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Chemical Structure| 202752-01-0

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Product Details of [ 202752-01-0 ]

CAS No. :202752-01-0
Formula : C37H32N2O3S
M.W : 584.73
SMILES Code : O=C(OCC1C2=C(C3=C1C=CC=C3)C=CC=C2)N[C@@H](CSC(C4=CC=CC=C4)(C5=CC=CC=C5)C6=CC=CC=C6)C(N)=O
MDL No. :MFCD30475790

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Application In Synthesis of [ 202752-01-0 ]

* 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 [ 202752-01-0 ]

[ 202752-01-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 202752-01-0 ]
  • [ 166737-85-5 ]
YieldReaction ConditionsOperation in experiment
92% With piperidine; In N,N-dimethyl-formamide; at 20℃; for 4h; A solution of the compound (R) - (9H-fluoren-9-yl) methyl (1-amino-1-oxo-3- (triphenylmethylthio) propan-2-yl) carbamate (4 g, 6.84 mmol )Was dissolved in N, N-dimethylformamide (20 ml)Piperidine (0.14 ml, 1.368 mmol) was added,Reaction at room temperature for 4 hours,TLC detection reaction is completed,The reaction mixture was washed with saturated brine,Extracted with dichloromethane,The organic phase was dried over sodium sulfate,concentrate,Column chromatography (methanol: dichloromethane = 1% -5%),The title product was obtained as a yellow oil (2.3 g, yield: 92%).
With pyrrolidine; In N,N-dimethyl-formamide; at 20℃; To a stirred solution of 9H-fluoren-9-ylmethyl {(li?)-2-amino-2-oxo-1-[(tritylthio)methyl]-ethyl} carbamate (380 mg, 0.65 mmol) in DMF (3 mL) was added pyrrolidine (11 muL, 0.13 mmol). The reaction was stirred at room temperature overnight. By TLC and mass spectrometry, the reaction was deemed complete. This DMF solution of the title compound was used as such in the next reaction (Step 5, Example 3).
 

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