Hydroxyamine hydrochloride → HCID 136166877, compound

HRID 1618038Notes

Reaction equation

HRID 1618038 reaction equation
[CH3:1][C:2]1[CH:7]=[C:6]([C:8](=O)[CH2:9][C@H:10]([C:18]2[CH:23]=[CH:22][C:21]([CH:24]3[CH2:27][N:26]([S:28]([NH2:31])(=[O:30])=[O:29])[CH2:25]3)=[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.[NH2:34][OH:35].C(=O)([O-])O.[Na+]>>[OH:35]/[N:34]=[C:8](/[C:6]1[CH:5]=[CH:4][N:3]=[C:2]([CH3:1])[CH:7]=1)\[CH2:9][C@H:10]([C:18]1[CH:23]=[CH:22][C:21]([CH:24]2[CH2:25][N:26]([S:28]([NH2:31])(=[O:29])=[O:30])[CH2:27]2)=[CH:20][CH:19]=1)[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=1[CH3:17]

Participants

4

Procedure

In analogy to example 1, step 2, from (R)-3-(4-(3-(2-methylpyridin-4-yl)-3-oxo-1-o-tolylpropyl)phenyl)azetidine-1-sulfonamide and hydroxylamine hydrochloride in the presence of sodium hydrogencarbonate was prepared the title compound as a white foam, MS (ESI+): m/z=465.3 ([M+H]+).

Sources & evidence

ORD record
ord-1da89eb28f5d4f188fdcbd2da7460be1
Source dataset
uspto-grants-2014_07
Patent number
US08765730B2

Reaction notes

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