AROMATIC 2-AMIN0-IMIDAZ0LE DERIVATIVES AS ALPHA-2A ADRENOCEPTOR AGONISTS

Field of the Invention

The present invention relates to substituted phenyl-2-amino-imidazoles. More particularly, the invention relates to such compounds which are useful in binding to and activating the 0C ₂ A adrenoreceptor which are therapeutically useful in the treatment of peripheral pain, elevated intraocular pressure and hypertension, as adjuncts in anesthesia, and as sedatives.

Background Of The Invention

A few phenyl-2-amino-imidazole derivatives are known in the pharmaceutical arts:

Jen, et al. in J. Med. Chem.. 18 £1), 90-99 (1975) made and tested the compounds below for antihypertensive and gastric antisecretory activity. These compounds were among a wider group of cyclic and acyclic amidines studied, however only the compounds shown have features in common with the present invention.

Both R groups are the same and are H, Cl, or CH3

U.S. Patent number 3,459,763 (to Gruenfeld) discloses a variety of substituted imidazole compounds, the main classes of compounds disclosed are regioisomers of the general structures: phenyl-2-amino-imidazoles and 1-N- phenyl-2-amino-imidazoles. Both classes of compounds appear to be produced by acid-induced cyclization from the same intermediates. Testing of the p _. -fluoro analog which is outside the scope of the present invention showed that it possessed modest hypotensive activity. It is not clear from the

specifϊcation whether both regioisomers are formed as a mixture and are separated by recrystallization or whether some intermediate structures favor formation of one regioisomer over the other.

The background of the division of adrenoceptors into differing categories and subtypes can be briefly described as follows. Historically, adrenoceptors were first divided in α and β types by Ahlquist in 1948. This division was based on pharmacological characteristics. Later, β-adrenoceptors were subdivided into βi and β ₂ subtypes, again based on a pharmacological definition by comparison of the relative potencies of 12 agonists. The α-adrenoceptors were also subdivided into αi and C ₂ subtypes, initially based on a presumed localization of αi receptors postsynaptically and 0C2 presynaptically. Now, however, this physiologic division is no longer used and it is generally accepted that the most useful way to subdivide the α-adrenoceptors is based on pharmacology using affinities for the antagonists yohimbine and prazosin. At αi receptors, prazosin is more potent than yohimbine, whereas at 06 ₂ receptors, yohimbine is more potent than prazosin. Bylund, et al. first suggested in 1981 that there possibly existed subtypes of the c^-adrenoceptors on the basis of radioligand binding studies. This initial work was done with various tissues taken from various species. While receptor heterogeneity among species is considered to be important, the term 'subtype' is usually reserved by pharmacologists for heterogeneity which can be demonstrated within the same species and ideally within a single tissue. Bylund and coworkers have later demonstrated that some regions of the human and rat brain contain two populations of α2-adrenoceptor sites which differ in their affinity for prazosin by 30- to 40-fold. This finding supports the division of the (X2 receptor into A and B subtypes.

Some examples of well known alpha ₂ (01 ₂ ) adrenergic receptor selective compounds known in the art are:

Clonidine Brimonidine

Clonidine is clinically useful as a hypotensive agent, and has been studied as a nasal decongestant and as an ocular hypotensive agent and as an anesthetic adjunct. The mechanism of action of clonidine has been described

as a centrally acting ot ₂ adrenergic partial agonist. Brimonidine (UK 14,308) is a newer, more lipophilic ot ₂ adrenergic agent that is also being studied as an antihypertensive, ocular hypotensive, and in other 0C2 agonist responsive conditions.

Still other examples of known 012 selective agonists that have been reported to have 0C ₂ A selectivity are:

Dexmedetomidine Oxymetazoline

Reports of studies of alpha 2A adrenoceptor activity for the compounds shown above are: Takano Y., et al., Eur. J. Pharmacol. 219 (3) pp. 465-68 (1992); Angel L, et al., J. Pharmacol. Exp. Ther. 254 (3) pp. 877-82 (1990), and Hirose, H., et al.. J. Lab. Clin. Med. 121(1) pp.11-12 (1993). The studies examined α2A receptors in relation to pain transmission and hyperglycemia.

A selective agonist as the term is used in this invention indicates a compound that binds to, and activates, a specific receptor subtype in preference to other receptors of related but different subtype(s). For example, a compound that binds to and activates the 0C ₂ A subtype receptor in preference to the ( ₂ B or CC2C subtype receptors is an 0C ₂ A selective agonist. Activation means that the receptor is induced to initiate a biochemical event that is controlled or operated by that particular receptor. Activation can further be thought of in terms of inducing the receptor to express its function.

The identification of subtypes of the alpha 2 receptors has progressed faster than the pharmacological and physiological characterization of these subtypes. However, the CX ₂ A receptor has been identified in the ciliary body of the eye , and so is postulated to have a controlling mechanism in glaucoma (see Jin, Y. et al., J. Qcύl. Pharmacol.. 10(1) pp. 359-69 (1994)). It has also

been studied in pain perception, or alternatively, pain alleviation (see Millan, M. J.. Eur. J. Pharmacol.. 215(2-3) pp. 355-6 (1992)).

Summary of the Invention

In the present invention, it has been found that compounds of the formula I, many of which are novel compounds, are selective agonists for C. ₂ A adrenoceptors.

I

The OC ₂ A selectivity of these compounds is greatly enhanced by a substituent present on the benzene or fused aromatic ring at the position occupied by group Ri in formula I. Without wishing to be held to a specific theory on this effect, it is believed that the ortho substituent induces a "twist" (variation in the angle made by the intersection of the planes of the phenyl and imidazole rings) of the imidazole ring relative to the benzene ring. Alpha2A selectivity is further enhanced when the substituents at Ri, R2, or R ₃ are capable of electron donation to the aromatic ring. In formula I, Ri is alkyl or alkenyl of 1 to 4 carbons, cyclopropyl, Cl, Br, I, -OR ₄ , -SR ₄ -NR ₄ R ₄ or -Si(R-i) ₃ wherein R ₄ represents alkyl or alkenyl of 1 to 4 carbon atoms or is hydrogen, R ₂ and R ₃ are selected from the group consisting of Ri and hydrogen; or Ri and R ₂ taken together form a fused ring with the phenyl moiety and are selected from the group consisting of -(CH ₂ )-i-, -NH(CH ₂ )2NH-, -0(CH ₂ )2θ-, -NH(CH ₂ ) ₂ 0-, -S(CH ₂ )2S-, -NH(CH ₂ )S-, and -0(CH ₂ )2S- and R ₃ is selected from the group consisting of Ri and hydrogen; or R ₂ and R ₃ taken together form a fused ring with the phenyl moiety and are selected from the group consisting of -(CH ₂ ) ₄ ~, -NH(CH ₂ ) ₂ NH-, -0(CH ₂ ) ₂ 0-, -NH(CH ₂ ) ₂ 0-, -S(CH ₂ ) ₂ S-. -NH(CH ₂ )S-, and -0(CH ₂ )2S-, -CH=CH-CH=CH-, -N=CH-CH=N- and -N=CH-N=CH-, or pharmaceutically acceptable salts thereof.

For the foregoing unsymmetrical atom strings representing R ₁ / ₂ or R ₂ R ₃ , the attachment atoms at either end can bind in either orientation to the ring. For example with -CH=N=CH=N-, the first carbon atom can bond to the benzene ring at ₂ and the ending nitrogen atom can bond at R ₃ , or the reverse is also possible (last nitrogen to R2 and first carbon to R ₃ ).

Further these compounds are useful in treating conditions which are linked to adrenergic control through the 0C2A receptor. Examples of conditions which can be treated are: peripheral pain, reduction or maintenance of intraocular pressure or the symptoms of glaucoma in at least one eye, and cardiovascular hypertension. Other therapeutic uses are for sedation, in treating hyperglycemia, and in augmentation of the effects of anesthetics.

Thus, the invention also relates to a method of selectively stimulating adrenergic OC ₂ A receptors in human or non-human mammals comprising administering to a mammal requiring 0C ₂ A adrenoceptor stimulation, a therapeutically effective amount of a compound or mixture of compounds of formula I or pharmaceutically acceptable salts thereof. The compounds of the present invention are useful to provide one or more desired therapeutic effects in a mammal.

Pharmaceutically acceptable salts of the compounds of formula I are also within the scope of the present invention. Pharmaceutically acceptable acid addition salts of the compounds of the invention are those formed from acids which form non-toxic addition salts containing pharmaceutically acceptable anions, such as the hydrochloride, hydrobromide, hydroiodide, sulfate, bisulfate, phosphate or acid phosphate, acetate, maleate, fumarate, oxalate, lactate, tartrate, citrate, gluconate, saccharate, or p-toluenesulfonate salts. A pharmaceutically acceptable salt may be any salt which retains the activity of the parent compound and does not impart any deleterious or untoward effect on the subject to which it is administered and in the context in which it is administered.

Organic amine salts may be made with amines, particularly ammonium salts such as mono-, di- and trialkyl amines or ethanol amines. Salts may also be formed with caffeine, tromethamine, and similar molecules. Where there is a nitrogen sufficiently basic as to be capable of forming acid addition salts such may be formed with any inorganic or organic acids or alkylating agent such as methyl iodide. Any of a number of simple organic acids such

as mono-, di-, or tri-acid may also be used. A pharmaceutically acceptable salt may be prepared for any compound of the invention having a functionality capable of forming such a salt, e.g., an acid salt of an amine functionality.

General Embodiments

Definitions

The compounds of the present invention all contain the (2-imidazolyl)amino structure as follows:

H this group is attached by the exocyclic nitrogen to an aromatic ring. Other adrenergic compounds are also known in the art which do not have the imidazole ring. Compounds such as the following: n ^* ^\ 15 exist as tautomers wherein the double bond

imidazolidines (from left to right). No tautomeric form of these compounds places a double bond at the 4-5 position of the imidazole ring.

The term "alkyl" as used here refers to and includes normal and branch chained alkyl groups. The term "lower alkyl", unless specifically stated otherwise, includes normal alkyl of 1 to 6 carbons, branch chained alkyl of 3 to 6 carbons. Similarly, the terms "alkenyl" and "alkynyl" include normal and branch chained groups having 2 to 6 carbons when the chains are normal, and 3 to 6 carbons when the chains are branched.

Detailed Description of the Invention

The preferred compounds of this invention, with reference to Formula I are those where Ri in the definition is not hydrogen, and are more preferred when Ri and/or R ₂ , and /or R ₃ are substituents which are capable of electron donation to the aromatic ring. Groups which are capable of electron

donation to the ring include rings fused to the aryl ring at the positions occupied by Ri and 2 or R2 and R ₃ .

An empirical measure of the electron-donating ability of single and multi- atom substituents on aromatic, particularly benzene rings, are Hammett values (taken from the sigma value in the Hammett equation :

Another measurement for individaul atoms is electronegativity. This is a measure of the electron donating or withdrawing capacity of individual atoms, however, these values are not available for multi-atoms substituents and measure the "pull" on electrons an atom makes in a covalent bond. The Hammett sigma values measure the influence of the substituent effect on reactivity of substrates and have been measured for substituents meta and para to the substrate group on benzene rings. Tables of these measurements can be found in organic and physical organic textbooks, for instance, Vogel's Handbook of Organic Chemistry. In many cases these values are measured by a comparison of the acid dissociation constants of the appropriately substituted aromatic carboxylic acid with the unsubstituted aromatic carboxylic acid. For substituents at the ortho position, owing to a neighbor effect from close proximity of the substituent to the reaction center on the ring, that σ ₀ rtho values cannot be reliably measured in every case and so are not published. However, for the purposes of defining this invention σ _me ta values give a measure of electron donation to the ring of a substituent at the ortho position, neighbor effects notwithstanding. The σ value for hydrogen is zero, as would be expected since these measurements are a comparison of a compound with substituents against the unsubstituted, i.e. "hydrogen substituted" compound. Applicants know of no better empirical measure of electron donation to an aromatic ring for defining the scope of the present invention, which includes multi-atom substituents and ring fusion. Therefore, the use of σ _me ta values as measured by means well known in the art are relied upon for a measure of the electron donation by substituents to both the phenyl and fused aromatic ring systems.

Descriptions of experimental methods for measuring σ values not available in published lists can be found in Advanced Organic Chemistry, J. March, McGraw Hill Book Company, pp. 251-253 (1977). For a review of the Hammett equation see Jaffe, Chem. Rev. 53, 191 (1953). Tables of rho (p) values for the equations can be found in Wells. Chem. Rev. 63, 171-218 (1963) and Bekkum ,Verkade and Wepster, Reel. Trav. Chim. Pays Bas 78, 821-827 (1959).

Preferred compounds of the invention are those compounds with an ortho substituent having a σ _me ta of 0.4 or less. Still more preferred are those compounds that have an electron donating group with <-> _me . _a values of about 0.15 or less (including those substituents that have negative σ values) at Ri. Even more preferred are those compounds with electron releasing groups located at R ₂ and / or R ₃ , as well as at Ri. Most preferred are those compounds which have a saturated heterocyclic ring fused to the benzene ring at the positions occupied by R2 and R ₃ in addition to an electron donating group with a σ _me ta value of about 0.15 or less (including those substituents that have negative σ values) at Ri.

Scheme I shows a general synthetic pathway to obtain the 2-amino- imidazole compounds of the present invention. RI, R2, and R3 are as defined in Formula I above. Briefly, an optionally substituted aniline

(aminobenzene) is treated with a strong base such as potassium hydride in tetrahydrofuran which then is allowed to react with phenylcyanate. The resulting N-cyano-aniline is refluxed with aminoacetaldehyde diethyl acetal in ethanol with methanesulfonic acid or another protic acid to produce the N-(2,2Diethoxyethyl)-N"-(anilino)guanidine. The diethoxy moiety is hydrolyzed in 20% HC1 and then cyclized to form the imidazole ring by treatment with an aqueous base such as NaOH to give the N-(2- imidazolyl)aminobenzene compounds with varying substituents on the benzene ring. By starting with a ring system which bears an amine group as an alternative to aminobenzenes , such as the 6-aminoquinoxaline ring, other compounds, in this instance the 6-(N-cyano)aminoquinoxaline, can be produced.

SCHEME I

The invention is further illustrated by the following non-limiting examples which are illustrative of a specific mode of practicing the invention and are not intended as limiting the scope of the appended claims.

Example 1: 2-N-(phenyl)ainino-lH---ii idazole

A.

N-cyanoaniline

Aniline (5.00g, 53.7 mmol) was dissolved in anhydrous ether (25 mL) and pentane (25 L) and cooled to 0° C. The cyanogen bromide 10.00 g, 105 mmol) was added to the cooled aniline solution and stirred overnight at room temperature. The mixture was concentrated to give a slurry product. Ether was added to the slurry and the resulting precipitate was filtered off. The filtrate was concentrated to give pure N-cyanoaniline (4.6 g, 72% yield).

B.

N-(2,2-diethoxyethyl)-N'-(phenyl)guanidine

The cyanamide (4.6 g, 39 mmol) was dissolved in anhydrous ethanol (100 mL). To this solution was added aminoacetaldehyde diethylacetal (Aldrich, 15.5 g 117 mmol) and methanesulfonic acid (Aldrich, 4.14 g, 39 mmol). The mixture was heated at reflux until starting material was no longer observed via thin layer chromatography (48 h). The crude reaction mixture was

concentrated in vacuo and purified by flash chromatography on silica with 5% methanol saturated with ammonia/chloroform to give N-(2,2- diethoxyethyl)-N'-(phenyl)guanidine (6.5 g, 66%) as a thick oil which was carried on to the next step without further purification.

2-N-(phenyl)amino-lH-imidazole

The acetal of previous step (1.3 g, 5.17 mmol) was dissolved in a solution of concentrated hydrochloric acid (Mallinkcrodt, 37%, 10 mL) and water (10 mL) at 0° C for 1 h. The solution was made basic (pH = 14) by the addition of 6N sodium hydroxide and stirred for 15 min. The resulting solution was extracted in methylene chloride, concentrated and purified by flash chromatography on silica with 5% methanol saturated with ammonia/chloroform to give 2-N-(phenyl)amino-lH-imidazole (35 mg, 4.5%).

Example 2; 5-Methyl-6-N-(2-imidazolyl)aminoquinoxaline (6)

A,

5-Methyl-6-(N-cyano)aminoquinoxaline (4)

To a slurry of potassium hydride (3.70g, 92.27 mmol) in anhydrous tetrahydrofuran (20 mL) at -78°C, 6-amino-5-methylquinoxaline (3) (6.37 g,

40.12 mmol)was added in THF (60 mL) via cannula. This mixture was stirred at 0°C for 1 h. After gas evolution had subsided, phenyl cyanate (5.25g, 44.13 mmol) was added via syringe. This mixture was stirred for an additional 4 h at 0°C. Anhydrous diethyl ether (30 mL) was added to the stirring solution and the resulting precipitate was filtered off, dissolved in H20, hot filtered, neutralized to pH 6 with HC1 (6N) and the resulting precipitate was filtered off. HC1 was also added dropwise to the mother liquor until a precipitate formed. The precipitate was filtered off, dissolved in H ₂ O, hot filtered, neutralized to pH 6 with HC1 and this precipitate was collected and combined with the other solids. The combined solids were slurried in diethyl ether for 1 h and filtered off. These solids were dried in vacuo to give pure 4 (4.98g) in 68% yield.

¹ H NMR(DMSO): 2.57 (s, 3h), 7.65 (d, J=9.3 Hz, 1H), 7.98 (d, J=3.9Hz, 1H), 8.83 (s, 1H), 8.90 (s, 1H), 9.90-10.10 (brs, 1H).

1 ³ C NMR(DMSO): 10.40, 112.32, 119.80, 120.36, 128.19, 137.10, 138.97, 141.54, 143.59, 145.18

IR(KBr): 3220, 2239, 1618, 1500 cm' ⁱ

MS: Exact mass calculated for Cι ₀ H ₈ N (M+) 184.0748, found 184.0762.

B,

N-(2,2Diethoxyethyl)-N"-[6-(5-methylquinoxalinyl)]guanidi ne (5)

To a slurry of 4 (1.43g, 7.76 mmol) in anhydrous ethanol (120 mL) in a 2-neck round-bottom flask equipped with reflux condenser and Drierite™ drying column was added aminoacetaldehyde diethylacetal (4.13g, 31.03 mmol) and methanesulfonic acid (Aldrich, 0.75g, 7.76 mmol). The mixture was heated at reflux until starting material was no longer observed by thin layer chromatography (48 h). The crude reaction mixture was concentrated in vacuo and purified by flash chromatography on silica with 10% methanol saturated with ammonia /chloroform to give 5. as a pale foam which was carried on to the next reaction without further purification.

^! H NMR(CDC1 ₃ ): 1.21 (t, J=7.0Hz, 6H), 2.55 (s, 3H), 3.43 (d, J=5.5Hz, 2H), 3.52-3.64 (m, 2H), 3.65-3.80 (m, 2H), 4.61 (t, J=5.5Hz, IH), 4.90-5.20 (brs, 3H), 7.37 (d, J=8.8Hz, IH), 7.72 (d, J=8.8Hz, IH), 8.55 (d, J=1.8Hz, IH), 8.65 (d, J=1.8Hz, IH).

MS: Exact mass calculated for C ₁₄ H ₁ 8N ₅ O ₂ (M+-C ₂ H5 ⁺ ) 288.1460, found 288.1458.

C

5-Methyl-6-N-(2-imidazolyl)aminoquinoxaline (6)

The acetal (5) was dissolved in a solution of concentrated HC1 (Mallinkrodt 37%, 15 mL) and water (15mL) at 0° C. Occasionally a colorless precipitate would form soon after the addition of HC1 and would be removed by filtration. The resulting solution was stirred for lh while warming to ambient temperature. The solution was made basic (pH=14) by addition of 6N sodium hydroxide and stirred for 15 min. before bringing the pH back to neutral by the

addition of IN HC1. The yellow precipitate was filtered off and filtered through silica using 5% ammonia saturated MeOH/CHCl ₃ to give pure product. The mother liquor was lyophilized and product remaining in the mother liquor residue was extracted into methanol and the NaCl was filtered off. This crude product was likewise filtered through silica and both pure portions were combined to give pure 6 (1.46g, 6.49 mmol) in 79% yield through two steps.

Elemental analysis: Calcd for C12H11N5: theoretical H 4.92 C 63.98 N 31.09 found H 4.83 C 63.74 N 30.95

IH NMR(DMSO): 2.62 (s, 3h), 6.70-6.90 (brs, 2H), 7.81 (d, J=9.3 Hz, IH), 8.30 (s,

IH), 8.44 (d, J=9.3 Hz, IH), 8.66 (d, J=1.8 Hz, IH), 8.80 (d, J=1.8Hz, IH), 11.0 (brs,

IH).

Example 3: 5-B-romo-β-N-(2-iι dazolyl)an^

A..

5-Bromo-6-(N-cyano)aminoquinoxaline, sodium salt

To a solution of 6-amino-5-bromoquinoxaline (6.61 g, 29.4 mmol) in anhydrous tetrahydrofuran (150 mL) at ambient temperature was added sodium hydride (Aldrich 60% suspension in oil, 1.77 g, 73.5 mmol) in portions. As gas evolution began to diminish the mixture was heated to reflux for 90 min with stirring. The reaction was cooled to ambient temperature and phenyl cyanate was added via syringe. This mixture was refluxed for an additional 2 h before concentrating to 50% of its original volume. The resulting precipitate was collected by filtration and rinsed with diethyl ether and dried in vacuo to give 5-bromo-6-(N-cyano) aminoquinoxaline, sodium salt (6.60 g), a yellow- green solid in 83% yield.

^! H NMR(DMSO): 7.57 (d, J= 9.1 Hz, IH), 7.64 (d, J= 9.1 Hz, IH), 8.36 (d, J=2.0 Hz, lH), 8.63 (d, J=2.0 Hz, lH).

MS: Exact mass calculated for C ₉ H ₅ BrN ₄ (M+) 247.9697, found 247.9700.

B.

N-(2,2-Diethoxyethyl)-N'-[6-(5-bromoquinoxalinyl)]guanidine

To a solution of 5-bromo-6-(N-cyano)aminoquinoxaline, sodium salt (0.26 g, 0.94 mmol) in anhydrous ethanol (25 mL) in a 2-neck round-bottom flask equipped with a reflux condenser and Drierite™ drying column was added aminoacetaldehyde diethylacetal (Aldrich, 0.19 g, 1.39 mmol) followed by methanesulfonic acid (Aldrich, 0.11 g, 1.13 mmol). The mixture was heated at reflux until starting material was no longer observed via thin layer chromatography (24 h). The crude reaction mixture was concentrated in vacuo, taken up in ethyl acetate, washed with saturated sodium bicarbonate, water and brine. The organic portions were filtered and re concentrated to a brown oil which was purified by flash chromatography on silica with 40% tetrahydrofuran/ethyl acetate to give N-(2,2-diethoxyethyl)-N'-[6-(5- bromoquin oxalinyl)]guanidine (0.27 g, 0.70 mmol) in 74% yield. Small amoimts of impurities were co-eluted with the product but did not interfere with subsequent reactions.

IH NMR(CDCL ₃ ): 1.23 (t, J= 7.0 Hz, 6H), 3.46 (d, J= 5.0 Hz, 2H), 3.55-3.70 (m, 2H), 3.71-3.83 (m, 2H) 4.70 (t, J= 5.0 Hz, IH), 4.90 (brs, IH), 5.25 (brs, 2H), 7.46 (d, J= 9.0 Hz, IH), 7.80 (d, J= 9.0 Hz, IH), 8.60 (d, J= 1.9 Hz, IH), 8.76 (d, J= 1.9 Hz, IH)

MS: Exact mass calculated for Ci ₃ Hι ₅ BrN5θ ₂ (M+-C ₂ H5+) 352.0409, found 352.0401.

5-Bromo-6-N-(2-imidazolyl)-aminoquinoxaline

The compound of example 6 (3.10 g, 8.14 mmol) was dissolved in a solution of concentrated hydrochloric acid (37%, 15 mL) and water (15 mL) at 0° C. The resulting solution was stirred for 2 h while warming to ambient temperature. The solution was then made basic (pH = 13) by the addition of 2N sodium hydroxide and stirred for 10 min. before bringing the pH back to neutral by the addition of IN hydrochloric acid. The yellow-green crude product was filtered off and the mother liquor was lyophilized. Crude product remaining in the mother liquor residue was extracted into methanol and the sodium chloride was removed by filtration. The crude product portions were combined and adhered to silica with methanol prior to flash

chromatography on silica with 10% methanol/chloroform to give pure 5- bromo-6-N-(2-imidazolyl)aminoquinoxaline (1.86 g, 6.41 mmol) in 79% yield

^! H NMR(DMSO): 6.65-6.70 (brs, 2H), 7.99 (d, J= 9.3 Hz, IH), 8.62 (s, IH), 8.73 (d, J=9.3 Hz, IH), 8.74 (d, J=1.9 Hz, IH), 8.89 (d, J=1.9 Hz, IH), 11.29 (brs, IH).

Elemental analysis: Calcd for CπHsBrNs: theoretical H 2.78 C 45.54 N 24.14 found H 2.82 C 45.73 N 23.90

Scheme II

Reagents: a) Br-CH ₂ -CH ₂ -Br, Nal (5 mol%), acetone; b) CH ₃ C(0)OC(0)CH ₃ , PPA; c) NaCIO; d) Et0 ₂ CCl, diisopropylethylamine; e) NaN ₃ ; f) benzyl alcohol, Δ; g) H ₂ , Pd-C; h) N,N-2,2-(diethoxy)-ethylcarbodiimide, CH ₃ SO ₃ H; i) HC1, H ₂ 0

Example 4 gives experimental details of the synthesis shown in Scheme II which provides 5-methyl-6-N-(2-imidazolyl)-amino-l,4-benzodioxane.

Example 4: 5-Methyl-6-N-(2-ύnidazolyl)-anιiιιo-l,4-benzodioxane _^ 5-Methyl-l,4-benzodioxane

A mixture of 3-methylcatechol (12.4 g, 100 mmol, Aldrich), 1,2-dibromoethane (9.5 mL, 110 mmol, Aldrich) and potassium carbonate (34.6 g, 0.25 mol) in acetone was warmed at reflux with mechanical stirring in a Morton Flask under argon overnight. Starting material was present so sodium iodide (0.75 g, 5.0 mmol) was added. The mixture was warmed for an additional 48 hrs. at which point the black slurry was poured into water and extracted with ether 3 times;

the ether layer was washed one time with 5% sodium thiosulfate, dried over M Sθ ₄ , passed through a pad 1 inch deep by 1/2 inch wide of silica (well washed with ether), concentrated and distilled (Kugelrohr, 80° C, 0.05 mm Hg) to afford 10.5 g gold-colored oil, which showed slight impurities by NMR. Flash chromatography (400 mL Siθ ₂ in a 2 inch by eight inch column, eluted with 5% ethyl acetate in hexane) afforded 9.0 g of pure product.

R 5-Methyl-6-acetyl-l,4-benzodioxane

A mixture of the benzodioxane (A) (60 mmol, 9.0 g) and acetic anhydride (60 mmol, 6.13 g, Aldrich) was treated with polyphosphoric acid (76.4 g) at 55 - 62° C in a heating bath with mechanical mixing under nitrogen for 90 minutes. The reaction was cooled and quenched by the addition of 100 mL of water. The reaction mixture was poured into water and extracted three times with ether.

* The combined ether fraction were washed two times with saturated NaHCU ₃ solution, one time with saturated NaCl solution, dried over MgSθ ₄ , and concentrated to afford an oily semi-solid. Chromatography (Siθ ₂ in a 2 inch by 6 inch column, eluted with 10% ethyl acetate in hexane) provided 4.0 g crystalline solid, 1.5 g of a pure oil and a 2 g mixture which was also an oil. IH NMR suggested that the crystalline fraction was the desired product. X-ray crystallography confirmed this assignment.

5-Methyl-6-carboxy- 1 ,4-benzodioxane

Fresh sodium hypochlorite was prepared by treating Ca(ClO)2 (80 mmol, 11.43 g) in 50 mL of water with Na2C0 ₃ (76 mmol, 8.05 g) and NaOH (24 mmol, 0.96 g) in 25 mL water. To this solution which resulted after warming with mixing and subsequent filtration was added solid acetophenone (example A, preceding) (20 mmol, 3.84 g). This mixture was warmed overnight at 60 ° C in a heating bath. The aqueous material was added to a separatory funnel and washed two times with dichloromethane. The material was then transferred to an Erlenmeyer Flask and treated dropwise with concentrated HC1 until the solution reached a pH of 3. The solid was collected by filtration and washed well with water. The NMR was consistent with the proposed product.

D.

5-Methyl-6-N-(2-imidazolyl)-amino-l,4-benzodioxane

A mixture of diisopropyl-ethylamine (25 mmol, 4.35 mL), and the acid from the preceding example (20 mmol, 3.95 g) in acetone was treated dropwise with ethyl chloroformate (21 mmol, 2.01 mL) in an ice bath over 10 minutes. After 30 minutes, at 0° C, a solution of NaN ₃ (40 mmol, 2.6 g, ACS Reagent) in water was added dropwise over 10 minutes. After 45 minutes at 0° C, the reaction mixture was poured into ice water and washed 3 times with dichloromethane. This solution was dried over Na2Sθ and concentrated to afford an oil that was warmed in toluene and benzyl alcohol at reflux for 2 hours. The reaction mixture was again concentrated to an oil to yield the 6-benzyl urethane of 5-methyl- benzodioxane. The amine was liberated by treatment of the urethane with 200 g of 10% Pd on carbon in THF and hydrogen gas.

Using the free amine (D), the named product was made analogously to Example 3 using the procedures described in Parts A, B, and C above.

H NMR(DMSO): 2.00 (s, 3H), 4.12-4.23 (dd, 4H, J= 7.14 Hz, 25.8 Hz), 6.55 (d, IH, J=11.48 Hz), 6.6 (s, 2H), 7.14 (d, IH, J=8.79 Hz), 7.45 (s, IH), 10.4 - 10.6 (s, IH).

^!3 C NMR(DMSO): 9.73, 63.52, 64.36, 110.83, 113.69, 114.56, 134.82, 137.63, 141.24, 146.48

MS: HRMS exact mass calcd. for C ₁₂ H ₁₃ N ₃ O2 (M+) 231.1007 found: 231.1008

Elemental analysis: Calcd for C ₁ 2H1 ₃ N ₃ O ₂ : theoretical H 5.67 C 62.32 N 18.17 found H 5.57 C 62.11N 18.08

Example 5: Experimental Assays: Binding Affinities and Receptor Activation

Receptor Binding Assays A.

Tissue preparation: Membrane suspensions were prepared from human cerebral cortex (HCC, for αi receptors) obtained from the UCI Organ and Tissue Bank. Briefly, tissues (lg) were homogenized in 25 mL of ice-cold 5 mM tris, pH 7.4 with a Polytron homogenizer for 30 sec at setting #7, and centrifuged for 10-12 minutes at 300 x g a 4°C. The supernatant was filtered through 2 layers of

gauze and diluted 1:2 with 50 mM Tris-HCl buffer, pH 7.4, then centrifuged at

49,000 x g for 20 minutes. The pellet fraction was washed 3 times (resuspended in Tris-HCl buffer and centrifuged for 20 minutes at 49,000 x g). The pellet was then stored at -80°C until the binding assay.

Cell preparation: Chinese hamster ovary (CHO) cells expressing the human

CC _2A and human ct ₂ C (CHO-C10 and CHO-C4 respectively) receptors and CHO cells (CHO-RNG) expressing the rat 0C ₂ B adrenoceptor were grown to near confluence in Dulbecco's modified Eagle's medium supplemented with 10% fetal bovine serum using standard cell culture methods. Cells were harvested by scraping and placed into cold buffer of the following composition: 50 mM Tris-HCl, 5 mM EDTA, pH 7.4). Cells were then homogenized with a Polytron homogenizer for 2 X 10 sec at setting #7, and centrifuged for 20 minutes at 49,000 x g. The pellet fraction was washed (resuspended in Tris-HCl, pH 8 buffer and centrifuged for 15-20 minutes at 49,000 x g) 2 times and stored at -100°C until binding assay.

Binding Studies: The radioligands [ ³ H]rauwolscine (specific activity 80 Ci/mmol) and [ ³ H]prazosin (specific activity 76 Ci/mmol) were obtained from New England Nuclear, Boston, MA. Frozen membrane pellet was resuspended in 25 mM gly cine /gly cine, pH 7.5 and incubated with radioligand under the following conditions: CHO-C10, CHO-RNG, CHO-C4- [ ³ H]rauwolscine, 22°C, 30 minutes; RKC-[ ³ H]rauwolscine, 0°C, 120 minutes; and, HCC-[ ³ H]prazosin, 22°C, 30 minutes in a final volume of 500 ul. At the end of the incubation period, the samples were filtered through glass filters (Whatman GF/B) in a 96 well cell harvester and rapidly washed four times with 4 mL of iced-cold 50 mM Tris-HCl buffer. The filters were then oven dried and transferred to scintillation vials containing 10 mL of Beckman's Ready Protein® scintillation cocktail for counting. Specific binding defined by 10 uM phentolamine for competition studies were as follows: 2.4 nM [ ³ H]brimonidine-RbICB 62%; 2.4 nM [ ³ H]rauwolscine-RbICB 75%; 2 nM [ ³ H]rauwolscine-RbKc 88%; 0.3 nM [ ³ H] rauwolscine-CHO-CIO 99%; 0.4 nM [ ³ H]rauwolsrine-CHO-RNG 99%, 0.3 nM [ ³ H]prazosin 87%; and 1 nM [ ³ H]rauwolscine-CHO-C4 90%. Protein concentrations were determined with a protein assay kit from Bio Rad. Binding isotherms, equilibrium dissociation and affinity constants were analyzed and determined by the non-linear least squares curve fitting programs EBDA (BioSoft) or AccuFit Competition/ Saturation by Beckman.

B.

Cell preparation: Chinese hamster ovary (CHO) cells expressing the human 0. _2A (CHO-C10) and the rat 0C2B(CHO-RNG) human 0C _2A adrenoceptors were grown to near confluence in Dulbecco's modified Eagle's medium supplemented with 10% fetal bovine serum using standard cell culture methods. Cells were harvested by scraping and placed into cold buffer of the following composition: 50 mM Tris-HCl, 5 mM EDTA, pH 7.4). Cells were then homogenized with a Polytron homogenizer for 2 X 10 sec at setting #7, and centrifuged for 20 minutes at 49,000 x g. The pellet fraction was washed (resuspended in Tris-HCl, pH 8 buffer and centrifuged for 15-20 minutes at 49,000 x g) 2 times and stored at -100°C until binding assay.

Binding studies: Determination of Ki

The radioligands [ ³ H]rauwolscine (specific activity 80 Ci/mmol) and [ ³ H]prazosin (specific activity 76 Ci/mmol) were obtained from New England Nuclear, Boston, MA. Frozen membrane pellet was resuspended in 25 mM glycine/ gly cine, pH 7.4 and incubated with radioligand under the following conditions: CHO-C10, CHO-RNG, CHO-C4-[ ³ H]rauwolscine, 22°C, 30 min.; and, HCC-[ H]prazosin, 22°C, 30 minutes in a final volume of 500 ul. At the end of the incubation period, the samples were filtered through glass fiber filters (Whatman GF/B) in a 96 well cell harvester and rapidly washed four times with 4 mL of iced-cold 50 mM Tris-CHl buffer. The filters were then oven dried and transferred to scintillation vials containing 5 mL of Beckman's Ready Protein® scintillation cocktail for counting. Specific binding defined by 10 uM phentolamine for competition studies were as follows: 0.3 nM[ ³ H] rauwolscine-CHO-CIO 99%; 0.4 nM [ ³ H]rauwolscine-CHO-RNG 99%, and 0.3 nM [ H] prazosin-HCC 87%. Protein concentrations were determined with a protein assay kit from Bio Rad. Binding isotherms, equilibrium dissociation and affinity constants were analyzed and determined by the non-linear least squares curve fitting programs AccuFit Competition/Saturation by Beckman.

Functional Experiments

Vas Deferens: The prostatic ends of the vas deferens (2-3 cm) were removed from albino rabbits and mounted between platinum electrodes in 9 mL organ baths containing Krebs-Hensleit solution of the following composition (mM): NaCl 119, KC1 .7, MgS0 ₄ 1.5, KH ₂ P0 ₄ 1.2. CaCl ₂ 2.5, NaHC0 ₃ 25 and glucose 11. This solution was maintained at 35° C and bubbled with 95% O ₂ and 5% CO ₂ . The tissue was equilibrated at 0.5 g tension for 30 minutes. The vas deferens

strips were then field stimulated at 0.1 Hz, 2 msec, 90 mA using a square wave stimulator (World Precision Instruments A310 Accupulser / A385 Stimulus Isolater), or a Grass S48 stimulator at 0.1 Hz, 2 msec, 70 volts. After 30 minutes of electrical stimulation, cumulative concentration-response curves in 0.25 log units were obtained with a 4 minute contact time for each concentration. Each tissue was used to evaluate only one drug. Tissue contractions produced by the field stimulation were measured isometrically using Grass FT-.03 force- displacement transducers and recorded on a Grass Model 7D physiograph. The reduction in electrically-evoked peak height by the drugs was measured and expressed as a percentage of the pre-drug peak height. The IC5 ₀ was determined as the concentration which produced a 50% reduction in peak height.

Representative compounds of the present invention were tested according to the procedures given above. Results of these tests are tabulated below. The receptor binding studies and K _\ are measures of the affinity of a compound for a particular receptor. The vas deferens assay is a measure of the degree of activation of the 0C2A affected when a compound binds to to that receptor. Rabbit vas deferens has been found to have predominantly the α _2A receptor subtype.

TABLE1

Table 1 (con't.)

Several modifications of the above described compounds, the processes disclosed for making them, and application of the disclosed processes to numerous compounds beyond the examples set forth above, may be practiced by those skilled in the art without departing from the scope and spirit of the present invention. Therefore the scope of the present invention should be interpreted solely from the following claims, as such claims are read in light of the present disclosure.