HCID 15027725, compound → HCID 14478192, compound

HRID 373155Notes

Reaction equation

HRID 373155 reaction equation
OC(C1C=CC(NS(C)(=O)=O)=CC=1)CCCN(CCC1C=CC=C(C)N=1)C.[OH:28][CH:29]([C:45]1[CH:50]=[CH:49][C:48]([NH:51][S:52]([CH3:55])(=[O:54])=[O:53])=[CH:47][CH:46]=1)[CH2:30][CH2:31][CH2:32][N:33]([CH2:36][CH2:37][C:38]1[CH:43]=[CH:42][CH:41]=[C:40]([CH3:44])[N:39]=1)[CH2:34][CH3:35]>>[CH2:34]([N:33]([CH2:36][CH2:37][C:38]1[CH:43]=[CH:42][CH:41]=[C:40]([CH3:44])[N:39]=1)[CH2:32][CH2:31][CH2:30][C:29]([C:45]1[CH:46]=[CH:47][C:48]([NH:51][S:52]([CH3:55])(=[O:53])=[O:54])=[CH:49][CH:50]=1)=[O:28])[CH3:35]

Participants

3

Reactant 2

HCID 15027725HCID 15027725, compoundHCID 15027726HCID 15027726, compound

Product 1

HCID 14478192HCID 14478192, compound

Procedure

The same procedure as that of Example 4-(2) was repeated except that N-[4-[1-hydroxy-4-[N-methyl-2-(6-methyl-2-pyridyl)ethylamino]butyl]phenyl]methanesulfonamide was replaced with N-[4-[1-hydroxy-4-[N-ethyl-2-(6-methyl-2-pyridyl)ethylamino]butyl]phenyl]methanesulfonamide obtained in the above step (1).

Workup

  1. customobtained in the above step (1)

Sources & evidence

ORD record
ord-c85fb30698d2461e870ad6c8db4d6c63
Source dataset
uspto-grants-1992_11
Patent number
US05162347

Reaction notes

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