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Chemical Structure| 905994-07-2 Chemical Structure| 905994-07-2

Structure of 905994-07-2

Chemical Structure| 905994-07-2

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Product Details of [ 905994-07-2 ]

CAS No. :905994-07-2
Formula : C28H35FN4O8S
M.W : 606.66
SMILES Code : O=C(N1CC2=C(C(F)=CC=C2)C1)O[C@H]3CN(C(OC(C)(C)C)=O)[C@H](C(N[C@@]4(C(NS(=O)(C5CC5)=O)=O)[C@H](C=C)C4)=O)C3

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Application In Synthesis of [ 905994-07-2 ]

* 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 [ 905994-07-2 ]

[ 905994-07-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 154350-29-5 ]
  • [ 1152020-87-5 ]
  • [ 905994-07-2 ]
YieldReaction ConditionsOperation in experiment
~ 100% Step 8B.; Compound 8A (265 mg, 0.526 mmol) and carbonyldiimidazole (195 mg, 1.16 mmol) were dissolved in 6 ml of anhydrous DMF and the resulting solution was stirred at 40 C. for 1 hour. Cyclopropylsulfonamide (130 mg, 1.07 mmol) was added to the reaction followed by DBU (0.150 ml, 1.0 mmol). The reaction mixture was stirred at 40 C. for 20 hour. The reaction mixture was diluted with ethyl acetate and washed with half-saturated-aqueous NaCl solution three times. The organic layer was dried over anhydrous (MgSO4) and concentrated to dryness to give compound 8B (100%)
Step 1c: Intermediate 1c; To a solution of the product of step1b (0.30 g, 0.6 mmol) in 10 mL of DCM was added CDI (0.16 g, 1.0 mmol) and the resulting solution was stirred at 40 C. for 1 hour. <strong>[154350-29-5]cyclopropylsulfonamide</strong> (0.18 g, 1.5 mmol) and DBU (0.16 g, 1.0 mmol) were added to the reaction mixture. The mixture was stirred at 40 C. for additional 10 hours. The solvent was then removed and the residue was diluted with EtOAc and was washed with aqueous NaOAc buffer (pH5, 2×10 mL), NaHCO3 solution and brine. After drying over Na2SO4 and removal of solvent, the residue was subjected to chromatography on silica gel using hexane/EtOAc (1:11:2). A total of 0.30 g of the title compound was obtained: Rf 0.1 (EtOAc:hexane=1:1), MS m/z: 605.0 (M-1).
  • 2
  • [ 159622-10-3 ]
  • [ 905994-07-2 ]
 

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