Cocaine receptor binding ligands

Abstract

Tropane derivatives having a high binding affinity and selectivity for dopamine transporters bear, on the tropane backbone either a carboxylic ester or isoxazole moiety, as well as a substituted phenyl moiety. The compounds have utility both as pharmaceutical and as imaging agents, when one or more atoms are radioactive.

Description

THE INVENTORS' PRIOR DISCLOSURES

[0002] The parent applications referenced above are directed to cocaine receptor binding ligands, which show enhanced affinity for binding to cocaine receptors, particularly dopamine transporter sites, although binding affinity is also high at serotonin transporters. These prior patents and patent applications are directed to compounds having the general formula: 1

[0003] Wherein Y=CH2R3, CO2R2, CONRR1, or 2

[0004] R1=hydrogen, C1-5 alkyl,

[0005] R2=hydrogen, C1-6 alkyl, C3-8 cycloalkyl, C1-4 alkoxy, C1-6 alkynyl, halogen or amine,

[0006] R3=OH, hydrogen, C1-6 alkyl, C3-8 cycloalkyl, C1-4 alkoxy, Cl, Br, I, CN, NH2, NHC1-6 alkyl, NC1-6 alkyl, OCOC1-6 alkyl OCOC1-3 alkylaryl,

[0007] A=S, O or N

[0008] X=H, C1-6 alkyl, C3-8 cycloalkyl, C1-4 alkoxy, C1-6 alkynyl, halogen, amino acylamido, and

[0009] Z=H, I, Br, Cl, F, CN, CF3NO2, N3, OR1, CO2NH2, CO2R1, C1-6 alkyl, NR4R5, NHCOF5, NHCO2R6

[0010] wherein R4-R6 are each C1-6 alkyl, R and R1 are independently H, C1-6 alkyl, C1-6 alkene, C1-6 alkyne, phenyl, phenyl substituted with 1-3 of C1-6 alkyl, alkene, alkyl or alkoxy, C1-6 alkoxy, phenoxy, amine, amine substituted with 1-2 of C1-6 alkyl, alkene, alkyne, alkoxy or phenyl or phenoxy or R and R1 may combine to form heterocyclic structure including pyrrolidinyl, piperidinyl and morpholino moieties, unsubstituted or substituted with 1-2 C1-6 alkyl, alkene, alkyne or alkoxy groups.

[0011] As is reflected in the parent applications and patents, due to the high binding affinity of these compounds, particularly as measured against the compound of the literature [3H]WIN 35,428 binding inhibition, these compounds have found particular use in both positron emission tomography (PET) as well as single photon emission computed tomography (SPECT). For PET use, one of the carbons of the molecule should be an [11C] labeled form, while SPECT imaging may employ a radioactive halogen label, such as the molecule on the phenyl ring of the general formula, either X or Z of the above-described general formula. In particular, the radioactive labels 123I, 125I and 131I may be used.

[0012] As this art has developed, it has proved difficult to determine what particular substitutions on the tropane backbone will yield high binding affinities while remaining pharmaceutically acceptable. The applicant has now discovered a new family of tropane derivatives, characterized by an aryl ring substituent, and either an isoxazole substituent or a carboxylic ester substituent. These particular compounds have been demonstrated to have a high dopamine transporter binding efficiency, and a high selectivity.

SUMMMARY OF THE INVENTION

[0013] Compounds of the general formula: 34

[0014] Wherein

[0015] R1 is hydrogen, C1-5 alkyl

[0016] Ra is phenyl, C1-6 alkyl, C1-6 alkyl-substituted phenyl

[0017] Rb is C1-6 alkyl, phenyl, C1-6 alkyl substituted phenyl and

[0018] Z is phenyl or naphtyl bearing 1-3 substituents selected from the group consisting of F, Cl, I, C1-6 alkyl, each substituent may be or include a radioactive label, fall within the scope of this invention.

[0019] These compounds have been demonstrated to have particular high binding affinity and selectivity for dopamine transporter sites.

[0020] The compounds of the invention can be prepared according to the methodologies established in the parent applications, incorporated herein by reference. The method of making the compound, per se, does not constitute an aspect of the invention. Particular measures for preparation of the isoxazole derivatives are shown herein. Nonetheless, other methods of making the compounds will occur to those of ordinary skill in the art, without the exercise of inventive faculty.

[0021] 3β-(4′-Chlorophenyl)-2β-(3′-phenylisoxazol-5-yl)tropane) (4,RTI-177)Hydrochloride

[0022] A soloution of n-butyl lithium in hexane (2.4M, 4.2 mL, 10.4 mmol) was added to a stirred solution of acetophenone oxime (0.703 g, 5.2 mmol) in a dry THF (10 mL) at 0° C. under nitrogen. After 1 h, a soloution of 3β-(4-chlorophenyl)tropane-2β-carboxylic acid methyl ester (1.18 g, 4 mmol) in dry THF (8 mL) was added, and the solution was allowed to warm to room temperature over 18 h. The mixture was poured into a stirred solution of concentrated sulfuric acid (2.28 g) in THF (12 mL) and water (2.8 mL) and was heated under reflux for 1 h. The cooled solution was basified using saturated aqueous potassium carbonate (10 mL) and extracted with 3×10 mL methylene chloride. The combined organic layer was dired and filtered. Removal of solvent under vacuum gave 1.46 g solid. Purification of the solid by flash column chromatography [20% (ether:triethylamine 9:1) in hexane] gave 0.75 g (50%) of pure 4 which was further purified by recrystallizing from ether:petroleum ether. 1H NMR (CDCl3) §1.74(m,3), 2.22 (m,3), 2.27 (s,3), 3.24 (m,2), 3.36 (m,2), 6.80 (s.1), 6.94 (m,2), 7.12 (m,2), 7.40 (m,3), 7.76 (m,2). IR (CHCl3)2940, 1600, 1590, 1490, 1405, 1350 cm−1.

[0023] The hydrochloride salt had mp 287° C. (dec); [α2D3 −97.5 (c 0.28, CH3OH). 1H NMR (CH3OD) α 2.35 (m,6), 2.84 (s,3), 3.73 (m,1), 4.09 (m,1), 4.21 (m,1), 6.12 (s,1), 7.14 (m,4), 7.34 (m,3), 7.57 (m,2).

[0024] Anal. Calcd for C23H24Cl2N20.0.25H2O: C,H,N.

[0025] 3α-(4′-Chlorophenyl)-2α-(5′-phenyl-1′,3′,4′-oxadiazol-2′-yl)tropane(5,RTI-188) Hydrochloride

[0026] To 0.59 g (2 mmol) of 8 in 2 mL of POCl3 was added 1.1 eq. of benzoic hydrazide, and the solution was reluxed under N2 for 2 h. The reaction miscture was cooled and poured into ice and basified to pH 7-8 using conc. NH4OH. To the aqueous layer was added 10 mL brince followed by extraction with 3×10 mL methylene chloride. The combined organic layer was dried (NaSO4), filtered, andthe solvent removed in vacuo to give 0.9 g residue. PUrification of this residue by flash column chromatography [50% (ether:triethylamine 9:1) in hexane gave 0.33 g (42%) of pure 5 which was recrystallized from ether:petroleum ether. 5

[0027] Well-established protocols for determining binding efficiency have shown selected compounds, pictured below, to have particularly high binding affinity, and selectivity, for dopamine transporter sites. 6

Comparison of Transporter Binding Potencies for
Selected 3β-(4-Substituted Phenyl)tropan-2β-carboxylic Acid Methyl Esters
7
	IC50(nM)
			DA	NE	5-HT	NE/DA	5-HT/DA
RTI No.	X	Y	[3H]WIN 35,428	[3H]Nisoxetine	[3H]Paroxetine	Ratio	Ratio
WIN 35,065-2	H	H	23	920	1962	40	85
WIN 35,428	F	H	13.9	835	692	60	50
RTI-32	CH3	H	1.71	60	240	35	140
RTI-31	Cl	H	1.12	37	44.5	33	40
RTI-55	I	H	1.26	36	4.21	29	3.3
RTI-51	Br	H	1.69	37.4	10.6	22	6
RTI-88	NH2	I	1.35	1329	120	984	89
RTI-111	Cl	Cl	0.79	17.96	3.13	67	4
RTI-112	Cl	CH3	0.81	36.2	10.5	45	13
RTI-318	8	0.51	21.1	0.80	41	1.6

[0028]

3β-(4′-Methylphenyl)-2β-(heterocyclic)tropane
9
	IC50(nM)
		DA	NE	5-HT	NE/DA	5-HT/DA
RTI No.	Het	[3H]WIN 35,428	[3H]Nisoxetine	[3H]Paroxetine	Ratio	Ratio
151	10	2.33	60	1074	26	461
171	11	0.93	254	3818	273	410
176	12	1.58	398	5110	252	3234
178	13	35.4	677	1699	19	48
194	14	4.45	253	4885	57	1098
195	15	47.48	1310	22,310	28	470
199	16	35.88	24,320	51,460	678	1434

[0029]

3β-(4′-Chlorophenyl)-2β-(heterocyclic)tropanes
17
	IC50(nM)
RTI		DA	NE	5-HT	NE/DA	5-HT/DA
No.	Het	[3H]WIN 35,428	[3H]Nisoxetine	[3H]Paroxetine	Ratio	Ratio
130	18	1.62	244.6	195	151	120
188	19	12.6	930	3304	74	262
200	20	15.3	4142	18,416	271	1203
165	21	0.59	181	572	307	970
177	22	1.28	504	2418	394	1889
189	23	19.7	496	1116	25	57
219	24	5.71	8563	10,342	1500	1811
202	25	1.37	403	1119	294	817
26	27
IC50(nM)	IC50(nM)
DA	5-HT	NE	DA	5-HT	NE
14	156	85	0.51	0.80	21
28	29
IC50(nM)	IC50(nM)
DA	5-HT	NE	DA	5-HT	NE
21	5062	1231	1.1	11.4	70.2

[0030] It should be noted that the compounds described and claimed herein are not useful solely as imaging compounds. The compounds are useful as surrogate agonists for treatment of cocaine abuse, as well as abuse of other psychostimulant drugs including amphetamines. The compounds of this invention exhibit a very slow onset of action, as well as a very long duration of action. Both of these attributes are desirable for appropriate substitute medication for psychostimulant abuse.

[0031] These compounds, because of their selectivity for the dopamine transporter are useful as antagonist drugs, or blockers of the actions of cocaine or other psychostimulants, blocking psychostimulant access but not inhibiting the functioning of the transporter. Further, treatment of neurodegenerative disorders may be affected through potentiation of neurotransmitter action. The compounds of the invention may be used to inhibit re-uptake in such situations. Finally, these compounds may find utility as analgesics. Accordingly, the compounds have utility in both their labeled and unlabeled forms.

[0032] This invention has been disclosed in terms of generic formula, as well as by specific example. Where examples are set forth, they are not intended, and should not be interpreted, as limiting. In particular, isomeric forms, as well as alternate substituents will occur to those of ordinary skill in the art without the exercise of inventive faculty, and remain within the scope of the invention, which is unlimited save by the recitation of the claims below.

Claims

1. A binding ligand having high binding affinity and selectivity for dopamine transporters, having the formula

2. The binding ligand of claim 1, wherein said compound is of one of the following formulas:

3. The binding ligand of claim 1, wherein said binding ligand bears a radioactive molecule selected from the group consisting of 11C, 123I, 125I, 131I.