# US 5,708,166 A · Macrocyclic chelants, their chelates and uses thereof in the diagnostic field > Agents: this data is available as JSON from the patentgrep API and MCP server — see https://patentgrep.com/llms.txt - Number: US 5,708,166 A - Document ID: US5708166A - Status: Granted - Kind: A - Application number: 08/783,609 - Filed: 1997-01-14 - Granted: 1998-01-13 - Earliest claimed: 1994-07-29 - Assignees: Dibra S.p.A. - Inventors: Fulvio Uggeri; Pier Lucio Anelli; Giuseppe Manfredi; Marino Brocchetta; Franco Fedeli - Web page: https://patentgrep.com/patent/US5708166A ## CPC - C07D 257/02: not condensed with other rings - A61K 49/06: Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations - C07D: HETEROCYCLIC COMPOUNDS (macromolecular compounds C08) - A61K: PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES (devices or methods specially adapted for bringing pharmaceutical products into particular physical or administering forms A61J3/00; chemical aspects of, or use of materials for deodorisation of air, for disinfection or sterilisation, or for bandages, dressings, absorbent pads or surgical articles A61L; soap compositions C11D) ## Abstract This invention relates to novel compounds able to chelate paramagnetic bi- or trivalent metal ions, their chelates with said metal ions and their use as contrast agents in magnetic resonance imaging (MRI). ## Claims ### Claim 1 A method for the preparation of a compound of formula (I) ##STR18## wherein A is a group of formula ##STR19## wherein X is a --O--R group where R is hydrogen, or a linear or branched (C.sub.1 -C.sub.5) alkyl group which can be substituted or not by 1-6 hydroxy and/or alkoxy groups, or X is a --NR.sub.2 R.sub.3 group where R.sub.2 and R.sub.3 can be same or different and are an hydrogen atom, a linear or branched (C.sub.1 -C.sub.10) alkyl group which can be substituted or not by 1-6 hydroxy and/or alkoxy groups, or a polyoxaalkyl group comprising 1-10 oxygen atoms and 3-30 carbon atoms, or --NR.sub.2 R.sub.3 group is a heterocyclic residue wherein R.sub.2 and R.sub.3, taken together, form a (C.sub.4 -C.sub.5) chain which can be interrupted or not by O, N, S, >N--CH.sub.3, and can be substituted or not by one or more hydroxy or hydroxyalkyl groups, B.sub.1, B.sub.2, B.sub.3 can be same or different and have the same meaning as A, or are a --CHYCOX group, wherein Y is a --CH.sub.2 OR.sub.1 group, wherein R.sub.1 is hydrogen, or a linear or branched (C.sub.1 -C.sub.5) alkyl group which can be substituted or not by 1-6 hydroxy and/or alkoxy groups, or R.sub.1 is a phenyl or benzyl residue which can be also mono or polysubstituted on the aromatic ring by halogen, hydroxy, alkoxy, carboxy, carbamoyl, alkoxycarbonyl, (C.sub.1 -C.sub.5) alkyl, (C.sub.1 -C.sub.5) hydroxyalkyl, amino, acylamino groups, or Y can also be a R.sub.1 residue as defined above, as well as the chelates of said compound of formula (I) with the metal ions having atomic number selected between 20 and 31, 39, 42, 43, 44, 49, or between 57 and 83, as well as their salts with physiologically acceptable organic bases selected from primary, secondary, tertiary amines or basic amino acids, or with inorganic bases whose cations are sodium, potassium, magnesium, calcium or their mixtures, or with anions of physiologically acceptable organic acids, selected from acetate, succinate, citrate, fumarate, maleate, oxalate, or with anions of inorganic acids such as the ions of hydrohalogen acids, such as chlorides, bromides, iodides exploiting the elimination of water or alcohol starting from the precursors of formula (V) ##STR20## wherein X, B.sub.1, B.sub.2, B.sub.3 are as defined above and R is H, a linear or branched alkyl group which contains 1-5 carbon atoms or an unsubstituted or substituted benzyl group, according to the following scheme: ##STR21## and the reaction is carried out in an aqueous medium or in a dipolar aprotic solvent or a mixture thereof, at a controlled pH ranging from 8 to 12, by addition of a suitable organic or inorganic base, at a temperature ranging from 80.degree. to 160.degree. C. ### Claim 2 (depends on 1) The method according to claim 1, wherein the reaction solvent is water. ### Claim 3 (depends on 1) The method according to claim 1, wherein the organic base is selected from the group consisting of ethanolamine, diethanolamine, glucamine, N,N-dimethylglucamine, N-methylglucamine. ### Claim 4 (depends on 1) The method according to claim 1, wherein the organic base is N-methylglucamine. ### Claim 5 (depends on 1) The method according to claim 1, wherein the pH is kept between 9 and 11. ### Claim 6 (depends on 1) The method according to claim 1, wherein the temperature ranges from 100.degree. to 130.degree. C. ### Claim 7 (depends on 1) The method according to claim 1, wherein the reaction is carried out in an autoclave.