4-Chlorobenzoyl chloride → HCID 14983034, compound
Reaction equation
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[CH:4][C:3]=1[C:9](=[O:11])[CH3:10].[Cl:12][C:13]1[CH:21]=[CH:20][C:16]([C:17](Cl)=O)=[CH:15][CH:14]=1.Br[CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28]Cl.[OH:30][CH:31]1[CH2:36][CH2:35][NH:34][CH2:33][CH2:32]1>>[Cl:12][C:13]1[CH:21]=[CH:20][C:16]([C:17]2[O:1][C:2]3[CH:7]=[CH:6][C:5]([O:8][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][N:34]4[CH2:35][CH2:36][CH:31]([OH:30])[CH2:32][CH2:33]4)=[CH:4][C:3]=3[C:9](=[O:11])[CH:10]=2)=[CH:15][CH:14]=1Participants
5
Procedure
The compound was prepared by a method similar to Example 11 from 2',5'-dihydroxyacetophenone, 4-chlorobenzoyl chloride, 1-bromo-6-chlorohexane, and 4-hydroxypiperidine: mp 127°-128° C.
Sources & evidence
- ORD record
- ord-47f84422ebdf43ab85248be896ee13e0
- Source dataset
- uspto-grants-1994_01
- Patent number
- US05278174
Reaction notes
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