Benzenesulfonyl chloride, 3,4-dichloro- → N-(6-(2-(Benzo[d]thiazol-2-yl)phenoxy)-5-chloropyridin-3-yl)-3,4-dichloro-benzenesulfonamide

HRID 1801858Notes

Reaction equation

HRID 1801858 reaction equation
[S:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[C:10]1[CH:24]=[CH:23][CH:22]=[CH:21][C:11]=1[O:12][C:13]1[N:18]=[CH:17][C:16]([NH2:19])=[CH:15][C:14]=1[Cl:20].[Cl:25][C:26]1[CH:27]=[C:28]([S:33](Cl)(=[O:35])=[O:34])[CH:29]=[CH:30][C:31]=1[Cl:32]>>[S:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[C:10]1[CH:24]=[CH:23][CH:22]=[CH:21][C:11]=1[O:12][C:13]1[N:18]=[CH:17][C:16]([NH:19][S:33]([C:28]2[CH:29]=[CH:30][C:31]([Cl:32])=[C:26]([Cl:25])[CH:27]=2)(=[O:35])=[O:34])=[CH:15][C:14]=1[Cl:20]

Participants

3

Reactant 2

HCID 7383Benzenesulfonyl chloride, 3,4-dichloro-HCID 668854446-(2-(Benzo[d]thiazol-2-yl)phenoxy)-5-chloropyridin-3-amine

Product 1

HCID 66885443N-(6-(2-(Benzo[d]thiazol-2-yl)phenoxy)-5-chloropyridin-3-yl)-3,4-dichloro-benzenesulfonamide

Procedure

The title compound was prepared by reacting 6-(2-(benzo[d]thiazol-2-yl)phenoxy)-5-chloropyridin-3-amine (obtained as per procedure described in preparation 4) and 3,4-dichlorobenzene-1-sulfonyl chloride.

Sources & evidence

ORD record
ord-48e8843508534fee83e885a0e996f2c3
Source dataset
uspto-grants-2013_01
Patent number
US08349862B2

Reaction notes

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