O-tert-butylhydroxylamine → 5-[[3-[(E)-(2-methylpropan-2-yl)oxyiminomethyl]phenyl]methyl-[(1S)-1,2,3,4-tetrahydronaphthalen-1-yl]carbamoyl]benzene-1,2,4-tricarboxylic acid

HRID 2307694Notes

Reaction equation

HRID 2307694 reaction equation
[CH:1]([C:3]1[CH:4]=[C:5]([CH:35]=[CH:36][CH:37]=1)[CH2:6][N:7]([C@@H:25]1[C:34]2[C:29](=[CH:30][CH:31]=[CH:32][CH:33]=2)[CH2:28][CH2:27][CH2:26]1)[C:8]([C:10]1[CH:15]=[C:14]([C:16]([OH:18])=[O:17])[C:13]([C:19]([OH:21])=[O:20])=[CH:12][C:11]=1[C:22]([OH:24])=[O:23])=[O:9])=O.[C:38]([O:42][NH2:43])([CH3:41])([CH3:40])[CH3:39]>>[C:38]([O:42]/[N:43]=[CH:1]/[C:3]1[CH:4]=[C:5]([CH:35]=[CH:36][CH:37]=1)[CH2:6][N:7]([C@@H:25]1[C:34]2[C:29](=[CH:30][CH:31]=[CH:32][CH:33]=2)[CH2:28][CH2:27][CH2:26]1)[C:8]([C:10]1[CH:15]=[C:14]([C:16]([OH:18])=[O:17])[C:13]([C:19]([OH:21])=[O:20])=[CH:12][C:11]=1[C:22]([OH:24])=[O:23])=[O:9])([CH3:41])([CH3:40])[CH3:39]

Participants

3

Procedure

The product from Example 76E and O-(tert-butyl)hydroxylamine were processed as described in Example 76F to provide the title compound.

Sources & evidence

ORD record
ord-a0fe25e684864a7b9e90bd18ee4a7aa3
Source dataset
uspto-grants-2004_12
Patent number
US06831193B2

Reaction notes

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