N-(3-Hydroxypropyl)oleamide → 3-(N-Oleoylamino)propyl 3-[N-(2,2,5,5-tetramethyl-1,3-dioxane-4-carbonyl)amino]propionate
反応式
[OH:1][CH2:2][CH2:3][CH2:4][NH:5][C:6](=[O:24])[CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13]/[CH:14]=[CH:15]\[CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23].[CH3:25][C:26]1([CH3:42])[O:31][CH:30]([C:32]([NH:34][CH2:35][CH2:36][C:37](O)=[O:38])=[O:33])[C:29]([CH3:41])([CH3:40])[CH2:28][O:27]1>>[CH3:25][C:26]1([CH3:42])[O:31][CH:30]([C:32]([NH:34][CH2:35][CH2:36][C:37]([O:1][CH2:2][CH2:3][CH2:4][NH:5][C:6](=[O:24])[CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13]/[CH:14]=[CH:15]\[CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23])=[O:38])=[O:33])[C:29]([CH3:41])([CH3:40])[CH2:28][O:27]1参加物
3
実験手順
N-(3-Hydroxypropyl)oleamide (3.54 g) and 2.59 g of 3-[N-(2,2,5,5-tetramethyl-1,3-dioxane-4-carbonyl)amino]propionic acid were reacted in the same manner as in Example 15 to obtain 5.05 g of the title compound (yield: 85%)
出典と根拠
- ORDレコード
- ord-f77721e0cb934d8c9d39477115b4d3a0
- 出典データセット
- uspto-grants-1992_06