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Chemical Structure| 954272-50-5 Chemical Structure| 954272-50-5

Structure of 954272-50-5

Chemical Structure| 954272-50-5

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Product Details of [ 954272-50-5 ]

CAS No. :954272-50-5
Formula : C12H19NO4
M.W : 241.29
SMILES Code : O=C(O)[C@@]1([C@@H](C1)C2CC2)NC(OC(C)(C)C)=O
MDL No. :MFCD30829621

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Application In Synthesis of [ 954272-50-5 ]

* 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 [ 954272-50-5 ]

[ 954272-50-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 154350-29-5 ]
  • [ 954272-50-5 ]
  • tert-butyl ((1S,2R)-2-((cyclopropylsulfonyl)carbamoyl)[1,1′-bi(cyclopropan)]-2-yl)carbamate [ No CAS ]
YieldReaction ConditionsOperation in experiment
20.1% the above product (1.52 g, 6.2 mmol) was dissolved in 60 mL of dry THF,CDI (1.13 g, 6.9 mmol) was added,Replaced with argon three times,The reaction solution was heated to 60 C for 4 hours,Cooled to room temperature,Cyclopropanesulfonamide (0.84 g, 6.9 mmol) was added,DBU (1.05 g, 6.9 mmol),Stir overnight at room temperature.The reaction mixture was diluted with 80 mL of ethyl acetate,Followed by washing twice with 30 mL of 10% citric acid,30 mL of saturated brine,The organic phase was dried over anhydrous sodium sulfate,filter,Filtrate spin dry,Silica gel column chromatography (PE: EA50: 1to 1: 1),The product was 0.43 g.The yield was 20.1%.
Compound 25; Step 1: Synthesis of (1R,2S)-1-amino-N-(cyclopropylsulfonyl) 2- cyclopropylcyclopropane carboxamide hydrochloride (Compound 25); ( IR,2S)- l-(tert-butoxycarbonylamino)-2-cyclopropylcyclopropane carboxylic acid (484 mg, 2.01 mmol), was dissolved in 20 niL THF, followed by addition of CDI (390 mg, 2.41 mmol) in one portion at rt. The reaction was stirred in a 60 C sandbath for 4 h, cooled to rt, and <strong>[154350-29-5]cyclopropanesulfonamide</strong> (292 mg, 2.41 mmol) and DBU (366 mg, 2.41 mmol) were added. The reaction was stirred at rt for overnight. The reaction was then diluted with 300 mL EtOAc and washed with 1 N HCI (2 x 15 niL), water, brine (10 mL each), and dried (Na2SO4), giving a white solid after removal of solvent (0.63 g, 91% yield). This crude product was determined to be fairly clean by 1H-NMR and LCMS (APCI+, 245.0, MH+-Boc), hence was directly used for the next de-protection step without further purification.
 

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