Acetic Anhydride → HCID 178474256, compound

HRID 24812Notes

Reaction equation

HRID 24812 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8]/[C:9](=[C:16]2\[C:17](=[O:28])[NH:18][C:19]3[C:24]\2=[CH:23][C:22]([N+:25]([O-:27])=[O:26])=[CH:21][CH:20]=3)/[C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[CH:4][CH:3]=1.[C:29](OC(=O)C)(=[O:31])[CH3:30]>C(O)(=O)C>[C:29]([NH:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8]/[C:9](=[C:16]2\[C:17](=[O:28])[NH:18][C:19]3[C:24]\2=[CH:23][C:22]([N+:25]([O-:27])=[O:26])=[CH:21][CH:20]=3)/[C:10]2[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=2)=[CH:4][CH:3]=1)(=[O:31])[CH3:30]

Participants

4

Reactant 2

HCID 7918Acetic AnhydrideHCID 178507734HCID 178507734, compound

Product 1

HCID 178474256HCID 178474256, compound

Reagents, catalysts & solvents 1

HCID 176Acetic AcidSolvent

Procedure

Prepared analogously to Example 31 from (Z)-3-[1-(4-aminophenylamino)-1-phenyl-methylidene]-5-nitro-2-indolinone and acetic anhydride in glacial acetic acid.

Sources & evidence

ORD record
ord-f88cfa5bfefb4053a3176796ee4a7f8d
Source dataset
uspto-grants-2005_02
Patent number
US06855710B2

Reaction notes

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