LY 213024 → HCID 72738706, compound

HRID 2254366Notes

Reaction equation

HRID 2254366 reaction equation
[C:1]([C:4]1[CH:5]=[C:6]([CH:31]=[CH:32][CH:33]=1)[C:7]([C:9]1[CH:10]=[CH:11][C:12]([O:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH3:30])=[C:13]([CH2:15][CH2:16][C:17]([OH:19])=[O:18])[CH:14]=1)=O)([OH:3])=[O:2].Cl.[NH2:35][OH:36]>>[C:1]([C:4]1[CH:5]=[C:6]([C:7](=[N:35][OH:36])[C:9]2[CH:10]=[CH:11][C:12]([O:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH3:30])=[C:13]([CH2:15][CH2:16][C:17]([OH:19])=[O:18])[CH:14]=2)[CH:31]=[CH:32][CH:33]=1)([OH:3])=[O:2]

Participants

3

Reactant 2

HCID 195214LY 213024HCID 443297Hydroxyamine hydrochloride

Product 1

HCID 72738706HCID 72738706, compoundYield 81%

Procedure

The title product was also prepared in 81% yield directly from 5-(3-carboxybenzoyl)-2-(decyloxy)benzenepropanoic acid upon treatment with hydroxylamine hydrochloride according to the procedure of Example 51.

Sources & evidence

ORD record
ord-73dd11d1e5d34b969294177bce8bbab5
Source dataset
uspto-grants-1993_08
Patent number
US05235064

Reaction notes

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