Hydroxyamine hydrochloride → HCID 58043335, compound

HRID 1617684Notes

Reaction equation

HRID 1617684 reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([CH:20]2[CH2:24][CH2:23][CH2:22][CH2:21]2)[CH2:9][C:10]([C:12]2[CH:13]=[CH:14][C:15](=[O:19])[N:16]([CH3:18])[CH:17]=2)=O)=[C:4]([F:25])[CH:3]=1.Cl.[NH2:27][OH:28].C([O-])(O)=O.[Na+]>>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([CH:20]2[CH2:24][CH2:23][CH2:22][CH2:21]2)[CH2:9]/[C:10](/[C:12]2[CH:13]=[CH:14][C:15](=[O:19])[N:16]([CH3:18])[CH:17]=2)=[N:27]\[OH:28])=[C:4]([F:25])[CH:3]=1

Participants

4

Reactant 3

HCID 443297Hydroxyamine hydrochlorideHCID 516892Sodium BicarbonateHCID 66669208HCID 66669208, compound

Product 1

HCID 58043335HCID 58043335, compound

Procedure

In analogy to example 151, step 3, 5-[3-(4-bromo-2-fluoro-phenyl)-3-cyclopentyl-propionyl]-1-methyl-1H-pyridin-2-one was reacted with hydroxylamine hydrochloride in the presence of NaHCO3 to give the title compound as a colorless solid, MS (ESI+): m/z=421.1 [M+H]+.

Sources & evidence

ORD record
ord-cda2a3c6829d42a78535a676ef1e18dd
Source dataset
uspto-grants-2014_07
Patent number
US08765730B2

Reaction notes

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