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7-Bromo-2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazine

  • CAS No. 946121-78-4

  • Cat. No. CS-0128559
  • Purity≥96%
  • MDL No.MFCD15527041

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

7-Bromo-2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazine|CS-0128559

Structure of 946121-78-4

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General Information

  • CAS No. 946121-78-4
  • Cat. No. CS-0128559
  • Purity ≥96%
  • MDL No. MFCD15527041
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₇BrN₂O
  • Molecular Weight 215.05
  • Synonym(s) 7-bromo-1H,2H,3H-pyrido[2,3-b][1,4]oxazine
  • SMILES BrC1=CN=C2OCCNC2=C1

Description

7-Bromo-2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazine features a brominated pyridooxazine scaffold with enhanced electrophilic character at the C7 position. This bench-stable heterocycle integrates readily into cross-coupling reactions and serves as a strategic intermediate in medicinal chemistry campaigns targeting CNS-active compounds and kinase inhibitors.

Application

7-Bromo-2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazine serves as a versatile heterocyclic building block for medicinal chemistry and materials science. Its bromine substituent enables palladium-catalyzed cross-coupling reactions, while the fused oxazine core provides structural rigidity and favorable pharmacophore geometry. The compound exhibits good bench stability and facilitates efficient functionalization in standard synthetic workflows.

Synthesis

  • Route1

    References

    • Ackermann, Jean; Bleicher, Konrad; Ceccarelli, Simona M.; Chomienne, Odile; Mattei, Patrizio; Sander, Ulrike Obst Patent: US2007/191603 A1, 2007 ; Location in patent: Page/Page column 37 ;

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   34.15
  • LogP   1.6484
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   0

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