Water → HCID 14458977, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][C:11]=1[Cl:12])[N:8]([CH2:13][C:14]([O:16][CH2:17][CH3:18])=[O:15])[C:7](=[O:19])[NH:6][C:5]2=[O:20].[H-].[Na+].[Br:23][C:24]1[CH:31]=[CH:30][C:27]([CH2:28]Br)=[C:26]([F:32])[CH:25]=1.O>CN(C)C=O>[Br:23][C:24]1[CH:31]=[CH:30][C:27]([CH2:28][N:6]2[C:5](=[O:20])[C:4]3[C:9](=[CH:10][C:11]([Cl:12])=[C:2]([Cl:1])[CH:3]=3)[N:8]([CH2:13][C:14]([O:16][CH2:17][CH3:18])=[O:15])[C:7]2=[O:19])=[C:26]([F:32])[CH:25]=1Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
To a suspension of ethyl 2-(6,7-dichloro-1,2,3,4-tetrahydro-2,4-dioxoquinazolin-1-yl)acetate (2.0 g) in N,N-dimethylformamide (50 ml) was added sodium hydride (60% in mineral oil, 288 mg) at room temperature with stirring and the mixture was stirred at the same temperature for 1 hour. To this mixture was added 4-bromo-2-fluorobenzyl bromide (1.93 g) at room temperature with stirring and the mixture was stirred at the same temperature for 2 hours. The solvent was removed to give a residue, which was poured into water. The resulting precipitates were collected by filtration and washed with n-hexane to give ethyl 2-[3-(4-bromo-2-fluorobenzyl)-6,7-dichloro-1,2,3,4-tetrahydro-2,4-dioxoquinazolin-1-yl]acetate (2.94 g).
Workup
- stirringthe mixture was stirred at the same temperature for 1 hour
- stirringwith stirring
- stirringthe mixture was stirred at the same temperature for 2 hours
- customThe solvent was removed
- customto give a residue, which
- customThe resulting precipitates
- filtrationwere collected by filtration
- washwashed with n-hexane
Sources & evidence
- ORD record
- ord-5dee23c96fb2412d9b0dca23c041375f
- Source dataset
- uspto-grants-1988_03
- Patent number
- US04734419
Reaction notes
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