W099/24405 published May 20,1999 discloses H3 receptor ligands of the imidazole type.

US 5,869,479 issued February 9,1999 discloses compositions for the treatment of the symptoms of allergic rhinitis using a combination of at least one histamine H1 receptor antagonist and at least one histamine H3 receptor antagonist.

In view of the art's interest in compounds which affect H3 receptors, novel compounds that are antagonists of H3 receptors would be a welcome contribution to the art. This invention provides just such a contribution.

Summary of the Invention The present invention provides novel compounds of structure I. or a pharmaceutical acceptable salt or solvate thereof, wherein: (A) R'is selected from : (1) aryl ; (2) heteroaryl ; (3) heterocycloalkyl (4) alkyl ; (5)-C (O) N (R) 2 ; (6) cycloalkyl ; (7) arylalkyl ; (8) heteroarylheteroaryl (e. g., isoxazoylthienyl or pyridylthienyl) ; or (9) a group selected from: said aryl (see (A) (1) above), heteroaryl (see (A) (2) above), aryl portion of arylalkyl (see (A) (7) above), phenyl ring of formula 11 (see (A) (9) above), phenyl ring of formula III (see (A) (9) above), phenyl rings of formula IVB (see (A) (9) above), or phenyl rings of formula IVD (see (A) (9) above) are optionally substituted with 1 to 3 substituents independently selected from: (1) halogen (e. g., Br, F, or Cl, preferably F or CI) ; (2) hydroxyl (i. e.,-OH); (3) lower alkoxy (e. g., Ci to C6 alkoxy, preferably C, to C4 alkoxy, more preferably Ci to C2 alkoxy, most preferably methoxy); (4)-aryl (i. e., aryloxy) ; (5)-SR22 ; (6)-CF3 ; (7)-OCF3 ; (8)-OCHF2; (9)-NR4R5 ; (10) phenyl ; (11) N02, (12)-C02R4 ; (13)-CON (R4) 2 wherein each R4 is the same or different; (14)-S (0) 2R22 ; (15)-S (O) 2N (R2°) 2 wherein each R20 is the same or different ; (16) -N(R24) S (0) 2R22 ; (17)-CN; (18)-CH20H ; (19) -OCH2CH2OR2; (20) alkyl (e. g., C, to C4, such as methyl) ; (21) substituted phenyl wherein said phenyl has 1 to 3 substituents independently selected from alkyl, halogen,-CN,-N02,-OCHF2,- Oalkyl ; (22)-Oalkylaryl (preferably-Oalkylphenyl or-Oalkyl-substituted phenyl, e. g.,-OCH2dichlorophenyl, such as-OCH2-2, 6- dichlorophenyl or-OCH2-2-chloro-6-fluorophenyl) wherein said aryl group is optionally substituted with 1 to 3 independently selected halogens ; or (23) phenyl ; (B) X is selected from alkyl (e. g., ;(CH2)q; or branched alkyl) or-S (O) 2- ; (C) Y represents (1) a single bond (i. e., Y represents a direct bond from M1 to M2) ; or (2) Y is selected from-C (O)-,-C (S)-, -(CH2)q-, or -NR4C(O)-; with the provisos that: (a) when M1 is N, then Y is not -NR4C(O)-; and (b) when Y is a bond, then M1 and M2 are both carbon; (D) M'and M2 are independently selected from C or N; (E) Z is selected from: C1-C6 alkyl, -SO2-, -C(O)- or -C(O)NR4-; (F) R2 is selected from : (1) a six-membered heteroaryl ring having 1 or 2 heteroatoms independently selected from N or N-O (i. e., N-oxide), with the remaining ring atoms being carbon ; (2) a five-membered heteroaryl ring having 1 to 3 heteroatoms selected from nitrogen, oxygen, or sulfur with the remaining ring atoms being carbon; or (3) an alkyl group, preferably a Ci to C4 alkyl group, more preferably methyl ; (4) an aryl group, e. g., phenyl or substituted phenyl (preferably phenyl), wherein said substituted phenyl is substituted with 1 to 3 substituents independently selected from: halogen,-Oalkyl, - OCF3,-CF3,-CN,-N02,-NHC (O) CH3, or-O (CH2) qN (R'°A) 2; (5)-N (R1'A) 2 wherein each R"A is independently selected from: H, alkyl (e. g., i-propyl) or aryl (e. g., phenyl), preferably one R"A is H and the other is phenyl or alkyl (e. g., i-propyl) ; (6) a group of the formula : (7) a heteroarylheteroaryl group, e. g., said five membered heteroaryl ring ( (F) (2) above) or six-membered heteroaryl ring ( (F) (1) above) is optionally substituted with 1 to 3 substituents selected from: (a) halogen ; (b) hydroxyl ; (c) lower alkyl ; (d) lower alkoxy ; (e)-CF3 ; (f)-NR4R5 ; (g) phenyl ; (h)-N02; (i)-C (O) N (R4) 2 (wherein each R4 is the same or different); 0)-C (0) 2R4 ; or (k) phenyl substituted with 1 to 3 substituents independently selected from: halogen,-Oalkyl,-OCF3,-CF3,-CN,-N02 or -O(CH2) qN (R10A) 2; (G) R3 is is selected from: (1) aryl ; (2) heteroaryl ; (3) heterocycloalkyl (4) alkyl ; or (5) cycloalkyl ; wherein said aryl or heteroaryl R3 groups is optionally substituted with 1 to 3 substituents independently selected from: (a) halogen (e. g., Br, F, or Cl, preferably F or Cl) ; (b) hydroxyl (i. e.,-OH); (c) lower alkoxy (e. g., Ci to C6 alkoxy, preferably Ci to C4 alkoxy, more preferably C, to C2 alkoxy, most preferably methoxy); (d)-Oaryl (i. e., aryloxy) ; (e) -SR22; (f)-CF3; (g)-OCF3 ; (h)-OCHF2; (i) -NR4R5 ; (j) phenyl ; (k) -NO2, -CO2R4; (m)-CON (R4) 2 wherein each R4 is the same or different; (n)-S (O) 2R22 ; (o)-S (O) 2N (R20) 2 wherein each R20 is the same or different; (p)-N (R24)S(O)2R22; (q)-CN; (r)-CH20H; (s) -OCH2CH2OR22 ; or (t) alkyl ; (H) R4 is selected from: (1) hydrogen; (2) C,-C6 alkyl ; (3) cycloalkyl ; (4) cycloalkylalkyl (e. g., cyclopropyl-CH2-or cyclohexyl-CH2-) ; (5) heterocycloalkylalky (e. g., tetrahydrofuranyl-CH2-); (6) bridged bicyclic cycloalkyl ring, such as, for example : (7) aryl having a fused heterocycloalkyl ring bound to said aryl ring, preferably the heteroatoms in said heterocycloalkyl ring are two oxygen atoms, e. g., phenyl having a heterocycloalkyl ring bound to said phenyl ring, such as (8) aryl ; (9) arylalkyl ; (10) alkylaryl ; (11) -(CH2) dCH (R'2A) 2 wherein d is 1 to 3 (preferably 1), and each R'2A is independently selected from phenyl or substituted phenyl, said substituted phenyl being substituted with 1 to 3 substituents independently selected from: halogen,-Oalkyl,-OCF3,-CF3,-CN, or -NO2, e. g., (12) heterocycloalkylheteroaryl, e. g., (13) -(C1 to C6) alkylene-O-R22 (e. g.,-C3H60CH3) ; wherein the aryl R4 group, the aryl portion of the arylalkyl R4 group, or the aryl portion of the alkylaryl R4 group is optionally substituted with 1 to 3 substituents independently selected from: (a) halogen ; (b) hydroxyl ; (c) lower alkyl ; (d) lower alkoxy ; (e)-CF3 ; -N(R20)(R24), (g) phenyl ; (h)-N02; (i)-C (O) N (R20) 2 (wherein each R20 is the same or different), (j) -C (O) R22; (i) -(CH2)k-cycloalkyl ; t)-(CH2) q-aryl ; or (k)-(CH2)m-OR22; (I) each R4B is independently selected from: H, heteroaryl (e. g., pyridyl), alkyl, alkenyl (e. g., allyl), a group of the formula arylalkyl (e. g., benzyl), or arylalkyl wherein the aryl moiety is substitued with 1-3 substituents independently selected from: halogen (e. g. -CH2-p-Clphenyl) ; preferably one R4B is H; (J) R5 is selected from: hydrogen, Ci-Ce alkyl,-C (O) R20 (e. g.,-C (O) alkyl, such as-C (O) CH3),-C (O) 2R2°,-C (O) N (R20) 2 (wherein each R20 is the same or different); (K) each R'°A is independently selected from H or C, to C6 alkyl (e. g., methyl), or each R10A, taken together with the nitrogen atom to which they are bound, forms a 4 to 7 membered heterocycloalkyl ring; (L) R12 iS (1) selected from alkyl, hydroxyl, alkoxy, or fluoro, provided that when R12 is hydroxy or fluoro then R12 is not bound to a carbon adjacent to a nitrogen ; or (2) R12 forms an alkyl bridge from one ring carbon to another ring carbon, an example of such a bridged ring system is: (M) R'3 is (1) selected from alkyl, hydroxyl, alkoxy, or fluoro, provided that when R13 is hydroxy or fluoro then R'3 is not bound to a carbon adjacent to a nitrogen; or (2) R'3 forms an alkyl bridge from one ring carbon to another ring carbon, an example of such a bridged ring system is: (N) R20 is selected from hydrogen, alkyl, or aryl, wherein said aryl group is optionally substituted with from 1 to 3 groups independently selected from: halogen, -CF3,-OCF3, hydroxyl, or methoxy ; or when two R20 groups are present, said two R20 groups taken together with the nitrogen to which they are bound form a five or six membered heterocyclic ring; (O) R22 is selected from: heterocycloalkyl (e. g., morpholinyl or pyrrolidinyl), alkyl or aryl, wherein said aryl group is optionally substituted with 1 to 3 groups independently selected from halogen, -CF3, -COF3, hydroxyl, or methoxy; (P) R24 is selected from: hydrogen, alkyl,-S02R22, or aryl, wherein said aryl group is optionally substituted with 1 to 3 groups independently selected from halogen,-CF3,-OCF3, hydroxyl, or methoxy; (Q) a is 0 to 2 ; (R) b is 0 to 2 ; (S) k is 1 to 5; (T) m is 2 to 5 ; (U) n is 1,2 or 3 with the proviso that when M'is N, then n is not 1; (V) p is 1,2 or 3 with the proviso that when M2 is N, then p is not 1; (W) q is 1 to 5 ; and (X) r is 1, 2, or 3 with the proviso that when r is 2 or 3, then M2 is C and p is 1.

This invention also provides a pharmaceutical composition comprising an effective amount of compound of Formula I, and a pharmaceutical acceptable carrier.

This invention further provides a method of treating : allergy, allergy-induced airway (e. g., upper airway) responses, congestion (e. g., nasal congestion), hypotension, cardiovascular disease, hypotension, diseases of the G ! tract, hyper and hypo motility and acidic secretion of the gastro-intestinal tract, obesity, sleeping disorders (e. g., hypersomnia, somnolence, and narcolepsy), disturbances of the central nervous system, attention deficit hyperactivity disorder ADHD), hypo and hyperactivity of the central nervous system (for example, agitation and depression), and/or other CNS disorders (such as Alzheimer's, schizophrenia, and migraine) comprising administering to a patient in need of such treatment (e. g., a mammal, such as a human being) an effective amount of a compound of Formula I.

This invention further provides a method of treating: allergy comprising administering to a patient in need of such treatment (e. g., a mammal, such as a human being) an effective amount of a compound of Formula I.

This invention further provides a method of treating: allergy-induced airway (e. g., upper airway) responses comprising administering to a patient in need of such treatment (e. g., a mammal, such as a human being) an effective amount of a compound of Formula I.

This invention further provides a method of treating: congestion (e. g., nasal congestion) comprising administering to a patient in need of such treatment (e. g., a mammal, such as a human being) an effective amount of a compound of Formula I.

This invention further provides a pharmaceutical composition comprising an effective amount of a compound of Formula I, and an effective amount of a H, receptor antagonist in combination with a pharmaceutical acceptable carrier.

This invention further provides a method of treating: allergy, allergy-induced airway (e. g., upper airway) responses, and congestion (e. g., nasal congestion) comprising administering to a patient in need of such treatment (e. g., a mammal, such as a human being) an effective amount of a compound of Formula I in combination with an effective amount of an H, receptor antagonist.

This invention further provides a method of treating: allergy comprising administering to a patient in need of such treatment (e. g., a mammal, such as a human being) an effective amount of a compound of Formula I in combination with an effective amount of an Hr receptor antagonist.

This invention further provides a method of treating: allergy-induced airway (e. g., upper airway) responses comprising administering to a patient in need of such treatment (e. g., a mammal, such as a human being) an effective amount of a compound of Formula I in combination with an effective amount of an H, receptor antagonist.

This invention further provides a method of treating: congestion (e. g., nasal congestion) comprising administering to a patient in need of such treatment (e. g., a mammal, such as a human being) an effective amount of a compound of Formula I in combination with an effective amount of an H, receptor antagonist.

DETAILED DESCRIPTION OF THE INVENTION As used herein, the following terms have the following meanings, unless indicated otherwise: alkyl- (including the alkyl portions of alkylamino, alkylaryl, arylalkyl, alkoxy and dialkylamino)-represents straight and branched carbon chains and contains from one to twenty carbon atoms, preferably one to six carbon atoms ; alkylaryl-represents an alkyl group, as defined above, bound to an aryl group, as defined below, wherein said aryl group is bound to the compound; aryl (including the aryl portion of alkylaryl and arylalkyl)-represents a carbocyclic group containing from 6 to 15 carbon atoms and having at least one aromatic ring (e. g., aryl is a phenyl or naphthyl ring), with all available substitutable carbon atoms of the carbocyclic group being intended as possible points of attachment, said carbocyclic group being optionally substituted with one or more (e. g., 1 to 3) substituents independently selected from: halo, alkyl, hydroxy, alkoxy, phenoxy, CF3, amino, alkylamino, dialkylamino,-COOR20 or-NO2 ; arylalkyl-represents an aryl group, as defined above, bound to an alkyl group, as defined above, wherein said alkyl group is bound to the compound; bridged bicyclic cycloalkyl rings-represents a cycloalkyl ring, as defined below, having an alkyl (as defined above) bridge from one ring carbon to another ring carbon thereby forming a bicyclic cycloalkyl ring, e. g., cycloalkyl-represents saturated carbocyclic rings of from 3 to 20 carbon atoms, preferably 3 to 7 carbon atoms; halo (halogen)-represents fluoro, chloro, bromo and iodo; and heteroaryl-represents cyclic groups, having at least one heteroatom selected from O, S or N, said heteroatom interrupting a carbocyclic ring structure and having a sufficient number of delocalized pi electrons to provide aromatic character, with the aromatic heterocyclic groups preferably containing from 2 to 14 carbon atoms; examples include but are not limited to isothiazolyl, isoxazolyl, oxazolyl, furazanyl, triazolyl,thiazolyi, thienyl, furanyl (furyl), pyrrolyl, pyrazolyl, pyranyl, pyrimidinyl, pyrazinyl, pyridazinyl, pyridyl (e. g., 2-, 3-, or 4-pyridyl), pyridyl N-oxide (e. g., 2-, 3-, or 4-pyridyl N-oxide), triazinyl, pteridinyl, indolyl (benzopyrrolyl), pyridopyrazinyl, isoqinolinyl, quinolinyl, naphthyridinyl, wherein said pyridyl N-oxide can be represented as: heterocycioalkyl-represents a saturated, carbocylic ring containing from 3 to 15 carbon atoms, preferably from 4 to 6 carbon atoms, which carbocyclic ring is interrupted by-1 to 3 hetero groups selected from-0-,-S-,-SO-,-S02 or-NR40- wherein R40 represents H, Cl to C6 alkyl, arylalkyl,-C (O) R,-C (O) OR, or C (O) N (R2°) 2 (wherein each R20 is independently selected) ; examples include but are not limited to 2-or 3-tetrahydrofuranyl, 2-or 3-tetrahydrothienyl, 2-, 3-or 4- piperidinyl, 2-or 3-pyrrolidinyl, 2-or 3-piperizinyl, 2-or 4-dioxanyl, 1,3-dioxolanyl, 1,3,5-trithianyl, pentamethylene sulfide, perhydroisoquinolinyl, decahydroquinolinyl, trimethylene oxide, azetidinyl, 1-azacycloheptanyl, 1,3-dithianyl, 1,3,5-trioxanyl, morpholinyl, thiomorpholinyl, 1,4-thioxanyl, and 1, 3,5-hexahydrotriazinyl, thiazolidinyl, tetrahydropyranyl ; heterocycloalkylheteroaryl-represents a heteroaryl group as defined above bound to a heterocycloalkyl as defined above; lower alkyl-represents an alkyl group, as defined above, that comprises 1 to 6 carbon atoms, preferably 1-4 carbon atoms; lower alkoxy-represents an alkoxy group whose alkyl moiety comprises 1 to 6 carbon atoms, preferably 1-4 carbon atoms; Ac-represents acetyl (i. e., CH3C (O)-) ; t-BOC-represents t-butyloxycarbonyl ; Ci/mmol-represents curie/mmol (a measure of specific activity); DCC-represents dicyclohexylcarbodiimide ; DEC-represents 2-diethylaminoethyl chloride hydrochloride ; DIC-represenets diisopropylcarbodiimide ; DMF-represents dimethylformamide ; DMSO-represents dimethylsulfoxide ; EtOAc-represents ethyl acetate; EtOH-represents ethanol ; FMOC-represents 9-fluorenylmethoxycarbonyl ; HOBT-represents 1-hydroxybenzotriazole ; Ki-represents inhibition constant for substrate/receptor complex ; LiOH-represents lithium hydroxide ; Me-represents methyl ; MeOH-represents methanol ; nM-represents nanomolar ; PyBOP-represents benzotriazole-1-yl-oxy-trispyrrol idino-phosphonium hexaflurophosphate ; TFA-represents trifluoroacetic acid; THF-represents tetrahydrofuran ; Also, as used herein,"upper airway"usually means the upper respiratory system--i. e., the nose, throat, and associated structures.

Also, as used herein,"effective amount"generally means a therapeutically effective amount.

Lines drawn into the rings indicate that the indicated bond may be attached to any of the substitutable ring carbon atoms.

Certain compounds of the invention may exist in different isomeric (e. g., enantiomers, diastereoisomers and geometric) forms. The invention contemplates all such isomers both in pure form and in admixture, including racemic mixtures. Enol forms are also included.

The compounds of this invention are ligands for the histamine H3 receptor.

The compounds of this invention can also be described as antagonists of the H3 receptor, or as H3 antagonists.

The compounds of the invention are basic and form pharmaceutical acceptable salts with organic and inorganic acids. Examples of suitable acids for such salt formation are hydrochloric, sulfuric, phosphoric, acetic, citric, oxalic, malonic, salicylic, malic, fumaric, succinic, ascorbic, maleic, methanesulfonic and other mineral and carboxylic acids well known to those skilled in the art. The salts are prepared by contacting the free base form with a sufficient amount of the desired acid to produce a salt in the conventional manner. The free base forms may be regenerated by treating the salt with a suitable dilute aqueous base solution such as dilute aqueous sodium hydroxide, potassium carbonate, ammonia and sodium bicarbonate. The free base forms differ from their corresponding salt forms somewhat in certain physical properties, such as solubility in polar solvents, but the salts are otherwise equivalent to their corresponding free base forms for purposes of this invention.

The compounds of Formula I can exist in unsolvated as well as solvate forms, including hydrated forms, e. g., hemi-hydrate. In general, the solvate forms, with pharmaceutical acceptable solvents such as water, ethanol and the like are equivalent to the unsolvated forms for purposes of the invention.

The compounds of this invention can be combined with an H, receptor antagonist (i. e., the compounds of this invention can be combined with an H, receptor antagonist in a pharmaceutical composition, or the compounds of this invention can be administered with H, receptor antagonist).

Numerous chemical substances are known to have histamine H, receptor antagonist activity and can therefore be used in the methods of this invention. Many H, receptor antagonist useful in the methods of this invention can be classified as ethanolamines, ethylenediamines, alkylamines, phenothiazines or piperidines.

Representative H, receptor antagonists include, without limitation : astemizole, azatadine, azelastine, acrivastine, brompheniramine, cetirizine, chlorpheniramine, clemastine, cyclizine, carebastine, cyproheptadine, carbinoxamine, descarboethoxyloratadine (also known as SCH-34117), diphenhydramine, doxylamine, dimethindene, ebastine, epinastine, efletirizine, fexofenadine, hydroxyzine, ketotifen, loratadine, levocabastine, meclizine, mizolastine, mequitazine, mianserin, noberastine, norastemizole, picumast, pyrilamine, promethazine, terfenadine, tripelennamine, temelastine, trimeprazine and triprolidine. Other compounds can readily be evaluated to determine activity at H, receptors by known methods, including specific blockade of the contractile response to histamine of isolated guinea pig ileum. See for example, W098/06394 published February 19, 1998.

Those skilled in the art will appreciate that the H, receptor antagonist is used at its known therapeutical effective dose, or the H, receptor antagonist is used at its normally prescribed dosage.

Preferably, said H1 receptor antagonist is selected from : astemizole, azatadine, azelastine, acrivastine, brompheniramine, cetirizine, chlorpheniramine, clemastine, cyclizine, carebastine, cyproheptadine, carbinoxamine, descarboethoxyloratadine, diphenhydramine, doxylamine, dimethindene, ebastine, epinastine, efletirizine, fexofenadine, hydroxyzine, ketotifen, loratadine, levocabastine, meclizine, mizolastine, mequitazine, mianserin, noberastine, norastemizole, picumast, pyrilamine, promethazine, terfenadine, tripelennamine, temelastine, trimeprazine or triprolidine.

More preferably, said H1 receptor antagonist is selected from: astemizole, azatadine, azelastine, brompheniramine, cetirizine, chlorpheniramine, clemastine, carebastine, descarboethoxyloratadine, diphenhydramine, doxylamine, ebastine, fexofenadine, loratadine, levocabastine, mizolastine, norastemizole, or terfenadine.

Most preferably, said H1 receptor antagonist is selected from: azatadine, brompheniramine, cetirizine, chlorpheniramine, carebastine, descarboethoxy- loratadine (also known as SCH-34117), diphenhydramine, ebastine, fexofenadine, loratadine, or norastemizole.

Even more preferably, said H, antagonist is selected from : loratadine, descarboethoxyloratadine, fexofenadine or cetirizine. Still even more preferably, said H, antagonist is loratadine or descarboethoxyloratadine.

In one preferred embodiment, said H, receptor antagonist is loratadine.

In another preferred embodiment, said H, receptor antagonist is descarboethoxyloratadine.

In still another preferred embodiment, said H, receptor antagonist is fexofenadine.

In yet another preferred embodiment, said H, receptor antagonist is cetirizine.

Preferably, in the above methods, allergy-induced airway responses are treated.

Also, preferably, in the above methods, allergy is treated.

Also, preferably, in the above methods, nasal congestion is treated.

In the methods of this invention wherein a combination of an H3 antagonist of this invention (compound of Formula I) is administered with a H, antagonist, the antagonists can be administered simultaneously, consecutively (one after the other within a relatively short period of time), or sequentially (first one and then the other over a period of time). In general, when the antagonists are administered consecutively or sequentially, the H3 antagonist of this invention (compound of Formula I) is administered first.

Compounds of Formula I include compounds of the formula : wherein R', X, n, M', R'2, a, Y, M2, R'3, b, p, Z and R2 are as defined for Formula I.

Compounds of Formula I also include compounds of the formula : wherein R', X, n, M', R12, a, Y, R'3, b, r, Z and R2 are as defined for Formula I.

R'is preferably selected from: (1) substituted aryl, more preferably substituted phenyl ; (2) substituted heteroaryl, more preferably substituted isoxazolyl ; or (3) formula IVA wherein each R3 is independently selected, more preferably each R3 is alkyl, most preferably each R3 is C1 to C4 alkyl, even more preferably each R3 is the same moiety, and still more preferably each R3 is methyl.

Preferably, when R'is a substituted phenyl group, the phenyl group has 1 to 3 substituents and the substituents are independently selected from: (1)-C (O) N (R4) 2, preferably each R4 is independently selected, more preferably each R4 is independently selected from H or arylalkyl (e. g.,-CH2CH2phenyl), most preferably one R4 is H and the other is arylalkyl, even more preferably one R4 is H and the other R4 is -CH2CH2phenyl; (2) halo, more preferably 1 to 3 halos independently selected from Br, Cl and F; (3)-S (O) 2R22, more preferably R22 is heterocycloalkyl, most preferably R22 is morpholinyl or pyrrolidinyl ; (4)-OCF3; (5)-OCHF2 ; or (6)-S (O) 2N (R2°) 2, more preferably each R20 is independently selected from alkyl or substituted phenyl, most preferably C1 to C4 alkyl or halo substituted phenyl, even more preferably methyl or chlorophenyl ; still more preferably each R20 is methyl or one R20 is methyl and the other R20 is chlorophenyl.

Preferably, when R'is a substituted isoxazolyl group the isoxazolyl group has 1 or 2 substituents independently selected from: (1) alkyl, more preferably Ci to C4 alkyl, most preferably methyl ; or (2) substituted phenyl, more preferably halo substituted phenyl (1 to 3 halo groups, preferably one halo group), most preferably chloro substituted phenyl (e. g., chlorophenyl).

More preferably the isoxazolyl is substituted with two alkyl groups (most preferably two methyl groups), or one halophenyl group (most preferably chlorophenyl).

Examples of R'groups include but are not limited to: Preferably X is selected from-CH2- (i. e., q is preferably 1) or -SO2-. More preferably X is-CH2-.

Preferably n is 2.

Preferably M'is N.

Preferably Y is-C (O)-.

Preferably M2 is C.

Preferably p is 2.

Preferably r is 1.

Preferably Z is a Cl to C6 alkyl group. More preferably Z is Most preferably Z is-CH2-.

Preferably R2 is a six membered heteroaryl ring or a substituted six membered heteroaryl ring, and more preferably the heteroaryl ring contains one nitrogen atom.

Preferably the substituted heteroaryl ring is substituted with one-NR4R5, and more preferably the substituent is-NH2. Most preferably R2 is selected from Even more preferably R2 is Preferably a is 0 and therefore there is no R12 group present.

Preferably b is 0 or 1, more preferably 0. When b is 1 R'3 is preferably-OH.

More preferably, when b is 1, R'3 is-OH bound to the M2 substituent and M2 is C.

Representative compounds of this invention include, but are not limited to: Compounds 18 (Example 1), 25 (Example 2), 26 (Example 3), 31 (Example 4), 33 (Example 5), 37 (Example 6), 41 (Example 7), 45 (Example 8), 49 (Example 9), 51 (Example 10), 52 (Example 11), 57 (Example 12), 58 to 67,73 to 84,89 to 157, 159 to 168, 212 to 269,271 to 272, 276 to 282,284,285,287 to 300, 306,309 to 319, 321 to 336, 338 to 340,342 to 349,351 to 361,363 to 371,374 to 377, 380 to 383, 387 to 390,392 to 406, and 408 to 410.

Preferred compounds are Compounds 93,276,306,317,331,332,333,336, 366,343,366,367,374, and 376 More preferred compounds are Compounds 306,332,333,336,366,374, and 376.

Structures for the above compounds are given below.

The following processes may be employed to produce compounds of the invention.

Step 1 1 2 3 In Step 1, compound 1, in which Q is a protecting group such as a carbamate, amide, or a substituted benzylic group, is allowed to react with compound 2, in which L is a leaving group such as a halogen atom, in a suitable solvent such as THF, DMSO or DMF in the presence of a base such as a tertiary amine or an inorganic base such as Na2CO3 at a temperature sufficient to achieve a reasonable reaction rate. R'2, M', n, a, R', and X are as defined above. Alternatively, in the case when X is- (CH2) q-, L can equal an aldehyde group, CHO and X is- (CH2) q-l-. In that case, compounds 1 and 2 are combined in a solvent such as trifluoroethanol in the presence of sieves. A reducing agent, such as NaBH (OAc) 3 or NaCNBH3 is added and the reaction stirred at a temperature suitable to complete the reaction.

Step 2 3 4 In Step 2, the protecting group Q is removed. When said protecting group is a carbamate such as t-BOC, dilute acid is used. In the case of a benzyl group, catalytic hydrogenation is used.

Step 3 When Y is C=O, amine 4 can be coupled to acid 5 (D is COsH, M2 is carbon) using a number of methods well known in the art such as DCC or PyBOP.

Alternatively, the acid 5 can be activated by conversion to the acid chloride or mixed anhydride and then reacted with the amine 4 to give 6. Suitable protecting groups for 5 include t-Boc or the like. Alternatively, when Y is-CH2-and M2 is carbon, D can be -CH2-L (where L is a halogen) and the reaction can be performed as in Step 1.

Step 4 Compound 6 in which the protecting group is a t-Boc can be deprotected under acidic conditions such as HCI in dioxane or TFA in CH2CI2 to give the amine 7.

Step 5 The amine 7 can be alkylated by reaction with the electrophile 8. In one case, L represents a carbonyl group and Z is a branched or straight chain alkyl group.

Compounds 7 and 8 are combined in a solvent such as CH2CI2 in the presence of sieves. After a suitable amount of time, a reducing agent such as NaBH (OAc) 3 is added to give the product 1. Alternatively, when L is a halogen atom such as Cl or Br, and Z is a branched or straight chain alkyl group or-SO2-7 and 8 are combined in a solvent such as DMF in the presence of a tertiary amine base to give the product I.

Alternative Synthesis An alternative approach to the synthesis of compounds of Formula I is given below.

Step 1 in the same manner as Step 5, compounds 8 and 9 can be converted to 10. In the case when M2 is carbon, D is C02alkyl and when M2 is nitrogen, D is a protecting group such as the BOC group.

Step 2 Compound 10 (D is C02alkyl) is saponified in a mixed solvent such as EtOH or MeOH and water, or THF, water, and MeOH using an alkali metal base such as LiOH or NaOH at a temperature of from 50 to 100°C to give 11.

Compound 11 can be combined with compound 4 as described in Step 3.

Step 3 (D is a protecting group) Compound 10, in which D is a protecting group such as t-Boc and MZ is nitrogen, can be deprotected under acidic conditions such as HCI in dioxane or TFA in CH2CI2 to give the amine 12.

Compound 12 can be coup) e0 w) tn compound 4 using a reagent sucn as carbonyl diimidazole or the like in a solvent such as THF, ether or the like at a temperature from 0 to 60°C to give compound I (Y is C=O, M'and M2 are nitrogen).

Step 5 Compound I (Y is C=O) can be converted to compound I (Y is C=S) by treatment of I with a reagent such as Lawesson's reagent in a solvent such as toluene at a temperature from 20 to 100°C.

Synthesis (M and M2 are carbon) Step 1 A solution of an excess of 13 in a solvent such as THF, CH2CI2 or the like is treated with a reagent such as BOC2O or an acid chloride or anhydride at a temperature of from-20° C to +30° C to produce 14A in which PG is a BOC group, or an amide. Alternatively, a solution of an excess of 13 in a solvent such as THF, CH2CI2 or the like is treated with a substituted or unsubstituted benzyl bromide in the presence of a base such as triethylamine to give 14A in which PG is a substituted benzyl group.

In Step 2, compound 14A, in which PG is a protecting group such as a carbamate, amide, or a substituted benzylic group, is allowed to react with compound 2, in which L is a leaving group such as a halogen atom, in a suitable solvent such as THF, DMSO or DMF in the presence of a base such as a tertiary amine or an inorganic base such as Na2CO3 at a temperature sufficient to achieve a reasonable reaction rate to give compound 15A. R'2, R'3, M', n, p, a, b, r, R', and X are as defined for formula 1. Alternatively, in the case when X is- (CH2) q-, L can equal an aldehyde group, CHO, and X is- (CH2) q-l-. In that case, compounds 14A and 2 are combined in a solvent such as trifluoroethanol in the presence of sieves and stirred for a suitable time. A reducing agent, such as NaBH (OAc) 3 or NaCNBH3 is added and the mixture stirred at a temperature suitable to complete the reaction.

Step 3 Compound 15A in which the protecting group is t-Boc can be deprotected under acidic conditions such as HCI in dioxane or TFA in CH2CI2 to give the amine 16A. Alternatively, when PG is a benzyl group, it can be removed by catalytic hydrogenation using a catalyst such as Pd/C.

Step 4 The amine 16A can be alkylated by reaction with the electrophile 8. In one case, L represents a carbonyl group and Z is a branched or straight chain alkyl group.

Compounds 16A and 8 are combined in a solvent such as CH2CI2 in the presence of sieves. After a suitable amount of time, a reducing agent such as NaBH (OAc) 3 is added to give the product 17A. Alternatively, when L is a halogen atom such as Cl or Br, and Z is a branched or straight chain alkyl group or-S02-16A and 8 are combined in a solvent such as DMF in the presence of a tertiary amine base to give the product 17A.

Compounds useful in this invention are exemplified by the following examples which should not be construed as limiting the scope of the disclosure. Alternative mechanistic pathways and analogous structures within the scope of the invention may be apparent to those skilled in the art.

Example 1 Step 1: Compound 14 (5 g, 43.8 mmol) and 2-bromobenzaldehyde (4.1 g, 22.2 mmol) were combined in CH2CI2 (130 mL) and stirred for 2 h. Na (OAc) 3BH (6.4 g, 30.2 mmol) was added and the mixture stirred overnight at room temperature. The reaction was then washed with saturated NaHCO3 and brine and dried. Filtration and concentration gave a residue which was purified by flash column chromatography (5% to 10% MeOH/NH3 in CH2CI2) to give 15 (3.44 g, 55%) Mass spectrum = 453 (M+H).

Step 2: A solution of 15 (2 g, 7.06 mmol), N-Boc isonipecotic acid (1.47 g, 6.42 mmol) and PyBOP (3.34 g, 6.42 mmol) in CH2CI2 (20 mL) was cooled to 0°C and diisopropyl ethyl amine (2.49 g, 19.3 mmol) was added. After 1 minute, the cooling bath was removed and the reaction stirred at room temperature for 48 hours. The reaction was washed with saturated NaHCO3, dried (Na2SO4), and concentrated and the residue was purified by flash column chromatography (30% to 50 % ethyl acetate in hexane) to give 16 (3 g, 60%).

Step 3: A solution of 16 (3 g, 6.07 mmol) in CH2CI2 (100 mL) at 0° C was treated with 4 N HCI (8 mL) and the reaction stirred at room temperature overnight. The solvent was removed in vacuo and the residue was dissolved in water and the pH adjusted to 8 by addition of aqueous NaOH. The water was removed in vacuo and the residue dissolved in MeOH, filtered and concentrated to give 17 as a white solid (3 g, >100%) which was used as is. Mass spectrum: 394 (M+H).

Step 4: In a manner similar to that described in Example 1, Step 1,17 (0.95 g, 2.4 mmol) and pyridine-4-carboxaldehyde (0.22 g, 2.02 mmol) was converted to 18 (0.57 g, 58%). Mass spectrum: 485 (M+H).

Example 2 Step 1: In a manner similar to that described in Example 1, Step 1, 19 (5 g, 26 mmol) and 2-bromobenzaldehyde (4.1 g, 21.7 mmol) was converted to 20 (6.2 g, 80%).

Step 2: in a manner similar to that described in Example 1, Step 3,20 (6.2 g, 17.5 mmol) was converted to 21 (5.5 g, 100%).

Step 3 In a manner similar to that described in Example 1, Step 1, 22 (0.45 g, 3.6 mmol) and ethyl isonipecotate (0.7,4.4 mmol) were converted to 23 (0.45 g, 64%).

Step 4: 23 24 A solution of 23 (0.45 g, 1.69 mmol) in MeOH (10 mL) was treated with 1 N KOH (5 mL) and the mixture was heated to 60° C overnight. The reaction was cooled and concentrated. The residue was dissolved in water and extracted with ethyl acetate. The pH of the aqueous phase was adjusted to 6-7 by addition of 1 N HCI.

The water was removed in vacuo and the residue taken up in MeOH, filtered and concentrated to give 24 which was used in the next step as is.

Step 5: In a manner similar to that described in Example 1, Step 2,21 (0.35 g, 1.39 mmol) and 24 (0.3 g, 1.26 mmol) was converted to 25 (0.50 g, 66%). Mass spectrum: 475 (M+H).

Example 3 To a solution of 25 (0.11 g, 0.23 mmol) in 2-propanol (6 mL) in a pressure vessel was added triethylamine (7 mL) and methylamine hydrochloride (3 g, 44.4 mmol) and the reaction heated to 95°C for 6 days. The reaction was cooled and the solvent removed in vacuo. The residue was dissolved in ethyl acetate and washed with half saturated NaHCO3. The organic layer was dried and concentrated, and the residue purified on a flash column (20% MeOH in ethyl acetate) to give 26 (40 mg, 36%). Mass spectrum: 486 (M+H).

Example 4 Step 1: 27 28 In a manner similar to that described in Example 1, Step 1,27 (2 g, 18.3 mmol) and ethyl isonipecotate (3.5,22 mmol) were converted to 28 (4.5 g, 99%).

Step 2: A solution of n-BuLi (3 mL of a 1.6 M solution in hexane, 4.8 mmol) in THF (25 mL) was treated at-25° C with (i-Pr) 2NH (0.49 g, 4.8 mmol). The reaction was stirred for 1 h at 0°C and then cooled to-70° C. Compound 28 (1.0 g, 4 mmol) in THF (3 mL) was added dropwise and the reaction stirred at-70°C for 2 h and-50° C for 2 h. The reaction was recooled to-70° C and (1 S)- (+)- (10- camphorsulfonyl) oxaziridine (1.04 g, 4.52 mmol) in THF (10 mL) was added. The reaction was stirred at-70° C for 2 h and slowly warmed to room temperature overnight. The reaction was quenched by the addition of saturated aqueous NH4CI and extracted with EtOAc. The organic layer was dried and concentrated, and the residue purified by column chromatography (4% MeOH in ethyl acetate) to give 29 (0.75 g, 71%).

Step 3: 29 30 In a manner similar to that described in Example 2, Step 4, 29 (0.35 g, 1.32 mmol) was converted to 30 (0.32 g, 99%).

Step 4: 30 31 In a manner similar to that described in Example 1, Step 2, 30 (0.2 g, 0.85 mmol) was converted to 31 (0.10 g, 25%). Mass spectrum : 473 (M+H).

Example 5 To a solution of 32 (0.52 g, 1.43 mmol ; synthesized in the same manner as compound 17) and 3-chloromethyloxadiazole (0.25g, 2.11 mmol) in toluene (10 mL) was added triethylamine (0.6 mL) and the reaction was heated to 75° C overnight.

The reaction was cooled, diluted with ethyl acetate and washed with saturated NaHCO3. The organic layer was dried and concentrated and the residue purified by flash column chromatography (10% MeOH in ethyl acetate) to give 33 (0. 2 g, 31 %) Mass spectrum: 448 (M+H).

Example 6 Step 1 34 35 In a manner similar to that described in Example 1, Step 2, compound 34 (1.2 g, 4.93 mmol) was coupled with compound 21 (1.4 g, 5.43 mmol) to give compound 35 (1.7 g, 74%).

Step 2 35 36 In a manner similar to that described in Example 1, Step 3, compound 35 (1.7 g, 3.54 mmol) was converted to 36 (1.3 g, 97%).

Step 3 In a manner similar to that described in Example 1, Step 1, compound 36 (0.41 g, 1.08 mmol) was converted to 37 (0.2 g, 45%). Mass Spectrum: 471 (M+H).

Example 7 Step1 38 39 To a stirred mixture of 38 (2.0 g, 12.5 mmol) and Na2CO3 (1.45 g, 13.7 mmol) in acetone (15 mL) was added chloroacetonitrile (1.05 g, 13.7 mmol) and the reaction mixture stirred for 3 h at room temperature. The solvent was removed in vacuo and the residue partitioned between ethyl acetate and water. The ethyl acetate layer was dried (Na2SO4) and concentrated to give 37 (2.3 g, 94%) which was used as is.

Step 2 To a solution of 39 (2.2 g, 11.2 mmol) in toluene (20 mL) was added n-Bu3Sn (5.7 g, 16.8 mmol) and the reaction heated to reflux for 48 h. Additional n-Bu3Sn (0. 5 mL) was added and the reaction was stirred at reflux for 6 h and at room temperature for 18 h. The reaction was cooled to room temperature, 5 N NaOH (35 mL) and hexane (35 mL) were added and the reaction was stirred for 2 h. The aqueous phase was separated and neutralized with concentrated HCI. The water was evaporated in vacuo and the residue taken up in MeOH, filtered, and the filtrate concentrated to give 40 (3.6 g) which was used in the next step without further purification.

Step 3 In a manner similar to that described in Example 1, Step 2, compound 40 (0.2 g, 0.95 mmol) was converted to 41 (0.2 g, 47%). Mass spectrum: 448 (M+H).

Example 8 Step 1 38 42 To a solution of 38 (2.57 g, 16 mmol) in THF (30 mL) was added propargyl bromide (1.34 g, 8.98 mmol) and the reaction heated to reflux overnight. After cooling to room temperature, the reaction was diluted with CH2CI2 and washed with 1 N NaOH. The organic layer was dried and concentrated to give a residue which was purified by flash column chromatography (5% ethyl acetate in hexane) to give 42 (1.31 g, 75%). Mass spectrum: 196 (M+H).

Step 2 42 43 To a solution of 42 (0.5 g, 2.56 mmol) in toluene (10 mL) was added trimethylsilyl azide (0.62 g, 5.12 mmol) and the reaction was heated to reflux for 18 h.

The reaction was cooled to room temperature, additional trimethylsilyl azide was added (0.7 mL). The reaction was stirred at 50° C for 8 days and 110° C for 10 days.

The solvent was evaporated in vacuo, MeOH (100 mL) was added, and the MeOH removed in vacuo. The residue so obtained was chromatographed (4% MeOH in ethyl acetate) to give 43 (0.5 g, 82%) Mass spectrum : 239 (M+H).

Step 3 43 44 In a manner similar to that described in Example 2, Step 4, Compound 43 (0.5 g, 2.1 mmol) was converted to compound 44 (0.44 g, 100%).

Step 4 1.2 mmol) and 21 (0.36,1.4 mmol) were converted to 45 (0.11 g, 20%). Mass spectrum: 447 (M+H).

Example 9 Step 1 46 47 A solution of compound 46 (2 g, 7.5 mmol), 19 (1.6 g, 8.2 mmol) and triethylamine (3.1 mL) in toluene (30 mL) was heated to reflux overnight. The solvent was evaporated and the residue partitioned between ethyl acetate and saturated NaHC03. The organic layer was dried and concentrated and the residue purified by flash column chromatography (30% ethyl acetate in hexane) to give 47 (1.6 g, 78%).

Step 2 47 48 In a manner similar to that described in Example 1, Step 3,47 (1.6 g, 4.3 mmol) was converted to 48 (1.5 g, 100%).

Step 3 In a manner similar to that described in Example 1, Step 2,48 (0.38 g, 1.1 mmol) was converted to 49 (0.15 g, 35%). Mass spectrum: 475 (M+H).

Example 10 To a suspension of 32 (0.5 g, 1.14 mmol) in acetonitrile (5 mL) was added diisopropylethylamine (0.59 g, 4.56 mmol) followed after 10 min by 50 (0.23 g, 1.37 mmol). The mixture was stirred at room temperature for 48 h. The acetonitrile was removed, xylene (10 mL) was added and the reaction refluxed overnight. The reaction was cooled, diluted with ethyl acetate and washed with water. The organic layer was dried and concentrated and chromatographed (10% to 20% MeOH in ethyl acetate) to give 51 (0.13 g, 25%). Mass spectrum: 463 (M+H).

Example 11 A solution of 25 (0.13 g, 0.27 mmol) in 1: 1 5% HCI in DME/water (4 mL) was heated to 60° C for 6 h. The reaction was cooled to room temperature, saturated NaHC03 and solid NaCI was added and the mixture was extracted with CH2CI2. The combined organic layers were dried, concentrated and the residue purified by flash column chromatography (5-10% NH3/MeOH in CH2CI2) to give 52 (40 mg, 31%).

Mass spectrum: 473 (M+).

Example 12 Step 1 53 54 Compound 53 (3.6 g, 29.1 mmol), ethyl isonipecotate (5.8 g, 36.4 mmol) and Ti (OiPr) 4 (10.3 g, 36.4 mmol) were combined and stirred at room temperature overnight. CH2CI2 (100 mL) was added followed by NaBH (OAc) 3 (8.6 g, 40.8 mmol) and the reaction stirred overnight. Saturated NaHC03 was added and the mixture filtered through Celite. The filter cake was washed with additional CH2CI2, and the combined filtrates were washed with saturated NaHCO3 and dried. Concentration gave a residue which was purified by flash column chromatography (8% MeOH in ethyl acetate) to give 54 (5 g, 83%). Mass spectrum: 277 (M+H).

Step 2 54 55 In a manner similar to that described in Example 4, Step 2, 54 (1 g, 3.6 mmol) was converted to 55 (0.4 g, 37%). Mass spectrum: 293 (M+H).

Step 3 55 56 In a manner similar to that described in Example 2, Step 4,55 (0.4 g, 1.4 mmol) was converted to 56 (0.4 g, 100%).

Step 4 In a manner similar to that described in Example 1, Step 2, 56 (0.38 g, 1.6 mmol) was converted to 57 (0.36 g, 47%). Mass spectrum: 505 (M+H).

Using the procedures described in Examples 1-12, the compounds in Table 1 were synthesized: TABLE 1 Compound Starting Material Product Number COsEt 58 OH H Chug 59 0 59 O 0 ber O bu F 60 F O 60 C 1'N l/ HO N-/ Ho bu F 61 H 3C q I H3 SJ _ I N B r J N /Y GZ \ H 3C N Cl Ha I CH3 Br N 63 0 zon ber CHO O 64 H3 \ N N NH I HN/CHO B HgC 0 65 H3 CH3 \ N N O I/, . 0 52 52 H3C H3C 0 NH /N N Br Br N 53 5 0 NH Bu ber N/ Br B Example 13 Step 1 Dissolved amine 68 (25.0 g, 0.134 mol) in CH2CI2 (500 mL) and added 3 A sieves (25 g), 3-chlorobenzaldehyde (28.3 g, 0.201 mol), and sodium triacetoxyborohydride (42.6 g, 0.201 mol). Stirred at 23° C for 16 h and filtered.

Washed filtrate with saturated NaHCO3 then saturated NaCl. Dried organic extract (MgS04), filtered, and concentrated. Purified by silica gel chromatography (eluant : 20% EtOAc-hexane) to give 31.0 g (0.100 mol, 74%) of the product 69 as a yellow oil. MS (ES for M+1) : m/e 312.

Step 2 Dissolved compound 69 (27.0 g, 0.087 mol) in CH2CI2 (500 mL) and added 1.0 N HCI in ether (275 mL, 0.275 mol). Stirred at 23° C for 96 h. Filtered and washed with ether to give 20.0 g of the dihydrochloride salt of compound 70.

Dissolved the dihydrochloride salt in 1 N NaOH (500 mL) and extracted with EtOAc.

Dried combined organic extracts (MgSO4), filtered, and concentrated to give 14.9 g (0.071 mol, 82%) of the product 70 as a yellow oil. MS (ES for M+1): m/e 211.

Step 3 Combined compound 70 (13.03 g, 0.062 mol), N-tBOC-isonipecotic acid (21.38 g, 0.093 mol), HOBT (16.28 g, 0.12 mol), and DEC (23.01 g, 0.12 mol) in CH2CI2 (400 mL). Stirred at 23° C for 4 h. Added 2 N NaOH and extracted with CH2CI2. Dried combined organic extracts (MgSO4), filtered, and concentrated.

Purified by silica gel chromatography (eluant : CH2CI2 then 2% MeOH with NH3- CH2CI2) to give 25.0 g (0.059 mol, 95%) of the product 71 as a yellow oil. MS (ES for M+1) : m/e 422.

Step 4 Dissolved compound 71 (20.0 g, 0.048 mol) in CH2CI2 (250 mL) and cooled to 0° C. Added TFA (50 mL) and stirred at 23° C for 3 h. Concentrated, added 6.25 N NaOH, and extracted with CH2CI2. Dried combined organic extracts (MgS04), filtered, and concentrated. Purified by silica gel chromatography (eluant : CH2CI2 then 5% MeOH with NH3-CH2CI2) to give 7.18 g (0.022 mol, 47%) of the product 72 as a yellow oil. MS (ES for M+1): m/e 322.

Step 5 72 73 Dissolved compound 72 (255 mg, 0.79 mmol) in CH2CI2 (10 mL) and cooled to 0° C. Added triethylamine (158 mg, 0.22 mL, 1.56 mmol) and mesyl chloride (115 mg, 0.078 mL, 1.01 mmol). Warmed to 23° C and stirred for 16 h. Added saturated NaHC03 and extracted with CH2CI2. Dried combined organic extracts (MgSO4), filtered, and concentrated. Purified by silica gel chromatography (eluant : CH2CI2 then 2% MeOH with NH3-CH2CI2) to give 164 mg (0.41 mmol, 52%) of the product 73 as a white foam. MS (ES for M+1): m/e 400.

Following the above procedure compound 74 was prepared: (MS (ES) 462 (M+1)).

Example 14 Dissolved compound 72 (250 mg, 0.78 mmol) and triethylamine (158 mg, 0.22 mL, 1.56 mmol) in CH2CI2 (10 mL) and cooled to 0° C. Added benzoyl chloride (142 mg, 0.12 mL, 1.01 mmol). Warmed to 23° C and stirred for 16 h. Added saturated NaHCO3 and extracted with CH2CI2. Dried combined organic extracts (MgS04), filtered, and concentrated. Purified by silica gel chromatography (eluant : CH2CI2 then 3% MeOH with NH3-CH2CI2) to give 191 mg (0.45 mmol, 58%) of the product 75 as a white foam. MS (ES for M+1): m/e 426.

Following the above procedure compound 76 was prepared: (MS (ES) 427 (M+1)).

Example 15 Dissolved compound 72 (250 mg, 0.78 mmol) and triethylamine (158 mg, 0.22 mL, 1.56 mmol) in dry THF (10 mL). Added phenylisocyanate (120 mg, 0.11 mL, 1.0 mmol) and stirred at 23° C for 16 h. Added water and extracted with EtOAc. Dried combined organic extracts (MgS04), filtered, and concentrated. Purified by silica gel chromatography (eluant : CH2CI2 then 3% MeOH with NH3-CH2CI2) to give 170 mg (0.39 mmol, 50%) of the product 77 as a white foam. MS (ES for M+1): m/e 441.

Following the above procedure compound 78 was prepared: (MS (ES) 407 (M+1)).

Example 16 Combined compound 72 (550 mg, 1.71 mmol), benzaldehyde (109 mg, 1.03 mmol), 0.5 g of crushed 3A sieves, and sodium triacetoxyborohydride (347 mg, 1.64 mmol) in 2: 1 CH2CI2 : EtOH (15 mL). Stirred at 23° C for 16 h. Added saturated NaHC03 and extracted with CH2CI2. Dried combined organic extracts (MgS04), filtered, and concentrated. Purified by silica gel chromatography (eluant : CH2CI2 then 3% MeOH with NH3-CH2CI2) to give 260 mg (0.63 mmol, 37%) of the product 79 as a white foam. MS (ES for M+1) : m/e 412.

Following the above procedure the compounds in Table 2 were prepared.

TABLE 2 Compound Compound MS (ES) Number 80 442 (M+1) cr,"N N N C OMe 81 469 (M+1) NCY lON N N C NHAc 82 413 (M+1) nord N N N C 83 413 (M+1) N N N C N 84 429 (M+1) N W J N roll, O Example 17: General procedure for reductive animation. Parallel synthesis.

87 A solution of the amine 85 (0.063 mmol) and the aldehyde 86 (0.32 mmol, 1.0 M in dichloroethane) is treated with NaBH (OAc) 3 (0.32 mmol, 0.5 M in dichloroethane) and placed on shaker for an average period of 18 h. Where needed more NaBH (OAc) 3 is added to force the reaction into completion. Amberlyst-15 resin (-100 mg) is added and the reaction mixture shaken for an additional hour while monitoring by TLC (10% NH3 saturated methanol in CH2CI2, Rf-0. 3) to ensure no amine product remained in solution. The resin is filtered and alternately washed six times with MeOH and dichloroethane. The resin is extracted by stirring twice, for 30 min, with 2N NH3/MeOH (2 ml) and rinsing twice with MeOH (2 ml). The combined extracts are concentrated in vacuo to provide the desired product 65.

Using this procedure, the compounds listed in Table 3 were synthesized. In Table 3 X, represents the moiety: 88 (i. e., the moiety 88 is compound 87 without the RrCH2-group).

TABLE 3 Compound R MS No. 89'w i I 471.1 (MH+) x, o 90 429. 1 (MH+) jazz 91 ° nx, 436. 1 (MH+) 0 X, o x, 92 H3 421. 1 (MH+) Xi H gt 93 r 459. 1581 (MH+) < 94 ax 379.1 (MH+) x "1 95 Ho 395.1 (MH+) Sx, 96 H3C--p-c-xi 423. 1 (MH+) H 3C 97 cox, 413.1 (MH+) 98 xi 407.1 (MH+) 99 N X 404. 1 (MH+) x 100 HO, >, 399. 1 (MH+) p 101 Sob 521. 1 (M) s cl 102 oH 423. 1 (MH+) 0 1 103/,-H3 439.1 (MH+) x, /PO X, 104 9\x, 393.1 (MH+) X 105 y"\x 409.1 (MH) H 3C H3C == 106 490. 1 (MH+) X, 6 o /I 'ON+ \ II O 107 H 3C, 409.1 (MH+) Xi I 108 409. 1 (MH+) H 3C OH OH 109 X, 437. 1 (MH) 0 CHs CH3 110 H3 407.1 (MH+) HsC- -Xi H 3C x 111 H3 459. 1 (MH+) xi 112 H3 421. 1 (Me dz 113 (tJ 553. 1 (M+) ci Fizz 114 X, 485. 1 (MH') CL 0 115 d 537. 1 (M+) I F cri CI 116 X, 473. 1 (M+) HO Br 117 xi 490.1 (MH') r-X, WlNI+ qu O- 118 xi 439. 1 (MH+) tY" 119 xi 485.1 (MH+) HO 120 439.1 (MH+) /x, 121 X, 488. 1 (MH+) /O Buzz 122 xi 415. 1 (MH) I F 123 437. 1 (MH+) 124 467. 1 (MH+) 125 455. 1 (MH+) 126 H3 423. 1 (MH+) o xi H 3C 127 415. 1 (MH) F eX, 128 S \ X 425. 1 (MH+) H 3C/ 129 x, 459. 1 (MH+) cl3 CHs I CH3 130 H 3C H3 437. 1 (MH+) p x H3C 131 o X, 467. 1 (MH+) "T1 CL3 CH3 132 X, 397. 1 (MH+) Zu 133 FX3 447 1 (MH+) F 134 xi 447.1 (MH+) F F F F 135 X, 397. 1 (MH+) F 136 407. 1 (MH+) H 3C 137//X'385. 1 (MH+) s 138//X'369. 1 (MH+) 0- 139 xi 591. 1 (MH) 0 6 140 395. 1 (MH+) Ht/ 141 41 424. 1 (MH) + , nit 0 0- 142 451. 1 (MH+) H3 CII-O 143 H34 407. 1 (MH+) ""A CHUG 144 ß 409. 1 (MH+) cl3 CH3 CH3 145 X, 439. 1 (MH+) oH 0 146 xi 393. 1 (MH) H 3cJf 147 xi 429. 1 (MH') X 148 I X'471. 1 (MH+) 1 149 Je 505. 1 (M+) a I ce 150 ß 527. 1 (MH+) ZU H go H 3C CH3 H 3C 151 4° 414. 1 (MH) #+_o- zu 152 Il 453. 1 (MH+) 0 HIC H gC "CHs 153 xi 464. 1 (M+) ci zon i 154 430. 1 (MH) sol s zozo - O 155 A 496. 1 (MH+) CHUG cl3 CHg 156 539. 1 (MH+) d F tuf F F 157 xi 485. 1 (MH+) H 3C HsC 159 395. 1 (MH+) OH OH 160 Cl 413. 1 (MH+) cri 161 xi 395. 1 (MH') HO 162 XI 435. 1 (MH+) I Hic H 3C CH3 H gC 163 < 469.1 (MH+) 164 X, 369. 1 (MH') 0 165 ¢ » x, 385.1 (MH+) s 166 424. 1 (MH) Õ il u 167 X, 418. 1 (MH+) CON 168 j 505 (MH+) xi I/ Thus, compounds in Table 3 have the formulas given in Table 4 below.

TABLE 4 Compound Structure No. 89 N-C, L,. Nr ZD 0,01 89 XCNJso 0 L 91 N 92 i HN 92 I N NN 93 jan . OJO B 94 N2j<N 2 94 0 N 95 95 rtt frT) rf kk k 96 c j< kjj' 'L rA I 98 I 99 ( 100 H O 101 ~< I c 12 M c @< zu v 103 i i i 104 105 H3C- 105 HsC'O \ (\ 105.) f Y frii jk< k<j '06 g 106 i 107 i . out3 "Di 109 H3Cso I < 108pop H 110 H3 110 H3/ H3 111 FOW 112 if 112 jazz CHg I CH3 113 i ci ci 114 tv xi N < 115 I i ° i N IN 116 zon fuzz N N HO Br Br 117 A4 po 118 1 HOf 119 i ho 119 120 121 i 121 11 I I r'i 11 f'r H3C-0 122 i F I FtF 123 i o 124 125 126 dz \/ 125 126 H3C- 129 Z @AS H3 ( : ' 130 "3 Fui Cl3 128 129 I H 129 B r/Y 130 H33$CH3 H3 0. CHa °CH3 1 H3Q v/ . uu< Y 1 q 2 b 13 : < 132 i 133 F')'6 \ 134 135 ri F fuzz 134 135 136 136 f "Y f"fT 137 zu </ rrri \<J LJUU) 138 / rrT \LJ LU 139 cor", 0 o 140 vu ho 141 142 H3+ t< i 142 H3 \ \ 143 H3/ I CH3 zon 145 ou DL tfT JN k 145 J' t!) r<"ri f" 146 i) OH 146 J J' [i fl ff 147 0 0, I 148 149 c zizi Tl ? p [i fAi 150 H3 H3 H3C 13C 151 -0 Q i _o / rfY . cU k. UU' 152 H, C- H3 H3XsCH3 153 CHO CHO 153 I 155 CI 156 154 . v I w zig 155 xi xi F I o I, ' , F 157 H3-al P f ? \ N \ 159 I 160 ci c I 161 ho, 6 \ H 162 Oh < H3C 163 i i I 164 h 164 i 165 166 o - a 0 167 158 f 168 6r N 168 i Example 18: Library preparation on solid phase Scheme 1 1. FMOC-Lys DIC/HOBT (J_H 2 N NH, 2. Piperazine/DMF o 169 o o o H HN . oY 0- ULar HOtOz CKNWAW Q Br - ber Bu DIC/HOBT 170 YCCN02 170 o TentaGel amino resin (1 eq.) was placed in a reaction vessel, dichloromethane, FMOC-Lysine (2 eq.) and HOBT (2.2 eq.) were added followed by the addition of DIC (2eq.). The mixture was shaken at room temperature for 12 hours, then drained and the resin was washed with dichloromethane twice and DMF three times, and treated with 20% piperazine in DMF (v/v) for 30 minutes. The resin was then washed with DMF twice, methanol twice and dichloromethane three times, and dried overnight in vacuo to give amine resin 169.

The amine resin 169 (1 eq.) was placed in a reaction vessel, dichloromethane, 4-bromomethyl-3-nitrobenzoic acid (2 eq.) and HOBT (2.2 eq.) were added followed by the addition of DIC (2eq.). The mixture was shaken at room temperature for 12 hours, then drained and the resin was washed with dichloromethane twice, methanol twice and dichloromethane three times, and dried overnight in vacuo to give bromoresin 170.

Scheme 2 The bromo resin 170 was divided into 24 portions, and each (1eq.) was treated with an amine (see 172 to 196 below) (5eq.) in THF. The mixture was shaken at room temperature overnight, drained and the resin was washed with THF twice, DMF twice and dichloromethane three times, and dried overnight in vacuo to give amine resin 171.

Scheme 3 CICOR2ACH2CI NiA R Cl q Lutidine, CH2CI2 A 2AV VNHRIA Õ 0 171 197 The amine resin 171 was divided into 3 portions, and each (1 eq.) was treated with an acid chloride (see 198 to 200 below) (2 eq.) and 2,6-lutidine (4 eq.) in dichloromethane. The mixture was shaken at room temperature for 30 minutes, drained and the resin was washed with dichloromethane twice, methanol twice and dichloromethane three times, and dried overnight in vacuo to give chlororesin 197.

Scheme 4 The chlororesin 197 was divided into 7 portions, and each (1 eq.) was treated with an appropriate amine (see 202 to 208 below) (5 eq.) in DMSO. The mixture was shaken at room temperature overnight, drained and the resin was washed with methanol twice, dichloromethane twice, methanol twice and dichloromethane three times, and dried in vacuo to give amine resin 201.

Scheme 5 201 209 The amine resin 201 was divided into 2 reaction vessels, and each was treated with 2% HOAc in DMF and an appropriate aldehyde (see 210-211 below). The mixture was shaken at room temperature for 30 minutes, and NaBH3CN was added to each reaction vessel. The mixture was shaken for overnight, drained, and the resin was washed with DMF twice, methanol three times and 10% HCI in methanol, and dried in vacuo to give resin 209.

In the above Schemes, RiA represents the substituents on R', R2A represents R', R3A represents R or R'3, and R4A represents R2.

Examples of compounds made by the above library procedure include : EXAMPLE 19 Compound 218 was prepared in solution in large quantity. The following is the procedure for the preparation of 218, which serves as the general protocol for preparation of other analogs.

To a solution of Phenylethyl amine (120 mg, 1 mmole) and triethyl amine (200 mg, 2 mmole) in CH2CI2 (10 mL) at 0 °C was added 4- (Chloromethyl) benzoyl chloride (230 mg, 1.2 mmole). After 30 min., the reaction mixture was poured into a separational funnel and washed with 1 N HCI (10 mL), 1 N NaOH (10 mL) and brine (10 mL). The organic layer was separated, dried over Na2SO4, and filtered. The filtrate was concentrated to give compound 273 as colorless oil (260 mg, 95%).

To a refluxed solution of compound 273 (260 mg, 0.95 mmole) in THF (10 mL) was added piperazine (430mg, 5 mmole). The mixture was under reflux for 1 h and cooled to room temperature. Solvent was removed and the residue was dissolved in EtOAc (20 mL), which was washed with H20 (2 x 10 mL), 1 N NaOH (10 mL) and brine (10 mL). The organic layer was separated, dried over Na2SO4, and filtered.

The filtrate was concentrated to give compound 274 as a slightly yellow oil (290 mg, 95%).

To a solution of Boc-isonipecotic acid (230 mg, 1 mmole) in EtOAc (10 mL) at 0° C was added DCC (206 mg, 1 mmole) followed by the addition of compound 274 (290 mg, 0.9 mmole) in EtOAc (5 mL). The reaction mixture was stirred at room temperature for 8h, and filtered. The filtrate was concentrated. Flash chromatography of the residue gave compound 275 as a colorless oil (390 mg, 80%) 2% HOAc/DMF, NaBH3CN To a solution of compound 275 (270 mg, 0.5 mmole) in CH2CI2 (5 mL) was added trifluoroacetic acid (0.5 mL). After 30 min., the mixture was concentrated, and the residue was dissolved in EtOAc (10 mL), which was washed with 1N NaOH (10 mL) and brine (10 mL). The organic layer was separated, dried over Na2SO4 and filtered. The filtrate was concentrated and the residue was dissolved in DMF (5 mL).

Acetic acid (0.2 mL), 4-pyridinecarboxaldehyde (64 mg, 0.6 mmole) and NaBH3CN (64 mg, 1 mmole) were added to the solution. The reaction mixture was kept at room temperature for 8h. EtOAc (15 mL) and H20 (10 mL) were added to the mixture, and the mixtures were poured into a separational funnel. The organic layer was washed with H2O (10 mL), 1N NaOH (10 mL) and brine (10 mL), separated and dried over Na2SO4. After filtration, the filtrate was concentrated. Flash chromatography of the residue to give compound 218 as a white foam (132 mg, 50%).

Following the procedure of Examples 1 to 17 the compounds in Table 5 were prepared.

TABLE 5 Compound Structure No. 276 ZON o i NJ J HN 277 0 eO"-N zu 279 0 N 278 9 279 1 NNI JN \ I H 280 1NLOAC H 280? 281 p- O C N c<oNt NJ C 282 I I 284 off T jn 285 \ IN CH3 p _ 287 N N N N BrCHs Br CH3 288 XNX XN N 0 zu N N 0 hic N O hic 290 Br CH3 I N N N IN O 291"0. i 292 OH zu zon bu F 293 N N N ION 294 Br N N N F 295 Br CH3 N N F ~ CNtl XN 0 296 H3C\N Bu N zizi ZON ! ! oh OU 0 buzz Br N N I N N yri 0 298 Br N 0 ! N O HN CH 299 299 Br CH3 299 §" r1 fT N N CH3 0 Br CH3 300 N) raj ici 0 I O 306 0 N N NJ N \ I NU2 ZIP F 309 i i"o 310 310 H zizi 311 Y'kJ' H F \ \ 'oxo 312 NU2 313 313 if 313 - cro 0 314 nu2 NHz o 315 F/j? '0 O 315 F F NH2 F 316 F NH2 F F 317 0 p, C NHz zozo ce 318- ? 319 NHz I 319 RUZ NH2 F F F F 322 i NHZ CI 322 I 3 Br NH2 Br 323 XI "nez Cl nu2 I \ F/ 324, <NHz 325 F 325 nu z F. O F T F 326 NH2 (nez NU2 /I \ 327 2 F 328 NH2 : 329 329 je F-, F/ CL 330 nu2 F-, Br /I Bu H3 CH3 O-N NH ou" Nu2 on o=s=o NH2 H3C"CH3 3 3 O-N 332 > NH2 joo)) C \ 1 NHZ -CUL 334 nu2 c C I 335 NH2 i NHz Nu2 ci 336 Ct 338 H H3 rye CI \ I 338 H' if CH3 H30t 0t 339 j ? Jf cri his I/ 340 i NH2 ceci i CI 342/ci \ I \ NHz o=s=o H-CHg 343 nu2 a NHz O 344 0 cri I r I NH zu SNH 344 NH2 345 345 °\\ NH 0==0 X,NH2 crv 346 346 c \ I \ NH2 0= 0 o=s=o 347 0 cri CL OH NHz SNH CI ci Fizz N ho ZU if0 o i, c ci 351 \, S HNH2 Nu2 351 Nu2 H Z f° w w NHZ O 352 NH2 Yk'k, o=ro 353 nu2 \ I \ NHz O U 6 354 H3C N H 2 v o CH3 355. j ? zozo 356 H2 zip I w 0 357 i Q 358 R ri 0 o po WW 357 su O CH3 359 » (O N q B v) P 360 w o Fiez 361 19, 0 . w I woo (Y , w o 3 4 , w 364 JJ 365 ! 3 Ha 0 cl3 366 , *, I N I/. nu2 cra 0 367 366 \ 1 NH2 c 367 i H3C" NH2 zozo CHEZ 3 r<T f! o I/NHz cU ° C 369 N H3C, NH 374 CSO JA NH2 % H3 H 3 3 0 NH2 xi hop b H_ cul 371 fut ° Cj cri 374 CI 374 N,,,'a NH2 fT cl 375 C % H2 NH2 0 Ci 376 rack-" NU2 0 Cl 377 NH2 0 0 380 380 o NH2 ° I 381 0 NH2 F 0 F 0 382 nu2 382 NH FI f ~ Hz 383 c NU, z QQQ H o rrT r ) LJ U. 0 387 P rfri , U kL, 387 388 j { zozo . UJ CH3 cl3 388 Asz 0 0 389 po ou 0-razz =O U 390 Cd / H2 392 0 i 'o R t\ O 393 Ir 39 f"fT O z O 394 OH O S N 1/ H C N J 396 9 O \\O xi nu2 0 396/ 0. O Co N H2 0 397 o 0 3 9 8 O <9 N H2 o o_ WHY VU zu 3 9 ans2 nu2 v0 0..,. J k Z J NH2 400 0 zozo PO I 4Mg 401 0 N N NJ zu 0 nu s HIC hic H3C 402 ° zu NHi O 403 ci ou NU ) 0 N ion S NJ N \ I s oNt I NU 404 % H3Co xOX NH2 thy "3 405 JJ' 0 405 C b NH2 406)} 405 nu Z I O 406 408 IN /NH \ I N N O 409 I N o 0 NH N NH 0-"-ON 1 410 T" 0 4 U N"--CN 410 O 410 0 r H3COHN I/J N I O General Procedure for Hg-Receptor Binding Assay The source of the H3 receptors in this experiment was guinea pig brain. The animals weighed 400-600 g. The brain tissue was homogenized with a solution of 50 mM Tris, pH 7.5. The final concentration of tissue in the homogenization buffer was 10% w/v. The homogenates were centrifuged at 1,000 x g for 10 min. in order to remove clumps of tissue and debris. The resulting supernatants were then centrifuged at 50,000 x g for 20 min. in order to sediment the membranes, which were next washed three times in homogenization buffer (50, 000 x g for 20 min. each). The membranes were frozen and stored at-70°C until needed.

All compounds to be tested were dissolved in DMSO and then diluted into the binding buffer (50 mM Tris, pH 7.5) such that the final concentration was 2 ug/ml with 0.1% DMSO. Membranes were then added (400 ug of protein) to the reaction tubes.

The reaction was started by the addition of 3 nM [3H] R-a-methyl histamine (8.8 Ci/mmol) or 3 nM [3H] Na-methyl histamine (80 Ci/mmol) and continued under incubation at 30°C for 30 min. Bound ligand was separated from unbound ligand by filtration, and the amount of radioactive ligand bound to the membranes was quantitated by liquid scintillation spectrometry. All incubations were performed in duplicate and the standard error was always less than 10%. Compounds that inhibited more than 70% of the specific binding of radioactive ligand to the receptor were serially diluted to determine a Kj (nM).

Compounds 89 to 157, 159 to 168,276 to 279,282,284,285,287 to 300,306, 309 to 319,321 to 336, 338 to 340, 342 to 349, 351 to 361,363 to 371, 374 to 377, 380 to 383,387 to 390,392 to 406, and 408 to 410 had a Ki within the range of about 0.2 to about 600 nM.

Preferred Compounds 93, 276, 306,317,328,331,332,333,336,343,366, 367,374 and 376 had a Ki within the range of about 0.2 to about 35 nM.

More preferred Compounds 306, 332,333,336,366,374 and 374 had a Ki within the range of about 2 to about 22 nM.

For preparing pharmaceutical compositions from the compounds described by this invention, inert, pharmaceutical acceptable carriers can be either solid or liquid.

Solid form preparations include powders, tablets, dispersible granules, capsules, cachets and suppositories. The powders and tablets may be comprised of from about 5 to about 95 percent active ingredient. Suitable solid carriers are known in the art, e. g. magnesium carbonate, magnesium stearate, talc, sugar or lactose. Tablets, powders, cachets and capsules can be used as solid dosage forms suitable for oral administration. Examples of pharmaceutically acceptable carriers and methods of manufacture for various compositions may be found in A. Gennaro (ed.), Remington's Pharmaceutical Sciences, 18th Edition, (1990), Mack Publishing Co., Easton, PA.

Liquid form preparations include solutions, suspensions and emulsions. As an example may be mentioned water or water-propylene glycol solutions for parenteral injection or addition of sweeteners and opacifiers for oral solutions, suspensions and emulsions. Liquid form preparations may also include solutions for intranasal administration.

Aerosol preparations suitable for inhalation may include solutions and solids in powder form, which may be in combination with a pharmaceutical acceptable carrier, such as an inert compressed gas, e. g. nitrogen.

Also included are solid form preparations which are intended to be converted, shortly before use, to liquid form preparations for either oral or parenteral administration. Such liquid forms include solutions, suspensions and emulsions.

The compounds of the invention may also be deliverable transdermally. The transdermal compositions can take the form of creams, lotions, aerosols and/or emulsions and can be included in a transdermal patch of the matrix or reservoir type as are conventional in the art for this purpose.

Preferably the compound is administered orally.

Preferably, the pharmaceutical preparation is in a unit dosage form. In such form, the preparation is subdivided into suitably sized unit doses containing appropriate quantities of the active component, e. g., an effective amount to achieve the desired purpose.

The quantity of active compound in a unit dose of preparation may be varied or adjusted from about 1 mg to about 150 mg, preferably from about 1 mg to about 75 mg, more preferably from about 1 mg to about 50 mg, according to the particular application.

The actual dosage employed may be varied depending upon the requirements of the patient and the severity of the condition being treated. Determination of the proper dosage regimen for a particular situation is within the skill of the art. For convenience, the total daily dosage may be divided and administered in portions during the day as required.

The amount and frequency of administration of the compounds of the invention and/or the pharmaceutical acceptable salts thereof will be regulated according to the judgment of the attending clinician considering such factors as age, condition and size of the patient as well as severity of the symptoms being treated. A typical recommended daily dosage regimen for oral administration can range from about 1 mg/day to about 300 mg/day, preferably 1 mg/day to 75 mg/day, in two to four divided doses.

While the present has been described in conjunction with the specific embodiments set forth above, many alternatives, modifications and variations thereof will be apparent to those of ordinary skill in the art. All such alternatives, modifications and variations are intended to fall within the spirit and scope of the present invention.