CA2356841A1 - Substituted nitrogen and sulfur alicyclic compounds, including methods for synthesis thereof - Google Patents

Abstract

The present invention provides new methods for preparation of various compounds that comprise alicyclic groups with nitrogen or sulfur as ring members, including 2,5-disubstituted tetrahydrothiophenes, 2,5-disubstituted pyrrolidines, 2,6-disubstituted thianes, 2,6-disubstituted hexahydropyridine s, 2,7-disubstituted thiepanes, 2,7-disubstituted hexahydroazepines, 2,8- disubstituted thiocanes and 2,8-disubstituted octahydroazocines. The inventi on further provides novel compounds and pharmaceutical compositions and therapeutic methods that comprise such compounds and compositions.

Description

SUBSTITUTED NITROGEN AND SULFUR .ALICYCLIC COMPOUNDS, INCLUDING METHODS FOR SYNTHESIS THEREOF
The present application claims the benefit of U.S. provisional application number 60/091,710, filed July 3, 1998, which is incorporated herein by reference in its entirety.
BACKGROUND
1. Field of the Invention The present invention provides new methods for preparation of various heterocyclic ring compounds (sulfur or nitrogen as alicyclic ring members) including 2,5-disubstituted tetrahydrothiophenes, 2,5-disubstituted pyrrolidines, 2,6-disubstituted thianes, 2,6-disubstituted hexahydropyridines, 2,7-disubstituted thiepanes, 2,7-disubstituted hexahydroazepines, 2,8-disubstituted thiocanes and 2,8-disubstituted octahydroazocines. The invention further provides novel compounds and pharmaceutical compositions and therapeutic methods that comprise such compounds.
2. Background Leukotrienes are recognized potent Iocal mediators, playing a significant role in inflammatory and allegeric responses, including artivritis, asthma, psoriasis and thrombotic disease. Leukotrienes are produced by th.e oxidation of arachidonic acid by lipoxygenase. More particularly, arachidonic acid is oxidized by 5-Iipooxygenase to the hydroperoxide, 5-hydroperoxy-eicosatetraenoic acid (5-HPETE), that is converted to leukotriene A4, that in turn can be converted to Ieukotriene B4, C4, or D4.
The slow-reacting substance of anaphylaxis is now known to be a mixture of leukotrienes Ca, Da and E4, all of which are potent bronchoconstrictors.
Efforts have been made to identify receptor antagonists or inhibitors of leukotriene biosynthesis, to prevent or minimize pathogenic inflammatory responses WO 00/O1b70 PCTIUS99/I5050 mediated by leukotrienes. For example, European Patent Application Nos.
901171171:0 and 901170171.0 report indole, benzofuran, and benz~othiophene lipoxygenase inhibiting compounds: Various 2,5-disubstituted tetrahydrothio~phenes and pyrrolidines have exhibited significant biological activity, including as llipoxygenase inhibitors. See U.S.
Patent Nos. 5;703,093; 5,681,966; 5,648,486; 5,434,151; and 5,358,938.
While such compounds can be useful therapeutic agents, current methods for synthesis of at least some of the compounds require lfngthy routes, and reagents and protocols that are less preferred in larger scale operations, such as to produce kilogram quantities.
It thus would be desirable to have improved methods to prepare tetrahydrothiophenes and pyrrolidines, particularly ne;w syntheses that facilitate larger scale production of such compounds.
SUMMARY OF THE INVENTION
We have now found new methods for preparation of cyclic sulfur compounds including 2,S-disubstituted tetrahydrothiophenes, 2,6-disubstituted thianes, 2,7-disubstituted thiepanes, and 2,7-disubstituted thiocan~es. We also have found new methods for preparation of cyclic nitrogen compoundls including 2,S-disubstituted pyrrolidines, 2,6-disubstituted hexahydropyridine, 2,'7-disubstituted hexahydroazepine and 2;8-disubstituted octahydroazocine. These methods utilize reagents and synthetic protocols that facilitate large scale manufacture, and ;provide increased yields relative to prior approaches.
The methods of.the invention are suitable for preparation of a variety of cyclic nitrogen or sulfur-containing compounds (i:e., alicyc:lic compounds having a nitrogen or sulfur ring member), including compounds of the following Formula I:
(Cw~)n'~/ ([~~ )F~
,Z/\X/ I
Ar WO 00/01670 PCTlUS99115050 wherein X is S, S(O), S(O)2, N or substituted N (including N-alkyl and N-oxide);
Ar is optionally substituted carbocyclic aryl o:r optionally substituted heteroaryl;
each R', Y and Y' is independently hydrogen or a non-hydrogen substituent such as halogen, hydroxyl, optionally substituted alkyl preferably having from 1 to about 20 carbon atoms, optionally substituted alkenyl preferably having from 2 to about 20 carbon atoms, optionally substituted alkynyl preferably having from 2 to about 20 carbon atoms, optionally substituted alkoxy preferably having from 1 to about 20 carbon atoms, optionally substituted alkylthio preferably having from 1 to about 20 carbon atoms, optionally substituted alkylsulfinyl preferably having; from 1 to about 20 carbon atoms, optionally substituted alkylsulfonyl preferably having; from 1 to about 20 carbon atoms, optionally substituted aminoalkyl preferably having i:rom 1 to about 20 carbon atoms, optionally substituted alkanoyl preferably having from 1 to about 20 carbon atoms, optionally substituted carbocyclic aryl having at Ieast about 6 ring carbons, or substituted or unsubstituted aralkyl having at least about 6 ring carbons, and the like;
Z is a chemical bond, optionally substituted alkylene, optionally substituted alkenylene, optionally substituted alkynylene, optionally substituted heteroalkylene, optionally substituted heteroalkenylene, optionally substituted heteroalkynylene, or a hetero atom such as O, S, S{O), S{O)2, or NRt wherein R' is the same as defined immediately above;
n is an integer from 1 to 11, and preferably is 1 to 9, more preferably 1 to 7;
p is an integer from 0 (where the a and (3 ring positions are fully hydrogen-substituted) to 4; and pharmaceutically acceptable salts thereof.
T'he methods of the invention are particularly suitable for synthesis of substituted 5-membered ring heterocycles, including cornpound~s of the following Formula II:

R~ R'' II
r/ Z ~. Y /W
n ~ X ~ )m wherein Ar and X are each the same as defined in Formula I above;
m is 0 or l; n is 1-6;
W is -AN{OM)C(O)N(R3)R4, -N(OM)C(O)N(R3)R4, -AN(R3)C{O)N(OM}R4, -N(R3)C{O)N(OM)R4, -AN(OM)C(O)R4, -N(OM)C(O)R4, -AC(O)N{OM)R4, -C(O)N(OM)R~, or -C(O)NHA; and A is lower alkyl,, lower alkenyl, lower alkynyl, alkylaryi or arylalkyl, wherein one or more carbons optionally can be replaced by N, O or S, however -Y-A-, -A-, or -AW- should not include two adjacent heteroatoms;
M is hydrogen, a pharmaceutically acceptablc; cation or a metabolically cleavable leaving group;
Y is O, S, S(O), S(O)z, NR3 or CHRS;
Z 1S O, S, S(O), S(O)2, OT NR3;
Rl and R2 are each independently hydrogen, lower alkyl, C3_$ cycloalkyl, halolower alkyl, halo or -COOH;
R3 and R4 are independently hydrogen, alkyl, alkenyi, alkynyl, aryl, arylalkyl, Ci_ 6alkoxy-C1_,oaikyl, Cm alkylthio-Cl_1o alkyl, heteroaryl, or heteroarylalkyl;
RS is hydrogen, lower alkyl, lower alkenyl, lower alkynyl, arylalkyl; alkaryl, -AN(OM)C(O)N(R3)R4, -AN(R3)C(O)N{OM)R4, -AN(OM)C(O)R4, -AC(O)N(OM)R4, -AS(O)XR3, -AS(O)XCHZC(O)R3, -AS(O)XCHZCH(O~H)R3, or-AC(O}NHR3, wherein x is 0-2; and pharmaceutically acceptable of such compounds.
Preferred compounds of Formula II include compounds where Ar is substituted by halo (including but not limited to fluoro}, Iower alkoxy (including methoxy), lower aryloxy (including phenoxy), W (as defined above in Formula II), cyano, or R3 (as -S_ defined above in Formula II). Those substituents are also preferred Ar group substituents for compounds of other formulae disclosed herein. Specifically suitable Ar groups for the above Formula II as well as the other formulae disclosed herein include phenyl, trimethoxyphenyl, dimethoxyphenyl, fluorophenyl (specifically 4-fluorophenyl), difluorophenyl, pyridyl, dimethoxypyridyl, quinolinyl, furyl, imidazolyl, and thienyl.
Additionally, in Formula II as well as other formulae disclosed herein, W
suitably is lower alkyl, such as a branched alkyl group, e.g. -{CFIZ)"C(alkyl)H-, wherein n is 1-5, and specifically -(CHZ)2C(CH3)H-, or lower alkynyl such as of the formula -C---C-CH(alkyl)-, including -C---C-CH{CH3)-.
In some instances, particularly for therapeutic applications, a selected stereoisomer of a compound of the above formulae m.ay be preferred.
Accordingly, methods of the invention include preparation of enanl;iomerically enriched compounds of Formula I.
In a first aspect, synthetic methods of the invention provide thio ring compounds and comprise reaction of an epoxyether substituted aryl compound with a thiolating reagent to form a thioepoxy ether. (As used herein, the term "aryl" as used herein refers to both carbocyclic aryl and hetoaromatic or heteroaryl groups, which terms in turn are further discussed below.) That thioepoxy ether is then reacted with an active methylene compound to form a thiolactone, preferably a 'y-thiol<~ctone. The active methylene compound can be a variety of agents. Diethyl and dvnethyl malonate are generally preferred, which provide an ethyl or methyl ester as a. thiolactone ring substituent. That ester group is then removed (particularly by hydrolysis and decarboxylation), and the lactone suitably reduced to a hydroxy(thioalicyclic)-aryl ether compound, particularly a hydroxy(tetrahydrothiophene)-aryl ether.
The hydroxy(tetrahydrothiophene)-aryl ether compound can be further functionalized as desired, particularly by activating the hydroxyl substituent of the WO 00/01b70 PCT/US99/15050 tetrahydrothiophene followed by substitution of the corresponding position of the thioalicyclic ring such as by a 1-alkyne reagent. Also, rather than directly activating the hydroxyl moiety, that group can be replaced with a halide, and the halide-substituted tetrahydrothiophene reacted with a benzylsulfonic acid reagent.
It also has been found that methods of the invention enable such substitution of the tetrahydrothiophene to proceed with extremely hil;h stereospecificity, e.g, at Ieast greater than about fi0 mole percent of one stereoisomE;r than the other, more typically greater than about 70 or 75 mole percent of one stereoisomer than the other isomer.
Recrystallization of the produced enantiomerically enriched mixture has provided very high optical parities, e.g. about 95 mole %, 97 mole °io or even 99 mole % or more of the single stereoisomer.
In a further aspect, synthetic methods of the invention provide nitrogen ring compounds and preferably comprise reaction of a sulfbnyl substituted hydroxyalkylaryl ether compound, in which the sulfonyl group is enantiomerically enhanced, either in the R or S configuration, with a reagent that will displace the sulfonyl with an azido group with inversion of configuration to form an azidohydroxyaryl ether. That azidahydroxy aryl ether is then oxidized to a 2,3-epoxide, preferably an optically active epoxide such as a (2S,3S) epoxide. That azidohydroxyaryl ether is further reacted with base and then triphenylphosphine to form a pyrrolidine compound which is further reacted to achieve carbon chain extension to yield an alkynylhydroxy arylether substituted pyrrolidine. The hydroxy pyrrolidine can be further functionalized as desired.
These methods surprisingly can proceed as a single step without isolation of intermediates to provide nitrogen ring compounds that have varying ring size as desired.
These methods are suitable for preparation of nitrogen ring compounds having from 5 to 12 or more ring members, and are particularly useful for synthesis of nitrogen ring compounds having from 5 to 8 or 9 ring members.

WO 00/01670 1'CT/US99/15050 More particularly, larger ring alkynyl-substituted compounds are readily provided through corresponding chain homologation of the epoxy reagent, i.e. by interposing additional "spacing" or alkylene chain members between the reagent's activated positions.
Thus, for example, to prepare an alkynyl-substrituted tetrahydopyridine, a reagent is employed that has at least a seven-carbon alkyl or aikylene chain that is activated at the 1- and 7- carbon positions e.g. by substitution by suitable leaving groups (such as those mentioned above), and the 2- and 3- positions of the chain form an epoxide ring. That compound is reacted with base to provide an alkynyl-:>ubstituted tetrahydropyridene.
Similarly, to prepare an alkynyl-substituted he:Kahydroazepine, a reagent is employed that has at least a seven-carbon alkyl or alkylene chain activated (particularly by leaving groups at the 1- and 8-carbon positions, amd the 2- and 3-postion of the chain form an epoxide ring. To prepare an alkynyl-substituted octahydroazocines compound, a reagent is employed that has at Least eight-carbon alkyl of alkylene chain activated at the 1- and 9-carbon positions, with the 2- and 3-positions of the chain forming an epoxide ring. Treatment of those respective reagents with appropriate base provides alkynyl-substituted hexahydroazepine and octahydroazocines compound.
In a yet further aspect of the invention, preparative methods are provided that include multiple reactions that surprisingly can proceed as a single step without isolation of intermediates to provide sulfur ring compounds that have varying ring size as desired.
These methods are suitable for preparation of sulfur ring compounds having from 5 to 12 or more ring members, and are particularly useful for synthesis of sulfur ring compounds having from 5 to 8 or 9 ring members.

-g_ Moreover, it has been surprisingly found that the one step procedure is enantivselective. Hence, if the starting reagent (a 2,3-thioepoxide) is optically active, the resulting substituted thio-ring compound also will be optically active.
More particularly, in this aspect of the invention the methods include formation, in a single step, of an alkynyl-substituted thio-ring compound. For preparation of an alkynyl-tetrahydrothiophene, a compound is reacted tihat has at least a six-carbon alkyl or alklyene chain that is activated at the 1- and 6-carbon positions such as by substitution by suitable leaving groups, and 2- and 3-carbon positions of the chain form a thioepoxide ring. The leaving groups of the 1- and 6-positions may be e.g. halo, such as chloro or bromo; or an ester, such as an alkyl or aryl sulfonic ester. Preferably, the 1-position is halo-substituted, particularly bromo-, iodo- or chloro-substituted, and the 6-position is substituted by an ester such as by a benzylsulfonyl group. That compound is reacted with a molar excess of a strong base such as an alkyllithium reagent that affords an alkynyl-substituted tetrahydrothiophene in a single step.
Larger ring aikynyl-substituted thio-ring compounds are readily provided through corresponding chain hornologation of the thioepoxy reagent, i.e. by interposing additional "spacing" or alkylene chain members between the reagent's activated positions.
Thus, for example, to prepare an alkynyl-substituted thiane, a reagent is employed that has at least a seven-carbon alkyl or alkylene chain that is activated at the l- and 7-caxbon positions e.g. by substitution by suitable leaving; groups (such as those mentioned above), and the 2- and 3- positions of the chain form a thioepoxide ring. That compound is reacted with base to provide an alkynyl-substituted thiane.
Similarly, to prepare an alkynyl-substituted thiepane, a reagent is employed that has at least a seven-carbon alkyl or alkylene chain activated (particularly by Ieawing groups) at the 1- and 8-carbon positions, and the 2- and 3-postion of the chain form a _g_ thioepoxide ring. To prepare an alkynyl-substituted thiocane compound, a reagent is employed that has at least eight-carbon alkyl of alkylene chain activated at the 1- and 9-carbon positions, with the 2- and 3-positions of the chain forming a thioepoxide ring.
Treatment of those respective reagents with appropriate base provides alkynyl-substituted thiane and thiocane compounds.
The invention further provides additional methods for synthesis of nitrogen ring compounds, which do not require use of an azide reagent. These methods include cyclization to provide a nitrogen ring compound, pre:Ferably having one or mare activated positions in the ring to facilitate functionalization of i:he formed heterocycle. For example, a ring carbon can have a carbonyl group as a direct ring member, or as a pendant group (e.g. pyrrolidinone, and/or pyrrolidino:ne with an acyl or other alkanoyl ring substituent), hydroxyl, haloalkyl as a pendant group, and the like.
Further provided are new routes to substituted hydroxy areas. In preferred aspects, these routes include reaction of a protected hydroxyurea (e.g., a compound of the formula NHzC(O)NHOR, where R is a hydroxy protecting group such as para-methoxybenzyl-) with a substituted alcohol, preferably in the presence of suitable dehydrating agents) to provide an amino ester, which is treated with ammonia and a Lewis acid to provide a hydroxy urea.
As mentioned above, compounds produced by the methods of the invention will be useful as pharmaceutical agents, including to treat disorders ar diseases mediated by S-lipoxygenase such as immune, allegeric and cardiovascular disorders and diseases, e.g.
general inflammation, hypertension, skeletal-muscular disorders, osteoarthritis, gout, asthma, lung edema, adult respiratory distress syndrome, pain, aggregation of platelets, shock, rheumatoid arthritis, psoriatic arthritis, psoriasis, autoimmune uveitis, allergic encephalomyelitis, systemic lupus erythematosis, acute; necrotizing hemmorrhagic encephalopathy, idiopathic thrombocytopenia, polychondritis, chronic active hepatitis, idiopathic sprue, Crohn's disease, Graves ophthalmop~athy, primary biliary cirrhosis, uveitis posterior, interstitial lung fibrosis, allergic asth~rna and inappropriate allergic responses to environmental stimuli.
S In other aspects, the invention provides new compounds as well as pharmaceutical compositions that comprise one or more of such compounds preferably with a pharmaceutically acceptable carrier. More particularly, compounds of the invention include those of Formula I above, where n is 2 or greater (i.e. compounds with alicyclic rings that have 6 or more ring members), which includes compounds of Formulae III, IIIa, IV, IVa, V, Va; as those formulae are defined below. The invention further provides methods for treatment and/or prophylaxis of various disorders and diseases including those disclosed above such as immune, allegoric and c~~rdiovascular disorders and diseases , the methods in general comprising administering an effective amount of one or mare compounds of Formula I above, where n is 2 or greater, to a subject, such as a mammal particularly a primate such as a human, that is, suffering from or susceptible to such a disorder or disease.
Compounds produced by the methods of the invention are useful as synthetic intermediates to prepare other compounds that will be useful for therapeutic applications.
Other aspects of the invention are disclosed infra.
DETAILED DESCRIPTION OF THE INVENTION
As discussed above, the invention provides methods that are particularly suitable for synthesis of compounds of the following Formula I:
~C~ ~n~/ ~R1 )P
I
Ar wherein Ar, Z, Y, Y', R', n and p are as defined above.
As discussed above, preferred compounds that. can be produced by the methods of the invention include substituted tetrahydrothiophenes, pyrrolidines, thianes, hexahydropyridines, thiepanes, hexahydroazepines, th.iocanes and octahydroazocines.
More particularly, preferred compounds produced by the methods of the invention include substituted thianes and hexahydropyridines including substituted thianes and hexahydropyridines of the following Formula III:
/(R~)q III
Ar-Z/\ X
wherein Ar, X, Z and RI are each the same as defined .above for Formula I, and q is an integer of from 0 to 9, and preferably q is 1, 2, 3 or 4; ;end pharmaceutically acceptable salts thereof.
Generally preferred are 2,6-disubstituted thianes and hexa,hydropyridines, such as compounds of the following Formula IIIa;
(R~)q, IIIa W
Ar-Z X (Y)m wherein Ar, X, Z, Y, W, RI and m are each the same as defined for Formula II
above, and q' is an integer of from 0 to 6 , and preferably q' is 0, I, 2, 3 or 4; and pharmaceutically acceptable salts thereof.
The methods are also particularly useful for preparations of substituted thiepanes and hexahydroazepines including compounds of the following Formula IV:
/ (R~)r IV
/~ X
Ar-Z
wherein Ar, X, Z and R' are each the same as defined above for Formula I, and r is an integer of from 0 to I I, and preferable r is I, 2, 3 .or 4; and pharmaceutically acceptable salts thereof.
Generally preferred are 2,7-disubstituted thiepa~zes and hexahydroazepines such as compounds of the following Formula IVa:
/(R1)r IVa _ .
Ar-Z
X (Y)rr~
wherein Ar, X, Z, Y, W, R' and m are each the same as def red for Formula II
above, and r' is an integer of from 0 to 10, and preferably r' is 0, I, 2, 3 or 4; and pharmaceutically acceptable salts thereof.

Still fmrther, methods of the invention can be especially useful for synthesis of substituted thiocanes and octahydroazocines, such as compounds of the following Formula V:
/ (R')s ,,r Ar-z~ x wherein Ar, X; Z and R' are each the same as defined above for Formula I, and s is an integer of from 0 to 13, and preferable s is 1, 2, 3 or 4; and pharmaceutically acceptable salts thereof.
Generally preferred are 2,8~disubstituted thioca~zes and octahydroazocines such as compounds of the following Formula Va:
j R')S
Va Ar-Z x .W
~Y)m vcvherein Ar, X, Z, Y, W, R' and m are each the same as defined for Formula II
above, and s is an integer of from 0 to 10, and preferably s is 0, 1, 2, 3 or 4; and pharmaceutically acceptable salts thereof.
The term alkyl, as used herein, unless otherwise specif ed, refers to a saturated straight, branched, or cyclic hydrocarbon preferably of C, to Clo, and specifically includes methyl, ethyl, propyl, isopropyl, butyl, isobutyl, t-butyl, pentyl, cyclopentyl, isopentyl, neopentyl, hexyl, isohexyl, cyclohexyl, 3-meth.ylpentyl, 2,2-dimethylbutyl, and 2,3-dimethylbutyl. The alkyl group can be optionally substituted with any appropriate group, including but not limited to R3 or one or more moieties selected from the group consisting of halo, hydroxyh amino, alkylamino, aryl;amino, alkoxy, aryloxy, nitro, cyano, sulfonic acid, sulfate, phosphonic acid, phosphate, or phosphonate, either unprotected, or protected as necessary, as known to those skilled in the art, for example, as disclosed in Greene et al., "Protective Groups in Organic Synthesis", John Wiley and Sons, Second Edition, Z 991.
The term halo, as used herein, refers to chlora" fluoro, iodo, or bromo.
The term lower alkyl, as used herein, and unless otherwise specified, refers to a C, to C6 saturated straight, branched, or cyclic (in the case of CS_6) hydrocarbon, and specif cally includes methyl, ethyl, propyl, isopropyl, butyl, isobutyl, t-butyl, pentyl, cyclopentyl, isopentyl, neopentyl, hexyl, isohexyl, cyc;lohexyl, 3-methylpentyl, 2,2-dimethylbutyl, and 2,3-dimethylbutyl, optionally substituted as described above for the alkyl groups.
The term alkenyl, as referred to herein, and uniless otherwise specified, refers to a straight, branched, or cyclic (in the case of CS_6) hydrocarbon preferably of C2 to Clo with at least one double bond, optionally substituted as described above.
The term lower alkenyl, as referred to herein, and unless otherwise specified, refers to an alkenyl group of C2 to C6, and specifically includes vinyl and allyl.
The term Iower alkylamino refers to an amino group that has one or two lower alkyl substituents.
The term allcynyl, as referred to herein, and unless otherwise specified, refers to preferably CZ to C,o straight or branched hydrocarbon with at least one triple bond, optionally substituted as described above. The term lower alkynyl, as referred to herein, and unless otherwise specified, refers to a CZ to C6 allcynyl group, specifically including acetylenyl, propynyl, and -C---C-CH(alkyl)-, including; -C=C-CH{CH3)-.
The term carbocyclic aryl, as used herein, and unless otherwise specified, refers to non-hetero aromatic groups that have 1 to 3 separate or fused rings and 6 to about 18 carbon ring atoms and include e.g. phenyl, napthyl, biiphenyl, phenanthryl, anthracyl, and the like. The carbocyclic aryl group can be optionally substituted with any suitable group, including but not limited to one or moieties sellected from the group consisting of halo, hydroxyl, amino, alkylamino, arylamino, alkoxy, aryloxy, nitro, cyano, sulfonic acid, sulfate, phosphonic acid, phosphate, or phospho:nate, either unprotected, or protected as necessary, as known to those skilled in the art, for example, as taught in Greene et al., "Protective Groups in Organic Synthesis", John Wiley and Sons, Second Edition, 1991, and preferably with halo {including bust not limited to fluoro), lower alkoxy (including methoxy), lower aryloxy (including; phenoxy}, W, cyano, or R3.
The term haloalkyl, haloalkenyl, or haloalkynwl refers to alkyl, alkenyl, or alkynyl group in which at least one of the hydrogens in the group has been replaced with a halogen atom.
The term heteroaryl, heterocycle or heteroaronnatic, as used herein, refers to an aromatic moiety that inchzdes at least one sulfur, oxygen, or nitrogen in the aromatic ring, which can optionally be substituted as described above for the aryl groups.
Non-limiting examples are pyrryl, furyl, pyridyl, 1,2,4-thiadiazolyl, pyrimidyl, thienyl, isothiazolyl, imidazolyl, tetrazolyl, pyrazinyl, pyrimidyl, quinolyl, isoquinolyl, benzofuran, benzothienyl, isobenzofuryl, pyrazolyl, indolyl, purin~,~l, carbazolyl, benzimidazolyl, and isoxazolyl. Suitable heteroaxomatic or heteroaryl groups will have 1 to 3 rings, 3 to 8 ring members in each ring and from 1 to 3 hetero atoms {N, O or S).

The term arylalkyl refers to a carbocyclic aryl group with an alkyl substituent.
The term alkylaryl refers to an alkyl group that has a carbocyclic aryl substituent.
The term organic or inorganic anion refers to .an organic or inorganic moiety that carries a negative charge and can be used as the negative portion of a salt.
The term "pharmaceutically acceptable canon" refers to an organic or inorganic moiety that carries a positive charge and that can be administered in association with a pharmaceutical agent, for example, as a counter catio;n. in a salt.
Pharmaceutically acceptable canons are known to those of skill in the art, and include but are not limited to sodium, potassium, and quaternary amine.
The term "metabolically cleavable leaving group" refers to a moiety that can be cleaved in vivo from the molecule to which it is attac3hed, and includes but it not limited to an organic or inorganic anion, a pharmaceutically acceptable canon, acryl (for example (alkyl)C{O), including acetyl, propionyl, and butyryl), alkyl, phosphate, sulfate and sulfonate.
Alkylene and heteroalkylene groups typically will have about 1 to about 8 atoms in the chain, more typically 1 to about 6 atoms in the :linkage. Alkenylene, heteroalkenylene, alkynylene and heteroalkynylene groups typically will have about 2 to about 8 atoms in the chain, more typically 2 to about 6 atoms in the linkage, and one or more unsaturated carbon-carbon bonds, typically one or two unsaturated carbon-carbon 2S bonds. A heteroalkylene, heteroalkenylene or heteroa~lkynylene group will have at least one hetero atom (N, O or S) as a divalent chain member.
The term alkanoyl refers to groups that in general formulae generally will have from 1 to about 16 carbon atoms and at least one carbonyl {C=O) moiety, more typically from 1 to about 8 carbon atoms, still more typically 1 to about 4-6 carbon atoms. The term alkylthio generally refers to moieties having onf; or more thioether linkages and preferably from 1 to about 12 carbon atoms, more prf;ferably from 1 to about 6 carbon atoms. The term alkylsulfinyl generally refers to rnoiieties having one or more sulfinyl (S(O)) linkages and preferably from 1 to about 12 ca~:bon atoms, more preferably from 1 to about 6 carbon atoms. The term alkylsulfonyl generally refers to moieties having one or more sulfonyl (S(O)2) linkages and preferably from I to about 12 carbon atoms, more preferably from 1 to about 6 carbon atoms. The term. aminoalkyl generally refers to groups having one or more N atoms and from 1 to about 12 carbon atoms, preferably from 1 to about 6 carbon atoms.
As discussed above, various substituent grout>s of the above formulae may be optionally substituted. Suitable groups that may be present on such a "substituted" group include e.g. halogen such as fluoro, chloro, bromo and iodo; cyano; hydroxyl;
vitro;
azido; sulfhydryl; alkanoyl e.g. C1~ alkanoyl group such as acetyl and the like;
carboxarnido; alkyl groups including those groups having 1 to about 12 carbon atoms, preferably from 1 to about 6 carbon atoms; alkenyl and alkynyl groups including groups having one or more unsaturated linkages and from 2 to about 12 carbon atoms, preferably from 2 to about 6 carbon atoms; alkoxy groups having one or more oxygen linkages and from I to about 12 carbon atoms, preferably 1 to about 6 carbon atoms; aryloxy such as phenoxy; alkylthio groups including those moieties having one or more thioether linkages and from 1 to about 12 carbon atoms, preferably from I to about 6 carbon atoms;
alkylsulfinyl groups including those moieties having one or more sulfinyl linkages and from 1 to about 12 carbon atoms, preferably from 1 t~o about 6 carbon atoms;
alkylsulfonyl groups including those moieties having one or more sulfonyl linkages and from 1 to about 12 carbon atoms, preferably from I Lo about 6 carbon atoms;
aminoalkyl groups such as groups having one or more N atoms and from 1 to about I2 carbon atoms, preferably from 1 to about 6 carbon atoms; carbocycl.ic aryl having b or more carbons, particularly phenyl; aryloxy such as phenoxy; aralkyl. having 1 to 3 separate or fused WO 00/01b70 PCTIUS99115050 rings and from 6 to about 18 carbon ring atoms, with benzyl being a preferred group;
aralkoxy having 1 to 3 separate or fused rings and from 6 to about 18 carbon ring atoms, with O-benzyl being a preferred group; or a heteroaromatic or heteroalicyclic group having 1 to 3 separate or fused rings with 3 to about 8 members per ring and one or more N, O or S atoms, e.g. cournarinyl, guinolinyl, pyridyl, pyrazinyl, pyrimidyl, fiiryl, pyrrolyl, thienyl, thiazolyl, oxazolyl, imidazolyl, indolyl, benzofuranyl, benzothiazolyl;
tetrahydrofuranyl, tetrahydropyranyl, piperidinyl, mo:rpholino and pyrrolidinyl: A
"substituted" group of a compound of the invention prepared by a method of the invention may be substituted at one or more available positions, typically 1 to about 3 positions, by one or more suitable groups such as those listed immediately above.
Particularly preferred preparative methods of l;he invention are exemplified in the following Schemes I through IV. Fox purposes of exemplification only, particularly preferred compounds and substituents are depicted in the Schemes, and it will be understood that a variety of other compounds can be employed in a similar manner as described below with respect to the exemplified compounds. Far instance, the carbocyclic aryl group of 4-fluorophenoI is depicted tlyroughout the Schemes, although a wide variety of other aryl groups could be employed in the same or similar manner as fluorophenyl. It should also be understood that references to "aryl" with respect to the Schemes includes those groups specified for the substituent Ar in Formula I
above and thus encompasses carbocyclic aryl such as phenyl and the like as well as heteroaryl groups. Additionally while compounds in the belo~av Scheme generally depict substitution at the ring carbons a to the ring hetero atom, other ring positions can be readily substituted e.g. by using appropriately substituted starting reagents.
Also, while various stereoisomers are depicted in the below Schemes, corresponding other stereoisomers can be readily obtained by use of the corresponding optically active reagents or enantiomertic selective reactions or separations.

_ 19_ cheme T
s _ ii O H2N_C_NH2 F ~ / Q~ _~ F - ~ $ CH2(COOEt)2 MeOH, RT ~ ~ ~
n-BuLi, reflux Q02~t DMA
F ~ , p/~ MgCi2.6H20 F Q
H O
g H O
_ 4 DIBAL-H F
H OH
Scheme I exemplifies a preferred preparative method of the invention wherein the enantiomericaliy pure epoxide _1 and thiourea react to form the cyclic sulfide (thiirane) 2 -maintaining the R configuration. Preferred epoxides are those that are enantiomerically enriched with R stereochemistry at the C2 carbon, such as the (R) glycidyl fluorophenyl 1 shown above. The preferred epoxide 1 and thiourea are reacted in a suitable solvent such as methanol for a time and temperature sufficient for reaction completion to provide thioaryl ether 2. See Example 1, Part 1 below for exemplary reaction conditions. The compound I and thiourea typically react in a suitable solvent, e.g. methanol, ethanol and the Like. Enantiomerically enriched epoxides suitable for conversion to a suitable (R) thioglycidyl ether are commercially available or can be headily prepared by known procedures. See, for instance, U.S. Patents Nos. 4,946,9'74 and 5,332,843 to Sharpless et al, for preparation of optically active derivatives of glyci~dol.

The thioepoxyaryl ether 2 then is reacted with an active methylene group, such as a diethyl or dimethyl malonate to provide thiobutyrol,actone 3. The exocyclic ester of 3 is then suitably cleaved, e.g. with reaction with magnesium chloride hexahydrate, to provide the corresponding carbonyl thiolactone ether 4. See Example 1, Part 3 which follows for an exemplary reaction conditions. The thiolactone 4_ is then reduced to the hydroxy-tetrahydrothiophene 5. Suitable reducing agents include e.g. DIBAL-H
and the like. See Example 1, Part 4, which follows.
Scheme II
PhSOZH - HC=CCH2CH20THP
F \ / '--.". F O~''~~.
CaCI \ /
H OH 2 ~ ~ iPrM Br, ZnBr r H S02Ph g 2. e~ux _5 8 OTHP
a F \ / O~°~' ~ t "/a HCI/ MeOH F 0,,,~~ / OH
H S H .'_'' ~~ S

Schemes II and III below exemplify further preferred methods of the invention for synthesis of alkynyl-substituted tetrahydrothiophene ethers. More specifically, the hydroxy substituent of tetrahydrothiophene 5_ is preferably activated, e.g. as an ether, tosyl, mesyl or benzene sulfinic acid derivative. Thus, a;s depicted in Scheme II, the hydroxy moiety of 5_ can be reacted with a suitable sulfin.ic or silyl reagent, e.g. to form the benzenesulfonyl derivative _6, or with reagents for sil;ylation, e.g. a silyl chloride such as TMSCI. See Example I, Part 5 and Example 2, Part 1 for suitable reaction conditions.

The activated aryltetrahydrothiophene ether fi can then react to provide the alkynyl-substituted tetrahydrothiophene 7 by treatment with a 1-alkyne in the presence of a strong base such an alkyllithium. Preferably the al)kyne reagent contains a protected hydroxy moiety such as an ether, e.g. a methoxyetho:xymethyl, methoxymethyl or tetrahydropyranyl ether 7 as depicted in the above Scheme. The hydroxy group can be readily deprotected after coupling of the alkynyl reagent to the tetrahydrothiophene ring, e.g. by treatment with dilute acid to yield the corresponding alcohol 8.
Typically, the alkyne reagent will contain a primary or secondary hyrdroxy moiety. See Example 1, Part 7 for suitable reaction conditions.
Scheme III
Purification _ OH ~PMB
$ bycrystallization F ' / O/~.~%~~ NH-C02Ph H S H PPh3, DEAD

OPMB
N'COOPh i..~..
O H S N , OH
H ~ i 10 _ F ~ / O~"'~~.. j N'CONH2 H S _ ,~ ~ H
As indicated in Scheme III, the enantiomericall.y enriched hydroxy tetrahydrothiophene _9 can be obtained by purif cation lby crystallization of the isomeric mixture 8. The hydroxy tetrahydrothiophene 9 can be further- functionalized as desired by amidation using a N,O-substituted hydroxylamine such as N-phenoxycarbonyl-O
p-methoxybenzyl-hydroxylamine in the presence of dehydrating reagents such as, triphenylphosphine and diethylazodicarboxylate, followed by treatment of the resulting intermediate 10 with ammonia to yield the hydroxylamine tetrahydrothiophene I
I. See Example 1, Part 9 and Part IO for optimal reaction conditions.
Schemes IV-VI below exemplify a further aspect of the invention that provides methods for synthesis of larger sulfur heterocyclic compounds such as thianes, thiepanes and thiocanes and an alternative method of obtaining substituted tetrahydrothiophenes.
This is accomplished by utilizing analogs of compound 1 S which have an extended alkyl chain of the appropriate length.
Scheme IV
Mg, CuCN
F O~ sr~/ F / ~~O OH
/

F ~ ~ O t7S02Ph OS02Ph oIBAL=H / ~ OS02Ph F~O / OEt --'~ F-"~'-O / OH

As shown in scheme IV, intermediate 15 is suitably obtained by reaction of arylepoxy ether l and the appropriate haloalkene utilizing Grignard conditions to obtain the alkene I2. Thus, to synthesize homoallylic alcohol 15, the arylepoxy ether _i and a haloalkene such as 4-bromo-1-butene, react in the presence of magnesium and a suitable catalyst system such as iodine and cuprous cyanide to provide the arylalkene ether 12.
The secondary hydroxyl group of 12 is suitably protected, e.g. preferably as a sulfonic ester to provide the terminal alkene 13. Alkene 13 is :further extended and fuctionalized by condensation to form the a,(3-unsaturated ester 14. The ester 14 is then reduced to an alcohol, typically by treatment with a strong base such as DIBAL-H to obtain intermediate homo allylic alcohol 15.
Scheme V
OS02Ph / \ OS02Ph O. H
F ~ ~ O / OH ----~ F-~0 ..,,~iOH
1( H
OS02Ph F ~ ~ O S ~.,t,OH

OS02Ph F ~ ~ O S .,, jCl ---~. \ Ow~~' H H

OOH
--.~ \ Ow.~,,.
H H
F ~

As shown in Scheme V, the homoallylic alcohol 15 is then enantioselectively oxidized to provide the epoxy group of 16. Scheme 'V shows the Sharpless asymmetric epoxidation of 15 to give the corresponding (2S,3S, tiS) arylether epoxide I6.
Other procedures may be used where in an optically active :Iigand or catalyst is used to promote enanteoselectivity of the oxidation of 15. The racemi.c epoxides may also be resolved, e.g. by chromatography using an optically active packing material. The arylether epoxide 16 is then converted to the corresponding thiirane I 7 by reaction with thiourea or phosphorous pentoxide. The Cl alcohol of compound 17 is then halogenated to provide the {2S,3S,6S) thiirane 18 where suitable halogens include chlorine and bromine.
Scheme V illustrates halogenation by in situ activation of the hydroxyl group to a rnesylate e.g. methane suIfonyl chloride with a nitrogen base such as pyridine or triethyl amine and can include catalysis by dimethylaminopyriidine. Subsequent substitution may be accomplished using the appropriate lithium salt e.g., lithium chloride or lithium bromide, dissolved in an appropriate solvent such as d;imethylfonnamide or THF. The arylether thiirane 17 could also be directly halogenatec! using an appropriate reagent.
Dehalogenation with concomitant rearrangeme~zt of compound 18 to the (3R) hydroxy alkyne 19 is accomplished by reaction with an; appropriate lithium base, such as lithium diisopropyl amine, in a suitable solvent e.g. TH:F. The alkyne 19 is extended by two carbons units by treatment with butyllithium in the presence of boron trifluoride diethyl etherate followed by ethylene oxide to yield the trans-tetrahydrothiophine _8.

Scheme VI
Mg, CuCN
,e0 _Br~'\~ OH
\ _ 21 ----..
F / \ OS02Ph S O
.,o\ .--,~, \ w.~w' S
CI ~ H _ 22 H ~ F ~ 23 This methodology may be used to synthesize tetrahydrothiophenes by reacting 1 and an appropriate alkene such as 4-bromo-I-butyene to obtain the necessary terminal alkene I2 for synthesis of tetrahydrothiophenes. Similarly preparation of key intermediates of thianes are obtained by reaction of 1 and an appropriate alkene such as 5-bromo-1-pentene, thiepanes by reaction of 1 and an appropriate alkene such as 6-bromo-I-hexene and thiocanes by reaction of 1 and an appropriate alkene such as 7-bromo-I-heptene. The resulting terminal alkenes of each of the above reactions are converted to the appropriate thiirane analogs of 22 and iEurther reacted to obtain the appropriate hydroxyalkynyl-sulfur heterocyclic compounds analogous to 23. The I S hydroxy alkynyl analogs of 23 are then converted to the appropriate substituted hydroxy areas by methods described above.

In a further aspect, routes to substituted hydroxy areas are provided. More particularly, a protected hydroxy urea (e.g., a compound of the formula NH2C(O)NHOR, where R is a hydroxy protecting group such as an alkyl, aryl or preferably aryalkyl ether such as an ether of an optionally substituted (phenyl)OCHZ-) is reacted with a substituted alcohol compound, such as analogues of ~ of Scheme III, preferably in the presence of suitable dehydrating agents) such as triphenyl phosphine and diethylazodicarboxylate (DEAD), to provide an amino ester, i.e. a moiety ofth.e formula-NRC(O)OR~R
where R
is as defined immediately above and R' is a non-hydrogen group such as aryl, particularly phenyl, alkyl, e.g. Cl_io alkyl, etc. That amino ester is then treated with ammonia and a Lewis acid such as boron trifluoride etherate and the like to provide a hydroxy urea. In a preferred method of hydroxy urea formation, para-methoxybenzyl- is utilized as the hydroxy protection group R.
In a second preferred aspect, synthetic methods of the invention include preparation of compounds useful as intermediates to prepare pyrrolidine compounds of the above Formula II (X being nitrogen in Formula II).

Scheme VII
oso2Pr, N

O / OH LiN3, DMF O / OH
w F / 15 F ' Sharpless Asymmetric Ns ~ H Ns ~ H
Epoxidation O ~.,, OH O ~.,, CI
1. MsCI, TF~1 ~
--..
26 H 2. Lift, DMF 1 / 27 H
F F

LDA (~ ~ Ph3P ' O\ H' w H H
1 , off ~ , OH
H_ /' n-BuLi, 8F3:Et20 O\. ''~~N ~~~H
~ , / H

Scheme VII exemplifies a preferred preparative; method of the invention wherein the enantiomerically enriched (6R) sufonic ester of the homo allylic alcohol 15 is transformed to an azide 25 with inversion to the S configuration at the C6 carbon.
Typically suifonic ester 15 and a suitable reagent such .as lithium azide react in a solvent such as dimethyl forrnarnide to yield the (6S) azide 25 The (6S) azido alcohol ~5 is then 10 enantioseiectively oxidized to provide the epoxy group of 26. Scheme VII
shows the Sharpless asymmetric epoxidation of 25 to give the corresponding {2S,3S, 6S) epoxyazide 26. Other procedures may be used where in an optically active ligand or catalyst is used to promote enanteoselectivity of the oxidation of 25. The racemic epoxides may also be resolved, e.g. by chromatography using an optically active packing material. The C 1 alcohol of compound 26 is then halogenated to provide the (2S,3S,6S)epoxy azide 27 where suitable halogens include chlorine and bromine.
Scheme IV illustrates halogenation by in situ activation of the hydroxyl group to a mesylate e.g. methane sulfonyl chloride with a nitrogen base such as pyridine or triethyl amine and can include catalysis by dimethylaminopyridine. Subsequent substitution may be accomplished using the appropriate lithium salt e.g. lithium chloride or lithium bromide, dissolved in an appropriate solvent such as dimethylformamide or THF.
The epoxy azide 26 could also be directly halogenated using an appropriate reagent.
Dehalogenation with concomitant rearrangement of compound 27 to the (3R) hydroxy alkyne 28 is accomplished by reaction within appropriate lithium base, such as lithium diisopropyl amine, in a suitable solvent e.g. T)=iF. The alkyne 28 is reacted with Z 5 triphenylphosphine in an appropriate manner to yield the trans-alkynyl-pyrrolidine 29.
The alkyne 29 is extended by two carbons units by treatment with butyllithium in the presence of boron trifluoride diethyl etherate followed by ethylene oxide to yield the traps-hydroxypyrrolidine 30.

-z9-Scheme VIII
Mg, Cu 1 25 ~ ,..
OSOzPh \ uN~ ~ ~ _ Ns 011 F~ O~w~OH

O N3 O --' ~ \ Ow.
-.--~. ,,. H
' SCI
28 H ~' F

As discussed above, in a further aspect the invention provides methods for synthesis of larger nitrogen heterocyclic compounds such as hexahydropyridines, hexahydroazepines, and octahydroazocines. This is accomplished by utilizing reagents akin to compound 15 (Scheme VII) which have an extrended alkyl chain of the appropriate length as previously described above and shown in Scheme VIII. The synthesis of hexahydropyridine by way of this method is outlined immediately above in Scheme VIII. Thus, to obtain the homoallylic alcohol 26, the arylepoxy ether 1 and and an appropriate haloalkene such as 5-bromo-1-pentene react in the presence of magnesium and a suitable catalyst system such as iodine and cuprous cyanide to provide the arylalkene ether 25. The secondary hydroxy group is suitably protected. e.g.
as an ester, preferrably a sulfonic ester and reacted as described for Scheme VII to obtain homo allylic alcohol 26. This methodology may be used to synthesize pyrrolidines by reacting 1 and an appropriate haloalkene such as 4-bromo-1-bu.tyene to obtain the necessary terminal alkene 12 necessary for synthesis of pyrrolidines. Similarly preparation of key intermediates of hexahydropyridines are obtained by reaction of 1_ and an appropriate haloalkene such as 5-bromo-I-pentene, hexahydroazepines by reaction of 1 and 6-bromo-1-hexene and octahydroazocines by reaction of 1 and an appropriate haloalkene such as 7-bromo-I-heptene. The resulting terminal alkenes o:Peach of the above reaction products are converted to the appropriate homo allylic; alcohol analogs of 15 and 25. The homo allylic alcohol can then be processed by methoolologies described for Scheme VII
to obtain the desired disubstituted nitrogen ring hetero~cycle.
In the following Schemes IX and X, the compound numerals in the below discussions of those Schemes are made in reference to the compound depicted in the particular Scheme.
In a further aspect, as generally exemplified in Scheme IX below, the invention includes methods to prepare nitrogen ring compounds of the invention without employing an azide intermediate. Thus, as depicted in Scheme IX below, an amino acid reagent is cyclized to provide a nitrogen ring compound (pyrrolid.inone 1 ), which can be functionalized to provide a desired aryl ring substituent: (fluorophenyl as exemplified in Scheme IX). The pyrrolidinone can be reduced, and functionalized as desired, e.g. to form an activated ring carbon by reaction with suifinic compound, such as an optionally phenyl sulfinic reagent, followed by nucleophilic substitution to that ring carbon, such as to provide alkyne 10 depicted in Scheme IX. See ExarrEple 2 below for exemplary preferred reaction conditions. That addition product can be further reacted as desired, including as discussed above to provide a hydroxy urea moiety, i.e. compound 13.
In the Scheme IX, the displacement reaction of compound 3_ to compound 4_ proceeds with an aryl nucleophile in the presence of a hydride reagent (base), such as potassium hydride or more preferably sodium hydride to yield the alcicyiic compound having an arylalkyl substituent, particularly an aryalkox;y substituent as depicted in the Scheme below. Preferred aryl nucelophiles include aryl compounds having one or more WO 00/O1G70 PCTft3S99/15050 hydroxy ring substituents (i.e. an aryl hydxoxy compound), preferably a carboxylic aromatic compound such as an optionally substituted. phenol, e.g. phenol optionally substituted by halo, Cl~ alkyl, C~_s alkoxy, cyano and the like. The aryl nucelophile is preferably reacted with a nitrogen alicyclic compound having an alkyl ring substituent, typically a C1_8 or Cl~ alkyl such as methyl and the Like that preferably has an activated carbon, e.g. a carbon substituted by a sulfonic ester (~e.g. tosylate, mesylate, etc.), where the aryl nucleophile reacts.
Additionally, the conversion of alicyclic compound having a hydroxy ring substituent to the corresponding sulfinic ester (exemplified as 7 to 9 below) can proceed via an alkoxy intermediate (e.g. Cr_8 alkoxy, more preferably Cl_3 alkoxy, more preferably methoxy) intermediate by esterfication of the hydxoxy ring moiety e.g. by reaction of the corresponding alcohol such as methanol and the like followed by reaction of alkoxy ring substituent with a sulfinic acid reagent, preferably an aryl reagent such as optionally substituted phenyl sulfinic acid. For example, the phenyl sulfinic acid reagent may be optionally substituted on the phenyl ring by Cl_8 alkyl preferably methyl, C1_8 alkoxy, cyano, halo and the like.

Sch NHz HO OH ~) Nagw4a M NOH HO Cat. SOCL~, MeOH
ii) EtOH, reflux H N O
O O O PMB
Me0 LiBH,,, THF-EtOH HO~\~~~~ TsCI, EtyN, DMAP TsO~\~~
H N O RT H N O '-.--~
O pMg DCM, RT H N O
PMB

~OH
/ ~O.~\~~~~ CAN Y
NaH, DMF F~ H PMB O CH3CN-H20 (10:9) ~ O H H BoCZO~~DMAP~
,/~ O THF, RT
F

O~\ J~O - DIBAL-H y O\~~~~OH PPTS, MeON~
BOC DCM, ~78oC ~ H B~ RT
F
s ~
i) BrMg- ~OTHP
O PhSOZH'~ Oy~i~ ZaBr2, THF, RT
DCM, RT H N SOzPh O $oC ii) PPTS, MeOH
BOC F
g 9 ~O\, h NH~(g) MeOH-THF, OoC
O O
H ~ H
F ~N NHz OH

Scheme X below depicts another route to nitrogen ring compounds of the invention without an azide intermediate compound. In this approach, an alcohol, which may be optically active to provide a resolved final product, can be provided by ring-opening of an epoxide (which may be optically active). The alcohol can be substituted be a variety of groups, including aryl groups, as exemplified in the below Scheme X. That alcohol (compound 3 below) then can be functionalized as desired to provide a nitrogen that can be cyclized to provide a nitrogen ring member. Thus, for example, as shown in the below Scheme X, the alcohol intermediate can be reacted with a phthalimide, followed by hydrazine to provide an amine which can be cyclized to provide a nitrogen ring, e.g. by ozonolysis of the terminal alkene to an aldehyde which then cyclizes to 7.
The amine group and alkene group can be spaced by additional carbons to provide nitrogen ring groups with additional carbon ring members. Thus, for example, to provide a six-member ring, four (typically saturated) carbons vvould be positioned between the amine and the alkene; to provide a seven-membered ring, five (typically saturated) carbons would be positioned between the amine and the alkene; and to prepare an eight-membered ring, six (typically saturated) carbons would be positioned between the amine and the allcene. The resulting compound can be further functionalized as discussed above and exemplified in Scheme X below. See also Example 3 below for exemplary preferred reaction conditions.

Scheme X
F~OH + Cf~O K~CO~, Aceton F~~O~O (R,RrC~(Salen~
reflux omp ex -"
F~O~OH + F-~-O~p OH
TPP,DEAD
F~O~O ~M~r ~~ F O O Phthalimide DEAD.
Dry Et20 ~ ~ OH TPP, THF

NH?NH2.H20, Et0 F~O _ F-~~0~~ (~oc)20--~
Reflux N~ Et3N, THF

F~O - Os , CH~~ F~-O PPTS. MeOH
NI-Bac H Boc OH

i) BrMg~OTHP
PhSO2H, CaC~ t)~\ J~Znsr2, THF, RT
H BoC O~ pCM, RT ~ H BoC S02Ph ;i? PPTS, MaOH

n O~
NH3(9) MeOH-THF, OoC
O
H H H \~ NH
N z In a preferred aspect, the invention provides new routes to substituted hydroxy wreas. More particularly, a protected hydroxy urea {e;.g., a compound of the f~rmula NH2C(O)NHOR, where R is a hydroxy protecting group such as an alkyl, aryl or preferably aryalkyl ether such as an ether of an optionally substituted (phenyl)OCH2-) is reacted with a substituted alcohol compound such as Z1 of Scheme IV in the presence of suitable dehydrating agents) such as triphenyl phosplhine and diethylazodicarboxylate (DEAD) to provide an amino ester, i.e. a moiety of the formula NRC(O)OR~R
where R
is as defined immediately above and Rf is a non-hydrogen group such as aryl, particularly phenyl, alkyl, e.g. Ct_~o alkyl, etc. That amino ester is then treated with ammonia and a IO Lewis acid such as boron trifluoride etherate and the like to provide a hydroxy urea. In a preferred method of hydroxy urea formation, para-methoxybenzyl- is utilized as the hydroxy protection group R.
Compounds of the invention that have substituted nitrogen or sulfur alicyclic ring members (e.g. compounds of Formulae I through V wherein X is -S(O)-, -S(O)2-, substituted N include -N{O)- can be readily prepared. For example, the prepared thin or nitrogen aIicyclic group can be oxidized to provide a ring member of -S(O)-, -S(O)2-, or -N(O)- by known techniques such as with H202 and/or sodium periodate. Where the nitrogen ring member is otherwise substituted, e.g. by an optionally substituted alkyl group, the preformed ring member can be reacted with an alkyl halide to provide the substituted nitrogen ring member.
As discussed above, compounds produced by the methods of the invention are useful for numerous therapeutic applications. The compounds can be administered to a subject, particularly a mammal such as human, in need of treatment, by a variety of routes. For example, the campound can be administered orally, parenterally, intravenously, intradermally, subcutaneously, or topically. For example, for parenteral application, particularly suitable are solutions, preferably oily or aqueous solutions as well as suspensions, emulsions, or implants, including suppositories. Ampules are convenient unit dosages. For enteral application, parl:icularly suitable are tablets, dragees or capsules e.g. having talc and/or carbohydrate carricr binder or the like, the carrier suitably being lactose and/or corn starch and/or potato starch.
. It often will be preferable to use an optically active or enantiomerically enriched mixture of a chiral compound of the invention for a given therapeutic application. As used herein, the term "enantiometrically enriched" typically refers to a compound mixture that is at least approximately 70 mole%, 80 oriole%, 85 mole% or 90 rnole% of a single stereoisomer, and preferably a compound mixh~re that contains approximately at ZO least about 92 mole%, 95 mole%, 97 mole%, 98 mole'%, 99 mole% or 100% of a single enantiomer of the compound.
The active compound may be administered to a subject as a pharmaceutically active salt, e.g. salts formed by addition of an inorganic acid such as hydrochloric acid, hydrobromic acid, phosphoric acid, etc., or an organic acid such as acetic acid, oxalic acid, tartaric acid, succinic acid, etc. Base addition salts also can be formulated if an appropriate acidic group is present on the compound. :for example, suitable base addition salts include those formed by addition of metal canons such as zinc, calcium, etc., or salts formed by addition of ammonium, tetraethylammoniurn, etc. Suitable dosages for a given therapy can be readily determined by the medical practitioner such as by standard dosing protocols. See also U.S. Patent 5,703,093.
All documents mentioned herein are incorporated herein by reference.
The following non-limiting examples are illustrative of the invention.

Example 1: Preparation of (25~(SR,~-2-(4-Fluorophenoxymethyl)-5-{4- N -hydroxy-ureidyl-I-butynyl)-tetrahydrothiophene (Scheme III, I 1~
Part I : (R}-ThiogyIcidyl-4-fluorophenyl ether 2 Thiourea (6.5 g, 0.085 mol.) was added to a 250 ml two neck flask containing ml of methanol and a magnetic stir bar. This solution 'was then cooled to 0 °C and (R)-glycidyl-4-fluorophenyl ether (13 g, 0.077 mol. in dry methanol) was added dropwise.
The reaction mixture, while stirnng, was allowed to w<~rm to room temperature and stirred an additional 6 hours. During this time the reaction was monitored by T'CL (ethyl acetate-light petroleum ether 1:4). Solvent was removc;d i~ vacuo and the residue was dissolved in ether, washed with brine, dried over Na2S(J4 and concentrated.
The crude product was purified on silica gel (9:1 hexane:ethyl acetate) to yield 10 g (70 %) of the ether 2, Scheme I. ja]D = +I3.3° (c 2.0, CHC13).
Part 2: (4,5~-2-Carboethoxy-(4-fluorophenoxym.ethyl)-y-thiobutyrolactone 3 Diethyl malonate (5.9 g, 0.0369 mol) and 40 m)L of dry THF were added to a I00 ml two neck round bottom flask (equipped with a reflux: condenser, nitrogen inlet and a septum). The reaction mixture was cooled to -78 °C and n-butyllithium was added dropwise and stirred for 45 minutes while allowed to warm. The mixture was then cooled to 0 °C and the fluorophenyl ether 2_, 5.66 g, 0.03~ 1 moL, dissolved in THF was added. The reaction mixture was refluxed for 18 hours and monitored by TLC
(ethyl acetate-light petroleum ether I :3}. The reaction was quenched with aqueous saturated ammonium chloride and solvent was removed. The resulting residue was dissolved in ethyl acetate, washed with brine then water, dried over Na2S04 and concentrated to yield (4S)-2-Carboethoxy- (4-fluorophenoxymethyl)-y-thiobutyrolactone 3 7.0 g. The crude product was purif ed on silica gel (ethyl acetate-light petroleum 1:8} to give 6.4 g (70 %) of 3,(Scheme I).

WO 00!01670 PCT/US99/15050 - 38 _ Part 3: {4S)-(4-Fluorophenoxymethyl)-y-thiobutyroactone 4 (Scheme I) (45)-2-Carboethoxy-(4-fluorophenoxymethyl)-y-thiobutyrolactone 3, 6 g, 0.020 mol., was added to a 50 ml round bottom flask containing 30 ml of N,N-dimethylacetarnide.
MgC12~6 H20 (4.08 g, 0.020 mol.) was added and the reaction mixture was refluxed for 6 hours. The reaction was diluted with water and extracted with ether. The organic layer was washed twice with water, brine and dried (Na2S04). The solvent was removed in vacuo to afford the thiobutyrolactone 4 in 78 % yield, 3.5 g, m.p. 73 °C, [a]D = +7g ° (c 1.49, CHCl3).
Part 4: (2,S')(SR,S)-2-(4-Fluorophenoxymethyl)~-5-hydroxy tetrahydrothiophene S_ (Scheme I) (4S~-(4-Fluorophenoxymethyl)-y-thiobutyrolac~tone _4, 2.57 g, 11.3 mol., in 25 ml of CH2C12 was added to a flame dried 50 ml two necked flask. The solution was cooled to -78 °C and DIBAL-H was added dropwise. The reaction was monitored by TLC
(ethyl acetate:light petroleum 1:2). After 2 hours, the reaction was quenched with a saturated aqueous solution of sodium-potassium tartratc; and extracted with CH2C12. The organic Layer was washed twice with water, brine, drieol (Na2SO4) and concentrated to afford the 5-hydroxy tetrahydrothiophene 5_ in 96 % yield, 2.5 g.
Part S: (2S)(SR,,S~-S-Benzensulfonyl-2-(4-fluorophenoxymethyl)-5-(4-hydroxybutyn-I-yl)-tetrahydrothiophene 6 (Scheme II).
Benzenesulfinic acid (2.34 g, 16.4 mmol.) CaCl2 ( 1.82 g, 16.4 mmol.) and 25 ml of CH2C12 were added to a SO ml round bottom flask. Tihe solution was cooled to 0 °C
and (2S)(SR,.S')-2-(4-Fluorophenoxymethyl)-5-hydroxy tetrahydrothiophene 5, 2.5 g, 0.011 mol., dissolved in dry CHZC12 was added. The reaction mixture was stirred and after 6 hours, filtered through celite and washed with CH~2CI2. The combined organic layers were washed with saturated aqueous Na2C03, water, brine and dried over NaZS04.
Solvent was removed in vacuo and the resulting crude product was crystallized from chloroform-hexane to give the pure benzensulfonyl-tetrahydrothiophene 6_ in 78 % yield, 3 g, m.p. = 84 °C.

Part 6: (2S}(SR,S}-2-(4-Fluorophenoxymethyl)-5-(4-tetrahydropyranoyl-I-butyne)-tetrahydrothiophene 7 (Scheme II).
Grignard grade magnesium, 0.81 g, 33.7 mmol, was added to a two necked round bottom flask and flamed dried under nitrogen. Dry THF, 70 mI, and I,2-dibromoethane (cat.) were added sequentially to the activated magnesium. Next, isopropyl bromide (2.07 g, 16.8 mol.) dissolved in THF was added dropwise over 10 minutes and the reaction was stirred for 1 hour. The resulting isopropyl magnesium bromide was cannulated into a 100 ml flame dried round bottom flask. 4-Tetrahydropyranoyl-butyne, 2.60 g, I6.8 mmol., was added and the reaction mixture was stirred at room temperature for 30 minutes and then cooled to 0 °C. ZnBr2, (10.12 ml, 1 M in THF) was added to the cooled mixture and stirred for 45 minutes. The reaction mixture was allowed to warm to room temperature and (2S~(SR,,S'}-5-Benzensulfonyl-2-(4-fluorophenoxymethyl)-5-(4-hydroxybutyn-1-yI)-tetrahydrothiophene 6 (2.97 g, 8.4 mmol.) in THF was added. The reaction mixture was refluxed till completion of reaction with monitoring by TCL (ethyl acetate:light petroleum 1:4). At the end of i 6 hours, the reaction was cooled to 0 °C and quenched with saturated aqueous NH4C1.
THF was removed in vacuo and the reaction mixture was partitioned between water and ethyl acetate: The organic layer was washed with water, brine, dried (NaZS04) and concentrated to yield 3 g of the crude tetrahydropyranoyl derivative 7.
Part 7: (2S'~(SR,S~-2-(4-Fluorophenoxymethyl)-5_{4-hydroxybutyn-1-yl)-tetrahydrothiophene 8_, (Scheme II}
Crude (2,5'}{SR,,S'}-2-(4-fluorophenoxymethyl)-5-(4-tetrahydropyranoyl-I-butyne)-tetrahydrothiophene 7 (3 g) was dissolved in 5 ml of methanol. A solution of 1 % HCl in methanol (10 ml) was added and the reaction was stirred at room temperature with monitoring by TLC (ethyl acetate:light petroleum ether I :1 ). At the end of 4 hours the reaction mixture was neutralized with saturated aqueous Na2C03 and methanol was removed in vacuo. The resulting solution was extracted with ethyl acetate, washed with WO 00/O1b70 PCT/US99/15050 water, brine, dried (Na2SO4) and concentrated. The reaction residue was dried in vacuo with warming to give (2,S)(SR,f)-2-(4-Fluorophenox~rmethyl)-5-(4-hydroxybutyn-1-yl)-tetrahydrothiophene 8_ in 86 % yield, 2.05 g.
Part 9: (2,S')(SR,.S~-2-(4-Fluorophenoxymethyl)-5-(4-N,O-biscarbophenoxy-1-butynyl)-tetrahydrothiophene 10 (Scheme III) A solution of dry THF (20 ml) and (2,S')(SR,,f)..2-{4-fluorophenoxymethyl)-5-(4-hydroxybutyn-1-yl)-tetrahydrothiophene _9, I.86 g 6.6 mol., was cooled to 0 °C.
Diethylazodicarboxylate, 1.4 g, 8.0 mol., was added d;ropwise followed by triphenylphosphine, 2.09 g; 8.0 mmoL, and the reaction mixture was stirred at 0 °C. N,O-biscarbophenoxy hydroxylamine, 2.18 g, 8.0 mmol, w;~.s added to the cooled reaction mixture and stirred for 6 hours with warming to room temperature. The reaction was monitored by TLC (hexane:ethyl acetate 3:1). Upon completion, solvent was removed in vacuo and the resulting crude residue was dissolved in ethyl acetate which was subsequently washed with water, brine, dried {Na2S04) and concentrated. The crude product was purified on silica gel (hexane:ethyl acetate 6:1) to give 3.4 g (96 %) of (2S)(SR,,f)-2-(4-Fluorophenoxymethyl)-5-(4- N,O-bisc~~rbophenoxy-1-butynyl)-tetrahydrothiophene I0.
Part 10: (2,S'){SR,S)-2-(4-Fluorophenoxymethyl)-.5-(4-N-hydroxy-ureidyl-1-butynyl)-tetrahydrothiophene 11 (Scheme III) A solution of methanol (S mI) and (2S}(SR,,S)-2-(~4-fluorophenoxymethyl)-5-(4-N,O-hiscarbophenoxy-1-butynyl)-tetrahydrothiophene 10 (3.0 g, 5.6 mmol.) was added to a 50 mI round bottom flask. Saturated NH3-MeOH, 1 S ml, was added to the reaction mixture and allowed to stir for 12 hours. Solvent was removed in vacuo and the resulting crude residue was crystallized from ethyl acetate-hexane to get pure {2,5~{SR,,S~-2-(4-Fluorophenoxymethyl)-5-{4- N -hydroxy-ureidyl- I -buty~t~yl)-tetrahydrothiophene 11 in 63 % yield, i.2g, m.p. = 1 I7 °C.

Example 2: Preparation of (2S,SS)-2-(4-flu~oro)phenoxymethyl-S_ 4-hydroxyureidyl-I-bu ( ~Yl)pyrrolidine References in this Example 2 to compound nwmerals (generally underli ned) designate the compounds depicted structurally in Scheme IX above.
Part l: (S)-5-Methoxycarbonyl-I-(4_methoxyb~enzyl)_2-pyri.oIidinone IX; 1_) : (Scheme To a solution of (S)-glutamic acid (SOg, 0.34 xrunol) in 300 mI. of 2M Na OH, was added a solution of p-anisaldehyde (46.3g, 0.34 mrnol) in ethanol (50m1 .
F
ollowing stirring for 30 min., the reaction mixture was cooled to ~0°C and sodi um barohydride (3~gg~ 0~ 1 moral) was added in portions. After being stirred for 2h at room temperature, an additional amount of p-arusaldehyde (4.6g, 0.033 viol) was added , follow ed by stirring for 30 min. and then addition of NaBH4 ( 0,25 g , 0.006 mmol . A$e r stirring for 30 min., the reaction mixture was extracted with ether (3x300 mI). The H of P the aqueous layer was adjusted to approximately 3 by dropwise addition of con °
c. IiCI at 0 C.
The precipitated solid was filtered off; dried and then dissolved in 700 ml of eth anol.
After refluxing for 5 hours, the solution was concentrated and the residue taken ' m methylene chloride to filter off the undissolved material. The clear solution on solv ent removal gave 20 g of crude product (24%).
To that crude product dissolved in 500 ml of dry methanol, under Nz atm., thion 1 Y
chloride (2m1) was added slowly for 2 min. After being stirred for 12 hours at room temperature, aqueous saturated NaHC03 was added dropwise ,until neutral pH.
The solvent was dried under vacuo and the residue was dissolved in ethyl acetate , washed with water and brine , dried over anhydrous Na2S04 and concentrat ed to afford the crude product which on purification by column chromatography (20% ethyl acetate in hexane 60-120 mesh gave 20 g ofp~e product as colorless oil (95'%) 1H NMR {200 MHz, CHCl3): b l.9 - 2.63 (m, 4 H), 3.65 (s, 3H), 3.77 (s, 3H), 3.83-4.00 (m, 2H), 4.82- 4.98 (d, 2H, J=13.6 Hz), 6.73-6.85 (d, 2H, J = 7.9 Hz), 7.02-7.16 (d, 2H, J= 7.9 Hz).
Part 2: (S)-S-hydroxymethyl-I-(4-methoxybenzyl)-2-pyrrolidinone (Scheme IX;
2):
Lithium chloride (8.17g, I90mmol) and sodium borohydride (7.2g, 190 mmol) were taken in a solvent mixture of ethanol (100 ml) and THF (60 ml) at 0°C. After vigorous stirring for 1 hour at room temperature, a solution of {S)-S-Methoxycarbonyl-1-(4-methoxybenzyl)-2-pyrrolidinone (20g, 76 mmol) (prepared as in Part 1 above) in 40 ml of THF was added at 0°C. The reaction mixture w,as stirred at room temperature for 6 hours. The solid was filtered off. The filtrate was neutralised to pH
approximately 7 by dropwise addition of saturated aqueous NH4CI solution at O°C. The solvent was removed under vaccuo. The residue was partitioned between ethyl acetate (500 ml) and water {500 ml). The organic extract was washed with brine, dried over anhydrous Na2S04, and concentrated zznder vaccuo to afford the crude product as colorless solid (I7g, 9S%) which was almost pure to be telescoped. llE3 NMR (200 MHz, CDC13) :

8 1.9 - 2.1 (m, 2H), 2.2-2.55 (m, 3H), 2.55-2.65 (1H, br s,-OH), 3.35-3.52 {m, 2H), 3.7-3.85 {d, 4H), 4.02-4.15 (d, IH, J=13.6 Hz), 4.70-4.85 (d, 1H, J==13.6 Hz), 6.73-6.85 (d, 2H, J= 7.9 Hz), 7.10-7.20 (d , 2H, J=7.9 Hz). TLC specification: mobile phase = 75% ethyl acetate in hexane; stat. phase = fsg 254; visual method = anisal stain, apm stain and uv; and Rf values = starting material : 0.2 and pdt. : 0.5.
Part 3: (S)-1-(4-methoxybenzyl)-5-p-tolunesulphonyloxymethyl-2-pyrrolidinone (Scheme IX; 3):
A mixture of (S)-5-hydroxymethyl-1-{4-methoxybenzyl)-2-pyrrolidinone (Sg, 21.28 mmol), p-tolunesulphonyl chloride (4.468, 23.Smmo1), triethylamine (4.3g, 42.56 mmol) in 75 mI of methylene chloride was stirred for 12 hours at room temperature. After washing with saturated aqueous NaHC03 and water, the; organic layer was dried over WO 00J01670 PCT/tJS99/15050 anhydrous NaZS04 and concentrated to afford the crude product which was filtered through a silica gel column (50% ethyl acetate in hexane, 60-120 mesh) to afford pure product as colorless solid in quantitative yield (7.Sg, 90%). 'H NMR (200MHz, CDC13) :8 1.73-1.93 (m, 1H), 1.96-2.18 (m, 1H), 2.24-2.60 (m, SH), 3.63 (sex, IH, J=3.SHz), 3.74 {d, 2H, J= 14 Hz), 3.8 (s, 3H), 3.90-4.1.0 (m, 213), 4.85 (d, 2H, J=14 Hz), 6.82 (d, 2H, J=8.13 Hz), 7.08 (d, 2H, J= 8.13 Hz), 7.38 (d, 21a, J=8.13 Hz), 7.75 (d, 2H, 8.13Hz) TLC specification ': mobile phase = pure ethyl acetate; stat. phase = fsg 254;
visual method= anisaldehyde stain, apm stain and uv; Rf values = starting material :
0.2 and pdt.
0.6.
to Part 4: (S)-1-(4-methoxybenzyl)-S-(4-fluoro)phenoxymethyl-2-pyrrolidinone (Scheme IX; ~:
To a solution of 4-fluorophenol (8.6g, 77mmol), in 50 ml of dry DMF, sodium hydride (3.08g, 77mmo1) was added spanning for 5 ruin. at 0°C under NZ
atmosphere.
Stirring for 15 min at room temperature was followed by the addition of a solution of (S)-1-(4-methoxybenzyl}-5-p-tolunesuiphonyloxymethyl-2-pyrrolidinone (2flg, 5I.3rnmo1) in 100 ml of dry DMF and TBAI (0.33g, 9mmo1). The reaction was stirred for 3 hours. Ice-cold water (500 ml) was then added followed by extraction with ethyl ether (3x500rn1).
The combined organic extract was washed with water and brine, dried over anhydrous NazSOa to afford a brown syrup which was purified by column chromatography (50%
ethyl acetate in hexane, 60-120 mesh) to afford the colorless solid {16g, 89%}
as pure product. 'H NMR (200MHz, CDCl3): 8 1.8-2.0 (m, :lH), 2.0-2.22 (m, IH), 2.24-2.64 (m, 2H), 3.67 (s, 3H), 3.72-3.83 (m, 3H), 4.02 (d, 2H, J=15.90 Hz), 4.78 (d, 2H, J=15.90Hz), 6.54-6.64 (m, 4H}, 6.84 (d, 2H, J=8.0 Hz), 7.07 (d, 2:Ei, J=8.OHz). '3C NMR
(50MHz, CDC13): b 21.68, 30.16, 44.2?, SS.14, 56.39, 69.15, 113.96, 115.34, 115.54, 116.0, 128.81, 129.24, 175.25. IR {CHCl3, cm'') : 2904, 1688, 1504, 1440, 1248, 1040, F.ABMS (m/z} :121, 204, 222, 330(M++1). HRMS : calcd. 330.150547, found 330.152029 , Melting point : 62-63°C. [a]D : 5.51 (C.' 6.02, CHCl3).
TLC specification:
mobile phase = 50% ethyl acetate in hexane (quadraple runs); stat. phase = fsg 254;

visual method = anisaldehyde stain, apm stain and uv; F;f values = starting material : 0.2 and pdt. : 0.6.
Part 5: (S)-5-(4-fluoro)phenoxymethyl-2-pyrrolidinone (Scheme IX; S) (S)-1-(4-methoxybenzyl)-5-{4-fluoro)phenoxymE;thyl-2-pyrrolidinone (llg, 54.4mmol), and ceric ammonium nitrate (89.58, 163.2rrvmol) were taken in a mixture of acetonitrile ( 160 ml) and water ( 16ml). The reaction mixture was stirred for 2 hours. The solvent was removed under vacuo. Ethyl acetate {300rn1) was added and the insoluble inorganic material was filtered off. The filtrate was washed with water, and brine, dried over anhydrous Na2S04, and concentrated under vacuo to leave a brown residue which on purification by column chromatography (pure ethyl acetate, 60-120 mesh) afforded 8.74 g of pure product (77%).'H NMR (200MHz, CDCl3) : 8 1.8-2.08 (m, 1H), 2.24-2.5 (m, 3H), 3.7-3.87(d, 1H, J=8.13Hz), 3.88-4.00 (dd, 1H, J1=9..3 Hz, J2=3.50Hz), 4.0-4.15 (m, 1H), 6.23-6.40 (br s, 1H), 6.72-6.90 (dd, 2H, 31=9.3Hz, J2=3.50Hz), 6.91-7.05 (t, 2H, 8.4Hz). 13C NMR (50MHz, CDC13): 8 23.13, 29.60, 53.:33, 71.90, 115.51, 115.63, 116.10, 178.10. IR ( neat, cni 1) : 820, 1204, 1352, 1648, 2876, 3212. EIMS
(m/z) 2I0(M++1), 117, 101, 84, 73, 60. HRMS : calcd. 210.093032 , found 209.085099 Melting point : 90-91°C. [a]D : 59.36 (C 0.85, CHC13}. TLC
specification: mobile phase = pure ethyl acetate; stat. phase = fsg 254; visual method = anisaldehyde, apm stain and uv; Rf values = starting material : 0.8 and pdt. : 0.3.
Part 6: {5S)-1-tent-butyloxycarbonyl-2-(4-fluoro)phenoxyrnethyl pyrrolidinone (Scheme IX; 6_) {S)-5-(4-fluoro)phenoxymethyl-2-pyrrolidinone (8.24 g, 39.8 mmol ) and DMAP
(4.86g, 39.8 mmol) were taken in 100 ml of dry THF under N2 atmosphere . Di-tert-butyl dicarbonate (17.4g, 79.6 mmol) was then added dropwise at RT. After a period of 5h stirring, the solvent was removed under vacuo. The residue was triturated with a mixture of ethyl acetate and petroleum ether {1 : 3 ratio, :Z00 rnI) and the precipitated material was filtered off. The filtrate was washed with b3rine, dried over anhydrous Na2S04 , and concentrated to afford the residue which was purified by column chromatography {5% ethyl acetate in hexane, 60-120 mesh) providing the pure product as a colourless oil (10.5g, 86% ). 1H NMR (200MHz, CDC13) : 8 1.54 (s, 9H), 2.13-2.36 (m, 2H), 2.38-2.58 (dddd, 1H, Jl= 2.04Hz, J2= 10.2 Hz, J3 =13.3 Hz), 2.69-2.91 (m, 1H), S 4.02-4.22 (m, 2H), 4.4-4..52 (m, IH), 6.82 {dd, 2H, :f 1= 4.08 Hz, J2= 10.2 Hz), 6.97 (t, 2H, J= 8.16Hz). a3C NMR {50MHz, CDCl3) :. 8 21.13, 28.05, 31.87, 56.63, 69.15, 96.11, 115.49, 115.65, 116.12, 160.00, 174.00. IR ( neat, cm 1) : 2992, 1792, 1712, 1504, 1472, 1376, 1312, 1264, 1200, 1152, 1024, 832. EIMS (m/z) :107,142, 152, 179, 210, 232, 254, 310{M++1). ARMS : calcd. 309.137637, found 309.136584. Melting point : 75 -76°C. [a]D : - 71.36 (C 3.08, CHC13). TLC specification: mobile phase =
pure ethyl acetate; stat. phase = fsg 254; visual method = anisaldehyde; apm stain and uv; Rf values = starting material : 0.3 and pdt.: 0.9.
Part 7: (5S)-1-tert-butyloxycarbonyl-5-(4-fluoro)phenoxymethylpyrrolidin-2-of (Scheme IX; 7) To a cooled solution of (5S)-1-tert-butyloxycarbonyl-5-(4-fluoro)phenoxymethyl pyrrolidinone (l Og, 32.3mmo1) at -78°C under NZ atmosphere in dry DCM
( 100m1) was added DIBAL-H ( 1M solution in toluene, 34 ml, :32.3mmol) dropwise. The reaction mixture was stirred for lhour. Saturated aqueous R.ochelle's salt solution (20m1) was added and the reaction mixture was stirred for Ih. 'The precipitated solid was f ltered off.
The filtrate was dried over anhydrous Na2S04 and concentrated to afford l Og of crude product as colorless oil (100%). IH NMR (200MHz, CDC13}: S 1.52 (s, 9H), 1.80-2.42 {m, 4H), 3.6-4.25 (m, 3H), 5.32-5.6 (m, 1H), 6.77-',t.3 (m, 4H). TLC
specification:
mobile phase = 20% ethyl acetate in hexane; stat. phase = fsg 254; visual method =
anisaldehyde, apm stain and uv; Rf values = starting material : 0.4 and pdt. :
0.8 w0 00101670 PCTlUS99lI5050 Part 8: (SS}-1-tert-butyloxy-5-(4-fluoro)phen:oxymethyl -2-methoxypyrrolidine (Scheme IX; 8_) (SS)-I-tent-butyloxycarbonyl-5-(4-fluoro)phenoxymethylpyrrolidin-2-ol(lOg,32.15mrno1) and PPTS (0.8g, 3.2mmol) were taken in 100 ml ofmethanol.
After 5- being stirred for 18h at RT, evaporation of the solvent gave the residue which on purification by column chromatography afforded l Og of pure product as colorless oiI
(96%). 1H NMR (200MHz, CDCI3) : 8 1.5 (s, 9H), 1.75-2.25 (m, 4H), 3.23-3.5 (m, 3H), 3.72-3.9 (m, 1H), 4.02-4.38 (m, 2H}, 5.1-5.5 (m, 1H), 6.76-7.02 (m, 4H). IR
(neat, cm 1):
2976,2944, 1696,1504,1392,1208, 1186, 1078,824. T'LC specification: mobile phase =
20% ethyl acetate in hexane; stat. phase = fsg 254; visual method = apm stain and uv; Rf values = starting material : 0.3 and pdt. : 0.5.
Part 9: (SS)-2-benzenesufonyl-1-tert-butyloxy -5-{4-fluoro)phenoxy methylpyrroilidine (Scheme IX; 9_):
I5 A solution of (SS)-1-tent-butoxy-5-{4-fluoro}pllenoxymethyl-2-methoxy pyrrolidine (9.8g, 30. l5mmol) in dry DCM (I00m1) containing powdered CaCI2 (Sg) was cooled to 0°C: Freshly prepared benzenesulfinic acid (4.3g, 30.15 mmol) was then added at once. T'he reaction mixture was, after being stirred for 2h at ambient temperature, was cooled back to 0°C. Aqueous saturated NaHC03 solution was added and the stirring was continued for lh. The suspension was filtered off and the filtrate was washed with water and brine, dried over anhydrous NaZS04 and concentrated to afford I 1.8g of pure product as colorless solid. (90%). rH NMR (200MHz, CDC13) : 8 1.20 (s, 9H), 2.1-2.57 (m, 3H), 2.7-2.83 (m, 1H), 4.07-4.52 (m, 3H), S:I-5.25 (m, 1H), 6.87-7.07 (m, 4H), 7.48-7.77 (m, 3H}, 7.85-7.97 (m, 2H). IR (neat, cm 1): 2976,1752,1504, 1488, 1456, 1368, 1312, 1216, I 152, 1088, 1040, 832, 768, 688, 560. FABMS (m/z) : 125,154, 194, 195; 194, 434, 435, 436 (Nt~+1). HRMS: calcd. 436.159398, found 436. 162468. Melting point: 113-114°C
TLC specification: mobile phase = 20% ethyl acetate in hexane; stat. phase =
fsg 254;
visual method= apm stain and uv; Rf values = starting material : 0.55 and pdt.
: 0.3;

Part i0: (2S,SS)-i-tert-butoxycarbonyl-2-(4-.fluoro)phenoxymethyl-5-{2-hydroxyethyl)ethynyl pyrrolidine (Scheme IX; 10) To a solution of 1-tetrahydropyranyloxy-3-butynylinagnesium bromide in THF
(prepared in situ by the addition of isopropylmagnesium bromide in THF) to 2-{3-butynyl-1-oxy)tetrahydropyran (1.0788, 7mmo1)), was added a solution of zinc bromide in THF (0.788, 3.Smmo1) at ambient temperature. T~o the colorless suspension, formed after 30 min. of stirring, was added (5S)-2-benzenesufonyl-1-tert-butoxycarbony-5-{4-fluoro)phenoxymethylpyn olidine {l.Sg, 3.5mmo1) irt 12 ml of THF. The reaction mixture was stirred for IO hours. The reaction mixture was quenched with aqueous NH4Cl solution (3ml) and partitioned between ether (300m1;1 and water (100m1). The organic part was washed with brine, dried over anhydrous NaZS04 and concentrated to afford the crude product which was dissolved in methanol (l5ml). PPTS (66mg, 0.2bmmol) was added and the reaction mixture was stirred at roam temperature overnight. The residue after the removal of methanol, was purified by colurrm chromatography (60-120mesh, 30% ethyl acetate in hexane) to afford the pure product as colorless oil (l.Og, 86%). zH
NMR(200 MHz,CDCl3) : b 1.49 (s,9H), 1.55-1.82{m,2H), 1.87-2.0(m, IH), 2.0-2.3(m,2H), 2.35-2.5(m,2H), 3.6-3.75(t,2H), 3.75-3.9(rn,lH), 3.95-4.25(m,2H), 4.44-4.58(m,lH), 6.77-7.0(m,4H). FABMS(m/z): 107, 136, 138, 154, 194, 238, 264, 308, 364.(M++1). TLC specification: mobile phase = 30°,~o ethyl acetate in hexane; stat. phase = fsg 254; visual method = apm stain and uv; Rf values = starting material :
0.85 and pdt.: 0.4.
Part l i : {2S,5S)-i-tert-butoxycarbonyl-2-(4-fluoro)phenoxymethyl-5-(4-N,O-bis-phenoxycarbonylhydroxyamino-1-butynyl)pyrrolidine (Scheme IX; 11):
To a solution of (2S,5S)-1-tert-butoxycarbom,~I-5-(2-hydroxyethyl)ethynyl-2-{4-fluoro)phenoxymethylpyrrolidine (820mg, 2.26mmo1), triphenyphosphine {712mg, 2.7mmol) and N,O-bis-phenoxycarbonylhydroxylamine {0.78, 2.7mmol) was added diethyl azodicarboxylate (0.47 g, 2.7mmo1) dropwise. After being stirred for 30 min. at 0°C, the stirring was continued for 6h at RT. The solvent removal under vacuo and the subjection of the residue to column purification (30°,~o ethyl acetate in hexane,60-120 mesh) to afford colorless semi-solid (1.12,80%). 1H NMR (200 MHz, CDCl3) : 8 1.5 (s, 9H}, 1.88-2.4 (m, 4H), 2.62-2.77 (t, 2H), 3.65-4.29 (in, 5H), 4.4-4.6 (m, 1H), 6.76-7.1 (m, 4H), 7.1-7.3 (m, 6H), 7.3-7.5 (m, 4H). TLC specification: mobile phase = 30%
ethyl acetate in hexane; stat. phase = fsg 254; visual method = apm stain and uv; Rf values =
starting material : 0.3and pdt. : 0.7.
Part 12: (2S,5S)-1-tent-butoxycarbonyl-5-(2-hydroxyethyl)ethynyl-2-(4-fluoro)phenoxymethyl-5-{4-hydroxyureidyl-1-butynyl}pyrrolidine (Scheme IX; 12) Ammonia gas was purged into a solution of (2S,5S}-1-tent-butoxycarbonyl-5-(2-hydroxyethyl)ethynyl-2-(4-fluoro}phenoxymethyl-5-(4-N,O-bis-phenoxycarbonylhydroxy amino-1-butynyl)pyrrolidime ( 1.4g, 2.26mmol) in a solvent mixture of methanol (30m1) and THF (10 ml) at 0°C for 15 minutes. The reaction mixture was stirred for 6 hours at room temperature overnight. Evaporation of the solvent and purification of the residue by column chromatography (30% ethyl acetate in hexane, 60-120 mesh) to afford 0.81 g of pure product as colorless liquid (85%). 1H
NMR (200MHz, CDCl3): 81.5 (s, 9H), 1.85-2.31 (m,, 4H), 2.36-2.5 (t, 2H), 3.5-3.68 (m, 1H}, 3.69-3.90 (m, 2H), 3.93-4.4 (dd, 1H, J= 7.9 Hz, J=3.4Hz), 4.07-4.2 (m, 1H), 4.35-4.55 (m, 1H), 5.1-5.35 (br.s, 2H}, 6.73-7.0 (m, 4H). lfR (neat, cm 1) : 3504, (br.), 2960, 1688, 1512, 1392, 1208,1160, 760. FAB:MS(m/z) : 153,194, 274, 322, 388, 422 (M++1). TLC specification: mobile phase = 30°~a ethyl acetate in hexane; stat. phase = fsg 254; visual method = apm stain and uv; Rf values = starting material :
0.9 and pdt.:
0.6.
Part 13: (2S,5S)-2-(4-fluoro)phenoxymethyl-_'>-(4-hydroxyureidyl-1-butynyl)pyrrolidine (Scheme IX; 13 Trifluoroacetic acid (O.SmI, 5.49mmo1) was added to a solution of substrate (0.8g, 1.83mmo1) in l Oml of DCM at 0°C. The reaction mixture was stirred for 3 hours at room temperature. Aqueous saturated NaHC03 was added at 0°C. After being stirred for 10 min. the organic layer was separated, washed with brine, dried over anhydrous Na2S04 and concentrated to afford the brown residue which was purified by column chromatography (10%methanol in ethyl acetate) to afford the colarless semi-solid (0.5Sg, 86%). ~H NMR(200 MHz,CDCl3) : s 1.5-1.97 (m, 4H), 2.01-2.25 (m, 2H), 2.38-2.6 (t, J=2.17Hz; 2H), 3.52-3.7 (t, J=6.54Hz, 2H), 3.72-4.04 (m, 4H), 6.73-7.6 (m, 4H).
FABMS(m/z) : 107, 120, 124, 136, 138, 154, 176, 194, 268, 279, 322 (M++1), TLC
specification: mobile phase = 5% methanol in ethyl acetate; stat. phase = fsg 254; visual method = apm stain and uv; Rf values = starting material : 0.2 and pdt. : 0.6 IO Example 3 Further preparation of (2S,5S)-2-(4-fluoro)phenoxymethyl-5-(4-hydroxyureidyl-1-butynyl)pyrrolidine References in this Example 3 to compound r.~umerals (generally underlined) designate the compounds depicted structurally in Scheme X above.
I5 Part l: (R)-1-(4-fluorophenyl) glycerol (Sch.eme X: 1):
To a solution of 4-fluorophenol (40g, 0.35m~mo1) in 400m1 acetone were added K2C03 (148g,1.05mmo1) and epichlorohydrin (98g, 1.05mmol). The reaction mixture was refluxed for 12 hr. Acetone was removed under vacuum, the residue was yl acetate, washed with water, dried over NaZS04 and concentrated . The crude residue was distilled 20 at 120°C, 2.0mm vacuum to get glycidyl-4-fluorophenyl ether product (52g, 85% yield).
To the racemic glycidyl-4-fluorophenyl ether (52g, 0.31mmo1) was added (R, R) Co-Salen complex (1.03g, 1.54mmo1). Distilled water (3.06m1, 0.17mmo1) was added dropwise to the reaction over a period of lh. The reaction was stirred for i2hr and completion of the reaction was judged by HPLC. Hexane was added in the reaction 25 mixture and the compound which got precipitated out was filtered and further washed with hexane to afford pure wh~te solid (R)-1-(4-fluorophenyl)glycerol (26.38g,49%
yield);TLC ethylacetate-hexane (1:3) Rf=0.2; [a]D-9.6° {c 1.6, EtOH) ;97% ee.

-SO-Part 2: (R)-Glycidyl-4-fluorophenyl ether (Sc:heme X; ~:
A mixture of (R)-1-(4-fluorophenyl)glycerol (26g, 0.14mmo1), triphenylphosphine (52g, 0.21mmo1) in dry benzene {250m1) were taken in a 5OOm1 R.B.
flask equipped with a spinbar, reflux condenser and ~utrogen inlet.
Diethylazodicarboxylate (DEAD) (33.3g, 0.21mmoi} was added to it and the reaction mixture was heated under reflux for 18h: Solvent was removed on rotavapor and the residue was dissolved in ether, washed with water, brine, dried over Na2SO4, concentrated and purified by silica gel column chromatography to give pure title product 2 (l2.Sg, 54.3% yield}: TLC: ethyl acetate-hexane (1:4), Rf=0.5; [a ]D-4.9° (c1.46, CHCI~) 1H NMR (CDC13, 200MHz): b 2.68 (dd, J = 4.5; 2.2 Hz, 1H), 2.85 (t, J =
4.58Hz,1H), 3.27 (m, 1H), 3.89 (dd, J =15.7, 6.7Hz, 1H), 4.11 (dd, J =15.7, 4.SHz, 1H), 6.74 -7.02 (m, 4H).
Part 3: (2R)-1-(4-fluorophenyl) hex-S-ene,2-of {Scheme X; 3_) A 500m1 two neck flask equipped with a ma~,metic stir bar, reflux condenser a septum and a nitrogen inlet, was charged with magnesium (8.5g, 0.35mmol) and flame dried along with magnesium. Dry ether (30m1) and dibromoethane (lml) were introduced. The reaction mixture was maintained at 0°C and ice water circulation was maintained through the condenser. Allyl bromide (9.1m1, 0.llmmol) in dry ether (50m1) was added dropwise. The reaction mixture was stirr<;d for lh and then CuCN
(130rng) was added. 4-fluorophenyl-glycidyl ether 2 (12g, 0.07mumol) in i 20m1 of dry ether was introduced slowly after 10 min. The reaction was completed in 20 min. as judged by TLC in 30% ethylacetate-hexane (Rf= 0.6}. Saturated ammonium chloride was added to quench the reaction and then the mixture was partitioned between water-ethylacetate.
Ethylacetate layer was washed with brine, dried over' Na2S04 and concentrated to give title product 3 (l3.Sg, 90 %), [a ]D-20.6 (cl.O,CHC1;;). IH-NMR (CDC13, 200MHz): 8 1.62-1.73 (m. 2H), 2.18-2.43 (q, J=6.8Hz, 2H), 3.75-4.09 (m, 3H}, 4.96-5.17 (m, 2H), 5.73-5.96 (m, 1H), 6.78-7.02 (m, 4H).

WO 00/O1b70 PCT/US99/15050 Part 4: {2S)-1-(4-flourophenyl)-2-phthalimido-hex-5-ene (Scheme X; 4_}
To a solution of compound 3 (8.4g, 0.04mmo1) in dry THF maintained at 0°C and under nitrogen, was added phthalirnide (7.Og, 0.048mmo1) and triphenylphosphine (12.6g, 0.48mmo1) . After lOmin DEAD (7.6m1, 0.048mmo1) was added dropwise.
The reaction was stirred for Sh and the completion was judged by TLC, 20% ethyl acetate -hexane (Rf= 0.7). THF was removed in vacuum and the residue was partitioned between water-ethyl acetate. The ethyl acetate layer was washed with brine, dried over Na2S04 and concentrated. The residue was purified on silica gel using ethyl acetate-hexane to give title product 4. 1H-NMR (CDC13, 200MHz) : 8 1.86-2.39 (m, 4H), 4.i2-4.21 (dd J=4.SHz, 13.6Hz , 1H), 4.43-4.55 (t, J=9Hz, 1H), 4.57-4.75(m, 1H), 4.89-5.14(m,2H), 5.65-5.87 (m, 1H), 6.69-7.05 (m, 4H), 7.63-798 (m, ~4H). Mass : 340 (M++1).
Part 5: (2S)-1-(4-flourophenyl)hex-5-ene-2-amine (Scheme X;
To a boiling solution of compound 4 (7.2g , 0.02mmo1) in 100 ml of ethanol was added hydrazine hydrate (l.Smi , 0.03mmol). The reaction mixture was refluxed for 4h and cooled to 0°C. Ethanol was removed under vacuum and partitioned between water-ethyl acetate. The ethyl acetate layer was separated, dried over NazSO4 , concentrated to get free amine 5 (4g} which was used as such for thc; next reaction. 1H-NMR
(CDCl3, 200MHz) : & 1.54-1.8 (m, 2H}, 2.12-2.38 (m, 2H}, 3.09-3.3 {broad s, 2H}, 3.64-3.78 (m, 1H), 3.8-3.98 (m, 2H), 4.95-5.18 (m, 2H}, 5.72-5.96 (m, 1H), 6.75-7.1 (m, 4H).
Part 6: (2S)-1-(4-fluorophenyi)hex-5-ene-2-N-tributyloxycarbonyl amine (Scheme X; 6}
To a solution of compound 5 (3.8g, O.Olmmol) in 40m1 THF was added triethyl amine (1.2m1, O.Olmmol) and (Boc)20 (2.1m1, 0.01:3mmol). The reaction mixture was stirred for 4h and the completion of the reaction was judged by TLC {15% ethyl acetate-hexane, Rf= 0.8) . The residue was concentrated, diluted with ethyl acetate, washed with water and brine, dried over NazS04 and concentrated under vacuum to give title product 6 {4.6g), which was purified on silicagel column. The overall yield of the two step i.e. from compound 4-6 is 70 %. ~H-N1V1R (CDCl3, 200MHz): ~ 1.38-1.43 (s, 9H), 1.67-1.82 (m , 2H), 2.I9-2.23 (q, J=4.SHz, 2H), 3.82-3.98 (s, 3H), 4.6-4.76 (broad s, 1H), 4.92-5.1 (m,2H), 5.7-5.9 (m, 1H), 6.74-7.03 (m, 4H). Mass : 310 (M++1) Part 7: (SS)-1-tert-butyloxycarbanyl-5-(4-fluoro)phenoxymethylpyrrolidin-2-of (Scheme X; 7) To a solution of compound 6 (3g) in dry methylene chloride (SOmI) was subjected to ozonolysis and stirred for 2 hours at -78°C. The completion of the reaction was judged by TLC in 20% ethylacetate-hexane (Rf = 0.8). The. reaction was quenched with dimethylsulphate, and concentrated to afford 10g of crude product (1.5g). 1H
NMR
(200MHz, CDCi3): 8 1.52 (s; 9H), 1.80-2.42 (m, 4H',~, 3.6-4.25 (m, 3H}, 5.32-5.6 (m, 1H), 6.77-7.3 (m, 4H). HRMS: cal :311.1532, found: 311.1545 Part 8: (SS}- I-tert-butoxycarbonyl -5-(4-fluoro)phenoxymethyl -2-methoxypyrrolidine (Scheme X; 8) (SS)-1-tert-butyloxycarbonyl-2-{4-fluoro)phe;noxymethylpyrrolidin-2-of (l.Og, 0.32mmol) and PPTS (8mg, 0.32mmo1) were taken :in l Oml of methanol. After being stirred for 18h at room temperature, evaporation of the solvent gave a residue which on purification on silicagel column afforded l.Og (96%;) of pure product, TLC :
20%
ethylacetate-hexane Rf= 0.5. 1H NMR (200MHz, CDCl3): 8 1.5 (s, 9H), 1.75-2.25 (rn, 4H), 3.23-3.5 (m, 3H), 3.72-3.9 (m, 1H), 4.02-4.38 (m, 2H), 5.1-5.5 (m, 1H), 6.76-7.02 (m, 4H).
Part 9: (SS)-2-benzenesufonyl-1-tent-butoxyc;arbony-5-{4-fluoro)phenoxymethyl pyrrolidine (Scheme X; 9_) A solution of (SS)-5-(4-fluoro)phenoxymethyl-1-tent-butoxycarbonyl-2-methoxypyrroladine (0.9g, 3.OISmmol) in dry DCM (lOml) containing powdered CaCl2 (O.Sg) was cooled to 0°C. Freshly prepared benzenesulfinic acid (0.43g, 3.015 mmol) was then added at once. The reaction mixture was starred for 2h at ambient temperature . and then cooled back to 0°C. Aqueous saturated NalFIC03 solution was added and the stirnng was continued for lhour. The suspension w<~s filtered and the filtrate was washed with water and brine, dried over anhydrous Na2S04.~nd concentrated to a ford 1.18g of pure product (90%), TLC was done in 20% ethylacetate-hexane, Rf = 0.4.
1H NMR (200MHz, CDCI3) : 8 I.20 (s, 9H), 2.1-2.S'7 (m, 3H), 2.7-2.83 (rn, IH), 4.07-4.52 (m, 3H), S.1-S.2S (m, iH), 6.87-7.07 (m, 4H), i'.48-7.77 (m, 3H), 7.85-7.97 (m, 2H) IR (neat, cm'1) : 2976,17S2,1S04, 1488, 1456, 1368, 1312, 1216, 1152, 1088, 1040, 832, 768, 688, 560. FABMS (m/z) : 12S,1S4, 194,195,194,434,435,436 (M++1) HRMS : calcd. 436.159398, found 436. 162468. Melting point : 1 I3-114°C.
Part 10: (ZS,SS)-1-tert-butoxycarbonyl-2-(4-~fluoro)phenoxymethyl-S-{2hydroxyethyl)ethynyl pyrrolidine (Scheme X; 10}
To a solution of I-tetrahydropyranyloxy-3-butynylmagnesium bromide in THF
[prepared in situ by the addition of isoprapylmagnesiium bromide in THF to 2-(3-butynyl-1-oxy)tetrahydropyran (O. I l g, 0.7mmo1)], was added a mixture of zinc bromide in .THF .
(78rng, 0.3Smmol} at ambient temperature. To the colorless suspension, farmed after 30 min. of stirnng, was added (SS)-2-benzenesulfonyl-1-tert-butaxycarbony-S-(4-fluoro) phenoxymethylpyrrolidine (0.1 Sg, 0.3Smmol) in 12 ml of THF. The reaction mixture was stirred for 10 hours. The reaction mixture was quenched with aqueous NH4C1 solution (0.3m1} and partitioned between ether (30m1} and water (lOml). The organic layer was washed with brine, dried over anhydrous NazS04 and concentrated to afford the crude product which was dissolved in methanol (I.SmI). PPTS (7mg, 0.026mmo1) was added and the reaction mixture was stirred at room temperature overnight. The residue after the removal of methanol, was purified by column chromatography (60-124mesh, 30% ethyl acetate in hexane) to afford the pure product as colorless oil (100mg, 86%) TLC: 30% ethyl acetate-hexane, Rf= 0.4; 1H NMR{200 Mhz, CDC13): 8 1.49 (s, 9H), 1.SS-1.82{m, 2H), 1.87-2.0(m, 1H}, 2.0-2.3(m, 2H), 2.35-2.S{m, 2H), 3.6-3.75(t, 2H), 3.75-3.9(m; 1H), 3.95-4.25(m, 2H), 4.44-4.58(m, 1H), 6.77-7.0(m, 4H).
FABMS(m/z) I07, 136, 138, 154, 194, 238, 264, 308, 364 (M++1) WO 00!01670 PCT/US99/15050 Part 11: (2S,SS)-1-tert-butoxycarbonyl-2-(4--fluoro)phenoxymethyl-5-(4-N,O-bis-phenoxycarbonylhydroxyarnino-1-butynyl)pyrrolidine (Scheme X; 11):
To a solution of (2S,SS)-I-tert-butoxycarbonyl-5-(2-hydroxyethyl)ethynyl-2-(4-fluoro)phenoxyrnethylpyrrolidine (82mg, 0.226mmo~1), triphenyphosphine {7lmg, 0.27mmo1) and N,O-bis-phenoxycarbonylhydroxyla~mine (70mg, 2.7mmol) was added diethyl azodicarboxylate {50mg, 0.27mmol) dropwise. The mixture was stirred for 30 min. at 0°C and then for 6 hours at room temperature;. The solvent was removed under vacuum and the residue was purified by column chromatography (30% ethyl acetate in hexane, Rc= 0.7) to afford colorless semi-solid (112mg, 80%). 1H NMR (200 MHz, CDC13) : 8 1.5 (s, 9H), 1.88-2.4 (m, 4H), 2.62-2.77 (t, 2H), 3.65-4.29 {m, SH), 4.4-4.6 (m, 1 H}, 6.76-7.1 (m, 4H), 7.1-7.3 {m, 6H), 7.3-7.5 (m, 4H).
Part 12: (2S,SS)-1-tent-butoxycarbonyl-2-{4iluoro)phenoxymethyl-I5 5-(4-hydroxyureidyl-1-butynyl)pyrrolidine (Scheme X; 12):
Ammonia gas was purged into a solution of {2S,SS)-1-tert-butoxycarbonyl-2-(4-fluoro)phenoxymethyl-5-(4-N,O-bis-phenoxycarbon,ylhydroxy amino-1-butynylpyrrolidine (100mg, 0.226mmol) in a solvent mixture of methanol (3m1) and THF
(I ml) at 0°C for 15 min. The reaction mixture was stirred for 6hours at room temperature. Evaporarion of the solvent and purification of the residue by column chromatography (30% ethyl acetate in hexane, Rf= C1.6) afforded 80mg of pure.product as colourless liquid (85%). 1H NMR {200MHz, CD(:13) : 8 1.5 {s, 9H), 1.85-2.31 (m, 4H}, 2.36-2.5 {t, 2H), 3.5-3.68 (m, 1H), 3.69-3.90 (m~, 2H), 3.93-4.4 (dd, 1H, J= 7.9, J=3.4Hz), 4.07-4.2 (m, 1H), 4.35-4.55 (m, 1H), 5.1-5.35 (br s, 2H), 6.73-7.0 (m, 4H).
IR (neat, crn 1) : 3504, 3450-3000 ( br), 2960, 1688, 1512, 1392, 1208,1160, 760.
FABMS{m/z) : 153,194, 274, 322, 388, 422 (M'~+1).

-SS-Part 13: (2S,SS) -(4-fluoro)phenoxymethyl-S~-(4-hydroxyureidyl-1-butynyl)pyrrolidine (Scheme X; 13 Trifluoroacetic acid (O.OSmI, O.S49mmo1) was added to a solution of substrate (80mg, 0.183mmo1) in irnl of CHZCIx at 0°C. The reaction mixture was stirred for 3h at S room temperature. Aqueous saturated NaHC03 was added at 0°C. After being stirred for min. the organic layer was separated, washed with. brine, dried over anhydrous Na2SOa and concentrated to afford the brown residue which was purified by column chromatography (10% methanol in ethyl acetate Rf= 0.6) to afford the colourless semi-solid (SSmg, 86%). 1H NMR (200 MHz,CDCl3): 8 l.S-i.97 (m, 4H), 2.01-2.25 (m, 2H), 10 2.38-2.6 (t, J=2.17Hz, 2H), 3.52-3.7 (t, J=6.S4Hz, 2H:), 3.72-4.04 (m, 4H), 6.73-7.6 (m, 4H). FABMS(m/z) : 107, 120, 124, 136, 138, 154, 1'76, 194, 268, 279, 322 (M++1) Example 4: Human whole blood assay The following compound of the invention was tested for Leukotriene B4 inhibition in the human whole blood assay detailed below.
0 ~~
~~~lVhfi i OH
Heparinized human whole blood was pre-incubated with selected concentrations of the test compound for 1S minutes at 37°C and stimulated with SO ~M
calcium ionphor for 30 minutes at 3?°C. The reaction was stopped by placing samples on ice and cold centrifugation at 4°C for 10 minutes at 1100 x g. Test sample plasma was diluted in buffer and assayed for LTB4 content. Test compound activity was determined as per Cayman LTD EIA and evaluated as ICso [nM]. The compound had an ICso of 2S6 nM.

The invention has been described in detail including preferred embodiments thereof. However, it will be understood that those sls:illed in the art, upon consideration of this disclosure, may make modifications and improvements thereon without departing from the spirit and scope of the invention as set forth, in the following claims.

Claims (84)

What is claimed is:

1. A method for preparing a hydroxy-substituted tetrahydrothiophene, comprising:
a) providing a thioepoxy-aryl ether;
b} reacting the epoxy-aryl ether with an active methylene compound to form a lactone; and c) reducing the lactone to provide a hydroxy-substituted tetrahydrothiophene.

2. The method of claim 1 wherein the aryl group of the thioepoxy-aryl ether is a carbocyclic aryl.

3. The method of claim 1 wherein the aryl group of the thioepoxy-aryl ether is a hetero aryl.

4. The method of claim 1 wherein the thioepoxy-aryl ether is optically active.

5. The method of claim 1 wherein the thioepoxy-aryl ether is racemic.

6. The method of claim 1 wherein the active methylene compound is a diester or a half ester thereof.

7. The method of claim 1 wherein the active methylene compound is a dialkyl malonate.

8. The method of claim 1 further comprising activating the hydroxy group of the hydroxy-substituted tetrahydrothiophene and substituting the activated tetrahydrothiophene position.

9. The method of claim 8 wherein the tetrahydrothiophene position is substituted with a nucleophilic compound.

10. The method of claim 10 wherein the tetrahydrothiophene position is substituted with a 1-alkynyl compound.

11. The method of any one of claims 8-10 wherein the substitution produces an enantiomeric excess of a stereoisomer.

12. The method of claim 11 wherein the substitution produces a stereoisomer that is present in at least about 60 percent relative to the other stereoisomer.

13. The method of claim 11 wherein the substitution produces a stereoisomer that is present in at least about 70 percent relative to the other stereoisomer.

14. The method of claim 11 wherein the substitution produces a trans stereoisomer that is present in at least about 60 percent relative to the cis stereoisomer.

15. The method of claim 11 wherein the substitution produces a trans stereoisomer that is present in at least about 70 percent relative to the cis stereoisomer.

16. The method of claim 11 wherein the substitution produces a cis stereoisomer that is present in at least about 60 percent relative to the trans stereoisomer.

17. The method of claim 11 wherein the substitution produces a cis stereoisomer that is present in at least about 70 percent relative to the trans stereoisomer,

18. The method of claim of claim 1 wherein the hydroxy-substituted tetrahydrothiophene is represented by the following formula:

wherein Ar is optionally substituted carbocyclic aryl or heteroaryl.

19. The method of claim 18 wherein Ar is optionally substituted carbocyclic aryl.

20. The method of claim 18 wherein Ar is optionally substituted phenyl.

21. A method for preparing an alkynyl-substituted tetrahydrothiopene, thiane, thiepane, or thiocane, comprising:
treating with base a compound comprising a substituted alkyl group to form an alkynyl-substituted tetrahydrothiopene, alkynyl-substituted thiane, alkynyl-substituted thiepane, or alkynyl-substituted thiocane, wherein the substituted alkyl group has 6, 7, 8, 9 or more carbon atoms, the 2,3-positions of alkyl group forming an epoxide ring, the 1-position of the alkyl group substituted with a first leaving group, and the 6-,7-, 8- or 9-position of the alkyl group substituted with a second leaving group.
22. The method of claim 21 wherein the substituted alkyl compound is treated with a molar excess of base.

22. The method of claim 21 wherein the substituted alkyl compound is treated with about a three molar excess of base.

23. The method of claim 21 wherein the base is an alkyllithium reagent, an amide salt or a hydride.

24. The method of claim 21 wherein the first and second leaving groups are each independently a halogen, a sulfonic alkyl ester, a sulfonic aryl ester or a sulfonic arylalkyl ester.

25. The method of claim 21 wherein one or both of the epoxide carbons are optically active.

26. The method of claim 21 wherein the formed tetrahydrothiopene, thiane, thiepane, or thiocane is optically active.

27. The method of claim 21 wherein both of the epoxide carbons are optically active.

28. The method of claim 27 wherein the two carbons adjacent to the ring sulfur of the formed tetrahydrothiopene, thiane, thiepane, or thiocane are each optically active.

29. The method of claim 27 wherein the tetrahydrothiopene, thiane, thiepane, or thiocane is formed from the substituted alkyl compound without isolation of intermediate compounds.

30. The method of claim 29 wherein the tetrahydrothiopene, thiane, thiepane, or thiocane is formed from the substituted alkyl compound in a single reaction step.

31. The method of claim 21 wherein the substituted alkyl compound is substituted at the 7, 8 or 9 carbons by an alkoxy, arylalkoxy or aryloxy group.

32. The method of claim 21 where the alkyl-substituted compound is substituted at the 6-position with the second leaving group, and treatment with base provides an alkynyl-substituted tetrahydrothiophene.

33. The method of claim 32 wherein a tetrahydrothiophene of the following formula is provided:
wherein Ar is optionally substituted carbocyclic aryl or heteroaryl.

34. The method of claim 21 where the alkyl-substituted compound is substituted at the 7-position with the second leaving group, and treatment with base provides an alkynyl-substituted thiane.

35. The method of claim 34 where the thiane is represented by the following formula:
wherein Ar is optionally substituted carbocyclic aryl or heteroaryl;
Z is a chemical bond, optionally substituted alkylene, optionally substituted alkenylene, optionally substituted alkynylene, optionally substituted heteroalkylene, optionally substituted heteroalkenylene, optionally substituted heteroalkynylene, or a hetero atom;

each R1 is independently hydrogen or a non-hydrogen substituent, at least one being present as a 1-alkynyl substituted on the thiane ring;.
q is an integer of from 1 to 9.

36. The method of claim 21 where the alkyl-substituted compound is substituted at the 8-position with the second leaving group, and treatment with base provides an alkynyl-substituted thiepane.

37. The method of claim 36 where the thiepane is represented by the following formula:
wherein Ar is optionally substituted carbocyclic aryl or heteroaryl;
Z is a chemical bond, optionally substituted alkylene, optionally substituted alkenylene, optionally substituted alkynylene, optionally substituted heteroalkylene, optionally substituted heteroalkenylene, optionally substituted heteroalkynylene, or a hetero atom;
each R1 is independently hydrogen or a non-hydrogen substituent, at least one being present as a 1-alkynyl substituted on the thiepane ring;.
r is an integer of from 1 to 9.

38. The method of claim 21 where the alkyl-substituted compound is substituted at the 9-position with the second leaving group, and treatment with base provides an alkynyl-substituted thiocane.

39. The method of claim 38 where the thiocane is represented by the following formula:
wherein Ar is optionally substituted carbocyclic aryl or heteroaryl;
Z is a chemical bond, optionally substituted alkylene, optionally substituted alkenylene, optionally substituted alkynylene, optionally substituted heteroalkylene, optionally substituted heteroalkenylene, optionally substituted heteroalkynylene, or a hetero atom;
each R1 is independently hydrogen or a non-hydrogen substituent, at least one being present as a 1-alkynyl substituted on the thiocane ring;.
s is an integer of from 1 to 11.

40. A method for preparing an alkynyl-substituted pyrrolidine, hexahydropyridine, hexahydroazepine or octahydroazocine, comprising:
treating with base a compound comprising a substituted alkyl group to form an alkynyl-substituted pyrrolidine, alkynyl-substituted hexahydropyridine , alkynyl-substituted hexahydroazepine, or alkynyl-substituted octahydroazocine, wherein the substituted alkyl group has 6, 7, 8, 9 or more carbon atoms, the 2,3-positions of alkyl group forming an epoxide ring, the 1-position of the alkyl group substituted with a leaving group, and the 6-,7-, 8- or 9-position of the alkyl group substituted with an azido group.

41. The method of claim 40 wherein the substituted alkyl compound is treated with a molar excess of base.

42. The method of claim 40 wherein the substituted alkyl compound is treated with about a three molar excess of base.

43. The method of claim 40 wherein the base is an alkyllithium reagent, an amide salt or a hydride.

44. The method of claim 40 wherein the leaving group is halogen, a sulfonic alkyl ester, a sulfonic aryl ester or a sulfonic arylalkyl ester.

45. The method of claim 40 wherein one or both of the epoxide carbons are optically active.

46. The method of claim 40 wherein the formed pyrrolidine, hexahydropyridine, hexahydroazepine or octahydroazocine is optically active.

47. The method of claim 40 wherein both of the epoxide carbons are optically active.

48. The method of claim 40 wherein the two carbons adjacent to the ring nitrogen of the formed pyrrolidine, hexahydropyridine, hexahydroazepine or octahydroazocine are each optically active.

49. The method of claim 40 wherein the pyrrolidine, hexahydropyridine, hexahydroazepine or octahydroazocine is formed from the substituted alkyl compound without isolation of intermediate compounds.

50. The method of claim 40 wherein the pyrrolidine, hexahydropyridine, hexahydroazepine or octahydroazocine is formed from the substituted alkyl compound in a single reaction step.

51. The method of claim 40 wherein the substituted alkyl compound is substituted at the 7, 8 or 9 carbons by an alkoxy, arylalkoxy or aryloxy group.

52. The method of claim 40 where the alkyl-substituted compound is substituted at the 6-position with the azido group, and treatment with base provides an alkynyl-substituted pyrrolidine.

53. The method of claim 52 wherein a pyrrolidine of the following formula is provided:
wherein Ar is optionally substituted carbocyclic aryl or heteroaryl.

54. The method of claim 40 where the alkyl-substituted compound is substituted at the 7-position with the azido leaving group, and treatment with base provides an alkynyl-substituted hexahydropyridine.

55. The method of claim 54 where the hexahydropyridine is represented by the following formula:
wherein Ar is optionally substituted carbocyclic aryl or heteroaryl;

Z is a chemical bond, optionally substituted alkylene, optionally substituted alkenylene, optionally substituted alkynylene, optionally substituted heteroalkylene, optionally substituted heteroalkenylene, optionally substituted heteroalkynylene, or a hetero atom;
each R1 is independently hydrogen or a non-hydrogen substituent, at least one being present as a 1-alkynyl substituted on the hexahydropyridine ring;.
q is an integer of from 1 to 9.

56. The method of claim 40 where the alkyl-substituted compound is substituted at the 8-position with the azido group, and treatment with base provides an alkynyl-substituted hexahydroazepine.

57. The method of claim 56 where the hexahydroazepine is represented by the following formula:
wherein Ar is optionally substituted carbocyclic aryl or heteroaryl;
Z is a chemical bond, optionally substituted alkylene, optionally substituted alkenylene, optionally substituted alkynylene, optionally substituted heteroalkylene, optionally substituted heteroalkenylene, optionally substituted heteroalkynylene, or a hetero atom;
each R1 is independently hydrogen or a non-hydrogen substituent, at least one being present as a 1-alkynyl substituted on the hexahydroazepine ring;
r is an integer of from 1 to 9.

58. The method of claim 40 where the alkyl-substituted compound is substituted at the 9-position with the azido group, and treatment with base provides an alkynyl-substituted octahydroazocine.

59. The method of claim 58 where the octahydroazocine is represented by the following formula:
wherein Ar is optionally substituted carbocyclic aryl or heteroaryl;
Z is a chemical bond, optionally substituted alkylene, optionally substituted alkenylene, optionally substituted alkynylene, optionally substituted heteroalkylene, optionally substituted heteroalkenylene, optionally substituted heteroalkynylene, or a hetero atom;
each R1 is independently hydrogen or a non-hydrogen substituent, at least one being present as a 1-alkynyl substituted on the octahydroazocine ring;.
s is an integer of from 1 to 11.

60. A method for preparing an N-hydroxy-substituted urea compound, comprising (a) reacting a urea compound where at least one of the urea nitrogens is protected with a methoxybenzyl group, (b) in the presence of a dehydrating agent, reacting the protected urea an alkyl or aryl group that comprises a hydroxy substituent, (c) treating the compound of step (b) with ammonia and a Lewis acid.

61. The method of claim 60 wherein the dehydrating agent is a triphenyl phosphine and diethylazodicarboxylate.

62. The method of claim 60 wherein the protecting group is para-methoxybenzyl.

63. The method of claim 60 wherein the Lewis acid is boron trifluoride.

64. A method for preparing an aryl-substituted alicyclic compound having a nitrogen ring member, comprising:
reacting an alicyclic compound having a nitrogen ring member and an alkyl ring substituent with an aryl nucleophile in the presence of a hydride reagent to yield the alicyclic compound having an arylalkyl substituent.

65. The method of claim 64 wherein the aryl nucleophile is an aryl hydroxy compound and the reaction yields an alicyclic compound having an aryloxyalkyl substituent.

66. The method of claim 64 or 65 wherein the aryl nucleophile is a carbocyclic aromatic compound.

67. The method of claim 66 wherein the aryl nucleophile is an optionally substituted phenol.

68. The method of claim 64 wherein alkyl ring substituent is a substituted methyl group.

69. The method of claim 64 wherein the alicyclic compound is a pyrrolidine, hexahydropyridine, hexahydroazepine or octahydroazocine compound.

70. A method for preparing a substituted alicyclic compound having a nitrogen ring member, comprising:
reacting an alicyclic compound having a nitrogen ring member and an alkoxy ring substituent with a sulfuric acid reagent to form a sulfonyl ring substituent.

71. The method of claim 70 wherein the alicyclic compound with sulfinic substituent is reacted with an alkynyl compound to yield an alicyclic compound having an alkynyl ring substituent.

72. The method of claim 70 wherein the an optionally substituted phenylsulfinic reagent is reacted with the alicyclic compound.

73. A compound of the following Formula I:
wherein X is S, S(O), S(O)2, N or substituted N (including N-alkyl and N-oxide);
Ar is optionally substituted carbocyclic aryl or optionally substituted heteroaryl;
each R1, Y and Y' is independently hydrogen or a non-hydrogen substituent;
Z is a chemical bond, optionally substituted alkylene, optionally substituted alkenylene, optionally substituted alkynylene, optionally substituted heteroalkylene, optionally substituted heteroalkenylene, optionally substituted heteroalkynylene, or a hetero atom such as O, S, S(O), S(O)2, or NR1 wherein R1 is the same as defined immediately above;
n is an integer from 2 to 11;
p is an integer from 0; and pharmaceutically acceptable salts thereof.

74. A compound of claim 73 wherein n is 1.

75. A compound of claim 73 wherein X is optionally substituted nitrogen or sulfur.

76. A compound of claim 73 wherein each R1, Y and Y' is independently hydrogen, as halogen, hydroxyl, optionally substituted alkyl, optionally substituted alkenyl preferably, optionally substituted alkynyl, optionally substituted alkoxy, optionally substituted alkylthio, optionally substituted alkylsulfinyl, optionally substituted alkylsulfonyl, optionally substituted aminoalkyl, optionally substituted alkanoyl, optionally substituted carbocyclic aryl having at least about 6 ring carbons, or substituted or unsubstituted aralkyl having at least about 6 ring carbons.

77. A compound of the following Formula III:
wherein X is S, S(O), S(O)2, N or substituted N;
Ar is optionally substituted carbocyclic aryl or optionally substituted heteroaryl;
each R1 is independently hydrogen or a non-hydrogen substituent;
Z is a chemical bond, optionally substituted alkylene, optionally substituted alkenylene, optionally substituted alkynylene, optionally substituted heteroalkylene, optionally substituted heteroalkenylene, optionally substituted heteroalkynylene, or a hetero atom such as O, S, S(O), S(O)2, or NR1 wherein R1 is the same as defined immediately above;
and q is an integer of from 0 to 9, and pharmaceutically acceptable salts thereof.

78. A compound of claim 77 wherein the compound is of the following Formula IIIa:
wherein Ar, X, Z, R1 and q' are the same as defined for Formula III;
W is -AN(OM)C(O)N(R3)R4, -N(OM)C(O)N(R3)R4, -AN(R3)C(O)N(OM)R4, -N(R3)C(O)N(OM)R4, -AN(OM)C(O)R4, -N(OM)C(O)R4, -AC(O)N(OM)R4, -C(O)N(OM)R4, or -C(O)NHA; and A is lower alkyl, lower alkenyl, lower alkynyl, alkylaryl or arylalkyl, wherein one or more carbons optionally can be replaced by N, O or S, however -Y-A-, -A-, or -AW- should not include two adjacent heteroatoms;
M is hydrogen, a pharmaceutically acceptable cation or a metabolically cleavable leaving group;
Y is O, S, S(O), S(O)2, NR3 or CHR5;
R3 and R4 are independently hydrogen, alkyl, alkenyl, alkynyl, aryl, arylalkyl, C1-6alkoxy-C1-10alkyl, C1-6 alkylthio-C1-10 alkyl, heteroaryl, or heteroarylalkyl;
R5 is hydrogen, lower alkyl, lower alkenyl, lower alkynyl; arylalkyl, alkaryl, -AN(OM)C(O)N(R3)R4, -AN(R3)C(O)N(OM)R4, -AN(OM)C(O)R4, -AC(O)N(OM)R4, -AS(O)x R3, -AS(O)x CH2C(O)R3, -AS(O)x CH2CH(OH)R3, or AC(O)NHR3, x is 0, 1 or 2;
m is 0 or 1; and pharmaceutically acceptable salts thereof.

79. A compound of the following Formula IV:
wherein X is S, S(O), S(O)2, N or substituted N;
Ar is optionally substituted carbocyclic aryl or optionally substituted heteroaryl;
each R1 is independently hydrogen or a non-hydrogen substituent;
Z is a chemical bond, optionally substituted alkylene, optionally substituted alkenylene, optionally substituted alkynylene, optionally substituted heteroalkylene, optionally substituted heteroalkenylene, optionally substituted heteroalkynylene, or a hetero atom such as O, S, S(O), S(O)2, or NR1 wherein R1 is the same as defined immediately above; and r is an integer of from 0 to 11; and pharmaceutically acceptable salts thereof.

80. A compound of claim 79 wherein the compound is of the Formula Formula IVa:
wherein Ar, Z, X, and R1 are the same as defined for Formula IV above;

W is -AN(OM)C(O)N(R3)R4, -N(OM)C(O)N(R3)R4, -AN(R3)C(O)N(OM)R4, -N(R3)C(O)N(OM)R4, -AN(OM)C(O)R4, -N(OM)C(O)R4, -AC(O)N(OM)R4, -C(O)N(OM)R4, or -C(O)NHA; and A is lower alkyl, lower alkenyl, lower alkynyl, alkylaryl or arylalkyl, wherein one or more carbons optionally can be replaced by N, O or S, however -Y-A-, -A-, or -AW- should not include two adjacent heteroatoms;
M is hydrogen, a pharmaceutically acceptable cation or a metabolically cleavable leaving group;
Y is O, S, S(O), S(O)2, NR3 or CHR5;
R3 and R4 are independently hydrogen, alkyl, alkenyl, alkynyl, aryl, arylalkyl, C1-6alkoxy-C1-10alkyl, C1-6 alkylthio-C1-10 alkyl, heteroaryl, or heteroarylalkyl;
R5 is hydrogen, lower alkyl, lower alkenyl, lower alkynyl, arylalkyl, alkaryl, -AN(OM)C(O)N(R3)R4, -AN(R3)C(O)N(OM)R4, -AN(OM)C(O)R4, -AC(O)N(OM)R4, -AS(O)x R3, -AS(O)x CH2C(O)R3, -AS(O)x CH2CH(OH)R3, or AC(O)NHR3, x is 0, 1 or 2;
and r' is an integer of from 0 to 10; and pharmaceutically acceptable salts thereof.

81. A compound of the following Formula V:
wherein X is S, S(O), S(O)2, N or substituted N;
Ar is optionally substituted carbocyclic aryl or optionally substituted heteroaryl;
each R1 is independently hydrogen or a non-hydrogen substituent;
Z is a chemical bond, optionally substituted alkylene, optionally substituted alkenylene, optionally substituted alkynylene, optionally substituted heteroalkylene, optionally substituted heteroalkenylene, optionally substituted heteroalkynylene, or a hetero atom such as O, S, S(O), S(O)2, or NR1 wherein R1 is the same as defined immediately above;

and s is an integer of from 0 to 13; and pharmaceutically acceptable salts thereof.

82. A compound of claim 81 wherein the compound is of the following Formula Va:
wherein Ar, X, Z, and R1 are each the same as defined for Formula V;
W is -AN(OM)C(O)N(R3)R4, -N(OM)C(O)N(R3)R4, -AN(R3)C(O)N(OM)R4, -N(R3)C(O)N(OM)R4, -AN(OM)C(O)R4, -N(OM)C(O)R4, -AC(O)N(OM)R4, -C(O)N(OM)R4, or -C(O)NHA; and A is lower alkyl, lower alkenyl, lower alkynyl, alkylaryl or arylalkyl, wherein one or more carbons optionally can be replaced by N, O or S, however -Y-A-, -A-, or -AW- should not include two adjacent heteroatoms;
M is hydrogen, a pharmaceutically acceptable cation or a metabolically cleavable leaving group;
Y is O, S, S(O), S(O)2, NR3 or CHR5;
R3 and R4 are independently hydrogen; alkyl, alkenyl, alkynyl, aryl, arylalkyl, C1-6alkoxy-C1-10 alkyl, C1-6 alkylthio-C1-10 alkyl, heteroaryl, or heteroarylalkyl;
R5 is hydrogen, lower alkyl, lower alkenyl, lower alkynyl, arylalkyl, alkaryl, -AN(OM)C(O)N(R3)R4, -AN(R3)C(O)N(OM)R4, -AN(OM)C(O)R4, -AC(O)N(OM)R4, -AS(O)x R3, -AS(O)x CH2C(O)R3, -AS(O)x CH2CH(OH)R3, or -AC(O)NHR3, x is 0, 1 or 2;
and s is an integer of from 0 to 10; and pharmaceutically acceptable salts thereof.

83. A pharmaceutical composition comprising a compound of any one of claims 73-82 and a pharmaceutically acceptable carrier.

84. A method of treating a disorder or disease associated with 5-lipoxygenase, comprising administering to a subject suffering from or susceptible to such a disease or disorder an effective amount of a compound or composition of any one of claims 73-83.
8s. A method of treating a immune, allergic or cardiovascular disorder or disease, comprising administering to a subject suffering from or susceptible to such a disease or disorder an effective amount of a compound of any one of claims 73-83.