HCID 21489186, compound → HCID 21489152, compound
Reaction equation
[N+:1]([C:4]1[CH:13]=[C:12]2[C:7]([C:8](=[O:21])[N:9]3[C:16]4[CH:17]=[CH:18][CH:19]=[CH:20][C:15]=4[NH:14][C:10]3=[N:11]2)=[CH:6][CH:5]=1)([O-:3])=[O:2].[C:22]12([C:30](Br)=[O:31])[CH2:29][CH2:28][CH2:27][CH:26]1[CH2:25][CH:24]=[CH:23]2>>[C:22]12([C:30]([N:14]3[C:10]4=[N:11][C:12]5[C:7]([C:8](=[O:21])[N:9]4[C:16]4[CH:17]=[CH:18][CH:19]=[CH:20][C:15]3=4)=[CH:6][CH:5]=[C:4]([N+:1]([O-:3])=[O:2])[CH:13]=5)=[O:31])[CH2:29][CH2:28][CH2:27][CH:26]1[CH2:25][CH:24]=[CH:23]2Participants
3
Procedure
6-(Bicyclo[3.3.0]octenoyl)-3-nitrobenzimidazo[2,1-b]-quinazolin-12(6H)one is prepared with 3-nitrobenzimidazo[2,1-b]-quinazolin-12(6H)one and bicyclo[3.3.0]octenoyl bromide.
Sources & evidence
- ORD record
- ord-f4f5eb5dad2a4e0fb668cd07c142a23e
- Source dataset
- uspto-grants-1976_12
- Patent number
- US04000275
Reaction notes
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