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[ CAS No. 1013920-62-1 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 1013920-62-1
Chemical Structure| 1013920-62-1
Structure of 1013920-62-1 * Storage: {[proInfo.prStorage]}
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Product Details of [ 1013920-62-1 ]

CAS No. :1013920-62-1 MDL No. :MFCD16621191
Formula : C11H20N2O3 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 228.29 Pubchem ID :-
Synonyms :

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Application In Synthesis of [ 1013920-62-1 ]

* 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 [ 1013920-62-1 ]

[ 1013920-62-1 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 122536-76-9 ]
  • [ 75-36-5 ]
  • [ 1013920-62-1 ]
YieldReaction ConditionsOperation in experiment
90% With triethylamine In dichloromethane at 20℃; for 4h; 8.1a Example 8: Preparation of 5-(5-Fluoro-2-oxo-l,2-dihydro-indol-(3Z)- ylidenemethyl]-2,4-dimethyl-lH-pyrrole-3-carboxylic acid ((S)-l-acetyl- pyrrolidin-3-yl)-amidePreparation of amines for examples 8 and 9:8b 8cBocNH'9b 9c Step Ia: Compound 8a (0.5g, 2.7mmol) and TEA (0.326g, 3.2mmol) were combined in 5mL of DCM. Acetyl chloride (0.253g, 3.2mmol) was added drop- wise. The resulting mixture was stirred at room temperature for 4h and evaporated under reduced pressure. The residue was dissolved in EA and washed with aqueous 5% NaHCO3 solution and brine. The organic layer was dried over anhydrous MgSO4 and evaporated to provide crude compound 8b (0.548g, 90%), which was used directly for the next step.
90% With triethylamine In dichloromethane at 20℃; for 4h; 8.1a Example 8 Preparation of 5-[5-Fluoro-2-oxo-1,2-dihydro-indol-(3Z)-ylidenemethyl]-2,4-dimethyl-1H-pyrrole-3-carboxylic acid ((S)-1-acetyl-pyrrolidin-3-yl)-amide Preparation of Amines for Examples 8 and 9 Step 1a: Compound 8a (0.5 g, 2.7 mmol) and TEA (0.326 g, 3.2 mmol) were combined in 5 mL of DCM. Acetyl chloride (0.253 g, 3.2 mmol) was added drop-wise. The resulting mixture was stirred at room temperature for 4 h and evaporated under reduced pressure. The residue was dissolved in EA and washed with aqueous 5% NaHCO3 solution and brine. The organic layer was dried over anhydrous MgSO4 and evaporated to provide crude compound 8b (0.548 g, 90%), which was used directly for the next step.
  • 2
  • [ 1013920-62-1 ]
  • [ 76-05-1 ]
  • [ 1013921-15-7 ]
YieldReaction ConditionsOperation in experiment
In dichloromethane at 20℃; for 2h; 8.2 Step 2: Compound 8b or 9b (1.0 eq.) was dissolved in DCM. TFA (10 eq.) was added slowly. The resulting mixture was stirred at room temperature for 2 h, evaporated to dryness under vacuum to provide compound 8c or 9c.
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