p-Chlorophenacyl bromide → HCID 70002262, compound
Reaction equation
[CH:1]1[C:6]([C:7]([CH2:9]Br)=[O:8])=[CH:5][CH:4]=[C:3]([Cl:11])[CH:2]=1.[CH3:12][O:13][C:14]1[CH:15]=[C:16]([C:22]2[C@H:31]3[C@H:26]([CH2:27][CH2:28][CH2:29][CH2:30]3)[C:25](=[O:32])[NH:24][N:23]=2)[CH:17]=[CH:18][C:19]=1[O:20][CH3:21].COC1C=C(C2[C@H]3[C@H](CCCC3)C(=O)N(C)N=2)C=CC=1OC>>[Cl:11][C:3]1[CH:4]=[CH:5][C:6]([C:7](=[O:8])[CH2:9][N:24]2[N:23]=[C:22]([C:16]3[CH:15]=[C:14]([O:13][CH3:12])[C:19]([O:20][CH3:21])=[CH:18][CH:17]=3)[C@H:31]3[C@H:26]([CH2:27][CH2:28][CH2:29][CH2:30]3)[C:25]2=[O:32])=[CH:1][CH:2]=1Participants
4
Procedure
Prepared from ω-bromo-4-chloroacetophenone and compound 1 as described for compound 8. Crystallized from methanol. M.p. 142°-144° C.
Workup
- customCrystallized from methanol
Sources & evidence
- ORD record
- ord-9b5ef27726854a0990ab774840b9b64e
- Source dataset
- uspto-grants-2000_08
- Patent number
- US06103718
Reaction notes
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