Hydroxyamine hydrochloride → HCID 136166895, compound

HRID 1617828Notes

Reaction equation

HRID 1617828 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]([C:24]3[CH:29]=[CH:28][C:27]([C:30]([OH:32])=[O:31])=[CH:26][CH: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]=[C:4]([CH3:34])[N:3]=1.Cl.[NH2:36][OH:37].C(=O)([O-])O.[Na+]>>[CH3:1][C:2]1[CH:7]=[C:6](/[C:8](=[N:36]/[OH:37])/[CH2:9][C@H:10]([C:18]2[CH:19]=[CH:20][C:21]([C:24]3[CH:25]=[CH:26][C:27]([C:30]([OH:32])=[O:31])=[CH:28][CH:29]=3)=[CH:22][CH:23]=2)[C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=2[CH3:17])[CH:5]=[C:4]([CH3:34])[N:3]=1

Participants

4

Procedure

In analogy to example 132, step 6, from 4′-[(R)-3-(2,6-dimethyl-pyridin-4-yl)-3-oxo-1-o-tolyl-propyl]-biphenyl-4-carboxylic acid and hydroxylamine hydrochloride in the presence of sodium hydrogencarbonate was prepared the title compound as a white semisolid, MS (ESI−): m/z=463.3 ([M−H]−).

Sources & evidence

ORD record
ord-7d0d231950a54ce9aadd9ea98cabe312
Source dataset
uspto-grants-2014_07
Patent number
US08765730B2

Reaction notes

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