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Water → 8-Carbamoyl-2-(2-n-propoxyphenyl)quinazolin-4(3H)-one

HRID 374777
Notes
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Reaction equation

HRID 374777 reaction equation
[CH2:1]([O:4][C:5]1[CH:13]=[CH:12][CH:11]=[CH:10][C:6]=1[C:7](Cl)=O)[CH2:2][CH3:3].[NH2:14][C:15]1[C:23]([C:24](=[O:26])[NH2:25])=[CH:22][CH:21]=[CH:20][C:16]=1[C:17]([NH2:19])=[O:18].[OH-].[Na+].O>N1C=CC=CC=1.C(O)C>[C:17]([C:16]1[CH:20]=[CH:21][CH:22]=[C:23]2[C:15]=1[N:14]=[C:7]([C:6]1[CH:10]=[CH:11][CH:12]=[CH:13][C:5]=1[O:4][CH2:1][CH2:2][CH3:3])[NH:25][C:24]2=[O:26])(=[O:18])[NH2:19]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 4

HCID 962WaterHCID 14798Sodium HydroxideHCID 102413842-Aminobenzene-1,3-dicarboxamideHCID 159219132-Propoxybenzoyl chloride

Product 1

HCID 1359851568-Carbamoyl-2-(2-n-propoxyphenyl)quinazolin-4(3H)-oneYield 40%

Reagents, catalysts & solvents 2

HCID 702
Ethanol
Solvent
HCID 1049PyridineSolvent

Procedure

2-n-Propoxybenzoyl chloride (7.27 g, 0.366 mol) was added dropwise to a stirred suspension of 2-amino-3-carbamoylbenzamide (Preparation 17; 2.63 g, 0.0147 mol) in pyridine (50 ml) at 0° C. The mixture was stirred at room temperature for 3 days, then the solvent evaporated under vacuum. The residue was treated with water (100 ml) and, on chilling the solution, colorless crystals formed. The product was collected by filtration and then suspended in a stirred mixture of sodium hydroxide (1.73 g, 0.043 mol), water (90 ml) and ethanol (20 ml). The mixture was heated under reflux for 3 hours, allowed to cool and filtered. The filtrate was acidified to pH 2 with concentrated hydrochloric acid and extracted with a methanoldichloromethane mixture (2:98, 3×100 ml). The organic extracts were combined, washed sequentially with saturated aqueous sodium carbonate solution (3×100 ml) and brine (3×50 ml), dried (Na2SO4) and evaporated under vacuum. Crystallization of the residue from ethyl acetate-methanol gave the title compound as a white solid (1 g, 40%), m.p. 226°-227° C. Found: C,67.00; H,5.40; N,12.90. C18H17N3O3 requires C,66.86; H,5.30; N,13.00%.

Workup

  1. customthe solvent evaporated under vacuum
  2. additionThe residue was treated with water (100 ml)
  3. temperatureon chilling the solution
  4. customformed
  5. filtrationThe product was collected by filtration
  6. temperatureThe mixture was heated
  7. temperatureunder reflux for 3 hours
  8. temperatureto cool
  9. filtrationfiltered
  10. extractionextracted with a methanoldichloromethane mixture (2:98, 3×100 ml)
  11. washwashed sequentially with saturated aqueous sodium carbonate solution (3×100 ml) and brine (3×50 ml)
  12. dry with materialdried (Na2SO4)
  13. customevaporated under vacuum
  14. customCrystallization of the residue from ethyl acetate-methanol

Sources & evidence

ORD record
ord-2f5129f333fa4bf3a50b422b6fdc2b27
Source dataset
uspto-grants-1996_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05482941

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes