Glyceraldehyde → HCID 73470855, compound

HRID 1292253Notes

Reaction equation

[Cl:1][C:2]1[CH:25]=[CH:24][C:5]([C:6]([N:8]2[C:16]3[C:11](=[CH:12][C:13]([O:17][CH3:18])=[CH:14][CH:15]=3)[C:10]([CH2:19][CH2:20][O:21][NH2:22])=[C:9]2[CH3:23])=[O:7])=[CH:4][CH:3]=1.[O:26]=[CH:27][CH:28]([CH2:30]O)[OH:29]>>[Cl:1][C:2]1[CH:25]=[CH:24][C:5]([C:6]([N:8]2[C:16]3[C:11](=[CH:12][C:13]([O:17][CH3:18])=[CH:14][CH:15]=3)[C:10]([CH2:19][CH2:20][O:21][N:22]=[CH:30][CH:28]([CH2:27][OH:26])[OH:29])=[C:9]2[CH3:23])=[O:7])=[CH:4][CH:3]=1

Participants

Reactant 2

HCID 751Glyceraldehyde

HCID 18914648HCID 18914648, compound

Product 1

HCID 73470855HCID 73470855, compound

Procedure

The title compound is prepared by reaction of O-2-[1-(4-chlorobenzoyl)-5-methoxy-2-methylindol-3-yl]ethylhydroxylamine with glyceraldehyde by the method of Example 1.

Sources & evidence

ORD record: ord-a1fab125dd584e7da5cc0a847f844bbd
Source dataset: uspto-grants-1998_05
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05756531

Reaction notes

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