HCID 19893582, compound → HCID 67794027, compound

HRID 892892Notes

Reaction equation

[C:1]([NH:20][C:21]1[CH:27]=[CH:26][C:24]([NH2:25])=[CH:23][CH:22]=1)(=[O:19])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8]/[CH:9]=[CH:10]\[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18].[C:28]([O:31][CH:32]([C:41]([CH3:48])([CH3:47])[CH2:42][O:43][C:44](=[O:46])[CH3:45])[C:33]([NH:35][CH2:36][CH2:37][C:38](O)=[O:39])=[O:34])(=[O:30])[CH3:29]>>[C:1]([NH:20][C:21]1[CH:27]=[CH:26][C:24]([NH:25][C:38](=[O:39])[CH2:37][CH2:36][NH:35][C:33](=[O:34])[CH:32]([O:31][C:28](=[O:30])[CH3:29])[C:41]([CH3:47])([CH3:48])[CH2:42][O:43][C:44](=[O:46])[CH3:45])=[CH:23][CH:22]=1)(=[O:19])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8]/[CH:9]=[CH:10]\[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18]

Participants

Reactant 2

HCID 19893582HCID 19893582, compound

HCID 68840460p-Oleoylaminoaniline

Product 1

HCID 67794027HCID 67794027, compoundYield 69%

Procedure

4-Oleoylaminoaniline (744 mg) and 606 mg of 3-[N-(2,4-diacetoxy-3,3-dimethyl-1-oxobutyl)amino]propionic acid were reacted in the same manner as in Example 1 to obtain 900 mg of the title compound (yield: 69%).

Sources & evidence

ORD record: ord-d57083bee97b4097a6037e2a0e9cbda3
Source dataset: uspto-grants-1992_06
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05120738

Reaction notes

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