3,5-Dimethylbenzoyl Chloride → HCID 21489183, compound

HRID 1974302Notes

Reaction equation

HRID 1974302 reaction equation
[CH3:1][O:2][C:3]1[CH:12]=[C:11]2[C:6]([C:7](=[O:20])[N:8]3[C:15]4[CH:16]=[CH:17][CH:18]=[CH:19][C:14]=4[NH:13][C:9]3=[N:10]2)=[CH:5][CH:4]=1.[CH3:21][C:22]1[CH:23]=[C:24]([CH:28]=[C:29]([CH3:31])[CH:30]=1)[C:25](Cl)=[O:26]>>[CH3:21][C:22]1[CH:23]=[C:24]([CH:28]=[C:29]([CH3:31])[CH:30]=1)[C:25]([N:13]1[C:9]2=[N:10][C:11]3[C:6]([C:7](=[O:20])[N:8]2[C:15]2[CH:16]=[CH:17][CH:18]=[CH:19][C:14]1=2)=[CH:5][CH:4]=[C:3]([O:2][CH3:1])[CH:12]=3)=[O:26]

Participants

3

Reactant 2

HCID 810883,5-Dimethylbenzoyl ChlorideHCID 178487725HCID 178487725, compound

Product 1

HCID 21489183HCID 21489183, compound

Procedure

6-(3,5-Dimethylbenzoyl)-3-methoxybenzimidazo[2,1-b]-quinazolin-12(6H)one is prepared with 3-methoxybenzimidazo[2,1-b]quinazolin-12(6H)one and 3,5-dimethylbenzoyl chloride.

Sources & evidence

ORD record
ord-eca3b78e85394b42a9f4fdf77e33b77b
Source dataset
uspto-grants-1976_12
Patent number
US04000275

Reaction notes

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