WO1993005779A1

WO1993005779A1 - Carbamate analogs of thiaphysovenine, pharmaceutical compositions, and method for inhibiting cholinesterases

Info

Publication number: WO1993005779A1
Application number: PCT/US1992/007085
Authority: WO
Inventors: Arnold Brossi; Xiao-Shu He; Stanley I. Rapoport; Nigel H. Greig; Malgarzota Brzostowska
Original assignee: The United States Of America Represented By The Secretary Department Of Health And Human Services
Priority date: 1991-09-26
Filing date: 1992-08-26
Publication date: 1993-04-01
Also published as: EP0605474A1; DK0605474T3; JP3193717B2; ATE254916T1; DE69233255T2; AU667318B2; EP0605474A4; US5378723A; CA2119782C; EP1251131A2; CA2119782A1; AU2504292A; DE69233255D1; EP0605474B1; EP1251131A3; JPH07505120A; ES2206449T3

Abstract

Substituted carbamates of tricyclic compounds which have a cyclic sulfer atom, provide highly potent and selective cholinergic agonist and blocking activity are useful as pharmaceutical agents. Cholinergic disease are treated with these compounds such as glaucoma, Myasthenia Gravis, Alzheimer's disease. Methods for inhibiting esterases, acetylcholinesterase and butyrylcholinesterase are also provided.

Description

CARBAMATE ANALOGS OF THIAPHYSOVENINE, PHARMACEUTICAL COMPOSITIONS, AND METHOD FOR INHIBITING CHOLINESTERASES

This application is a Continuation-in-Part of U.S. patent application 07/765,766, filed September 26, 1991.

Technical Field

The present invention relates to inhibitors of cholinesterases, pharmaceutical compositions and method of use thereof. More particular, the invention relates to thiaphysovenine and carbamate analogs and a method of using these potent inhibitors of cholinesterases.

Background Art

Physostigmine, also called eserine, and particular derivatives of physostigmine are anti- cholinesterase inhibitors which are well known. Such well known compounds are also useful in the treatment of glaucoma, Myasthenia Gravis, Alzheimer's disease and as antidotes against poisoning with organophosphates.

It has been discovered that the natural isomer of physostigmine has blocking properties as well as agonist properties at the neuromuscular AChR. By contrast (+)-physostigmine shows only negligible inhibition of cholinesterase (ChE). See Brossi et al., FEBS Lett., Vol. 201, pages 190-192 (1986).

Even though (+)-physostigmine has only negligible ChE inhibitory activity, it is as effective as a protective pretreatment drug against multiple lethal doses of sarin, see Albuquerque et al, Fundam. Appl. Caltoxicol., Vol. 5, pages 182-203 (1985). The observed beneficial protection appears to be due to direct interactions of the carbamates with the postsynaptic nicotinic AChR. The protective effectiveness of the carbamates against organophosphates appears to be related to the direct ability of the carbamates to decrease the hyperactivation caused by accumulation of the neurotransmitter.

The above information, available due to the research in this field, is important in the evaluation of potential new pharmacological agents for treating cholinergic disorders, for example, Myasthenia Gravis and Alzheimer's disease. Potential agents can be evaluated for potency in vitro by testing the agents against electric eel acetylcholinesterase (AChE) and human plasma butyrylcholinesterase (BChE).

Of the two enzymes known to hydrolyze acetylcholine (ACh) in vivo, AChE, which is found in red blood cells, in the brain and in nerve tissues, seems to be more specific than BChE which is found in serum, pancreas and in the liver. It, however, has not previously been shown in the art that compounds which selectively inhibit one of the two enzymes more than the other would offer a medical advantage. The natural alkaloid (-)-physostigmine, its potential metabolite

(-)-(N1)-norphysostigmine, and the natural alkaloid physovenine which are used as biological standards in this art area, inhibit AChE and BChE in vitro similarly at similar concentrations.

Accordingly, there is need in the art for highly selective agents active against one of AChE and BChE while not being potent against the other so as to lead to better treatment of a particular cholinergic disorder and minimize negative side effects. Such compounds would be of great medical importance in the treatment of cholinergic disorders.

Summary of the Invention

It is an object of the present invention to provide highly potent and selective cholinergic agonist and blocking compounds.

It is a further object of the present invention to provide improvements in therapy relative to cholinergic diseases such as glaucoma, Myasthenia Gravis, Alzheimer's disease, and organophosphate poisoning.

It is a still further object of the present invention to provide compounds with selective acetylcholinesterase and butyrylcholinesterase activity.

It is an even further object of the present invention to provide (3aS-cis) isomer compounds with absolute configuration identical to that of natural physostigmine, which is a compound of the formula

wherein R¹ is H or a linear or branched chain C₁ - C₁₀ alkyl group; and R² is selected from the group consisting of wherein R³ and R⁴ are independently selected from the group consisting of H and a linear or branched chain C₁ - C₁₀ - alkyl group;

and with the proviso that when one of R¹ or R² is a H or a methyl group, the other of R¹ or R² is not H; including optical isomers. Brief Description of the Figures

Figure 1 illustrates the in vivo inhibiton rates and duration of activity for inhibiting the enzyme acetylcholinesterase (AChE) by Tacrine (THA), (-)- Physostigmine, and (-)-Thiaphysovenine.

Figure 2 compares the in vivo inhibition rates and duration of activity for thiaphysovenine and thiaphysovenol phenylcarbamates in inhibiting AChE.

Description of Preferred Embodiments

In accordance with this invention there are disclosed compounds of the formula I

wherein R¹ is H or a linear or branched chain C₁ - C₁₀ alkyl group; and R² is selected from the group consisting of a linear or branched chain -C₁ - C₁₀ alkyl group, or

wherein R³ and R⁴ are independently selected from the group consisting of H and a linear or branched chain

C₁ - C₁₀ - alkyl group;

and with the proviso that when one of R¹ or R² is a H or a methyl group, the other of R¹ or R² is not H;

including optical isomers.

Preferred are compounds wherein

R¹ is H and R² is C₄ - C₁₀ alkyl;

R¹ and R² are independently C₁ -C₁₀ alkyl; or

R¹ is H and R² is a group of the formula

wherein

R ³ and R⁴ are both H or a -CH₃ group;

R ³ is selected from the group consisting of a methyl, ethyl, or isopropyl group and R ⁴ is H; or

R ³ is H and R⁴ is an isopropyl group.and R² is a structure of the formula

wherein

R ³ is independently H or a -C₁-C₅-alkyl group and R⁴ is independently H or a -C₁-C₅-alkyl group. Even more preferred are compounds wherein R³ is selected from the group of radicals consisting of H, -CH₃, -CH₂-CH₃,

-CH₂-CH₂-CH₃, and -CH(-CH₃)₂, and R⁴ is H, -CH₃, or

-CH(-CH₃)₂.

The above compounds are thiaphysovenol carbamic acid derivatives having high potency in the inhibition of acetylcholinesterase and butyrylcholinesterase.

Some of the carbamates were more specific for AChE whereas others were more highly specific for BChE.

Other cholinesterase inhibitors are known in the prior art. Physostigmine and physovenine are optically active alkaloids with a (3aS)-absolute configuration at the chiral carbon atom C(3a). Both of these compounds are potent inhibitors of cholinesterases in vitro and in vivo, blocking the conversion of acetylcholine into choline reversibly. Physostigmine has been found to have useful medical applications in disorders which result to a malfunction of this process.

Surprisingly, the thiaphysovenol carbamates according to the present invention have shown high potency. Thus, carbamates with longer aliphatic side chains are long acting and appear to be less toxic than carbamate analogs of physovenine and physostigmine.

Accordingly, the present compounds represent a significant advancement in the prior art.

Compositions within the scope of the invention include compositions wherein the active ingredient is contained in an effective amount to achieve its intended purpose. The compounds can be administered in any pharmaceutically acceptable amount, for example, in amounts ranging from 0.001 gram to about 1 gram per kilogram of body weight. Based on the information which is presented herein, the determination of effective amounts is well within the skill of the ordinary practitioner in the art. The compounds are generally useed in pharmaceutical compositions (wt%) containing the active ingredient with a carrier or vehicle in the composition in an amount of about 0.1 to 99 wt% and preferably about 25-85 wt%.

Either fluid or solid unit dosage forms can be readily prepared for oral administration. For example, the compounds of Formula I can be. admixed with conventional ingredients such as dicalcium phosphate, magnesium aluminum silicate, magnesium stearate, calcium sulfate, starch, talc, lactose, acacia, methyl cellulose and functionally similar materials as pharmaceutical excipients or carriers. A sustained release formulation may optionally be used. In older or incoherent patients sustained release formulations may even be preferred. Capsules may be formulated by mixing the compound with a pharmaceutical diluent which is inert and inserting this mixture into a hard gelatin capsule having the appropriate size. If soft capsules are desired, a slurry of the compound with an acceptable vegetable, light petroleum or other inert oil can be encapsulated by forming into a gelatin capsule.

Suspensions, syrups and elixirs may be used for oral administration of fluid unit dosage forms. A fluid preparation including oil may be used for oil soluble forms. A vegetable oil such as corn oil, peanut oil or safflower oil, for example, together with flavoring agents, sweeteners and any preservatives produces an acceptable fluid preparation. A surfactant may be added to water to form a syrup for fluid unit dosages. Hydro-alcoholic pharmaceutical preparations may be used having an acceptable sweetener, such as sugar, saccharin or a biological sweetener and a flavoring agent in the form of an elixir.

Pharmaceutical compositions for parenteral and suppository administration can also be obtained using techniques standard in the art.

Preferred uses of the compounds according to the invention are as pharmaceutical agents suitable for oral administration. Another preferred use of the compounds is in transdermal parenteral formulations, which are particularly useful in treating cholinergic disorders such as glaucoma, Myasthenia Gravis, Alzheimer's disease, and organophosphate poisoning. Accordingly, compositions suitable for administration to these areas are particularly included within the invention. The above parenteral solutions or suspensions may be administered transdermally and delivered with a skin patch. If desired they may be given by injection in an appropriate vehicle such as sesame oil.

Accordingly, incorporation of the active compounds and a slow release matrix may be implemented for administering transdermally. The compounds may be administered transdermally in amounts of about 0.01 to 99% of the composition and preferably about 25 to 85 wt% of the active ingredient in the vehicle or carrier.

Transdermal th-erapeutic systems are self- contained dosage forms that, when applied to intact skin, deliver drug(s) at a controlled rate to the systemic circulation. Advantages of using the transdermal routing include: enhanced therapeutic efficacy, reduction in the frequency of dosing, reduction of side effects due to optimization of blood- concentration vs. time profile, increased patient compliance due to elimination of multiple dosing schedules, bypassing the hepatic "first pass" metabolism, avoiding gastro-intestinal incompatibilities and providing a predictable and extendable duration of activity. However, the main function of the skin is to act as a barrier to entering compounds. As a consequence, transdermal therapy has been preferred for a limited number of drugs that possess the desirable physiochemical properties for diffusion across the skin barrier. One effective method δf overcoming the barrier function of the skin is to include a penetration enhancer in the formulation of the transdermal therapeutic system.

The penetration enhancer is a chemical compound that, when included in a formulation, temporarily increases the permeability of the skin to a drug line allowing more of the drug to be absorbed in a shorter period of time. Several different types of penetration enhancers have been reported such as dimethylsulfoxide, n-decylmethylsulfoxide, N,N-dimethylacetamide N,N- dimethylformamide, 1-dodecylazacycloheptane-2-one (Azone), propylene glycol, ethanol, pyrrolidones such as N-methyl-2-pyrrolidone (NMP) and surfactants.

The above compounds can be present in the reservoir alone or in combination with pharmaceutical carriers. The pharmaceutical carriers acceptable for the purposes of this invention are the known art carriers that do not adversely effect the drug, the host, or the material comprising the drug delivery device. Suitable pharmaceutical carriers include sterile water, saline, dextrose, dextrose in water or saline; condensation products of castor oil and ethylene oxide combining about 30 to 35 moles of ethylene oxide per mole of castor oil, liquid acid, lower alkanols, oils such as corn oil, peanut oil, sesame oil and the like, with emulsifiers such as mono- or di-glyceride of a fatty acid; or a phosphatide, e.g., lecithin, and the like; glycols, polyalkylene glycols, aqueous media in the presence of a suspending agent, for example, sodium carboxymethyl cellulose, sodium alginate, poly(vinylpyrrolidone), and the like, alone, or with suitable dispensing agents such as lecithin, polyoxyethylene stearate, and the like. The carrier may also contain adjuvants such as preserving agents, stabilizing agents, wetting agents, emulsifying agents and the like together with penetration enhancer and the compounds of this invention.

The effective dose for mammals may vary due to such factors as age, weight, activity level or condition of the subject being treated. Typically, an effective dosage of a compound according to the present invention is about 1 to 800 milligrams when administered by either oral or rectal dose from 1 to 3 times daily. This is about .002 to about 50 milligrams per kilogram of the subject's weight administered per day. Preferably about 10 to about 300 milligrams are administered orally or rectally 1 to 3 times a day for an adult human. The required dose is considerably less when administered parenterally. Preferably about .01 to about 150 milligrams may be administered intramuscularly or transdermally, one or two times a day for an adult human. Compounds of the present invention may be administered topically in amounts of about .01 to about 99 wt% of the composition, and preferably about 25 to 85 wt% . The present compounds are also useful in a method for treating cholinergic disorders such as glaucoma, Myasthenia Gravis, Alzheimer's disease, and as an antidote against poisoning with organo phosphates. The method according to the invention comprises administering an effective amount of a compound according to the invention or an effective amount of a pharmaceutical composition according to the invention to a mammal in need of such treatment.

Surprisingly, the compounds according to the invention have shown selective cholinergic agonist and blocking activity. Of the two enzymes known to hydrolyze acetylcholine in vivo, acetylcholinesterase (AChE) which is found in red blood cells, in the brain, and in nerve tissues, seems to be more specific then butyrylcholinesterase (BChE) which is found in serum, pancreas and in the liver. It, however, was never shown that compounds which selectively inhibit one of the two enzymes more than the other, would offer a medical advantage.

The present invention relates to selective inhibition as follows: The natural alkaloid (-)- physostigmine, its potential metabolite (-)-(N1)- norphysostigmine and the natural alkaloid physovenine which were used as biological standards in the inhibited AChE and BChE in vitro similarly at similar concentrations.

Below are three sections illustrating compounds.

The first section (COMPARATIVE) shows standard compounds (A, B, and C), whose biological activity is used to compare with the compounds according to the present invention.

The second section (SCHEME 1) is a flow chart showing a general reaction which produces compounds according to the present invention and avoid separation of isomers by preserving the (3aS-cis)- absolute structure.

The third section (SCHEME 2) is a flow chart showing a general reaction scheme for a complete synthesis for producing compounds according to the present invention.

COMPARATIVE COMPOUNDS

(-)-PHYSOSTIGMINE

(-)-N(1)-NORPHYSOSTIGMINE

(-)-PHYSOVENINE

The thiaphysovenol carbamates according to the invention are produced by the following general procedure according to reaction Scheme 1, which is illustrated above.

The starting material in the reaction Scheme 1, (-)-eseroline, is obtained form natural (-)-physostigmine of the (3aS-cis)-absolute configuration by the procedure described by Yu et al. (Heterocycles, 26, page 1271 (1987)). This (-)-eseroline is then subjected to a Hofmann degradation using an alkyl halide, a dialkyl halide, a dialkyl sulfate, a benzyl halide, or the like. Preferred Hofmann reagents are methyl bromide, methyl iodide and benzyl bromide. This reaction affords a carbinolamine, which on reaction, for example, with methyl iodide yields a quaternary salt as an intermediate in the reaction shown in Scheme 1. In this intermediate, the phenolic group of the first reaction product in Scheme 1 has also been converted to an ether, e.g., a methyl ether. (In the intermediates of reaction Schemes 1 and 2, R is used to represent the ether substituent group, e.g., a methyl group.)

This second structure intermediate of reaction scheme 1 is treated with the nucleophile -SH (e.g., sodium hydrogen sulfide) in water which results in the formation of the thiehoindole ring system and provides a crucial intermediate in the synthesis of thiaphysovenines. It ((-)-thiaphysovenol methyl ether) is a crystalline solid having a high negative specific rotation. Specifically, for example, a substitution reaction with 7 N sodium mercaptide results in ring closure and leads to a 50-60% yield of crystalline thioether, which is fully characterized by spectral data. The methyl ether portion of the tricyclic structure is reacted to cleave the methyl ether group and convert the phenol into thiaphysovenol carbamates.

The same reaction also can be applied to other ethers of thiaphysovenol, such as the ethyl ether or the benzyl ether. Preferred reagents for the cleavage are

Lewis acids such as AlCl₃ or BBr₃. These Lewis acids also cleave other aromatic ethers such as ethyl ethers or benzyl ethers, which may be preferred over the methyl ether. The (-)-thiaphysovenol intermediate structure is the third structure shown in reaction

Scheme 1.

Further reaction of the thiaphysovenol in Scheme 1 with an isocyanate (R²-N=C=O) or a disub-stituted- carbamoyl halide ((R¹, R²) =N-C(=O)-X, with X representing a halide leaving group), by standard protocol (see for example, Yu et al., Heterocycles, 27, page 745 (1988), results in carbamates according to the fourth structure shown in reaction Scheme 1.

As is apparent from reaction Scheme 1, the absolute (3aS-cis) configuration present in (-)- eseroline is preserved in the final thiaphysovenol carbamates.

Accordingly, the present invention includes a process for producing compounds by using a process according to reaction Scheme 1. This invention process is described as follows:

A process for preparing a compound according to the present invention as set forth above which avoids the separation of isomers by preserving the (3aS-cis)- absolute configuration throughout the synthetic procedure, which process comprises (a) subjecting (-)-eseroline, having the (3aS- cis)-absolute configuration

to Hofmann degradation using an alkyl halide, a dialkyl halide, a dialkyl sulfate, a benzyl halide, or the like, which by an elimination reaction yields a bicyclic carbinolamine, which is reacted with the alkyl halide, dialkyl halide, dialkyl sulfate, or the like to yield the quaternary salt having the following formula

wherein R is an alkyl or benzyl group,

(b) treating the quaternary ammonium salt of step (a) with sodium hydrogen sulfide in water which results in ring closure and the formation of the thienoindole ring system to provide a compound of the following formula

(c) treating the R ether intermediate of step (b) with a Lewis acid to cleave the R ether group to yield a phenol intermediate compound named (-)- thiaphysovenol having the following formula

(d) reacting the (-)-thiaphysovenol of step (c) with a compound of the formula

wherein X is a leaving group to provide a thiaphysovenol carbamate compound according to the present invention having the absolute (3aS-cis) configuration.

A second route for producing the compounds according to the present invention is a total synthetic procedure as shown by reaction Scheme 2, set forth above.

The first structure in reaction Scheme 2 is a bicyclic nitrile compound whose phenolic group on the benzo portion has been etherified (Julian et al., J.A.C.S., 57 , page 563 (1935); and Schonenberger et al., Helv. Chim. Acta., 69, page 1486 (1986)). This first structure is reacted by published protocol (Yu et al., Heterocycles, 27 , page 1709 (1988)) to afford a racemic N(1)-noreseroline ether, e.g., a methyl ether in the second sturucture shown in reaction Scheme 2. For example, this racemic N(1)-noreseroline methyl ether can be prepared from the nitrile by reacting it with lithiumalumium hydride, diisobutyl-aluminum hydride (DIBAH), or a similar reducing agent, in tetrahydrofuran.

The second structure (racemic N(1)-noreseroline) shown in reaction Scheme 2, is then subjected to ether cleavage and reacting the phenol with isocyanates or disubstituted carbamoyl halides.

First racemic N(1)-noreseroline methyl ether of reaction Scheme 2 is subjected to Hofmann degradation and reaction with methyl iodide as in reaction Scheme 1, to yield a racemic quaternary ammonium salt. This salt corresponds to the second structure shown in reaction Scheme 1, but it is optically inactive. This salt is a mixture of the compound shown in Scheme 1 with the (3aS)-absolute structure and its enantiomer (optical isomer).

The next step follows protocol used in the series of the optically active (3aS)-isomers shown in Scheme 1: reaction of the reacemic quaternary ammonium salt with the nucleophile SH- (sodium hydrogen sulfide) in water results in the formation of racemic thiaphysovenol methyl ether, and the corresponding phenol (racemic thiaphysovenol) is obtained upon treatment with Lewis acid, preferentilly carried out in a solvent such as methylene chloride or carbon tetrachloride. Reaction of this phenol with isocyanates or disubstituted carbamoyl chlorides affords the desired racemic carbamate esters. They are purified by chromatography. The racemic esters can be resolved into optical isomers on chiral cholumns, or by chromatography on cellulose triacetate as described in the literature for racemic physovenine derivatives (see, for example, Yu et al., Helv. Chim. Acta, 74, page 761 (1991)).

The reaction step of both reaction Schemes 1 and 2 that reacts the quaternary ammonium salt with the -SH nucleophile (e.g., sodium hydrogen sulfide) to yield the thienoindoline structure is an important novel reaction step. This step is essential for preparing the carbamates covered by the present application. This procedure has also not previously been reported in the literature. The quaternary ammonium carbinolamines can be separated or reacted with an -SH nucleophile to yield a thienoindoline structure.

Although conversion of pyrrolindoles into furanoindoles to produce physovenines was executed without isolation of the intermediate quaternary carbinolamines, it was shown that they are indeed the ultimate precursors in this reaction (Dale et al., J. Pharm. Pharmacol. 22, page 889 (1970)).

As described above in discussing reaction Schemes 1 and 2, the general procedures reported in the literature for making carbamates of the physovenine series and the physostigmine series can be followed to produce the carbamates according to the present invention. For example, in reaction Schemes 1 and 2, the N-disubstituted carbamates were prepared from (-)- thiaphysovenol or its racemic equivalents by reaction with dimethyl carbamoyl chloride, as reported in the physostigmine series. Also, the NH-carbamates are obtained with (-)-thiaphysovenol or its racemic equivalents by reaction with substituted isocyanates. Accordingly, the present invention also includes a process for making the compounds of the racemic series according to the present invention using the reaction Scheme 2 as described above, followed by resolution of the racemic mixture. The procedures are as follows.

A total synthetic process for producing compounds according to present invention first produces a racemic carbamate derivative followed by separation of the compounds according to the present invention from the racemate, which process comprises:

(a) reaction of a ether substituted bicyclic nitrile compound, wherein R represents the substituent attached to the oxygen atom to form the ether group (R is methyl, for example, but it may be replaced by another alkyl group such as ethyl, which was used by Julians total synthesis (Julian et al., J.A.C.S. 57, page 563 (1935)) or benzyl, wherein the ether substituted nitrile compound has the following formula

wherein R is a removable alkyl or benzyl phenol protecting group, with lithium aluminum hydride, DIBAH, or the like in an inert solvent to produce a racemic N(1)-noreseroline methyl ether compound having the following formula

(b) the racemic N(1)-noreseroline R ether, which is produced by step (a) is then subjected to Hofmann degradation using an alkyl halide, a dialkyl halide, a dialkyl sulfate, a benzyl halide, or the like, which by an elimination reaction yields a bicyclic carbinolamine, which is reacted with the alkyl halide, dialkyl halide, dialkyl sulfate, benzyl halide or the like to yield the racemic quaternary salt having the following formula

(c) treating the quaternary ammonium salt of step (b) with sodium hydrogen sulfide in water which results in ring closure and the formation of the thienoindole ring system to provide a racemic compound of the following formula

(d) the R ether intermediate of step (c) is then

(i) treated to remove the R ether group and yield a phenolic intermediate of formula

; and ; and (ii) the phenolic intermediate compound of step (d:i) is then reacted with a compound of the formula

wherein X is a leaving group; or (iii) the phenol of step (d:i) is reacted with a substituted isocyanate

compound of the formula

in the presence of an alkaline metal catalyst in an inert solvent

to provide a racemic thiaphysovenol carbamate compound of formula

wherein R¹ and R² are defined as above ; and

(e) separating the racemic mixture to yield a thiaphysovenine compound having the absolute (3aS-cis) configuration. Compounds according to the invention are listed in Table I.

Experimental Data

M.p. (uncorrected): Fisher-Johns apparatus; H- NMR spectra (300 MHz): Varian XL-300 spectrometer, δ in ppm rel. to TMS (=0.0 ppm) as internal standard; Mass spectra for chemical ionization (CI-MS, m/z): Finnigan- 1015D mass spectrometer, and for electron impact (EI- MS) and high resolution mass measurement (HRMS): VG- Micro Mass 7070F mass spectrometer; Optical rotation ([α]_D): Perkin-Elmer-241 MC automatic polarimeter; silica gel plates were purchased from Analtech Inc., Newark, N.J.; Column chromatology (GHLF): Merck 60 (230-400 mesh); solvent systems used for TLC: (A) CHCl₃/CH₃OH/NH₄OH = 90/9/1; (B) CHCl₃/CH₃OH = 96/4.

(-)-Eseroline (the first structure in reaction Scheme 1) is prepared from (-)-physostigmine by a procedure well known in the art as discussed above.

Experiment 1

(-) -3,3a,8,8a-Tetrahydro-3a,8-dimethyl-2H-thieno-

[2,3-b]indole-5-ol methyl ether.

(-)-Eseroline (2.66 g, 12.10 mmol) was dissolved in DMSO (150 ml) under N₂-atmosphere at R.T. Powdered KOH (2.80 g, 49.9 mmol) was added. After stirring for 5 minutes at R.T. in N₂-atmosphere, CH₃I (3.59 g, 25.3 mmol) was added, and the stirring continued for 1 hour. Then CH₃I (7.3 g, 51.4 mmol) was added and the reaction mixture stirred for another hour. It was washed with Et₂O (50 ml x 2) to remove excess CH₃I and some DMSO, and the remaining solution evaporated in vacuo to remove low boiling solvents, then added with 7 N NaHS (115 ml) and refluxed for 2 hours. After cooling, the reaction mixture was extracted with Et₂O (100 ml x 3). The combined extracts were washed with 10% citric acid (50 ml x 3) and brine (50 ml x 2), dried (anh. Na₂SO₄) and evaporated in vacuo to give a yellowish oil 2.33 g which was passed through a column chromatography [silica gel, eluted by CH₂Cl₂/CH₃OH (250/1)] to give 1.82 g (63.6%) of the methyl ether as colorless crystals: m.p. 40-41°C; CI-MS: MH⁺ 236; ¹H-NMR (CDCl₃): δ 1.45 (s, 3H, C(3a)-CH₃), 2.21-2.85 (m, 4H, 2, 3-CH₂), 2.79 (s, 3H, N-CH₃), 3.78 (s, 3H, O-CH₃), 5.10 (s, 1H, C(8a)-H), 6.39 (d, 1H, J = 8.2, 7-H), 6.66 (d, 1H, J

=2.5, 4-H), 6.70 (dd, 1H, J = 2.5, 8.2, 6-H) ppm; [ α]_D -246.14° (c 1.33, EtOH).

Anal. Calc. for C₁₃H₁₇NSO (235.341): C 66.34, H 7.28, N. 5.95. S 13.62; Found: C 66.30, H 7.32, N 5.93, S 13.53. Experiment 2

Production of thiaphysovenol from the methyl ether produced in Experiment 1.

(-)-3,3a,8,8a-Tetrahydro-3a,8-dimethyl-2H-thieno

[2,3-b]indole-5-ol.

The methyl ether from Experiment 1 (1.87 g. 8 mmol) was dissolved in CH₂Cl₂ (80 ml) and then the solution of BBr₃ (7 ml) in CH₂Cl₂ (30 ml) added dropwise with stirring under N₂-atmosphere at R.T. After 2 h, MeOH was added cautiously under cooling (a water bath), and volatile gases released by opening the reaction vessel. The solvent was evaporated in vacuo. The residue was dissolved in H₂O (22 ml), made alkaline by the addition of 10% NaHCO₃, and extracted with Et₂O (100 ml x 3). The Et₂O phase was washed with brine (30 ml x 2), dried (anh. Na₂SO₄) and evaporated in vacuo to give a yellowish foam 1.57 g which was subjected to a flash chromatography (silica gel, eluted by CH₂Cl₂) to give pink crystals which was triturated in iso-octane to give 1.2 g of thiaphysovenol as off-white crystals (67.9%): m.p. 112-113°C; CI-MS: MH⁺ 222; ¹H-NMR (CDCl₃): δ 1.41 (s, 3H, C(3a)-CH₃), 2.18-2.81 (m, 4H, 2,3-CH₂), 2.75 (s, 3H, N-CH₃), 4.28 (s, 1H, exchanges with D₂O, O-H), 5.07 (s, 1H, C(8a)-H), 6.30-6.60 (m, 3H Ar-H) ppm; [α]_D -262.92° (c 0.99, EtOH). Anal. Calc. for C₁₂H₁₅NSO (221.31): C 65.12, H 6.83, N 6.33, S 14.49; Found: C 65.06, H 6.87, N 6.29, S 14.42.

Experiment 3

Production of carbamates of thiaphysovenol,

(-)-3, 3a, 8, 8a-tetrahydro-3a, 8-dimethyl-2H-thieno- [2,3-b]indole-5-ol butyl carbamate.

Thiaphysovenol (1 mmol) was dissolved in anhydrous ether (20 ml) and a small piece of sodium (ca. 1 mg) added. After stirring for 5 minutes at R.T. in N₂-atmosphere, N-butylisocyanate (1.1 mmol) was added. The reaction mixture was stirred for 20 hours at R.T. under N₂-atmosphere, then sodium was removed, the solvent was evaporated in vacuo and the residue was dissolved in EtOAc. The EtOAc phase was washed with 0.1 N NaOH, brine, dried (and. Na₂SO₄) and evaporated in vacuo to give pink foam which was subjected to a column chromatography (silica gel, CH₂Cl₂/CH₃OH (250/1)] to give the butyl carbamate. It was crystallized with EtOAc-hexane to give the butyl carbamate as colorless crystals (47.5%): m.p. 92-93°C; CI-MS: MH⁺ 321; ¹H-NMR (CDCl₃) : δ 0.95 (t, 3H, J = 7.2, chain-CH₃), 1.43 (s, 3H, C(3a)-CH₃), 1.37-1.57 (m, 4H, chain-CH₂CH₂-CH₃), 2.18-2.81 (m, 4H, 2, 3-CH₂), 2.79 (s, 3H, N(8)-CH₃), 3.25 (q, 2H, J = 6.8, chain-N- CH₂), 4.90 (br, 1H, N-H), 5.07 (s, 1H, C(8a)-H), 6.35- 6.85 (m, 3H, Ar-H) ppm; [α]_D -217.97° (c 0.76, EtOH).

Anal. Calc. for C₁₇H₂₄N₂SO₂ (320.444): C 63.71, H 7.55, N 8.74, S 10.01; Found: C 63.65, H 7.61, N 8.74, S 10.09.

Experiment 4

The production of (-)-3, 3a, 8, 8a-tetrahvdro-3a,8- dimethyl-2H-thieno[2,3-b]indole-5-ol heptylcarbamate from thiaphysovenol.

The same general procedure was followed as in Experiment 3, but N-heptylisocyanate was used as the reactant instead of N-butylisocyanate. It was triturated with hexane to give the heptyl carbamate as colorless crystals (45.1%): m.p. 84°C; CI-MS: MH⁺ 363; ¹H-NMR (CDCl₃): δ 0.89 (t, 3H, chain-CH₃), 1.43 (s, 3H, C(3a)-CH₃), 1.29-1.57 (m, 10H, chain-CH₂)₅-CH₃), 2.18- 2.82 (m, 4H, 2,3-CH₂), 2.79 (s, 3H, N-CH₃), 3.22 (q, 2H, J = 6.6, chain-N-CH₂), 4.93 (s, 1H, N-H), 5.08 (s, 1H, C(8a)-H), 6.36-6.85 (m, 3H, Ar-H) ppm; [α]_D- 216.36° (c 1.05, CHCl₃). Anal. Calc. for C₂₀H₃₀N₂SO₂ (362.524): C 66.26, H

8.34, N 7.73, S 8.84; Found: C 66.37, H 8.35, N 7.75, S 8.93.

Experiment 5

Production of (-)-3, 3a, 8, 8a-tetrahydro-3a, 8- dimethyl-2H-thieno[2,3-b]indole-5-ol phenylcarbamate from thiaphysovenol.

The same general procedure was followed as in Experiment 3, but N-phenylisocyanate was used as the reactant. The resulting carbamate was crystallized with ether to give the phenyl carbamate as colorless crystals (69.0%): m.p. 175-176°C; CI-MS: MH⁺ 341; ¹H- NMR (CDCl₃); δ 1.45 (s, 3H, C(3a)-CH₃), 2.81 (s, 3H, N- CH₃), 2.15-2.82 (m, 4H, 2, 3-CH₂), 5.09 (s, 1H, C(8a)- H), 6.38-6.93 (m, 3H, Ar-H), 7.07-7.45 (m, 5H, Ar-H) ppm; [α]_D -258.76° (c 0.84, CHCl₃).

Anal. Calc. for C₁₉H₂₀N₂SO₂ (340.434): C 67.03, H 5.92, N 8.23, S 9.42; Found: C 66.94, H 5.95, N 8.26, S 9.48.

Experiment 6

The production of (-)-3, 3a, 8,8a-tetrahydro-3a, 8- dimethyl-2H-thieno[2,3-b]indole-5-ol 2'-methylphenyl- carbamate from thiaphysovenol.

The same general procedure was followed as in Experiment 3, but N-(2-methylphenyl)isocyanate was used as the reactant. The resulting carbamate was a colorless foam (66.5%): CI-MS; MH⁺ 355; ¹Η-NMR (CDCl₃): δ 1.45 (s, 3H, C(3a)-CH₃), 2.32 (s, 3H, chain-2'-CH₃), 2.80 (s, 3H, N-CH₃), 2.18-2.83 (m, 4H, 2,3-CH₂), 5.09(s, 1H, C(8a)-H), 6.38-6.94 (m, 3H, Ar-H), 7.03- 7.25 (m, 4H, Ar-H) PPM; [α]_D -148.53° (c 0.68, CHCl₃).

Anal. Calc. for C₂₍₎H₂₂N₂SO₂ ·0.75 H₂O (367.979): C 65.28, H 6.44, N 7.61, S 8.71; Found: C 65.66, H 6.20, N 7.57, S 8.68.

Experiment 7

Production of (-)-3, 3a, 8, 8a-tetrahydro-3a, 8- dimethyl-2H-thieno[2,3-b]indole-5-ol 2'-ethylphenyl- carbamate from thiaphysovenol.

The same general procedure was followed as in Experiment 3, but N-(2-ethylphenyl)isocyanate was used as the reactant. It was a colorless foam (70.5%): CI- S: MH⁺ 369, 222 (100%); ¹H-NMR (CDCl₃); δ 1.28 (t, 3H, J = 7.57, chain-2'-C-CH₃), 1.44 (s, 3H, C(3a) -CH₃), 2.15-2.84 (m, 6H, 2,3-CH₂ and chain -2'-CH₂- CH₃), 2.80 (s, 3H, N-CH₃), 5.09 (s, 1H, C(8a)-H), 6.38- 6.93 (m, 3H, Ar-H), 7.08-7.23 (m, 4H, Ar-H) ppm; [α]_D- 237.7° (c 0.27, CHCl₃).

Anal. Calc. for C₂₁H₂₄N₂SO₂·0.25 H₂O (372.989): C 67.62, H 6.62, N 7.51, Found: C 67.59, H 6.60, N 7.52.

Experiment 8

Production of (-)-3, 3a, 8, 8a-tetrahydro-3a, 8- dimethyl-2H-thieno[2,3-b]indole-5-ol 2'-isopropyl- phenylcarbamate from thiaphysovenol.

The same general procedure was followed as in Experiment 3, but N-(2-isopropylphenyl)isocyanate was used as the reactant. It was a colorless oil (86.5%): CI-MS: MH⁺ 383, 222 (100%); ¹Η-NMR (CDCl₃): δ 1.29 (d, 6H, chain-2'-C-(CH₃)₂), 1.44 (s, 3H, C(3a)-CH₃), 2.20 (m, 1H, chain-2'-CH-Me₂), 2.54-2.83 (m, 4H, 2,3-CH₂), 2.80 (s, 3H, N-CH₃), 5.09 (s, 1H, C(8a)-H), 6.38-6.94 (m, 3H, Ar-H), 7.16-7.31 (m, 4H, Ar-H) ppm; [α]_D

-211.22° (c 0.41, CHCl₃).

Anal. Calc. for C₂₂H₂₆N₂SO₂ (382.514): C 69.07, H 6.85, N 7.33, S 8.38; Found: C 68.93, H 6.90, N 7.26, S 8.28. Experiment 9

Production of ( - )-3, 3a, 8, 8a-tetrahydro-3a, 8- dimethyl-2H-thieno[2,3-b]indole-5-ol 4'-isopropyl- phenylcarbamate from thiaphysovenol.

The same general procedure was followed as in

Experiment 3, but N-(4-isopropylphenyl)isocyanate was used as the reactant. It was triturated with etherhexane to give the 4'-isopropylphenylcarbamate as colorless crystals (41.7%): m.p. 198-200°C; EI-MS: MH⁺

221, 161 (100%), 146,128; ¹H-NMR (CDCl₃); δ 1.23 (d,

6H, chain-4'-C-(CH₃)₂), 1.44 (s, 3H, C(3a)-CH₃), 2.15-

2.93 (m, 5H, 2,3-CH₂ and chain -4'-CH-((CH₃)₂), 2.80

(s, 3H, N-CH₃), 5.09 (s, 1H, C(8a)-H), 6.38-6.92 (m,

3H, Ar-H), 7.17-7.36 (dd, 4H, Ar-H) ppm; [α]_D -221.25°

(c 0.65, CHCl₃).

Anal. Calc. for C₂₂H₂₆N₂SO₂·0.75 H₂O (396.029):

C 66.72, H 7.00, N 7.08, S 8.10; Found: C 66.71, H 6.74, N 7.12, S 8.04.

Experiment 10

Production of (-)-3, 3a, 8, 8a-tetrahydro-3a, 8- dimethyl-2H-thieno[2,3-b]indole-5-ol 2',4'-dimethyl- phenylcarbamate from thiaphysovenol.

The same general procedure was followed as in Experiment 3, but N-(2,4-dimethylphenyl)isocyanate was used as the reactant. It was an off-white foam (58.2%): m.p. 51-53°C; CI-MS: MH⁺ 369; ¹H-NMR (CDCl₃): δ 1.44 (s, 3H, C(3a)-CH₃), 2.29 (d, 6H, chain-2',4'- CH₃), 2.15-2.83 (m, 4H, 2,3-CH₂), 2.80 (s, 3H, N-CH₃), 5.09 (s, 1H, C(8a)-H), 6.38-6.93 (m, 3H, Ar-H), 7.01- 7.04, (d, 3H, Ar-H) ppm; [α]_D -193.5° (c 1.18, EtOH)

Anal. Calc. for C₂₁H₂₄N₂SO₂ (368.484): C 68.45, H 6.56, N 7.60, S 8.70; Found: C 68.45, H 6.57, N 7.57, S 8.76.

Experiment 11

Production of (-)-3, 3a, 8, 8a-tetrahvdro-3a, 8- dimethyl-2H-thieno[2,3-b]indole-5-ol N.N-dimethyl- carbamate.

Freshly prepared thiaphysovenol (350 mg, 1.58 mmol) was dissolved in 5 ml of pyridine, and 860 mg (8 mmol) of N,N-dimethylcarbamoyl chloride added. The reaction mixture was stirred at 50°C under N₂ - atmosphere overnight, and after the addition of 0.2 ml of Et₃N kept for 3 additional hours at 50°C. The solvent was evaporated in high vacuum to give an orange glass-like compound which was dissolved in EtOAc/H₂O (100 ml/50 ml). The EtoAc phase was washed with 2 N HCl, brine, dried (anh. Na₂SO₄) and evaporated in vacuo to give a colorless oil. The oil was flash chromotographed on a silica gel column [CH₂Cl₂/CH₃OH (250/1)] to give 260 mg of the N,N-dimethylcarbamate as a colorless oil (64.5%) (and 50 mg of starting material, thiaphysovenol): CI-MS: MH⁺ 293; ¹H-NMR (CDCl₃): δ 1.43 (s, 3H, C(3a)-CH₃), 2.17-2.77 (m, 4H,

2,3-CH₂), 2.79 (s, 3H, N(8)-CH₃), 3.03 (d, 6H,

N-(CH₃)₂), 5.07 (s, 1H, C(8a)-H), 6.38-6.84 (m, 3H, Ar-

H) ppm; [α]_D -208.11° (c 1.15, EtOH).

Anal. Calc. for C₁₅H₂₀N₂SO₂(292.394): C 61.61, H

6.89, N 9.58, S 10.97; Found: C 61.51, H.6.93, N 9.49,

S 10.90.

The complete synthetic procedure according to

Scheme 2 is indicated by the following experiments.

Experiment 12

Production of fumarate salt of racemic (±)-O- methyl-N(1)-noreseroline.

To a stirred solution of LiAlH₄ in THF (91 ml, 1.0 M solution) was added, dropwise, a solution of nitrile having the formula shown by the first structure of reaction Scheme 2, (10.5 g, 45.6 mmol) in THF (25 ml) at R.T. under N₂-atmosphere. The reaction mixture was first stirred at R.T. for 1 hour and then refluxed for an additional one-half hour. After cooling, the reaction mixture was diluted with THF (92 ml), treated with H₂O (3.9 ml), 15% NaOH aqueous solution (3.9 ml) and H₂O (11 ml) in ice bath. It was stirred for 15 minutes, then filtered. The filtrate was evaporated in vacuo to give brown oil, which was dissolved in 2 N HCl. The acidic aqueous solution was washed with Et₂O (50 ml x 2 ) , then, adjusted to pH 9 with K₂CO₃ and extracted with Et₂O (100 ml x 3). The combined extracts were washed with brine (40 ml x 2), dried (anh. Na₂SO₄) and concentrated to about 50 ml, a saturated EtOH solution of fumaric acid 5.28 g was added. Recrystallization of the salt from EtOH gave the fumarate of (±)-O-Methyl-N(1)-noreseroline (7.6 g, 50%): m.p. 201-203°C (d); CI-MS: MH⁺ 219; ¹H-NMR (CDCl₃); δ 1.42 (s, 3H, C(3a)-CH₃), 1.74-3.09 (m, 4H, 2,3-CH₂), 2.79 (s, 3H, N(8)-CH₃), 3.75 (s, 3H, O-CH₃), 4.42 (s, 1H, C(8a)-H), 6.25-6.68 (m, 3H, Ar-H) ppm.

Anal. Calc. for C₁₃H₁₈N₂O·C₄H₄O₄ (334.37): C 61.06, H 6.63, N 8.38; Found: C 60.99, H 6.60, N 8.35.

Experiment 13

Preparation of ( ± ) - 3 , 3a, 8, 8a-tetrahvdro-3a, 8- dimethyl-2H-thieno[2,3-b]indole-5-ol methyl ether.

The free base of the (±)-O-methyl-N(1)- noreseroline fumarate from Experiment 12 was obtained by adjusting the pH to 8. The same general procedure as for the Experiment 1 was followed, but using the free base (±)-O-Methyl-N(1)-noreseroline as the starting material instead of (-)-eseroline, and CH₃I was added after instead of before the KOH was added. The procedure results in (±)-3, 3a, 8, 8a-tetrahydro-3a, 8- dimethyl-2H-thieno[2,3-b]indole-5-ol methyl ether as a colorless oil (27%). TLC, MS, H-NMR were identical with the 3aS-cis compound yielded by Experiment 1, above; HRMS M⁺ (calc. for C₁₃H₁₇NSO): 235.1031, M⁺ (found) 235.1039.

Experiment 14

Production of (±)-3, 3a, 8, 8a-tetrahvdro-3a, 8- dimethyl-2H-thieno[2,3-b]indole-5-ol ((±)-thiaphysovenol) from the methyl ether.

The methyl ether was demethylated as described in Experiment 2, above. Workup resulted in an oil (66.2%): TLC, MS, ¹H-NMR were identical with

(-)-thiaphysovenol; HRMS M⁺ (calc. for C₁₂H₁₅NSO): 221.0874, M⁺ (found): 221.0880.

Experiment 15

Production of (±)-3, 3a, 8, 8a-Tetrahydro-3a,8- dimethyl-2H-thieno[2,3-b]indole-5-ol 2 ' ,4'-dimethyl- phenylcarbamate from racemic thiaphysovenol.

The same procedure is followed as in Experiment 10, but racemic thiaphysovenol is used as the starting material. Workup yielded a colorless oil (43.8%). TLC, MS, H-NMR were identical with the (-)-isomer described in Experiment 10.

Anal. Calc. for C₂₁H₂₄N₂SO₂ 0.75 H₂O (381.999): C 66.02, H 6.73, N 7.34, S 8.39; Found: C 66.29, H 6.52, N 7.40, S 8.32.

Experiment 16

The resolution of (±)-3, 3a, 8, 8a-tetrahvdro-3a,8- dimethyl-2H-thieno[2,3-b]indole-5-ol 2'-methylphenyl- carbamate.

The optical resolution of the racemic mixture is accomplished by chromatography on cellulose triacetate columns as described for physovenine (Yu et al., Helv. Chim. Acta, 74, page 761 (1991)). Upon resolution the resulting TLC, MS, H-NMR and optical rotation are identical with (-)-3,3a,8,8a-Tetrahydro-3a,8-dimethyl- 2H-thieno[2,3-b]indole-5-ol 2'-methylphenylcarbamate prepared in Experiment 6, above. Experiment 17

Production of (±)-3,3a,8,8a-tetrahydro-3a,8- dimethyl-2H-thieno[2,3-b]indole-5-ol 4'-isopropyl- phenylcarbamate from racemic thiaphysovenol.

The same procedure was used as in Experiment 9, but racemic thiaphysovenol was used. It was obtained as colorless crystals (from ether-hexane, 78.5%); m.p. 184-185 °C; CI-MS: MH⁺ 383, 222 (100%); TLC, ¹H-NMR were identical with the corresponding optically active compound of Experiment 9.

Anal. Calc. for C₂₂H₂₆N₂SO₂ (382.514): C 69.07, H 6.85, N 7.33, S 8.38; Found: C 69.14, H 6.91, N 7.37, S 8.42.

Experiment 18

Resolution of (±)-3,3a,8,8a-tetrahvdro-3a,8-di- methyl-2H-thieno[2,3-b]indole-5-ol 4'-isopropylphenyl- carbamate.

The optical resolution of the racemic mixture obtained in experiment 17 is accomplished as described in Experiment 16, above. Upon resolution the resulting TLC, MS, H-NMR, and optical rotation are identical with (-)-3,3a,8,8a-tetrahydro-3a,8-dimethyl-2H- thieno[2,3-b]indol-e-5-ol 4'-isopropylphenylcarbamate prepared in Experiment 9, above. Biological Experimental

In Vitro Assay of Human Anti-AChE and -BChE activity, IC₅₀

A classical enzyme inhibition assay was undertaken to quantitate the activity of the control compounds (A, B, and C) derivatives against AChE and BChE. Anti-cholinesterase activity was determined against human erythrocyte AChE and plasma BChE in 0.1 M Na₃PO₄ buffer (pH 8.0), using the spectrophotometric method of Ellman et al. (Biochem. Pharmacol. 7 , page 88, (1961)). Freshly collected blood was centrifuged (6000 x g, 10 min, 4 °C), the plasma was separated and diluted 1:125 with 0.1 Na₃PO₄ (pH 7.4). Erythrocytes were washed three times in isotonic saline, lysed by the addition of 9 volumes of Na₃PO₄ containing 0.5% Triton-X (Sigma Chemical Co., St. Louis, MO) (pH 7.4 on ice for 30 min) and diluted with 19 volumes of 0.1M Na₃PO₄ (pH 7.4), to a final dilution of 1:200. Acetyl- β-methylthiocholine (0.5 mM) (Sigma) and s-Butyrylthiocholine (0.5 mM) (Sigma) were used as specific substrates for the assay of AChE and BChE, respectively. For each cholinesterase preparation

25 μl of enzyme were added to a final incubation volume of 0.75 ml. The compounds tested were initially dissolved in Tween 80/EtOH (3:1, V:V, 75 μl total volume), diluted with 0.1 M Na₃PO₄ (pH 8.0) in half log-intervals to a final concentration range of between 1 x 10^-5 M and 3 x 10^-10 M, and were preincubated with enzyme (30 min at 21 °C) prior to addition of substrates. The Tween 80/EtOH was diluted in excess of 1:1000 and did not affect either AChE or BChE activity. Following a 25 min incubation, at 37 °C, production of a yellow thionitrobenzoate anion was measured with a spectrophotometer set to 412 nm wavelength. Nonspecific substrate hydrolysis was determined under conditions of complete enzyme inhibition (by addition of physostigmine 1 x 10^-5 M), and the associated change in absorbance was subtracted from that observed with the test compounds. Furthermore, the activity of each compound was assessed alongside that of physostigmine, as an external standard, whose activity has been previously reported (See, Yu et al., Helv. Chim. Acta 74, page 761 (1991) and Yu et al., 31, page 2297 (1988)).

The pharmacological activity of each compound was expressed as an IC₅₀, which is defined as the

concentration, in nanomoles, required to inhibit 50% of the enzyme activity of AChE and BChE, separately. For determination of IC₅₀ values, the enzyme activity of each concentration was expressed as a percent of that determined in the absence of each compound . This then was transformed into a logit format, where logit = In (% activity/ [100 - % activity]), and was plotted as a function of the log concentration of the compound. IC_5fJ values (i.e., logit = In (50/ [100 - 50] = 0) were determined only from correlation coefficients of less than -0.985, and when more than 50% inhibition was achieved from duplicate samples.

Each compound was analyzed between 4 and 8 occasions. A two-tailed student's t-test was performed to compare two means (see. Miller, Simultaneous Statistical Inferences, McGraw-Hill,

New York, NY, page 76 (1966)). When more than two means were compared, one-way analysis of variance and the Bonferroni multiple t-test were used (see, Miller, Simultaneous Statistical Inferences, McGraw-Hill,

New York, NY, page 76 (1966)). Statistical significance was taken at the level of p < 0.05.

Table II below lists the important biological data for compounds according to the invention. The IC₅₀ values and the activity levels for AChE and BChE inhibition are listed as compared to the prior art standard compounds. The compound numbers Ex. 1-9 refer to the same compounds structures that were listed as compounds 1-9 in Table I, above.

In Vivo Duration of Activity Studies

Catheters, filled with heparinized saline, were tied into the right femoral vein and artery of anesthetized male rats, which then were restrained in a plaster cast and allowed to recover from anesthesia in a temperature-controlled enclosure. Plasma samples were withdrawn to quantitate untreated levels of AChE activity. At 90 min after surgery, hexamethonium bromide (5 mg/kg, i.p.) was administered, followed by atropine methylbromide (4 mg/kg, s.c.) 10 min later. These quaternary nicotinic and muscarinic antagonists, do not enter brain and inhibit peripheral cholinergic overdrive associated with cholinesterase inhibition, which may be deleterious to the animal. Two hours after surgery, either (i) physostigmine, (ii) physostigmine derivatives, or (iii) THA was administered i.v. Plasma samples were removed at intervals between 2 min and 8 hour, immediately frozen to -70 °C and then assayed for cholinesterase inhibition. AChE inhibition was measured as described above, with necessary modifications required for quantitation from rat plasma.

All drugs were formulated in a manner consistent with i.v. administration. Specifically, drugs were dissolved in Tween 80/EtOH (3:1, V:V), approximately 100 vl, and then were diluted in excess of 1:9 (V:V) with isotonic saline. The use of Tween 80/EtOH did not affect either AChE or BChE inhibitory activity of compounds in in vitro studies (Yu et al., Helv. Chim. Acta 74, pages 761-766, (1991)). Doses were determined in prior studies involving the measurement of rectal temperature and tremor; two centrally-mediated actions of cholinesterase inhibitors and cholinergic agonists.

Figure 1 demonstrates the in vivo inhibition of the enzyme acetylcholinesterase (AChE), i.e., the activity of cholinesterase inhibitiors such as (-)- physostigmine and (-)-thiaphysovenine possess good inhibition properties (as predicted from in vitro studies), but their duration of action is short. Compared to THA (tacrine); THA inhibition is achieved only at a high dose (close to toxicity), but is of longer duration.

Figure 2 shows AChE inhibition by I.V. (-)- thiaphysovenine, (-)-Phenyl- and (-)-2',4'-di- methylphenyl-thiaphysovenine in rat plasma. The activity and persistence of 5 mg/kg doses of the tested compounds were compared for a 480 minute period. Figure 2 shows that whereas (-)-thiaphysovenine has a short duration of action (also see Figure 1), carbamates, i.e., phenylcarbamates, possess high inhibition of long duration. This is achieved at doses without side-effects or toxicity. Such results are surprising and provide potent new in vivo AChE inhibitors.

Another unexpected and surprising discovery was made for the dimethylcarbamate of (-)-thiaphysovenol ((-)-3, 3a, 8, 8a-Tetrahydro-3a, 8-dimethyl-2H- thieno[2,3b]indole-5-ol dimethylcarbamate. Surprisingly, the dialkyl carbamate possesses long- lasting inhibiting properties. The mono-substituted carbamate (thiaphysovenine) has good inhibition properties but does not persist.

The foregoing description of the specific embodiments will so fully reveal the general nature of the invention that others can, by applying current knowledge, readily modify and/ or adapt for various applications such specific embodiments without departing from the generic concept and therefore such adaptations are intended to be comprehended within the meaning and range of equivalents of the disclosed embodiments. It is to be understood that the phraseology or terminology employed herein is for the purpose of description only and not of limitation.

Claims

1 . A compound of the formula

wherein R¹ is H or a linear or branched chain C₁ - C₁₀ alkyl group; and R² is selected from the group consisting of

a linear or branched chain -C₁ - C₁₀ alkyl group, or

C₁ - C₁₀ - alkyl group;

and with the proviso that when one of R ¹ or R² is a H or a methyl group;

including optical isomers of the 3aS series.

2. A compound according to claim 1, wherein

R ¹ is H and R² is C₄ - C₁₀ alkyl;

R ¹ and R² are independently C₁ -C₁₀ alkyl; or R ¹ is H and R² is a group of the formula

wherein

R ³ and R⁴ are both H or a -CH₃ group;

R³ is selected from the group consisting of a methyl, ethyl, or isopropyl group and R⁴ is H; or

R ³ is H and R⁴ is an isopropyl group.

3. A racemic compound according to the formula

a linear or branched chain -C₁ - C₁₀ alkyl group, or

C₁ - C₁₀ - alkyl group; and with the proviso that when one of R¹ or R² is a H or a methyl group, the other of R¹ or R² is not H;

including optical isomers

4. A compound according to claim 3, wherein

R¹ is H and R² is C₄ - C₁₀ alkyl;

R ¹ and R² are independently C₁ -C₁₀ alkyl; or

R¹ is H and R² is a group of the formula

wherein

R³ and R⁴ are both H or a -CH₃ group;

R³ is H and R⁴ is an isopropyl group.

5. A process for preparing a compound of claim 1, which avoids the separation of isomers by preserving the (3aS-cis)-absolute configuration throughout the synthetic procedure, which process comprises

(a) subjecting (-)-eseroline, having the (3aS- cis)-absolute configuration

to Hofmann degradation using an alkyl halide, a dialkyl halide, a benzyl halide, or a dialkyl sulfate, which by an elimination reaction yields a bicyclic carbinolamine, which is reacted with a member from the group consisting of an alkyl halide, a dialkyl halide, a benzyl halide, or a dialkyl sulfate to yield the quaternary salt having the following formula

wherein R is an alkyl or benzyl group,

(c) the R ether intermediate of step (b) then then treated with a Lewis acid to cleave the R ether group to yield a phenol intermediate compound named (- )-thiaphysovenol having the following formula

(d) the (-)-thiaphysovenol of step (c) is then reacted with a compound of the formula

wherein X is a leaving group to provide a thiaphysovenol carbamate compound according to claim 1 having the absolute (3aS-cis) configuration.

6. A total synthetic process for producing a compound according to claim 1 by first producing a racemic carbamate derivative followed by separation of the compounds according to claim 1 from the racemate, which process comprises:

(a) reaction of a ether substituted bicyclic nitrile compound of the formula

wherein R is a removable phenol protecting group selected from the group consisting of alkyl and benzyl, with lithium aluminum hydride or DIBAH in an inert solvent to produce a racemic N(1)-noreseroline ether compound having the following formula

(b) the racemic N(1)-noreseroline R ether, which is produced by step (a) is then subjected to Hofmann degradation, which by an elimination reaction yields a bicyclic carbinolamine, which is reacted with a member from the group consisting of an alkyl iodide, a dialkyl halide, a benzyl halide, or a dialkyl sulfate to yield the racemic quaternary salt having the following formula

wherein R is alkyl or benzyl,

(d) the R ether intermediate of step (c) is then

(i) treated to remove the R ether group and yield a phenolic intermediate

of formula

; and (ii) the phenolic intermediate compound of step (d:i) is then reacted with a compound of the formula

compound of the formula

in the presence of an alkaline metal catalyst in an inert solvent

to provide a racemic thiaphysovenol carbamate compound of formula

wherein R ¹ and R² are defined as in claim 1; and

(e) separating the racemic mixture to yield a thiaphysovenol carbamate compound according to claim 1 having the absolute (3aS-cis) configuration.

7. A compound according to claim 1, wherein R³ is independently selected from the group consisting of H, -CH₃, -CH₂-CH₃, and -CH(-CH₃)₂, and R⁴ is independently selected from the group consisting of H, -CH₃, and -CH(-CH₃)₂.

8. A pharmaceutical composition comprising a pharmaceutically effective amount of a compound according to claim 1 and a carrier.

9. A method for treating cholinergic disorders comprising administration of an effective amount of a compound according to claim 1 to a mammal in need of such treatment.

10. A method according to claim 9, wherein the cholinergic disorder is selected from the group consisting of glaucoma, Myasthenia Gravis, Alzheimer's disease.

11. A method for inhibiting acetylcholinesterase activity comprising administering an effective amount of a compound according to claim 1 to a mammal in need thereof.

12. A method f or inhibiting acetylcholinesterase activity comprising transdermally administering an effective amount of a compound according to claim 1 to a mammal in need thereof.

13. A method for inhibiting butyrylcholinesterase activity comprising administering an effective amount of a compound according to claim 1 in a mammal.

14. A method for treating organophosphate poisoning in a mammal comprising administering an effective amount of a compound according to claim 1.