Hydroxyamine hydrochloride → HCID 136359987, compound

HRID 1617512Notes

Reaction equation

HRID 1617512 reaction equation
[CH3:1][C:2]1[CH:7]=[C:6]([C:8](=O)[CH2:9][CH:10]([C:18]2[CH:23]=[CH:22][C:21]([CH2:24][C:25]([OH:27])=[O:26])=[CH:20][CH:19]=2)[C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=2[CH3:17])[CH:5]=[CH:4][N:3]=1.Cl.[NH2:30][OH:31].C([O-])(O)=O.[Na+]>>[OH:31][N:30]=[C:8]([C:6]1[CH:5]=[CH:4][N:3]=[C:2]([CH3:1])[CH:7]=1)[CH2:9][CH:10]([C:18]1[CH:23]=[CH:22][C:21]([CH2:24][C:25]([OH:27])=[O:26])=[CH:20][CH:19]=1)[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=1[CH3:17]

Participants

4

Reactant 3

HCID 443297Hydroxyamine hydrochlorideHCID 516892Sodium BicarbonateHCID 67015534HCID 67015534, compound

Product 1

HCID 136359987HCID 136359987, compound

Procedure

In analogy to example 74, step 7, from {4-[3-(2-methyl-pyridin-4-yl)-3-oxo-1-o-tolyl-propyl]-phenyl}-acetic acid and hydroxylamine hydrochloride in the presence of NaHCO3 was prepared the title compound as a mixture of E and Z isomers (3.6:1) as a colorless oil, MS (ESI+): m/z=389.19 ([M+H]+).

Sources & evidence

ORD record
ord-bdf2019a8e9c45c9b45483e9b4040a4d
Source dataset
uspto-grants-2014_07
Patent number
US08765730B2

Reaction notes

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