4-Bromo-2-chlorobenzenesulfonyl chloride → HCID 66837908, compound

HRID 73100Notes

Reaction equation

HRID 73100 reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([S:8](Cl)(=[O:10])=[O:9])=[C:4]([Cl:12])[CH:3]=1.[CH3:13][N:14]1[C:22]2[C:17](=[CH:18][C:19]([CH2:23][NH2:24])=[CH:20][CH:21]=2)[CH:16]=[N:15]1>>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([NH:24][CH2:23][C:19]2[CH:18]=[C:17]3[C:22](=[CH:21][CH:20]=2)[N:14]([CH3:13])[N:15]=[CH:16]3)(=[O:10])=[O:9])=[C:4]([Cl:12])[CH:3]=1

Participants

3

Reactant 2

HCID 27347664-Bromo-2-chlorobenzenesulfonyl chlorideHCID 230001565-(Aminomethyl)-1-methyl-1H-indazole

Product 1

HCID 66837908HCID 66837908, compound

Procedure

The titled compound was prepared according to the procedure described in step-1 of Example 1 from 4-bromo-2-chlorobenzene-1-sulfonyl chloride and (1-methyl-1H-indazol-5-yl)methanamine.

Sources & evidence

ORD record
ord-ccfaa05d768e4ceda809b8ae2d641243
Source dataset
uspto-grants-2014_09
Patent number
US08829026B2

Reaction notes

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