Process for the direct preparation of N,N-disubstituted derivatives for 4,13-diaza-18-crown-6

Claim 2

A process for the direct preparation of N,N-disubstituted derivatives of 4,13-diaza-18-crown-6 in which the both nitrogen atoms in the ring have identical substituents and derive originally from an amine, comprising reacting a 1,8-diiodo-3,6-dioxaoctane or alkyl or aryl derivatives thereof with a molar equivalent of a primary amine having 1-12 carbon atoms in the molecule in the presence of an alkali metal or alkaline earth metal carbonate base and a nitrile, formamide or sulfoxide solvent at a temperature of 25° to 175° C. for a period of 12 to 60 hours, wherein the concentration of amine and diiodide in the solvent are in the range 0.1 to 0.5 molar and the amount of base relative to the amine is 4-6 molar equivalents.

Claim 3

A process according to claim 1 wherein the deriatives of 1,8-diiodo-3,6-dioxaoctane are selected from the group having the following typical substitutents: 2-alkyl, 4-alkyl, 2,4-dialkyl, 2,4,5-trialkyl and 2,4,5,7-tetralkyl, 4,5-benzo, or 2-aryl, 4-aryl, 2,4-diaryl, 2,4,5-triaryl, 2,4,5,7-tetraaryl and alkyl or aryl derivatives thereof; wherein the alkyl groups are carbon residues containing 1-12 carbons, or are benzyl or substituted benzyl groups.

Claim 4

The process according to claim 2 wherein the diiodo derivatives are selected from the group 1,8-diiodo-3,6-dioxaoctane, 4,5-benzo-1,8-diiodo-3,6-dioxaoctane, 2-methyl-1, 8-diiodo-3,6-dioxaoctane, 4-methyl-1,8-diiodo-3,6-dioxaoctane, 4-ethyl-1,8-diiodo-3,6-dioxaoctane and 4,5-dipropyl-1,8-diiodo-3,6-dioxaoctane.

Claim 5

The process according to claim 1 wherein the primary amine is selected from the group aminoalkanes, benzylamine and alkyl substituted derivatives thereof, 2-methoxybenzylamine and positional isomers thereof, 2-alkyloxybenzylamine and positional isomers thereof, benzylamine derivatives having alkyl substituents and one or more functional groups selected from the group alkyl, alkoxyalkyl, thioalkoxyalkyl, halogen, cyano, nitro, carboalkoxy, azo and carbocyclic aryl; allylamine and alkyl substituted derivatives thereof, 2-(aminoethyl)-furan and positional isomers and alkyl substituted derivatives thereof, 2-(aminomethyl)thiophene and alkyl substituted derivatives and positional isomers thereof, 2-ethanolamine, 3-propanolamine, 4-butanolamine, 5-pentanolamine, 6-hexanolamine, 7-heptanolamine, 8-octanolamine, 9-nonanolamine, 10-decanolamine, 11-undecanolamine, 12-dodecanolamine and alkyl derivatives thereof, 2-(aminomethyl)pyridine and positional isomers and alkyl derivatives thereof, said alkyl groups containing 1-12 carbon atoms.

Claim 6

The process according to claim 4 in which the primary amine is selected from a group consisting of: benzylamine, 2-methoxybenzylamine, allylamine, 2-ethanolamine, 2-(aminomethyl)furan and 2-(aminomethyl)-pyridine.

Claim 7

The process according to claim 1 wherein the base comprises an alkali metal or alkaline earth metal carbonate selected from the group consisting essentially of lithium carbonate, sodium carbonate, potassium carbonate, strontium carbonate, rubidium carbonate, cesium carbonate, magnesium carbonate, calcium carbonate and barium carbonate.

Claim 8

The process according to claim 6 wherein the carbonate is sodium carbonate.

Claim 9

The process according to claim 1 wherein the solvent is acetonitrile, propionitrile, N,N-dimethylformamide or dimethylsulfoxide.

Claim 10

The process according to claim 8 wherein the solvent is acetonitrile.