4-(3,3-Diethyl-ureido)-benzenesulfonyl chloride → 3-Amino-3-(2-chlorophenyl)-5-ethoxy-1-[4-(N',N'-diethylureido)benzenesulfonyl]-1,3-dihydroindol-2-one

HRID 234514Notes

Reaction equation

HRID 234514 reaction equation
[NH2:1][C:2]1([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=2[Cl:21])[C:10]2[C:5](=[CH:6][CH:7]=[C:8]([O:11][CH2:12][CH3:13])[CH:9]=2)[NH:4][C:3]1=[O:14].[CH2:22]([N:24]([CH2:38][CH3:39])[C:25](=[O:37])[NH:26][C:27]1[CH:32]=[CH:31][C:30]([S:33](Cl)(=[O:35])=[O:34])=[CH:29][CH:28]=1)[CH3:23]>>[NH2:1][C:2]1([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=2[Cl:21])[C:10]2[C:5](=[CH:6][CH:7]=[C:8]([O:11][CH2:12][CH3:13])[CH:9]=2)[N:4]([S:33]([C:30]2[CH:29]=[CH:28][C:27]([NH:26][C:25]([N:24]([CH2:38][CH3:39])[CH2:22][CH3:23])=[O:37])=[CH:32][CH:31]=2)(=[O:35])=[O:34])[C:3]1=[O:14]

Participants

3

Procedure

This compound is prepared according to the procedure described in EXAMPLE 30 from 3-amino-3-(2-chlorophenyl)-5-ethoxy-1,3-dihydroindol-2-one and 4-(N',N'-diethylureido)benzenesulfonyl chloride.

Workup

  1. customThis compound is prepared

Sources & evidence

ORD record
ord-78998dca7f1f45859a18c7493d041abb
Source dataset
uspto-grants-1997_01
Patent number
US05594023

Reaction notes

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