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Phosphorus oxychloride → HCID 57465578, compound

HRID 1042981
Notes
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Reaction equation

HRID 1042981 reaction equation
[CH3:1][C:2]1[C:6]([C:7]2[CH:16]=[C:15]3[C:10]([C:11](O)=[C:12]([N+:17]([O-:19])=[O:18])[CH:13]=[N:14]3)=[CH:9][CH:8]=2)=[C:5]([CH3:21])[O:4][N:3]=1.O=P(Cl)(Cl)[Cl:24]>>[Cl:24][C:11]1[C:10]2[C:15](=[CH:16][C:7]([C:6]3[C:2]([CH3:1])=[N:3][O:4][C:5]=3[CH3:21])=[CH:8][CH:9]=2)[N:14]=[CH:13][C:12]=1[N+:17]([O-:19])=[O:18]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 24813Phosphorus oxychlorideHCID 178434743HCID 178434743, compound

Product 1

HCID 57465578HCID 57465578, compoundYield 75%

Procedure

A suspension of 7-(3,5-dimethyl-4-isoxazolyl)-3-nitro-4-quinolinol (for a preparation see intermediate 15, 5 g, 17 mmol) in POCl3 (50 ml) was refluxed overnight. After cooling the solvent was evaporated in vacuo. The resulting residue was poured over saturated aqueous Sodium hydrogen carbonate, extracted with DCM, washed with water, dried over Na2SO4. The solvent was evaporated under reduce pressure to give the title compound as a light brown solid (4 g, 75%). 1H NMR (300 MHz, CDCl3, ppm) δ: 9.23 (s, 1H), 8.45 (d, J=8.9 Hz, 1H), 8.04 (d, J=1.5 Hz, 1H), 7.67 (dd, J=8.9, 1.5 Hz, 1H), 2.47 (s, 3H), 2.32 (s, 3H).

Workup

  1. temperaturewas refluxed overnight
  2. temperature
After cooling the solvent
  • customwas evaporated in vacuo
  • additionThe resulting residue was poured over saturated aqueous Sodium hydrogen carbonate
  • extractionextracted with DCM
  • washwashed with water
  • dry with materialdried over Na2SO4
  • customThe solvent was evaporated
  • Sources & evidence

    ORD record
    ord-fcf879bc50724d63a9fa418f30d41e48
    Source dataset
    uspto-grants-2013_10
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US08557984B2

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes