p-Bromobenzenesulfonyl chloride → 4-Bromo-N-[2-(1H-imidazol-1-yl)ethyl]benzenesulfonamide

HRID 64857

Reaction equation

HRID 64857 reaction equation
[N:1]1([CH2:6][CH2:7][NH2:8])[CH:5]=[CH:4][N:3]=[CH:2]1.[Br:9][C:10]1[CH:15]=[CH:14][C:13]([S:16](Cl)(=[O:18])=[O:17])=[CH:12][CH:11]=1>>[Br:9][C:10]1[CH:15]=[CH:14][C:13]([S:16]([NH:8][CH2:7][CH2:6][N:1]2[CH:5]=[CH:4][N:3]=[CH:2]2)(=[O:18])=[O:17])=[CH:12][CH:11]=1

Participants

3

Reactant 2

HCID 7396p-Bromobenzenesulfonyl chlorideHCID 4306672-(1H-imidazol-1-yl)ethanamine

Product 1

HCID 136873114-Bromo-N-[2-(1H-imidazol-1-yl)ethyl]benzenesulfonamide

Procedure

When 1H-imidazole-1-ethanamine was treated with 4-bromobenzenesulfonyl chloride by the procedure of Example 20, the compound of this example, mp 165°-167° C., was obtained.

Sources & evidence

ORD record
ord-b2d2a8b7c3874c64be8a0b528b437629
Source dataset
uspto-grants-1986_09
Patent number
US04610981

Linked notes

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