Acetic Anhydride → HCID 178474194, compound

HRID 24762Notes

Reaction equation

HRID 24762 reaction equation
[NH2:1][C:2]1[CH:3]=[C:4]([NH:8]/[C:9](=[C:16]2\[C:17](=[O:25])[NH:18][C:19]3[C:24]\2=[CH:23][CH:22]=[CH:21][CH:20]=3)/[C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[CH:5]=[CH:6][CH:7]=1.[C:26](OC(=O)C)(=[O:28])[CH3:27]>C(O)(=O)C>[C:26]([NH:1][C:2]1[CH:3]=[C:4]([NH:8]/[C:9](=[C:16]2\[C:17](=[O:25])[NH:18][C:19]3[C:24]\2=[CH:23][CH:22]=[CH:21][CH:20]=3)/[C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[CH:5]=[CH:6][CH:7]=1)(=[O:28])[CH3:27]

Participants

4

Procedure

Prepared analogously to Example 31 from (Z)-3-[1-(3-aminophenylamino)-1-phenyl-methylidene]-2-indolinone and acetic anhydride in glacial acetic acid.

Sources & evidence

ORD record
ord-8d4d919ef9b64a7080f25268eaceba65
Source dataset
uspto-grants-2005_02
Patent number
US06855710B2

Reaction notes

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