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Phosphorus oxychloride → 4-Chloro-8-iodo-7-methylquinazoline

HRID 1668923
Notes
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Reaction equation

HRID 1668923 reaction equation
P(Cl)(Cl)([Cl:3])=O.[I:6][C:7]1[C:8]([CH3:18])=[CH:9][CH:10]=[C:11]2[C:16]=1[N:15]=[CH:14][NH:13][C:12]2=O>>[Cl:3][C:12]1[C:11]2[C:16](=[C:7]([I:6])[C:8]([CH3:18])=[CH:9][CH:10]=2)[N:15]=[CH:14][N:13]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 24813Phosphorus oxychlorideHCID 1357422708-Iodo-7-methylquinazolin-4(3H)-one

Product 1

HCID 584664844-Chloro-8-iodo-7-methylquinazolineYield 92.1%

Procedure

Phosphorous oxychloride (19.5 mL, 210 mmol) and 8-iodo-7-methylquinazolin-4(3H)-one (2.00 g, 6.99 mmol) were added to a round bottomed flask. The reaction mixture was heated at reflux for 2 h. Upon cooling, excess POCl3 was removed under reduced pressure and the remaining crude product dissolved in DCM (100 mL) and washed with ice-cold water (300 mL) to remove excess acid. The crude residue dissolved in DCM was then dried over anhydrous sodium sulfate and concentrated in vacuo to give 4-chloro-8-iodo-7-methylquinazoline (1.96 g, 92%) as an amorphous brown solid. MS (M+H)+ 305.

Workup

  1. temperatureThe reaction mixture was heated
  2. temperature
at reflux for 2 h
  • temperatureUpon cooling
  • customexcess POCl3 was removed under reduced pressure
  • dissolutionthe remaining crude product dissolved in DCM (100 mL)
  • washwashed with ice-cold water (300 mL)
  • customto remove excess acid
  • dissolutionThe crude residue dissolved in DCM
  • dry with materialwas then dried over anhydrous sodium sulfate
  • concentrationconcentrated in vacuo
  • Sources & evidence

    ORD record
    ord-5431aab719d340fea363d8eb6c42cf1c
    Source dataset
    uspto-grants-2011_08
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US07989461B2

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes