1-((Pyridin-4-yl)methyl)piperazine → HCID 57496151, compound

HRID 1797963Notes

Reaction equation

HRID 1797963 reaction equation
[C:1]([C:3]1[CH:4]=[C:5]([NH:9][C:10](=[O:33])[NH:11][C:12]2[CH:17]=[CH:16][C:15]([S:18]([NH:21][CH2:22][C:23]3[CH:28]=[CH:27][C:26]([S:29](=[O:32])(=[O:31])[NH2:30])=[CH:25][CH:24]=3)(=[O:20])=[O:19])=[CH:14][CH:13]=2)[CH:6]=[CH:7][CH:8]=1)#[N:2].[N:34]1[CH:39]=[CH:38][C:37]([CH2:40][N:41]2[CH2:46][CH2:45][NH:44][CH2:43][CH2:42]2)=[CH:36][CH:35]=1>>[NH:2]=[C:1]([N:44]1[CH2:45][CH2:46][N:41]([CH2:40][C:37]2[CH:36]=[CH:35][N:34]=[CH:39][CH:38]=2)[CH2:42][CH2:43]1)[C:3]1[CH:4]=[C:5]([NH:9][C:10](=[O:33])[NH:11][C:12]2[CH:17]=[CH:16][C:15]([S:18]([NH:21][CH2:22][C:23]3[CH:28]=[CH:27][C:26]([S:29](=[O:32])(=[O:31])[NH2:30])=[CH:25][CH:24]=3)(=[O:20])=[O:19])=[CH:14][CH:13]=2)[CH:6]=[CH:7][CH:8]=1

Participants

3

Reactant 2

HCID 8087151-((Pyridin-4-yl)methyl)piperazineHCID 574961804-(3-(3-cyanophenyl)ureido)-N-(4-sulfamoylbenzyl)benzenesulfonamide

Product 1

HCID 57496151HCID 57496151, compoundYield 11%

Procedure

The title compound was prepared from 4-(3-(3-cyanophenyl)ureido)-N-(4-sulfamoylbenzyl)benzenesulfonamide following procedure C and using 2 equivalents of 1-(pyridin-4-ylmethyl)piperazine as secondary amine. The product was purified by preparative HPLC.

Workup

  1. customThe product was purified by preparative HPLC

Sources & evidence

ORD record
ord-ab10137f42064bd2ab41600e7b5961c1
Source dataset
uspto-grants-2013_01
Patent number
US08343963B2

Reaction notes

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