trans-2-Decenoic acid → HCID 117920382, compound
Reaction equation
[C:1]([OH:12])(=O)/[CH:2]=[CH:3]/[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10].Cl.Cl.[N:15]1([C:21]2[CH:33]=[CH:32][C:24]([O:25][CH2:26][C:27]([O:29][CH2:30][CH3:31])=[O:28])=[CH:23][CH:22]=2)[CH2:20][CH2:19][NH:18][CH2:17][CH2:16]1>>[C:1]([N:18]1[CH2:17][CH2:16][N:15]([C:21]2[CH:22]=[CH:23][C:24]([O:25][CH2:26][C:27]([O:29][CH2:30][CH3:31])=[O:28])=[CH:32][CH:33]=2)[CH2:20][CH2:19]1)(=[O:12])/[CH:2]=[CH:3]/[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10]Participants
3
Procedure
The same procedures as in Example 2 were carried out using (E)-2-decenoic acid and ethyl 2-[4-(1-piperazinyl)phenoxy]acetate dihydrochloride as starting raw materials, to produce ethyl 2-[4-[4-((E)-2-decenoyl)piperazin-1-yl]phenoxy]acetate (ethyl ester of Compound 47).
Sources & evidence
- ORD record
- ord-b73dca25459c483e9e5e802cd946a50a
- Source dataset
- uspto-grants-2016_08
- Patent number
- US09428477B2
Reaction notes
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