Oleic Acid → N-[2-(Oleoyloxy)phenyl]-3-[N-(2,2,5,5-tetramethyl-1,3-dioxane-4-carbonyl)amino]propanamide
Reaction equation
[OH:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[NH:8][C:9](=[O:25])[CH2:10][CH2:11][NH:12][C:13]([CH:15]1[C:20]([CH3:22])([CH3:21])[CH2:19][O:18][C:17]([CH3:24])([CH3:23])[O:16]1)=[O:14].[C:26](O)(=[O:44])[CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33]/[CH:34]=[CH:35]\[CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH3:43]>>[C:26]([O:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[NH:8][C:9](=[O:25])[CH2:10][CH2:11][NH:12][C:13]([CH:15]1[C:20]([CH3:21])([CH3:22])[CH2:19][O:18][C:17]([CH3:24])([CH3:23])[O:16]1)=[O:14])(=[O:44])[CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33]/[CH:34]=[CH:35]\[CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH3:43]Participants
3
Procedure
N-(2-Hydroxyphenyl)-3-[N-(2,2,5,5-tetramethyl-1,3-dioxane-4-carbonyl)amino]propanamide (350 mg) and 282 mg of oleic acid were reacted in the same manner as in Example 15 to obtain 411 mg of the title compound (yield: 67%).
Sources & evidence
- ORD record
- ord-b665a17c5a2b42d3b594e6c4b8497588
- Source dataset
- uspto-grants-1992_06
- Patent number
- US05120738
Reaction notes
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