1,3-Dimethylimidazolium Iodide → 6,7-Dimethoxyquinazoline

HRID 276791Notes

Reaction equation

HRID 276791 reaction equation
Cl[C:2]1[C:11]2[C:6](=[CH:7][C:8]([O:14][CH3:15])=[C:9]([O:12][CH3:13])[CH:10]=2)[N:5]=[CH:4][N:3]=1.BrC1C=C(C=CC=1)C=O.[I-].C[N+]1C=CN(C)C=1.[H-].[Na+]>O1CCOCC1>[CH3:13][O:12][C:9]1[CH:10]=[C:11]2[C:6](=[CH:7][C:8]=1[O:14][CH3:15])[N:5]=[CH:4][N:3]=[CH:2]2

Participants

6

Reactant 4

HCID 203341,3-Dimethylimidazolium IodideHCID 24758Sodium hydrideHCID 765833-BromobenzaldehydeHCID 27693644-Chloro-6,7-dimethoxyquinazoline2×

Product 1

HCID 30316616,7-Dimethoxyquinazoline

Reagents, catalysts & solvents 1

HCID 312751,4-DioxaneSolvent

Procedure

The lead compound 4-(3′-bromobenzoyl)-6,7-dimethoxyquinazoline WHI-P164 was synthesized by reacting 4-chloro-6,7-dimethoxyquinazoline 5 with the commercially available 3-bromobenzaldehyde in the presence of 1,3-dimethylimidazolium iodide and sodium hydride in refluxing dioxane for 4 hours (Scheme 2) (32,33). The remaining 6,7-dimethoxyquinazoline derivatives were synthesized by condensing 4-chloro-6,7-dimethoxyquinazoline 5 with the corresponding substituted anilines as shown in Scheme 3.

Sources & evidence

ORD record
ord-14890fafc978493bb7e02c26e7a55fa8
Source dataset
uspto-grants-2002_03
Patent number
US06355645B2

Reaction notes

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