4-[N-(2-dimethylamino-ethyl)-N-methylsulphonyl-amino]-aniline → HCID 178456774, compound

HRID 1007423Notes

Reaction equation

HRID 1007423 reaction equation
C([N:4]1[C:12]2[C:7](=[CH:8][C:9]([O:15][CH3:16])=[C:10]([O:13][CH3:14])[CH:11]=2)[C:6](=[C:17](OCC)[CH2:18][CH3:19])[C:5]1=[O:23])(=O)C.[CH3:24][N:25]([CH3:40])[CH2:26][CH2:27][N:28]([S:36]([CH3:39])(=[O:38])=[O:37])[C:29]1[CH:34]=[CH:33][C:32]([NH2:35])=[CH:31][CH:30]=1>>[CH3:24][N:25]([CH3:40])[CH2:26][CH2:27][N:28]([C:29]1[CH:30]=[CH:31][C:32]([NH:35]/[C:17](=[C:6]2\[C:5](=[O:23])[NH:4][C:12]3[C:7]\2=[CH:8][C:9]([O:15][CH3:16])=[C:10]([O:13][CH3:14])[CH:11]=3)/[CH2:18][CH3:19])=[CH:33][CH:34]=1)[S:36]([CH3:39])(=[O:38])=[O:37]

Participants

3

Procedure

Prepared from 1-acetyl-3-(1-ethoxy-1-ethyl-methylidene)-5,6-dimethoxy-2-indolinone and N-(2-dimethylamino-ethyl)-N-methylsulphonyl-p-phenylenediamine

Sources & evidence

ORD record
ord-0a3151021298453e8bac93b917537c7a
Source dataset
uspto-grants-2004_09
Patent number
US06794395B1

Reaction notes

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