HCID 178470667, compound → HCID 178525177, compound

HRID 24742Notes

Reaction equation

HRID 24742 reaction equation
C([O:3][C:4]([CH2:6][C:7]1[CH:8]=[C:9]([NH:13]/[C:14](=[C:21]2\[C:22](=[O:30])[NH:23][C:24]3[C:29]\2=[CH:28][CH:27]=[CH:26][CH:25]=3)/[C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[CH:10]=[CH:11][CH:12]=1)=[O:5])C>[OH-].[Na+]>[C:4]([CH2:6][C:7]1[CH:8]=[C:9]([NH:13]/[C:14](=[C:21]2\[C:22](=[O:30])[NH:23][C:24]3[C:29]\2=[CH:28][CH:27]=[CH:26][CH:25]=3)/[C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[CH:10]=[CH:11][CH:12]=1)([OH:5])=[O:3]

Participants

3

Procedure

Prepared analogously to Example 8 by saponification of (Z)-3-[1-(3-ethoxycarbonylmethyl-phenylamino)-1-phenyl-methylidene]-2-indolinone in sodium hydroxide solution.

Sources & evidence

ORD record
ord-a6070f2d8623488c8cef2cade4573e68
Source dataset
uspto-grants-2005_02
Patent number
US06855710B2

Reaction notes

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