CA2494632A1

CA2494632A1 - 3-amino-2-hrydroxyalkanoic acids and their prodrugs

Info

Publication number: CA2494632A1
Application number: CA002494632A
Authority: CA
Inventors: Nwe Y. Bamaung; Richard A. Craig; Jack Henkin; Megumi Kawai; Xenia B. Searle; George S. Sheppard; Jieyi Wang
Original assignee: Individual
Current assignee: Abbott Laboratories
Priority date: 2002-08-06
Filing date: 2003-08-05
Publication date: 2004-02-12
Also published as: EP1546087A1; MXPA05001467A; JP2005534702A; WO2004013085A1

Abstract

Compounds having the formula are useful for treating conditions which arise from or are exacerbated by angiogenesis. Also disclosed are pharmaceutical compositions comprising the compounds, methods of treatment using the compounds, methods of inhibiting angiogenesis, and methods of treating cance r.

Description

Technical Field The present invention relates to novel compounds having methionine aminopeptidase-2 inhibitory (MetAP2) activity useful for treating conditions which arise from or are exacerbated by angiogenesis, pharmaceutical compositions comprising the compounds, l0 methods of treatment using the compounds, methods of inhibiting angiogenesis, and methods of treating cancer.
Packground of the Invention Angiogenesis is the fundamental process by which new blood vessels are formed and 15 is essential to a variety of normal body activities (such as reproduction, development, and wound repair). Although the process is not completely understood, it is believed to involve a complex interplay of molecules which both stimulate and inhibit the growth of endothelial cells, the primary cells of the capillary blood vessels. Under normal conditions these molecules appear to maintain the microvasculature in a quiescent state (i.e., one of no 2o capillary growth) for prolonged periods that may last for weeks, or in some cases, decades.
However, when necessary, such as during wound repair, these same cells can undergo rapid proliferation and turnover within as little as five days.
Although angiogenesis is a highly regulated process under normal conditions, many diseases (characterized as "angiogenic diseases") are driven by persistent unregulated 25 angiogenesis. Otherwise stated, unregulated angiogenesis may either cause a particular disease directly or exacerbate an existing pathological condition. Thus, there is a continuing need for compounds which demonstrate antiangiogenic activity.
Summary of the Invention 3o In its principle embodiment, the present invention provides a compound of formula (17 OH
( or a therapeutically acceptable salt thereof, wherein Rl is selected from the group consisting of alkyl, alkylsulfanylalkyl, aryl, arylalkyl, 35 cycloalkyl, (cycloalkyl)alkyl, (heterocycle}alkyl, and hydroxyalkyl; and R2 is selected from the group consisting of hydrogen, alkenyl, alkyl, alkylcarbonyloxyalkyl, alkylcarbonylalkyl, aryl, arylalkyl, cycloalkyl, (cycloalkyl)alkyl, heterocycle, and (heterocycle)alkyl.
In another embodiment, the present invention provides a phal-maceutical composition comprising a compound of formula (I), or a therapeutically acceptable salt thereof, in combination with a therapeutically acceptable carrier.
In another embodiment, the present invention provides a method of inhibiting angiogenesis in a mammal in recognized need of such treatment comprising administering to the mammal a pharmaceutically acceptable amount of a compound of formula (1?.
i0 In another embodiment, the present invention provides a method for treating cancer in a patient in recognized need of such treatment comprising administering to the patient a therapeutically acceptable amount of a compound of formula (I), or a therapeutically acceptable salt thereof.
15 Detailed Description of the Invention As used herein, the singular forms "a", "an", and "the" include plural reference unless the context clearly dictates otherwise.
As used in the present specification the following terms have the meanings indicated:
The term "alkenyl," as used herein, refers to a monovalent straight or branched chain 20 group of one to ten carbon atoms containing at least one carbon-carbon double bond.
The term "alkoxy," as used herein, refers to an alkyl group attached to the parent molecular moiety through an oxygen atom.
The term "alkyl," as used herein, refers to a group derived from a straight or branched chain saturated hydrocarbon of one to ten atoms.
25 The term "alkylcarbonyl," as used herein, refers to an alkyl group attached to the parent molecular moiety through a carbonyl group.
The term "alkylcarbonyloxy," as used herein, refers to an alkyIcarbonyl group attached to the parent molecular moiety through an oxygen atom.
The term "alkylcarbonyloxyaIkyl," as used herein, refers to an alkylcarbonyloxy group 30 attached to the parent molecular moiety through an alkyl group.
The teim "alkylsulfanyl," as used herein, refers to an alkyl group attached to the parent molecular moiety through a sulfur atom.
The term "alkylsulfanylalkyl," as used herein, refers to an alkylsulfanyl group attached to the parent molecular moiety through an alkyl group.
35 The term "amino," as used herein, refers to -NRaRb, wherein Ra and Rb are independently selected from the group consisting of hydrogen, alkyl, alkylcarbonyl, cycIoalkyl, (cycioaIkyI)alkyI, and unsubstituted aryl.

The term "aryl," as used herein, refers to a phenyl group, or a bicyclic or tricyclic fused ring system wherein one or more of the fused rings is a phenyl group.
Bicyclic fused ring systems are exemplified by a phenyl group fused to a monocyclic cycloalkenyl group, as defined herein, a monocyclic cycloalkyl group, as defined herein, or another phenyl group.
Tricyclic fused ring systems are exemplified by a bicyclic fused ring system fused to a monocyclic cycloalkenyl group, as defined herein, a monocyclic cycloalkyl group, as defined herein, or another phenyl group. Representative examples of aryl include, but are not limited to, anthracenyl, azulenyl, fluorenyl, indanyl, indenyl, naphthyl, phenyl, and tetrahydronaphthyl. The aryl groups of the present invention can be optionally substituted to with one, two, three, four, or five substituents independently selected from the group consisting of alkoxy, alkyl, alkylcarbonyl, amino, carboxy, cyano, halo, haloalkoxy, haloalkyl, vitro, and oxo.
The term "arylalleyl," as used herein, refers to an aryl group attached to the parent molecular moiety through an alkyl group. The alkyl part of the arylalkyl can be optionally substituted with an amino group.
The term "carbonyl," as used herein, refers to -C(O)-.
The term "carboxy," as used herein, refers to -C02H.
The term "cyano," as used herein, refers to -CN.
The term "cycloalkenyl," as used herein, refers to a non-aromatic cyclic or bicyclic 2o ring system having three to ten carbon atoms and one to three rings, wherein each five-membered ring has one double bond, each six-membered ring has one or two double bonds, each seven- and eight-membered ring has one to three double bonds, and each nine-to ten-membered ring has one to four double bonds. Examples of cycloalkenyl groups include, but are not limited to, cyclohexenyl, octahydronaphthalenyl, and norbornylenyl.
The term "cycloalkyl," as used herein, refers to a saturated monocyclic, bicyclic, or tricyclic hydrocarbon ring system having three to twelve carbon atoms.
Examples of cycloalkyl groups include, but are not limited to, cyclopropyl, cyclopentyl, bicyclo[3.1.1]heptyl, and adamantyl.
The term "(cycloalkyI)alkyl," as used herein, refers to a cycloalkyl group attached to 3o the parent molecular moiety through an alkyl group.
The term "halo," or "halogen," as used herein, refers to F, Cl, Br, or I.
The term "haloalkoxy," as used herein, refers to a haloalkyl group attached to the parent molecular moiety through an oxygen atom.
The term "haloalkyl," as used herein, refers to an alkyl group substituted by one, two, three, or four halogen atoms.
The term "heterocycle," as used herein, refers to a five-, six-, or seven-membered ring containing one, two, or three heteroatoms independently selected from the group consisting of nitrogen, oxygen, and sulfur. The five-membered ring has zero to two double bonds and the six- and seven-membered rings have zero to three double bonds. The term "heterocycle" also includes bicyclic groups in which the heterocycle ring is fused to a phenyl group, a monocyclic cycIoalkenyl group, as defined herein, a monocyclic cycloalkyl group, as defined herein, or another monocyclic heterocycle group, as defined herein; and tricyclic groups in which a bicyclic system is fused to a phenyl group, a monocyclic cycloalkenyl group, as defined herein, a monocyclic cycloalkyl group, as defined herein, or another monocyclic heterocycle group. The heterocycle groups of the present invention can be attached to the parent molecular moiety through a carbon atom or a nitrogen atom in the group.
Examples of heterocycles include, but are not limited to, benzothienyl, furyl, imidazolyl, indolinyl, indolyl, isothiazolyl, isoxazolyl, morpholinyl, oxazolyl, piperazinyl, piperidinyl, pyrazolyl, pyridinyl, pyrrolidinyl, pyrrolopyridinyl, pyrrolyl, thiazolyl, thienyl, and.thiomorpholinyl. The heterocycle groups of the present invention can be optionally substituted with one, two, three, four, or five substituents independently selected from the group consisting of alkoxy, alkyl, alkylcarbonyl, amino, carboxy, cyano, halo, haloalkoxy, haloalkyl, nitro, and oxo.
The term "(heterocycle)alkyl," as used herein, refers to a heterocycle group attached to the parent molecular moiety through an alkyl group.
The term "nitro," as used herein, refers to -h.T02.
The term "oxo," as used herein, refers to =O.
2o The compounds of the present invention can exist as therapeutically acceptable salts.
The term "therapeutically acceptable salt," as used herein, represents salts or zwitterionic forms of the compounds of the present invention which are water or oil-soluble or dispersible, which are suitable for treatment of diseases without undue toxicity, irritation, and allergic response; which are commensurate with a reasonable benefit/risk ratio, and which are effective for their intended use. The salts can be prepared during the final isolation and purification of the compounds or separately by reacting an amino group with a suitable acid.
Representative acid addition salts include acetate, adipate, alginate, citrate, aspartate, benzoate, benzenesulfonate, bisulfate, butyrate, camphorate, camphorsulfonate, digluconate, glycerophosphate, hemisulfate, heptanoate, hexanoate, formate, fumarate, hydrochloride, 3o hydrobromide, hydroiodide, 2-hydroxyethansulfonate, lactate, maleate, mesitylenesulfonate, methanesulfonate, naphthylenesulfonate, nicotinate, 2-naphthalenesulfonate, oxalate, pamoate, pectinate, persulfate, 3-phenyIproprionate, picrate, pivalate, propionate, succinate, tartrate, trichloroacetate, trifluoroacetate, phosphate, glutamate, bicarbonate, para-toluenesulfonate, and undecanoate. Also, ammo groups in the compounds of the present invention can be quaternized with methyl, ethyl, propyl, and butyl chlorides, bromides, and iodides; dimethyl, diethyl, dibutyl, and diamyl sulfates; decyl, Iauryl, myristyl, and steryl chlorides, bromides, and iodides; and benzyl and phenethyl bromides. Examples of acids which can be employed to form therapeutically acceptable addition salts include inorganic acids such as hydrochloric, hydrobromic, sulfuric, and phosphoric, and organic acids such as oxalic, malefic, succinic, and citric.
Basic addition salts can be prepared during the final isolation and purification of the compounds by reacting a carboxy group with a suitable base such as the hydroxide, carbonate, or bicarbonate of a metal cation or with ammonia or an organic primary, secondary, or tertiary amine. The cations of therapeutically acceptable salts include lithium, sodium, potassium, calcium, magnesium, and aluminum, as well as nontoxic quaternary amine cations such as ammonium, tetramethylammonium, tetraethylammonium, methylamine, dimethylamine, trimethylamine, triethylamine, diethylamine, ethylamine, tributylamine, pyridine, N,N-dimethylaniline, N-methylpiperidine, N-methylmorpholine, dicyclohexylamine, procaine, dibenzylamine, N,N-dibenzylphenethylamine, 1-ephenamine, and N,N'-dibenzylethylenedianune. Other representative organic amines useful for the formation of base addition salts include ethylenediamine, ethanolamine, diethanolamine, piperidine, and piperazine.
The present compounds can also exist as therapeutically acceptable prodrugs.
The term "therapeutically acceptable prodrug," refers to those prodrugs or zwitterions which are suitable for use in contact with the tissues of patients without undue toxicity, irritation, and allergic response, are commensurate with a reasonable benefit/risk ratio, and are effective for their intended use. The term "prodrug," refers to compounds which are rapidly transformed in vivo to parent compounds of formula (I) for example, by hydrolysis in blood. Prodrugs of the present invention are compounds of formula (I] where R2 is other than hydrogen (i.e., carboxylic esters). Representative prodrugs include, but are not limited to, methyl (3R)-3-amino-2-hydroxy-5-(methylsulfanyl)pentanoate; methyl (2RS,3R)-3-amino-4-cyclohexyl-2-hydroxybutanoate; (1S,2R)-2-amino-2,3-dihydro-1H inden-1-yl (2RS,3R)-3-amino-4--cyclohexyl-2-hydroxybutanoate; benzyl (2S,3R)-3-amino-3-cyclopentyl-2-hydroxypropanoate; benzyl (2S,3R)-3-amino-3-cycloheptyl-2-hydroxypropanoate;
(2S)-2-(methylamino)-2-(1-naphthyl)ethyl (2S,3R)-3-amino-5-(ethylsulfanyl)-2-hydroxypentanoate;
(2R)-2-(methylanuno)-2-(1-naphthyl)ethyl (2S,3R)-3-amino-5-(ethylsulfanyI)-2-3o hydroxypentanoate; 2-(methylamino)-2-(1-naphthyl)propyl (3R)-3-amino-5-(ethylsulfanyl)-2-hydroxypentanoate; (2R)-2-(methylamino)-2-(1-naphthyl)ethyl (2S,3R)-3-amino-4-cyclohexyl-2-hydroxybutanoate; (2R)-2-(methylamino)-2-(1-naphthyl)ethyl (2S,3R)-3-amino-2-hydroxy-5-phenylpentanoate; methyl (2RS,3R)-3-amino-5-(ethylsulfanyl)-2-hydroxypentanoate; benzyl (2RS,3R)-3-amino-5-(ethylsulfanyl)-2-hydroxypentanoate; butyl (2RS,3R)-3-amino-5-(ethylsulfanyl)-2-hydroxypentanoate; isopropyl (2S,3R)-3-amino-2-hydroxy-5-(isopropylsulfanyl)pentanoate; isopropyl (2RS,3R)-3-amino-5-(ethylsulfanyl)-2-hydroxypentanoate; [(2,2-dimethylpropanoyl)oxy]methyl (2RS,3R)-3-amino-5-(ethylsulfanyl)-2-hydroxypentanoate; sec-butyl (2RS,3R)-3-amino-5-(ethylsulfanyl)-2-hydroxypentanoate; (1,3-dioxo-1,3-dihydro-2H isoindol-2-yl)methyl (2RS,3R)-3-amino-5-(ethylsulfanyl)-2-hydroxypentanoate; sec-butyl (2RS,3R)-3-amino-2-hydroxy-5-(isopropylsulfanyl)pentanoate; [(2,2-dimethyIpropanoyI)oxy]methyl (2S,3R)-3-amino-2-hydroxy-5-(isopropylsulfanyl)pentanoate; (I,3-dioxo-I,3-dihydro-ZH isoindol-2~yI)methyl (2S,3R)-3-amino-2-hydroxy-5-(isopropylsulfanyl)pentanoate; and 3-oxo-I,3-dihydro-2-benzofuran-I-yl (2S,3R)-3-amino-2-hydroxy-5-(isopropylsulfanyI)pentanoate.
Asymmetric centers exist in the compounds of the present invention. These centers are designated by the symbols "R" or "S," depending on the configuration of substituents around the chiral carbon atom. It should be understood that the invention encompasses all stereochemical isomeric forms, or mixtures thereof, which possess the ability to inhibit angiogenesis. Individual stereoisomers of compounds can be prepared synthetically from commercially available starting materials which contain chiral centers or by preparation of mixtures of enantiomeric products followed by separation such as conversion to a mixture of diastereomers followed by separation or recrystallization, chromatographic techniques, or direct separation of enantiomers on chiral chromatographic columns. Starting compounds of particular stereochemistry are either commercially available or can be made and resolved by techniques known in the art.
In accordance with methods of treatment and pharmaceutical compositions of the invention, the compounds can be administered alone or in combination with other anticancer agents. When using the compounds, the specific therapeutically effective dose level for any particular patient will depend upon factors such as the disorder being treated and the severity of the disorder; the activity of the particular compound used; the specific composition employed; the age, body weight, general health, sex, and diet of the patient;
the time of administration; the route of administration; the rate of excretion of the compound employed;
the duration of treatment; and drugs used in combination with or coincidently with the compound used. The compounds can be administered orally, parenterally, osmotically (nasal sprays), rectally, vaginally, or topically in unit dosage formulations containing carriers, adjuvants, diluents, vehicles, or combinations thereof. The term "parenteral"
includes infusion as well as subcutaneous, intravenous, intramuscular, and intrasternal injection.
Parenterally administered aqueous or oleaginous suspensions of the compounds can be formulated with dispersing, wetting, or suspending agents. The injectable preparation can also be an injectable solution or suspension in a diluent or solvent. Among the acceptable diluents or solvents employed are water, saline, Ringer's solution, buffers, monoglycerides, diglycerides, fatty acids such as oleic acid, and fixed oils such as monoglycerides or diglycerides.

WO 2004/013085 PCT/US2003/024396.
The antiangiogenic effect of parenterally administered compounds can be prolonged by slowing their absorption. One way to slow the absorption of a particular compound is administering injectable depot forms composing suspensions of crystalline, amoyhous, or otherwise water-insoluble forms of the compound. The rate of absorption of the compound is dependent on its rate of dissolution which is, in turn, dependent on its physical state. Another way to slow absorption of a particular compound is administering injectable depot forms comprising the compound as an oleaginous solution or suspension. Yet another way to slow absorption of a particular compound is administering injectable depot forms comprising microcapsule matrices of the compound trapped within liposomes, rnicroemulsions, or biodegradable polymers such as polylactide-polyglycolide, polyorthoesters or polyanhydrides.
Depending on the ratio of drug to polymer and the composition of the polymer, the rate of drug release can be controlled.
Transdermal patches can also provide controlled delivery of the compounds. The rate of absorption can be slowed by using rate controlling membranes or by trapping the compound within a polymer matrix or gel. Conversely, absorption enhancers can be used to increase absorption.
Solid dosage forms for oral administration include capsules, tablets, pills, powders, and granules. In these solid dosage forms, the active compound can optionally comprise diluents such as sucrose, lactose, starch, talc, silicic acid, aluminum hydroxide, calcium silicates, polyamide powder, tableting lubricants, and tableting aids such as magnesium stearate or microcrystalline cellulose. Capsules, tablets, and pills can also comprise buffering agents, and tablets and pills can be prepared with enteric coatings or other release-controlling coatings. Powders and sprays can also contain excipients such as talc, silicic acid, aluminum hydroxide, calcium silicate, polyamide powder, or mixtures thereof. Sprays can additionally contain customary propellants such as chlorofluorohydrocarbons or substitutes therefore.
Liquid dosage forms for oral administration include emulsions, microemulsions, solutions, suspensions, syrups, and elixirs comprising inert diluents such as water. These compositions can also comprise adjuvants such as wetting, emulsifying, suspending, sweetening, flavoring, and perfuming agents.
Topical dosage forms include ointments, pastes, creams, lotions, gels, powders, solutions, sprays, inhalants, and transdermal patches. The compound is mixed under sterile conditions with a carrier and any needed preservatives or buffers. These dosage forms can also include excipients such as animal and vegetable fats, oils, waxes, paraffins, starch, tragacanth, cellulose derivatives, polyethylene glycols, silicones, bentonites, silicic acid, talc and zinc oxide, or mixtures thereof. Suppositories for rectal or vaginal administration can be prepared by mixing the compounds with a suitable non-irritating excipient such as cocoa butter or polyethylene glycol, each of which is solid at ordinary temperature but fluid in the rectum or vagina. Ophthalmic formulations comprising eye drops, eye ointments, powders, and solutions are also contemplated as being~within the scope of this invention.
The total daily dose of th.e compounds administered to a host in single or divided doses can be in amounts from about 0.1 to about 200 mg/kg body weight or preferably from about 0.25 to about 100 mg/kg body weight. Single dose compositions can contain these amounts or submultiples thereof to make up the daily dose.
Determination of Biol ~ical Activity Proc. Natl. Acad. Sci. USA 94: 6099-6103 (1997) and Chemistry and Biolo~y, 4(6):
461-471 (1997) report that both AGM-1470 and ovalicin, a sequiterpene isolated from the fungus Pseudorotiuaax ocalis have been found to bind to a common bifunctional protein, type 2-methionine aminopeptidase (MetAP-2) and conclude that MetAP2 plays a critical role in the proliferation of endothelial cells and may serve as a promising target for the development of new anti-angiogenic drugs.
Assays for the inhibition of catalytic activity of MetAP2 were performed in 96-well microtiter plates. Compounds to be tested (compounds of formula (>] where R2 is hydrogen) were dissolved in dimethyl sulfoxide at 10 mM and diluted ten-fold in assay buffer (50 mM
HEPES, pH 7.4, 100 mM NaCI). Ten microliters of solution of each compound to be tested for inhibition were introduced into each cell of the plate. hero inhibition of enzyme activity 2o was taken to be the result obtained in cells in which 10 mL of assay buffer was placed. A
mixture totaling 90 mL per well and made up of 84 rnL of assay buffer containing 100 mM
MnCl2, 1 rnL of L-amino acid oxidase (Sigma Catalog No. A-9378, ~11 mg/mL), 1 mL of horseradish peroxidase (Sigma Catalog No. P-8451, dissolved in assay buffer at a concentration of 10 mg/mL), 1 mL of the tripeptide Met-Ala-Ser (Sachem) dissolved in assay buffer at concentration of 50 mM, 1 mL of oYtho-dianisidine (Sigma Catalog No.
D-1954, freshly made solution in water at a concentration of 10 mg/mL), and MetAP2 at a final concentration of 1.5 mg/mL was rapidly mixed and added to each cell containing test or control compound. The absorbence at 450 nanometers was measured every 20 seconds over a period of twenty minutes using an automatic plate reader (Molecular Devices, CA, USA).
3o The Vmax in mOD/min, calculated for each well, was used to represent MetAP2 activity.
The ICSO for each inhibitor was obtained by plotting the remaining activity versus inhibitor concentrations. Representative compounds of the present invention had ICSO's between about 0.030 ~M and about 1.80 ~,M. Preferred compounds of the present invention had IC5o's between about 0.030 and about 0.05 ~,M.
As tlxe literature has established a casual link between inhibition of MetAP2 and the resultant inhibition of endothelial cell proliferation and angiogenesis, it can be inferred that the compounds of the invention, including, but not limited to those specified in the examples, _g_ possess antiangiogenic activity. As angiogenesis inhibitors, such compounds are useful in the treatment of both primary and metastatic solid tumors, including carcinomas of breast, colon, rectum, lung, oropharynx, hypopharynx, esophagus, stomach, pancreas, liver, gallbladder and bile ducts, small intestine, urinary tract (including kidney, bladder, and urothelium), female genital tract (including cervix, uterus, and ovaries as well as choriocarcinoma and gestational trophoblastic disease), male genital tract (including prostate, seminal vesicles, testes, and germ cell tumors), endocrine glands (including the thyroid, adrenal, and pituitary glands), and skin, as well as hemangiomas, melanomas, sarcomas (including those arising from bone and soft tissues as well as Kaposi's sarcoma) and tumors of the brain, 'nerves, eyes, and meninges l0 (including astrocytomas, gliomas, glioblastomas, retinoblastomas, neuromas, neuroblastomas, Schwannomas, and meningiomas). Such compounds may also be useful in treating solid tumors arising from hematopoietic malignancies such as leukemias (i.e., chloromas, plasmacytomas and the plaques and tumors of mycosis fungosides and cutaneous T-cell lymphoma/leukemia) as well as in the treatment of lymphomas (both Hodgkin's and non-Hodgkin's lymphomas). In addition, these compounds may be useful in the prevention of metastases from the tumors described above either when used alone or in combination with radiotherapy andlor other chemotherapeutic agents. The compounds of the invention can also be useful in the treatment of the aforementioned conditions by mechanisms other than the inhibition of angiogenesis.
Further uses include the treatment and prophylaxis of autoimmune diseases such as rheumatoid, immune and degenerative arthritis; various ocular diseases such as diabetic retinopathy, retinopathy of prematurity, corneal graft rejection, retrolental fibroplasia, neovascular glaucoma, rubeosis, retinal neovascularization due to macular~degeneration, hypoxia, angiogenesis in the eye associated with infection or surgical intervention, and other abnormal neovascularization conditions of the eye; skin diseases such as psoriasis; blood vessel diseases such as hemagiomas, and capillary proliferation within atherosclerotic plaques; Osler-Webber Syndrome; myocardial angiogenesis; plaque neovascularization;
telangiectasia; hemophiliac joints; angiofibroma; and wound granulation. Other uses include the treatment of diseases characterized by excessive or abnormal stimulation of endothelial 3o cells, including not limited to intestinal adhesions, Crohn's disease, atherosclerosis, scleroderma, and hypertrophic scars, i.e., keloids. Another use is as a birth control agent, by inhibiting ovulation and establishment of the placenta. The compounds of the invention are also useful in the treatment of diseases that have angiogenesis as a pathologic consequence such as cat scratch disease (Rochele minutesalia qui~ztasa) and ulcers (He~icobacter~ylori).
The compounds of the invention are also useful to reduce bleeding by administration prior to surgery, especially for the treatment of resectable tumors.

Synthetic Methods Abbreviations which have been used in the descriptions of the scheme and the examples that follow are: BOC for tart-butoxycarbonyl; PCC for pyridinium chlorochromate;
,EDC for 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride; HOAT for hydroxy-7-azabenzotriazole; DCC for 1,3-dicyclohexylcaxbodiimide; HC?BT for 1-hydroxybenzotriazole; DMSO for dimethylsulfoxide; BOC-ON for [2-(tert-butoxycarbonyloxyimino)-2-phenylacetonitrile; and THF for tetrahydrofuran.
The compounds and processes of the present invention will be better understood in connection with the following synthetic schemes which illustrate the methods by which the compounds of the invention may be prepared. Starting materials can be obtained from commercial sources or prepared by well-established literature methods known to those of ordinary skill in the art. The groups Rl, and R2 are as defined above unless otherwise noted below.
This invention is intended to encompass compounds having formula (1~ when prepared by synthetic processes or by metabolic processes. Preparation of the compounds of the invention by metabolic processes include those occurring in the human or animal body (~32 vivo) or processes occurring in vitro.
Schegne 1 By Rt OH ~OH
BOCHN ~ BOCNN
O
(2) (3) p p BOCHN
OH O
(Ia) (4) 2o As shown in Scheme 1, compounds of formula (2) can be converted to compounds of formula (3) by treatment with a reducing agent. Examples of reducing agents include sodium bis(2-methoxyethoxy)aluminum hydride (Red-Al~), lithium aluminum hydride, and borane.
Oxidation of compounds of formula (3) can be accomplished by treatment with an oxidizing agent such as sulfur trioxide pyridine complex, PCC, or the Dess-Martin periodinane to provide compounds of formula (4). Conversion of compounds of formula (~) to compounds of formula (4) may also be achieved by conversion to the N-methoxy-N
methylamide using N, O-dimethyIhydroxylamine and an activating agent such as DCC or EDCI, followed by treatment with a reducing agent such as lithium aluminum hydride. Reacting compounds of formula (4) with trimethylsilylcyanide or sodium bisulfate and potassium cyanide provides the cyanohydxin which can be treated ira situ with a strong acid such as HCl to simultaneously hydrolyze the cyano group and remove the protecting group, providing compounds of formula (Ia) (compounds of formula (I) where R2 is hydrogen).
Scheme 2 O O

HO H H OOH OH
BOCHN
S-S
O
(6) (2a) Compounds of formula (2a) can be prepared according to the procedure shown in Scheme 2. Reduction of compounds of formula (6) with liquid ammonia and sodium 1o followed by treatment with an alkyl halide provides compounds of'formula (2a) where R3 is alkyl. Alternatively, compounds of formula (2a} can be prepared by treating compounds of formula (6) with liquid ammonia and sodium followed by a strong acid (such as HCl) and an appropriately substituted alcohol (R30H).
Scheme 3 O O BOCHN O
R1/ \H R1 ~ ORa ~ Ry OR4 {9) OH
HZN O BOCHN O
R' OH Ri OH
OH OH
15 (ta) (10) Scheme 3 shows the synthesis of compounds of formula (Ia). Compounds of formula (7) can be converted to compounds of formula (8) (R4 is an alkyl group) by treatment with the appropriately substituted phasphonate in the presence of a base such as sodium hydride, potassium hydride, or lithium hexamethyldisilazide. Conversion of compounds of formula 2o (8) to compounds of formula (9) can be accomplished by treatment with tart-butylcarbamate, tent-butylhypochlorite, and NaOH, followed by treatment with potassium osmate and either hydroquinine 1,4-phthalazinediyl diether or 1,4-phthalazinediyl diether (depending on which -11_-enantiomer is desired). Hydrolysis of the ester can be accomplished by methods known to those of ordinary skill in the aut (for example, lithium hydroxide and hydrogen peroxide) to provide cornpounds of formula (10), which can be deprotected using conditions kno~rn to those of ordinary skill in the ant (such as HCl) to provide compounds of formula (Ia).
Scheme 4 R~ O R~ O
BOCHN OH ~ BOCHN ORz OH OH
(S) (11) R~ O
NH2 ~ ~ORZ
OH
(~) Compounds of formula (Ib) can be prepared by the methods shown in Scheme 4.
Compounds of formula (5) can be esterified by treatment with an aIkylating agent such as trimethylsilyldiazomethane or by coupling with the corresponding alcohol (R20H) in the to presence of a coupling agent such as EDC and H(~AT or DCC and HOBT to provide compounds of formula (11). Conversion of compounds of formula (I1) to compounds of formula (Ib) (compounds of formula (I) where Ra is other than hydrogen) can be accomplished by methods known to those of ordinary skill in the art (for example, treatment with HCl).
Scheme 5 BOCHN ~ ~OR2 OH
(11) (12) H2N ~ ~OR2 OH
(Ib) (14) (13) Compounds of formula (Ib) can also be prepared by the procedures described in Scheme 5. Compounds of formula (11) can be treated with 2,2-dirnethoxypropane in the presence of an acid such as methylbenzenesulfonic acid or p-toluenesulfonic acid to provide compounds of formula (12). Hydrolysis of the ester using conditions known to those of ordinary skill in the art (for example, lithium hydroxide) provides compounds of formula (13). Esterification of compounds of formula (13) can be accomplished by treatment with an appropriately substituted alcohol (R20H) and a coupling agent such as EDC and HOAT or DCC and HOBT. Compounds of formula (14) can be treated with a strong acid such as HCl l0 in the presence of water to provide compounds of formula (Ib}.
The present invention will now be described in connection with certain preferred embodiments which are not intended to limit its scope. On the contrary, the present invention covexs all alternatives, modifications, and equivalents as can be included within the scope of the claims. Thus, the following examples, which include preferred embodiments, will 15 illustrate the preferred practice of the present invention, it being understood that the examples are for the purposes of illustration of certain preferred embodiments and are presented to provide what is believed to be the most useful and readily understood description of its procedures and conceptual aspects.
Compounds of the invention were named by ACD/ChemSketch version 5.fl 20 (developed by Advanced Chemistry Development, Tnc., Toronto, ON, Canada) or were given names which appeared to be consistent with ACD nomenclature.
Example 1 (2RS,3.R)-3-amino-2-h droxy-5-(methylsulfan~pentanoic acid Example lA

tent-butt(1R)-1-(hydroxymethyl)-3-(methylsulfanyl)propylcarbamate A solution of N (tent-butoxycarbonyl)-D-methionine (12.47 g, 50 mmol) and sodium bis(2-methoxyethoxy)aluminum hydride (Red-Al~) (50 mmol) in day toluene (1~5 mL) was stirred at 0 °C for 30 minutes, then at ambient temperature for 1 hour.
The mixture was treated with aqueous Rochelle salt and extracted with diethyl ether. The extract was washed sequentially with brine and aqueous NaHC03, dried (MgSO~.), filtered, and concentrated to provide the desired product (9.05 g).
Example 1B
1o tert-butyl (1R)-1-formyl-3-(meth lsulfanyl)~ropylcarbamate A solution of Example lA (9.05 g, 38.5 mmol), sulfur trioxide pyridine complex (30.64 g,192.5 mmol), and triethylamine (26.8 mL, 192.5 mmol) in DMSO (30 mL) was stirred at ambient temperature for 30 minutes, cooled to 0 °C, treated sequentially with water (20 xnL) and saturated aqueous KHSOq. (120 mL), and extracted with ethyl acetate. The I5 extract was washed sequentially with saturated aqueous KHS04 and brine, dried (MgS04), filtered, and concentrated to provide the desired product (9.00 g).
Example 1C
2RS,3R)-3-amino-2-hydrox~5-(methylsulfanyl)pentanoie acid 2o A solution of Example 1B (9.00 g, 38.5 mmol) and sodium bisulfate (3.80 g, 36.6 mrnol) in water (200 rnL) was stirred at 5 °C for 72 hours, warmed to ambient temperature, treated with a mixture of potassium cyanide (2.51 g, 38.6 mmol) in ethyl acetate (250 mL), and stirred for 4 hours. The separated ethyl acetate layer was washed sequentially with water and brine, dried (MgS04), filtered, and concentrated. The concentrate was dissolved in 25 dioxane (75 mL) and 12M HCl~(75 mL), heated to reflux for 16 hours, concentrated, dissolved in water (8 imL) and acetone (300 mL), adjusted to pH 5.5 with 1M
NaOH, and filtered. The filter cake was dried under vacuum to provide the desired product (5.81 g).
MS (ESI(+)Q1MS) m/e 180 (M+H)+, 202 (M+ Na)~; MS (ESI(-)) m!e 178 (M-H) ;1H
NMR
(300 MHz, D20) 8 4.25 (d, O.SH), 4.14 (d, 4.5H), 3.78 (m, O.SH), 3.66 (m, 0.5H), 2.65 (m, 30 2H), 2.13 (s, 1.5H), 2.09 (s, 1.5H), 1.93 (m, 2IT).
Example 2 (2RS,3R)-3-amino-5-(eth Isu~IfanyI)-2-h~xy~entanoic acid 35 Example 2A
(2RSi3R)-3-f(teat-butoxycarbonYl)aminol-5-(eth ls~ ulfanyI)-2-hydroxypentanoic acid The desired product was prepared by substituting (2R)-2-((tert-butoxycarbonyl)amino)-4-(ethylsulfanyl)butanoic acid for (2R)-2-((tert-butoxycarbonyl)amino)-3-cyclohexylpropanoic acid in Examples 3A-3C. MS (ESI) mle 294 (M+H)+.
Exam In a 2B
(2RS,3R)-3-amino-5-(ethylsulfan~l -2-hydroxypentanoic acid The desired product was prepared by substituting Example 2A for Example 3C in Example 3D. MS (ESI] mle 194 (M+H)+;1H NMR (300 MHz, DMSO-d6) S 8.14 (br s, l0 0.6H), 7.95 (br s, 1.4H), 4.35 (d, 0.3H), 4.16 (d, 0.7H), 3.70 (m, 0.3H), 3.46 (m, 0.7H), 2.63 (m, 2I~, 2.49 (m, 2H), 1.84 (m, 2H), 1.18 (m, 3H).
Example 3 (2RS,3R)-3-amino-4-cyclohexyl-2-hydroxybutanoic acid Exam lp a 3A
tef~-butyl (1R)-2-cyclohexyl-1-(hydroxymeth~rl)eth~lcarbamate A solution of (2R)-2-((tent-butoxycarbonyl)amino)-3-cyclohexylpropanoic acid (30.4 g,112 mmol) in toluene (300 mL) at 0 °C was treated with sodium bis(2-2o rnethoxyethoxy)aluminum hyd~~de (Red-AI~) (115 mmol) over 45 minutes. The mixture was stirred for 30 minutes, warmed to room temperature, stirred for 1 hour, treated with aqueous Rochelle salt, and extracted with diethyl ether. The extract was washed sequentially with brine and aqueous NaHC03, dried (MgSO4), filtered, and concentrated to provide the desired product.
Exam lp a 3B
tent-butyl (1R)-2-c clohexyl-1-forrilylethylcarbamate A solution of Example 3A (25.8 g,100 mmol), sulfur trioxide pyridine complex (79.6 g, 500 mmol), and triethylamine (69.7 mL, 500 mmol) in DMSO (70 mL) at room 3o temperature was stirred for 30 minutes, cooled to 0 °C, treated with water and saturated aqueous KHS04, and extracted with ethyl acetate. The extract was washed sequentially with saturated aqueous KHS04 and brine, dried (MgS04), filtered, and concentrated to provide the desired product.
Example 3C
(2RS 3R)-3-f (tart-butoxycarbonyl)aminol-4-c clue 1-~2-hydrox~utanoic acid A solution of Example 3B (19.7 g, 77.1 mmol) and sodium bisulfate (8.0 g, 77.1 mmol) in water (500 mL) at 5 °C was stirred for 24 hours, warmed to room temperature, treated v~ith a solution of potassium cyanide (5.I g, 78.8 mmol) in ethyl acetate (350 mL), and stirred for 5 hours. The aqueous phase was separated and extracted with ethyl acetate. The .
combined extracts were washed sequentially with water and brine, dried (MgS04), filtered, and concentrated. The concentrate was dissolved in dioxane (150 mL), treated with I2M HCl (150 mL), heated to reflux, stirred for 21 hours, and cooled to room temperature. The mixture was concentrated, dissolved in a mixture of water (30 mL) and acetone (200 mL), adjusted to pH 5.5 with 1M NaOH, treated with acetone (3.5 L), and cooled to l0 0 °C for 4 hours. The resulting precipitate was collected by filtration. The filter cake was dried, dissolved in 1:1 water/dioxane, treated with BOC-ON (1.2 eq.), and triethylamine (2 eq.), heated to 45 °C, stirred for 15 hours, treated with 10% aqueous KHS04, and extracted with ethyl acetate. The extract was washed sequentially with water and brine, dried (MgSO~.), filtered, and concentrated to provide the desired product.
Example 3D
(2RS,3R)-3-amino-4-~clohex 1-~2-hydroxybutanoic acid A solution of Example 3C (75 mg, 0.25 mmol) in 4M HCI in dioxane (2 mL) at room temperature was stirred for 1 hour, concentrated, then purified by reverse phase HPLC with 2o acetonitrile/water to provide the desired product. MS (ESI] m/e 202 (M+IT)~; 1H NMR (300 MHz, DMSO-d6) ~ 7.81 (br s, 2I-~, 4.07 (d, 1H), 3.35 (m, 1H), 1.80-1.67 (m, 5H), 1.57-1.51 (m, l~, 1.46-1.17 (m, 5H), 1.00-0.90 (m, 2H); Anal. Calcd. for CloFi2oC1NO3:
C, 50.52; H, 8.48; N, 5.89. Found: C, 50.18; H, 8.56; N, 5.67.
Example 5 f2RS,3R)-3-amino-3-cyclohexyl-2-hydroxy~ro~anoic acid The desired product was prepared by substituting (2R)-2-((tert-butoxycarbonyl)amino)-2-(cyclohexyl)ethanoic acid for (2R)-2-((tent-butoxycarbonyl)amino)-3-cyclohexylpropanoic acid in Examples 3A-3D. MS {ESn m/e 188 (M+H)+;1H NMR
(300 MHz, DMSO-d6) S 7.92 (br s, 0.6H), 7.77 (br s, 1.4H), 4.31 (d, 0.3H), 4.12 (d, 0.7H), 3.69 (m, 0.7H), 3.48 (m, 0.3H), 1.85-1.70 (m, 4H), 1.70-1.51 (m, 2H), 1.46-1.17 (m, 3H), 1.00-0.90 (m, 2H}.
Example 6 (ZRS,3R)-3-amino-2-h~drox r-~5-pheny~entanoic acid Example 6A

(2RS,3R)-3-f(tert-butox ca~bonyl~aminol-2-h drox~-5-phenylpentanoic acid The desired product was prepared by substituting (2R)-2-((tert-butoxycarbonyl}amino)-4-(phenyl)butanoic acid for (2R)-2-((tent-butoxycarbonyl)amino)-3-cyclohexylpropanoic acid in Examples 3A-3C. MS {ES>] m/e 310 (M+H)+.
Example 6B
(2RS,3R)-3-amino-2-h droxy-5-nhenyl~entanoic acid The desired compound was obtained by substituting Example 6A for Example 3C in Example 3D. MS (ESI(+)) m/e 210 (M+H)+; 1H NMR (300MHz, DMSO-d6) b 7.34-7.16 (m, io 5H), 4.19 (br d, 1H), 2.76-2.65 (m, 2H), 1.97-1.68 (m, 2H).
Example 7 (2RS,3R)-3-amino-2-hydro~-5-(isoprop lsulfanyl)~entanoic acid 15 Example 7A
~2R)-2-f(tert-butox cy arbonyl)aminol-4-fisoprop ls~yl)butanoic acid A solution of D-homocystine (20 g, 75 mmol) in liquid ammonia (600 mL) was treated sequentially with sodium (8.9 g, 390 mmol) and 2-bromopropane (20 mL, 210 mmol).
The ammonia was allowed to evaporate under a stream of nitrogen, and the residue was 2o dissolved in 1:1 2-propanol/water (500 mL), treated with di-ten-butyl dicarbonate (50 g, 230 mmol), stirred at room temperature for 6 hours, then concentrated. The residue was dissolved in water and the pH was adjusted to 10 with 50°lo NaOH. The solution was washed twice with diethyl ether, adjusted to pH 2 with 12M HCI, and extracted twice with ethyl acetate.
The extracts were dried (MgSO4}, filtered, then concentrated to provide the desired product.
25 MS (ESI) m/e 279 (M+H)+.
Example 7B
(2RS 3R)-3-f(tert-butox carbonyl)aminol-2-hydroxy-5-(isopropylsulfan~pentanoic acid The desired product was prepared by substituting Example 7A for (2R)-2-((tert butoxycarbonyl)amino)-3-cyclohexylpropanoic acid in Examples 3A-3C. MS
(ESI(+}) mle 30 308 (M+H)+.
Example 7C
(2RS,3R)-3-amino-2-hydrox -5-(iso ropylsulfanyl)pentanoic acid The desired product was prepared by substituting Example 7B for Example 3C in 35 Example 3D. MS (ESJ] m/e 208 (M+H)~; iH NMR (300 MHz, DMSO-d6) & 7.34 (br s, 0.6H), 7.20 (br s, 1.4H), 4.10 (d, 0.3I~, 4.02 (d, 0.7H), 3.70 {m, 0.7H), 3.46 (m, 0.3H), 2.92 (m, 1H), 2.61 (m, 2H), 1.83-1.75 (m, 2H), 1.21 (d, 2.1H), 1.19 (d, 0.9H).

Example 8 (~S 3R 4S)-3-amino-~-hydrox~4-(3-hydroxypropyl)-7-methyloctanoic acid Example 8A
5-methylhexanoyl chloride A mixture of 5-methylhexanoic acid (25 mL~ 175 mmol) and thionyl chloride (50 znL, 0.69 mol) was stirred at reflux for 90 minutes. The mixture was concentrated, then distilled at reduced pressure to give the desired product (22.35 g).
Example 8B
(4R)-4-benzyl-3-(5-meth~hexanoyl)-1 3-oxazolidin-2-one To a -78 °C solution of 4(R)-benzyl-2-oxazolidinone (21.28 g, 0.12 mol) in THF (360 mL) was added ~a-butyllithium (48 mL, 2.5M in hexane, 120 mmol). After 10 minutes Example 8A (19.76 g, 0.134 mol) was added. After 30 minutes the mixture was warmed to 0 °C, and quenched with saturated ammonium chloride. The supernatant was decanted and concentrated. The residue was partitioned between water and ethyl acetate and the organic layer was washed sequentially with water,1M sodium bicarbonate, water, and brine, dried (MgSO4), filtered, and concentrated to provide the desired product. MS (ESA
m/e 290 (M+~~.
Example 8C
~R~-4-benzyl-3-f (2~-2-(3-methylbutyl)-4-~entenoyll-13-oxazolidin-2-one To a stirred -78 °C solution of Example 8B (15.65 g, 54.2 mmol) in THF
(I60 mL) was added sodium bis(trimethylsilyl)amide (55 mL, 1M in THF). The reaction mixture was stirred for 45 minutes and a11y1 bromide (5.3 mL, 60.9 mmol) was added. The reaction mixture was stirred for 90 minutes, warmed to 0 °C, and stirred an additional 90 minutes.
The reaction was quenched with saturated ammonium chloride, concentrated, and partitioned between water and ethyl acetate. The organic layer was washed sequentially with water, 1M
3o sodium bicarbonate, water, and brine, dried (MgS04), filtered, and concentrated to provide the desired product. MS (ESZ] m/e 330 (M+I~~.
Example 8D
~25~' -2-(3-methylbutyl)-4-pentenoic acid To a 0 °C solution of Example 8C (17.3 g, 52.6 mmol) in THF (200 mL) was added water (25 mL) and 30°Io hydrogen peroxide (25 mL, 220 mmol). A solution of lithium hydroxide monohydrate {4.38 g, 104 mmol) in water (100 mL) was added and the resulting solution was stirred for 12 hours. ~l rie mixture was quenched with aqueous NaHS03 then concentrated and made basic with 5M NaOH. The aqueous phase was washed with ethyl acetate, then acidified with concentrated HCI to pH 3 and extracted twice with ethyl acetate.
The combined extracts were dried (MgS04), filtered, and concentrated to provide the desired product. MS (ESI(+)) mle 171 (M+H)+.
Example 8E
(2S)-N methoxy-N-methyl-2-(3-meth~lbut 1~4-pentenamide A solution of Example 8D (4.54 g, 26.7 mmol), N, O-dimethyl hydroxylamine l0 hydrochloride (5.6 g, 57 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (5.19 g, 27 mmol), 1-hydroxybenzotriazole (4.I2 g, 30.5 mmol), and N
methylmorpholine (7.0 mL, 64 mmol) in dichloromethane (270 mL) at room temperature was stirred for 4 hours, diluted with dichlor~methane, washed sequentially with aqueous NaHC03, brine, 10% KHS04, and brine, dried (MgSO~.), filtered, and concentrated. Flash 15 column chromatography (silica gel, 10% ethyl acetate/hexanes) provided the desired product.
MS (ESI(+)) m/e 214 (M+H)~.
Example 8F
(2S)-2-(3-hydroxypropyl)-N methoxy-N,5-dimethylhexanamide 2o A solution of Example 8E (2.31 g, 10.8 mmol), and THF-borane complex (12.0 mL, 1.OM in THF) in THF (10 mL) at 0 °C was stirred for 2.5 hours, treated with 30% aqueous hydrogen peroxide (I0 mL, 88 mmol) and pH 7 buffer solution (20 mL), stirred vigorously for 90 minutes, diluted with dichloromethane, washed with pH 7 buffer, dried {Na2S04), filtered, and concentrated to provide the desired product. MS (ESI] m/e 232 (M+H)+.
Exam l~p a 8G
~2S)-2-(3-1 ~tert-butyl(dimethyl)silyllox~propyl)-N methoxy-N 5-dimethylhexanamide A solution of Example 8F (2.58 g, 11.1 mmol), tent-butyldimethylsilyl trifluoromethanesulfonate (2.8 mL, 12 mmol), and 2,6-lutidine (1.5 mL, 13 mmol) in 3o dichloromethane (100 mL) at 0 °C was stirred for 2 hours; diluted with dichloromethane, washed sequentially with IO% KHS04, aqueous NaHC03, and brine, dried (MgS04), filtered, and concentrated to provide the desired product. MS (ESl~ m/e 346 (M+H)+.
Example 8H
~2S)-2-(3-~ ftert-butyl(dimeth 1)sil~loxylpropyl)-5-methylhexanal A solution of Example 8F (3.16 g, 9.16 mmol) and lithium aluminum hydride (0.34 g, 9.2 mmol) in diethyl ether (100 mL) at room temperature was stirred 30 minutes, treated with 1M NaHS04, diluted with diethyl ether, washed sequentially with 10% NaHSO~, and brine, dried (MgS04), filtered, and concentrated to provide the desired product. MS
(ESI) n~le 287 (M+H)~.
Example SI
benzyl (2E,4S)-4-(3-l ftert-butyl(dimethyl)silylloxy)pro~yl)-7-meth-2-octenoate A solution of Example 8H (2.6I g, 9.I6 mmol), benzyl diethylphosphonoacetate (2.83 g, 9.90 mmol), and sodium hydride (0.24 g, IO mmoI) in benzene (40 mL) at room temperature was stirred 2 hours, diluted with ethyl acetate, washed sequentially with saturated l0 aqueous NH4C1 and pH 7 buffer, dried (MgSO~), filtered, and concentrated.
Flash column chromatography (silica gel, 2:1 hexanes/CH2C12) provided the desired product.
MS (ESI) mle 419 (M+H)+.
Example 8J
15 benzyl (2S,3R,4,S7-3-f(tent-butoxycarbonyl)aminol-4-(3-dftert-butyl(dimeth 1)siIylloxylprop~l)-2-l~droxy-7-methyloctanoate The desired product was prepared by substituting Example 8I for Example 9B in Example 9C. Flash column chromatography (silica gel, 10% ethyl acetate/hexanes) provided the purified product. MS (ESTj mle 552 (M+H)+.
Exam 1P a 8I~
(2S,3R,45~-3-amino-2-h'rdrox -~4-(3-h~oxypropyl)-7-meth~loctanoic acid A mixture of Example 8J (15 mg, 0.027 mmol) and 10% PdlC in THF (5 mL) under a hydrogen atmosphere at room temperature was stirred for 3.5 hours and filtered. The filtrate 2S was treated with tetrabutylammonium fluoride (0.25 mL, 1.OM in TIC for 18 hours, diluted with diethyl ether, washed twice with 1M HCI, dried (Na25O4), filtered, and concentrated.
The concentrate was dissolved in 4M HGl in dioxane (2 mL), stirred for 1 hour, and concentrated to provide the desired product. MS (ESI) m/e 248 (M+H)~; 1H NMR
(300 MHz, DMSO-d6) ~ 4.21 (d, 1H), 3.73 (m, 1H), 3.67 (rn, 1H), 3.56 (m, 1H), 1.60-1.48 (m, 4H), 1.43-1.37 (m, 2H), 1.35-1.23 (m, 4H), 0.91 (d, 6H).
Example 9 2S,3R)-3-amino-2-hydroxy-6-phenylhexanoic acid Example 9A
4- henylbutanal A solution of 4-phenylbutyric acid (1.64 g, 10.0 mmol), N,O-dimethyl hydroxylamine hydrochloride (1.58 g, 16 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (2.06 g, 10.7 mmol), 1-hydroxybenzotriazole (1.56 g, 11.6 mmol), and N-methylmorpholine (2.8 mL, 26 mmol) in dichloromethane (40 mL) at room temperature was stirred for 16 hours, diluted with dichloromethane, washed sequentially with aqueous NaHC03, brine, 10% KHSO~., and brine, dried (MgS04), filtered, and concentrated. A
mixture of the concentrate and lithium aluminum hydride (9.0 mmol, 1 equiv.) in diethyl ether (49 mL) at room temperature was stirred for 90 minutes, treated with 1M
NaHS04, diluted with diethyl ether, washed sequentially with 10% KHS04, and brine, dried (MgS04), l0 filtered, and concentrated to provide the desired product. MS (ESI) m/e 148 (M+H)+.
Exam lp a 9B
ethyl (2E)-6-phenyl-2-hexenoate A solution of Example 9A (1.17 g, 7.9 mmol), triethyl phosphonoacetate (1.05 mL, 7.9 mmol), lithium bromide (0.70 g, 8.1 mmol), and triethylamine (1.1 mL, 7.8 mmol) in THF (80 mL) at room temperature was stirred for 16 hours, quenched with water, stirred for 15 minutes, diluted with ethyl acetate, washed sequentially with pH 7 buffer and brine, dried (MgS04), filtered, and concentrated. The concentrate was purified by flash column chromatography on silica gel with 1:1/dichloromethane:hexanes to provide the desired product. MS (ESI) mle 218 (M+H)+.
Example 9C
ethyl (2S,3R)-3-f(tef~-butoxycarbonyl)anv.nol-2-h dery-6-phenylhexanoate A solution of tef-t-butylcarbamate (1.00 g, 8.55 mmol), tart-butylhypochlorite (0.96 mL, 8.5 mmol}, and 0.5M NaOH (17 mL, 8.5 mmol) in 1-propanol (30 mL) at room temperature was stirred for 15 minutes. Example 9B (0.614 g, 2.82 mmol), potassium osrnate dihydrate (0.030 g, 0.08 mmol) and hydroquinine 1,4-phthalazinediyl diether (0.109 g, 0.14 mmol) were added, and the mixture was stirred at 0 °C for 2 hours, diluted with ethyl acetate, washed sequentially with water, 1M HCl, aqueous NaHC03, and brine, dried (MgSO~.), 3o filtered, and concentrated. The concentrate was purified by flash column chromatography on silica gel with 1:4/ethyl acetate:hexanes to provide the desired product. MS
(ESI) m/e 352 (M+H)+.
Exam Ip a 9D
(2S 3R)-3-f (tart-butoxycarbonyl)aminol-2-h~y-6-phenylhexanoic acid A solution of Example 9C (0.316 g, 0.90 mmol), 30% hydrogen peroxide (0.40 mL, 3.5 mmol), and lithium hydroxide monohydrate (0.076 g, 1.8 mmol) in 3:1 tetrahydrofuranlwater (8 mL) was stirred at 0 °C for 3 hours and concentrated. The concentrate was dissolved in water and the pH adjusted to 10 with 1M NaOH. The solution was washed twice with diethyl ether, adjusted to pH 2 with 1M HCl, and extracted twice with ethyl acetate. The combined extracts were dried (MgS04), filtered, and concentrated ~to provide the desired product. MS (ESI] m/e 324 (M+H)~.
Example 9E
(2S,3R)-3-amino-2-hydroxy-6-t~henylhexanoic acid A solution of Example 9D (25.7 mg, 0.08 mmol) in 4M HCl in dioxane (2 mL) was stirred at room temperature for 1 hour and concentrated to provide the desired product. MS
(ESI] m/e 224 (M+H)~; IH NMR (300 MHz, DMSO-d~) S 7.29 (rn, 2H), 7.18 (m, 3H), 4.11 (d, 1H), 3.69 (m, 1H), 2.57 (m, 2H), 1.73-1.49 (m, 4H).
Exam lp a 10 (2RS,3R)-3-amino-5-(tart-butylsulfanyl)-2-hydroxypentanoic acid Example l0A
(2R)-2-f(tern-butoxycarbonyl)aminol-4-(tart bu~lsulfanyl)butanoic acid A solution of D-homocystine (3.0 g, l l mmol) in liquid ammonia (I00 mL) was 2o treated with sodium (1.3 g, 56 mmol). The ammonia was allowed to evaporate under a stream of nitrogen, and the residue was dissolved in 1M HCl (10 mL). The pH
was adjusted to 0 with concentrated HCI, treated with tart-butanol (5 mL, S3 mmol), heated to reflux for 16 hours, and concentrated. The concentrate was dissolved in 1:1 2-propanollwater (80 mT.~), treated with di-tart-butyl dicarbonate (20.2 g, 92.7 mmol), stirred at room temperature for 16 hours, and concentrated. The concentrate was dissolved in water adjusted to pH

10 with 50%
NaOH. The solution was washed twice with diethyl ether, adjusted to pH 2 with HCI, and extracted twice with ethyl acetate. The combined extracts were dried (MgS04), f ltered, then concentrated to provide the desired product. MS (ESI) m/e 292 (IV!+H)~.
3o Example lOB
(2RS,3R)-3-amino-5-(tent-butylsulfan Iy )J2-hydroxypentanoic acid The desired product was prepared by substituting Example l0A for (2R)-2-((tert-butoxycarbonyl)amino)-3-cyclohexylpropanoic acid in Examples 3A-3D. MS (ESn m/e 222 (M+I~~; IH NMR (300 MHz, DMSO-d6) S 4.38 (d, 0.5H), 4.28 (d, 5H), 3.73-3.66 (m, 1H), 2.72-2.63 (m, 2H), 1.95-1.84 (m, 2H), 1.34 (s, 4.5H), 1.32 (s, 2.5H).
Example 11 methyl (3R)-3-amino-2-h droxy-5-(methylsulfan~pentanoate Exam lp a 11A
(3R)-3-f(tent-butoxycarbonyl)aminol-2-h~oxy-5-(methylsuIfanyl)pentanoic acid A solution of Example 1C (2.68 g, 12.5 mmol), triethylamine (3.47 ml, 75.0 mmol), and 2-(tent-butyoxycarbonyloxyimino)-2-phenylacetonitrile (3.22 g, 13.0 mmol) in 30%
aqueous dioxane was heated to 50 °C for 6 hours, cooled to ambient temperature, and concentrated. The residue was diluted with aqueous sodium hydroxide (0.25M, 50 mL) and extracted twice with ethyl acetate. The aqueous layer was acidified to pH 3 with IM H3P04 to and extracted five times with chloroform. The combined extracts were washed with brine, dried (MgS04), filtered, and concentrated to provide the desired product (1.62 g). MS (ESI]
m/e 27 8 (M-H)-.
Example I lB
(3R)-3-r(tert butoxycarbonyl)aminol-5-(methylsulfanyl)-2-(tetrahydro-2H pyran-loxy)pentanoic acid A solution of Example 11A (1.62 g, 5.8 mmol), 3,4-dihydro-2FI-pyran (0.64 mL, mmol), and pyridinium p-toluenesulfonate (0.15 mL, 0.60 mmol) in dichloromethane (30 mL) was heated to 35 °C for 16 hours and concentrated. The concentrate was diluted with aqueous sodium hydroxide (0.25M, 15 mL) and extracted twice with ethyl acetate. The aqueous layer was adjusted to pH 3 with aqueous H3P04 (1.OM) and extracted three times with ethyl acetate. These three extracts were combined, washed sequentially with water (20 mL) and brine (20 mL), dried (MgS04), filtered, and concentrated to provide the desired product (0.6I g). MS (APCI(+)) m/e 364. (M+H)+
Example I1C
methyl (3R)-3-((tart-butoxycarbonyl)amino)-~-h droxy-5-(methylthio)pentanoate A solution of Example 11B (0.25g, 0.68 mmol) and trimethylsilyldiazomethane (2.OM
in hexanes, 15 mL) in THF at room temperature was stirred for 4 hours, treated with acetic acid (1 mL), and concentrated. The residue was dissolved in methanol, treated with p-toluenesulfonic acid (10 mg), and heated to 55 °C for 16 hours. The mixture was concentrated and purified by flash column chromatography on silica gel with 25% ethyl acetate/hexanes to provide the desired product. MS (APCI(+)) m/e 294 (M+I~t.
Example 11D
methyl (3R)-3-amino-2-h d~ roxy-5-(methylsulfa~l)pentanoate A solution of Example 11C in 4M HCI in dioxane (10 mL) at room temperature was stirred for 4 hours and concentrated to provide the desired product. MS
(APCI(+)) m/e 194 (M-H) ; 1H NMR (300 MHz, DMSO-d6) 8 8.09 (br s, 2H), 7.94 (br s, 1H), 6.58 (m, O.SH), 6.42 (m, 0.5H), 4.48 (m, 0.5H), 4.30 (m, 0.5H), 3.72 (s, 3H), 2.58 (m, 2H), 2.04 (s, 1.SH), 2.02 (s, I.5H), 1.82 (m, 2H).
Example 12 methyl (2RS,3R)-3-amino~4-cyclohexyl-2-h~oxybutanoate to Example 12A
methyl (2RS,3R)-3-(tart-butoxycarbonyl)amino-4-cyclohexyl-2-h droxybutanoate A solution of Example 3C (10.234 g, 34 mmol), and trimethylsilyldiazomethane (2.0M in hexanes, 25 mL) in 3.5:1 benzene/methanol (232 mL) at room temperature was stirred at 0 °C for I hour, warmed to ambient temperature, stirred for 1 hour, quenched by the dropwise addition of acetic acid, concentrated to provide the desired product.
MS (ES'1) mle 316 (M+H)+.
Example 12B
methyl (2RS,3R)-3-amino-4-cyclohexyl-2-h droxybutanoate 20. The desired product was prepared by substituting Example 12A for Example 3C in Example 3D. MS (ES17 mle 216 (M+H)~; 1H NMR (300 MHz, CD30D) 8 4.42 (d, 0.3H), 4.22 (d, 0.7H), 3.80 (s, 2.1H), 3.77 (s, 0.9H), 3.~4 (m, 1H), 1.80-1.67 (m, 5H), 1.57-1.51 (m, 1H), 1.46-1.I7 (m, 5H), 1.00-0.90 (m, 2H).
2s Exam Ip a 13 (IS,2R)-2-amino-2,3-dihydro-1H inden-1-yl (2RS 3R)-3-amino-4-cyclohex hydroxybutanoate A solution of Example 3C (0.10 g, 0.33 mmol), (IS,2R)-1-amino-2-hydroxyindane (0.086 g, 0.58 mmol), 1-(3-dimethylaxninopropyl)-3-ethylcarbodiimide hydrochloride (0.080 3o g, 0.41 mmol), 1-hydroxybenzotriazole (0.061 g, 0.45 mmol), and N
methylmorpholine (0.05 mL , 0.46 mmol) in 3:1 dichloromethane/DMF (4 mL) at room temperature was stirred for 16 hours, diluted with dichloromethane, washed sequentially with aqueous NaHC03, brine, 10%
KHSO4, and brine, dried (MgS04), filtered, and concentrated. The residue was dissolved in 4M HCl in dioxane (3 mL), stirred for I hour, concentrated, then purified by reverse phase 35 HPLC with acetonitrile/water to provide the desired product. MS (ESl~ m/e 333 (M+I~+; 1H
NMR (300 MHz, DMSO-d6) 8 7.81 (br s, 2H), 7.40-7.17 (m, 4H), 6.65 (d, 1H), 5.52 (m, 1H), 4.18 (d, 1H), 3.14 (m, 1H), 2.55-2.45 (m, 2H), 1.80-1.67 (m, 5H), 1.57-1.51 (m, 1H), 1.46-1.17 (m, 5H), 1.00-0.90 (m, 2H).
Example 14 benzyl (2S,3R)-3-amino-3-c~pent~2-h droxypropanoate Example 14A
bend (2E~-3-c~pentylacrylate A solution of cyclopentanecaboxaldehyde (0.069 g, 0.70 mmol), benzyl (diethylethyl io phosphono)acetate (0.100 g, 0.35 mmol), lithium bromide (0.030 g, 0.35 nunol), and triethylamine (0.049 mL, 0.35 mmol) in THF (1 mL) at room temperature was stirred for 16 hours, quenched with water, stirred for 15 minutes, diluted with ethyl acetate, washed sequentially with pH 7 buffer and brine, dried (MgS04), filtered, and concentrated to provide the desired product. MS (ESI] m/e 231 (M+H)+.
Example 14B
benzyl (2S,3R)-3-f (tart-butox cy arbon~)aminol-3-cyclopentyl-2-h~ypropanoate The desired product was prepared by substituting Example 14A for Example 9B in Example 9C. MS (ESI) m/e 364 (M+H)+.
Example 14C
benzyl (2S,3R)-3-amino-3-cyclopent~ydroxypropanoate The desired product was prepared by substituting Example 14B fox Example 3C in Example 3D. MS (ESl] mle 264 {M+H)+; 1H NMR (300 MHz, CD30D) b 7.39 (m, 5H), 5.29 (dd, 2H), 4.04 (d, 1H), 3.88 (dd, 1H), 3.6'6 (s, 1H), 1.96 (m, 1H), 1.86 (m, 1H), 1.68 (m, 2H), 1.58 (m, 2H), 1.43 (m, IH), 1.23 (m, 1H).
Example 15 benzyl (2S,3R)-3-amino-3-cycloheptyl-2-h~ypropanoate 3o The desired product was grepared by substituting cycloheptanecarboxaldehyde for cyclopentanecarboxaldehyde in Examples 14A-C. MS (ES>:) m/e 292 (M+H)+;1H NMR
(300 MHz, CD30D) 8 7.39 (m, 5H), 5.29 (dd, 2H), 4.09 (d, 1H), 3.78 (dd, 1H), 3.66 (s, 1H), 1.84 (m, 1H), 1.65 (m, 2H), 1.57 (m, 2H), 1.52 (m, 2H), 1.46 (m, 2H), 1.41 (m, 2H), 1.33 (m, 2H).
Exam lp a 16 12,t'1-~-(methylamino)-2-(1-naphthyl)ethyl (2S 3R)-3-amino-5-(eth lsy ulfanyl)-h droxypentanoate Example 16A
teat-butyl (IR)-2-hydroxy-1-(1-naphth l~ l(iyethyl)carbamate and ter-t-butyl (1RS)-2 h~droxy-1-methyl-1-(1-naphthyl)ethyl(methyl)carbamate A mixture of sodium hydride (dispersion in 60% mineral oiI , 440 mg, 10.9 mmol) and methyl (2R)-[{tert-butoxycarbonyl)amino](1-naphthyl)acetate (1.43 g, 4.54 mmol) in THF (20 mL) was stirred at 0 °C for 15 minutes, treated with methyl iodide (1.978 mL, 31.8 mmol), stirred at 0 °C for 2 hours, warmed to room temperature, and stirred for 16 hours.
The mixture was diluted with ethyl acetate, washed sequentially with 10%
aqueous KHS04 and brine, dried (MgS04), filtered, and concentrated to provide a mixture of mono- and di-methylated product (ratio: 4:1). The mixture (2.0 g) was dissolved in THF (20 mL), cooled to 0 °C, treated with sodium bis(2-methoxyethoxy)aluminum hydride (Red-Al~) {6 mL), stirred for 1 hour, warmed to room temperature, stirred for 1 hour, quenched with aqueous Na2S04 (10 mL), and extracted three times with ethyl acetate. The combined extracts were washed twice with brine, twice with 10% KHS04, once more with brine, twice with IO%
sodium hydrogen carbonate, three additional times with brine, dried (MgSO~.), filtered, and concentrated. The concentrate was purified by flash column chromatography on silica gel with 10% ethyl acetate/hexanes to provide the desired products MS(ESI(+)) m!e 302 (M+H)+
and 316 (M+H)+.
Example I6B
~2R)-2-(meth~amino)-2-(1-nanhthyl)ethyl (2S,3R~3-amino-5-(ethylsulfanyl)-2 hydroxypentanoate The desired product was prepared by substituting tert-butyl (1R)-2-hydroxy-I-(1 naphthyl)ethyl(methyl)carbamate from Example 16A and Example 2A for (IS,2R)-I-amino-2-hydroxyindane and Example 3C, respectively, in Example 13. The crude product was purified by reverse phase HPLC with acetonitrile/water to provide the desired product. MS
(ESI(+)) m/e 377 (M+I-~~; 1H-NMR (300MHz, DMSO-d6) 8 8.29-8.19 (m, 1H), 8.06-8.00 (m, 3H), 7.71-7.58 (m, 3H), 6.48 (d, 1H), 5.60 (br s, 1H), 4.75-4.66 (m, 1H), 4.60-4.53 (m, 21~, 3.72-3.56 (m, 1H), 2.60 (br s, 3H), 2.48-2.26 (m, 3H, includes 2.33 (q)), 1.77-1.44 (m, 2I~, 1.05 (t, 3I~.
Example I7 (2R~2-(methylamino)-2-(1-naphth ly )ethyl (2S 3R)-3-amino-5-(ethylsulfanyl)-2 h droxyperztanoate The desired compound u~as obtained by substituting methyl (2S)-[(tert butoxycarbonyl)amino](1-naphthyl)acetate for methyl (2R)-[(te3~'-butoxycarbonyl)amino](1-naphthyl)acetate in Examples 16A-B. MS (ESI(+)) mle 377 (M+H)t; 'H-NMR
(300MHz, DMSO-d~) 8 8.32-8.25 (m, 1H), 8.08-7.99 (m, 3H), 7.72-7.54 (m, 3H), 6.63 (d, 1H), 5.62 (br s, 1H), 4.71-4.55 (m, 2H), 4.45-4.40 (m, 1H), 3.73-3.64 (m, 1H), 2.62 (br s, 3H), 2.53-2.42 (m, 3H, overlapped with solvent peaks), 1.94-1.70 (m, 2H), I.17 (t, 3H).
Example 18 2-(methylamino)-2-(1-na~ht~l)propyl (3R)-3-amino-5-(eth~sulfan l~ydroxypentanoate The desired product was prepared by substituting ter t-butyl (IRS)-2-hydroxy-1 methyl-1-(1-naphthyl)ethyl(methyl)carbamate from Example 16A and Example 2A
for to (1S,2R)-1-amino-2-hydroxyindane and Example 3C, respectively, in Example 13. MS
(ESI(+)) m/e 391 (M+H]~; 1H-NMR (300MHz, DMSO-d6) 8 8.I5-8.03 (br s, 3I-~, 7.93-7.82 (br s, 3H), 7,66-7.56 (br s, 1H), 6.54 (d, 0.7H}, 6.45 (d, 0.3H), 4.25-4.17 (br s, 0.3H), 4.13-4.05 (br s, 0.7H), 3.54-3.40 (m, 1H), 2.60 (br s, 3H), 2.67-2.43 (m, includes solvent peaks), I.93-1.59 (m, 2H), I.2I-I.07 (m, 6H).
z5 Example I9 (2R)-2-~methylamino -2-) (I-naphthyl)ethyl (2S,3R)-3-amino-4-c~clohexyl-2 h droxybutanoate The desired product was prepaxed by substituting tef-t-butyl (1R)-2-hydroxy-1-(1-2o naphthyl)ethyl(methyl)carbamate from Example 16A for (1S,2R)-1-amino-2-hydroxyindane in Example 13. The crude product was purified by reverse phase HPLC with acetonitxile/watex to provide the desired product. MS (ESI) m/e 385 (M+H)+; 1H
NMR (300 MHz, DMSO-d6) 8 I0.I7 (br s,lH}, 9.8 (6x s, 1H), 8.28 (d, 1H), 8.08-7.95 (m, 4H}, 7.7-7.55 (m, 3H), 6.56 (d, IH), 5.63 (br s, IH), 4.69 (dd, 1H), 4.57 (dd, 1H), 4.3 (m, 1H), 3.5 (br s, 25 IH), 2.6 (s, 3H), I.7-I.5 (m, 6H), 1.45-1.35 (m, 3H), I.22-1.05 (m, 3H), 0.88-0.73 (m, 1H).
Example 20 (2R)-2-(methylamino)-2-(1-naphthyl)ethyl (2S,3R)-3-amino-2-h droxy-5-phenylpentanoate The desired compound was obtained by substituting ten-butyl (1R)-2-hydroxy-1-(1-3o naphthyl)ethyl(methyl)carbamate from Example I6A and Example 6A for (IS,2R)-1-amino-2-hydroxyindane and Example 3C, respectively, in Example 13. The crude pxoduct was purified by reverse phase HPLC to provide the desired product. MS (ESI) mle 393 (M+H)+;
1H NMR (300 MHz, DMSO-d6} S 10.2 (br s,lH), 9.8 (br s, IH), 8.29 (d, IH), 8.15 (br s, 2IT), 8.04 (m, 3H), 7.7-7.58 (m, 3H),7.34-7.I6 (m, 4H), 6.63 (d, 1H), 5.63 (br s, 1H), 4.7-4.56 (m, 35 2H), 4.48 (br s, Il~, 3.58 (br s, zH), 2.78-2.53 (m, 2H), 2.6 (s, 3I-~, 1.95-I.75 (m, 2H).
Exam Ip a 21 _27_ methyl (2RS,3R)-3-amino-5-(ethylsulfan l~ydroxypentanoate Example 21A
methyl (2RS,3R)-3-f(tent-6utoxycarbonyl)aminol-5-(eth lsulfanyl)-2-h~droxypentanoate The desired product was prepared by substituting Example 7B and diazomethane for Example 3C and trimethylsilyldiazomethane, respectively, in Example 12A.
Example 21B
methyl (2RS,3R)-3-amino-5-(ethylsulfan~-hydroxypentanoate The desired product was prepared by substituting Example 21A for Example 3C in Example 3D. MS (ESI] m!e 208 (M+H)+; III NMR (300 MHz, DMSO-db) S 8.15 (br s, 0.6H), 7.99 (br s, 1.4H), 6.53 (d, 0.7H~, 6.39 (d, 0.3H), 4.48 (m, 0.3ITj, 4.29 (m, 0.7H), 3.70 (s, 2.1H), 3.53 (s, 0.9H), 2.63 (m, 2IT), 2.49 (m, 2H), 1.90-1.80 (m, 2IT), 1.20-1.14 (m, 3H).
Exam Ip a 22 benzyl (2RS,3R)-3-amino-5-(ethylsuIfanyI)-2-hydroxypentanoate Example 22A
3-tent-butyl 5-methyl (4R 5RS)-4-f2-(ethylsulfan Iy )ethyll-Z 2-dimeth~-1 3-oxazolidine-3 5-2o dicarboxylate A mixture of Example 21A (1.12 g, 3.65 mmol) and catalytic 4-methylbenzenesulfonic acid (15 mg) in 2,2-dimethoxypropane (35 mL) at ambient temperature was stirred for 36 hours, diluted with ethyl acetate, washed sequentially with aqueous NaHC03 and pH 7 buffer, dried (MgS04), filtered, and concentrated.
Flash column chromatography (silica gel, 10% acetone/hexanes) provided the desired product.
MS (ESI) m/e 348 (M+H)+.
Exam lie 2-2B
4R.5RS)-3-(tent-butoxycarbonyl)-4- f 2-(ethylsulfanyl)ethyl)-2,2-dimethvl-1,3-oxazolidine-5-3o carboxylic acid A 0 °C solution of Example 22A (0.65 g, 1.87 mmol) in THF (6 mL) was treated with a solution of lithium hydroxide monohydrate (0.088 g, 2.1 mmol) in water (2 mL), stirred fox 2 hours, concentrated, and diluted with wafer. The aqueous phase was washed with diethyl ether, adjusted to pH 4 with 0.5M citric acid, and extracted twice with ethyl acetate. The combined extracts were dried (Na2S0~.), filtered, and concentrated to provide the desired product. MS (ES>) m/e 334 (M+1~~.
_28_ Example 22C
benzyl (2RS 3R)-3-amino-5-(eth lsulfanyl)-2-hydroxypentanoate A solution of Example 22B (0.11 g, 0.33 mmol), benzyl alcohol (0.07 mL, 0.7 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (0.080 g, 0.41 mmol), HOAT
(0.045 g, 0.33 mmol), and N methylmorpholine (0.055 mL , 0.50 mmol) in 3:1 dichloromethane/DMF (4 mL) at room temperature was stirred for 16 hours, diluted with dichIoromethane, washed sequentially with aqueous NaHC03, brine, 0.5M citric acid, and brine, dried (MgS04), filtered, and concentrated. The residue was dissolved in 4M HCl in dioxane (2 mL), stirred for 1 hour, treated with water (1 mL), stirred for 1 hour, concentrated, to and purified by reverse phase HPLC with acetonitrilelwater to provide the desired product.
MS (ESl] m/e 284 (M+H)+; 1H NMR (300 MHz, DMSO-d6) b 7.43-7.37 (m, 5H), 5.20 (s, 1.4H), 5.19 (m, 0.6H), 4.44 (m, 0.3H), 4.32 (m, 0.7H), 3.53 (m, 1H), 2.63 (m, 2H), 2.43 (m, 2H), 1.90-1.75 (m, 2H), 1.20-1.12 (m, 3H).
15 Example 23 butyl (2RS 3R)-3-amino-5-(eth lsu~lfanyl)-2-hydroxypentanoate The desired product was prepared by substituting 1-butanol for benzyl alcohol in Example 22C. MS (ESn m/e 250 (M+H)+; 1H NMR (300 MHz, DMSO-d6) 8 7.87-7.80 (br s, 2H), 6.53 (m, 0.7H), 6.33 (d, 0.3H), 4.40 (m, 0.3H), 4.24 (m, 0.7H), 4.12 (t, 2H), 3.53 (m, 20 1H), 2.63 (m, 2H), 2.48 (m, 2H), 1.90-1.75 (m, 2H), 2.66-1.57 (m, 2H), 1.44-1.33 (m, 2H), 1.22-1.16 (m, 3H) 0.92 (t, 3H).
Example 24 isopropyl (2S 3R)-3-amino-2-hydroxy-5-(isoprop lsy ulfanyl)pentanoate 25 The desired product was prepared by substituting 2-propanol and Example 7B
for (1S,2R)-1-amino-2-hydroxyindane and Example 3C, respectively, in Example 13.
The crude product was purified by reverse phase HPLC with acetonitrile/water to provide the desired product. MS (ESA m/e 250 (M+H)+; 1H NMR (300 MHz, DMSO-d6) b 7.97 (br s, 2H), 6.62 (d, 1H), 5.02-4.92 (m, 1H), 4.18 (t, 1H), 3.73-3.63 (m, 1H), 3.53-3.38 (m, 2H), 2.98-2.85 (m, 30 1H), 2.7-2.55 (m~ IH), I.8 (q, 1H), 1.25 (d, 6H), 1.2 (d, 6H).
Example 25 isopropyl (2RS 3R)-3-amino-5-(eth lsy ulfan l~ydroxypentanoate The desired product was prepared by substituting 2-propanol for benzyl alcohol in 35 Example 22C. MS (ESA m/e 236 (M+H)+; 1H NMR (300 MHz, DMSO-d~) 8 7.73 (br s, 2H), 4.97 (m, 1H), 4.15 (d, 1H), 3.44 (m, 1H), 2.63 (m, 2H), 2.49 (m, 2H), 1.79 (m, 2H), 1.23 (d, 6H), 1.18 (m, 3H).
_29-Example 26 ((2,2-dimeth~lwopanoyl)oxylmethyl (2RS 3R)-3-amino-5-(ethylsulfan~?-2 hydroxypentanoate A solution of Example 22B (0.102 g, 0.3I mmol), cesium carbonate (0.1I l g, 0.34 mmol), and chloromethyl pivalate (0.055 mL, 0.38 mmol) in DMF (3 mL) at room temperature was stirred for 24 hours; diluted with ethyl acetate, washed sequentially with water, aqueous NaHC03, pH 7 buffer, and brine, dried (MgS04), filtered, and concentrated.
The residue was dissolved in 4M HCl in dioxane (2 mL), stirred for 1 hour, treated with water (1 mL), stirred for 1 hour, concentrated, and purified by reverse phase HPLC
with acetonitrile/water to provide the desired product. MS (ES)) m/e 308 (M+H)+; 1H
NMR (300 MHz, DMSO-d6) 8 7.87-7.80 (br s, 2H), 6.53 (m, 0.7H), 6.33 (d, 0.3H), 4.40 (m, 0.3H), 4.24 (m, 0.7H), 4.28 (s, 0.6H), 4.26 (s, 1.4H), 3.53 (m, 1H), 2.63 (m, 2H), 2.48 (m, 2H), 1.90-1.75 (m, 2H), 1.22-1.16 (m, 12H).
is Example 27 sec-butyl (2RS,3R)-3-amino-S-(ethylsulfan ly )-2-hydroxypentanoate The desired product was prepared by substituting 2-butanol for benzyl alcohol in Example 22C. MS (ES)] m/e 250 (M+H)+; tH NMR (300 MHz, DMSO-d6) S 7.87-7.80 (br 2o s, 2H), 6.53 (m, 0.7H), 6.33 (d, 0.3H), 4.83 (m, 1H), 4.40 (m, 0.3H), 4.24 (m, 0.7H), 3.53 (m, 1H), 2.63 (m, 2H), 2.48 (m, 2H), 1.90-1.75 (m, 2H), 1.28-1.17 (m, 7H), 0.92-0.84 (m, 3H).
Example 28 (I,3-dioxo-I,3-dihydro-2H isoindol-2- 1)Y methyl (2RS,3R)-3-amino-5-(ethylsulfanyI)-2-25 h~y~entanoate The desired product was prepared by substituting N (bromomethyl)phthalimide for chloromethyl pivalate in Example 26. MS (ESI) m/e~ 353 (M+H)+; 1H NMR (300 MHz, DMSO-d6) 8 7.99-7.82 (m, 4H), 6.64 (d, 0.7H), 6.48 (d, 0.3H), 5.73 (s, 1H), 4.97 (s, 1H), 4.30 (m, 0.7H), 4.18 (m, 0.3H), 3.53 (m, 1H), 2.63 (m, 2H), 2.48 (m, 2H), 1.90-1.75 (m, 2H), 30 1.22-1.16 (m, 3H).
Example 29 sec-but I (~2RS 3R)-3-amino-2-hYdrox -~5- isopropylsulfan~)pentanoate 35 Examt~le 29A
(4R,SRS~3-(tern-butoxycarbo~l)-4-f2-(isoprop ls~ulfanyl)ethyll-2 2-dimethyl-1 oxazolidine-5-carboxylic acid The desired product was prepared by substituting Example 7B for Example 21A in Examples 22A and 22B.
Exam lp a 29B
sec-butyl (2RS 3R)-3-amino-2-h dy roxy-5-(isoprop ls~ ulfanyl)pentanoate The desired product was prepared by substituting 2-butanol and Example 29A for benzyl alcohol and Example 22B, respectively, in Example 22C. MS (ESI) m/e 264 (M+H)+;
iH NMR (300 MHz, DMSO-d6) 8 7.97 (br s, 2H), 6.60-5.55 (m, 1H), 4.83 (m, 1H), 4.18 (m, 1H), 3.73-3.63 (m, 1H), 3.53-3.38 (m, 2H), 2.98-2.85 (m, 1H), 2.70-2.55 (m, 1H), 1.87-1.78 to (m, 3H), 1.25 (m, 3H), 1.20 (d, 6H), 0.89-0.83 (m, 3H).
Example 30 L(2 2-dimeth~nropanoyl)ox l~methyl (2S,3R)-3-amino-2-hydroxy-5 isoprop ls~yl)pentanoate 15 The.desired product was prepared by substituting Example 29A for Example 22B in Example 26. The crude product was purified by reverse phase HPLC with acetonitrile/water to provide the desired product. MS (ESI) m/e 322 (M+H)+;1H NMR (300 MHz, DMSO-d6) 8 7.97-7.83 (br m, 2H), 6.73 (d, 1H), 5.78 (dd, 2H), 4.33 (t, 1H), 4.16 (m, 1H), 3.73-3.63 (m, 1H), 3.53-3.38 (m, 1H), 2.98-2.85 (m, 1H), 2.70-2.55 (m,1H), 1.87-1.78 (m, 1H), 1.20 (d, 20 6H), 1.12 (s, 9H).
Example 31 (1,3-dioxo-1 3-dihydro-2H isoindol-2- 1)m~ethyl (2S 3R)-3-amino-2-hydroxy-5 (isopropylsulfan~pentanoate 25 The desired product was prepared by substituting N
(brornomethyl)phthalimide and Example 29A for chloromethyl pivalate and Example 22B, respectively, in Example 26. The crude product was purified by reverse phase HPLG with acetonitrile/water to provide the desired product. MS (ESI) m/e 367 (M+H)+; 1H NMR (300 MHz, DMSO-d6) S 7.97-7.83 (m, 6H), 6.63 (d, 1H), 5.72 (s, 1H), 4.97 (s, 1H), 4.32 (t, 1H), 4.17 (m, 1H), 3.73-3.63 (m, 30 1H), 3.53-3.38 (m, 1H), 2.98-2.85 (m, 1H), 2.70-2.55 (m, 1H), 1.87-1.78 (m, 1H), 1.20 (d, 6H).
Example 32 3-oxo-1 3-dihydro-2-benzofuran-1-yl (2S 3R)-3-anuno-2-hydroxy-5-35 (isoprop, lsy ulfanyl)pentanoate The desired product was prepared by substituting 3-bromophthalide and Example for chloromethyl pivalate and Example 22B, respectively, in Example 26. The crude product was purified by reverse phase HPLC with acetonitrile/water to provide the desired product.
MS (ESI) m/e 340 (M+H)+; IH NMR (300 MHz, DMSO-d~) b 8.03-7.92 (m, 3H), 7.83-7.78 (m, 2H), 7.66 (d, 1H), 6.63 (s, 1H), 4.28 (m, 1H), 4.18 (d, 1H), 3.73-3.63 (111, 1H), 3.53-3.38 (m, 1H), 2.98-2.85 (m, 1H), 2.70-2.55 (m, 1H), 1.87-1.78 (m, 1H), 1.20 (d, 6H).
It will be evident to one skilled in the art that the present invention is not limited to the foregoing illustrative examples, and that it can be embodied in other specific forms without departing from the essential attributes thereof. It is therefore desired that the examples be considered in all respects as illustrative and not restrictive, reference being made to the appended claims, rather than to the foregoing examples, and all changes which come within the meaning and range of equivalency of the claims are therefore intended to be embraced therein.

Claims

WHAT IS CLAIMED IS

1. A compound of formula (I) or a therapeutically acceptable salt thereof, wherein R1 is selected from the group consisting of alkyl, alkylsulfanylalkyl, aryl, arylalkyl, cycloalkyl, (cycloalkyl)alkyl, (heterocycle)alkyl, and hydroxyalkyl; and R2 is selected from the group consisting of hydrogen, alkenyl, alkyl, alkylcarbonyloxyalkyl, alkylcarbonylalkyl, aryl, arylalkyl, cycloalkyl, (cycloalkyl)alkyl, heterocycle, and (heterocycle)alkyl.

2. The compound of claim 1 wherein R2 is hydrogen.

3. The compound of claim 2 wherein R1 is alkylsulfanylalkyl.

4. The compound of claim 3 selected from the group consisting of (2RS,3R)-3-amino-2-hydroxy-5-(methylsulfanyl)pentanoic acid;
(2RS,3R)-3-amino-5-(ethylsulfanyl)-2-hydroxypentanoic acid;
(2RS,3R)-3-amino-2-hydroxy-5-(isopropylsulfanyl)pentanoic acid; and (2RS,3R)-3-amino-5-(tert-butylsulfanyl)-2-hydroxypentanoic acid.

5. The compound of claim 2 wherein R1 is selected from the group consisting of arylalkyl, cycloalkyl, (cycloalkyl)alkyl, and hydroxyalkyl.

6. The compound of claim 5 selected from the group consisting of (2RS,3R)-3-amino-4-cyclohexyl-2-hydroxybutanoic acid;
(2RS,3R)-3-amino-3-cyclohexyl-2-hydroxypropanoic acid;
(2RS,3R)-3-amino-2-hydroxy-5-phenylpentanoic acid;
(2S,3R,4S)-3-amino-2-hydroxy-4-(3-hydroxypropyl)-7-methyloctanoic acid; and (2S,3R)-3-amino-2-hydroxy-6-phenylhexanoic acid.

7. The compound of claim 1 wherein R2 is arylalkyl.

8. The compound of claim 7 wherein R1 is alkylsulfanylalkyl.

9. The compound of claim 8 selected from the group consisting of (2S)-2-(methylamino)-2-(1-naphthyl)ethyl (2S,3R)-3-amino-5-(ethylsulfanyl)-2-hydroxypentanoate;
(2R)-2-(methylamino)-2-(1-naphthyl)ethyl (2S,3R)-3-amino-5-(ethylsulfanyl)-2-hydroxypentanoate;
2-(methylamino)-2-(1-naphthyl)propyl (3R)-3-amino-5-(ethylsulfanyl)-2-hydroxypentanoate;
and benzyl (2RS,3R)-3-amino-5-(ethylsulfanyl)-2-hydroxypentanoate.

10. The compound of claim 7 wherein R1 is selected from the group consisting of arylalkyl, cycloalkyl, and (cycloalkyl)alkyl.

11. The compound of claim 10 selected from the group consisting of benzyl (2S,3R)-3-amino-3-cyclopentyl-2-hydroxypropanoate;
benzyl (2S,3R)-3-amino-3-cycloheptyl-2-hydroxypropanoate;
(2R)-2-(methylamino)-2-(1-naphthyl)ethyl (2S,3R)-3-amino-4-cyclohexyl-2-hydroxybutanoate; and (2R)-2-(methylamino)-2-(1-naphthyl)ethyl (2S,3R)-3-amino-2-hydroxy-5-phenylpentanoate.

12. The compound of claim 1 wherein R2 is alkyl.

13. The compound of claim 12 selected from the group consisting of methyl (3R)-3-amino-2-hydroxy-5-(methylsulfanyl)pentanoate;
methyl (2RS,3R)-3-amino-4-cyclohexyl-2-hydroxybutanoate;
methyl (2RS,3R)-3-amino-5-(ethylsulfanyl)-2-hydroxypentanoate;
butyl (2RS,3R)-3-amino-5-(ethylsulfanyl)-2-hydroxypentanoate;
isopropyl (2S,3R)-3-amino-2-hydroxy-5-(isopropylsulfanyl)pentanoate;
isopropyl (2RS,3R)-3-amino-5-(ethylsulfanyl)-2-hydroxypentanoate;
sec-butyl (2RS,3R)-3-amino-5-(ethylsulfanyl)-2-hydroxypentanoate; and sec-butyl (2RS,3R)-3-amino-2-hydroxy-5-(isopropylsulfanyl)pentanoate.

14. The compound of claim 1 wherein R2 is selected from the group consisting of alkylcarbonyloxyalkyl, aryl, heterocycle, and (heterocycle)alkyl.

15. The compound of claim 14 selected from the group consisting of (1S,2R)-2-amino-2,3-dihydro-1H-inden-1-yl (2RS,3R)-3-amino-4-cyclohexyl-2-hydroxybutanoate;
[(2,2-dimethylpropanoyl)oxy]methyl (2RS,3R)-3-amino-5-(ethylsulfanyl)-2-hydroxypentanoate;
(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl (2RS,3R)-3-amino-5-(ethylsulfanyl)-2-hydroxypentanoate;
[(2,2-dimethylpropanoyl)oxy]methyl (2S,3R)-3-amino-2-hydroxy-5-(isopropylsulfanyl)pentanoate;
(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl (2S,3R)-3-amino-2-hydroxy-5-(isopropylsulfanyl)pentanoate; and 3-oxo-1,3-dihydro-2-benzofuran-1-yl (2S,3R)-3-amino-2-hydroxy-5-(isopropylsulfanyl)pentanoate.

16. A pharmaceutical composition comprising a compound of claim 1 or a therapeutically acceptable salt thereof, in combination with a therapeutically acceptable carrier.

17. A method of inhibiting angiogenesis in a mammal in recognized need of such treatment comprising administering to the mammal a pharmaceutically acceptable amount of a compound of claim 1.

18. A method for treating cancer in a patient in recognized need of such treatment comprising administering to the patient a therapeutically acceptable amount of a compound of claim 1, or a therapeutically acceptable salt thereof.