Cocaine receptor binding ligands

Description

PARENT APPLICATIONS

This application is a Continuation of U.S. patent application Ser. No. 08/506,541, filed on Jun. 24, 1995, now abandoned, which is a Continuation-In-Part of U.S. patent application Ser. No. 08/436,970, filed May 8, 1995, now U.S. Pat. No. 5,736,123 and U.S. patent application Ser. No. 08/164,576, filed Dec. 10, 1993, now U.S. Pat. No. 5,496,953. The latter application is in turn a Continuation-In-Part of U.S. patent application Ser. No. 07/792,648, filed Nov. 15, 1991, now abandoned, which is in turn a Continuation-In-Part of U.S. patent application Ser. No. 07/564,755, filed Aug. 9, 1990, now U.S. Pat. No. 5,128,118 and U.S. patent application Ser. No. 07/972,472, filed Mar. 23, 1993, now U.S. Pat. No. 5,413,779, based on PCT Application PCT/US91/05553, filed Aug. 9, 1991, now U.S. Pat. No. 5,413,979. The entire disclosure of U.S. Pat. Nos. 5,496,953, 5,413,779, 5,380,848 and 5,128,118 are incorporated herein by reference.

THE INVENTORS' PRIOR DISCLOSURES

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:
Wherein Y=CH₂R₃, CO₂R₂, CONRR¹, or

• R₁=hydrogen, C_1-5 alkyl,
• R₂=hydrogen, C_1-6 alkyl, C_3-8 cycloalkyl, C_1-4 alkoxy, C_1-6 alkynyl, halogen or amine,
• R₃=OH, hydrogen, C_1-6 alkyl, C_3-8 cycloalkyl, C_1-4 alkoxy, Cl, Br, I, CN, NH₂, NHC_1-6 alkyl, NC_1-6 alkyl, OCOC_1-6 alkyl OCOC_1-3 alkylaryl,
• A=S, O or N
• X=H, C_1-6 alkyl, C_3-8 cycloalkyl, C_1-4 alkoxy, C_1-6 alkynyl, halogen, amino acylamido, and
• Z=H, I, Br, Cl, F, CN, CF₃NO₂, N₃, OR₁, CO₂NH₂, CO₂R₁, C_1-6 alkyl, NR₄R₅, NHCOF₅, NHCO₂R₆,
  wherein R₄–R₆ are each C_1-6 alkyl, R and R¹ are independently H, C_1-6 alkyl, C_1-6 alkene, C_1-6 alkyne, phenyl, phenyl substituted with 1–3 of C_1-6 alkyl, alkene, alkyl or alkoxy, C_1-6 alkoxy, phenoxy, amine, amine substituted with 1–2 of C_1-6 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 C_1-6 alkyl, alkene, alkyne or alkoxy groups.

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.

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

Compounds of the general formula:

Wherein

• R₁ is hydrogen, C_1-5 alkyl
• R_a is phenyl, C_1-6 alkyl, C_1-6 alkyl-substituted phenyl
• R_b is C_1-6 alkyl, phenyl, C_1-6 alkyl substituted phenyl and
• Z is phenyl or naphtyl bearing 1–3 substituents selected from the group consisting of F, Cl, I, C_1-6 alkyl, each substituent may be or include a radioactive label, fall within the scope of this invention.

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

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.

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

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.

The hydrochloride salt had mp 287° C. (dec); [α²_D3 −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 (s, 1), 7.14 (m, 4), 7.34 (m, 3), 7.57 (m, 2).

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

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

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.

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.

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.

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.

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.