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Chemical Structure| 150109-42-5 Chemical Structure| 150109-42-5

Structure of 150109-42-5

Chemical Structure| 150109-42-5

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Product Details of [ 150109-42-5 ]

CAS No. :150109-42-5
Formula : C9H16ClNO4
M.W : 237.68
SMILES Code : C[C@H](NC(OC(C)(C)C)=O)C(OCCl)=O
MDL No. :MFCD12165899

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Application In Synthesis of [ 150109-42-5 ]

* 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 [ 150109-42-5 ]

[ 150109-42-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1174046-72-0 ]
  • [ 150109-42-5 ]
  • C32H30ClF2N5O7 [ No CAS ]
YieldReaction ConditionsOperation in experiment
With potassium carbonate; In N,N-dimethyl-formamide; at 20.0℃; Examples 3 tol 1 were prepared using the following General Procedure: To a mixture of N-(4-(2-amino-3-chloropyridin-4-yloxy)-3-fluorophenyl)-5-(4- <n="41"/>fluorophenyl)-4-oxo-l,4-dihydropyridine-3-carboxamide (Example 1, 0.1 mmol) and potassium carbonate (0.4 mmol) in DMF (1 mL), was added the corresponding chloromethyl ester derivative (0.3 mmol, for preparation, see Synth. Commun., 14:857-864 (1984)). The reaction mixture was stirred at rt for 1-3 h, diluted with DCM, and washed with aq. KH2PO4 solution. The organic layer was dried over MgSO4 and the N-Boc-protected intermediate was purified by column chromatography (SiCh, using a DCM/EtOAc gradient elution). [00100] The N-Boc-protected intermediate was then treated with 30% TFA/DCM (2 mL) for 1 h. The solvents were removed in vacuo, and the product was purified by preparative-HPLC to afford the title compound as a TFA salt.
 

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