HCID 15010988, compound → HCID 19893625, compound

HRID 892908Notes

Reaction equation

HRID 892908 reaction equation
[OH:1][CH2:2][CH2:3][CH2:4][NH:5][C:6](=[O:16])[CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH3:15].[CH3:17][C:18]1([CH3:34])[O:23][CH:22]([C:24]([NH:26][CH2:27][CH2:28][C:29](O)=[O:30])=[O:25])[C:21]([CH3:33])([CH3:32])[CH2:20][O:19]1>>[CH3:17][C:18]1([CH3:34])[O:23][CH:22]([C:24]([NH:26][CH2:27][CH2:28][C:29]([O:1][CH2:2][CH2:3][CH2:4][NH:5][C:6](=[O:16])[CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH3:15])=[O:30])=[O:25])[C:21]([CH3:33])([CH3:32])[CH2:20][O:19]1

Participants

3

Reactant 2

HCID 15010988HCID 15010988, compoundHCID 189385173-[N-(2,2,5,5-Tetramethyl-1,3-dioxane-4-carbonyl)amino]propionic acid

Product 1

HCID 19893625HCID 19893625, compoundYield 98.1%

Procedure

N-(3-Hydroxypropyl)decanamide (2.29 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 4.61 g of the title compound (yield: 98%)

Sources & evidence

ORD record
ord-7b36c30d19e2437084183ec54dee310a
Source dataset
uspto-grants-1992_06
Patent number
US05120738

Reaction notes

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