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Chloroform → 6-Methoxy-1-methyl-2-phenyl-1H-quinazolin-4-one

HRID 557133
Notes
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Reaction equation

HRID 557133 reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([NH:12][CH3:13])=[C:7]([CH:11]=1)[C:8]([NH2:10])=[O:9].C(Cl)(=O)[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1.Cl[CH:24](Cl)Cl>>[CH3:1][O:2][C:3]1[CH:11]=[C:7]2[C:6](=[CH:5][CH:4]=1)[N:12]([CH3:24])[C:13]([C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)=[N:10][C:8]2=[O:9]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 6212ChloroformHCID 7412Benzoyl chlorideHCID 669916645-Methoxy-2-methylamino-benzamide

Product 1

HCID 669907996-Methoxy-1-methyl-2-phenyl-1H-quinazolin-4-one

Procedure

1.00 g (5.55 mmol) 5-Methoxy-2-methylamino-benzamide were dissolved in 25 ml trichloromethane and 2.34 g (1.93 ml, 16.6 mmol) benzoyl chloride were added. The mixture was boiled for 90 min. After filtration the residue was dissolved in trichloromethane and saturated sodium bicarbonate solution. The organic solution was dried over magnesium sulfate and evaporated under vacuum.

Workup

  1. filtrationAfter filtration the residue
  • dissolutionwas dissolved in trichloromethane
  • dry with materialThe organic solution was dried over magnesium sulfate
  • customevaporated under vacuum
  • Sources & evidence

    ORD record
    ord-17071fecd7ff4903b8121cd23762b920
    Source dataset
    uspto-grants-2011_11
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US08058431B2

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes