2,4-Dichlorobenzoyl chloride → HCID 21489184, compound
Reaction equation
[CH2:1]([O:3][C:4]1[CH:5]=[CH:6][C:7]2[NH:21][C:11]3=[N:12][C:13]4[C:18]([C:19](=[O:20])[N:10]3[C:8]=2[CH:9]=1)=[CH:17][CH:16]=[CH:15][CH:14]=4)[CH3:2].[Cl:22][C:23]1[CH:31]=[C:30]([Cl:32])[CH:29]=[CH:28][C:24]=1[C:25](Cl)=[O:26]>>[Cl:22][C:23]1[CH:31]=[C:30]([Cl:32])[CH:29]=[CH:28][C:24]=1[C:25]([N:21]1[C:11]2=[N:12][C:13]3[C:18]([C:19](=[O:20])[N:10]2[C:8]2[CH:9]=[C:4]([O:3][CH2:1][CH3:2])[CH:5]=[CH:6][C:7]1=2)=[CH:17][CH:16]=[CH:15][CH:14]=3)=[O:26]Participants
3
Procedure
6-(2,4-Dichlorobenzoyl)-9-ethoxybenzimidazo[2,1-b]-quinazolin-12(6H)one is prepared with 9-ethoxybenzimidazo[2,1-b]-quinazolin-12(6H)one and 2,4-dichlorobenzoyl chloride.
Sources & evidence
- ORD record
- ord-8966787df8b84a359d030c1ff17093cb
- Source dataset
- uspto-grants-1976_12
- Patent number
- US04000275
Reaction notes
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