IP Library Granted Patent US 10,450,267
Granted Patent B2
US 10,450,267 · App. 16/204,413 · Granted Oct 22, 2019

Method for preparing N-[4-(2-{[2-(4-methane sulfonamidophenoxy) ethyl] (methyl)amino}ethyl)phenyl]methanesulfonamide (dofetilide)

Inventor: Marek Stancl (Brno, CZ)
Assignee: Farmak, A.S.
C07C311/08C07C303/36
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Quick Facts
Patent No.
US 10,450,267
App. No.
16/204,413
Granted
Oct 22, 2019
Kind
B2
Abstract

A method for preparing 1-(4-methanesulfonamidophenoxy)-2-[N-(4-methanesulfonamidophenethyl)-N-methylamino]ethane (Dofetilide) of formula I by sulfonylation of 1-(4-aminophenoxy)-2-[N-(4-aminophenethyl)-N-methylamino]ethane of formula II with N-methylsulfonyl-N′-methylimidazolium chloride of formula III.

Claims (7)

1. A method for preparing 1-(4-methanesulfonamidophenoxy)-2-[N-(4-methane-sulfonamidophenethyl)-N-methylamino]ethane (Dofetilide) of formula I

by sulfonylation of 1-(4-aminophenoxy)-2-[N-(4-aminophenethyl)-N-methylamino]ethane of formula II,

characterized in that the sulfonylation is carried out with N-methylsulfonyl-N′-methylimidazolium chloride of formula III

in an organic solvent.

2. The method according to claim 1 , characterized in that N-methylsulfonyl-N′-methylimidazolium chloride prepared by reaction of 1-methylimidazole with methanesulfonyl chloride is used.

3. The method according to claim 1 , characterized in that the organic solvent is N-methylpyrrolidone, N,N-dimethylformamide, N,N-dimethylacetamide or their mixture.

4. The method according to claim 1 , characterized in that the reaction is carried out at a temperature of −20 to −5° C.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 3, 2018
From: STANCL, MAREK
To: FARMAK, A.S.
Reel/Frame 047648/0218 →
Priority Claims (1)
CZ 2017-772 · Dec 1, 2017 · national
Continuity (1)
Related Publication 20190169121A1 · Jun 6, 2019
Cited By (4)
US 12,390,431 US 12,396,970 US 12,403,109 US 12,740,947