg) and intermediate 12 (31 mg) in dry 1,2-dichloroethane (5 mL) and acetonitrile (1 mL) was stirred at r.t. for 30 minutes under a nitrogen atmosphere. Then, sodium triacetoxyborohydride (42 mg) was added and the mixture was stirred at 23 C. for 24 hours. The solution was diluted with AcOEt and washed with water. The organic layer was dried and concentrated in vacuo to a residue which was purified by flash chromatography (AcOEt/MeOH 9:1) to give: [0379] example 11a (2 mg-T.I.c.: AcOEt/MeOH 8:2 Rf=0.33), [0380] example 11b (7 mg-T.I.c.: AcOEt/MeOH 8:2 Rf=0.16).
 

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