AU726604B2

AU726604B2 - Cascade polymer complexes, process for their production and pharmaceutical agents containing said complexes

Info

Publication number: AU726604B2
Application number: AU47393/99A
Authority: AU
Inventors: Thomas Frenzel; Andreas Muhler; Johannes Platzek; Bernd Raduchel; Heribert Schmitt-Willich
Original assignee: Schering AG
Current assignee: Bayer Pharma AG
Priority date: 1995-07-04
Filing date: 1999-09-06
Publication date: 2000-11-16
Anticipated expiration: 2016-06-20
Also published as: AU4739399A

Description

Our Ref: 745102 P/00/011 Regulation 3:2

AUSTRALIA

Patents Act 1990

ORIGINAL

COMPLETE SPECIFICATION STANDARD PATENT

S..

W, IP Auot-rl"§ Documents receicd on: 6; e.

C

*5 St.

Batch No: Applicant(s): Schering Aktiengesellschaft Mullerstrasse 178 D-13353 Berlin

GERMANY

DAVIES COLLISON

CAVE

Patent Trade Mark Attorneys Level 10, 10 Barrack Street SYDNEY NSW 2000 Address for Service: Invention Title: Cascade polymer complexes, process for their production and pharmaceutical agents containing said complexes The following statement is a full description of this invention, including the best method of performing it known to me:- 5020 -1- Cascade Polymer Complexes, Process for their Production and Pharmaceutical Agents Containing Said Complexes This application is a divisional of Australian patent Application No. 63586/96. The invention of this divisional application relates to a novel compound of general formula I'A 3' 1' 2 R R OOC-R HC N -CH, -CH, -N

I

CH

2

CH,

(I

CH

2

CH,

I I N-CH,-CH N 2 1 CHR -CO OR CHR -CO OR o* whereby R independently of one another, stand for a hydrogen atom, a metal ion equivalent of atomic numbers 20-29, 39, 42-44 or 57-83 or an acid protective group,

R

2 stands for a hydrogen atom, a methyl or an ethyl radical, which optionally is substituted with 1-2 hydroxy or 1 carboxy group(s),

R

3 stands for a

R

4

R

2 I I -CH-CO-N -U6_T- group,

R

4 stands for a straight-chain, branched, saturated or unsaturated

C,-C

30 alkyl chain, which optionally is interrupted by 1-10 oxygen atoms, 1 phenylene group, 1 phenylenoxy group and/or optionally is substituted by hydroxy, 1-3 carboxy, 1-phenyl group(s),

U

6 stands for a straight-chain, branched, saturated or unsaturated C,-C20 alkylene group optionally containing imino, 1-3 phenylene, 1-3 phenylenoxy, 1-3 phenylenimino, 1-5 amide, 1-2 hydrazide, 1-5 carbonyl, ethylenoxy, 1 urea, 1 thiourea, 1-2 carboxyalkylimino, 1-2 ester groups; 1-10 oxygen, sulfur and/or 1-5 nitrogen atom(s) and/or optionally .is substituted by 1-5 hydroxy, 1-2 mercapto, 1-5 oxo, 1-5 thioxo, 1-3 carboxy, 1-5 carboxyalkyl, 1-5 ester and/or 1-3 amino group(s), whereby the phenylene groups 15 that are-optionally contained can be substituted by 1-2 carboxy, 1-2 sulfo or 1-2 hydroxy groups, T' stands for a -COOH, -N=C=O or -N=C=S group, and C*O stands for an activated carboxyl group.

The ensuing description is substantially identical to the description of "parent" No. 63586/96.

The parent description has been fully readopted to facilitate identification of the parent/divisional relationship. It is reiterated that the invention of this divisional application is as defined above, and in the ensuing claims.

The invention relates to the object characterized in the claims, new cascade polymer complexes, agents that contain these compounds, the use of the complexes in diagnosis and therapy, and a process for the production of these compounds and agents.

-Ib- The contrast media that are now used in clinical practice for the modern imaging processes of nuclear spin tomography

(MRI)

and computer tomography- (CT) (Magnevist Pro Hance(R), Ultravist(R) and Omniscan()] are dispersed in the entire extracellular space of the body (intravascular space and interstitium). This dispersion space comprises about 20% of the volume of the body.

In clinical practice, extracellular MRI contrast media were first used successfully in the diagnosis of cerebral and spin l disease processes since here a quite special situation exists 1 with respect to the regional dispersion space. In the brain and spinal cord, extracellular contrast media in healthy tissue do not leave the intravascular space because of the blood-brain barrier. In the case of pathological processes with disruption of the blood-brain barrier malignant tumors, inflammations, demyelinating diseases, etc.), regions with elevated blood-vessel permeability then develop inside the brain for these extracellular contrast media (Schmiedl et al., MRI of 2 Blood-Brain Barrier Permeability in Astrocytic Gliomas: Application of Small and Large Molecular Weight Contrast Media, Magn. Reson. Med. 22: 288, 1991). Affected tissue can be identified with high contrast relative to healthy tissue by exploiting this disruption of vascular permeability.

Outside of the brain and the spinal cord, however, no such permeability barrier exists for the above-mentioned contrast media (Canty et al., First-Pass Entry of Nonionic Contrast Agent into the Myocardial Extravascular Space. Effects on Radiographic Estimate of Transit Time and Blood Volume. Circulation 84: 2071, 1991). Thus, the concentration of the contrast medium is 9 no longer dependent-on vascular permeability, but only on the size of the extracellular space in the corresponding tissue.

Delimitation of the vessels relative to the surrounding interstitial space using this contrast medium is not possible.

A contrast medium that is dispersed exclusively in the 1 vascular space would be desirable, particularly for the 9 visualization of vessels. The purpose of such a blood-pool a ent is to make it possible, with the aid of nuclear spin tomograpy, to delimit tissue with sufficient blood supply from tissue with insufficient blood supply, and thus to diagnose an ischemia.

Infarcted tissue can also be delimited, based on its anemia, from surrounding healthy or ischemic tissue if a vasal contrast medium is used. This is of special importance if, the point is to distinguish a myocardial infarction from an ischemia.

To date, most of the patients in whom there is suspicion of cardiovascular disease (this disease is the most frequent cause of death in Western industrialized countries) have to undergo invasive diagnostic tests. In angiography at present, diagnostic radiology with the aid of iodine-containing contrast media is used in particular. These tests suffer from various drawbacks: they are associated with the risk of radiation exposure, as well as with difficulties and stresses, which therefore particularly have the effect that the iodine-containing contrast media, as compared with NMR contrast media, have to be used in much higher concentrations.

There is therefore a need for NMR contrast media which can mark the vascular space (blood-pool agents). These compounds are to be distinguished-by good compatibility and by high effectiveness (high increase of signal intensity with MRI).

Thus far, the attempt to solve at least a part of this problem by using complexing agents that are bonded to macromolecules or biomolecules has been successful only to a limited extent.

Thus, for example, the number of paramagnetic centers in the complexes that are described in European Patent Applications 0 088 695 and No. 0 150 844 is not sufficient for satisfactory imaging.

If the number of metal ions required is increased by repeated introduction of complexing units into a macromolecular biomolecule, this is associated with an intolerable impairment of the affinity and/or specificity of this biomolecule Nucl.

Med. 24, 1158 (1983)].

Macromolecules can generally be suitable as contrast media for angiography. Twenty-four hours after intravenous injection in rats, however, albumin-GdDTPA (Radiology 1987; 162: 205), shows a concentration in the liver tissue that constitutes almost 30% of the dose. In addition, only 20% of the dose is eliminated in 24 hours.

The macromolecule polylysine-GdDTPA (European Patent Application, Publication No. O 233 619) has also proved suitable as a blood-pool agent. Because of production, however, this compound consists of a mixture of molecules of different sizes.

In excretion tests in rats, it was shown that this macromolecule is excreted unchanged by glomerular filtration through the kidneys. Due to factors related to synthesis, however, polylysine-GdDTPA may also contain macromolecules that are so large that they cannot pass through the capillaries of the S. kidneys in the case of glomerular filtration and thus remain in the body.

Also, macromolecular contrast media based on carbohydratis, dextran, have been described (European Patent Application, Publication No. 0 326 226). The drawback of these compounds lies in the fact that the latter generally carry only about 5% of the signal-enhancing paramagnetic cation.

The polymers described in European Patent Application No. O 430 863 as well as the polymers described in German laid-open specification DE 43 44 460 already represent a step toward bloodpool agents since they no longer exhibit the size and molecular weight relative to heterogeneity that are characteristic of the previously mentioned polymers. Much like the compounds disclosed by Wiener et al. in an article in "Magnetic Resonance in Medicine" of January 1994 (pages 1 to however, they leave something to be desired as regards complete elimination, compatibility, and/or effectiveness.

The object was therefore to make available new diagnostic tools particularly to identify and locate vascular diseases that do not have the aboe-mentioned drawbacks. This object is achieved by this invention.

:It has been found that complexes which consist of nitrogencontaining cascade polymers that are provided with complexing ligands, at least 16 ions of an element of atomic numbers 20-29, 39, 42, 44 or 57-83, and optionally cations of inorganic and/or organic bases, amino acids or amino acid amides, and which optionally contain acylated amino groups, are surprisingly very well Suited for the production of NMR and x-ray diagnostic agents without exhibiting the above-mentioned drawbacks.

S S S 4.

S S C. S S S C. C C *S S

S

CC..

S.

C C

**CS

Macromolecules can generally be suitable as contrast media for angiography. Twenty-four hours after intravenous injection in rats, however, albumin-GdDTPA (Radiology jqj; 162: 205), shows a concentration in the liver tissue that constitutes almost 30% of the dose. In addition, only 20% of the dose is eliminated in 24 hours.

The macromolecule polylysine-GdDTPA (European Patent Application, Publication No. 0 233 619) has also proved suitable as a blood-pool agent. Because of production, however, this compound consists of a mixture of molecules of different sizes.

In excretion tests in rats, it was shown that this macromolecule is excreted unchanged by glomerular filtration through the kidneys. Due to factors related to synthesis, however, polylysine-GdDTPA may also contain macromolecules that are so large that they cannot pass through the capillaries of the kidneys in the case of glomerular filtration and thus remain in the body.

Also, macromolecular contrast media based on carbohydrates, dextran, have been described (European Patent Application, Publication No. 0 326 226). The drawback of these compounds lies in the fact that the latter generally carry only about 5% of the signal-enhancing paramagnetic cation.

The polymers described in European Patent Application No. 0 430 863 already represent a step toward blood-pool agents since they no longer exhibit the size and molecular weight relative to heterogeneity that are characteristic of the previously mentioned polymers. They leave something to be desired, however, as regards complete elimination, compatibility, and/or effectiveness.

The object was therefore to make available new diagnostic tools particularly to identify and locate vascular diseases that do not have the above-mentioned drawbacks. This object is achieved by this invention.

It has been found that complexes which consist of nitrogencontaining cascade polymers that are provided with complexing ligands, at least 16 ions of an element of atomic numbers 20-29, r 39, 42, 44 or 57-83, and optionally cations of inorganic and/or organic bases, amino acids or amino acid amides, and which optionally contain lycylated amino groups, are surprisingly very well suited for the production of NMR and x-ray diagnostic agents without exhibiting the above-mentioned drawbacks.

The complexing cascade polymers according to the invention can be described by general formula

I

W-K )y]x1 in which A stands for a nitrogen-containing cascade nucleu off base multiplicity a, X and Y, independently of one another, stand for a direct bond or a cascade reproduction unit of reproduction multiplicity x or y, Z and W, independently of one another, stand for a cascade reproduction unit of reproduction multiplicity z or w, K stands for the radical of a complexing agent, a stands for numbers 2 to 12, x, y, z and w, independently of one another, stand for numbers 1 to 4, provided that at least two reproduction units are different and that 16 <5 a x ,y *z w :5 64 holds true for the product of the multiplicities.

As cascade nucleus A, the following are suitable: nitrogen atom, N- H U 2 1 1 2 22

NN

2

U

H-C2-N 2 H2 N 1 2

CH

2 -N -CH 2 10H 2 -N -C2CH2 12 12 2CH2 -N 4 2 -0(H 2 -N CH 2

CH

2 12 12 u

U

-N

*0 OS 00 S 0

OS

@0 00 50 S. 0 0 u1 u2 IN N 0

M

12 12 u

U

0005 *0 00 S 0000 5 4000 00 0 5005

I-N

u 2N-M

U

M-N

23 U U2 U'

NJ~

NN~N

U N\ 2 0*

NE

in which mn and n stand for numbers 1 to p -stands, for numbers 0 to

U

1 stands for Q' or E,

U

2 stands for Q 2 or E with E meaning the group Q 2 1210 LI '2 1 whereby o stands for numbers 1 to 6, Q stands for a hydrogen atom or Q 2 and

Q

2 stands for a direct bond, M stands for a alkylene chain which optionally is interrupted by 1 to 3 oxygen atoms and/or optionally is substituted with 1 to 2 oxo groups, R° stands for a branched or unbranched

C

1

-C

10 alkyl radical, a nitro, amino, carboxylic acid group or for M

U

M-N

U-

whereby number Q 2 corresponds to base multiplicity a.

The nitrogen atom, whose three bonds (base multiplicity a 3) in a first "inner layer" (generation 1) are occupied by three reproduction units X or Y (if X stands for a direct bond) or Z (if X and Y in each case stand for a direct bond), represents the simplest case of a cascade nucleus; in other words: the thr hydrogen atoms of the basic cascade starter ammonia A(H)a have been substituted by three reproduction units X or Y or Z.

In this case, number Q 2 contained in cascade nucleus A represents base multiplicity a.

Reproduction units X, Y, Z and W contain

-NQIQ

2 groups, in which Q 1 means a hydrogen atom or Q 2 and Q 2 means a direct bond.

The number Q 2 contained in the respective reproduction unit X) corresponds to the reproduction multiplicity of this unit x in the case of The product of all multiplicities a x y z w indicates the number of complexing agent radicals K bonded in the cascade polymers. The polymers according to the invention contain at least 16 and at most 64 radicals K in the molecule, which in each case can bond one ion to a maximum of three ions (in the case of divalent ions), preferably one ion, to an element of the above-mentioned atomic numbers.

The last generation, reproduction unit W bonded to complexing agent radical K, is bonded to K with NH groups (-NQQ 2 with Q 1 meaning a hydrogen atom and Q 2 direct bond), while the S* preceding reproduction units can be linked together both by NHQ 2 groups by ac-ylation reactions) and by NQ 2

Q

2 groups by alkylation reactions).

SThe cascade polymer complexes according to the invention exhibit a maximum of 10 generations more than just one of reproduction units X, Y and Z can also be present in the molecule in each case), but preferably 2 to 4 generations, whereby at least two of the reproduction units in the molecule are different.

As preferred cascade nuclei A, those are indicated which fall under the above-mentioned general formulas if m stands for numbers 1-3, especially preferably for number 1, n stands for numbers 1-3, especially preferably for number 1, P stands for numbers 0-3, especially preferably for number 1, 9.

.9 9 9. 0 stands for number 1, H stands f or a -CH 2 -CO or -CH 2 CO group and

R

0 stands f or a -CH 2

NU

1

U

2

CH

3 or NO 2 group.

As further preferred cascade starters A(H)ai there can be listed, e.g.: (In the parentheses, base multiplicity a is indicated for the case where subsequent mono- or disubstitution is used in building the next generation)- Tris (aminoethyl) amine (a 6 or 3); tris (aminopropyl) amine (a 6 or 3); diethylenetriamine (a 5 or 3); triethylenetetramine (a 6 or 4); tetraethylenepentamflne (a 7 or 1,3, 5-tris(aminomethyl) benzene (a 6 or 3); triiuesic acid triamide (a 6 or 3); 1,4, 7-triazacyclononane (a 3); 1,4,7, lO-tetraazacyclododecane (a 4); 1,4,7,10, l 3 -pentaazacyclopentadecane (a 1,4,8, ll-tetraazacyclotetradecane (a 4); 1,4,7,10, l 3 ,l 6 -hexaazacyclooctadecane (a 6); lI 4 7 ,lO,13,16,19,22,25,28-decaazacyclotriacontane (a tetrakis (aminomethyl) methane (a 8 orL1); 1,1, 1-tris (aminomethyl) ethane (a 6 or 3); tris (aminopropyl) -nitromethane (a 6 or 3); 2,4, 6-triamino-1, 3, 5-triazine (a 6 or 3); li 3 ,5, 7 -adamantanetetracarboxylic acid amide (a 8 or 4); -diphenylether-tetracarboxylic acid amide (a 8 or 4); 1, 2-bis [phenoxyethane] -3 31,' 5 S-tetracarboxylic acid amide (a 8 or 4); l, 4 7 hlOl 3 ,16,21,24-octaazabicyclo[8.8.8]hexacosane (a 6).

It can be pointed out that the definition as cascade nucleus A and thus the separation of cascade nucleus and first reproduction unit can be selected by purely formal means and thus independently of the actual synthesis of the desired cascade polymer complexes. Thus, the tris(aminoethyl)amine used in Example 4 can be considered as cascade nucleus A itself (compare the general formula, indicated first for A, with m n p 1,

U

1 E with o meaning number 1 and U 1

U

2

Q

2 but also as a nitrogen atom cascade nucleus which as a first generation exhibits three reproduction units /CH2

N

(compare the definition of E).

Cascade reproduction units X, Y, Z and W are determined, independently of one another, by

E,

U

3 U-N 2 U1

NU

4 N 2 3 U U

U-V

U 1 U N U2 "^2 1 3

U

U-N

U -N

U

2 in which

U

1 stands for Q 1 or E,

U

2 stands for Q 2 or E with 1 E meaning the group -CH2-N 2 whereby o stands for numbers 1 to 6,

Q

1 stands for a hydrogen atom or Q2, Q* Q stands for a direct bond,

U

3 stands for a C,-C 20 alkylene chain, which optionally is interrupted by 1 to 10 oxygen atoms and/or 1 to 2 -N(CO)q-R 2 radicals, 1 to 2 phenylene radicals and/I 1 to 2 phenylenoxy radicals and/or optionally is substituted by 1 to 2 oxo, thioxo, carboxy,

C

1

-C,

alkylcarboxy,

C

1

-C

5 alkoxy, hydroxy,

C

1

-C

5 alkyl groups, whereby q stands for numbers 0 or 1 and

R

2 stands for a hydrogen atom, a methyl or an ethyl radical, which optionally is substituted with 1-2 hydroxy or 1 carboxy group(s), L stands for a hydrogen atom or the group

U

3/

U-N

UI

V stands for methine group UI, if at the same time U 4 means a direct bond or group M and Us has one of the meanings of u 3 orCO 0* V stands for group if at the same time U 4 and U1 are identical and mean the direct bond or group

M.

Preferred cascade reproduction units X, Y, Z and W are those in which in the above-mentioned general formulas, radical U 3 stands f or

-COCH

2

OCH

2 CO-,

-COCH

2

-CH

2

CH

2

-CONHC

6

H

4

-COCH

2 CH.CO-,

-COCH

2

-CH

2

CH

2 COCH 2

CH

2

CH

2

CHCO-'

radical U4 stands for a direct bond, for -CH 2

CO-,

radical

U

5 stands for a direct bond, for -(CH2) 4

-CH

2

CO-,

-CH(COOH)-,

CH

2

OCH

2

CH

2

-CH

2

C

6

H

4

CH

2

-C

6

H

4

OCH

2

CH

2 radical E stands for a group -Qq2 2 cHN Cascade reproduction units X, Y, Z and W that are-referred to as examples can be cited:

-CH

2

CH

2 NH-; -CH 2

CH

2

N<;

-COCH(NH-)(CH

2 4 -COCH(Nc )(CH 2 4 Nc; -COCH 2

OCH

2

CON(CH

2

H

2

-COCH

2 0CH 2

CON(CH

2

CH

2 N< )2; -COCH2N(CH 2

CH

2 NH); -COCH 2

N(CH

2

CH

2 N< )2;

-COCH

2 NH-; -COCH 2 N<

-COCH

2

CH

2

CON(CH

2

CH

2

NH-)

2

-COCH

2

CH

2 CoN(cH 2

CH

2 N< )2; -COCH2OCH2CONH-C 6

H

4

.CH[CH

2

CON(CHCHNH-)

2 ]2 ppCOCH2CH2CONH-C 6

H

4

CH[CHCON(CH

2

CHN)];

p CONH2CZ.HC 6

H

4 -C

[CH

2 CON(CHH-212

*CONH-C

6

H

4

.'CH[CH

2

CON(CH

2

CH

2

NH)

2 ]2; -COCH(NH..)CH(COOH)NH..; -COCH(N<

)CH(COOH)N<.

CON(GH

2

OH

2

NH-)

2

-COCK

2 Oat 2

CONH

2 2

CON(CH

2 OHi 2

NH-)

2

CON(CH

2

CH

2 N< )2 -C O H 20 O N HCO N

H

2

OH

2 N 2 CON H2HNH-) 2 -CON

CON(CH

2

CH

2

N.)

2 cON(OHCH 2 )2NH *-CONH2 \ON -CO~c-ICONC

C

2

N<)

2

"-OOH

2

CH

2 CONH OON(C3ZH 2 cH 2 N< )2 OC2HNH- OCH2HNH- 2 0 2

NH-

00I 2

CH

2

NH-

OCH

2

CH

2

N<

00H 2 a-I 2

N<

-C-0012 2N< .9 9 *9*9 .9 9* 9 9* 999.

9.

9@

O(CNH

2 (O)-HOcHNH.

(cP 2

C

2 O 2

CH

2

HNH.

0(012 CH 2 0) 2

CH

2

CH

2

NH-

0(CH 2

CH

2

O)

2

CH.

2

CH

2

N<

/00\

(CH

2

CH

2

O)

2 Oi 2

CH

2

N<

O(OHCH

2

Q-

2 H2C 2

N<

Complexing agent radicals K are described by general formulas IA and IB: 1 2 R OOO-R HC\

NO-H

2 2 -N -cH 2

-H

2

-N

/2 1 CHR -CO OR '2 '2 H R -C O O R

(IA),

R

R'OOC-H C CH-CO-a

CH-COOR'

I 1 I N -CH, CH, N-CHCH,--N

R'OOC-HI

2 C

CH

2

-COOR'

in which

R

I

independently of one another, stand for a hydrogen atom or a metal ion equivalent of atomic numbers 20-29, 39, 42-44 or 57-83,

R

2 stands for a hydrogen atom, a methyl or an ethyl radical which optionally is substituted with 1-2 hydroxy or 1 carboxy group(s),

R

3 stands for a

R

4

R

2 -CH-CO-N-U--T- group,

R

4 stands for a straight-chain, branched, saturated orC unsaturated

C

1 0 C alkyl chain, which optionally is interrupted by 1-10 oxygen atoms, 1 phenylene group, 1 phenylenoxy group and/or optionally is substituted by hydroxy, 1-3 carboxy, 1-phenyl group(s),

R

5 stands for a hydrogen atom or for R 4 U6 stands for a straight-chain, branched, saturated or unsaturated

C

1

-C

2 0 alkylene group optionally containing imino, 1-3 phenylene, 1-3 phenylenoxy, 1-3 phenylenimino, 1-5 amide, 1-2 hydrazide, 1-5 carbonyl, ethylenoxy, 1 urea, 1 thiourea, 1-2 carboxyalkylimino, 1-2 ester groups; 1-10 oxygen, sulfur and/or 1-5 nitrogen atom(s) and/or optionally substituted by 1-5 hydroxy, 1-2 mercapto, 1-5 oxo, thioxo, 1-3 carboxy, 1-5 carboxyalkyl, 1-5 ester and/or 1-3 amino group(s), whereby the phenylene groups that optionally can be contained can be substituted by 1-2 carboxy, 1-2 sulfa or 1-2 hydroxy groups, *T stands for a -CO-a, -NHCO-a or -NHCS-a group, and stands for the binding site to the terminal nitrogen atoms-of-the -last generation, of reproduction unit W.

As preferred complexing agent radicals K, those can bementioned in which in above-indicated formula IA, the C 1

-C

20 and preferably

C

1 -c 12 alkylene chain that stands f or U 6 contains the groups 2

-CH

2 NHCO, -NHCOCH 2 O, -NHCOCH 2

OC

6

H

4 -N (CH 2

CO

2 H)

:-NHCOCH

2

C

6

H

4

-NHCSNHC

6 4

-CH

2

OC

6

H

4 I -CH 2

CH

2 O and/or is substituted by groups -COOH, -CH 2

COOH.

As examples of U6, the following groups can be cited:

-CHT

2

-CH

2

CH

2 -CH2CH CHA~

-C

6 4

-C

6

H

1 0

*CH

2

C

6

H

5

-CH

2 NHCOCH2CH(CH 2

CO

2

H).C

6

H

4

-CH

2

NHCOCH

2

OCH

2

-CH

2

NHCOCH

2

C

6

H

4

-CH

2

NHCOCH

2 C0 2

H

-2NHCSNHC 6

H

4

-CH(CH

2 COOH)C~i 2 -C2OC6H 4

-N(CHCOOH)CH

2 r, -C2NHCOCH2O(CH 2

CH

2 4 'c 6

H

4 -cH 2 0-C 6

H

4 -C2CH2O-CH 2 CH2-,

-CH

2

CH

2

-O.CH

2

CHO

2 CHQj, S0 3 H C2 A s m l s f J h o l wi g g o p a e i d c t d *C3 *CH5 .C2CO Siasl osa o examplesoR, the oloin rous can b indIated cobalt-CM 3 ni

C

6 1{ 5 I, -cperI)-COOHdmimII) If the agent according to the invention is intended for use inN diagnosis aig, the central ion fatheocomple esaltemustob an element of higher atomic number in order to achieve sufficient absorption of the x rays. It has been found that for this purpose, diagnostic agents which contain a physiologically compatible complex salt with central ions of elements of atomic numbers between 21-29, 39, 42, 44, 57-83 are suitable; these are, for example, the lanthanum(III) ion and the above-mentioned ions of the lanthanide series.

The cascade polymer complexes according to the invention contain at least 16 ions of an element of the above-mentioned atomic numbers.

The remaining acid hydrogen atoms, those which were *not substituted by-he central ion, optionally can be replaced completely or partially by cations of inorganic and/or organic S bases, amino acids, or amino acid amides.

Suitable inorganic cations are, for example, the lithium ion, the potassium ion, the calcium ion, the magnesium ion, and especially the sodium ion. Suitable cations of organic bases are, those of primary, secondary, or tertiary amines, s ch as, for example, ethanolamine, diethanolamine, morpholine, glucamine, N,N-dimethylglucamine, and especially

N-

methylglucamine. Suitable cations of amino acids are, for example, those of lysine, arginine, and ornithine, as well as the amides of otherwise acidic or neutral amino acids.

The compounds according to the invention, which have a molecular weight of 10,000-80,000 D, preferably 15,000-40,000

D,

exhibit the desired properties described above. They contain the large number, required for their use, of metal ions bonded in a stable manner to the complex.

They accumulate in regions with high vascular permeability, such as, in tumors, they make it possible to make statements regarding the perfusion of tissues, and they provide the possibility of determining the blood volume in tissues, of shortening selectively the relaxation times or densities of the blood, and of graphically representing the permeability of blood vessels. Such physiological data cannot be obtained through the use of extracellular contrast media, such as, Gd-DTPA [MagnevistR)]. From these standpoints, there also follow the uses in the modern -maging processes of nuclear spin tomography and computer tomography: more specific diagnoses of malignant tumors, early therapy monitoring in cases where cytostatic, antiphlogistic, or vasodilative therapy is used, early identification of underperfused regions in the myocardium), angiography in vascular diseases, and identification and diagnosis of (sterile or infectious) inflammations.

The cascade polymer complexes according to the invention are also extremely well suited for (interstitial and i.v.) lymphography.

As further advantages relative to extracellular contrast media, such as, Gd-DTPA [Magnevist(R)], the greater effectiveness as contrast media for nuclear spin tomography (higher relaxivity) must be emphasized; this ensures a marked reduction of the diagnostically required dose. At the same time, the contrast media according to the invention can be formulated as solutions in an isoosmolar manner in the blood and thus reduce the osmotic stress of the body, which is reflected in a reduced toxicity on the part of the substance (higher toxic threshold).

Smaller doses and higher toxic thresholds result in a significant increase of the reliability of contrast medium use in modern imaging processes.

In comparison with macromolecular contrast media based on carbohydrates, dextran (European Patent Application, Publication No. 0 326 226), which carry as mentioned generally only about 5% of the signal-enhancing paramagnetic cation, the polymer complexes according to the invention exhibit 9 9w a content of the-paramagnetic cation of generally about Thus, the macromolecules according to the invention produce much better signal enhancement per molecule, which simultaneously has the effect that the dose necessary for nuclear spin tomography is considerably smaller relative to macromolecular contrast media based on carbohydrates.

With the polymer complexes according to the invention, it has been possible to design and produce macromolecules in sucl a way that the latter have a uniformly defined molecular weight.

It is thus possible, surprisingly enough, to control the size of the macromolecules in such a way that the latter are large enough to be able to leave the vascular space only slowly, but at the same time small enough to be able to pass through the capillaries of the kidneys, which are 300-800 A in size.

In comparison to the other mentioned polymer compounds of the prior art, the cascade polymer complexes according to the invention are distinguished by improved excretion behavior, greater effectiveness, greater stability, and/or better compatibility.

Another advantage of this invention lies in the fact that now complexes with hydrophilic or lipophilic, macrocyclic or open-chain, low-molecular, or high-molecular ligands have become accessible. As a result, the possibility exists for controlling the compatibility and pharmacokinetics of these polymer complexes by chemical substitution.

The production of the cascade polymer complexes according to the invention is carried out in that compounds of general formula I, W-B) )yxa in which SA stands for a nitrogen-containing cascade nucleus of base multiplicity a, X and Y, independently of one another, stand for a direct bond or a cascade reproduction unit of reproduction multiplicity x or y, Z and W, independently of one another, stand for a cascade reproduction unit of reproduction multiplicity z or w, a stands for numbers 2 to 12, x, y, z and w, independently of one another, stand for numbers 1 to 4 and B stands for the binding site of the terminal NH groups of the last generation, of reproduction unit W provided that at least two reproduction units are different, and that for the product Of multiplicities, 16 <9 a *x ,y ,z *w 5 64, holds true, are reacted with a complex or complexing agent K' of general formula I'A or I'B 4. 9. 9 94 99 9 9949 49 99 9 99 9 4 R OOCR 2HC 3.

R

N~H -H2 -N c 2

C

I

-H

2 cH /2 1., CHR -00COR

H

2

H

2 (V A) a2 -CR R 1 00C-H. C

CIH

2 -COOR 1 I I I R"OOC-H 2

C

CH

2 -C OOR' whereby

R

1 independently of one another, stand for a hydrogen atom, a metal ion equivalent of atomic numbers 20-29, 39, 42-44, or 57-83 or an acid protective group,

R

3 stands for a

R

4

R

2 I

I

-CH -CO -N group,

R

4 stands for a straight-chain, branched, saturated or unsaturad CI-CO alkyl chain, which optionally is interrupted by 1-10 oxygen atoms, 1 phenylene group, 1 S• phenylenoxy group and/or optionally is substituted by hydroxy, 1-3 carboxy, l-phenyl group(s),

R

5 stands for a hydrogen atom or for R 4

U

6 stands for a straight-chain, branched, saturated or unsaturated CI-C 2 0 alkylene group optionally contain'g imino, 1-3 phenylene, 1-3 phenylenoxy, 1-3 phenylenimino, 1-5 amide, 1-2 hydrazide, 1-5 carbonyl, ethylenoxy, 1 urea, 1 thiourea, 1-2 carboxyalkylimino, 1-2 ester groups; 1-10 oxygen, sulfur and/or 1-5 nitrogen atom(s) and/or optionally substituted by 1-5 hydroxy, 1-2 mercapto, 1-5 oxo, thioxo, 1-3 carboxy, 1-5 carboxyalkyl, 1-5 ester and/or 1-3 amino group(s), whereby the phenylene groups that are optionally contained can be substituted by 1-2 carboxy, 1-2 sulfo or 1-2 hydroxy groups, T' stands for a -COOH, -N=C=O or -N=C=S group, and C*O stands for an activated carboxyl group, provided that if K' stands for a complex at least two (in the case of divalent metals) or three (in the case of trivalent metals) of substituents R 1 stand for a metal ion equivalent of the above-mentioned elements and that optionally other carboxyl groups are present in the form of their salts with inorganic and/or organic bases, amino acids or amino acid amides, optionally present -rot6ective groups are cleaved off, the thus obtained cascade polymers if K' stands for a complexing agent are reacted in a way known in the art with at least one metal

S

S oxide or metal salt of an element of atomic numbers 20-29, 39, 42, 44, or 57-83 and then optionally in the cascade polymer complexes thus obtained, acid hydrogen atoms that are still present are completely or partially substituted by cations of inorganic and/or organic bases, amino acids, or amino acid amides, and optionally still present free terminal amino groups are optionally acylated before or after the metal complexing.

Another aspect of this invention is represented by the new compounds of general formula I'A 3.

1' 2

R

R OOC-R HC.

I

CHCH

I I P^ CH2 N--CH,--CH N (I'A) CHR -COOR CHR -OOR whereby R independently of one another, stand for a hydrogen atom, a metal ion equivalent of atomic numbers 20-29, 39, 42-44 or 57-83 or an acid protective group,

R

3 stands for a

R

4

R

2 I

I

-CH-CO-N group,

R

4 stands for a straight-chain, branched, saturated or unsaturated

C

1

-C

U

6 stands for a straight-chain, branched, saturated or unsaturated

C,-C

20 alkylene group optionally containing imino, 1-3 phenylene, 1-3 phenylenoxy, 1-3 phenylenimino, 1-5 amide, 1-2 hydrazide, 1-5 carbonyl, ethylenoxy, 1 urea, 1 thiourea, 1-2 carboxyalkylimino, 1-2 ester groups; 1-10 oxygen, sulfur and/or 1-5 nitrogen atom(s) and/or optionally substituted by 1-5 hydroxy, 1-2 mercapto, 1-5 oxo, thioxo, 1-3 carboxy, 1-5 carboxyalkyl, 1-5 ester and/or 1-3 amino group(s), whereby the phenylene groups that are optionally contained can be substituted by 1-2 carboxy,-1-2 -sulfo or 1-2 hydroxy groups, T' stands for a -COOH, -N=C=O or -N=C=S group, and C*O stands for an activated carboxyl group.

They are used as important intermediate products for the production of the cascade polymer complexes of general formula I.

As an example of an activated carbonyl group C*O in complexes or complexing agents anhydride, p-nitrophenyl ester, N-hydroxysuccinimide ester, pentafluorophenyl ester, d acid chloride can be mentioned.

The addition or acylation that is carried out to introduce the complexing agent units is performed with substrates that contain desired substituents K (optionally bonded to a leaving group) or from which the desired substituent is generated by the reaction.

As examples of addition reactions, the reaction of isocyanates and isothiocyanates can be mentioned, whereby the reaction of isocyanates is preferably performed in aprotic solvents, such as, THF, dioxane, DMF, DMSO, methylene chloride at temperatures of between 0 and 100 0 C, preferably between 0 and 50 0 C, optionally with the addition of an organic base such as triethylamine, pyridine, lutidine,

N-

ethyldiisopropylamine, N-methylmorpholine. The reaction with isothiocyanates is generally performed in solvents, such as, water or lower alcohols, such as, methanol, ethanol, isopropanol or their mixtures, DMF or mixtures of DMF and water at temperatures of between 0 and 100 0 C, preferably between 0 and 50°C, optionally with the addition of an organic or inorganic -base, such as, triethylamine, pyridine, lutidine,

N-

ethyldiisopropylamine, N-methylmorpholine, or alkaline-earth hydroxides, alkali hydroxides, such as, lithium, sodium, potassium, calcium hydroxide, or their carbonates, such as, e.g., magnesium carbonate.

As examples of acylation reactions, the reaction of free carboxylic acids according to the methods known to one skille in the art J. P. Greenstein, M. Winitz, Chemistry of the Amino Acids, John Wiley Sons, N.Y. (1961), pp. 943-945] can be mentioned. It has proven advantageous, however, to convert the carboxylic acid group before the acylation reaction into an activated form, such as, anhydride, active ester or acid chloride E. Gross, J. Meienhofer, The Peptides, Academic Press, N.Y. (1979), Vol. 1, pp. 65-314; N. F. Albertson, Org.

React. 12, 157 (1962)].

In the case of reaction with active ester, the literature known to one skilled in the art Houben-Weyl, Methoden der organischen Chemie [Methods of Organic Chemistry], Georg Thieme Verlag, Stuttgart, Volume E 5 (1985), 633] can be cited. This reaction can be performed under the conditions indicated above for the anhydride reaction. However, aprotic solvents, such as, methylene chloride, chloroform, can also be used.

In the case of acid chloride reactions, only aprotic solvents, such as, methylene chloride, chloroform, toluene or THF, at temperatures of between -20 to 50 0 C, preferably of between 0 to 30 0 C, are used. Further, literature known to one skilled in the art-[e.g., Houben-Weyl, Methoden der Organischen Chemie, Georg-Thieme-Verlag, Stuttgart, (1974), Volume 15/2, pp.

4 355-364] can be cited.

If R 1 stands for an acid protective group, lower alkyl, S aryl and aralkyl groups, for example, the methyl, ethyl, propyl, butyl, phenyl, benzyl, diphenylmethyl, triphenylmethyl, bis-(pnitrophenyl)-methyl groups, as well as trialkylsilyl groups, suitable.

The optionally desired cleavage of the protective groups is carried out according to the processes known to one skilled in the art, for example by hydrolysis, hydrogenolysis, alkaline saponification of esters with alkali in aqueous-alcoholic solution at temperatures of 0oC to 50 0 C or in the case of tertbutyl esters with the aid of trifluoroacetic acid.

Terminal amino groups that are optionally incompletely acylated with ligands or complexes can optionally be converted into amides or semiamides. The reactions with acetic anhydride, succinic anhydride or diglycolic anhydride can be mentioned as examples.

The introduction of the desired metal ions is carried out in the way in which it was disclosed in, German laid-open specification 34 01 052, by the metal oxide or a metal salt (for example, the nitrate, acetate, carbonate, chloride or sulfate) of the element of atomic numbers 20-29, 42, 44, 57-83 being dissolved or suspended in water and/or a lower alcohol (such as m: ethanol, ethanol or isopropanol) and being reacted with the solution or suspension of the equivalent amount of complexing -ligand and then optionally existing acid hydrogen atoms of the acid groups being substituted by cations of inorganic and/or organic bases, amino acids or amino acid amides.

The introduction of the desired metal ions can be carried out both in the stage of complexing agent I'A or I'B, i.e., before the coupling to the cascade polymers, and after coupling of unmetalated ligands I'A or I'B.

o In this case, the neutralization is carried out with theaid of inorganic bases (for example, hydroxides, carbonates or bicarbonates) of, for example, sodium, potassium, lithium, magnesium or calcium and/or organic bases, such as, i.a., primary, secondary and tertiary amines, such as, for example, ethanolamine, morpholine, glucamine, N-methyl and N,Ndimethylglucamine, as well as basic amino acids, such as, for example, lysine, arginine and ornithine or of amides of originally neutral or acidic amino acids, such as, for example, hippuric acid, glycine acetamide.

For the production of neutral complex compounds, enough of the desired bases can be added, for example, to the acid complex salts in aqueous solution or suspension that the neutral point is reached. The obtained solution can then be evaporated to the dry state in a vacuum. Often, it is advantageous to precipitate the neutral salts formed by adding water-miscible solvents, such as, for example, lower alcohols (methanol, ethanol, isopropanol and others), lower ketones (acetone and others), polar ethers (tetrahydrofuran, dioxane, 1,2-dimethoxyethane and others) and thus to obtain easily ibolated and readily purified crystallizates. It has proven especially advantageous to add the desired bases as early as during the complexing of the reaction mixture and thus to save a process step.

If the acid complex compounds contain several free acid groups, it is often suitable to produce neutral mixed salts, which contain both inorganic and organic cations as counterios.

This can happen, for example, by the complexing ligands aqueous suspension or solution being reacted with the oxide or salt of the element yielding the central ion and half of the amount of an organic base required for neutralization, the complex salt formed being isolated, optionally purified and then mixed with the required amount of inorganic base for complete neutralization. The sequence of the addition of base can also be reversed.

The purification of the thus obtained cascade polymer complexes is carried out, optionally after adjusting the pH to 6 to 8, preferably about 7, by adding an acid or base, preferably by ultrafiltration with membranes of suitable pore size Amicon("RYMl0, Amicon(R)YM3) or gel filtration on, suitable Sephadex R) gels.

In the case of neutral complex compounds, it is often advantageous to provide the polymeric complexes with an anion exchanger, for example, IRA 67 (OH" form) and optionally in addition with a cation exchanger, for example, IRC 50 form) for the separation of ionic components.

The production'of the cascade polymers carrying terminal amino groups required for the coupling to complexing agents K' Si °(or else the corresponding metal-containing complexes) generally proceeds from nitrogen-containing cascade starters A(H)a that can be produced by commercially available methods or according to or analogously to methods known in the literature. The introduction of generations X, Y, Z and W is carried out according to meth-ds known in the literature J. March, Advanced Organic

J

Chemistry, 3rd ed.; John Wiley Sons, (1985), 364-381] by acylation or alkylation reactions with protected amines exhibiting the desired structures, which contain functional groups capable of bonding to the cascade nuclei, such as, e.g., carboxylic acids, isocyanates, isothiocyanates or activated carboxylic acids (such as, anhydrides, active esters, acid chlorides) or halides (such as, chlorides, bromides, iodides), aziridine, mesylates, tosylates or other leaving groups known to one skilled in the art.

It can be stressed, however, that the differentiation between cascade nucleus A and reproduction units is purely formal. It can be advantageous synthetically that formal cascade starter is not used, but rather the nitrogen atoms forming part of the cascade nucleus by definition are introduced firt together with the first generation. Thus, for synthesis of the compound described in Example ib), it is more advantageous not to alkylate the formal cascade nucleus trimesic acid triamide with, benzyloxycarbonylaziridine (six-fold), but rather to react trimesic acid-trichloride with bis[2- (benzyloxycarbonylamino)-ethyl]-amine (three-fold).

As amino protective groups, the benzyloxycarbonyl, tertbutoxycarbonyl, trifluoroacetyl, fluorenylmethoxycarbonyl, benzyl and formyl groups familiar to one skilled in the art [Th. W.

Greene, P. G. M. Wuts, Protective Groups in Organic Syntheses, 2nd ed., John Wiley and Sons (1991), pp. 309-385] can be mentioned. After cleavage of these protective groups, which I~so is carried out according to methods known in the literature, the next desired generation can be introduced into the molecule. In addition to this synthesis of a generation consisting of two reaction stages in each case (alkylation or acylation and protective group cleavage), the simultaneous introduction of two, or several generations, X-[Y-(Z)y]x is also possible with only two reaction stages. The synthesis of these multi-generation units is carried out by alkylation or acylation of unprotected amines ("reproduction amine") exhibiting the structures of the desired reproduction units, with a second reproduction amine, whose amine groups are present in protected form.

The compounds of general formula A(H)a required as cascade starters are commercially available or can be produced according to or analogously to methods known in the literature Houben-Weyl, Methoden der Org. Chemie, Georg-Thieme-Verlag, Stuttgart (1957), Vol. 11/1; M4. Micheloni et al., Inorg. Chem.

(1985), 24, 3702; T. J. Atkins et al., Org. Synth., Vol.. 58 (1978), 86-98; The-Chemistry of Heterocyclic Compounds: J. S.

Bradshaw et a1. ,'AZ-Crbwn-4acrocycles, John Wiley Sons, N.Y.

(1993)]. As examples, there can be cited: Tris(aminoethyl)amine Fluka Chemie (Fluka Chemistry) AG, Switzerland; Aldrich-Chemie (Aldrich Chemistry), Germany); tris(aminopropyl)amine C. Woerner et al., Angew.

.*.Chem. (Applied Chem.] Int. Ed. Engl. (1993), 22, 1306]; diethylenetriamine Fluka; Aldrich]; triethylenetetramine Fluka; Aldrich]; tetraethylenepentamine Fluka; Aldrich]; 1, 3 ,S-tris(aminomethyl)benzene T. H. Garrett et al., J. Am. Chem. Soc. (1991), 113, 2965]; trimesic acid triamide H. Kurihara; Jpn. Kokai Tokyo Koho JP 04077481; CA 117, 162453]; 1, 4 ,7-triazacyclononane Fluka; Aldrich]; l, 4 7 ,lO,l 3 -pentaazacyclopentadecane K. W. Aston, Eur. Pat. Appi. 0 524 161, CA 120, 44580]; 1,4,7, lO-tetraazacyclotiodecane Aldrich] 1,4,8, ll-tetraazacyclotetradecane Fluka; Aldrich]; 1, 4 7 ,lOl 3 ,16,19,22,25,28-decaazacyclotriacontane A. Andres et al., J. Chem. Soc. Dalton Trans. (1993), 35073; l,l,1-tris(aminomethyl)ethane R. J. Geue et al., Aust. J. Chem. (1983), 927]; tris(aminopropyl).nitromethane G. R. Newkome et al., Angew. Chem. 103, 1205 (1991) analogously to Larock, Comprehensive Organic Transformations, VCH Publishers,

N.Y.

(1989), 419-420]--- 1,3,5, 7 -adamantanetetracarboxylic acid amide

H.

:Stetter et al., Tetr. Lett. 1967, 1841]; 1, 2 -bis~phenoxyethane-3', 3"1, "-tetracarboxylic acid amide J. P. Coliman et al.; J. Am. Chem. Soc. (1988), 110, 3477-86 analogously to the instructions for Example 1b)]; l 4 7 ,1O,l 3 ,16,21,24-octaazabicyclor8.88]hexacosne P. H. Smith et al., J. Org. Chem. (1993), 58, 7939].

The production of the reproduction amines that contain the above-mentioned functional groups required for the synthesis of generations is carried out according to or analogously to the instructions described in the experimental part or according to processes known in the literature.

As examples, there can be mentioned: NC-Di-benzyloxycarbonyl-.lyinepnitrophenl ester (see instructions for Example 1c));

HOOC-CH

2

OCH

2 CO-N (CH 2

CH

2

NH-CO-O-CH

2

C

6 H) 2

HOOC-CH

2 N (CH 2

CH

2

NH-CO--CH

2

C

6 5) 2

HOOC-CH

2

CH

2 CO-N (CH 2

CH

2

NH-COCF

3 2 (to be produced according to instructions for Example 3a), by starting from bis (trif luoroacetylaminoethyl) amine instead of bis(benzyloxycarbonylaminoethyl)amine and from succinic anhydride.

instead of diglycolic anhydride];

HOOC-CH

2

OCH

2

CONH-C

6

H

4 -CH CH 2 CON (CH 2

CH

2 NH-CO-0-CH 2

C

6

H

5 2 1 2 (to be produced analogously to instructions for Example 3a];

O=C=N-C

6 4 -C (C 2 CON (CH 2

CH

2 NH-CO-o-CH 2

C

6 5) 2 1 2 .0-H..H 6

NH-CO-O-CH

2

C.H.

CON (CH2CH 2 NHCO-0O.CH 2 CaH)2 CON(C(CH2CHHNHO..ON2H 2

H

6 H2 N-benzyloxycarbonyl-aziridine to be produced according to M.

Zinic et al., J. Chem. Soc, Perkin Trans 1, 21-26 (1993) N-benzyloxycarbonyl-glycine commercially available in, e.g., Bachem, California

OCH

2

CH

2 NHCO-O-CH2

CH

HOOC OCH2CH 2

NHCO-OCH

2

C

6 Hs

OCH

2 CH NHCO-O-CH 2 Hs a to be produced according to C. J.

Cavallito et al., J. Amer. Chem. Soc.

1943, 65, 2140, by starting from N-CO-O-

CH

2

C

6

H

5 -(2-bromoethyl)amine instead of benzyl chloride R. Jacobson et al., J. Med. Chem. (1991), 34, 2816].

The production of the complexes and complexing agents oft general formula I'A and I'B is carried out according to or analogously to the instructions described in the experimental part or according to methods known in the literature (see, e.g., European Patent Applications Nos. 0 512 661, 0 430 863, 0 255 471 and 0 565 930.

Thus, the production of compounds of general formula I'A can be carried out, in that a group T" is used as a precursor of functional group either in the meaning of a protected acid function, which can be converted into the free acid function independently of acid protective groups R 1 according to the above-indicated process, or in the meaning of a protected amine function, which unblocks according to processes known in the literature [Th. W. Greene, P. G. M. Wuts, Protective Groups in Organic Synthesis, 2nd Edition, John Wiley Sons (1991), pp.

309-385] and then can be converted into the isocyanates or isothiocyanates [Methoden der Org. Chemie (Houben-Weyl), E 4, pp.

742-749, 837-843, Georg Thieme Verlag, Stuttgart, New York (1983)]. Such compounds can be produced according to or analogously to the instructions that are described in the experimental part By mohoalkylation of cyclene with suitable ahaloacid amides [in aprotic solvents, such as, chloroform].

The production of compounds of general formula I'B can be carried out, for example, in that a protected acid function is S. o used as a precursor of the activated carboxyl group-C*O, which can be converted into the free acid function independently of acid protective groups R 1 according to the above-indicated processes and can be activated according to the process tha are known in the literature and are also described above. Such compounds can be produced according to or analogously to the instructions that are described in the experimental part or, for example, in that an amino acid derivative of general formula

II

R

HN C(II) HN

COV'

in which

R

5 has the meaning indicated for R 5 whereby hydroxy or carboxy groups that are optionally contained in R 5 are optionally present in protected form, and

V

1 is a straight-chain or branched C1-C6 alkyl group, a benzyl, trimethylsilyl, triisopropylsilyl, 2,2,2trifluoroethoxy or 2,2,2-trichloroethoxy group, whereby

V

I is different from is reacted with an alkylating agent of general formula III C CO R S I I l too. 2 Hal COR"' eeoc in which

R

1 stands for a protective group, and *9 Hal stands for a halogen atom, such as Cl, Br or I, but preferably Cl [see also M. A. Williams, H.

Rapoport, J. Org. Chem. 58, 1151 (1993)].

Preferred amino acid derivatives are the esters of natur lly occurring a-amino acids.

The reaction of compound (II) with compound (III) is carried out preferably in a buffered alkylation reaction, whereby an aqueous phosphate-buffer solution is used as a buffer. The reaction is carried out at a pH of 7-9, but preferably at a pH of 8. The buffer concentration can be between 0.1-2.5 M, but preferably a 2 M phosphate-buffer solution is used. The temperature of the alkylation can be between 0 and 50 0 C; the preferred temperature is room temperature.

The reaction is carried out in a polar solvent, such as, acetonitrile, tetrahydrofuran, 1,4-dioxane or 1,2dimethoxyethane. Preferably, acetonitrile is used.

The production of the pharmaceutical agents according to the invention is also carried out in a way known in the art, by the complex compounds according to the invention optionally with the addition of the additives that are commonly used in galenicals being suspended or dissolved in aqueous medium and then the suspension or solution optionally being sterilized.

Suitable additives are, for example, physiologically harmless buffers (such as, for example, tromethamine), additives of complexing agents or weak Complexes (such as, for example, diethylenetriaminepentaacetic acid or the corresponding Cacascade polymer complexes) or if necessary electrolytes, such as, for example, sodium chloride or if necessary antioxidants, such as, for example, ascorbic acid.

9 If suspensions or solutions of the agents according to the invention in water or physiological salt solution are desired for enteral administration or other purposes, they are mixed withkne or more adjuvant(s) that are commonly used in galenicals [for example, methyl cellulose, lactose, mannitol] and/or surfactant(s) [for example, lecithins, TweenR), Myrjc)] and/or flavoring substance(s) for taste correction [for example, ethereal oils].

In principle, it is also possible to produce the pharmaceutical agents according to the invention even without isolating the complex salts. In any case, special care must be used to undertake the chelation so that the salts and salt solutions according to the invention are practically free of noncomplexed metal ions having a toxic effect.

This can be ensured, for example, with the aid of color indicators such as xylenol orange by control titrations during the production process. The invention therefore also relates to processes for the production of complex compounds and their salts. As a last precaution, there is a purification of the isolated complex salt.

The pharmaceutical agents according to the invention contain preferably 1 mol-1.3 mol/l of the complex salt and are generally dosed in amounts--of--0.001-5 mmol/kg. They are intended for enteral and parenteral administration. The complex compounds according to the invention are used 1. for NMR diagnosis and diagnostic radiology in the form 0* 6* of their complexes with the ions of elements with atomic numbers 21-29, 39, 42, 44 and 57-83; 2. for radiodiagnosis and radiotherapy in the form of their complexes with radioisotopes of the elements lith atomic numbers 27, 29, 31, 32, 37-39, 43, 49, 62, 64, 75 and 77.

The agents according to the invention meet the varied requirements for suitability as contrast media for nuclear spin tomography. Thus, they are very well suited, after oral or parenteral administration, for improving the image, obtained with the aid of nuclear spin tomographs, in its informative value by increasing the signal intensity. Further, they show the great effectiveness which is necessary to load the body with the fewest possible amounts of foreign substances, and the good compatibility which is necessary to maintain the noninvasive nature of the studies.

The good water solubility and low osmolality of the agents according to the invention makes it possible to produce highly concentrated solutions, so that the volume load of the circulatory system can be held within reasonable limits, and to compare the dilution through the bodily fluid, NMR diagnostic agents must be 100- to 1000-fold better water-soluble S than for NMR spectroscopy. Further, the agents according to the invention exhibit not-only high stability in vitro, but also surprisingly high stability in vivo, so that a release or an S S exchange of the ions toxic in themselves not covalently bonded in the complexes is carried out only extremely slowly within the time in which the new contrast media are again completely excreted.

In general, the agents according to the invention for use as NMR diagnostic agents are dosed in amounts of 0.0001 5 mmol kg, preferably 0.005-0.5 mmol/kg. Details of use are discussed, for example, in Weinmann et al., Am. J. of Roentgenology 142, 619 (1984).

Especially low dosages (under 1 mg/kg of body weight) of organ-specific NMR diagnostic agents can be used, for example, to detect tumors and myocardial infarction.

Further, the complex compounds according to the invention are used advantageously as susceptibility reagents and as shift reagents for in vivo NMR spectroscopy.

The agents according to the invention are also suitable as radiodiagnostic agents because of their advantageous radioactive properties and the good stability of the complex compounds contained in them. Details of their use and dosage are described in, "Radiotracers for Medical Applications," CRC Press, Boca Raton, Florida.

Another imaging methcd with radioisotopes is positron emission tomography, which uses positron-emitting isotopes, such as, 43 Sc, "Sc;- 52 Fe, 55 Co and 8 Ga (Heiss, W. Phelps, M.

Positron Emission Tomography of Brain, Springer Verlag Berlin, Heidelberg, New York 1983).

The compounds according to the invention are also suitable, surprisingly enough, for differentiating malignant and benign tumors in areas without blood-brain barriers.

They are also distinguished in that they are eliminated completely from the body and thus are well-tolerated.

J

Since the substances according to the invention are concentrated in malignant tumors (no diffusion in healthy tissue, but high permeability of tumor vessels), they can also assist in the radiation therapy of malignant tumors. The latter is distinguished from the corresponding diagnosis only by the amount and type of the isotope used. The object, in this case, is the destruction of tumor cells by high-energy shortwave radiation with a smallest possible range of action. For this purpose, 46 interactions of the metals contained in the complexes (such as, iron or gadolinium) are used with ionizing radiations x rays) or with neutron rays. By this effect, the local radiation dose is significantly increased on the spot where the metal complex is found in tumors). To produce the same radiation dose in the malignant tissue, the radiation exposure for healthy tissue can be considerably reduced with the use of such metal complexes and thus side effects that are stressful to the patients are avoided. The metal complex conjugates according to the invention are therefore suitable also as radiosensitizing substances in radiation therapy of malignant tumors use of Mossbauer effects of in neutron capture therapy). Suitable Bemitting ions are, for example, 4 6 Sc, 47Sc, 48 Sc, 7Ga, "Ga and 9Y.

Suitable a-emitting ions exhibiting short half-lives are, for example, 211 Bi, 212 Bi, 213 Bi and 21 4Bi, whereby 212 Bi is preferred. A suitable photon- and electron-emitting ion is 1 58 Gd, which can be obtained from 1 57 Gd by neutron capture.

If the agent according to the invention is intended for e in the variant of radiation therapy proposed by R. L. Mills al. (Nature Vol. 336, (1988), p. 787), the central ion must be derived from a Mossbauer isotope, such as, for example, 57Fe or 151Eu.

In the in vivo administration of the therapeutic agents according to the invention, the latter can be administered together with a suitable vehicle, such as, for example, serum, or physiological common salt solution and together with another protein, such as, for example, human serum albumin. In this case, the dosage depends on the type of cellular disorder, the metal ion used and the type of imaging method.

The therapeutic agents according to the invention are administered parenterally, preferably i.v.

Details of use of radiotherapeutic agents are discussed in, R. W. Kozak et al. TIBTEC, October 1986, 262.

The agents according to the invention are extremely well suited as x-ray contrast media, especially for computer tomography whereby it is especially to be emphasized that no signs of the anaphylaxis-like reactions, known from the iodine-containing contrast media, can be detected with them in biochemical-pharmacological studies. They are especially .9C9 .valuable because of the advantageous absorption properties in the areas of higher tube voltages for digital subtraction techniques.

In general, the agents according to the invention are dosed for use as x-ray contrast media analogously to, for example, meglumine-diatrizoate in amounts of 0.1-5 mmol/kg, preferably 0.25-1 mmol/kg.

Details of use f x-ray contrast media are discussed in,-for example, Barke, RSntgenkontrastmittel [X-Ray Contrast Media], G.

Thieme, Leipzig (1970) and P. Thurn, E. Bucheler "Einfuhrung in die R8ntgendiagnostik [Introduction to Diagnostic Radiology]," G. Thieme, Stuttgart, New York (1977).

In general, it has been possible to synthesize new complexing agents, metal complexes and metal complex salts, which open up new possibilities in diagnostic and therapeutic medicine.

48 The following examples are used for a more detailed explanation of the object of the invention: *q q S. S. Sq Sq..

SS

S. S *S S

S.

qe S S q Sq Example 1 a) Bis[2-(benzyloxycarbonylamino)-ethyl]-amine 51.5 g (500 mmol) of diethylenetriamine and 139 ml (1 mol) of triethylamine are dissolved in dichloromethane and mixed at 0 C with 161 g of benzyl cyanoformate (Fluka) in dichloromethane and then stirred overnight at room temperature.

After the reaction is completed, concentration by evaporation is performed during draw-off, the residue is taken up in diethyl ether, the organic phase is washed with sodium carbonate solution and dried with sodium sulfate. The filtrate is mixed with o* hexane, the precipitate is filtered out and dried.

Yield: 163.4-g (88% of theory) Elementary analysis: Cld: C 64.67 H 6.78 N 11.31 Fnd: C 64.58 H 6.83 N 11.28 b) N,N,N',N',N",N"-Hexakis[2-(benzyloxycarbonylamino)-ethylttrimesic acid triamide 13.27 g (50 mmol) of trimesic acid trichloride (Aldrich) and 34.7 ml (250 mmol) of triethylamine are dissolved in dimethylformamide (DMF) and mixed at O0C with 65.0 g (175 mmol) of the amine described in Example la) and then stirred overnight at room temperature. The solution is concentrated by evaporation in a vacuum, and the residue is chromatographed on silica gel with ethyl acetate.

Yield: 39.4 g (62% of theory) Elementary analysis: Cld: C 65.24 H 5.95 N 9.92 Fnd: C 65.54 H 5.95 N 9.87 c) Na,Nt-Bis(N,N'-dibenzyloxycarbonyl-lysyl)-lysine, protected "tri-lysine" 3.6 g (20 mmol) of lysine-hydrochloride and 6.95 ml mmol) of triethylamine are dissolved in DMF, mixed with 26.8 g mmol) of Na, N-dibenzyloxycarbonyl-lysine-p-nitrophenylester (Bachem) and stirred for 2 days at room temperature. After the reaction is completed, it is concentrated by evaporation in a vacuum, the residue-is taken up in ethyl acetate and shaken out with dilute hydrochloric acid. The organic phase is dried with sodium sulfate, the solvent is concentrated by evaporation, and the residue is chromatographed with ethyl acetate/ethanol in a step gradient.

Yield: 10.7 g (57% of theory) .o Elementary analysis: Cld: C 63.95 H 6.65 N 8.95 Fnd: C 63.63 H 6.69 N 8.93 d) Completely protected benzyloxycarbonyl-24-polyamine based on N,N,N',N',N",N"-hexakis[2-(trilysyl-amino)-ethyl]-trimesic acid triamide 1.27 g (1 mmol) of the hexa-benzyloxycarbonylamine described in Example Ib) is dissolved in glacial acetic acid and mixed with 33% hydrogen bromide in glacial acetic acid while being stirred.

After 60 minutes, the incipient precipitation is completed with diethyl ether, the hexaamine-hydrobromide produced is washed with ether, dried in a vacuum and used in the subsequent reaction described below without further purification.

Yield: 0.95 g (quantitative) g (7.5 mmol) of the protected "tri-lysine" described in Example Ic), 1.2 g (7.5 mmol) of l-hydroxybenzotriazole and 2.4 g (7.5 mmol) of 2 -(lH-benzotriazol-l-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate (TBTU; Peboc Limited, UK) are dissolved in DMF and stirred for 15-minutes. This solution is then mixed with 5.16 ml (30 mmol) of N-ethyldiisopropylamine and with 0.95 g (1 mmol) of the hexaamine-hydrobromide described above, and it is stirred overnight at room temperature. After the reaction is completed, it is concentrated by evaporation in a vacuum, and the residue is chromatographed on silica gel with ethyl acetate/ethanol Yield: 4.55 g (76% of theory) Elementary analysis: Cld: C 64.35 H 6.71 N 10.52 Fnd: C 64.08 H 6.57 N 10.29 e) 2 -Bromopropionylglycine-benzyl ester 55.9 g (326.1 mmol) of 2 -bromopropionic acid chloride is added in drops at 0 C to 100 g (296.4 mmol) of glycine benzyl ester-p-toluenesulfonic acid salt and 33.0 g (326.1 mmol) of triethylamine in 400 ml of methylene chloride. The temperature is not allowed to exceed 5 0 C. After addition is completed, it is stirred for one hour at 0°C, then for 2 hours at room temperature. 500 ml of ice water is added, and the water phase is set at pH 2 with 10% aqueous hydrochloric acid. The organic phase is separated, washed once each with 300 ml of 5% aqueous soda solution and 400 ml of water. The organic phase is dried on magnesium sulfate and evaporated to the dry state in a vacuum.

The residue is recrystallized from diisopropyl ether.

Yield: 68.51 g (75% of theory) of a colorless crystalline powder Melting point: 69-70 0

C

Elementary analysis: Cld: C 46.76 H 7.19 N 4.54 Br 25.92 :'Fnd: C 46.91 H 7.28 N 4.45 Br 25.81 f) 1-[4-(Benzyloxycarbonyl)-l-methyl-2-oxo-3-azabutyl]- 1,4,7,10-tetraazacyclododecane g (162.2 mmol) of the title compound of Example le) is added to 55.8 g (324.4 mmol) of 1, 4 7 dissolved in 600 ml of chloroform, and it is stirred overnight at room temperature. 500 ml of water is added, the organic phase is separated and in each case washed twice with 400 ml of water.

The organic phase is dried on magnesium sulfate and evaporated to the dry state in a vacuum. The residue is chromatographed on silica gel (mobile solvent: chloroform/methanol/aqueous ammonia 10:5:1).

Yield: 40.0 g [63% of theory relative to the le) used] of a slightly yellowish viscous oil.

Elementary analysis: Cld: C 61.36 H 8.50 N 17.89 Fnd: C 61.54 H 8.68 N 17.68 g) 10-[4-(Benzyloxycarbonyl)-l-methyl-2-oxo-3-azabutyl]-1,4,7tris(tert-butoxycarbonylmethyl)-1,4,7,10tetraazacyclododecane (sodium bromide complex) 33 g (169 mmol) of bromoacetic acid-tert-butyl ester is added to 20 g (51.08 mmol) of the title compound of Example If) and 17.91 g (169 mmol) of sodium carbonate in 300 ml of acetonitrile, and it is stirred for 24 hours at 60 0 C. It is *oo cooled to 0 C, the salts are filtered out, and the filtrate is evaporated to the dry state. The residue is chromatographed silica gel (mobile solvent: ethyl acetate/ethanol: 15:1). TL fractions that contain the product are concentrated by evaporation, and the residue recrystallizes from diisopropyl ether.

Yield: 34.62 g (81% of theory) of a colorless crystalline powder Melting point: 116-117 0

C

Elementary analysis: Cld: C 54.54 H 7.59 N 8.37 Na 2.74 Br 9.56 Fnd: C 54.70 H 7.65 N 8.24 Na 2.60 Br 9.37 h) 10-(4-Carboxy-l-methyl-2-oxo-3-azabutyl)-1,4,7-tris(tertbutoxycarbonylmethyl)-1,4,7,10-tetraazacyclododecane (sodium bromide complex) g (35.85 mmol) of the title compound of Example ig is dissolved in 500 ml of isopropanol, and 3 g of palladium catalyst (10% Pd/C) is added. It is hydrogenated overnight at room temperature. Catalyst is filtered out, the filtrate is evaporated to the dry -state in a vacuum and recrystallized from acetone.

Yield: 22.75 g (85% of theory) of a colorless crystalline powder Melting point: 225 C (decomposition) Elementary analysis: Cld: C 49.86 H 7.69 N 9.38 Na 3.07 Br 10.71 Fnd: C 49.75 H 7.81 N 9.25 Na 2.94 Br 10.58 i) 24-mer N-(5-DO3A-yl-4-oxo-3-azahexanoyl)-cascade polyamide based on N,N,N',N',N",N"-hexakis[2-(trilysylamino)-ethyl]trimesic acid triamide*) g (1 mmol) of the poly-benzyloxycarbonylamine described in Example Id) is dissolved in glacial acetic acid and mixed with 33% hydrogen bromide in glacial acetic acid while being stirred.

After 3 hours, the incipient precipitation is completed with diethyl ether, the 24 -amine-hydrobromide produced is washed with ether and dried in a vacuum.

35.84 g (48 mmol) of the acid described in Example Ih) above is dissolved in DMF, mixed with 7.35 g (48 mmol) of 1- 9 hydroxybenzotriazole, with 15.41 g (48 mmol) of TBTU (Peboc Limited, UK) and with 49.3 ml (288 mmol) of Nethyldiisopropylamine, and it is stirred for 20 minutes at room S temperature. This solution is then mixed with the (1 mmol) 24amine-hydrobromide described above, and it is stirred for 4 days at room temperature. The solution is concentrated by evaporation S in a vacuum, the remaining oil is cooled in an ice bath and m*xed with trifluoroacetic acid, stirred overnight at room temperatkre and then precipitated with diethyl ether. The precipitate is dried in a vacuum, taken up in water, set at pH 7, a DO3A 1, 4 7 -tris(carboxymethyl)-1,4,7,10tetraazacyclododecane YM3 Amicon(R)-ultrafiltration membrane is used to remove lowmolecular portions, and the retentate is ultimately membranefiltered and freeze-dried.

Yield: 13.5 g (83% of theory)

H

2 0 content (Karl-Fischer): 6.2% Elementary analysis (relative to anhydrous substance): Cld: C 45.82 H 6.09 N 15.07 Na 10.79 Fnd: C 45.56 H 6.15 N 14.80 Na 10.52 k) 24-mer-Gd-complex of N-(5-DO3A-yl-4-oxo-3-azahexanoyl)cascade polyamide based on N,N,N',N',N",N"-hexakis[2- (trilysylamino)-ethyl]-trimesic acid triamide 8.13 g (0.5 mmol) of the complexing agent acid described in :0 Example li) above is set at pH 3 in water with dilute hydrochloric acid, mixed with 2.17 g (6 mmol) of GdzO 3 stirred for 30 minutes at 80 0 C, set at pH 7 after cooling and desalinated with a YM3 AMICON R) ultrafiltration membrane. The retentates ultimately membrane-filtered and freeze-dried.

Yield: 8.89 g (92.1% of theory)

H

2 0 content (Karl-Fischer): 9.6% Gd determination (AAS): 19.6% Elementary analysis (relative to anhydrous substance): Cld: C 40.26 H 5.35 N 13.24 Gd 21.62 Fnd: C 39.98 H 5.51 N 13.42 Gd 21.37 Example 2 a) 2 -Bromopropionyl-B-alanine-benzyl ester 53.65 g (313 mmol) of 2 -bromopropionic acid chloride is added in drops at 0 C to 100 g (285 mmol) of B-alanine-benzyl ester-p-toluenesulfonic acid salt and 31.67 g (313 mmol) of triethylamine in 400 ml of methylene chloride. The temperature is not allowed to exceed 5 0 C. After addition is completed, if is stirred for 1 hour at oOC, then for 2 hours at room temperature.

500 ml of ice water is added, and the water phase is set at pH 2 with 10% aqueous hydrochloric acid. The organic phase is separated, washed once each with 300 ml of 5% aqueous hydrochloric acid,-300 ml of 5% aqueous soda solution and 400 ml of water. The organic phase is dried on magnesium sulfate and evaporated to the dry state in a vacuum. The residue is recrystallized from diisopropyl ether.

Yield: 71.36 g (78% of theory) of a colorless crystalline powder Elementary analysis: Cld: C 48.46 H 7.51 N 4.35 Br 24.80 Fnd: C 48.29 H 7.65 N 4.25 Br 24.61 b) l-[5-(Benzyloxycarbonyl)-l-methyl-2-oxo-3-azapentyl]- 1,4,7,10-tetraazacyclododecane g (155.2 mmol) of the title compound of Example 2a) is added to 53.32 g (310 mmol) of 1, 4 7 dissolved in 600 ml of chloroform, and it is stirred overnight at room temperature. 500 ml of water is added, the organic phase is separated, and it is washed twice in each case with 400 ml of water. The organic phase is dried on magnesium sulfate and evaporated to the dry state in a vacuum. The residue is chromatographed on silica gel (mobile solvent: chloroform/methanol/aqueous 25% ammonia: 10/5/1).

Yield: 38.39 g [61% of theory relative to the 2a) usedfof a light yellowish viscous oil.

Elementary analysis: Cld: C 62.20 H 8.70 N 17.27 Fnd: C 62.05--H 81 N 17.15 c) 10-15-(Benzyloxycarbonyl)-l-methyl-2-oxo-3-azapentyl]-1,4,7tris(tert-butoxycarbonyl-methyl)-1,4,7,10tetraazacyclododecane (sodium bromide complex) 31.8 g (163 mmol) of bromoacetic acid-tert-butyl ester is added to 20 g (49.32 mmol) of the title compound of Example 2) and 17.28 g (163 mmol) of sodium carbonate in 300 ml of acetonitrile, and it is stirred for 24 hours at 60 0 C. It is cooled to OOC, salts are filtered out, and the filtrate is evaporated to the dry state. The residue is chromatographed on silica gel (mobile solvent: ethyl acetate/ethanol 10/1). The fractions that contain the product are concentrated by evaporation, and the residue recrystallizes from diisopropyl ether.

Yield: 31.89 g (76% of theory) of a colorless, crystalline powder Elementary analysis: Cld: C 55.05 H 7.70 N 8.23 Na 2.69 Br 9.40 Fnd: C 55.17 H 7.85 N 8.10 Na 2.51 Br 9.30 d) 10- 5-(Carboxy)-l-methyl-2-oxo-3-azapentyl]-1,4,7-tris(tertbutoxycarbonylmethyl)-1,4,7,10-tetraazacyclododecane (sodium bromide complex) 30 g (35.26 mmol) of the title compound of Example 2c) is dissolved in 500-ml--of isopropanol, and 3 g of palladium catalyst (10% Pd/C) is added. It is hydrogenated overnight at room temperature. Catalyst is filtered out, the filtrate is evaporated to the dry state in a vacuum and recrystallized from acetone.

Yield: 24.41 g (91% of theory) of a colorless, crystalline powder Elementary analysis: Cld: C 50.52 H 7.82 N 9.21 Na 3.01 Br 10.52 Fnd: C 50.41 H 7.95 N 9.10 Na 2.91 Br 10.37 e) 24-mer N-( 6 -DO3A-yl-5-oxo-4-azaheptanoyl)-cascade polyamide based on NN,N',N',N",N"-hexakis[2-(trilysylamino)-ethyl]trimesic acid triamide g (1 mmol) of the poly-benzyloxycarbonylamine described in Example id) is dissolved in glacial acetic acid and mixed with 33% hydrogen bromide in glacial acetic acid while being stirred.

36.52 g (48 mmol) of the acid described in Example 2d) above is dissolved in DMF, mixed with 7.35 g (48 mmol) of 1hydroxybenzotriazole, with 15.41 g (48 mmol) of TBTU (Peboc Limited, UK) and with 49.3 ml (288 mmol) of Nethyldiisopropylamine, and it is stirred for 20 minutes at room temperature. This solution is then mixed with the (1 mmol) 24amine-hydrobromide described above and stirred for 4 days at room temperature. The solution is concentrated by evaporation in a vacuum, the remaining oil is cooled in an ice bath and mixed ith trifluoroacetic acid, stirred overnight at room temperature ad then precipitated with diethyl ether. The precipitate is dried in a vacuum, taken up in water, set at pH 7, a YM3 Amicon( R ultrafiltration membrane is used to remove low-molecular portions, and the retentate is ultimately membrane-filtered and freeze-dried.

Yield: 14.4 g (85% of theory) content (Karl-Fischer): 8.7% Elementary analysis (relative to anhydrous substance): Cld: C 46.82 H 5.98 N 14.79 Na 10.59 Fnd: C 47.04 H 6.23 N 14.96 Na 10.26 f) 24-mer-Gd Complex of N-( 6

-DO

3 A-yl-5-oxo-4-azaheptanoyl)cascade polyamide based on N,N,N',N',N",N"-hexakis(2- (trilysylamino)-ethyl]-trimesic acid triamide g (0.5 mmol) of the complexing agent acid described in Example 2e) above is set at pH 3 in water with dilute hydrochloric acid, mixed with 2.17 g (6 mmol) of Gd0 3 stirred for 30 minutes at 80 0 C, set at pH 7 after cooling and desalinated with a YM3 AMICON(RLultrafiltration membrane. The retentate is ultimately membrane-filtered and freeze-dried.

Yield: 8.50 g (88% of theory) content (Karl-Fischer): 7.9% Gd determination (AAS): 19.4% Elementary analysis (relative to anhydrous substance): t.

Cld: C 41.12 H 5.52 N 12.99 Gd 21.21 Fnd: C 40.86 H 5.34 N 13.25 Gd 20.95 Example 3 a) N,N'-Bis(benzyloxycarbonyl)-3-[carboxymethoxyacetyl]-3- 37.14 g (100 mmol) of the bis(benzyloxycarbonyl-aminoethyl)amine described in Example la) is dissolved in DMF, mixed in an ice bath with 17.4 g (150 mmol) of diglycolic anhydride (Janssen 62 Chimica) and 21 ml (150 mmol) of triethylamine and then stirred overnight at room temperature. The solution is concentrated by evaporation in a vacuum, the residue is taken up in ethyl acetate and shaken out with dilute hydrochloric acid. The organic phase is dried with sodium sulfate and after the drying agent is filtered, it is crystallized by adding hexane.

Yield: 41.4 g (85% of theory) Elementary analysis: Cld: C 59.13 H 6.00 N 8.62 Fnd: C 58.99 H 5.93 N 8.70 S b) N,N' ,N",N"'-Tetrakis{8-(benzyloxycarbonylamino)-6-[(2- (benzyloxycarbonylaminoethyl]-5-oxo-3-oxaoctanoyl}cyclene 345 mg (2 mmol) of 1, 4 ,7,10-tetraazacyclododecane (cyclene; Fluka) is azeotropically dehydrated with toluene. A solution of 4.88 g (10 mmol) of N,N'-bis(benzyloxycarbonyl)-3- [carboxymethoxyacetyl]-3-azapentane-1,5-diamine [Example 3a)] in tetrahydrofuran (THF) as well as 2.47 g (10 mmol) of 2-ethoxylethoxycarbonyl-1,2-dihydroquinoline (EEDQ; Fluka) are added to the cooled solution of cyclene in toluene at room temperature, and it is stirred overnight. After the reaction is completed, the product is precipitated by adding hexane, decanted from solvent and reprecipitated once more from THF/hexane and then from THF/toluene. After drying in a vacuum, 2.78 g (68% of theory) of a pale yellow solid is obtained.

Elementary analysis: Cld: C 60.93 H 6.29 N 10.93 Fnd: C 60.68 H 6.40 N 10.97 c) Completely protected benzyloxycarbonyl-32-polyamine based on 32-amine condensed with N,N-bis(lysyl)-lysine ("trilysine) from N,N',N",N"'-tetrakis{8benzyloxycarbonylamino)-6-[2-(benzyloxycarbonylamino)ethyl]-5-oxo-3-oxaoctanoyl}cyclene 2.05 g (1 mmol) of the octa-benzyloxycarbonylamine described in Example 3b) is dissolved in glacial acetic acid and mixed with 33% hydrogen bromide in-glacial acetic acid while being stirred.

After 90 minutes, the incipient precipitation is completed with diethyl ether, the octa-amine-hydrobromide produced is washed with ether, dried in a vacuum and used in the subsequent reaction described below without further purification.

Yield: 1.6 g (quantitative) .9.4 g (10 mmol) of the protected "tri-lysine" described

L

Example Ic), 1.5 g (10 mmol) of 1-hydroxybenzotriazole and 3.2 g mmol) of 2 -(1H-benzotriazol-l-yl)-1,1,3,3,-tetramethyluronium tetrafluoroborate (TBTU; Peboc Limited, UK) are dissolved in DMF and stirred for 15 minutes. This solution is then mixed with 5.16 ml (30 mmol) of N-ethyldiisopropylamine and with 1.6 g (1 mmol) of the octaamine-hydrobromide described above, and it is stirred overnight at room temperature. After the reaction is completed, it is concentrated by evaporation in a vacuum, and the 64 residue is chromatographed on silica gel with dichloromethane/methanol (10:1).

Yield: 6.0 g (72% of theory) Elementary analysis: Cld: C 63.32 H 6.76 N 10.74 Fnd: C 62.98 H 6.91 N 10.43 d) 32-mer N-(5-DO 3 A-yl-4-oxo-3-azahexanoyl)-cascade polyamide *based on the 32-mer amine described in Example 3c) above 8.35 g (1 mmol) of the 32 -mer-benzyloxycarbonylamine described in Example 3c) is dissolved in glacial acetic acid and mixed with 33% hydrogen bromide in glacial acetic acid while :being stirred. After 3 hours, the incipient precipitation is completed with diethyl ether, the 3 2-amine-hydrobromide produced is washed with ether and dried in a vacuum.

47.8 g (64 mmol) of the acid described in Example Ih) is dissolved in DMF, mixed with 9.8 g (64 mmol) of 1hydroxybenzotriazole, with 20.5 g (64 mmol) of TBTU (Peboc Limited, UK) and with 65.7 ml (384 mmol) of N-ethyldiisopropylamine, and it is stirred for 20 minutes at room temperature. This solution is then mixed with the (1 mmol) 32amine-hydrobromide described above and stirred for 4 days at room temperature. The solution is concentrated by evaporation in a vacuum, the remaining oil is cooled in an ice bath and mixed with trifluoroacetic acid, stirred overnight at room temperature and then precipitated with diethyl ether. The precipitate is dried in a vacuum, taken up in water, set at pH 7, a YM3 Amicon(R) ultrafiltration membrane is used to remove low-molecular portions, and the retentate is ultimately membrane-filtered and freeze-dried.

Yield: 17.2 g (76.4% of theory)

H

2 0 content (Karl-Fischer): 7.6% Elementary analysis (relative to anhydrous substance): Cld: C 45.73 H 6.12 N 15.08 Na 10.61 Fnd: C 45.89 H 6.30 N 14.84 Na 10.31 e) 32-mer-Gd Complex of N-(5-D03A-yl-4-oxo-3-azahexanoyl)boot cascade polyamide based on the 32-mer amine described in Example 3c) 10.4 g (0.5 mmol) of the complexing agent acid described in Example 3d) above is set at pH 3 in water with dilute hydrochloric acid, mixed with 2.89 g (8 mmol) of Gd 3 stirred for 30 minutes at 80C, set at pH 7 after cooling and desalinated with a YM3 AMICON(") ultrafiltration membrane. The retentate ultimately membrane-filtered and freeze-dried.

Yield: 12.1 g (91.1% of theory)

H

2 0 content (Karl-Fischer): 11.0% Gd determination (AAS): 18.6% Elementary analysis (relative to anhydrous substance): Cld: C 40.26 H 5.39 N 13.28 Gd 21.30 Fnd: C 40.10 H 5.21 N 13.04 Gd 21.03 The ytterbium complex is obtained analogously with Yb 2

(CO

3 Elementary analysis (relative to anhydrous substance): Cld: C 39.42 H 5.28 N 13.00 Yb 22.94 Fnd: C 39.29 H 5.40 N 12.81 Yb 22.65 Example 4 a) Hexaethylene glycol monomethyl ether-p-toluenesulfonic acid ester 14.3 g (75 mmol) of p-toluenesulfonic acid chloride is added in portions at OOC to 20 g (67.49 mmol) of hexaethylene glycol monomethyl ether-and 7.59 g (75 mmol) of triethylamine in 200 ml of chloroform, and it is then stirred for 4 hours at this S temperature. It is evaporated to the dry state in a vacuum, and the residue is chromatographed on silica gel (mobile solvent: chloroform/methanol 5/1).

Yield: 27.67 g (91% of theory) of a sheetlike, vitreous solid Elementary analysis: Cld: C 53.32 H 7.61 S 7.12 Fnd: C 53.15 H 7.70 S 7.03 b) 1-Benzyloxy-5-(benzyloxycarbonyl)-2-chloro-3-oxo-4azapentane 76 g (326.1 mmol) of 2 -chloro-3-(benzyloxy)-propionic acid chloride (produced according to Inorg. Chem. Vol. 31; 2422, 1992) is added in drops to 100 g (296.4 mmol) of glycine benzyl esterp-toluenesulfonic acid salt and 33.0 g (326.1 mmol) of triethylamine in 400 ml of methylene chloride at 0°C, and it is stirred for 2 hours at this temperature. 500 ml of ice water is added, and the water phase is set at pH 2 with 10% aqueous hydrochloric acid. The organic phase is separated, washed once each with 300 ml of 5% aqueous hydrochloric acid, 300 ml of aqueous soda solution and 400 ml of water. The organic phase is dried on magnesium sulfate and evaporated to the dry state in a vacuum. The residue is chromatographed on silica gel (mobile solvent: methylene chloride/hexane/acetone 15/5/1).

Yield: 75.07 g (70% of theory) of a pale yellow-colored viscous oil o Elementary analysis: Cld: C 63.07 H 5.57 N 3.87 Cl 9.80 Fnd: C 63.17 H 5.65 N 3.75 Cl 9.63 c) 1-[ 4 -(Benzyloxycarbonyl)-1-(benzyloxymethyl) -2-oxo-3azabutyl]-1,4,7,10-tetraazacyclododecane g (193.5 mmol) of the title compound of Example 4b) and 11.1 g (64.5 mmol) of 1,4,7,10-tetraazacyclododecane are dissolved in 70 ml of dimethylformamide and stirred for 2 days at 0 C. It is evaporated to the dry state in a vacuum, the residue is taken up in 700 ml of water and extracted twice with 250 ml of chloroform each. The organic phase is dried on magnesium sulfate and evaporated to the dry state in a vacuum. The residue is chromatographed on silica gel (mobile solvent: aqueous ammonia 10/5/1).

Yield: 13.16 g (41% of theory relative to cyclene) of a viscous, colorless oil Elementary analysis: Cld: C 65.17 H 7.90 N 14.07 Fnd: C 65.24 H 7.77 N 14.18 d) 10-[4-(Benzyloxycarbonyl)--(benzyloxymethyl)-2-oxo-3azabutyl]-1,4,7-tris(tert-butoxycarbonylmethyl)-1,4,7,10tetraazacyclododechne (sodium bromide complex) 16.81 g (86.2 mmol) of bromoacetic acid-tert-butyl ester is added to 13 g (26.12 mmol) of the title compound of Example 4c) and 9.14 g (86.2 mmol) of sodium carbonate in 200 ml of acetonitrile, and it is stirred for 24 hours at 60 0 C. It is cooled to OOC, salts are filtered out, and the filtrate is evaporated to the dry state. The residue is chromatographed silica gel (mobile solvent: ethyl acetate/ethanol 15/1).

Yield: 19.46 g (79% of theory) of a waxy solid Elementary analysis: Cld: C 57.32 H 7.38 N 7.43 Na 2.43 Br 8.47 Fnd: C 57.22 H 7.51 N 7.27 Na 2.33 Br 8.29 69 e) 10-[4-Carboxy-2-oxo-l-hydroxymethyl-3-azabutyl]-1,4,7tris(tert-butoxycarbonylmethyl)-1,4,7,10tetraazacyclododecane (sodium bromide complex) 3 g of palladium catalyst (10% Pd/C) is added to 19 g (20.15 mmol) of the title compound of Example 4d) in 300 ml of isopropanol and hydrogenated overnight at room temperature.

Catalyst is filtered out, the filtrate is evaporated to the dry state in a vacuum, and the residue is recrystallized from acetone.

Yield: 13.06 g (85% of theory) of a colorless, crystalline powder Elementary analysis: Cld: C 48.82 H 7.53 N 9.18 Na 3.00 Br 10.49 FFnd: C 48.71 H 7.68 N 9.03 Na 2.81 Br 10.23 f) 10[ 4 -(Benzyloxycarbonyl) (hydroxymethyl)-2-oxo-3azabutyl]-1,4,7-tris(tert-butoxy-carbonylmethyl)-1,4,7,10tetraazacyclododecane 3.42 g (20 mmol) of benzyl bromide is added to 13 g (17.04 mmol) of the title compound of Example 4e) and 6.11 g (18.75 mmol) of anhydrous cesium carbonate in 70 ml of dimethylformamide, and it is stirred overnight at 50 0 C. It is cooled to 0 C, and 700 ml of water is added. Then, it is extracted twice with 300 ml of methylene chloride each. The combined organic phases are washed twice with water, dried on magnesium sulfate and evaporated to the dry state in a vacuum.

The residue is chromatographed on silica gel (mobile solvent: ethyl acetate/ethanol).

Yield: 9.97 g (78% of theory) of a colorless, viscous oil Elementary analysis: Cld: C 60.86 H 8.47 N 9.34 Fnd: C 60.95 H 8.61 N 9.21 g) 10-[ 4 -(Benzyloxycarbonyl)-1-(2,5,8, 11 ,14,17, 20 -heptaoxaheneicosanoyl)- 2 -oxo-3-azabutyl]-1,4,7-tris(tertbutoxycarbonylmethyl)-1,4,7,10-tetraazacyclododecane .9.7 g (12.93 mmol)- of the title compound of Example 4f) is dissolved in 50 ml of THF, and 0.43 g (14.22 mmol) of sodium hydride (80% in paraffin) is added at -10C. It is stirred for 30 minutes at 0C. Then, 11.65 g (25.86 mmol) of the title compound of Example 4a) and 3.46 g (25.86 mmol) of lithium iodide Sare added. It is stirred for 24 hours at room temperature. 3 ml of water is carefully added and then evaporated to the dry st te.

The residue is chromatographed on silica gel (mobile solvent:i chloroform/methanol 10:1).

Yield: 12.1 g (91% of theory) of a vitreous solid Elementary analysis: Cld: C 59.57 H 8.72 N 6.81 Fnd: C 59.65 H 8.91 N 6.62 h) 10-[1-(2-8,11,14,17,20-Heptaoxa-heneicosanoyl)-2-oxo-3-aza- 4-(carboxy)-butyl]-1,4,7-tris(tert-butoxycarbonylmethyl)- 1,4,7,10-tetraazacyclododecane 12 g (11.67 mmol) of the title compound of Example 4g) is dissolved in 300 ml of isopropanol and 2 g of palladium catalyst Pd/C) is added. It is hydrogenated overnight at room temperature. Catalyst is filtered out, and the filtrate is evaporated to the dry state. The residue is recrystallized from acetone/diisopropyl ether.

Yield: 10.18 g (93% of theory) of a waxy solid Elementary analysis: Cld: C 56.33 H 8.92 N 7.46 Fnd: C 56.20 H 9.03 N 7.35 i) 24-mer Gd complex of N-(5-DO3A-yl-4-oxo-3-aza- 7110,13,16,19,22, 25 -heptaoxa-hexacosanoyl)-cascade polyamide based on N,N,N',N',N",N"-hexakis[2-(trilysylamino)-ethyl trimesic acid triamide g (1 mmol) of the 24 -mer-benzyloxycarbonylamine described in Example ld) is dissolved in glacial acetic acid and mixed with 33% hydrogen bromide in glacial acetic acid while being stirred. After 3 hours, the incipient precipitation is completed with diethyl ether, the 24 -amine-hydrobromide produced is washed with ether and dried in a vacuum. 45.03 g (48 mmol) of the acid described in Example 4h) above is dissolved in DMF, mixed with 7.35 g (48 mmol) of 1-hydroxybenzotriazole, with 15.41 g (48 mmol) of TBTU (Peboc Limited, UK) and with 49.3 ml (288 mmol) of N-ethyldiisopropylamine and stirred for 20 minutes at room temperature. This solution is then mixed with the above described (1 mmol) 24-amine hydrobromide and stirred for 4 days at room temperature. The solution is concentrated by evaporation in a vacuum, the remaining oil is cooled in an ice bath and mixed with trifluoroacetic acid, stirred overnight at room temperature and then precipitated with diethyl ether. The precipitate is dried in a vacuum, taken up in water, set at pH 3 with dilute hydrochloric acid, mixed with 8.70 g (24 mmol) of Gd 2 0 3 stirred for 4 hours at 80 0 C, set at pH 7 after cooling, and a YM3 AMICON ultrafiltration membrane is used to remove low-molecular portions, and the retentate is ultimately membrane-filtered and freeze-dried.

Yield: 19.6 g (73.3% of theory) HO0 content (Karl-Fischer): 8.3% Gd determination (AAS): 14.0% Elementary analysis (relative to anhydrous substance): t Cld: C 43.94 H 6.38 N 9.43 Gd 15.39 Fnd: C 44.27 H 6.22 N 9.29 Gd 15.09 Example a) 1,7-Bis(trifluoroacetyl)-1,4, 7 -triazaheptane 113.3 g (790 mmol) of trifluoroacetic acid ethyl ester is added in drops to a solution consisting of 41.14 g (390 mmol) of 1, 4 7 -triazaheptane in 350 ml of tetrahydrofuran at 80 0 C and under nitrogen. It is allowed to stir overnight at room temperature, concentrated by evaporation in a vacuum. The remaining oil is crystallized from hexane.

Yield: 115 g (99.9% of theory) Melting point: 68 70 0

C

Elementary analysis: Cld: C 32.55 H 3.76 F 38.62 N 14.24 Fnd: C 32.63 H 3.75 F 38.38 N 14.19 b) 1,7-Bis(trifluoroacetyl)-4 -benzyloxycarbonyl-1,4,7triazaheptane 14.75 g (50 mmol) of the trifluoroacetyl compound produced under Example 5a) as well as 8.3 ml (60 mmol) of triethylamine are dissolved in 120 ml of dichloromethane and cooled to OOC.

While being stirred, 7.5 ml (53 mmol) of benzyl chloroformate S- dissolved in 20 ml of dichloromethane, is now added in drops. It is allowed to stir overnight at room temperature, he salts are extracted with distilled water, the dichloromethane h solution is dried on sodium sulfate, evaporated to the dry state in a vacuum, and the residue is crystallized from ether/hexane.

Yield: 18.40 g (85.7% of theory) Melting point: 131 132 0

C

Elementary analysis: Cld: C 44.76 H 3.99 F 26.55 N 9.79 Fnd: C 44.87 H 4.03 F 26.62 N 9.61 c) 3,9-Bis(tert-butoxycarbonylmethyl)-6-benzyloxycarbonyl- 3,6,9-triazaundecanedicarboxylic acid-di-tert-butyl ester 4.29 g (10 mmol) of the trifluoroacetyl derivative produced under Example 5b) is dissolved in 30 ml of ethanol and mixed with 800 mg (20 mmol) of sodium hydroxide solution in 10 ml of distilled water. It is stirred for 3 hours at room temperature, evaporated to the dry state in a vacuum at a bath temperature-of 0 C, residual water is removed by azeotropic distillation with isopropanol and taken up in 30 ml of dimethylformamide. 6.9 g (50 mmol) of potassium carbonate as well as 9.7 g (50 mmol) of bromoacetic acid-tert-butyl ester are then added to it, and the 4-benzyloxycarbonyll ,4-,7-triazaheptane is alkylated at room temperature overnight. The dimethylformamide is then drawn off in an oil pump vacuum, the residue is dispersed between water and dichloromethane, the organic solution is dried on sodium sulfate, evaporated to the dry state in a vacuum, and the residue is purified by chromatography on silica gel. The title compound is eluted with ethyl acetate/hexane. It is obtained as foam.

Yield: 6.49 g (93.6% of theory) Elementary analysis: Cld: C 62.32 H 8.57 N 6.06 Fnd: C 62.41 H 8.66 N 6.01 d) 3, 9 -Bis(tert-butoxycarbonylmethyl)-3,6,9triazaundecanedicarboxylic acid-di-tert-butyl ester g (5 mmol) of the compound produced under Example 5c) is dissolved in 100 ml of ethanol, mixed with 200 mg of Pearlman's catalyst (Pd 20% on activated carbon) and hydrogenated until the calculated amount of hydrogen is taken up. Catalyst is suctioned off and evaporated to the dry state in a vacuum. The title compound is obtained as a white foam.

Yield: 2.80 g (99.9% of theory) Elementary analysis:

S

Cld: C 60.98--H 9-.54 N 7.51 Fnd: C 60.02 H 9.62 N 7.56 3,9-Bis(tert-butoxycarbonylmethyl)-6-[1-(ethoxycarbonyl)ethyl]-3,6, 9 -triazaundecanedioic acid-di-tert-butyl ester 5.60 g (10 mmol) of the amino compound produced under Example 5d) is dissolved in 30 ml of dimethylformamide. 1.66 q (12 mmol) of potassium carbonate as well as 2.17 g (12 mmol) f 2-bromopropionic acid ethyl ester are then added to it at room temperature, and it is stirred overnight. It is then poured onto ice water, extracted with ethyl acetate, the organic solution is dried on sodium sulfate, evaporated to the dry state in a vacuum, and the title compound is obtained by chromatography on silica gel. A mixture of ethyl acetate/hexane is used as eluant.

Yield: 4.18 g (63.4% of theory) Elementary analysis: Cld: C 60.07 H 9.32 N 6.37 Fnd: C 60.18 H 9.40 N 6.31 f) 3,9-Bis(tert-butoxycarbonylmethyl)-6-[l-(carboxy)-ethyl]- 3,6,9-triazaundecanedioic acid-di-tert-butyl ester 6.60 g (10 mmol) of the compound produced under Example e) is dissolved in 50 ml of ethanol. The solution of 400 mg mmol) of sodium hydroxide in 5 ml of distilled water is then 4* added to it, and it is stirred for 3 hours at 50 0 C. According to *4 the thin-layer chromatogram, the saponification is quantitative.

It is evaporated td'the dry state in a vacuum, traces of water are removed by codistillation with ethanol, and the residue is dried at 40 0 C in a vacuum. The title compound is obtained as a white powder. The remaining white residue is dissolved in 80 ml of wet ethanol and mixed with the solution of 535 mg mmol) of ammonium chloride in 10 ml of distilled water while being stirred. It is evaporated to the dry state in a vacuum, the soluble portions in butanol are taken up and again evapo ted to the dry state in a vacuum. The residue is extracted with toluene. The organic solution is evaporated to the dry state in a vacuum, and the title compound is obtained as foam.

Yield: 5.35 g (84.7% of theory) Elementary analysis: Cld: C 58.93 H 9.09 N 6.65 Fnd: C 59.01 H 9.16 N 6.60 g) 24-mer N-{N,N-Bis[2-(N,N-bis(carboxymethyl))-aminoethyl]alanyl}-cascade-polyamide based on hexakis[2-(trilysylamino)-ethyl]-trimesic acid triamide, sodium salt g (1 mmol) of the poly-benzyloxycarbonylamine described in Example Id) is dissolved in glacial acetic acid and mixed with 33% hydrogen bromide in glacial acetic acid while being stirred.

After 3 hours, the incipient precipitation is completed with diethyl ether, the 24-amine-hydrobromide produced is washed with ether and dried in a vacuum.

30.33 g (48 mmol) of the acid described in Example 5f) above is dissolved in DMF; mixed with 7.35 g (48 mmol) of 1hydroxybenzotriazole, with 15.41 g (48 mol) of TBTU (Peboc Limited, UK) and with 49.3 ml (288 mmol) of Nethyldiisopropylamine, and it is stirred for 20 minutes at room temperature. This solution is then mixed with the (1 mmol) 24amine-hydrobromide described above, and it is stirred for 4 days at room temperature. The solution is concentrated by evaporation

S~

in a vacuum, the remaining oil is cooled in an ice bath and xed with trifluoroacetic acid, stirred overnight at room temperature and then precipitated with diethyl ether. The precipitate is dried in a vacuum, taken up in water, set at pH 7, a YM3 Amicon ultrafiltration membrane is used to remove low-molecular portions, and the retentate is ultimately membrane-filtered and freeze-dried.

Yield: 11.0 g (86.3% of theory) content (Karl-Fischer): 8.2% Elementary analysis (relative to anhydrous substance): Cld: C 42.87 H 5.41 N 11.96 Na 12.08 Fnd: C 42.78 H 5.66 N 12.11 Na 11.89 h) 24-mer-Gd complex of N-{N,N-bis[2-(N,N-bis(carboxymethyl))aminoethyl]-alanyl}-cascade polyamide based on N,N,N',N',N",N"-hexakis[2-(trilysylamino)-ethyl]-trimesi' acid triamide, sodium salt 8.13 g (0.5 mmol) of the complexing agent acid described in Example 5g) above is set at pH 3 in water with dilute hydrochloric acid, mixed with 2.17 g (6 mmol) of Gdz 3 stirred for 30 minutes at 8"°C,-set at pH 7 after cooling and desalinated with a YM3 AMICONR) ultrafiltration membrane. The retentate is ultimately membrane-filtered and freeze-dried.

Yield: 8.0 g (90.5% of theory) HzO content (Karl-Fischer): 00** "Gd determination (AAS): 21.0% -Elementary analysis (relative to anhydrous substance): Cld: C 35.93 H 4.38 N 10.03 Gd 23.09 Na 3.38 Fnd: C 35.71 H 4.65 N 9.88 Gd 22.84 Na 3.50 Example 6 a) 3,9-Bis(tert-butoxycarbonylmethyl)-6benzyloxycarbonylmethyl-3, 6 9 -triazaundecanedioic acid-ditert-butyl ester 5.60 g (10 mmol) of the amino compound produced under Example 5d) is dissolved in 30 ml of dimethylformamide. 1.66 g (12 mmol) of potassium carbonate as well as 2.58 g (12 mmol) of bromoacetic acid benzyl ester are then added to it at room temperature, and it is stirred overnight. It is then poured onto ice water, extracted with ethyl acetate, the organic solution is S" dried on sodium sulfate, evaporated to the dry state in a vacuum, and the title compound is obtained by chromatography on silica gel. A mixture of ethyl acetate/hexane is used as eluant.

Yield: 6.32 g (89.3% of theory) Elementary analysis: Cld: C 64.65 H 9.00 N 5.95 Fnd: C 64.62 H 9.07 N 5.90 b) 3,9-Bis(tert-butoxycarbonylmethyl)-6-carboxymethyl-3,6,9triazaundecanedioic acid-di-tert-butyl ester 7.08 g (10 mmol) of the benzyl ester produced under 6a) is dissolved in 100 ml of ethanol and mixed with 0.4 g of Pearlman's catalyst (Pd 20%, It is hydrogenated until 224 ml of hydrogen is taken up, catalyst is suctioned out, rewashed well with ethanol, and the solution is evaporated to the dry state in a vacuum. The product is obtained as foam, which crystallizes from ether/hexane.

Yield: 6.87 g (97.3% of theory) Melting point: 73 75 0

C

Elementary analysis: Cld: C 57.85 H 9.00 N 5.95 Fnd: C 57.91 H 9.11 N 6.01 c) 32-mer N-{N,N-Bis[2-(N,N-bis(carboxymethyl))-aminoethyl]glycyl}-cascade-polyamide based on the 32-mer amine described in Example 3c), sodium salt 8.35 g (1 mmol) of the 3 2-mer-benzyloxycarbonylamine described in Example 3c) is dissolved in glacial acetic acid and mixed with 33% hydrogen bromide in glacial acetic acid while being stirred. After 3 hours, the incipient precipitation is *C C completed with diethyl ether, the 32-amine-hydrobromide produced is washed with ether and dried in a vacuum.

C39.5 g (64 mmol) of the acid described in Example 6b) ale is dissolved in DMF, mixed with 9.8 g (64 mmol) of 1hydroxybenzotriazole, with 20.5 g (64 mmol) of TBTU (Peboc Limited, UK) and with 65.7 ml (384 mmol) of Nethyldiisopropylamine, and it is stirred for 20 minutes at room temperature. This solution is then mixed with the (1 mmol) 32amine-hydrobromide described above, and it is stirred for 4 days at room temperature. The solution is concentrated by evaporation in a vacuum, the remaining oil is cooled in an ice bath and mixed with trifluoroacetic acid, stirred overnight at room temperature and then precipitated with diethyl ether. The precipitate is dried in a vacuum, taken up in water, set at pH 7, a YM3 Amicon(R) ultrafiltration membrane is used to remove low-molecular portions, and the retentate is ultimately membrane-filtered and freeze-dried.

Yield: 15.7 g (78.6% of theory)

H

2 0 content (Karl-Fischer): Elementary analysis (relative to anhydrous substance): Cld: C 41.77 H 5.24 N 12.33 Na 12.14 Fnd: C 41.49-H 5-.36 N 12.49 Na 11.93 d) 32 -mer-Gd-complex of the N-{N,N-bis[2-(N,Nbis(carboxymethyl))-aminoethyl]-glycyl}-cascade polyamide based on the 32-mer amine described in Example 3c), sodium salt 10.0 g (0.5 mmol) of the complexing agent acid described in Example 6c) above is set at pH 3 in water with dilute hydrochloric acid, mixed with 2.89 g (8 mmol) of Gd 2 0 3 stirred for 30 minutes at 80 0 C, set at pH 7 after cooling and desalinated with a YM3 AMICON a ultrafiltration membrane. The retentate is ultimately membrane-filtered and freeze-dried.

Yield: 10.9 g (90.9% of theory) content (Karl-Fischer): Gd determination (AAS): 20.9% 82 Elementary analysis (relative to anhydrous substance): Cld: C 34.98 H 4.24 N 10.33 Gd 23.19 Na 3.39 Fnd: C 35.20 H 4.08 N 10.46 Gd 22.89 Na 3.60 83 Example for an In Vivo Comparison with an Extracellular Contrast ledium The suitability of the compound described in Example 1k) as a blood-pool-agent is shown in the following test.

As test animals, five male (Schering-SPF) rats that are 300- 350 g.in weight are used. Before the test, the abdomen is opened, the intestines are shifted and then the renal vessels (arterial venous) of both sides are ligated through the rear peritoneum with a surgical needle. Then, the abdominal cavity is closed again. 0.3 ml (respectively 50 mmol/L) of the following •o contrast medium soltion per animal is then administered intravenously: mixture of 1 part each of the compound of Example named compound 1 below, and the dysprosium complex of 10-(1hydroxymethyl-2,3-dihydroxypropyl)-1,4,7-tris(carboxymethyl)- S 1, 4 7 ,10-tetraazacyclododecane, produced analogously to the instructions in European Patent Application EP 448 191, named compound 2 below. Blood samples are taken with a catheter in the common carotid artery at the following times: 15, 30, 45, 60 seconds, 3, 5, 10, 15 minutes p.i. In the blood samples obtained, the concentrations of gadolinium (Gd) and dysprosium (Dy) are measured with the aid of atomic emission spectrometry (ICP-AES) in each case in a parallel manner. The portion of the injected contrast medium of compound 1 (Gd) and compound 2 (Dy, comparison substance), remaining in the blood space, can be compared in the same animals by the different marking. Since renal excretion is not possible, the decrease in the blood 84 concentration can be attributed only to a dispersion in the blood spaces and to the diffusion in the interstitial tissue.

Resut: The diffusion of compound 1 in the interstitium is considerably slowed-down in comparison to an extracellular contrast medium compound 2 (see Figure 1).

The extracellular contrast medium (compound 2) diffuses quickly into the interstitial spaces of the body, so that as early as after 3-5 minutes an equilibrium is reached (displayed by constant blood level). In contrast to this, not only are constantly higher blood concentrations measured with the cascade polymer (compound 1) (reference to smaller volume of distribution), in addition no equilibrium is reached over the entire examination period of 15 minutes (reference to diffusion into interstitial tissue proceeding only very slowly). This means that compound 1 behaves as a blood-pool contrast medium.

f Measured blood concentrations of Gd (compound 1) and Dy (compound 2) in rats (n 5) with ligated renal vessels (Key:] Zeit [min. =Time [minutes p-i.] Gd Gd(±t STD- Dy Dy(* STD' *AS

AB*ABW

400- 350- 300 250- 200- .150- 100- 0 0 5 ~Zelt [mi. p.1.1 1 Example of an MR Angiography on Rabbits The compound cited under Example 1k was studied on rabbits (CH. R. Kisslegg, 4 kg of body weight) in an MR angiography experiment (Ganzkbrper [Whole-Body] MRT System Siemens Vision, tesla, FISP 3D; TR: 400 ms; TE 15 ms; flip angle: 450; coronal).

In the precontrast picture (see photo), only one to two major vessels are visible abdominal aorta) in relatively poor contrast (signal intensity SI of these vessels against the background). After i.v. administration of 50 Amol of Gd/kg of body weight of the compound described in Example 1k, a marked increase in contrast (SI of the vessels/SI of the background) and a wide variety of minor blood vessels and capillaries

A.

and V. femoralis, A. and V. mesenterica caudalis, A. and V.

renalis, A. and V. subrenalis, etc.), which could not be detected before the administration of contrast medium, are visible.

M. a.

87 Example of Lymph Node Accumulation in Guinea Pigs The compound according to the invention that is cited under Example 1k was studied 30 minutes to 24 hours after subcutaneous administration (10 Amol of gadolinium/kg of body weight, hind paw in stimulated guinea pigs (complete Freund's adjunct; in each case 0.1 ml i.m. in the right and left upper and lower legs; 2 weeks before administration of the test substances) to determine its lymph node accumulation in three successive lymph node stations (popliteal, inguinal, iliac). In this case, the results listed below (determination of gadolinium accumulation with the aid of ICP-AES) were obtained: e*.

S..

Time of Lymph Node Removal min p.i min p.i.

4 h p.i.

24 h p.i.

I

Gadolinium Concentration in Three Successive Lymph Node Stations [mol/1] of Dose/g of Tissue] Popliteal Inguinal Iliac Ratic 921 pmol/1 387 Amol/1 215 Amol/l 10:4.2: 20.1% 8.5% 4.7% 659 pmol/1 120 Amol/l 68 Amol/1 10:1.8: 14.4% 2.6% 176 Amol/1 79 Amol/1 47 Amol/1 10:4.5: 3.9% 1.7% 62 Amol/l 13 Amol/1 28 Mmol/1 10:2.1:4 1.4% 0.3% 0.6% 2.3 2.7 ii P \WVPDOCS\CRNMSPBCI\745102.TCdoc-30/08/0 87a The reference to any prior art in this specification is not, and should not be taken as, an acknowledgement or any form of suggestion that the prior art forms part of the common general knowledge in Australia.

0*00 a a a0 0 a a 0044a

Claims

102.SPE 6/9/99 88- The claims defining the invention are as follows: 1. Compounds of the general formula I'A R OOC-R HC N CH, -CH, -N .Cl' 2 CH., V CH 2 H N CH,-CH 2 -N /2 2f12 CHR -CO OR CHR -CO OR whereby R' 1 independently of one another, stand for a hydrogen atom, a'metal ion equivalent of atomic numbers 20-29, 39, 42-44 or 57-83 or an acid protective group, R 2 stands for a hydrogen atom, a methyl or an ethyl radical, which optionally is substituted with 1-2 hydroxy or 1 carboxy group(s), R' stands for a R R 1 1 -CH -CO-N -u 6 '-zL group, R 4 stands for a straight-chain, branched, saturated or unsaturated C 1 -C 30 alkcyl chain, which optionally is interrupted by 1-10 oxygen atoms, 1 phenylene group, 1 phenylenoxy group and/or optionally is substituted by hydroxy, 1-3 carboxy, 1-phenyl group(s), P:\WPDOCS\CRN\SPEC1\745102.SPE 619199 -89- U 6 stands for a straight-chain, branched, saturated or unsaturated C 1 -C 20 alkylene group optionally containing 1-5 imino, 1-3 phenylene, 1-3 phenylenoxy, 1-3 phenylenimino, 1-5 amide, 1-2 hydrazide, 1-5 carbonyl, ethylenoxy, 1 urea, 1 thiourea, 1-2 carboxyalkylizino, 1-2 ester groups; 1-10 oxygen, V sulfur and/or 1-5 nitrogen atom(s) and/or optionally is substituted by 1-5 hydroxy, 1-2 mercapto, 1-5 oxo, thioxo, 1-3 carboxy, 1-5 carboxyalkyl, 1-5 ester and/or 1-3 amino group(s), whereby the phenylene groups that are cptionally contained can be substituted by 1-2 toS 15 carboxy, 1-2 sulfo or 1-2 hydroxy groups, stands for a -COOH, -N=C=O or -N=C=S group, and *C*O stands for an activated carboxyl group. DATED This 6th day of September, 1999 SCHERING AKTIENGESELLSCHAFT By its Patent Attorneys DAVIES COLLISON CAVE