4-[(Methylsulfonyl)amino]benzoyl chloride → N-[(1-Methyl-4-phenylpiperazin-2-yl)methyl]-4-[(methylsulfonyl)amino]benzamide

HRID 1589039Notes

Reaction equation

HRID 1589039 reaction equation
[CH3:1][N:2]1[CH2:7][CH2:6][N:5]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH2:4][CH:3]1[CH2:14][NH2:15].[CH3:16][S:17]([NH:20][C:21]1[CH:29]=[CH:28][C:24]([C:25](Cl)=[O:26])=[CH:23][CH:22]=1)(=[O:19])=[O:18]>>[CH3:1][N:2]1[CH2:7][CH2:6][N:5]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH2:4][CH:3]1[CH2:14][NH:15][C:25](=[O:26])[C:24]1[CH:28]=[CH:29][C:21]([NH:20][S:17]([CH3:16])(=[O:19])=[O:18])=[CH:22][CH:23]=1

Participants

3

Reactant 2

HCID 117911194-[(Methylsulfonyl)amino]benzoyl chlorideHCID 149987831-Methyl-4-phenyl-2-piperazinemethanamine

Product 1

HCID 14998865N-[(1-Methyl-4-phenylpiperazin-2-yl)methyl]-4-[(methylsulfonyl)amino]benzamide

Procedure

In a manner similar to preparation 3, react 1-methyl-4-phenyl-2-piperazinemethanamine with 4-[(methylsulfonyl)amino]benzoyl chloride to obtain the title compound.

Workup

  1. customIn a manner similar to preparation 3

Sources & evidence

ORD record
ord-081bdec4f52542cca6ba7bf782dc43da
Source dataset
uspto-grants-1993_06
Patent number
US05223623

Reaction notes

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