Hydroxyamine hydrochloride → HCID 58043611, compound

HRID 1617872Notes

Reaction equation

HRID 1617872 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([C:20]2[CH:25]=[CH:24][C:23]([S:26]([CH2:29][CH3:30])(=[O:28])=[O:27])=[CH:22][CH: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:31])[CH:3]=1.Cl.[NH2:33][OH:34].C(=O)([O-])O.[Na+]>>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([C:20]2[CH:21]=[CH:22][C:23]([S:26]([CH2:29][CH3:30])(=[O:27])=[O:28])=[CH:24][CH:25]=2)[CH2:9]/[C:10](/[C:12]2[CH:13]=[CH:14][C:15](=[O:19])[N:16]([CH3:18])[CH:17]=2)=[N:33]\[OH:34])=[C:4]([F:31])[CH:3]=1

Participants

4

Procedure

In analogy to example 151, step 3, 5-(3-(4-chloro-2-fluorophenyl)-3-(4-(ethylsulfonyl)-phenyl)propanoyl)-1-methylpyridin-2(1H)-one was reacted with hydroxylamine hydrochloride in the presence of sodium hydrogencarbonate to give the title compound as a colourless solid, MS (ESI+): m/z=477.0 [M+H]+.

Sources & evidence

ORD record
ord-8637de75c3e849fa931485b27b5d04ed
Source dataset
uspto-grants-2014_07
Patent number
US08765730B2

Reaction notes

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