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(S)-Hexahydropyrrolo[1,2-a]pyrazin-6(2H)-one

  • CAS No. 151763-88-1

  • Cat. No. CS-0053989
  • Purity≥95%
  • MDL No.MFCD11506232

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

(S)-Hexahydropyrrolo[1,2-a]pyrazin-6(2H)-one|CS-0053989

Structure of 151763-88-1

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General Information

  • CAS No. 151763-88-1
  • Cat. No. CS-0053989
  • Purity ≥95%
  • MDL No. MFCD11506232
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₁₂N₂O
  • Molecular Weight 140.18
  • Synonym(s) (S)-tetrahydropyrrolo[1,2-a]pyrazin-6(1H,2H,7H)-one
  • SMILES O=C1CC[C@@]2([H])CNCCN21

Description

(S)-Hexahydropyrrolo[1,2-a]pyrazin-6(2H)-one is a chiral heterocyclic scaffold featuring a saturated pyrazine ring fused to a pyrrolidine moiety. This rigid, electron-rich structure serves as a key building block in medicinal chemistry, offering enhanced metabolic stability and defined stereochemistry for targeted ligand design.

Application

(S)-Hexahydropyrrolo[1,2-a]pyrazin-6(2H)-one serves as a valuable chiral building block in medicinal chemistry, offering a rigid, saturated heterocyclic scaffold with defined stereochemistry. Its amide-like functionality enables selective derivatization and facilitates incorporation into bioactive molecules. The compound exhibits good bench stability and compatibility with standard coupling reactions, supporting efficient synthesis of complex nitrogen-containing architectures.

Synthesis

  • Route1
    • null|null
      865717-07-3
    • ~81%
    • In-stock
      (S)-Hexahydropyrrolo[1,2-a]pyrazin-6(2H)-one|CS-0053989
      151763-88-1

    References

    • Neurotune AG Patent: EP2098526 A1, 2009 ; Location in patent: Page/Page column 11 ;

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS05
Signal Word : Danger
UN#: 3259
Class : 8
Packing Group : Ⅲ
Hazard Statements : H314
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

Quality Control

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Computational Chemistry Data

  • TPSA   32.34
  • LogP   -0.4194
  • H_Acceptors   2
  • H_Donors   1
  • Rotatable_Bonds   0

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