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Chemical Structure| 483366-11-6 Chemical Structure| 483366-11-6

Structure of 483366-11-6

Chemical Structure| 483366-11-6

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Product Details of [ 483366-11-6 ]

CAS No. :483366-11-6
Formula : C12H15FN2O3S
M.W : 286.32
SMILES Code : N#C[C@H]1NC[C@@H](F)C1.O=S(C2=CC=C(C)C=C2)(O)=O
MDL No. :MFCD16875451

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Application In Synthesis of [ 483366-11-6 ]

* 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 [ 483366-11-6 ]

[ 483366-11-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 483366-11-6 ]
  • [ 218609-00-8 ]
  • tert-butyl N-[(2R)-4-[(2S,4S)-2-cyano-4-fluoropyrrolidin-1-yl]-1-(4-fluorophenyl)-4-oxobutan-2-yl]carbamate [ No CAS ]
YieldReaction ConditionsOperation in experiment
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In N,N-dimethyl-formamide; at 20.0℃; for 20.5h; General procedure: A solution of (3R)-3-[[(tert-butoxy)carbonyl]amino]-4-phenylbutanoic acid (compound 17a, 108mg, 0.385mmol) in DMF (5mL) was added HOBt (166mg, 1.225mmol) and EDCI (154mg, 0.805mmol). After stirring for 30min compound 16 (100mg, 0.35mmol) and additional TEA (0.17mL, 1.225mmol) were added. This solution was allowed to stir at room temperature for 20h and then the saturated NaHCO3 was added. The mixture was extracted with EtOAc and washed with saturated NaCl, dried over Na2SO4 and concentrated. The residue was purified with flash chromatography on silica gel, eluted with a mixture of PE/EA (4/1, v/v) to afford 18a (112mg, 85%) as a white solid.
  • 2
  • [ 483366-11-6 ]
  • [ 218609-00-8 ]
  • (2S,4S)-1-[(3R)-3-amino-4-(4-fluorophenyl)butanoyl]-4-fluoropyrrolidine-2-carbonitrile [ No CAS ]
 

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