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Phosphorus oxychloride → 4-Chloro-6-iodoquinoline-3-carbonitrile

HRID 1297629
Notes
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Reaction equation

HRID 1297629 reaction equation
[I:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[NH:8][CH:7]=[C:6]([C:12]#[N:13])[C:5]2=O.P(Cl)(Cl)([Cl:17])=O>>[Cl:17][C:5]1[C:4]2[C:9](=[CH:10][CH:11]=[C:2]([I:1])[CH:3]=2)[N:8]=[CH:7][C:6]=1[C:12]#[N:13]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 24813Phosphorus oxychlorideHCID 289765906-Iodo-4-oxo-1,4-dihydroquinoline-3-carbonitrile

Product 1

HCID 224667694-Chloro-6-iodoquinoline-3-carbonitrileYield 98%

Procedure

A mixture of 6 6-iodo-4-oxo-1,4-dihydro-quinoline-3-carbonitrile (example 14b) (100 g, 0.34 mol) in phosphorus oxychloride (300 mL) was refluxed under N2 for 7 h. After cooling, the solvent was removed by rotary evaporator and then by the oil pump. Sat. sodium bicarbonate (200 mL) and ice water were slowly added. The solid was collected by filtration, washed with sat. sodium bicarbonate, water and dried to obtain 4-chloro-6-iodo-quinoline-3-carbonitrile (58 g, 98%) as a yellow solid. LC-MS m/e 315 (MH+).

Workup

  1. temperaturewas refluxed under N2 for 7 h
  2. temperatureAfter cooling
On this pageParticipantsProcedureWorkupSources & evidenceReaction notes
custom
the solvent was removed by rotary evaporator
  • additionSat. sodium bicarbonate (200 mL) and ice water were slowly added
  • filtrationThe solid was collected by filtration
  • washwashed with sat. sodium bicarbonate, water
  • customdried
  • Sources & evidence

    ORD record
    ord-2fda928f72ed4c278ade8f07219a366f
    Source dataset
    uspto-grants-2007_07
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US07250515B2

    Reaction notes

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