Benzenesulfonamide, 4-amino-N,N-dimethyl- → HCID 178486143, compound

HRID 24952

Reaction equation

HRID 24952 reaction equation
C([N:4]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[C:6](=[C:13](OCC)[C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[C:5]1=[O:23])(=O)C.[CH3:24][N:25]([CH3:36])[S:26]([C:29]1[CH:34]=[CH:33][C:32]([NH2:35])=[CH:31][CH:30]=1)(=[O:28])=[O:27]>>[CH3:24][N:25]([CH3:36])[S:26]([C:29]1[CH:34]=[CH:33][C:32]([NH:35]/[C:13](=[C:6]2\[C:5](=[O:23])[NH:4][C:12]3[C:7]\2=[CH:8][CH:9]=[CH:10][CH:11]=3)/[C:14]2[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=2)=[CH:31][CH:30]=1)(=[O:27])=[O:28]

Participants

3

Reactant 2

HCID 74369Benzenesulfonamide, 4-amino-N,N-dimethyl-HCID 542378881-Acetyl-3-(1-ethoxy-1-phenylmethylidene}-2-indolinone

Product 1

HCID 178486143HCID 178486143, compound

Procedure

Prepared analogously to Example 1c from 1-acetyl-3-(1-ethoxy-1-phenyl-methylidene)-2-indolinone and 4-aminobenzenesulphonic acid-dimethylamide.

Sources & evidence

ORD record
ord-269bd2e836f64ed6b0464e450ce23f23
Source dataset
uspto-grants-2005_02
Patent number
US06855710B2

Linked notes

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