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1-Acetyl-6-amino-3,3-dimethylindoline

  • CAS No. 453562-71-5

  • Cat. No. CS-M3748
  • Purity≥97%
  • MDL No.MFCD07636699

*For research and further manufacturing use only, not for direct human use.

1-Acetyl-6-amino-3,3-dimethylindoline|CS-M3748

Structure of 453562-71-5

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General Information

  • CAS No. 453562-71-5
  • Cat. No. CS-M3748
  • Purity ≥97%
  • MDL No. MFCD07636699
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₂H₁₆N₂O
  • Molecular Weight 204.27
  • Synonym(s) 1-(6-Amino-3,3-dimethylindolin-1-yl)ethanone
  • SMILES NC1=CC2=C(C=C1)C(C)(C)CN2C(C)=O

Description

1-(6-Amino-3,3-dimethylindolin-1-yl)ethanone features a sterically hindered indolinone core with a pendant amino group, enabling direct integration into peptide and heterocyclic scaffolds. The acetyl moiety provides a reactive handle for derivatization under mild conditions, while the electron-rich aromatic system enhances solubility in polar organic solvents. This compound serves as a key building block for bioactive molecule synthesis.

Application

1-(6-Amino-3,3-dimethylindolin-1-yl)ethanone serves as a versatile building block in medicinal chemistry, enabling the construction of indoline-based scaffolds prevalent in kinase inhibitors and CNS-targeted therapeutics. The acetamide functionality provides a handle for derivatization via acylation or reductive amination, while the 3,3-dimethyl substitution enhances metabolic stability and modulates solubility. Bench-stable and compatible with standard purification methods, it functions effectively in multi-step syntheses requiring functional group tolerance and predictable reactivity.

Synthesis

  • Route1

    References

    • WO2010/71828 A2, ; Page/Page column 15-16 ;
  • Route2
    • null|null
      453562-67-9
    • ~%
    • In-stock
      1-Acetyl-6-amino-3,3-dimethylindoline|CS-M3748
      453562-71-5

    References

    • US2011/98311 A1, ;
  • Route3

    References

    • US2011/98311 A1, ;

Safety Information

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Hazard Statements : N/A
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Computational Chemistry Data

  • TPSA   46.33
  • LogP   1.9129
  • H_Acceptors   2
  • H_Donors   1
  • Rotatable_Bonds   0

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