10-Undecenoyl chloride → HCID 18694928, compound
Reaction equation
[C:1]([N:4]1[CH2:9][C:8](=[O:10])[N:7]([C:11](=[O:20])[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH3:19])[CH2:6][C:5]1=[O:21])(=[O:3])[CH3:2].[C:22](Cl)(=O)[CH2:23]CCCCCCCC=C>>[C:1]([N:4]1[CH2:9][C:8](=[O:10])[N:7]([C:11](=[O:20])[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH:22]=[CH2:23])[CH2:6][C:5]1=[O:21])(=[O:3])[CH3:2]Participants
3
Procedure
##STR27## Synthesized as for 1-Acetyl4-nonanoyl-2,5-piperazinedione in EXAMPLE I using 10-undecenoyl chloride in place of nonanoyl chloride.
Sources & evidence
- ORD record
- ord-acf45aef18024630b924eea42df8cad2
- Source dataset
- uspto-grants-2000_08
- Patent number
- US06096098
Reaction notes
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