HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

Phosphorus oxychloride → 7-Bromo-2-chloro-1,5-naphthyridine

HRID 509654
Notes
Print preview

Reaction equation

HRID 509654 reaction equation
[Br:1][C:2]1[CH:11]=[C:10]2[C:5]([CH:6]=[CH:7][C:8](=O)[NH:9]2)=[N:4][CH:3]=1.O=P(Cl)(Cl)[Cl:15]>>[Br:1][C:2]1[CH:11]=[C:10]2[C:5]([CH:6]=[CH:7][C:8]([Cl:15])=[N:9]2)=[N:4][CH:3]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 24813Phosphorus oxychlorideHCID 57815430HCID 57815430, compound

Product 1

HCID 583105447-Bromo-2-chloro-1,5-naphthyridineYield 62.9%

Procedure

7-bromo-1,5-naphthyridin-2(1H)-one (C-4) (3.1 g, 13.78 mmol, 1.0 eq) was dissolved in POCl3 (20 mL) and the resulting mixture was stirred at reflux for 1 h. The reaction was complete based on TLC analysis. The mixture was concentrated in vacuo to remove POCl3. The residue was poured into ice water (30 mL) and neutralized with saturated aqueous Na2CO3 solution to adjust the pH value to 7-8 while keeping the temperature below 10° C. The resulting mixture was extracted with ethyl acetate (3×30 mL), the combined organic layer was washed with brine, dried over Na2SO4 and filtered. The filtrate was concentrated in vacuo to afford the desired product 7-bromo-2-chloro-1,5-naphthyridine (F-31) (2.11 g, 62.9% yield). ESI-MS m/z: 242.9 [M+H]+.

Workup

  • temperatureat reflux for 1 h
  • concentrationThe mixture was concentrated in vacuo
  • customto remove POCl3
  • additionThe residue was poured into ice water (30 mL)
  • customthe temperature below 10° C
  • extractionThe resulting mixture was extracted with ethyl acetate (3×30 mL)
  • washthe combined organic layer was washed with brine
  • dry with materialdried over Na2SO4
  • filtrationfiltered
  • concentrationThe filtrate was concentrated in vacuo
  • Sources & evidence

    ORD record
    ord-27a28933b9164875b84cbc516f4380af
    Source dataset
    uspto-grants-2015_08
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US09096590B2

    Reaction notes

    Loading…

    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes