Sodium Hydroxide → HCID 178483748, compound

HRID 24896Notes

Reaction equation

HRID 24896 reaction equation
C([N:4]1[C:12]2[C:7](=[CH:8][C:9]([N+:13]([O-:15])=[O:14])=[CH:10][CH:11]=2)[C:6](=[C:16](OCC)[C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[C:5]1=[O:26])(=O)C.[CH3:27][N:28]([CH3:43])[CH2:29][CH2:30][N:31]([C:36]1[CH:42]=[CH:41][C:39]([NH2:40])=[CH:38][CH:37]=1)[S:32]([CH3:35])(=[O:34])=[O:33].[OH-].[Na+]>CN(C=O)C.CO>[CH3:27][N:28]([CH3:43])[CH2:29][CH2:30][N:31]([C:36]1[CH:37]=[CH:38][C:39]([NH:40]/[C:16](=[C:6]2\[C:5](=[O:26])[NH:4][C:12]3[C:7]\2=[CH:8][C:9]([N+:13]([O-:15])=[O:14])=[CH:10][CH:11]=3)/[C:17]2[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=2)=[CH:41][CH:42]=1)[S:32]([CH3:35])(=[O:34])=[O:33]

Participants

6

Reactant 3

HCID 14798Sodium HydroxideHCID 225696634-[N-(2-dimethylamino-ethyl)-N-methylsulphonyl-amino]-anilineHCID 542801041-Acetyl-3-{1-ethoxy-1-phenylmethylidene}-5-nitro-2-indolinone

Product 1

HCID 178483748HCID 178483748, compound

Reagents, catalysts & solvents 2

HCID 887MethanolSolventHCID 6228DimethylformamideSolvent

Procedure

Prepared analogously to Examples 1 and 187 from 1-acetyl-3-(1-ethoxy-1-phenyl-methylidene)-5-nitro-2-indolinone and 4-[N-(2-dimethylamino-ethyl)-N-methylsulphonyl-amino]-aniline in DMF and subsequent treatment with sodium hydroxide solution in methanol.

Sources & evidence

ORD record
ord-a13496f3a51843c998cd99dc7fe78f9a
Source dataset
uspto-grants-2005_02
Patent number
US06855710B2

Reaction notes

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