4-Bromo-2-methylbenzenesulfonyl chloride → 4-Bromo-2-methyl-N-((1-methyl-1H-indol-5-yl)methyl)benzenesulfonamide

HRID 73073

Reaction equation

HRID 73073 reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([S:8](Cl)(=[O:10])=[O:9])=[C:4]([CH3:12])[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]=[CH: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])[CH:15]=[CH:16]3)(=[O:10])=[O:9])=[C:4]([CH3:12])[CH:3]=1

Participants

3

Reactant 2

HCID 27813384-Bromo-2-methylbenzenesulfonyl chlorideHCID 18525752(1-methyl-1H-indol-5-yl)methylamine

Product 1

HCID 668378594-Bromo-2-methyl-N-((1-methyl-1H-indol-5-yl)methyl)benzenesulfonamide

Procedure

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

Sources & evidence

ORD record
ord-dfa7f917077c4245b2e224bef4d1c03a
Source dataset
uspto-grants-2014_09
Patent number
US08829026B2

Linked notes

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