Process for producing 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid and complexes thereof

Patent metadata

Field	Value
Publication number	US-9458117-B2
Application number	US-201414763550-A
Country	US
Kind code	B2
Filing date	Jan 22, 2014
Priority date	Jan 28, 2013
Publication date	Oct 4, 2016
Grant date	Oct 4, 2016

Abstract

A process for producing 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid (DOTA) including salts and hydrates thereof of general formula (I) from the respective cyclen.

The process involves the use of cationic- and anionic exchange resins and solvent treatments to remove the organic and inorganic contaminants. Any cations present in the raw DOTA or other contaminants resulting from the reaction of cyclen are largely reduced in early stages of the process allowing to obtain good yields of DOTA in a purified grade and in an easier and reliable way. The process is useful for the production of DOTA, of macrocyclic compounds including metal ions complexes thereof and of compositions including the macrocyclic compounds that can be used as contrast agents for magnetic resonance imaging.

First claim

The invention claimed is:

1. A process for preparing 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid (DOTA) or a salt or a hydrate thereof and having formula (I):

the process comprising the steps of:
a) reacting 1,4,7,10-tetra-azacyclododecane and a halo-acetic acid with a base at a pH ≧10 so as to obtain the DOTA;
b) crystallizing the DOTA obtained in step a) by adding an acid to achieve a pH ≦3, followed by a heating step and a cooling step, wherein the heating step is performed at a temperature in a range from 50° C. to 100° C. for at least 5 minutes, and the cooling step is performed at a temperature in a range from 5° C. to 25° C. for at least 5 minutes so as to obtain a raw material;
c) treating the raw material obtained in step b) with a cationic resin and then desorbing the DOTA with a volatile base solution;
d) further treating a solution resulting from step c) with an anionic resin; and
e) washing a product produced in step d) in a two-stage wash including a first stage with a first organic volatile acid with a pKa less than 5 until the DOTA starts to be released from the anionic resin, and a second stage with an organic volatile acid with a pKa less than or equal to the pKa of the first organic volatile acid and/or with a higher concentration than the first organic volatile acid to release the DOTA from the anionic resin.

2. The process according to claim 1 , wherein step a) is performed at a pH ≧13.

3. The process according to claim 1 , wherein an amount of the halo-acetic acid in step a) is at least 4 equivalents with regard to an initial amount of cyclen and an amount of the base is at least two times a number of equivalents of the halo-acetic acid.

4. The process according to claim 1 , wherein the halo-acetic acid is selected from the group consisting of iodoacetic acid, bromoacetic acid, and chloroacetic acid.

5. The process according to claim 1 , wherein the base in step a) is an alkali metal hydroxide.

6. The process according to claim 1 , wherein the acid added in step b) is selected from the group consisting of HCI, H 2 SO 4 , HNO 3 , HBr, HI, and HCIO 4 .

7. The process according to claim 1 , wherein the heating and cooling steps in step b) occur, respectively, at a temperature in a range from 50 to 60° C. and a temperature in a range from 5 to 10° C.

8. The process according to claim 1 , further comprising performing a washing step with a mixture of water and a water miscible low boiling organic solvent selected from the group of acetone, ethanol, methanol, and iso-propanol in a ratio from 1:1.5 to 1:3 (weight/weight) between step b) and step c).

9. The process according to claim 1 , wherein, in step e), the organic volatile acid used in the first stage is formic acid or acetic acid in an aqueous solution at a concentration between 0.01-0.1% or 0.1-0.3% respectively, and the organic volatile acid used in the second stage is formic acid in an aqueous solution at a concentration in a range from 1 to 20%.

10. A process for preparing gadoterate meglumine, the process comprising the steps of:
performing the process as described in claim 1 ;
f) adding Gd 2 O 3 to the DOTA so as to form a DOTA-Gd complex; and
g) adding meglumine to the DOTA-Gd complex.

Assignees

• Agfa Healthcare Nv

Inventors

• Buffel Diederik
• Ganorkar Rakesh
• Burt Jennifer
• Boi Xavier

Classifications

• A61K49/108

  the metal complex being Gd-DOTA · CPC title

• C07D457/04

  with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 8 · CPC title

• C07D257/02 Primary

  not condensed with other rings · CPC title