WO2004043339A2

WO2004043339A2 - Substituted cycloalkyl p1' hepatitis c virus inhibitors

Info

Publication number: WO2004043339A2
Application number: PCT/US2003/015780
Authority: WO
Inventors: Jeffrey Allen Campbell; Stanley V. D'andrea; Andrew Good; Jianqing Li; Fiona Mcphee; Amy Ripka; Paul Michael Scola; Yong Tu
Original assignee: Bristol-Myers Squibb Company
Priority date: 2002-05-20
Filing date: 2003-05-20
Publication date: 2004-05-27
Also published as: EP1505945B1; EP1505945A2; JP4271148B2; JP2006501307A; EP1505945A4; IS7531A; WO2004043339A3; AU2003301959A8; DE60324552D1; PL373374A1; ES2315568T3; ATE413411T1; PL213029B1; AU2003301959A1; NO20044895L; US20040077551A1; US6878722B2

Abstract

The present invention relates to tripeptide compounds, compositions and methods for the treatment of hepatitis C virus (HCV) infection. In particular, the present invention provides novel tripeptide analogs, pharmaceutical compositions containing such analogs and methods for using these analogs in the treatment of HCV infection.

Description

SUBSTITUTED CYCLOALKYL PI' HEPATITIS C VIRUS INHIBITORS

FIELD OF THE INVENTION

The present invention is generally directed to antiviral compounds, and more specifically directed to compounds which inhibit the functioning of the NS3 protease encoded by Hepatitis C virus (HCV), compositions comprising such compounds and methods for inhibiting the functioning of the NS3 protease.

BACKGROUND OF THE INVENTION

HCV is a major human pathogen, infecting an estimated 170 million persons worldwide - roughly five times the number infected by human immunodeficiency virus type 1. A substantial fraction of these HCV infected individuals develop serious progressive liver disease, including cirrhosis and hepatocellular carcinoma. (Lauer, G. M.; Walker, B. D. N Engl. J. Med. (2001), 345. 41-52).

Presently, the most effective HCV therapy employs a combination of alpha-interferon and ribavirin, leading to sustained efficacy in 40% of patients. (Poynard, T. et al. Lancet (1998), 352, 1426-1432). Recent clinical results demonstrate that pegylated alpha-interferon is superior to unmodified alpha- interferon as monotherapy (Zeuzem, S. et al. N Engl. J. Med. (2000), 343, 1666- 1672). However, even with experimental therapeutic regimens involving combinations of pegylated alpha-interferon and ribavirin, a substantial fraction of patients do not have a sustained reduction in viral load. Thus, there is a clear and long-felt need to develop effective therapeutics for treatment of HCV infection.

HCV is a positive-stranded RΝA virus. Based on a comparison of the deduced amino acid sequence and the extensive similarity in the 5' untranslated region, HCV has been classified as a separate genus in the Flaviviridae family. All members of the Flaviviridae family have enveloped virions that contain a positive stranded RNA genome encoding all known virus-specific proteins via translation of a single, uninterrupted, open reading frame.

Considerable heterogeneity is found within the nucleotide and encoded amino acid sequence throughout the HCV genome. At least six major genotypes have been characterized, and more than 50 subtypes have been described. The major genotypes of HCV differ in their distribution worldwide, and the clinical significance of the genetic heterogeneity of HCV remains elusive despite numerous studies of the possible effect of genotypes on pathogenesis and therapy.

The single strand HCV RNA genome is approximately 9500 nucleotides in length and has a single open reading frame (ORF) encoding a single large polyprotein of about 3000 amino acids. In infected cells, this polyprotein is cleaved at multiple sites by cellular and viral proteases to produce the structural and non- structural (NS) proteins. In the case of HCV, the generation of mature non-structural proteins (NS2, NS3, NS4A, NS4B, NS5A, and NS5B) is effected by two viral proteases. The first one, as yet poorly characterized, cleaves at the NS2-NS3 junction; the second one is a serine protease contained within the N- terminal region of NS3 (henceforth referred to as NS3 protease) and mediates all the subsequent cleavages downstream of NS3, both in cis, at the NS3-NS4A cleavage site, and in trans, for the remaining NS4A- NS4B, NS4B-NS5A, NS5A- NS5B sites. The NS4A protein appears to serve multiple functions, acting as a cofactor for the NS3 protease and possibly assisting in the membrane localization of NS3 and other viral replicase components. The complex formation of the NS3 protein with NS4A seems necessary to the processing events, enhancing the proteolytic efficiency at all of the sites. The NS3 protein also exhibits nucleoside triphosphatase and RNA helicase activities. NS5B is a RNA- dependent RNA polymerase that is involved in the replication of HCV. Among the compounds that have demonstrated efficacy in inhibiting HCV replication, as selective HCV serine protease inhibitors, are the peptide compounds disclosed in U.S. Patent No. 6,323,180.

SUMMARY OF THE INVENTION

The present invention provides compounds, or pharmaceutically acceptable salts, solvates or prodrugs thereof, having the structure of formula I

wherein:

(a) R* is trialkylsilane; halo; C_3-7 cycloalkyl, C - cycloalkenyl; C_6-1o aryl; C_7-14 alkylaryl; C_6-10 aryloxy; C_7-14 alkylaryloxy; C_8-15 alkylarylester; Het; or C_1-8 alkyl optionally substituted with C_1-6 alkoxy, hydroxy, halo, C_2-10 alkenyl, C_2-10 alkynyl, C_3-7 cycloalkyl,

C - cycloalkenyl, C_6-1o aryl, C_7-1 alkylaryl, C_6-1o aryloxy, C _-1 alkylaryloxy, C_8-15 alkylarylester or Het; o — C-R₈ wherein R₈ is C_3-7 cycloalkyl, C_4-7 cycloalkenyl; C_6-10 aryl; C_7-1 alkylaryl; C_6-1o aryloxy; C_7-1 alkylaryloxy; C_8-15 alkylarylester; Het; or C_1-8 alkyl optionally substituted with C_1-6 alkoxy, hydroxy, halo, C_2-10 alkenyl, C_2-10 alkynyl, C_3-7 cycloalkyl, C _-7 cycloalkenyl, C_6-10 aryl, C_7-1 alkylaryl, C_6-10 aryloxy, C_7-1 alkylaryloxy, C_8-15 alkylarylester or Het; O

I I

— C-ORg wherein R is C _-7 cycloalkyl, C_4-7 cycloalkenyl; C_6-10 aryl; C_7-1 alkylaryl; C_6-10 aryloxy; C_7-1 alkylaryloxy; C_8-15 alkylarylester; Het; or C_1-8 alkyl optionally substituted with C_1-6 alkoxy, hydroxy, halo, C_2-10 alkenyl, C_2-1o alkynyl, C_3- cycloalkyl, C_4-7 cycloalkenyl, C_6-10 aryl, C_7-14 alkylaryl, C_6-10 aryloxy, C_7-14 alkylaryloxy, C_8-15 alkylarylester or Het; o — C— NR10R11 , wherein R*o and Rπ are each independently C_3-7 cycloalkyl, C_4-7 cycloalkenyl; C_6-1o aryl; C _-14 alkylaryl; C_6-1o aryloxy; C _-14 alkylaryloxy; C_8-15 alkylarylester; Het; or C_1-8 alkyl optionally substituted with C_1-6 alkoxy, hydroxy, halo, C_2-10 alkenyl, C_2-1o alkynyl, C_3-7 cycloalkyl, C_4-7 cycloalkenyl, C_6-10 aryl, C_7-1 alkylaryl, C_6-10 aryloxy, C_7-14 alkylaryloxy, C_8-15 alkylarylester or Het; -SO₂R₁₂ wherein R₁₂ is C_3-7 cycloalkyl, C _-7 cycloalkenyl; C_6-10 aryl; C_7-1 alkylaryl; C_6-ι₀ aryloxy; C _-1 alkylaryloxy; C_8-15 alkylarylester; Het; or C_1-8 alkyl optionally substituted with C_1-6 alkoxy, hydroxy, halo, C _-10 alkenyl, C_2-10 alkynyl, C_3- cycloalkyl, C_4-7 cycloalkenyl, C₆-₁₀ aryl, C_7-14 alkylaryl, C_6-1o aryloxy, C_7-14 alkylaryloxy, C_8-15 alkylarylester or Het; o or — OCR13 wherein R₁₃ is C_3- cycloalkyl, C_4- cycloalkenyl; C_6-10 aryl; C_7-1 alkylaryl; C_6-1o aryloxy; C_7-14 alkylaryloxy; C_8-15 alkylarylester; Het; or C_1-8 alkyl optionally substituted with C_1-6 alkoxy, hydroxy, halo, C_2-10 alkenyl, C_2-1o alkynyl, C_3- cycloalkyl, C_4- cycloalkenyl, C₆.₁₀ aryl, C_7-ι alkylaryl, C_6-10 aryloxy, C_7-14 alkylaryloxy, C₈.*₅ alkylarylester or Het;

(b) R₂ is C_1-6 alkyl, C_2-6 alkenyl or C₃.₇ cycloalkyl, each optionally substituted from one to three times with halogen; or R₂ is H; or R₂ together with the carbon to which it is attached forms a 3, 4 or 5 membered ring; (c) R₃ is Cι-₈ alkyl optionally substituted with halo, cyano, amino, C_1-6 dialkylamino, C_6-10 aryl, C_7-14 alkylaryl, C_1-6 alkoxy, carboxy, hydroxy, aryloxy, C_7-14 alkylaryloxy, C_2-6 alkylester, C_8-15 alkylarylester; C_3-12 alkenyl, C_3- cycloalkyl, or C_4-10 alkylcycloalkyl, wherein the cycloalkyl or alkylcycloalkyl are optionally substituted with hydroxy, C_1-6 alkyl, C_2-6 alkenyl or C_1-6 alkoxy; or R₃ together with the carbon atom to which it is attached forms a C_3-7 cycloalkyl group optionally substituted with C_2-6 alkenyl; (d) R is H, C_1-6 alkyl, C_3-7 cycloalkyl, C_1-6 alkoxy, C_3-7 cycloalkoxy, halo-C_!-₆ alkyl, CF₃, mono-or di- halo-C_1-6 alkoxy, cyano, halo, thioalkyl, hydroxy, alkanoyl, NO₂, SH, , amino, C_1-6 alkylamino, di (Ci-β) alkylamino, di (C*-₆) alkylamide, carboxyl, (C--₆) carboxyester, C_1-6 alkylsulfone, C_1-6 alkylsulfoxide, C_1-6 alkylsulfonamide or di (Ci-₆) alkyl(alkoxy)amine;

(e) R₇ is H, Ci-₆ alkyl, C_3-7 cycloalkyl, Cβ-io aryl, C_7-1 alkylaryl; C_6-10 aryloxy; C_7-14 alkylaryloxy; C_8-15 alkylarylester or Het;

(f) m is 1 or 2;

(g) n is 1 or 2; (h) p is 1, 2 or 3;

(i) Y is H, phenyl substituted with nitro, pyridyl substituted with nitro, or C_1-6 alkyl optionally substituted with cyano, OH or C_3-7 cycloalkyl; provided that if R₄ or R₅ is H then Yis H;

(j) B is H, C_1-6 alkyl, R -(C=O)-, R₄θ(C=O)-, R₄-N(R₅)-C(=O)-, R₄-N(R₅)-C(=S)-, R₄SO-.-, or R₄-N(R₅)-SO₂-;

(k) R is (i) C_1-10 alkyl optionally substituted with phenyl, carboxyl,

C_1-6 alkanoyl, 1-3 halogen, hydroxy, -OC(O)C_1-6 alkyl, C_1-6 alkoxy, amino optionally substituted with C_1-6 alkyl, amido, or (lower alkyl) amido; (ii) C_3-7 cycloalkyl, C_3-7 cycloalkoxy, or C_4-10 alkylcycloalklyl, each optionally substituted with hydroxy, carboxyl, (C_1-6 alkoxy)carbonyl, amino optionally substituted with C_1-6 alkyl, amido, or (lower alkyl) amido; (iii) C_6-1o aryl or C_7-16 arylalkyl, each optionally substituted with C_1-6 alkyl, halogen, nitro, hydroxy, amido, (lower alkyl) amido, or amino optionally substituted with C_1-6 alkyl; (iv) Het; (v) bicyclo(l.l.l)pentane; or (vi) -C(O)OC_1-6 alkyl, C_2-6alkenyl or C_2-6 alkynyl; and. (1) R₅ is H; C_1-6 alkyl optionally substituted with 1-3 halogens; or C_1-6 alkoxy provided R is C^o alkyl;

or a pharmaceutically acceptable salt, solvate or prodrug thereof.

The present invention also provides compositions comprising the compounds or pharmaceutically acceptable salts, solvates or prodrugs thereof and a pharmaceutically acceptable carrier. In particular, the present invention provides pharmaceutical compositions useful for inhibiting HCV NS3 comprising a therapeutically effective amount of a compound of the present invention, or a pharmaceutically acceptable salt, solvate or prodrag thereof, and a pharmaceutically acceptable carrier.

The present invention further provides methods for treating patients infected with HCV, comprising administering to the patient a therapeutically effective amount of a compound of the present invention, or a pharmaceutically acceptable salt, solvate or prodrag thereof. Additionally, the present invention provides methods of inhibiting HCV NS3 protease by administering to a patient an effective amount of a compound of the present invention.

By virate of the present invention, it is now possible to provide improved drugs comprising the compounds of the invention which can be effective in the treatment of patients infected with HCV. Specifically, the present invention provides peptide compounds that can inhibit the functioning of the NS3 protease, e.g., in combination with the NS4A protease. DETAILED DESCRIPTION OF THE INVENTION

Stereochemical definitions and conventions used herein generally follow McGraw-Hill Dictionary of Chemical Terms, S. P. Parker, Ed., McGraw-Hill Book Company, New York (1984) and Stereochemistry of Organic Compounds, Eliel, E. and Wilen, S., John Wiley & Sons, Inc., New York (1994). Many organic compounds exist in optically active forms, i.e., they have the ability to rotate the plane of plane-polarized light. In describing an optically active compound, the prefixes D and L or R and S are used to denote the absolute configuration of the molecule about its chiral center(s). The prefixes d and 1 or (+) and (-) are employed to designate the sign of rotation of plane-polarized light by the compound, with (-) or 1 meaning that the compound is levorotatory and (+) or d, meaning the compound, is dextrorotatory. For a given chemical structure, these compounds, called stereoisomers, are identical except that they are mirror images of one another. A specific stereoisomer of a mirror image pair may also be referred to as an enantiomer, and a mixture of such isomers is often called an enantiomeric mixture.

The nomenclature used to describe organic radicals, e.g., hydrocarbons and substituted hydrocarbons, generally follows standard nomenclature known in the art, unless otherwise specifically defined. Combinations of groups, e.g., alkylalkoxyamine, include all possible stable configurations, unless otherwise specifically stated. Certain radicals and combinations are defined below for purposes of illustration.

The terms "racemic mixture" and "racemate" refer to an equimolar mixture of two enantiomeric species, devoid of optical activity.

The term "chiral" refers to molecules which have the property of non- superimposability of the mirror image partner, while the term "achiral" refers to molecules which are superimposable on their mirror image partner. The term "stereoisomers" refers to compounds which have identical chemical composition, but differ with regard to the arrangement of the atoms or groups in space.

The term "diastereomer" refers to a stereoisomer which is not an enantiomer, e.g., a stereoisomer with two or more centers of chirality and whose molecules are not mirror images of one another. Diastereomers have different physical properties, e.g. melting points, boiling points, spectral properties, and reactivities. Mixtures of diastereomers may separate under high resolution analytical procedures such as electrophoresis and chromatography.

The term "enantiomers" refers to two stereoisomers of a compound which are non-superimposable mirror images of one another.

The term "pharmaceutically acceptable salt" is intended to include nontoxic salts synthesized from a compound which contains a basic or acidic moiety by conventional chemical methods. Generally, such salts can be prepared by reacting the free acid or base forms of these compounds with a stoichiometric amount of the appropriate base or acid in water or in an organic solvent, or in a mixture of the two; generally, nonaqueous media like ether, ethyl acetate, ethanol, isopropanol, or acetonitrile are preferred. Lists of suitable salts are found in Remington's Pharmaceutical Sciences, 18th ed., Mack Publishing Company, Easton, PA, 1990, p. 1445. The compounds of the present invention are useful in the form of the free base or acid or in the form of a pharmaceutically acceptable salt thereof. All forms are within the scope of the invention.

The term "therapeutically effective amount" means the total amount of each active component that is sufficient to show a meaningful patient benefit, e.g., a sustained reduction in viral load. When applied to an individual active ingredient, administered alone, the term refers to that ingredient alone. When applied to a combination, the term refers to combined amounts of the active ingredients that result in the therapeutic effect, whether administered in combination, serially or simultaneously.

The term "compounds of the invention", and equivalent expressions, are meant to embrace compounds of Formula I, and pharmaceutically acceptable salts, and solvates, e.g. hydrates. Similarly, reference to intermediates, is meant to embrace their salts, and solvates, where the context so permits. References to the compound of the invention also include the preferred compounds of Formula II and iπ.

The term "derivative" means a chemically modified compound wherein the modification is considered routine by the ordinary skilled chemist, such as an ester or an amide of an acid, protecting groups, such as a benzyl group for an alcohol or thiol, and tert-butoxycarbonyl group for an amine.

The term "solvate" means a physical association of a compound of this invention with one or more solvent molecules, whether organic or inorganic. This physical association includes hydrogen bonding. In certain instances the solvate will be capable of isolation, for example when one or more solvent molecules are incorporated in the crystal lattice of the crystalline solid. "Solvate" encompasses both solution-phase and isolable solvates. Exemplary solvates include hydrates, ethanolates, methanolates, and the like.

The term "prodrug" as used herein means derivatives of the compounds of the invention which have chemically or metabolically cleavable groups and become, by solvolysis or under physiological conditions, the compounds of the invention which are pharmaceutically active in vivo. A prodrug of a compound may be formed in a conventional manner with a functional group of the compounds such as with an amino, hydroxy or carboxy group when present. The prodrug derivative form often offers advantages of solubility, tissue compatibility, or delayed release in a mammalian organism (see, Bundgard, H., Design of Prodrugs, pp. 7-9, 21-24, Elsevier, Amsterdam 1985). Prodrugs include acid derivatives well known to practitioners of the art, such as, for example, esters prepared by reaction of the parent acidic compound with a suitable alcohol, or amides prepared by reaction of the parent acid compound with a suitable amine.

The term "patient" includes both human and other mammals.

The term "pharmaceutical composition" means a composition comprising a compound of the invention in combination with at least one additional pharmaceutical carrier, i.e., adjuvant, excipient or vehicle, such as diluents, preserving agents, fillers, flow regulating agents, disintegrating agents, wetting agents, emulsifying agents, suspending agents, sweetening agents, flavoring agents, perfuming agents, antibacterial agents, antifungal agents, lubricating agents and dispensing agents, depending on the nature of the mode of administration and dosage forms. Ingredients listed in Remington's Pharmaceutical Sciences, 18^th ed., Mack Publishing Company, Easton, PA (1999) for example, may be used.

The phrase "pharmaceutically acceptable" is employed herein to refer to those compounds, materials, compositions, and/or dosage forms which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of patients without excessive toxicity, irritation, allergic response, or other problem or complication commensurate with a reasonable risk benefit ratio.

The term "treating" refers to: (i) preventing a disease, disorder or condition from occurring in a patient which may be predisposed to the disease, disorder and/or condition but has not yet been diagnosed as having it; (ii) inhibiting the disease, disorder or condition, i.e., arresting its development; and (iii) relieving the disease, disorder or condition, i.e., causing regression of the disease, disorder and/or condition.

The term "substituted" as used herein includes substitution at from one to the maximum number of possible binding sites on the core, e.g., organic radical, to which the subsitutent is bonded, e.g., mono-, di-, tri- or tetra- substituted, unless otherwise specifically stated.

The term "halo" as used herein means a halogen substituent selected from bromo, chloro, fluoro or iodo. The term "haloalkyl" means an alkyl group that in substituted with one or more halo substituents.

The term "alkyl" as used herein means acyclic, straight or branched chain alkyl substituents and includes, for example, methyl, ethyl, propyl, butyl, tert- butyl, hexyl, 1-methylethyl, 1-methylpropyl, 2-methypropyl, 1,1-dimethylethyl. Thus, C_1-6 alkyl refers to an alkyl group having from one to six carbon atoms. The term "lower alkyl" means an alkyl group having from one to six, preferably from one to four carbon atoms. The term "alkylester" means an alkyl group additionally containing on ester group. Generally, a stated carbon number range, e.g., C_2-6 alkylester, includes all of the carbon atoms in the radical.

The term "alkenyl" as used herein means an alkyl radical containing at least one double bond, e.g., ethenyl (vinyl) and alkyl.

The term "alkoxy" as used herein means an alkyl group with the indicated number of carbon atoms attached to an oxygen atom. Alkoxy includes, for example, methoxy, ethoxy, propoxy, 1-methylethoxy, butoxy and 1,1- dimethylethoxy. The latter radical is referred to in the art as tert-butoxy. The term "alkoxycarbonyl" means an alkoxy group additionally containing a carbonyl group.

The term "cycloalkyl" as used herein means a cycloalkyl substituent containing the indicated number of carbon atoms and includes, for example, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl and spiro cyclic groups such as spirocyclopropyl as spirocyclobutyl. The term "cycloalkoxy" as used herein means a cycloalkyl group linked to an oxygen atom, such as, for example, cyclobutyloxy or cyclopropyloxy. The term "alkylcycloalkyl" means a cycloalkyl group linked to an alkyl group. The stated carbon number range includes the total number of carbons in the radical, unless otherwise specfically stated. This a C_4-10 alkylcycloalkyl may contain from 1-7 carbon atoms in the alkyl group and from 3-9 carbon atoms in the ring, e.g., cyclopropylmethyl or cyclohexylethyl.

The term "aryl" as used herein means an aromatic moiety containing the indicated number of carbon atoms, such as, but not limited to phenyl, indanyl or naphthyl. For example, C_6-1o aryl refers to an aromatic moiety having from six to ten carbon atoms which may be in the form of a monocyclic or bicyclic structure. The term "haloaryl" as used herein refers to an aryl mono, di or tri substituted with one or more halogen atoms. The terms "alkylaryl", "arylalkyl" and "aralalkyl" mean an aryl group substituted with one or more alkyl groups. Thus, a C₇.-_.4 alkylaryl group many have from 1-8 carbon atoms in the alkyl group for a monocyclic aromatic and from 1-4 carbon atoms in the alkyl group for a fused . aromatic. The aryl radicals include those substituted with typical substituents known to those skilled in the art, e.g., halo, hydroxy, carboxy, carbonyl, nitro, sulfo, amino, cyano, dialkylamino haloalkyl, CF₃, haloalkoxy, thioalkyl, alkanoyl, SH, alkylamino, alkylamide, dialkylamide, carboxyester, alkylsulfone, alkylsulfonamide and alkyl(alkoxy)amine. Examples of alkylaryl groups include benzyl, butylphenyl and 1-naphthylmethyl. The terms "alkylaryloxy" and "alkylarylester" mean alkylaryl groups containing an oxygen atom and ester group, respectively.

The term "carboxyalkyl" as used herein means a carboxyl group (COOH) linked through an alkyl group as defined above and includes, for example, butyric acid.

The term "alkanoyl" as used herein means straight or branched 1-oxoalkyl radicals containing the indicated number of carbon atoms and includes, for example, formyl, acetyl, 1-oxopropyl (propionyl), 2-methyl-l-oxopropyl, 1-oxohexyl and the like. The term "amino aralkyl" as used herein means an amino group substituted with an aralkyl group, such as the following amino aralkyl

The term "alkylamide" as used herein means an amide mono-substituted with an alkyl, such as

The term "carboxyalkyl" as used herein means a carboxyl group (COOH) linked through a alkyl group as defined above and includes, for example, butyric acid.

The term "heterocycle", as used herein means a monovalent radical derived by removal of a hydrogen from a five-, six-, or seven-membered saturated or unsaturated (including aromatic) heterocycle containing from one to four heteroatoms selected from nitrogen, oxygen and sulfur. Furthermore, the term heterocycle includes heterocycles, as defined above, that are fused to one or more other ring stracture. The heterocycles of the present invention include those substituted with typical substituents known to those skilled in the art on any of the ring carbon atoms, e.g., one to three substituents. Examples of such substituents include C_1-6 alkyl, C_3-7 cycloalkyl, C-.g alkoxy, C_3-7 cycloalkoxy, halo-C--g alkyl, CF₃, mono-or di- halo-C*.g alkoxy, cyano, halo, thioalkyl, hydroxy, alkanoyl, NO₂, SH, , amino, C-.g alkylamino, di (C--₆) alkylamino, di (C--₆) alkylamide, carboxyl, (C--₆) carboxyester, C_1-6 alkylsulfone, C_1-6 alkylsulfonamide, C_1-6 alkylsulfoxide, di (C--₆) alkyl(alkoxy)amine, C_6-1o aryl, C_7- ₁₄ alkylaryl, and a 5-7 membered monocyclic heterocycle. Examples of suitable heterocycles include, but are not limited to, pyrrolidine, tetrahydrofuran, thiazolidine, pyrrole, thiophene, diazepine, lH-imidazole, isoxazole, thiazole, tetrazole, piperidine, 1,4-dioxane, 4-morpholine, pyridine, pyrimidine, thiazolo[4,5-b]-pyridine, quinoline, or indole, or the following heterocycles:

The term "alkyl-heterocycle" as used herein, means a heterocyclic radical as defined above linked through a chain or branched alkyl group, wherein alkyl as defined above containing the indicated number of carbon atoms. Examples of C_\. g alkyl-Het include:

The term "heteroaryl" as used herein means an aromatic five- or six- membered cyclic organic group having at least one O, S and/or N atom.

Furthermore, the term "heteroaryl" includes heteroaryl groups as defined about that fused to one or more other ring structures. Examples of heteroaryl groups include pyridyl, thienyl, thiazolyl, imidazolyl, isoxazolyl, isothiazolyl, furyl, pyrimidinyl, pyrazinyl, or pyridazinyl.

Where used in naming compounds of the present invention, the designations "PI', PI, P2, P3 and P4", as used herein, map the relative positions of the amino acid residues of a protease inhibitor binding relative to the binding of the natural peptide cleavage substrate. Cleavage occurs in the natural substrate between PI and PI' where the nonprime positions designate amino acids starting from the C-terminus end of the peptide natural cleavage site extending towards the N-terminus; whereas, the prime positions emanate from the N-terminus end of the cleavage site designation and extend towards the C-terminus. For example, PI' refers to the first position away from the right hand end of the C-terminus of the cleavage site (ie. N-terminus first position); whereas PI starts the numbering from the left hand side of the C-terminus cleavage site, P2: second position from the C-terminus, etc.)(see Berger A. & Schechter I., Transactions of the Royal Society London series. (1970), B257, 249-264].

Thus in the compounds of formula I, the "PI' to P4" portions of the molecule are indicated below:

P2

As used herein the term "1-aminocyclopropyl-carboxylic acid" (Acca) refers to a compound of formula:

As used herein the term "tert-butylglycine" refers to a compound of the formula:

The term "residue" with re erence to an amino acid or amino acid derivative means a radical derived from the corresponding α-amino acid by eliminating the hydroxyl of the carboxy group and one hydrogen of the α-amino acid group. For instance, the terms Gin, Ala, Gly, He, Arg, Asp, Phe, Ser, Leu, Cys, Asn, Sar and Tyr represent the "residues" of L-glutamine, L-alanine, glycine, L-isoleucine, L-arginine, L-aspartic acid, L-phenylalanine, L-serine, L-leucine, L- cysteine, L-asparagine, sarcosine and L-tyrosine, respectively.

The term "side chain" with reference to an amino acid or amino acid residue means a group attached to the α-carbon atom of the α-amino acid. For example, the R-group side chain for glycine is hydrogen, for alanine it is methyl, for valine it is isopropyl. For the specific R-groups or side chains of the α-amino acids reference is made to A.L. Lehninger's text on Biochemistry (see chapter 4).

For compounds of the present invention, it is preferred that m is 2. It is also preferred that n is 1. It is additionally preferred that R₂ is ethyl or ethenyl.

In accordance with one aspect of the present invention, R- may be trialkylsilane; halo; C_3-7 cycloalkyl, C_4-7 cycloalkenyl; C_6-10 aryl; C_7-1 alkylaryl; C_6-10 aryloxy; C_7-14 alkylaryloxy; C_8-15 alkylarylester; Het; or C_1-8 alkyl optionally substituted with C-.g alkoxy, hydroxy, halo, C_2-10 alkenyl, C_2-10 alkynyl, C_3- cycloalkyl, C_4-7 cycloalkenyl, C_6-10 aryl, C₇.₁₄ alkylaryl, C₆.₁₀ aryloxy, C_7-14 alkylaryloxy, C_8-i5 alkylarylester or Het. In accordance with another aspect of the present invention, R- may o be — C-R₈ wherein R₈ is C_3-7 cycloalkyl, C_4-7 cycloalkenyl; C_6-1o aryl; C_7-14 alkylaryl; C_6-10 aryloxy; C_7-14 alkylaryloxy; C_8-15 alkylarylester; Het; or C_1-8 alkyl optionally substituted with C-.g alkoxy, hydroxy, halo, C_2-10 alkenyl, C_2-10 alkynyl,

C_3-7 cycloalkyl, C_4-7 cycloalkenyl, C_6-10 aryl, C_7-14 alkylaryl, C_6-10 aryloxy, C_7-14 alkylaryloxy, C_8-15 alkylarylester or Het.

In accordance with another aspect of the present invention, R₁ may be o

II — C-OR₉ wherein R is C_3-7 cycloalkyl, C_4-7 cycloalkenyl; C_6-10 aryl; C_7-14 alkylaryl; Cg_-10 aryloxy; C _-14 alkylaryloxy; C_8-15 alkylarylester; Het; or C_1-8 alkyl optionally substituted with C_1-6 alkoxy, hydroxy, halo, C_2-10 alkenyl, C_2-10 alkynyl, C_3- cycloalkyl, C - cycloalkenyl, Cg_-10 aryl, C_7-14 alkylaryl, C_6-1o aryloxy, C_7-1 alkylaryloxy, C_8-15 alkylarylester or Het.

In accordance with another aspect of the present invention, R_t may be o

11

— C— R10R1₁ , wherein R₁₀ and Rπ are each independently C_3-7 cycloalkyl, C_4-7 cycloalkenyl; C_6-10 aryl; C_7-14 alkylaryl; Cg_-10 aryloxy; C_7-14 alkylaryloxy; C_8-15 alkylarylester; Het; or C_1-8 alkyl optionally substituted with -g alkoxy, hydroxy, halo, C_2-10 alkenyl, C_2-10 alkynyl, C_3-7 cycloalkyl, C_4-7 cycloalkenyl, Cg_-10 aryl, C_7- ₁₄ alkylaryl, Cg_-10 aryloxy, C_7-1 alkylaryloxy, C_8-15 alkylarylester or Het.

In accordance with another aspect of the present invention, R- may be - SO₂R₁₂ wherein R₁₂ is C_3- cycloalkyl, C_4-7 cycloalkenyl; Cg_-10 aryl; C_7-14 alkylaryl; Cg_-10 aryloxy; C_7-1 alkylaryloxy; C_8-15 alkylarylester; Het; or C_1-8 alkyl optionally substituted with C_1-6 alkoxy, hydroxy, halo, C_2-10 alkenyl, C_2-10 alkynyl, C_3-7 cycloalkyl, C_4-7 cycloalkenyl, C_6-10 aryl, C_7-14 alkylaryl, C_6-10 aryloxy, C_7-14 alkylaryloxy, C_8-15 alkylarylester or Het. In accordance with another aspect of the present invention, R- may be o

I I

— OCR13 wherein R₁₃ is C_3-7 cycloalkyl, C_4-7 cycloalkenyl; C_6-10 aryl; C_7-14 alkylaryl; Cg_-10 aryloxy; C _-14 alkylaryloxy; C_8-15 alkylarylester; Het; or C_1-8 alkyl optionally substituted with C_1-6 alkoxy, hydroxy, halo, C_2-1o alkenyl, C _-10 alkynyl, C_3-7 cycloalkyl, C_4-7 cycloalkenyl, Cg_-10 aryl, C_7-14 alkylaryl, C_6-10 aryloxy, C_7-14 alkylaryloxy, C_8-i₅ alkylarylester or Het.

Preferably, Ri is C_1-8 alkyl optionally substituted with C_1-6 alkoxy, hydroxy, halo, C_2-1o alkenyl, C_2-10 alkynyl, C_3-6 cycloalkyl, C _-7 cycloalkenyl, Cg. ₁₀ aryl, C_7-14 alkylaryl, Cg_-10 aryloxy, C_7-14 alkylaryloxy, C_8-i₅ alkylarylester or Het. More preferably, R_t is C_1-8 alkyl optionally substituted with C_1-6 alkoxy, hydroxy, halo, C_2-10 alkenyl, C _-10 alkynyl, C_3-6 cycloalkyl, C_4-7 cycloalkenyl, C_6- *o aryl, C_7-14 alkylaryl, C_6-10 aryloxy, C_7-14 alkylaryloxy, or C_8-15 alkylarylester.

In accordance with the present invention, R may be C-.g alkyl, C_2-6 alkenyl or C_3-7 cycloalkyl, each optionally substituted from one to three times with halogen; or R₂ is H; or R₂ together with the carbon to which it is attached forms a 3, 4 or 5 membered ring. Preferably, R is C-.g alkyl, C_2-g alkenyl or C_3- cycloalkyl. More preferably, R₂ is C _-6 alkenyl. Most preferably, R₂ is vinyl

In accordance with the present invention, R₃ may be C_1-8 alkyl optionally substituted with halo, cyano, amino, C-.g dialkylamino, C_6-1 aryl, C_7-14 alkylaryl, C-.g alkoxy, carboxy, hydroxy, aryloxy, C_7-1 alkylaryloxy, C_2-g alkylester, C_8-15 alkylarylester; C_3-12 alkenyl, C_3-7 cycloalkyl, or C_4-10 alkylcycloalkyl, wherein the cycloalkyl or alkylcycloalkyl are optionally substituted with hydroxy, C g alkyl,

C_2-6 alkenyl or C_1-6 alkoxy; or R₃ together with the carbon atom to which it is attached forms a C_3-7 cycloalkyl group optionally substituted with C_2-6 alkenyl. Preferably, R₃ is C _1-8 alkyl optionally substituted with Cgaryl, C_1-6 alkoxy, carboxy, hydroxy, aryloxy, C_7-1 alkylaryloxy, C_2-6 alkylester, C_8-15 alkylarylester; C_3-12 alkenyl, C_3-7 cycloalkyl, or C _-10 alkylcycloalkyl. More preferably, R₃ is C*. s alkyl optionally substituted with C_1-6 alkoxy; or C_3-7 cycloalkyl. Most preferably, R₃ is t-butyl. In accordance with the present invention, Y may be H, phenyl substituted with nitro, pyridyl substituted with nitro, or C-.₆ alkyl optionally substituted with cyano, OH or C_3-7 cycloalkyl; provided that if R or R₅ is H then Yis H. Preferably, Y is H.

In accordance with the present invention, B may be H, C_1-6 alkyl, R₄-(C=O)-, R₄O(C=O)-, R₄-N(R₅)-C(=O)-, R₄-N(R₅)-C(=S)-, R₄SO₂-, or R₄-N(R₅)-SO₂-. Preferably, B is H, C_1-6 alkyl, R₄-(C=O)-, R₄O(C=O)-, R₄-N(R₅)-C(=O)-, R₄-N(R₅)-C(=S)-, R₄SO₂-, or R₄-N(R₅)-SO₂-. More preferably, B is R₄-(C=O)-, R₄O(C=O)-, or R₄-N(R₅)-C(=O)-. Most preferably, B is R₄θ(C=O)- .

In accordance with the present invention, R may be (i) C_MO alkyl optionally substituted with phenyl, carboxyl, C*.g alkanoyl, 1-3 halogen, hydroxy, -OC(O)C_1-6 alkyl, C_1-6 alkoxy, amino optionally substituted with C-.g alkyl, amido, or (lower alkyl) amido; (ii) C_3-7 cycloalkyl, C_3- cycloalkoxy, or C _-1o alkylcycloalklyl, each optionally substituted with hydroxy, carboxyl, ( .g alkoxy)carbonyl, amino optionally substituted with C_1-6 alkyl, amido, or (lower alkyl) amido; (iii) Cg.*o aryl or C_7-16 arylalkyl, each optionally substituted with C_1-6 alkyl, halogen, nitro, hydroxy, amido, (lower alkyl) amido, or amino optionally substituted with C_1-6 alkyl; (iv) Het; (v) bicyclo(l.l.l)pentane; or (vi) -C(O)OC_1-g alkyl, C_2-6alkenyl or C_2-6 alkynyl. Preferably, R₄ is (i) C_1-10 alkyl optionally substituted with phenyl, carboxyl, C_1-6 alkanoyl, 1-3 halogen, hydroxy, C_1-6 alkoxy; (ii) C_3-7 cycloalkyl, C_3-7 cycloalkoxy, or C _-10 alkylcycloalklyl; or (iii) Cg-*o aryl or C_7-16 arylalkyl, each optionally substituted with C_1-6 alkyl or halogen. More preferably, R₄ is (i) C_1-10 alkyl optionally substituted with 1-3 halogen or C_1-6 alkoxy; or (ii) C_3-7 cycloalkyl or C_4-10 alkylcycloalkyl. Most preferably, R is t-butyl.

In accordance with the present invention, R₅ may be H; C_1-6 alkyl optionally substituted with 1-3 halogens; or C_1-6 alkoxy provided R is C-.-Q alkyl. Preferably, H or C_1-6 alkyl optionally substituted with 1-3 halogens. More preferably, R₅ is H.

In accordance with the present invention Rg may be H, C-.g alkyl, C_3-7 cycloalkyl, C-.g alkoxy, C_3-7 cycloalkoxy, halo-C--₆ alkyl, CF₃, mono-or di- halo- C_1-6 alkoxy, cyano, halo, thioalkyl, hydroxy, alkanoyl, NO₂, SH, , amino, C_1-6 alkylamino, di (C--g) alkylamino, di (C--g) alkylamide, carboxyl, (Cι~β) carboxyester, C_1-6 alkylsulfone, C_1-6 alkylsulfoxide, C_1-6 alkylsulfonamide or di (d-₆) alkyl(alkoxy)amine. Preferably, Rgis C_1-6 alkyl, C_3- cycloalkyl, or C-.g alkoxy. More preferably, R₆ is C_1-6 alkoxy.

In accordance with the present invention, R may be H, C--₆ alkyl, C_3-7 cycloalkyl, C_6-10 aryl, C_7-1 alkylaryl; C_6-10 aryloxy; C_7-14 alkylaryloxy; C_8-15 alkylarylester or Het. '

The substituents from each grouping may be selected individually and combined in any combination which provides a stable compound in accordance with the present invention. Also, more than one substituent from each group may be substituted on the core group provided there are sufficient available binding sites. For example, more than one Rg substituent can be present on the ring shown in Formula 1, e.g., 3 different Rg substitutents.

In a preferred embodiment, compounds of the present invention have the stracture of Formula II

wherein R₃, R₆, R₇, R_1; m, B and Y are as defined in Formula I while R₁ is C_1-6 alkyl, C_2-6 alkenyl or H. The present invention further comprises salts or solvates compounds of Formula II, as well as pharmaceutical compositions comprising compounds of Formula π, or salts or solvates thereof.

In another preferred embodiment, compounds of the present invention have the stracture of Formula III

wherein R₃, B, R-, Rg, R₇, m and Y are as defined in Formula I. The present invention further comprises salts or solvates of compounds of Formula III, as well as pharmaceutical compositions comprising compounds of Formula III, or salts or solvates thereof.

In another preferred embodiment, compounds of the present invention have the structure of Formula IV

Formula IV wherein R₃, B, R_1; R₆, R₇, m and Y are as defined in Formula I. The present invention further comprises salts or solvates of compounds of Formula IV, as well as pharmaceutical compositions comprising compounds of Formula IV, or salts or solvates thereof.

Preferred embodiments of the present invention include the following compounds, including their pharmaceutically acceptable solvates or salts:

The compounds of the present invention, when in a basic form, can form salts by the addition of a pharmaceutically acceptable acid. The acid addition salts are formed from a compound of Formula I and a pharmaceutically acceptable inorganic acid, including but not limited to hydrochloric, hydrobromic, hydroiodic, sulfuric, phosphoric, or organic acid such as p-toluenesulfonic, methanesulfonic, acetic, benzoic, citric, malonic, fumaric, maleic, oxalic, succinic, sulfamic, or tartaric. Thus, examples of such pharmaceutically acceptable salts include chloride, bromide, iodide, sulfate, phosphate, methanesulfonate, citrate, acetate, malonate, fumarate, sulfamate, and tartrate.

Salts of an amine group may also comprise quaternary ammonium salts in which the amino nitrogen carries a suitable organic group such as an alkyl, alkenyl, alkynyl or aralkyl moiety.

Compounds of the present invention, which are substituted with an acidic group, may exist as salts formed through base addition. Such base addition salts include those derived from inorganic bases which include, for example, alkali metal salts (e.g. sodium and potassium), alkaline earth metal salts (e.g. calcium and magnesium), aluminum salts and ammonium salts. In addition, suitable base addition salts include salts of physiologically acceptable organic bases such as trimethylamine, triethylamine, morpholine, pyridine, piperidine, picoline, dicyclohexylamine, N,N'-dibenzylethylenediamine, 2-hydroxyethylamine, bis-(2-hydroxyethyl)amine, tri-(2-hydroxyethyl)amine, procaine, dibenzylpiperidine, N-benzyl-β-phenethylamine, dehydroabietylamine, N,N'-bishydroabietylamine, glucamine, N-methylglucamine, collidine, quinine, quinoline, ethylenediamine, ornithine, choline, N,N'-benzylphenethylamine, chloroprocaine, diethanolamine, diethylamine, piperazine, tris(hydroxymethyl)aminomethane and tetramethylammonium hydroxide and basic amino acids such as lysine, arginine and N-methylglutamine. These salts may be prepared by methods known to those skilled in the art.

Certain compounds of the present invention, and their salts, may also exist in the form of solvates with water, for example hydrates, or with organic solvents such as methanol, ethanol or acetonitrile to form, respectively, a methanolate, ethanolate or acetonitrilate. The present invention includes each solvate and mixtures thereof. In addition, compounds of the present invention, or a salt or solvate thereof, may exhibit polymorphism. The present invention also encompasses any such polymorphic form.

The compounds of the present invention also contain two or more chiral centers. For example, the compounds may include PI cyclopropyl element of formula

PI

wherein and C₂ each represent an asymmetric carbon atom at positions 1 and 2 of the cyclopropyl ring. Not withstanding other possible asymmetric centers at other segments of the compounds, the presence of these two asymmetric centers means that the compounds can exist as racemic mixtures of diastereomers, such as the diastereomers wherein R₂ is configured either syn to the amide or syn to the carbonyl as shown below.

(1R, 2S) (IS, 2R)

R₂ is syn to carbonyl R₂ is syn to carbonyl

(1R, 2R) (IS, 2S)

R₂ is syn to amide R₂ is syn to amide

The present invention includes both enantiomers and mixtures of enantiomers such as racemic mixtures.

The enantiomers may be resolved by methods known to those skilled in the art, for example, by formation of diastereoisomeric salts which may be separated by crystallization, gas-liquid or liquid chromatography, selective reaction of one enantiomer with an enantiomer-specific reagent. It will be appreciated that where the desired enantiomer is converted into another chemical entity by a separation technique, then an additional step is required to form the desired enantiomeric form. Alternatively, specific enantiomers may be synthesized by asymmetric synthesis using optically active reagents, substrates, catalysts or solvents, or by converting one enantiomer into the other by asymmetric transformation.

The compounds of the present invention may be in the form of a prodrag. Simple aliphatic or aromatic esters derived from, when present, acidic groups pendent on the compounds of this invention are preferred prodrugs. In some cases it is desirable to prepare double ester type prodrugs such as (acyloxy) alkyl esters or (alkoxycarbonyl)oxy)alkyl esters.

Certain compounds of the present invention may also exist in different stable conformational forms which may be separable. Torsional asymmetry due to restricted rotation about an asymmetric single bond, for example because of steric hindrance or ring strain, may permit separation of different conformers. The present invention includes each conformational isomer of these compounds and mixtures thereof.

Certain compounds of the present invention may exist in zwitterionic form and the present invention includes each zwitterionic form of these compounds and mixtures thereof.

The starting materials useful to synthesize the compounds of the present invention are known to those skilled in the art and can be readily manufactured or are commercially available.

The compounds of the present invention can be manufactured by methods known to those skilled in the art, see e.p., US Patent No. 6,323,180 and US Patent Appl. 20020111313 Al. The following methods set forth below are provided for illustrative purposes and are not intended to limit the scope of the claimed inyention. It will be recognized that it may be preferred or necessary to prepare such a compound in which a functional group is protected using a conventional protecting group then to remove the protecting group to provide a compound of the present invention. The details concerning the use of protecting groups in accordance with the present invention are known to those skilled in the art.

The compounds of the present invention may, for example, be synthesized according to a general process as illustrated in Scheme I (wherein CPG is a carboxyl protecting group and APG is an amino protecting group): Scheme I

PI Pl-CPG + APG-P2 APG-P2-P1-CPG

APG-P3-P2-P1-CPG P2-P1-CPG + APG-P3

B-P3-P2-P1 B-P3-P2-P1-P1'

Briefly, the PI, P2, and P3 can be linked by well known peptide coupling techniques. The PI, P2, and P3 groups may be linked together in any order as long as the final compound corresponds to peptides of the invention. For example, P3 can be linked to P2-P1; or PI linked to P3-P2.

Generally, peptides are elongated by deprotecting the α-amino group of the N-terminal residue and coupling the unprotected carboxyl group of the next suitably N-protected amino acid through a peptide linkage using the methods described. This deprotection and coupling procedure is repeated until the desired sequence is obtained. This coupling can be performed with the constituent amino acids in stepwise fashion, as depicted in Scheme I.

Coupling between two amino acids, an amino acid and a peptide, or two peptide fragments can be carried out using standard coupling procedures such as the azide method, mixed carbonic-carboxylic acid anhydride (isobutyl chloroformate) method, carbodiimide (dicyclohexylcarbodiimide, diisopropylcarbodiimide, or water-soluble carbodiimide) method, active ester (p-nitrophenyl ester, N-hydroxysuccinic imido ester) method, Woodward reagent K-method, carbonyldiimidazole method, phosphorus reagents or oxidation-reduction methods. Some of these methods (especially the carbodiimide method) can be enhanced by adding 1-hydroxybenzotriazole or 4-DMAP. These coupling reactions can be performed in either solution (liquid phase) or solid phase.

More explicitly, the coupling step involves the dehydrative coupling of a free carboxyl of one reactant with the free amino group of the other reactant in the present of a coupling agent to form a linking amide bond. Descriptions of such coupling agents are found in general textbooks on peptide chemistry, for example, M. Bodanszky, "Peptide Chemistry", 2^nd rev ed., Springer- Verlag, Berlin, Germany, (1993). Examples of suitable coupling agents are N,N'-dicyclohexylcarbodiimide, 1-hydroxybenzotriazole in the presence of N,N'-dicyclohexylcarbodiimide or N-ethyl-N'-[(3-dimethylamino)propyl]carbodiimide. A practical and useful coupling agent is the commercially available

(benzotriazol- 1 -yloxy)tris-(dimethylamino)phosphonium hexafluorophosphate, either by itself or in the present of 1-hydroxybenzotriazole or 4-DMAP. Another practical and useful coupling agent is commercially available 2-(lH-benzotriazol-l-yl)-N, N, N' , N'-tetramethyluronium tetrafluoroborate. Still another practical and useful coupling agent is commercially available O-(7-azabenzotrizol-l-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate. The coupling reaction is conducted in an inert solvent, e.g. dichloromethane, acetonitrile or dimethylformamide. An excess of a tertiary amine, e.g. diisopropylethylamine, N-methylmorpholine, N-methylpyrrolidine or 4-DMAP is added to maintain the reaction mixture at a pH of about 8. The reaction temperature usually ranges between 0 °C and 50 °C and the reaction time usually ranges between 15 min and 24 h.

The functional groups of the constituent amino acids generally must be protected during the coupling reactions to avoid formation of undesired bonds. Protecting groups that can be used are listed, for example, in Greene, "Protective Groups in Organic Chemistry", John Wiley & Sons, New York (1981) and "The Peptides: Analysis, Synthesis, Biology", Vol. 3, Academic Press, New York (1981), the disclosures of which are hereby incorporated by reference.

The α-amino group of each amino acid to be coupled to the growing peptide chain must be protected (APG). Any protecting group known in the art can be used. Examples of such groups include: 1) acyl groups such as formyl, trifluoroacetyl, phthalyl, and p-toluenesulfonyl; 2) aromatic carbamate groups such as benzyloxycarbonyl (Cbz or Z) and substituted bensyloxycarbonyls, and 9-fluorenylmethyloxycarbonyl (Fmoc); 3) aliphatic carbamate groups such as tert-butyloxycarbonyl (Boc), ethoxycarbonyl, diisopropylmethoxycarbonyl, and allyloxycarbonyl; 4) cyclic alkyl carbamate groups such as cyclopentyloxycarbonyl and adamantyloxycarbonyl; 5) alkyl groups such as triphenylmethyl and benzyl; 6)trialkylsilyl such as trimethylsilyl; and 7) thiol containing groups such as phenylthiocarbonyl and dithiasuccinoyl.

The preferred α-amino protecting group is either Boc or Fmoc. Many amino acid derivatives suitably protected for peptide synthesis are commercially available. The α-amino protecting group of the newly added amino acid residue is cleaved prior to the coupling of the next amino acid. When the Boc group is used, the methods of choice are trifluoroacetic acid, neat or in dichloromethane, or HCl in dioxane or in ethyl acetate. The resulting ammonium salt is then neutralized either prior to the coupling or in situ with basic solutions such as aqueous buffers, or tertiary amines in dichloromethane or acetonitrile or dimethylformamide. When the Fmoc group is used, the reagents of choice are piperidine or substituted piperidine in dimethylformamide, but any secondary amine can be used. The deprotection is carried out at a temperature between 0°C and room temperature (rt or RT) usually 20-22°C.

Any of the amino acids having side chain functionalities must be protected during the preparation of the peptide using any of the above-described groups. Those skilled in the art will appreciate that the selection and use of appropriate protecting groups for these side chain functionalities depend upon the amino acid and presence of other protecting groups in the peptide. The selection of such protecting groups is important in that the group must not be removed during the deprotection and coupling of the α-amino group.

For example, when Boc is used as the α-amino protecting group, the following side chain protecting group are suitable: p-toluenesulfonyl (tosyl) moieties can be used to protect the amino side chain of amino acids such as Lys and Arg; acetamidomethyl, benzyl (Bn), or tert-butylsulfonyl moieties can be used to protect the sulfide containing side chain of cysteine; bencyl (Bn) ethers can be used to protect the hydroxy containing side chains of serine, threonine or hydroxyproline; and benzyl esters can be used to protect the carboxy containing side chains of aspartic acid and glutamic acid.

When Fmoc is chosen for the α-amine protection, usually tert-butyl based protecting groups are acceptable. For instance, Boc can be used for lysine and arginine, tert-butyl ether for serine, threonine and hydroxyproline, and tert-butyl ester for aspartic acid and glutamic acid. Triphenylmethyl (Trityl) moiety can be used to protect the sulfide containing side chain of cysteine.

Once the elongation of the peptide is completed all of the protecting groups are removed. When a liquid phase synthesis is used, the protecting groups are removed in whatever manner is dictated by the choice of protecting groups. These procedures are well known to those skilled in the art.

Further, the following guidance may be followed in the preparation of compounds of the present invention. For example, to form a compound where 1^.-0(0)-, R -S(O)₂„ a protected P3 or the whole peptide or a peptide segment is coupled to an appropriate acyl chloride or sulfonyl chloride respectively, that is either commercially available or for which the synthesis is well known in the art. In preparing a compound where 1^0-0(0)-, a protected P3 or the whole peptide or a peptide segment is coupled to an appropriate chloroformate that is either commercially available or for which the synthesis is well known in the art. For Boc-derivatives (Boc)₂O is used. For example:

[P-_j-Pi.] -COOEt

Cyclopentanol is treated with phosgene to furnish the corresponding chloroformate.

The chloroformate is treated with the desired NH₂-tripeptide in the presence of a base such as triethylamine to afford the cyclopentylcarbamate.

In preparing a compound where' R -N(R₅)-C(O)-, or R -NH-C(S)-, a protected P3 or the whole peptide or a peptide segment is treated with phosgene followed by amine as described in SynLett. Feb 1995; (2); 142-144 or is reacted with the commercially available isocyanate and a suitable base such as triethylamine.

In preparing a compound where R -N(R5)-S(O₂), a protected P3 or the whole peptide or a peptide segment is treated with either a freshly prepared or commercially available sulfamyl chloride followed by amine as described in patent Ger. Offen.(1998), 84 pp. DE 19802350 or WO 98/32748.

The α-carboxyl group of the C-terminal residue is usually protected as an ester (CPG) that can be cleaved to give the carboxylic acid. Protecting groups that can be used include: 1) alkyl esters such as methyl, trimethylsilylethyl and t-butyl, 2) aralkyl esters such as benzyl and substituted benzyl, or 3) esters that can be cleaved by mild base treatment or mild reductive means such as trichloroethyl and phenacyl esters.

The resulting α-carboxylic acid (resulting from cleavage by mild acid, mild base treatment or mild reductive means) is coupled with a R-SO₂NH₂ [prepared by treatment of R-SO₂Cl in ammonia saturated tetrahydrofuran solution] in the presence of peptide coupling agent such as GDI or ED AC in the presence of a base such as 4-dimethylaminopyridine (4-DMAP) and/or l,8-diazabicyclo[5.4.0]undec-7-ene (DBU) to incorporate the PI' moiety, effectively assembling the tripeptide PI '-P1-P2-P3-APG. Typically, in this process, 1-5 equivalents of PI' coupling agents are used.

Furthermore, if the P3 protecting group APG is removed and replaced with a B moiety by the methods described above, and the resulting α-carboxylic acid resulting from cleavage (resulting from cleavage by mild acid, mild base treatment or mild reductive means) is coupled with a RiSO₂NH₂ [prepared by treatment of RiSO₂Cl in ammonia saturated tetrahydrofuran solution or alternative methods described herein] in the presence of peptide coupling agent such as GDI or ED AC in the presence of a base such as 4-dimethylaminopyridine (4-DMAP) and/or l,8-diazabicyclo[5.4.0]undec-7-ene (DBU) to incorporate the PI' moiety, the tripeptide P1'-P1-P2-P3-B is prepared. Typically, in this process, 1-5 equivalents of PI' coupling agents are used.

Compounds of the present invention can be prepared by many methods including those described in the examples, below, and as described in U.S. Patent

No. 6,323,180 and U.S. Patent Application No. 10/001,850 filed on November 20, 2001. The teachings of U.S. Patent No. 6,323,180 and U.S. Patent Application No. 10/001,850 are incorporated herein, in their entirety, by reference. The present invention also provides compositions comprising a compound of the present invention, or a pharmaceutically acceptable salt, solvate or prodrug thereof, and a pharmaceutically acceptable carrier. Pharmaceutical compositions of the present invention comprise a therapeutically effective amount of a compound of the invention, or a pharmaceutically acceptable salt, solvate or prodrug thereof, and a pharmaceutically acceptable carrier, with a pharmaceutically acceptable carrier, e.g., excipient, or vehicle diluent.

The active ingredient, i.e., compound; in such compositions typically comprises from 0.1 weight percent to 99.9 percent by weight of the composition, and often comprises from about 5 to 95 weight percent.

The pharmaceutical compositions of this invention may be administered orally, parenterally or via an implanted reservoir. Oral administration or administration by injection are preferred. In some cases, the pH of the formulation may be adjusted with pharmaceutically acceptable acids, bases or buffers to enhance the stability of the formulated compound or its delivery form. . The term parenteral as used herein includes subcutaneous, intracutaneous, intravenous, intramuscular, , intra- articular, intrasynovial, intrasternal, intrathecal, and intralesional injection or infusion techniques.

The pharmaceutical compositions may be in the form of a sterile injectable preparation, for example, as a sterile injectable aqueous or oleaginous suspension. This suspension may be formulated according to techniques known in the art using suitable dispersing or wetting agents and suspending agents. The details concerning the preparation of such compounds are known to those skilled in the art.

When orally administered, the pharmaceutical compositions of this invention may be administered in any orally acceptable dosage form including, but not limited to, capsules, tablets, and aqueous suspensions and solutions. In the case of tablets for oral use, carriers which are commonly used include lactose and corn starch. Lubricating agents, such as magnesium stearate, are also typically added. For oral administration in a capsule form, useful diluents include lactose and dried corn starch. When aqueous suspensions are administered orally, the active ingredient is combined with emulsifying and suspending agents. If desired, certain sweetening and/or flavoring and/or coloring agents may be added.

Other suitable carriers for the above noted compositions can be found in standard pharmaceutical texts, e.g. in "Remington's Pharmaceutical Sciences", 19 th ed., Mack Publishing Company, Easton, Penn., 1995. Further details concerning the design and preparation of suitable delivery forms of the pharmaceutical compositions of the invention are known to those skilled in the art.

Dosage levels of between about 0.01 and about 1000 milligram per kilogram ("mg/kg") body weight per day, preferably between about 0.5 and about 250 mg/kg body weight per day of the compounds of the invention are typical in a monotherapy for the prevention and treatment of HCV mediated disease.

Typically, the pharmaceutical compositions of this invention will be administered from about 1 to about 5 times per day or alternatively, as a continuous infusion. Such administration can be used as a chronic or acute therapy. The amount of active ingredient that may be combined with the carrier materials to produce a single dosage form will vary depending upon the host treated and the particular mode of administration.

As the skilled artisan will appreciate, lower or higher doses than those recited above may be required. Specific dosage and treatment regimens for any particular patient will depend upon a variety of factors, including the activity of the specific compound employed, the age, body weight, general health status, sex, diet, time of administration, rate of excretion, drug combination, the severity and course of the infection, the patient's disposition to the infection and the judgment of the treating physician. Generally, treatment is initiated with small dosages substantially less than the optimum dose of the peptide. Thereafter, the dosage is increased by small increments until the optimum effect under the circumstances is reached. In general, the compound is most desirably administered at a concentration level that will generally afford antivirally effective results without causing any haπnful or deleterious side effects.

When the compositions of this invention comprise a combination of a compound of the invention and one or more additional therapeutic or prophylactic agent, both the compound and the additional agent are usually present at dosage levels of between about 10 to 100%, and more preferably between about 10 and 80% of the dosage normally administered in a monotherapy regimen.

When these compounds or their pharmaceutically acceptable salts, solvates or prodrugs are formulated together with a pharmaceutically acceptable carrier, the resulting composition may be administered in vivo to mammals, such as man, to inhibit HCV NS3 protease or to treat or prevent HCV virus infection. Such treatment may also-be achieved using the compounds of this invention in combination with agents which include, but are not limited to: immunomodulatory agents, such as interferons; other antiviral agents such as ribavirin, amantadine; other inhibitors of HCV NS3 protease; inhibitors of other targets in the HCV life cycle such as helicase, polymerase, metalloprotease, or internal ribosome entry site; or combinations thereof. The additional agents may be combined with the compounds of this invention to create a single dosage form. Alternatively these additional agents may be separately administered to a mammal as part of a multiple dosage form.

Accordingly, another aspect of this invention provides methods of inhibiting HVC NS3 protease activity in patients by administering a compound of the present invention or a pharmaceutically acceptable salt or solvate thereof, wherein the substituents are as defined above.

In a preferred embodiment, these methods are useful in decreasing HCV NS3 protease activity in the patient. If the pharmaceutical composition comprises only a compound of this invention as the active component, such methods may additionally comprise the step of administering to said patient an agent selected from an immunomodulatory agent, an antiviral agent, a HCV protease inhibitor, or an inhibitor of other targets in the HCV life cycle such as, for example, helicase, polymerase, or metalloprotease. Such additional agent may be administered to the patient prior to, concurrently with, or following the administration of the compounds of this invention.

In an alternate preferred aspect, these methods are useful for inhibiting viral replication in a patient. Such methods can be useful in treating or preventing HCV disease.

The compounds of the invention may also be used as laboratory reagents. Compounds may be instrumental in providing research tools for designing of viral replication assays, validation of animal assay systems and structural biology studies to further enhance knowledge of the HCV disease mechanisms.

The compounds of this invention may also be used to treat or prevent viral contamination of materials and therefore reduce the risk of viral infection of laboratory or medical personnel or patients who come in contact with such materials, e.g., blood, tissue, surgical instraments and garments, laboratory instraments and garments, and blood collection or transfusion apparatuses and materials.

Examples

The specific examples that follow illustrate the syntheses of the compounds of the instant invention, and are not to be construed as limiting the invention in sphere or scope. The methods may be adapted to variations in order to produce compounds embraced by this invention but not specifically disclosed. Further, variations of the methods to produce the same compounds in somewhat different manner will also be evident to one skilled in the art.

Chemical abbreviations commonly used to identify chemical compounds in the literature include Bn: benzyl; Boc: tert-butyloxycarbonyl {Me₃COC(O)}; BSA: bovine serum albumin; CDI: carbonyldiimidazole; DBU: 1,8-diazabicy- clo[5.4.0]-undec-7-ene; CH₂C1₂=DCM: methylene chloride; DEAD: diethylazodicarboxylate; DIAD: diisopropylazodi-carboxylate; DIEA: diisopropylethylamine; DIPEA: diisopropylethylamine; 4-DMAP: 4- dimethylaminopyridine; DCC: l,3-dicyclohexyl-carbodiimide; DMF: dimethylformamide; DMSO: dimethylsulfoxide; DPPA: diphenylphosphoryl azide; ED AC: ethyldimethylaminopropylcarbodimide hydrochloride; EDTA: ethylenediaminetetraacetic acid; Et: ethyl; EtOH: ethanol; EtOAc: ethyl acetate; Et₂O: diethyl ether; Grubb's Catalyst: bis(tricyclohexylphosphine)benzylidene ruthenium (IV) dichloride; HATU: [O-7-azabenzotriazol-l-yl)-l, HBTU: [O-(lH- benzotriazol-l-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; PYBROP: Bromo-tris-pyrrolidino-phosphonium hexafluorophosphate; HO AT, l-hydroxy-7-azabenzotriazole; HPLC: high performance liquid chromatography; MS: mass spectrometry; Me: methyl; MeOH: methanol; NMM: N- methylmorpholine; NMP: N-methylpyrrol-idine; Pr: propyl; Succ: 3- carboxypropanoyl; PPA: polyphosphoric acid; TBAF: tetra-n-butyl ammonium fluoride; 1,2-DCE or DCE: 1,2-dichloroethane; TBTU:2-(lH-benzotriazole-l-yl)- 1,1,3,3-tetramethyluronium tetrafluoroborate; TFA: trifluoroacetic acid; THF: ■ tetrahydrofuran Solution percentages express a weight to volume relationship, and solution ratios express a volume to volume relationship, unless stated otherwise. Nuclear magnetic resonance (NMR) spectra were recorded either on a Bruker 300, 400 or 500 MHz spectrometer; the chemical shifts (δ) are reported in parts per million. Flash chromatography was carried out on silica gel (SiO₂) evident to one skilled in the art. All Liquid Chromatography (LC) data were recorded on a Shimadzu LC-10AS liquid chromatograph using a SPD-10AV UV-Vis detector and Mass Spectrometry (MS) data were determined with a Micromass Platform for LC in electrospray mode (ES+). Flash chromatography was carried out on (SiO₂) silica gel evident to one skilled in the art (see W.C. Still et al., J. Org. Chem., (1978), 43, 2923).

All Liquid Chromatography (LC) data were recorded on a Shimadzu LC- 10AS liquid chromatograph using a SPD-10AV UV-Vis detector and Mass Spectrometry (MS) data were determined with a Micromass Platform for LC in electrospray mode (ES+).

The following describes the construction of representative compounds of the present invention. It should be noted that this portion of the patent is broken down into sections, namely Section A, Section B etc. It should also be noted that the numbers of Compounds found in the present invention is not contiguous. Such a break in numbering is marked by a new section, (eg. in going from Section B to Section C) Section A: Unless otherwise noted, each compound was analyzed, by LC/MS, using one of seven methodologies, having the following conditions. Columns: (Method A) - YMC ODS S7 C18 3.0x50 mm

(Method B) - YMC ODS-A S7 C18 3.0x50 mm

(Method C) - YMC S7 C18 3.0x50 mm (Method D) - YMC Xterra ODS S7 3.0x50 mm

(Method E) - YMC Xterra ODS S7 3.0x50 mm

(Method F) - YMC ODS-A S7 C18 3.0x50 mm

(Method G) - YMC C18 S5 4.6x50 mm]

(Method H) - Xterra S7 3.0x50 mm (Method I) - Xterra S7 C18 3.0x50 mm

Gradient: 100% Solvent A/0% Solvent B to

0% Solvent A/100% Solvent B Gradient time: 2 min. (A, B, D, F, G, H, I); 8 min. (C, E) Hold time: 1 min. (A, B, D, F, G, H, I); 2 min. (C, E) Flow rate: 5 mL/min

Detector Wavelength: 220 nm

Solvent A: 10% MeOH / 90% H₂O / 0.1% TFA

Solvent B: 10% H₂O / 90% MeOH / 0.1% TFA.

The compounds and chemical intermediates of the present invention, described in the following examples, were prepared according to the following methods.

Example 1 Boc-(4R)-(2-phenyl-7-methoxyquinoline-4-oxo)-5-proline, shown below, was prepared as described in Steps la-c.

Step la: Preparation of 4-hydroxy-2-phenyl-7-methoxyquinoline, shown below.

To a solution of m-anisidine (300g, 2.44mole) and ethyl benzoylacetate

(234.2g, 1.22mole) in toluene (2.0 L) was added HCl (4.0 N in dioxane, 12.2 mL, 48.8 mmole). The resulting solution was refluxed for 6.5 hr using a Dean-Stark apparatus (about 56 ml of aqueous solution was collected). The mixture was cooled to rt, partitioned multiple times with aqueous HCl (10%, 3x500mL), aqueous NaOH (1.0 N, 2x200mL), water (3x200 mL), and the organic layer dried (MgSO₄) and concentrated in vacuo to supply an oily residue (329.5g). The crude product was heated in an oil bath (280 °C) for 80 min using a Dean-Stark apparatus (about 85 mL liquid was collected). The reaction mixture was cooled down to rt, the solid residue triturated with CH₂C1₂ (400 mL), the resulting suspension filtered, and the filter cake washed with more CH₂C1 (2x150 mL). The resulting solid was dried in vacuo (50 °C; 1 torr; 1 day) affording analytically pure 4-hydroxy-7-methoxy -2-phenylquinoline as a light brown solid (60.7g, 20% overall). 1H NMR δ (DMSO): 3.86 (s, 3H), 6.26 (s, IH), 6.94 (dd, J=9.0, 2.4 Hz, IH), 7.21 (d, J=2.4 Hz, IH), 7.55-7.62 (m, 3H), 7.80-7.84 (m, 2H), 8.00 (d, J=9.0 Hz, IH), 11.54 (s, IH); ¹³C NMR (DMSO-dg) δ: 55.38, 99.69, 107.07, 113.18, 119.22, 126.52, 127.17, 128.97, 130.34, 134.17, 142.27, 149.53, 161.92, 176.48. LC-MS (retention time: 1.26, method D), MS m/z 252 (M⁺+l).

Step lb: Preparation of 4-chloro-7-methoxy-2-phenyIquinoline, shown below.

The product of Step la (21.7g, 86.4mmole) was suspended in POCl₃ (240 mL). The suspension was refluxed for 2 hours. After removal of the POCl₃ in vacuo, the residue was partitioned between EtOAc (IL), and cold aqueous NaOH (generated from 1.0N 200 mL NaOH and 20 mL 10.0 N NaOH) and stirred for 15 min. The organic layer was washed with water (2x200mL), brine (200mL), dried (MgSO ), and concentrated in vacuo to supply 4-chloro-2-phenyl-7- methoxyquinoline (21. Og, 90%) as a light brown solid. 1H NMR (DMSO-d_ό) δ: 3.97 (s, 3H), 7.36 (dd, 7=9.2, 2.6 Hz, IH), 7.49-7.59 (m, 4H), 8.08 (d, 7=9.2 Hz, IH), 8.19 (s, IH), 8.26-8.30 (m, 2H); ¹³C NMR (DMSO-dg) δ: 55.72, 108.00, 116.51, 119.52, 120.48, 124.74, 127.26, 128.81, 130.00, 137.58, 141.98, 150.20, 156.65, 161.30. LC-MS (retention time: 1.547, Method D), MS m/z 270 (MM). Step lc: Preparation of Boc-(4R)-(2-phenyl-7-methoxy-quinoline-4- oxo)-S-proline, shown below.

To a suspension of Boc-4_--hydroxyproline (16.44g, 71.1mmol) in DMSO (250mL) was added t-BuOK (19.93g, 177.6mmol) at 0 °C. The generated mixture was stirred for 1.5 hour and then the product of Step lb (21.02g, 77.9 mmol) was added in three portions over 1 h. The reaction was stirred for one day, the reaction mixture was poured into cold water (1.5L) and washed with Et₂O (4x200mL). The aqueous solution was acidified to pH 4.6, filtered to obtain a white solid, and dried in vacuo to supply the product, Boc (4R)-(2-phenyl-7- methoxyquinoline-4-oxo)proline (32.5g, 98%). 1H NMR (DMSO-d₆) δ 1.32, 1.35 (two s (rotamers) 9H), 2.30-2.42 (m, IH), 2.62-2.73 (m, IH), 3.76 (m, 2H), 3.91 (s, 3H), 4.33-4.40 (m, IH), 5.55 (m, IH), 7.15 (dd, 7=9.2, 2.6 Hz, IH), 7.37 (d, 7=2.6 Hz, IH), 7.42-7.56 (m, 4H), 7.94-7.99 (m, IH), 8.25, 8.28 (2s, 2H), 12.53 (brs, IH); LC-MS (retention time: 1.40, Method D), MS m/z 465 (M⁺+l).

Example 2

(1R,2S) PI isomer of l-{[l-2-tert-Butoxycarbonylamino-3,3- dimethylbutyryl)-4-(7-methoxy-2-phenylquinolin-4-yloxy)pyrrolidine-2- carbonyl]amino}-2-vinylcyclo-propanecarboxylic acid, shown below, was prepared as described in Steps 2a-e.

Step 2a: Preparation of (l--,2S)/(15,2__)-l-amino-2-vinylcyclopropane carboxylic acid ethyl ester hydrochloride, shown below.

ons Base,

A3/B) HCl

(1R, 2S) / (1S, 2R)

Method A_: R=H ₍From Step Al₎ ^{Stθp 2a} (Overall Preparation⁾ Method B_: R=Ph (Aldrich) ^Fro Method A (steps A1-A3⁾ or

Method B (One-pot procedure)

The named compound was made by each of the following methods A and B.

Method A

A.l) Preparation of N-benzyl inline of glycine ethyl ester, shown below.

Glycine ethyl ester hydrochloride (303.8 g, 2.16 mole) was suspended in tert-butylmethyl ether (1.6 L). Benzaldehyde (231 g, 2.16 mole) and anhydrous sodium sulfate (154.6 g, 1.09 mole) were added and the mixture cooled to 0 °C using an ice-water bath. Triethylamine (455 mL, 3.26 mole) was added dropwise over 30 min and the mixture stirred for 48 h at rt. The reaction was then quenched by addition of ice-cold water (1 L) and the organic layer was separated. The aqueous phase was extracted with tert-butylmethyl ether (0.5 L) and the combined organic phases washed with a mixture of saturated aqueous NaHCO₃ (1 L) and brine (1 L). The solution was dried over MgSO , concentrated in vacuo to afford 392.4 g of the N-benzyl imine product as a thick yellow oil that was used directly in the next step. 1H ΝMR (CDC1₃, 300 MHz) δ 1.32 (t, 7=7.1 Hz, 3H), 4.24 (q, 7=7.1 Hz, 2H), 4.41 (d, 7=1.1 Hz, 2H), 7.39-7.47 (m, 3H), 7.78-7.81 (m, 2H), 8.31 (s, IH).

A.2) Preparation of racemic N-Boc-(lR,2S)/(15,2R)-l-amino-2- vinylcyclopropane carboxylic acid ethyl ester

To a suspension of lithium tert-butoxide (84.06 g, 1.05 mol) in dry toluene (1.2 L), was added dropwise a mixture of the N-benzyl imine of glycine ethyl ester (100.4 g, 0.526 mol) and tr n_-l,4-dibromo-2-butene (107.0 g, 0.500 mol) in dry toluene (0.6 L) over 60 min. After completion of the addition, the deep red mixture was quenched by addition of water (1 L) and tert-butylmethyl ether (TBME, 1 L). The aqueous phase was separated and extracted a second time with TBME (1 L). The organic phases were combined, 1 Ν HCl (1 L) was added and the mixture stirred at room temperature for 2 h. The organic phase was separated and extracted with water (0.8 L). The aqueous phases were then combined, saturated with salt (700 g), TBME (1 L) was added and the mixture cooled to 0 °C. The stirred mixture was then basified to pH 14 by the dropwise addition of 10 Ν ΝaOH, the organic layer separated, and the aqueous phase extracted with TBME (2 x 500 mL). The combined organic extracts were dried (MgSO₄) and concentrated to a volume of IL. To this solution of free amine, was added di- tert-butyldicarbonate (131.0 g, 0.6 mol) and the mixture stirred 4 days at rt. , Additional di-tert-butyldicarbonate (50 g, 0.23 mol) was added to the reaction, the mixture refluxed for 3 h, and was then allowed cool to room temperature overnite. The reaction mixture was dried over MgSO and concentrated in vacuo to afford 80 g of crude material. This residue was purified by flash chromatography (2.5 Kg of SiO₂, eluted with 1% to 2% MeOH/CH₂Cl₂) to afford 57 g (53%) of racemic N-Boc-(iR,2S)/(lS,2R)-l-amino-2-vinylcyclopropane carboxylic acid ethyl ester as a yellow oil which solidified while sitting in the refrigerator. 1H ΝMR (CDC1₃, 300 MHz) δ 1.26 (t, 7=7.1 Hz, 3H), 1.46 (s, 9H), 1.43-1.49 (m, IH), 1.76-1.82 (br m, IH), 2.14 (q, 7=8.6 Hz, IH), 4.18 (q, 7=7.2 Hz, 2H), 5.12 (dd, 7=10.3, 1.7 Hz, IH), 5.25 (br s, IH), 5.29 (dd, 7=17.6, 1.7 Hz, IH), 5.77 (ddd, 7=17.6, 10.3, 8.9 Hz, IH); MS m/z 254.16 (M⁺-1).

A.3 Preparation of Racemic (1__,2S)/(1S,2Z?) l-amino-2-vinylcyclopropane carboxylic acid ethyl ester hydrochloride

N-Boc-(l_-,2S/lS,2R)-l-amino-2-vinylcyclopropane carboxylic acid ethyl ester (9.39 g, 36.8 mmol) was dissolved in 4NHCl/dioxane (90ml, 360 mmol) and was stirred for 2 h at rt. The reaction mixture was concentrated to supply (l_-,2S/lS,2R)-l-amino-2-vinylcyclopropane carboxylic acid ethyl ester hydrochloride in quanitative yield (7 g, 100%). 1H ΝMR (Methanol-d₄) δ: 1.32 (t, 7=7.1, 3H), 1.72 (dd, 7=10.2, 6.6 Hz, IH), 1.81 (dd, 7=8.3, 6.6 Hz, IH), 2.38 (q, 7=8.3 Hz, IH), 4.26-4.34 (m, 2H), 5.24 (dd, 10.3, 1.3 Hz, IH) 5.40 (d, 7=17.2, IH), 5.69-5.81 (m, IH).

Method B

To a solution of potassium tert-butoxide (11.55 g, 102.9 mmol) in THF (450 mL) at -78°C was added the commercially available NN-dibenzyl imine of glycine ethyl ester (25.0 g, 93.53 mmol) in THF (112 mL). The reaction mixture was warmed to 0 °C, stirred for 40 min, and was then cooled back to -78 °C. To this solution was added trans- l,4-dibromo-2-butene (20.0 g, 93.50 mmol), the mixture stirred for 1 h at 0 °C and was cooled back to -78 °C. Potassium tert- butoxide (11.55 g, 102.9 mmol) was added, the mixture immediately warmed to 0 °C, and was stirred one more hour before concentrating in vacuo. The crude product was taken up in Et O (530 mL), IN aq. HCl solution (106 mL, 106 mmol) added and the resulting biphasic mixture stirred for 3.5 h at rt. The layers were separated and the aqueous layer was washed with Et₂O (2x) and basified with a saturated aq. NaHCO₃ solution. The desired amine was extracted with Et₂O (3x) and the combined organic extract was washed with brine, dried (MgSO₄), and concentrated in vacuo to obtain the free amine. This material was treated with a 4N HCl solution in dioxane (100 mL, 400 mmol) and concentrated to afford (l_.,2S)/(lS,2R)-l-amino-2-vinylcyclopropane carboxylic acid ethyl ester hydrochloride as a brown semisolid (5.3 g, 34% yield) identical to the material obtained from procedure A, except for the presence of a small unidentified aromatic impurity (8%).

Step 2b: Preparation of the (1R,25) PI isomer of 2-(l- Ethoxycarbonyl-2-vinylcyclopropylcarbamyl-4-(7-methoxyl-2- phenylquinolin-4-yloxy)pyrrolIindine-l-carboxylic acid tert-butyl ester or alternative designation 2(5)-(l(__)-ethoxycarbonyl-2(5)-vinyl- cyclopropylcarbamoyl)-4(R)-(7-methoxy-2-phenyl-quinoIin-4-yloxy)- pyrrolidine-1-carboxylic acid tert-butyl ester, shown below.

To a solution of Boc-4(R)-(2-phenyl-7-methoxyquinoline -4-oxo)proline from Step lc (11.0 g, 23.7 mmole), HCl salt of a racemic mixture of (1R,2S) and (1S,2R) PI derived diastereomers from Step 2a, (5.40 g, 28.2 mmole), NMM (20.8 mL; 18.9 mmole) in 500 mL of 50% CH₂C1₂/THF was added the coupling reagent PyBrop or Bromotrispyrrolidino-phosphonium hexafluorophosphate (16.0 g, 34.3 mmole) in three portions in 10 min at 0 °C. The solution was stirred at rt for'one day and then was washed with pH 4.0 buffer (4x50 mL). The organic layer was washed with saturated aqueous NaHCO₃ (100 mL), the aqueous washing extracted with ethyl acetate (150 mL), and the organic layer backwashed with pH 4.0 buffer (50 mL), and saturated aqueous NaHCO₃ (50 mL). The organic solution was dried (MgSO ), concentrated and purified using a Biotage 65M column (eluted with 50% EtOAc/Hexanes) to provide over 7.5 g of a 1:1 mixture of (1R,2S) and (1S,2R) PI isomers of 2-(l-Ethoxycarbonyl-2- vinylcyclopropylcarbamyl-4-(7-methoxyl-2-phenylquinolin-4- yloxy)pyrrollindine-l-carboxylic acid tert-butyl ester (50% overall) or alternatively elution over a Biotage 65M column using a slow to 15% to 60% EtOAc in hexanes gradient to supply 3.54 g (25%) of the high Rf eluted (1R,2S) PI isomer, and 3.54 g (25%) of the low Rf eluted (1S,2R) PI isomer. Data for (1R,2S) PI isomer: 1H NMR (CDC1₃) δ 1.21 (t, 7=7 Hz, 3H),

1.43 (s, 9H), 1.47-1.57 (m, IH), 1.88 (m, IH), 2.05-2.19 (m, IH), 2.39 (m, IH), 2.88 (m, IH), 3.71-3.98 (m, 2H), 3.93 (s, 3H), 4.04-4.24 (m, 2H), 4.55 (m, IH), 5.13 (d, 7=10 Hz, IH), 5.22-5.40 (m, IH), 5.29 (d, 7=17 Hz, IH), 5.69-5.81 (m, IH), 7.02 (brs, IH), 7.09 (dd, 7=9, 2 Hz, IH), 7.41-7.52 (m, 4H), 7.95 (d, 7=9 Hz, IH), 8.03, 8.05 (2s, 2H); ¹³C NMR (CDC1₃) δ: 14.22; 22.83, 28.25, 33.14, 33.58, 39.92, 51.84, 55.47, 58.32, 61.30, 75.86, 81.27, 98.14, 107.42, 115.00, 117.84, 118.27, 122.63, 123.03, 127.50, 128.72, 129.26, 133.39, 140.06, 151.23, 159.16, 160.34, 161.35, 169.78, 171.68. LC-MS (retention time: 1.62, method D), MS m/z 602 (M⁺+1). Data for the (1S,2R) PI isomer: 1H NMR δ 1.25 (t, 7=7 Hz, 3H), 1.44 (s,-

9H), 1.46-1.52 (m, IH), 1.84 (m, IH), 2.12-2.21 (m, IH), 2.39 (m, IH), 2.94 (m, IH), 3.82 (m, 2H), 3.97 (s, 3H), 4.05-4.17 (m, 2H), 4.58 (m, IH), 5.15 (d, 7=10.8 Hz, IH), 5.33 (d, 7=17 Hz, IH), 5.30-5.43 (m, IH), 5.72-5.85 (m, IH), 7.05 (s, IH), 7.13 (dd, 7=9, 2 Hz, IH), 7.46-7.60 (m, 4H), 7.98 (d, 7=9, IH), 8.06-8.10 (m, 2H). LC-MS (retention time: 1.66, method D), MS m/z 602 (M⁺+l).

Alternative Step 2b: Preparation of 2(5)-(l(R)-ethoxycarbonyl-2(5)- vinyl-cyclopropylcarbamoyl)-4(__)-(7-methoxy-2-phenyl-quinolin-4-yloxy)- pyrrolidine-1-carboxylic acid tert-butyl ester, shown below.

The product of Step 2a, (lR,2S)/(lS,2__)-l-amino-2-vinylcyclopropane carboxylic acid ethyl ester hydrochloride (7.5 g, 39.1 mmol), was combined with diisopropylethylamine (32.5 mL, 186 mmol) in dichloromethane (150 mL). To the resulting mixture was added HOBT hydrate (6.85 g, 44.7 mmol) and the product from Step lc, Boc-4(i?)-(2-phenyl-7-methoxyquinoline-4-oxo)proline (17.3 g, 37.3 mmol), followed by addition of HBTU (16.96 g, 44.7 mmol). A slight exotherm occurred immediately, and the mixture was stirred at room temperature overnight. The mixture was then concentrated in vacuo and redissolved in ethyl acetate (600 mL). The solution was washed with water (2 x 200 mL), then with 10% aqueous sodium bicarbonate (2 x 200 mL), then with water (150 mL) and finally with brine (150 mL). The organic was dried over anhydrous magnesium sulfate and filtered, and the filtrate was concentrated in vacuo to a beige glassy solid. Purification was performed in multiple batches (7 g each) by flash chromatography on a Biotage Flash 75M cartridge (66% hexanes/ethyl acetate) to provide the (1R,2S) vinyl Acca PI isomer of 2-(l- Ethoxycar-bonyl-2-vinylcyclopropylcarbamoyl)-4-(7-methoxy-2-phenyl- quinolin-4-yloxy)-pyrrolidine-l-carboxylic acid ethyl ester as the initial eluted isomer (9.86 g total, 44.0% yield), followed by elution of the (1S,2R) vinyl acca PI isomer of 2-(l-Ethoxycarbonyl-2-vinylcyclopropylcarbamoyl)-4-(7-methoxy- 2-phenyl-quinolin-4-yloxy)-pyrrolidine-l-carboxylic acid ethyl ester as the second eluted isomer (10.43 g total, 46.5% yield). A total of 1.97 g of mixed fractions were recovered to give an overall conversion of 99.3% to the two diastereomers.

(1R,2S) isomer - 1H NMR: (methanol-d₄) δ 1.23 (t, 7= 7.2 Hz, 3H), 1.4 (s, 4H), 1.45 (s, 6H), 1.73 (dd, 7= 7.9, 1.5 Hz, 0.4H), 1.79 (dd, 7= 7.8, 2.4 Hz, 0.6H), 2.21 (q, 7 = 8.2 Hz, IH), 2.44-2.49 (m, IH), 2.66-2.72 (m, 0.4H), 2.73- 2.78 (m, 0.6H), 3.93-3.95 ( , 2H), 3.96 (s, 3H), 4.10-4.17 (m, 2H), 4.44 (q, 7 = 7.8 Hz, IH), 5.13 (d, 7 = 10.7 Hz, IH), 5.31 (d, 7 = 17.7Hz, OAK), 5.32 (d, 7 = 17.4 Hz, 0.6H), 5.49 (bs, IH), 5.66-5.82 (m, IH), 7.16 (dd, 7= 9.2, 2.5 Hz, IH), 7.26 (s, IH), 7.42 (d, 7= 2.4 Hz, IH), 7.48-7.55 (m, 3H), 8.02-8.05 (m, 3H); MS m/z 602 (M⁺+l)

Step 2c: Preparation of the (1R,2S) PI diastereomer of l-{[4-(7- Methoxy-2-phenylquinolin-4yloxy)pyrrolidine-2-carbonyl]-l-amino}-2- vinylcyclo-propanecarboxylic acid ethyl ester, dihydrochloride, shown below.

The product of Step 2b (5.88g, 9.77mmol), the (1R,2S) vinyl Acca PI isomer of 2-(l-Ethoxycarbonyl-2-vinylcyclopropylcarbamoyl)-4-(7 -methoxy-2- phenyl-quinolin-4-yloxy)pyrrolidine-l -carboxylic acid ethyl ester, was dissolved in HCl/dioxane (4.0M; 200ml) and was stirred for 2.5 h at rt. The reaction mixture was concentrated to supply the titled product. 1H NMR (Methanol-d₄) δ 1.24 (t, 7=7 Hz, 3H), 1.50 (dd, 7=10, 5 Hz, IH), 1.78 (dd, 7=8.4, 5.5 Hz, IH), 2.24-2.33 (m, IH), 2.56-2.66 (m, IH), 3.05 (dd, 7=14.6, 7.3 Hz, IH), 3.98 (s, 2H), 4.06 (s, 3H), 4.15 (q, 7=7 Hz, 2H), 4.76 (dd, 7=10.6, 7.3 Hz, IH), 5.13 (dd, 7=10.2, 1.8 Hz), 5.32 (dd, 7=17, 2 Hz), 5.70-5.83 (m, IH), 6.05 (m, IH), 7.48 (dd, 7=9, 2 Hz, IH), 7.65-7.79 (m, 5H), 8.12-8.15 (m, 2H), 8.54 (d, 7=9.5 Hz, IH);

¹³C NMR (methanol-d₄) δ: 14.77, 23.23, 34.86, 37.25, 41.19, 43.90, 52.66, 60.35, 62.32, 62.83, 68.27, 72.58, 73.70, 81.21, 100.70, 102.44, 116.13, 118.67, 122.25, 126.93, 130.27, 130.94, 133.19, 134.14, 134.89, 143.79, 158.39, 166.84, 167.44, 169.57, 171.33. LC-MS (retention time: 1.55, Method D), MS m z 502 (M⁺+l) Step 2d: Preparation of the (1R,25) PI isomer of l-{[l-2-.er.-

Butoxycarbonylamino-3,3-dimethyl-butyryl)-4-(7-methoxy-2- phenylquinolin-4-yloxy)p-pyrrolidine-2-carbonyl]amino}-2-vinyl- cyclopropanecarboxylic acid ethyl ester, shown below.

To a suspension of the product of Step 2c, the (1R,2S) vinyl Acca PI isomer of 2-(l-Ethoxycarbonyl-2-vinylcyclopropylcarbamoyl)-4-(7-methoxy-2- phenyl-quinolin-4-yloxy)pyrrolidine-l -carboxylic acid ethyl ester (1.95g; 3.4mmol), N-BOC-L-tert-leucine (0.94g, 4.08mmol), MM (1.87ml, 17mmol) in DMF (15mL) was added HATU (1.55g, 4.08 mmol) at 0 °C. After being stirred for 2 days, the reaction mixture was diluted with EtOAc (200 mL), washed with pH 4.0 buffer (2x30 mL), saturated aqueous NaHCO₃ (30 mL), brine (30mL), dried (MgSO₄), purified by a Biotage 40 M column (eluted with 15% to 60% EtOAc in Hexanes) to supply the titled product as a white solid (2.21g, 90%). 1H NMR (CDC1₃) δ 1.05 (s, 9H), 1.20 (t, 7=7 Hz, 3H), 1.38-1.43 (m, IH), 1.41 (s, 9H), 1.80-1.85 (m, IH), 2.08-2.16 (m, IH), 2.39-2.47 (m, IH), 2.90-2.99 (m, IH), 3.90-4.01 (m, IH), 3.93 (s, 3H), 4.12 (q, 7=7 Hz, 2H), 4.36 (d, 7=10 Hz, IH), 4.45 (d, 7=12 Hz, IH), 4.75-4.85 (m, IH), 5.09-5.13 (m, IH), 5.21-5.34 (m, 2H), 5.69-5.81 (m, IH), 7.00-7.09 (m, 2H), 7.42-7.54 (m, 5H), 8.01-8.05 (m, 3H); ¹³C NMR (CDC1₃) δ 14.30, 22.85, 26.40, 28.25, 32.20, 34.09, 35.39, 39.97, 53.86, 55.47, 58.28, 58.96, 61.29, 75.94, 79.86, 97.98, 107.43, 115.06, 117.98, 118.38, 123.03, 127.52, 128.76, 129.24, 133.40, 140.26, 151.44, 155.74, 159.16, 160.09, 161.32, 169.55, 170.64, , 172.63. LC-MS (retention time: 1.85, Method D), MS m/z 715 (M⁺+l).

Step 2e: Preparation of the titled product, Example 2, the (1R,2S) PI isomer of l-{[l-2-.eri'-Butoxycarbonylan_ino-3,3-dimethylbutyryl)-4-(7- methoxy-2-phenylquinolin-4-yloxy)pyrrolidine-2-carbonyl]-amino}-2- vinylcyclopropanecarboxylic acid. To a suspension of the product of Step 2d, the (1R,2S) PI isomer of l-{ [1-

2-tert-Butoxycarbonylamino-3,3-dimethylbutyryl)-4-(7-methoxy-2- phenylquinolin-4-yloxy)pyrrolidine-2-carbonyl]amino}-2-vinyl- cyclopropanecarboxylic acid ethyl ester (2.63g, 3.68 mmol) in THF(150 mL), CH₃OH (80 mL), and H₂O (20 mL) was added LiOH (1.32g, 55.2 mmol). The reaction mixture was stirred for two days, acidified to neutral pH, and concentrated in vacuo until only the aqueous layer remained. The resulting aqueous residue was acidified to pH 3.0 by addition of 1.0 N aqueous HCl, and extracted with EtOAc (4x200mL). Combined organic solvent was washed by brine (20 mL), dried (Na₂SO ), filtered, and concentrated in vacuo to supply the titled product, Example 2, the (1R,2S) PI isomer of l-{ [1-2-tert-

Butoxycarbonylamino-3,3-dimethylbutyryl)-4-(7-methoxy-2-phenylquinolin-4- yloxy)pyrrolidine-2-carbonyl]-amino}-2-vinylcyclopropanecarboxylic acid as white solid (2.41g, 96%). 1H NMR (CDCl₃/Methanol-d₄) δ 0.98, 1.01 (two s (rotamers) 9H), 1.40, 1.42 (two s (rotamers) 9H), 1.35-1.47 (m, IH), 1.89-1.93 (m, IH), 2.03-2.14 (m, IH), 2.45-2.52 (m, IH), 2.64-2.78 (m, IH), 3.94 (s, 3H), 3.96-4.12 (m, IH), 4.34 (d, 7=10 Hz, IH), 4.52 (d, 7=11 Hz, IH), 4.58-4.64 (m, IH), 5.10 (d, 7=12 Hz, IH), 5.24 (d, 7=16 Hz, IH), 5.34 (m, IH), 5.68-5.86 (m, 2H), 7.02-7.05 (m, IH), 7.32 (m, IH), 7.40-7.54 (m, 4H), 7.97-8.03 (m, 3H); LC- MS (retention time: 1.64, method D), MS m/z 687 (M⁺+l).

la) tBuNH₂

Method I (Steps a-d). Preparation of 1-Substituted Cyclopropanesulfonamides Required For N-acylsulfonamide Coupling Steps 3e-8e (Examples 3-8 used to Prepare Compounds 1-6 Respectively).

Step la: N-ter--Butyl-(3-chIoro)propylsulfonamide.

Step la) A neat solution of tert-Butylamine (315.3 mL, 3.0 mol) was dissolved in THF (2.5 L), cooled to -20 °C, and 3-Chloropropanesulfonyl chloride (182.4 mL, 1.5 mol) was added slowly. The reaction mixture was allowed to warm to rt and stirred for 24 h. The mixture was filtered, and the filtrate was concentrated in vacuo. The residue was dissolved in CH₂C1₂ (2.0 L). The resulting solution was washed with 1 N HCl (1.0 L), water (1.0 L), brine (1.0 L) and dried over Na₂SO . It was filtered and concentrated in vacuo to give a slightly yellow solid which was crystallized from hexane to afford the product as a white solid (316.0 g, 99%): 1H NMR (CDC1₃) δ 1.38 (s, 9H), 2.30-2.27 (m, 2H), 3.22 (t, 7= 7.35 Hz, 2H), 3.68 (t, 7= 6.2 Hz, 2H), 4.35 (bs, IH).

Steps 3Ib-3Ic: Preparation of N--er.-Butyl-(l-methyl)cyclopropyl- sulfonamide.

Steps 3Ib-3Ic) A solution of N-tert-Butyl-(3-chloro)propylsulfonamide (4.3 g, 20 mmol) was dissolved in dry THF (100 mL) and cooled to - 78 °C. To this solution was added rc-BuLi (17.6 mL, 44 mmol, 2.5 M in hexane) slowly. The dry ice bath was removed and the reaction mixture was allowed to warm to rt over a period of 1.5 h. This mixture was then cooled to - 78°C, and a solution of n-BuLi (20 mmol, 8 mL, 2.5 M in hexane) was added. The reaction mixture was warmed to rt, recooled to -78 °C over a period of 2 h and a neat solution of methyliodide (5.68 g, 40 mmol) added. The reaction mixture was allowed to warm to rt overnight, quenched with saturated ΝFL-Cl (100 mL) at rt. It was extracted with EtOAc (100 mL). The organic phase was washed with brine (100 mL), dried (MgSO₄), and concentrated in vacuo to give a yellow oil which was crystallized from hexane to afford the product as a slightly yellow solid (3.1 g, 81%): 1H ΝMR (CDC1₃) δ 0.79 (m, 2H), 1.36 (s, 9H), 1.52 (m, 2H), 1.62 (s, 3H), 4.10 (bs, IH)

Step 3Id: Preparation of Example 3, 1-methylcyclopro-pylsulfonamide. Step 3Id) A solution of N-tert-ButyH 1 -methyl)cyclopropylsulfonamide

(1.91 g, 10 mmol) was dissolved in TFA (30 mL), and the reaction mixture stirred at rt for 16 h. The solvent was removed in vacuo to give a yellow oil which was crystallized from EtOAc / hexane (1 : 4, 40 mL) to yield Example 3, 1- methylcyclopropylsulfonamide, as a white solid (1.25 g, 96%): 1H NMR (CDC1₃) δ 0.84 (m, 2H), 1.41 (m, 2H), 1.58 (s, 3H), 4.65 (bs, 2H). Anal. Calcd. For C₄H₉NO₂S: C, 35.54; H, 6.71; N, 10.36. Found: C, 35.67; H, 6.80; N, 10.40.

Steps 4Ib-4Ic: Preparation of N-tert-Butyl-(l-aIIyl)cyclopropylsulfonamide.

Steps 4Ib-4Ic) This compound, N-tert-Butyl-(l- allyl)cyclopropylsulfonamide, was obtained in 97% yield according to the procedure described in the synthesis σ/N-tert-Butyl-(l-methyl)cyclopropylsul- fonamide except 1.25 equivalents of allyl bromide were used as electrophile. The compound was taken directly into the next reaction without purification: 1H ΝMR (CDC1₃) δ 0.83 (m, 2H), 1.34 (s, 9H), 1.37 (m, 2H), 2.64 (d, 7= 7.3 Hz, 2H), 4.25 (bs, IH), 5.07-5.10 (m, 2H), 6.70-6.85 (m, IH).

Steps 4Id: Preparation of Example 4, 1-allylcyclopro-pylsulfonamide.

Step 4Id) This compound, Example 4, 1-allylcyclopropylsulfonamide, was obtained in 40% yield from N-tert-butyl-(l-allyl)cyclopropylsulfonamide according to the procedure described in the synthesis of 1-

Methylcyclopropylsulfonamide. The compound was purified by column chromotography over SiO₂ using 2% MeOH in CH₂C1₂ as the eluent: 1H ΝMR (CDC1₃) δ 0.88 (m, 2 H), 1.37 (m, 2 H), 2.66 (d, 7=7.0 Hz, 2 H), 4.80 (s, 2 H), 5.16 (m. 2 H), 5.82 (m, 1 H); ¹³C ΝMR (CDC1₃) δ 11.2, 35.6, 40.7, 119.0, 133.6.

Steps 5Ib-5Ic: Preparation of N-tert-Butyl-[l-(l-hydroxy)cyclohexyl]- cyclopropylsulfonamide.

Steps 5Ib-5Ic) This compound was obtained in 84% yield using to the procedure described for the synthesis of N-tert-Butyl-(l-methyl)cyclopropylsul- fonamide except 1.30 equivalents of cyclohexanone were used, followed by recrystallization from the minimum amount of 20% EtOAc in hexane: 1H ΝMR (CDC1₃) δ 1.05 (m, 4H), 1.26 (m, 2H), 1.37 (s, 9H), 1.57-1.59 (m, 6H), 1.97 (m, 2H), 2.87 (bs, IH), 4.55 (bs, IH).

Steps 5Id: Preparation of Example 5, l-(l-cyclohexenyl)cycIopropyl- sulfonamide.

Step 5Id) This compound, l-(l-cyclohexenyl)-cyclopropylsulfonamide, Example 5, was obtained in 85% yield from N-tert-butyl-[l-(l-, hydroxy)cyclohexyl]-cyclopropylsulfonamide using the procedure described for the synthesis of 1-methylcyclopropylsulfonamide, followed by recrystallization from the minimum amount of EtOAc and hexane: 1H ΝMR (DMSO-d₆) δ 0.82 (m, 2 H), 1.28 (m, 2 H), 1.51 (m, 2 H), 1.55 (m, 2 H), 2.01 (s, 2 H), 2.16 (s, 2 H), 5.89 (s, 1 H), 6.46 (s, 2 H); ¹³C ΝMR (DMSO-dg) δ 11.6, 21.5, 22.3, 25.0, 27.2, 46.9, 131.6, 132.2; LR-MS (ESI): 200 (M⁺-1).

O c ^H ^phJ

Steps 6Ib-6Ic: Preparation of N-tert -Butyl- (l-benzoyl)cyclopropyl- sulfonamide.

Steps 6Ib-6Ic) This compound was obtained in 66% yield using the procedure described for the synthesis of N-tert-Butyl-(l- methyl)cyclopropylsulfonamide except 1.2 equivalents of methyl benzoate was used as the electrophile. The compound was purified by column chromatography over SiO₂ using 30% to 100% CH₂C1₂ in hexane: 1H NMR (CDC1₃) δ 1.31 (s, 9H), 1.52 (m, 2H), 1.81 (m, 2H), 4.16 (bs, IH), 7.46 (m, 2H), 7.57 (m, IH), 8.05 (d, 7= 8.5 Hz, 2H).

Steps 6Id: Preparation of Example 6, 1-benzoylcyclo-propylsulfonamide. Steps 6Id) This compound, Example 6, 1-benzoylcyclopropyl- sulfonamide, was obtained in 87% yield from N-tert-butyl(l- benzoyl)cycloρropylsul-fonamide using the procedure described for the synthesis of 1-Methylcyclopropylsulfonamide, followed by recrystallization from the minimum amount of EtOAc in hexane: 1H ΝMR (DMSO-dg) δ 1.39 (m, 2 H), 1.61 (m, 2 H), 7.22 (s, 2 H), 7.53 (t, 7=7.6 Hz, 2 H), 7.65 (t, 7=7.6 Hz, 1 H), 8.06 (d, 7=8.2 Hz, 2 H); ¹³C ΝMR (DMSO-d₆) δ 12.3, 48.4, 128.1, 130.0, 133.4, ■ 135.3, 192.0.

Steps 7Ib-7Ic: Preparation of N-ter.-Butyl-(l-benzyl)cyclopropyl- sulfonamide.

Steps 7Ib-7Ic) This compound was obtained in 60% yield using the procedure described for the synthesis of N-tert-Butyl-(l- methyl)cyclopropylsulfonamide except 1.05 equivalents of benzyl bromide were used, followed by trituration with 10% EtOAc in hexane: 1H ΝMR (CDC1₃) δ

0.92 (m, 2H), 1.36 (m, 2H), 1.43 (s, 9H), 3.25 (s, 2H), 4.62 (bs, IH), 7.29-7.36

(m, 5H).

Steps 7Id: Preparation of Example 7, 1-Benzylcyclo-propylsulfonamide.

Step 7Id) This compound, Example 7, 1-Benzylcyclopropylsulfonamide, was obtained in 66% yield from N-tert-butyl(l-benzyl)cyclopropylsul-fonamide using the procedure described for the synthesis of 1-

Methylcyclopropylsulfonamide, followed by recrystallization from the minimum amount of 10% EtOAc in hexane: 1H ΝMR (CDC1₃) δ 0.90 (m, 2H), 1.42 (m, 2 H), 3.25 (s, 2 H), 4.05 (s, 2 H), 7.29 (m, 3 H), 7.34 (m, 2 H); ¹³C ΝMR (CDC1₃) δ 11.1, 36.8, 41.9, 127.4, 128.8, 129.9, 136.5.

Steps 8Ib-8Ic: Preparation of N-tert-Butyl-(l-phenylaminocarboxy)- cyclopropylsulfonamide. Steps 8Ib-8Ic) This compound was obtained in 42% yield using the procedure described for the synthesis of N-tert-Butyl-(l- methyl)cyclopropylsulfonamide using 1 equivalent of phenylisocyanate, followed by recrystallization from the minimum amount of EtOAc in hexane^!H ΝMR (CDC1₃) δ 1.38 (s, 9H), 1.67-1.71 (m, 4H), 4.30 (bs, IH), 7.10 (t, 7= 7.5 Hz, IH), 7.34 (t, 7 = 7.5 Hz, 2H), 7.53 (t, 7 = 7.5 Hz, 2H).

Steps 8Id: Preparation of Example 8, l-(Phenylamino-carboxy)cyclopropyl- sulfonamide.

Step 8Id) This compound, Example 8, 1- (Phenylaminocarboxy)cyclopropylsulfonamide, was obtained in 75% yield from N-tert-butyl(l-phenylaminocarboxy)cycloρropylsulfonamide using the procedure described for the synthesis of 1-Methylcyclopropylsulfonamide, followed by recrystallization from the minimum amount of EtOAc in hexane: 1H NMR (CDCI₃) δ 1.70 (m, 2 H), 1.75 (m, 2 H), 4.85 (s, 2 H), 7.16 (t, 7=7.6 Hz, 1 H), 7.35 (t, 7=7.6 Hz, 2 H), 7.53 (d, 7=8.2 Hz, 2 H), 9.25 (s, 1 H).

Compound 1, Example 9 Compound 1, Example 9, BOCNH-P3(L-^-BuGly)-P2[(4R)-(2-phenyl-7- methoxyquinoline-4-oxo)-S-proline]-Pl(l__,2S Vinyl Acca)-CONHSO₂(l- methylcyclopropan-1-yl) or alternate designation, Compound 1, the (1R,2S) PI isomer of (l-{4-(7-Methoxy-2-phenylquinolin-4-yloxy)-2-[l-(l- methylcyclopropanesulfonyIaminocarbonyl)-2- vinyIcyclopropylcarbamoyI]pyrrolidine-l-carbonyI}-2,2- dimethylpropyl)carbamic acid tert -butyl ester, shown below, was prepared as follows.

Step 9f) A solution of CDI (0.068g, 0.43 mmol) and the product of Step 2e (.250g, 0.364 mmol) in THF (5 mL) was refluxed for 60 min and allowed to cool down to rt. A total of 0.069 g (0.51 mmol) of 1- methylcyclopropanesulfonamide (prepared according to Example 3), followed by the addition of a solution of neat DBU (0.078 mL, 0.51 mmol). The reaction was stirred for 18 h, diluted with EtOAc (30 mL) and washed pH 4.0 buffer (3xl0mL), dried (MgSO₄), concentrated and purified over three 1000 DM preparative TLC plate from Analtech (20X40 cM, eluted sequentially with 1% to 4% MeOH in CH₂C1₂) to supply Example 9, Compound 1 (0.1374 g, 47%): 1H NMR (methanol-04, 300MHz) D 0.70-0.80 (m, 2H), 1.03 (s, 9H), 1.24-1.29 (m, 11H), 1.43-1.47 (m, IH), 1.52 (s, 3H), 1.77-1.89 (m, IH), 2.15 (m, IH), 2.44 (m, IH), 2.72 (m, IH), 3.94 (s, 3H), 4.04-4.16 (m, IH), 4.22-4.28 (m, IH), 4.49-4.64 (m, 3H), 5.00-5.08 (m, IH), 5.23 (d, 7=17 Hz, IH), 5.55 (m, IH), 5.73-5.93 (m, IH), 7.05-7.09 (m, IH), 7.25 (s, IH), 7.39 (m, IH), 7.48-7.56 (m, 3H), 8.03-8.12 (m, 3H). LC-MS (retention time: 1.59, Method D), MS m/z 804 (MM).

Compound 2, Example 10 Compound 2, Example 10, BOCNH-P3(L-^-BuGly)-P2[(4R)-(2-phenyl-7- methoxyquinoline-4-oxo)-S-proline]-Pl(lR,25 Vinyl Acca)-CONHSO₂(l- allylcyclopropan-1-yl) or alternate designation, Compound 2, the (1R,2S) PI isomer of {l-[2-[l-(l-AUylcyclopropanesul-fonylaminocarbonyl)-2- vinyIcycIopropylcarbamoyl]-4-(7-methoxy-2-phenylquinolin-4-yloxy)- pyrrolidine-l-carbonyl]-2,2-dimethylpropyl}carbamic acid tert-butyl ester. Step lOf) This compound was prepared in 83% yield from tripeptide acid product of step 2e (Example 2) in analogous fashion to the procedure of Example 9 except that 1-allylcyclopropanesulfonamide (prepared in Example 4) was used in place of 1-methylcyclopropanesulfonamide: 1H NMR (CDCl₃/methanol-d ) D 0.80-0.82 (m, 2H), 1.00 (s, 9H), 1.26-1.28 (m, 2H), 1.31 (s, 9H), 1.38 (m, IH), 1.74-1.85 (m, IH), 1.90-2.07 (m, IH), 2.38-2.52 (m, IH), 2.56-2.65 (m, 3H), 3.90 (s, 3H), 3.96-4.13 (m, IH), 4.26 (m, IH), 4.43 (d, 7=11.6 Hz, IH), 4.56 (m, IH), 4.90-5.00 (m, 2H), 5.07-5.15 (m, 2 H), 5.34 (m, IH), 5.54-5.91 (m, 3H), 6.98-7.04 (m, 2H), 7.33-7.36 (m, IH), 7.41-7.49 (m, 3H), 7.93-8.00 (m, 3H). HRMS m/z (M+H)⁺ calcd for C₄₄H5₆N₅SO₉: 830.3799 found: 830.3812. LC-MS (retention time: 1.68, Method I), MS m/z 830 (M⁺+l).

Compound 2A, Example 10A Compound 2, Example 11, BOCNH-P3(L-.-BuGly)-P2[(4R)-(2-phenyl-7- methoxyquinoline-4-oxo)-S-proline]-Pl(l__,2S Vinyl Acca)-CONHSO₂(l- cyclopropan-1-yl) Hydrochloride Salt or alternate designation, Compound 2A, the (1R,25) PI isomer of {l-[2-[l-(l-AUyl- cyclopropanesulfonylaminocarbonyl)-2-vinylcyclopropyl-carbamoyl]-4-(7- methoxy-2-phenylquinolin-4-yloxy)-pyrro!idine-l-carbonyl]-2,2- dimethylpropyl}carbamic acid tert-butyl ester hydrochloride.

HCl Salt of Product of Step lOf) This compound was prepared in quantitative yield from Compound 2 (Example 10) by dissolving in CH₂C1₂ (-50 mg/mL), cooling to -78 °C, adding 5 molar equivalents of 4N HCl/dioxane and then immediately concentrating in vacuo: 1H NMR (methanol-d₄) D 0.83-0.98 (m, 2H), 1.04 (s, 9H), 1.19 (s, 9H), 1.36-1.60 (m, 3H), 1.81-1.88 (m, IH), 2.22- 2.35 (m, IH), 2.38-2.50 (m, IH), 2.59-2.70 (m, 2H), 2.75-2.84 (m, IH), 4.05 (s, 3H), 4.08-4.16 (m, 2H), 4.61-4.69 (m, 2H), 5.16-5.18 (m, 3H), 5.28-5.37 (m, IH), 5.63-5.80 ( , 2H), 5.82-5.89 ( , IH), 7.38 (d, 7=9.5, 2.2 Hz, IH), 7.57 (d, 7=2.2 Hz, IH), 7.64 (s, IH), 7.69-7.76 (m, 3H), 8.08-8.11 (m, 2H), 8.34 (d, 7=9.5 Hz, IH). HRMS m/z (M+H)⁺ calcd for C₄ H₅₆N₅SO₉: 830.3799 found: 830.3812.

LC-MS (retention time: 1.68, Method D with hold time changed from 2 to 3 min), MS m/z 830 (M⁺+l).

Compound 3, Example 11 Compound 3, Example 11, BOCNH-P3(L-/ BuGly)-P2[(4R)-(2-phenyI-7- methoxyquinoline-4-oxo)-5-proline]-Pl(lR,25 Vinyl Acca)-CONHSO₂(l- Cyclohex-1-enyl-cyclopropan-l-yl) or alternate designation, Compound 1, the (1R,2S) PI isomer of {l-[2-[l-(l-Cyclohex-l-enyl- cyclopropanesuIfonylaminocarbonyl)-2-vinylcyclopropyIcarbamoyl]-4-(7- methoxy-2-phenyl-quinolin-4-yloxy)pyrrolidine-l-carbonyl]-2,2-dimethyl- propyl}carbamic acid tert-butyl ester.

Step llf) This compound was prepared in 74% yield from tripeptide acid product of step 2e (Example 2) in analogous fashion to the procedure of Example 9 except that l-(l-cyclohexenyl)cyclόpropylsulfonamide (prepared in Example 5) was used in place of 1-methylcyclopropanesulfonamide: 1H NMR (CDCl₃/methanol-d₄) D 0.70-1.10 (m, 3H), 1.00 (s, 9H), 1.17-1.61 (m, 6H), 1.32 (s, 9H), 1.87-2.27 (m, 5H), 2.34-2.52 (m, IH), 2.54-2.69 (m, IH), 3.90 (s, 3H), 4.00-4.04 (m, IH), 4.26 (m, IH), 4.35-4.48 (m, IH), 4.48-4.66 (m, IH), 4.88-5.03 (m, IH), 5.07-5.20 (m, 1 H), 5.34 (m, IH), 5.73-5.94 ( , IH), 6.99 (m, 2H), 7.36 (s, IH), 7.41-7.51 (m, 3H), 7.93-7.99 (m, 3H). HRMS m/z (M+H)⁺ calcd for C₄₇H₆₀N₅O₉S: 870.4112 found: 870.4119. LC-MS (retention time: 1.82, Method I), MS m/z 870 (MM).

Compound 4, Example 12 Compound 4, Example 12, BOCNH-P3( ^-BuGly)-P2[(4R)-(2-phenyl-7- methoxyquinoline-4-oxo)-5-proline]-Pl(lR,2S Vinyl Acca)-CONHSO₂(l- Benzoylcyclopropan-1-yl) or alternate designation, Compound 4, the (1R,25) PI isomer of {l-[2-[l-(l-Benzoylcyclopropanesulfonyl-aminocarbonyl)-2- vinyl-cyclopropylcarbamoyl]-4-(7-methoxy-2-phenylquinolin-4-yloxy)- pyrrolidine-l-carbonyl]-2,2-dimethylpropyl}-carbamic acid tert-butyl ester. Step 12f) This compound was prepared in 77% yield from tripeptide acid product of step 2e (Example 2) in analogous fashion to the procedure of Example 9 except that 1-benzoylcyclo-propylsulfonamide (prepared in Example 6) was used in place of 1-methylcyclopropanesulfonamide: 1H NMR (CDCl₃/methanol- ( ) □ 0.95 (s, 9H), 1.13-1.35 (m, 3H), 1.29 (s, 9H), 1.54-1.75 (m, 3H), 1.81-1.98 (m, IH), 2.38-2.59 (m, 2H), 3.87 (s, 3H), 3.99-4.02 (m, IH), 4.20-4.26 (m, IH), 4.33-4.41 (m, IH), 4.45-4.55 (m, IH), 4.77-4.90 (m, IH), 4.99-5.11 (m, IH), 5.22-5.30 (m, IH), 5.52-5.72 (m, IH), 6.94-7.00 (m, 2H), 7.20-7.47 (m, 7H), 7.91-7.98 (m, 3H), 7.98-8.04 (m, 2H). HRMS m/z (M+H)⁺ calcd for C₄₈H₅₆N₅O₉S: 894.3748 found: 894.3756. LC-MS (retention time: 1.72, Method I), MS m/z 894 (M⁺+l). 66

Compound 5, Example 13 Compound 5, Example 13, BOCNH-P3(L-,-BuGly)-P2[(4R)-(2-phenyl-7- methoxyquinoline-4-oxo)-5-proline]-Pl(lR,25 Vinyl Acca)-CONHSO₂(l- Benzylcyclopropan-1-yl) or alternate designation, Compound 5, the (1R,25) PI isomer of {l-[2-[l-(l-Benzylcyclopropanesulfonyl-aminocarbonyι)-2- vinyl-cyclopropylcarbamoyl]-4-(7-methoxy-2-phenylquinoIin-4-yloxy)- pyrrolidine-l-carbonyl]-2,2-dimethylpropyl}-carbamic acid tert-butyl ester. Step 13f) This compound was prepared in 26% yield from tripeptide acid product of step 2e (Example 2) in analogous fashion to the procedure of Example 9 except that 1-benzylcyclo-propylsulfonamide (prepared in Example 7) was used in place of 1-methylcyclopropanesulfonamide: 1H NMR (CDCl₃/methanol-d₄) D 0.80-1.42 (m, 5H), 1.02 (s, 9H), 1.35 (s, 9H), 1.75-2.08 (m, 2H), 2.41-2.54 (m, IH), 2.57-2.71 (m, IH), 3.26-3.30 (m, 2H), 3.93 (s, 3H), 4.03-4.18 (m, IH), 4.45 (d, 7=12 Hz, H), 4.47-4.67 (m, IH), 4.96-5.04 (m, IH), 5.11-5.20 (m, IH), 5.34 (m, IH), 5.78-6.04 (m, IH), 6.99-7.20 (m, 6H), 7.38-7.50 (m, 5H), 7.95-8.05 (m, 3H). HRMS m z (M+H)+ calcd for C₄₈H₅₈N₅O₉S: 880.3955, found: 880.3939. LC-MS (retention time: 1.78, Method I), MS m/z 880 (M⁺+l).

Compound 6, Example 14 Compound 6, Example 14, BOCNH-P3(L-.-BuGly)-P2[(4R)-(2-phenyl-7- methoxyquinoIine-4-oxo)-5-proline]-Pl(lR,2S Vinyl Acca)-CONHSO₂(l- phenylcarbamoyl-cyclopropan-1-yl) or alternate designation, Compound 6, the (1R,2S) PI isomer of (l-{4-(7-Methoxy-2-phenyl-quinolin-4-yloxy)-2-[l- (l-phenylcarbamoyl-cyclopropane-sulfonylaminocarbonyl)-2-vinylcycIopro- pylcarbamoyl] -pyrrolidine- l-carbonyl}-2,2-dimethyl-propyl)carbamic acid tert-butyl ester.

Step 14f) This compound was prepared in 78% yield from the tripeptide acid product of step 2e (Example 2) in analogous fashion to the procedure of Example 9 except that 1-phenylcarbamoylcyclopropanesulfonamide (prepared in Example 8) was used in place of 1-methylcyclopropanesulfonamide: 1H NMR (CDCl₃/methanol-d₄) D 0.97 (s, 9H), 1.19-1.40 (m, IH), 1.30 (s, 9H), 1.40-1.60 (m, 4H), 1.61-1.74 (m, IH), 1.89-1.94 (m, IH), 2.30-2.38 (m, IH), 2.43-2.53 (m, IH), 3.90 (s, 3H), 4.17-4.24 (m, IH), 4.37-4.49 (m, IH), 4.81-4.89 (m, IH), 5.05- 5.11 (m, IH), 5.16 (m, IH), 5.81-5.88 (m, IH), 6.93-7.06 (m, 3H), 7.13-7.17 (m, 2H), 7.35 (m, IH), 7.43-7.56 (m, 5H), 7.92-8.06 (m, 3H). HRMS m z (M+H)⁺ calcd for C₄₈H₅₇N₆O₁₀S: 909.3857, found: 909.3857. LC (retention time: 1.73, Method I). LRMS m/z 909 (M⁺+l). lla) NH₃ (aq) lib) BOC₂0, Et₃N, 4-DMAP (cat.) lie) π-BuLi (2 eq.); pH 3 workup

Example 16; R=CH₂cyclopropane

Example 17,

Example 18, R= (C=0)NH(4-yl-3,5-diMe isoxazole)

Method II (Steps a-e). Preparation of 1-Substituted Cyclopropanesulfonamides Required For N-acylsulf-onamide Coupling Steps 15e-18e (Examples 15-18 used to Prepare Compounds 7-10, Respectively).

Step Ha: 3-chloropropylsulfonamide. Step Ila) A solution of 3-Chloropropanesulfonyl chloride (55 g, 310.7 mmol) was dissolved in THF (200 mL) and added dropwise over 30 min to a solution of ΝH4OH (200 mL) cooled to 0 °C. The reaction mixture was warmed to rt, stirred 1 h, and the aqueous layer partioned multiple time with CH C1₂ (4 X 500-mL). The combined CH₂C1₂ layer was washed with 1 N HCl (150 mL), water (150 mL), dried over MgSO₄ and concentrated in vacuo. The crude solid was recrystallized from the minimum amount of CH₂C1₂ in hexanes to afford 3- chloropropylsulfonamide as a white solid (45.3 g, 93%). 1H NMR (CDC1₃) δ 2.34 (m, 2 H), 3.32 (t, 7=7.3 Hz, 2 H), 3.70 (t, 7=6.2 Hz, 2 H), 4.83 (s, 2 H); ¹³C NMR (CDC1₃) δ 27.10, 42.63, 52.57.

Step lib: 3-chloropropylsulfonylamine .e/t-butylcar-bamate.

Step lib) To a solution of 3-chloropropylsulfonamide (30.2 g, 191.5 mmol), Et₃N (30.2 mL, 217.0 mmol), and 4-DMAP (2.40g, 19.6 mmol) in CH₂C1₂ (350 mL) cooled to 0 °C was added slowly dropwise a solution of BOC₂O (47.2g, 216.9 mmol) in CH₂C1₂ (250 mL) over 30 min. The reaction mixture was allowed to warm to rt, stirred an additional 3 h and was partioned with 1 N HCl (300 mL), water (300 mL), brine (300 mL), dried over MgSO and concentrated in vacuo to afford the crude product. This material was triturated with 70 mL of 5% CH₂C1₂ in hexanes to afford 3-chloropropylsulfonylamine tert- , butylcarbamate as an offwhite solid (47.2 g, 96%): 1H NMR (CDC1₃) δ 1.51 (s, 9 H), 2.33 (m, 2 H), 3.60 (t, 7=7.3 Hz, 2 H), 3.68 (t, 7=6.21 Hz, 2 H); ¹³C NMR (CDCI₃) δ 26.50, 27.95, 42.37, 50.40, 84.76, 149.53.

Step He: Preparation of cyclopropylsulfonylamine tert-butyl carbamate.

Step He) A solution of /z-BuLi (74.7 mL, 119.5 mmol, 1.6 M in hexane) was dissolved in dry THF (105 mL) and cooled to -78 °C under a Argon atmosphere. To this solution was added a solution of 3- chloropropylsulfonylamine tert-butylcarbamate (14 g, 54.3 mmol) in dry THF

(105 mL) slowly dropwise over 20-30 min. The dry ice bath was removed and the reaction mixture was allowed to warm to rt over a period of 2 h. The reaction mixture was quenched with glacial AcOH (3.4 mL), concentrated in vacuo, and partitioned between CH C1₂ (100 mL) and water (100 mL). The organic phase was washed with brine (100 mL), dried (MgSO ), and concentrated in vacuo to afford the cyclopropylsulfonylamine tert-butyl carbamate as a waxy offwhite solid (12.08 g, 100%): 1HNMR (CDC1₃) δ 1.10 (m, 2 H), 1.34 (m, 2 H), 1.50 (s, 9 H), 2.88 (m, 1 H), 7.43 (s, 1 H). ¹³C NMR (CDC1₃) δ 6.21, 28.00, 31.13, 84.07, 149.82.

Step 15IId: Preparation of 1-methoxymethylcyclopropyl-sulfonylamine tert- butylcarbamate. Step 15IId) To a solution of cyclopropylsulfonylamine tert-butyl carbamate (1.0 g, 4.5 mmol) dissolved in THF (30 mL) cooled to -78 °C, was added n-BuLi (6.4 mL, 10.2 mmol, 1.6 M in hexane) and the reaction mixture was stirred for 1 h. To this solution was added a neat solution of chloromethyl methyl ether (0.40 mL, 5.24 mmol), and the mixture was slowly allowed to warm to room temperature overnite. The solution pH was adjusted to 3 using IN aqueous HCl and was then extracted with EtOAc (4 x 50 mL portions). The combined extracts were dried (MgSO₄) and concentrated to afford Example 18, 1- methoxy-methylcyclopropylsulfonylamine tert-butylcarbamate, as a waxy solid (1.20 g, 100%) which was taken directly into the next reaction without further purification: 1H NMR (CDC1₃) δ 1.03 (m, 2 H), 1.52 (s, 9 H), 1.66 (m, 2H), 3.38 (s, 3 H), 3.68 (s, 2 H), 7.54 (s,,l H); ¹³C NMR (CDC1₃) δ 11.37, 28.29, 40.38, 58.94, 73.43, 83.61, 149.57.

Step 15IIe: Preparation of Example 15, 1-methoxy-methylcyclopropy- sulfonamide.

Step 15IIe) A solution of 1-methoxy-methylcycloρropylsulfonylamine tert-butylcarbamate (1.14 g, 4.30 mmol) was dissolved in a solution of 50%TFA CH₂C1₂ (30 mL) and was stirred stirred at rt for 16 h. The solvent was removed in vacuo and the residue chromatographed over 80g of SiO₂ (eluting with 0% to 60% EtOAC Hexanes to afford Example 15, 1- methoxymethylcyclopropylsulfonamide, as a white solid (0.55 g, 77% overall over two steps): 1H NMR (CDC1₃) δ 0.95 (m, 2 H), 1.44 (m, 2 H), 3.36 (s, 3 H), 3.65 (s, 2 H), 4.85 (s, 2 H); ¹³C NMR (CDC1₃) δ 11.17, 40.87, 59.23, 74.80; LRMS m/z 183 (M⁺+NH-).

Q ^H

V^NvV

^C ϊ ^

Step 16IId: Preparation of l-cyclopropylmethylcyclo-propylsulfonylamine tert-butylcarbamate.

Step 16IId) This compound, 1-cyclopropyl- methylcyclopropylsulfonylamine tert-butylcarbamate, was obtained in 92% yield according to the procedure described in the synthesis of 1-methoxymethylcyclo- propylsulfonylamine tert-butylcarbamate (Step 15IId) except 1.10 equivalents of cyclopropylmethyl bromide were used as electrophile. The compound was taken directly into the next reaction without purification: 1H NMR (CDC1₃) δ 0.10 (m, 2 H), 0.51 (m, 2 H), 0.67 (m, 1 H), 1.10 (m, 2 H), 1.49 (s, 9 H), 1.62 (m, 2 H), 1.87 (d, 7=7.0 Hz, 2 H).

Steps 16IIe: Preparation of Example 16, l-cyclopropylmethyl- cyclopropylsulfonamide. Step 16IId) This compound, Example 16, 1- cyclopropylmethylcyclopropylsulfonamide, was obtained in 65% yield from 1- cyclopropylmethylcyclo-propylsulfonylamine tert-butylcarbamate (from step 16IId) according to the procedure described for the synthesis of 1- Methoxymethylcyclopropylsulfonamide (step 15IIe). The compound was purified by column chromotography over SiO₂ using 0% to 60% EtOAc in

Hexanes as the eluent: 1H NMR (CDC1₃) δ 0.15 (m, 2 H), 0.51 (m, 2 H), 1.01 (m, 2 H), 1.34 (m, 3 H), 1.86 (d, 7=7.0 Hz, 2 H), 4.83 (s, 2 H); ¹³C NMR (CDC1₃) δ 4.65, 7.74, 11.26, 35.62, 41.21; LRMS m/z 193 (M'+NEU).

Step 17IId: Preparation of 1-propylcarbamoylcyclopro-panesulfonamide ter.-butylcarbamate. Step 17IId) This compound, 1-propylcar- bamoylcyclopropanesulfonamide tert-butylcarbamate, was obtained in a crude 100% yield according to the procedure described for the synthesis of l- methoxymethylcyclopropylsulfonylamine tert-butyl-carbamate (Step 15IId) except that 1.10 equivalents of n-propyl isocyanate was used as the electrophile. The compound was taken directly into the next reaction without purification: 1H NMR (CDC1₃) δ 0.10 (m, 2 H), 0.51 (m, 2 H), 0.67 (m, 1 H), 1.10 (m, 2 H), 1.49 (s, 9 H), 1.62 (m, 2 H), 1.87 (d, 7=7.0 Hz, 2 H).

Steps 17IIe: Preparation of Example 17, 1-propylcarbamoylcyclopropane- sulfonamide.

Step 17IIe) This compound, Example 17, 1- propylcarbamoylcyclopropanesulfonamide, was obtained in an optimized 50% yield from 1-propylcar-bamoylcyclopropanesulfonamide tert-butylcarbamate (from step 17IId) according to the procedure described for the synthesis of 1- Methoxymethylcyclopropylsulfonamide (step 15IIe), except that no chromatography was used as the material was recrystallized from the minimum amount of CH₂C1₂/Hexanes: 1H NMR (CDC1₃) δ 0.15 (m, 2 H), 0.51 (m, 2 H), 1.01 (m, 2 H), 1.34 (m, 3 H), 1.86 (d, 7=7.0 Hz, 2 H), 4.83 (s, 2 H); ¹³C NMR (CDCI3) δ 4.65, 7.74, 11.26, 35.62, 41.21; LRMS m/z 193 ( NH^*).

Step 18IId: Preparation of l-(3,5-dimethylisoxazol-4-yl)carbamoyl- cyclopropanesulfonairύde tertf-butylcar-bamate. Step 18IId) This compound, l-(3,5-dimethylisoxazol-4- yl)carbamoylcyclopropanesulfonamide tert-butylcarbamate, was obtained in a crude 100% yield according to the procedure described for the synthesis of l- methoxymethylcyclopropylsulfonylamine tert-butylcarbamate (Step 15IId) except that 1.20 equivalents of 3,5-dimethylisoxazole-4-isocyanate was used as the electrophile. The compound was taken directly into the next reaction without purification.

Steps 18IIe: Preparation of Example 18, l-(3,5-dimethylisoxazol- 4yl)carbamoylcyclopropanesulfonamide.

Step 18IIe) This compound, Example 18, l-(3,5-dimethylisoxazol- 4yl)carbamoylcyclopropanesulfonamide, was obtained in 50% yield (580 mg) from 1.62g (4.52 mmol) of l-(3,5-dimethylisoxazol-4-yl)carbamoylcyclo- propanesulfonamide tert-butylcarbamate using 30 mL (120 mmol) of 4N HCl/dioxanes, stirring overnite, concentration and chromatography over a Biotage 40M column (eluting with 0% to 5% MeOH/CH₂Cl₂: 1H NMR (methanol-d-) δ 1.57 (m, 2 H), 1.61 (m 2 H), 2.15 (s, 3 H), 2.30 (s, 3 H), 4.84 (s, 3 H); ¹³C NMR (methanol-d₄) δ 9.65, 10.94, 15.01, 46.11, 114.82, 159.45, 165.55, 168.15; LRMS m/z 260 (M⁺+H).

(>95%)

(Array Biopharma)

R=tBu (from step la) or or tBu R= BOC (from Step Mb ii) TFA

(>95%)

General Processes For The Preparation of Unsubstituted Cyclopropylsulfonamide (Method A or Method B) Method A: To a solution of 100 mL of THF cooled to 0 °C was bubbled in gaseous ammonia until saturation was reached. To this solution was added a solution of 5 g (28.45 mmol) of cyclopropylsulfonyl chloride (purchased from Array Biopharma) in 50 mL of THF, the solution warmed to rt overnite and stirred one additional day. The mixture was concentrated until 1-2 mL of solvent remained, applied onto 30 g plug of SiO₂ (eluted with 30% to 60%

EtOAc/Hexanes) to afford 3.45g (100%) of cyclopropylsulfonamide as a white solid.

Method B, Step i (R=tBu) A solution of rc-BuLi (86.7 mL, 138.8 mmol, 1.6 M in hexane) was dissolved in dry THF (120 mL) and cooled to -78 °C under a Argon atmosphere. To this solution was added a solution of N-tert-

Butyl-(3-chloro)propylsulfonamide from Step la (14.5 g, 67.8 mmol) in dry THF (160 mL) slowly dropwise over 60 min. The dry ice bath was removed and the reaction mixture was allowed to warm to rt over a period of 2 h. The reaction mixture was quenched with glacial AcOH (3.4 mL), concentrated in vacuo, and partitioned between CH₂C1₂ (100 mL) and water (100 mL). The organic phase was washed with aqueous IN NaOH (150 mL), brine (100 mL), dried (MgSO ), and concentrated in vacuo to afford the N-tert-Butyl cyclopropylsulfonamide as a waxy offwhite solid (12 g, 100%): 1HNMR (CDC1₃) δ 0.98 (m, 2H), 1.17 (m,

2H), 1.38 (s, 9H), 2.45 (m, IH), 4.45 (bs, IH). ¹³C NMR (CDC1₃) δ 6.5, 30.6,

33.5, 54.2. MS (ESI) 176 (M⁺-H).

Method B, Step ii (R=tBu to H) A yield >95% was routinely obtained of cyclopropylsulfonamide following the same TFA deprotection procedure used in step 3Id, except that of N-tert-Butyl cyclopropylsulfonamide was used in place of

N-tert-Butyl-(l-methyl)cyclopropyl-sulfonamide.

Method B, Step i same as Step lie (R=BOC) The preparation of cyclopropylsulfonylamine tert-butyl carbamate from 3- chloropropylsulfonylamine tert-butylcarbamate is described already in Step lie

(100%).

Method B, Step ii (R=BOC to R=H) The preparation of cyclopropylsulfonylamine tert-butyl carbamate. A yield >95% was routinely obtained of cyclopropylsulfonamide following the same TFA deprotection procedure used in step 31d, except that of cyclopropylsulfonylamine tert-butyl carbamate was used in place of N-tert-Butyl-(l-methyl)cyclopropyl-sulfonamide.

Data for cyclopropylsulfonamide: 1H ΝMR (methanol-d ) δ 0.94-1.07 (m, 4H),

2.52-2.60 (m, IH); 1H ΝMR (DMSO-dβ) δ 0.88 (m, 2H), 0.92 (m, 2H), 2.47 (m,

IH), 6.70 (bs, 2H); ¹³C ΝMR (methanol-d-) δ 5.92, 33.01; ¹³C ΝMR (DMSO-d₆) δ 4.85, 31.80. Anal. Calcd. For C₃H₇ΝO₂S: C, 29.74; H, 5.82; N, 11.56. Found:

C, 29.99; H, 5.89, N, 11.50.

Alternative Preparation of Product of Step lie

Alternative Preparation Of The Product of Step lie: Cyclopropylsulfonylamine fert-butyl carbamate

Step ii) To a solution of cyclopropylsulfonamide (6.0 g, 50.0 mmol) in CH₂C1₂ (50 mL) was added BOC₂O (13.0 g, 59.0 mmol), Et₃N (7.5 mL, 74 mmol), and 4-DMAP (0.30 g, 2.5 mmol). The reaction mixture was stirred overnite at rt, diluted with EtOAc (300 mL), partitioned with 1 N HCl (3 x 100 mL), dried over MgSO₄ and concentrated in vacuo to afford 9.3g (85%) of cyclopropylsulfonylamine tert-butylcarbamate as a white solid having identical data to its preparation in Step He.

Compound 7, Example 19 Compound 7, Example 19, BOCNH-P3(L-.-BuGly)-P2[(4__)-(2-phenyl-7- methoxyquinoline-4-oxo)-S-proline]-Pl(lR,25 Vinyl Acca)-CONHSO₂(l- methoxymethyl-cyclopropan-1-yl) or alternate designation, Compound 7, the (1R,25) PI isomer of {l-[2-[l-(l-

MethoxymethylcyclopropanesulfonylaminocarbonyI)-2- vinylcycIopropylcarbamoyl]-4-(7-methoxy-2-phenyl-quinolin-4- yloxy)pyrrolidine-l-carbonyI]-2,2-dimeth-ylpropyI}-carbamic acid tert-butyl ester.

Step 19f) This compound was prepared in 63.4% yield from the tripeptide acid product of step 2e (Example 2) in analogous fashion to the procedure of Example 9 except that 1-methoxymethylcyclopropanesulfonamide (prepared in Example 15) was used in place of 1-methylcyclopropanesulfonamide: 1H NMR (methanol- ) D 0.94-1.11 (m, IH), 1.05 (s, 9H), 1.28 (s, 9H), 1.38-1.66 (m, 3H), 1.78-1.87 (m, 2H), 1.97-2.00 (m, IH), 2.17-2.36 (m, 2H), 2.63-2.71 (m, IH), 3.94 (s, 3H), 4.08 (d, 7=10 Hz, IH), 4.24-4.27 (m, IH), 4.52-4.57 (m, 2H), 5.09 (d, 7=11 Hz, IH), 5.22-5.31 (m, IH), 5.56 (m, IH), 5.71-5.86 (m, IH), 7.07 (d, 7=9, 2 Hz, IH), 7.25 (s, IH), 7.38 (d, 7=2 Hz, IH), 7.47-7.57 (m, 3H), 8.04- 8.12 (m, 3H). HRMS m/z (M-H) calcd for C₄₃H₅₄N₅O₁₀S: 832.3591, found: 832.3592. LC-MS (retention time: 1.61, Method A), MS m/z 833 (MM).

Compound 8, Example 20 Compound 8, Example 20, BOCNH-P3(L-t-BuGIy)-P2[(4R)-(2-phenyI-7- methoxyquinoline-4-oxo)-5-proline]-Pl(lR,25 Vinyl Acca)-CONHSO₂(l- cyclopropylmethyl-cyclopropan-1-yl) or alternate designation, Compound 8, the (1R,25) PI isomer of {l-[2-[l-(l-Cyclopropylmethyl- cyclopropanesulfonylaminocarbonyl)-2-vinyl-cyclopropylcarbamoyl]-4-(7- methoxy-2-phenyl-quinoIin-4-yloxy)-pyrrolidine-l-carbon l]-2,2-dime- thylpropyl}-carbamic acid tert-butyl ester.

Step 20f) This compound was prepared in 71% yield from the tripeptide acid product of step 2e (Example 2) in analogous fashion to the procedure of Example 9 except that 1-cyclopropylmethylcyclopropanesulfonamide (prepared in Example 16) was used in place of 1-methylcyclopropanesulfonamide: 1H NMR (methanol-d-) D 0.00-0.14 (m, 2H), 0.38-0.53 (m, 2H), 0.61-0.74 (m, IH), 0.83- 1.65 (m, 5H), 1.04 (s, 9H), 1.28 (s, 9H), 1.72-1.96 (m, 3 H), 2.18-2.40 (m, 2H), 2.63-2.73 (m, IH), 3.95 (s, 3H), 4.10 (d, 7=10 Hz, IH), 4.26 (d, 7=9 Hz, IH), 4.46-4.59 (m, 2H), 5.09 (d, 7=11 Hz, IH), 5.23-5.33 (m, IH), 5.57 (m, IH), 5.65- 5.77 (m, IH), 7.08 (dd, 7=9, 2 Hz, IH), 7.25 (s, IH), 7.39 (d, 7= 2 Hz, IH), 7.47- 7.57 (m, 3H), 8.04-8.09 (m, 3H). HRMS m/z (M-H) calcd for C₄₅H₅₆N₅O₉S:

844.3955, found: 844.3804. LC-MS (retention time: 1.76, Method I), MS m/z 844 (M⁺+l).

Compound 9, Example 21 Compound 9, Example 21, BOCNH-P3( -^-BuGly)-P2[(4__)-(2-phenyl-7- methoxyquinoline-4-oxo)-5-proline]-Pl(lR,25 Vinyl Acca)-CONHSO₂(l- propylcarbamoyl-cyclopropan-1-yi) or alternate designation, Compound 9, the (1R,25) PI isomer of (l-{4-(7-Methoxy-2-phenylquinolin-4-yloxy)-2-[l-(l- propylcarbamoyl-cyclopropanesulfonylaminocarbonyl)-2-vinylcyclopro- pylcarbamoyl]pyrrolidine-l-carbonyl}-2,2-dimethyl-propyl)carbamic acid tert-butyl ester.

Step 21f) This compound was prepared in 59% yield from the tripeptide acid product of step 2e (Example 2) in analogous fashion to the procedure of Example 9 except that 1-propylcarbamoylcyclopropanesulfonamide (prepared in Example 17) was used in place of 1-methylcyclopropanesulfonamide: 1H NMR (methanol-d₄) D 0.89-0.96 (m, 3H), 1.05 (s, 9H), 1.21 (s, 9H), 1.29-1.85 (m,

8H), 2.20-2.30 (m, IH), 2.42-2.54 (m, IH), 2.76-2.83 (m, IH), 3.14-3.25 (m, 2H), 4.05 (s, 3H), 4.10-4.18 (m, 2H), 4.60-4.71 (m, 2H), 5.10-5.15 (m, IH), 5.23-5.33 (m, IH), 5.58-5.71 (m, IH), 5.83 (m, IH), 7.36 (dd, 7=9, 2.2 Hz, IH), 7.54 (d, 7=2.2 Hz, IH), 7.63 (s, IH), 7.68-7.77 (m, 3H), 8.07-8.10 (m, 2H), 8.34 (d, 7=9 Hz, IH). HRMS m/z (M-H) calcd for C₄₅H₅₇N₅O₁₀S: 873.3857, found: 873.3895. LC-MS (retention time: 1.69, Method I), MS m/z 875 (M^+l).

Compound 10, Example 22 Compound 10, Example 22, BOCNH-P3(L-.-BuGly)-P2[(4RM2-phenyl-7- methoxyquinoIine-4-oxo)-5-proline]-Pl(lR,25 Vinyl Acca)-CONHSO₂(l- propylcarbamoyl-cyclopropan-1-yl) or alternate designation, Compound 10, the (1R,25) PI isomer of {l-[2-{l-[l-(3,5-Dimethylisoxazql-4- ylcarbamoyl)cyclopropanesul-fonylaminocarbonyl]-2- vinylcyclopropylcarbamoyl}-4-(7-methoxy-2-phenyIquinolin-4- yloxy)pyrrolidine-l-carbon-yl]-2,2-dimethylpropyl}carbamicacid tert-butyl ester.

Step 22f) This compound was prepared in 53% yield from the tripeptide acid product of step 2e (Example 2) in analogous fashion to the procedure of Example 9 except that l-(3,5-Dimethylisoxazol-4-ylcarbamoyl)cycloρro- panesulfonamide (prepared in Example 18) was used in place of 1- methylcyclopropanesulfonamide: 1H NMR (methanol-cLi.) δ 0.98 (s, 9H), 1.01 (m, IH), 1.27-1.41 (m, 2H), 1.30 (s, 9H), 1.43-1.49 (m, IH), 1.54-1.59 (m, IH), 1.61-1.67 (m, 2H), 2.04-2.09 (m IH), 2.14, 2.16 (2s, 3H), 2.29 (s, 3H), 2.46-2.51 (m, IH), 2.68 (dd, J=14, 8 Hz, IH), 3.83-3.86 (m, IH), 3.93 (s, 3H), 4.20-4.24 (m, IH), 4.46 (d, J=12 Hz, IH), 4.51-4.54 (m, IH), 4.92-4.95 (m, IH), 5.11-5.18 (m, IH), 5.44 (m, IH), 5.84-5.99 (m, IH), 7.02-7.04 (m, IH), 7.20-7.25 (m, IH), 7.36-7.38 (m, IH), 7.47-7.55 (m, 3H), 8.05-8.09 (m, 3H). HRMS m z (M-H) calcd for C₄₇H₅₆N₇OπS: 926.3786, found: 926.3777. LC (retention time: 1.35, Method I). Method III (Steps IHa-IIIb). Formation of Example 23, 1- Bromocyclopropanesulfonamide:

. Ilia) S0₂CI₂, PhH, hv Br O

D -^{Br ►} // lllb) NH₃, THF t H NH₂

Step Ilia: Formation of 1-Bromocyclopropanesulfonyl choride:

Br O

CI o Step Ilia) Cyclopropyl bromide (lOmL, 125 mmol) was dissolved in benzene (11.2 mL). To this solution was added 2 drops of pyridine. The resulting mixture was stirred and irradiated with a 250W lamp, two inches from the flask while sulfuryl chloride (5.0 mL, 62.4 mmol) was added dropwise over 14 minutes. After 15 addition minutes of stirring with irradiation, the reaction was concentrated in vacuo. Upon standing for one hour, crystals formed which were filtered off and discarded. The residual oil was then distilled under high vacuum (60°C, 0.05mm) to yield the titled product 1.18g (4.3%) as a yellow oil: 1H NMR (CDC1₃,) δ 1.73 (2H, t), 2.15 (2H, t): ¹³C NMR (CDC1₃) 49.1, 20.3.

Step IHb: Formation of Example 23, 1-Bromocyclopropanesulfonamide:

Br O P II NH₂ O

Step Hlb) 1-Bromocyclopropanesulfonyl chloride (0.9g, 4.10 mmol) was dissolved in 15 mL of THF saturated with NH₃. The solution was stirred overnight and then the NH-C1 was filtered away. The filtrate was concentrated to yield Example 23, 1-Bromocyclopropanesulfonamide, 980 mgs (91%) as a tan solid: 1H NMR (acetone-dg) δ 1.70 (2H, t), 1.41 (2H, t). MS m/z 201 (M+H). Compound 11, Example 24 Preparation of Compound 11, Example 24, BocNH-P3(.-BuGly)-P2[(4RM2- phenyl-7-methoxyquinoline-4-oxo)-S-proline]-Pl(lR,2S Vinyl Acca)- CONHSO₂(l -bromo- cyclopropan-1-yl) or alternate designation, Compound 11, the (1R,25) PI isomer of {l-[2-[l-(l-Bromocyclopropanes- ulfonylaminocarbonyl)-2-vinylcy-clopropylcarbamoyI]-4-(7-methoxy-2- phenylquinoIin-4-yloxy)pyrrolidine-l-carbonyl]-2,2-dimethylpropyl}- carbamic acid tert-butyl ester:

Step 24f) The Product of Example 2 (Step 2e), BocNH-P3(t-BuGly)- P2[(4R)-(2-phenyl-7-methoxyquin-oline-4-oxo)-S-proline)]-Pl(l_.,2S Vinyl Acca)-OH (18 mgs, 0.026 mmol) was dissolved in 500 μ L THF. To this solution was added DBU (8 μL, 0.052 mmol) and CDI (6 mgs, 0.034 mmol. The resulting mixture was refluxed for 40 minutes and cooled to room temperature. 1- bromocyclopropanesulfonamide (13 mgs, 0.066 mmol) prepared in Example 23 using Method III (Steps a-b), was then added and the solution brought to reflux for 24 hours. After cooling, the solution was diluted with ethyl acetate, washed with IN HCl and brine and dried over Na₂SO₄. The volatiles were removed in vacuo. The product was purified by a Biotage 40M silica column eluting with 95: 5 ethyl acetate: methanol to yield Compound 11, Example 24, 19 mgs (83%) as a white solid: 1H NMR (methanol-c ) δ 8.03-8.09 (m, 3H), 7.48-7.54 (m, 3H), 7.37 (m, IH), 7.25 (s, IH), 7.07 (m, IH), 6.57 (d, IH, 7=8.9 Hz), 5.99 (m, IH), 5.54 (bs, IH), 5.21 (m, IH), 5.02 (d, IH, 7=10.4 Hz), 4.50-4.58 (m, IH), 4.24 (m, IH), 4.11 (m, IH), 3.93 (s, IH), 2.72 (m, IH), 2.55 (m, IH), 2.12 (m, IH), 1.73-1.81 (m, 3H), 1.45 (m, IH), 1.31-1.36 (m, 2H), 1.27 (s, 9H), 1.04 (s, 9H), 0.91 (m, 2H). MS m/z 868.47 (M+H).

Compound 12, Example 25 Compound 12, Example 25, (cyclopentyl-O(C=O)NH-P3(L-^-BuGly)- P2[(4R)-(2-phenyl-7-methoxyquinoline-4-oxo)-5-proline]-Pl(lR,25 Vinyl Acca)-CONHSO₂(l-methyl-l-cyclopropane) or alternate designation, Compound 12, the (1R,25) PI isomer of (l-{4-(7-Methoxy-2-phenyl-quinolin- 4-yIoxy)-2-[l-(l-methylcycIopropanesulfonyl-an_inocarbonyl)-2-vinyl- cycIopropyIcarbamoyl]-pyrrolidine-l-carbonyI}-2,2- dimethylpropyl)carbamic acid cyclopentyl ester.

Preparation of cyclopentyl Chloroformate

This procedure was used for the preparation of non- commercially available chloroformates. To a solution of (5.8g, 67.6 mmol) of commercially available (Aldrich) reagents of cyclopentanol and pyridine (5.8 mL; 72 mmol) in THF (150 mL) cooled to 0 °C was added a 1.93 M solution of phosgene in toluene (48 mL, 92.6 mmol over 10 min under argon. The resulting solution was allowed to warm to rt over 2 h, the resulting solid filtered, and the mother liquor carefully concentrated in vacuo at room temperature until theoretical mass was obtained. The resulting residue was dissolved in 100 mL of THF to prepare a 0.68M stock solution of cyclopentyl chloroformate that could be stored in the freezer until use. In analogous fashion, other commercially available alcohols could be converted to 0.68M stock solutions of the corresponding chloroformates.

Step 25g) A solution of 172 mg (0.214 mmol)of the product of Step 2f, (1R,2S) PI diastereomer of (l-{4-(7-Methoxy-2-phenylquinolin-4-yloxy)-2-[l- (l-methyl-cyclopropanesulfonylaminocarbonyl)-2-vinylcyclo- ropylcarbamoyl]pyrrolidine-l-carbonyl}-2,2-dimethyl-propyl)carbamic acid tert- butyl ester was treated with 8mL (32 mmol) of 4N HCl in dioxane for 2 h and then concentrated in vacuo to afford 168 mg of the Bis HCl product. LC-MS (retention time: 1.23, Method A (hold time changed from 2 min to 3 min), MS m/z 704 (M⁺+1).

Step 25h) To a slurry of 80 mg (0.103 mmol) of the Bis HCl salt product of Step 25g and 67 mg (0.52 mmol) of DIPEA in 2 mL of CH₂C1₂, was added 0.34 mL (0.24 mmol) of a 0.68M solution of cyclopentyl chloroformate, and the mixture stirred overnite. MeOH was added and the mixture concentrated. The crude was then resubjected to reaction conditions and MeOH added to quench. The mixture was concentrated in vacuo and the residue chromatographed over two lOOOμ PTLC plates from Analtech (each 20X40 cm, eluted sequentially with 0% to 3% MeOH in CH₂C1₂) to afford 40 mg (48%) of the desired P4 carbamate, Compound 12, Example 25, the (1R,2S) PI isomer of (l-{4-(7-Methoxy-2- phenyl-quinolin-4-yloxy)-2-[l-(l -methylcyclopropanesulfonyl-aminocarbonyl)- 2-vinylcyclopropylcarbamoyl]-pyrrolidine-l-carbonyl}-2,2- dimethylpropyl)carbamic acid cyclopentyl ester: ^!H NMR (methanol-α^) δ 0.63- 0.80 (m, 2H), 0.87-0.95 (m, 2H), 1.02 (s, 9H), 1.10-1.85 (m, 13H), 2.06-2.17 (m, IH), 2.41-2.57 (m, IH), 2.68-2.77 (m, IH), 3.92, 3.93 (two s, 3H), 3.99-4.12 (m, IH), 4.28 (s, IH), 4.45-4.50 (m, IH), 4.56-4.61 (m, IH), 4.67-4.74 (m, IH),

4.94-5.06 (m, IH), 5.20 (d, 7=17 Hz, IH), 5.53 (m, IH), 5.82-6.05 (m, IH), 7.06 (dd, 7=9, 2 Hz, IH), 7.23 (m, IH), 7.37-7.38 (m, IH), 7.46-7.54 (m, 3H), 8.04- 8.08 (m, 3H).

Compound 13 Example 26 Preparation of P4(cyclopropylCH₂(C=O)NH)-P3(L-^-BuGly)-P2[(4R)-(2- phenyl-7-methoxyquinoline-4-oxo)-S-proline]-Pl(l_-,25 Vinyl Acca)-

CONHSO₂(l-methyl-l-cyclopropane) or alternate designation, Compound 13 the (1R,25) PI isomer of l-[2-(2-Cyclopropyl-acetyIamino)-3,3-dimethyl- butyryl]-4-(7-methoxy-2-phenylquinolin-4-yloxy)-pyrrolidine-2-carboxyIic acid [l-(l-methylcyclopropanesulfonylaminocarbonyl)-2- vinylcyclopropyl]amide.

Step 26h) To a slurry of 80 mg (0.103 mmol) of the Bis HCl salt product of Step 25g, 19 mg (0.12 mmol) of HOBT.H₂O, 12.4 mg (0.124 mmol) of cyclopropyl acetic acid (Aldrich) and 67 mg (0.52 mmol) of DIPEA in 2 mL of CH₂C1₂, was added 47 mg (0.124 mmol) of HATU, and the mixture stirred overnite. The mixture was concentrated in vacuo and the residue chromatographed over two lOOOμ PTLC plates from Analtech (each 20X40 cm, eluted sequentially with 0% to 3% MeOH in CH₂C1₂) to afford 51 mg (63%) of the desired P4 carbamate, Compound 13, Example 26, the (1R,2S) PI isomer of l-[2-(2-Cyclopropylacetylamino)-3,3-dimethyl-butyryl]-4-(7-methoxy-2-phenyl- quinolin-4-yloxy)-pyrrolidine-2-carboxylic acid [1-(1- methylcyclopropanesulfonylaminocarbonyl)-2-vinylcyclopropyl] amide: 1H NMR (methanol-d*) δ 0.09-0.13 (m, 2H), 0.39-0.46 (m, 2H), 0.74-0.98 (m, 5H), 1.06 (s, 9H), 1.34-1.39 (m, IH), 1.84 (dd, 7=7.9, 5.2 Hz, IH), 1.98-2.03 (m, IH), 2.13- 2.20 (m, IH), 2.36-2.48 (m, IH), 2.66-2.75 (m, IH), 3.94 (s, 3H), 4.08-4.16 (m, IH), 4.42-4.46 (m, IH), 4.54-4.59 (m, 2H), 4.63-4.66 (m, IH), 5.03-5.08 (m, IH), 5.23-5.27 (m, IH), 5.56 (m, IH), 5.76-5.84 (m, IH), 7.08-7.10 (m, IH), 7.23-7.25 (m, IH), 7.30 (d, 7=2 Hz, IH), 7.47-7.55 (m, 3H), 8.01-8.06 (m, 3H). Section B

The following columns and conditions were used in the Examples cited in

Section B.

Columns: (Method A) - YMC ODS S7 C18 3.0x50 mm (Method B) - YMC ODS-A S7 C18 3.0x50 mm (Method C) - YMC S7 C18 3.0x50 mm (Method D) - YMC Xterra ODS S7 3.0x50 mm (Method E) - YMC Xterra ODS S7 3.0x50 mm (Method F) - YMC ODS-A S7 C18 3.0x50 mm

(Method H), - Xterra S7 3.0x50 mm (Method I) - Xterra S7 C18 3.0x50 mm (Method G) - YMC C18 S5 4.6x50 mm (Method J) - Xterra ODS S7 3.0x50 mm (Method K) - YMC ODS-A S7 C18 3.0x50 mm

(Method L) - Xterra ODS S7 3.0x50 mm (Method M) - Xterra ODS S5 3.0x50 mm (Method N) - Xterra C-18 S5 4.6x50 mm

Gradient: 100% Solvent A/0% Solvent B to

0% Solvent A/100% Solvent B

Gradient time: 2 min. (A, B, D, F, G, H, I, L); 8 min. (C, E); 4 min (J); 3 min (K)

Hold time: 1 min. (A, B, D, F, G, H, I, J, K, L, N); 2 min. (C, E)

Flow rate: 5 mL/min (A, B, C, D, E, F, G) Flow rate: 4 mL/min (J, K, N)

Detector Wavelength: 220 nm

Solvent A: 10% MeOH / 90% H₂O / 0.1% TFA

Solvent B: 10% H₂O / 90% MeOH / 0.1% TFA. Compound 27 Example 27

compound 27

Compound 27, Example 27, BOCNH-P3(L-t-BuGly)-P2[(4R)-(2-phenyl-7- methoxyquinoline-4-oxo)-S-proline]-Pl(lR,2S Vinyl Acca)-CONHSO₂(l- trimethylsilanylcyclopropan-1-yl) or alternate designation, Compound 27, example 27, {l-[2-[2-Ethyl-l-(l-trimethylsilanyl- cyclopropanesulfonylaminocarbonyl)-cyclopropylcarbamoyl]-4-(7-methoxy- 2-phenyI-quinolin-4-yloxy)-pyrrolidine-l-carbonyl]-2,2-dimethyl-propyl}- carbamic acid tert-butyl ester

Step 27a: N-tert-Butyl-(l-trimethylsilanyl)cvclopropylsulfonamide o ^H

(HsC'aSi^ST ^ Δ ° compound 27a

Step 27a) This compound was obtained in 84% yield from N-tert-Butyl-(3- chloro) propylsulfonamide according to the procedure of Steps 3Ib-3Ic (Example 2) described in the synthesis of Ν-tert-Butyl-(l-methyl) cyclopropylsulfonamide and 2.0 equivalents of trimethylsilyl chloride was used 4sed as electrophile. The compound was used as crude.

Step 27b: Preparation of (l-trimethylsilanyl)cvclopropylsulfonamide

°^*- -NH,

Δ ° compound 27b

Step 27b) This compound was obtained in 73% yield from N-tert-butyl- (l-trimethylsilanyl)cyclopropylsulfonamide according to the procedure of Steps 3Id (Example 2) described in the synthesis of 1-methylcyclopropylsulfonamide. The compound was recrystallized from EtOAc/hexanes: 1H NMR (CHLOROFORM-D) δ ppm 0.17 (s, 9 H), 0.91 (m, 2 H), 1.33 (m, 2 H), 4.47 (s, 2 H).

Step 27c: Preparation of Comppound 27. example 27. BOCNH-P3(L-t-BuGlv)-

P2r(4_-)-(2-phenyl-7-methoxyquinoline-4-oxo)-S-proline]-Pl(l_..2S Vinyl Acca -

CONHSO^fl-trimethylsilanyl-cvclopropan-l-yl) or alternate designation.

Compound 27. example 27. ( l-r2-r2-Ethyl-l-(l-trimethylsilanyl- cyclopropanesulfonylaminocarbonyl)-cvclopropylcarbamoyl]-4-(7-methoxy-2- phenyl-quinolin-4-yloxy)-pyrrolidine- 1 -carbonyl] -2,2-dimethyl-propyl I -carbamic acid tert-butyl ester

compound 1₄

Step 27c) To a solution of the tripeptide acid (0.080 g, 0.116 mmol) of the product of step 2e (Example 2) in THF (2 mL) was added CDI (0.0264 g, 0.16 mmol), and the resulting solution was heated at 72 °C for 1 h and allowed to cool down to rt. 1-Trimethylsilanylcyclopropylsulfonamide (0.027g, 0.14 mmol) and neat DBU (0.024 mL, 0.16 mmol) were added. The reaction mixture was stirred for 16 h, diluted with EtOAc (150 mL) and washed pH 4.0 buffer (2x30 mL), dried (Na₂SO₄ MgSO₄), concentrated. The residue was purified over 20X40 cM 1000 D Analtech PTLC plates (MeOHyCH₂Cl₂: 2 to 4%) to afford the desired product (Compound 27) 0.0811 g (88%) as a white foam: 1H NMR (CDCl₃/methanol-04) D ppm 0.12 (s, 9 H), 1.04 (m, 24 H), 1.76 (m, 1 H), 1.98 (m, 1 H), 2.59 (m, 1 H), 3.90 (s, 3 H), 4.03 (m, 1 H), 4.25 (d, 7=4.88 Hz, 1 H), 4.43 (d, 7=11.29 Hz, 1 H), 4.58 (s, 1 H), 4.96 (s, 1 H), 5.12 (m, 1 H), 5.34 (s, 1 H), 5.84 (m, 1 H), 7.02 (m, 2 H), 7.36 (m, 1 H), 7.46 (m, 3 H), 7.95 (m, 3 H). HRMS m/z (M+H)⁺ calcd for GwHeoNsSSiO.,: 862.3881 found: 862.3888. LC- MS (retention time: 1.78, Method I), MS m/z 862(M⁺+1).

Compound 28 Example 28

I compound 28

Step 28a: Preparation of N-tert-Butyl-l-ethyl-cyclopropylsulfonamide o ^H

compound 28a

Step 28a) This compound was prepared form N-tert-Butyl-(3-chloro) propyl sulfonamide (59 g, 276 mmol) and ethyl iodide (86.11 g, 552 mmol) according to the procedure of Steps 3Ib-3Ic (Example 2) described in the synthesis of Ν-tert-Butyl-(l-methyl) cyclopropylsulfonamide. The compound was used as crude: 1H NMR (CHLOROFORM-D) D ppm 0.82 (m, 2 H), 0.99 (t, 7=7.48 Hz, 3 H), 1.33 (m, 11 H), 1.92 (q, 7=7.53 Hz, 2 H), 3.91 (s, 1 H). Step 28b: Preparation l-ethyl-cyclopropylsulfonamide

compound 28b

Step 28b) This compound was obtained in 49% yield (19 g) in two steps according to the procedure of Steps 3Id (Example 2) described in the synthesis of 1-methylcyclopropylsulfonamide. The compound was recrystallized from EtOAc/hexanes as a white solid: 1H NMR (CHLOROFORM-D) δ ppm 0.85 (m, 2 H), 1.03 (t, 7=7.48 Hz, 3 H), 1.34 (m, 2 H), 1.96 (q, 7=7.32 Hz, 2 H), 4.61 (s, 2 H).

Step 28c: Preparation of compound 28, Example 28, BOCNH-P3(L-t-BuGlv)-

P2r(4_,)-(2-phenyl-7-methoxyquinoline-4-oxo)-S-prolinel-Pl (1R,2S Vinyl Acca)-

CONHSO^d-ethyl-cvclopropan-l-yl) or alternate designation Compound 28, example 28, I l-r2-r2-Ethyl-l-(l-ethyl-cvclopropanesulfonylaminocarbonyl)- cvclopropylcarbamoyl1-4-(7-methoxy-2-phenyl-quinolin-4-yloxy)-pyrrolidine-l- carbonvH-2,2-dimethyl-propyl}-carbamic acid tert-butyl ester

compound 28

Step 28c) Compound 28 was prepared in 63% yield (0.1878 g) from tripeptide acid (0.25 g, 0.36, mmol) of the product of step 2e (Example 2) in analogous fashion to the procedure of Step 27c of Example 27 except that 1- ethyl-cyclopropanesulfonic acid amide was used in place of 1-trimethylsilanyl- cyclopropanesulfonamide: 1H NMR (methanol-d ) D ppm 0.91 (m, 2 H), 0.96 (t, 7=7.48 Hz, 3 H), 1.04 (s, 9 H), 1.27 (s, 9 H), 1.47 (m, 3 H), 1.83 (m, 2 H), 1.95 (m, 1 H), 2.26 (m, 2 H), 2.67 (m, 1 H), 3.94 (s, 3 H), 4.08 (d, 7=10.38 Hz, 1 H), 4.24 (dd, 7=16.79, 9.16 Hz, 1 H), 4.52 (m, 2 H), 5.10 (m, 1 H), 5.28 (m, 1 H), 5.53 (s, 1 H), 5.68 (m, 1 H), 7.06 (d, 7=8.85 Hz, 1 H), 7.22 (s, 1 H), 7.38 (s, 1 H), 7.51 (m, 3 H), 8.05 (m, 3 H). HRMS m/z (M-H)^" calcd for C₄₃H₅₄N₅SO₉: 816.3642 found: 816.3651. LC-MS (retention time: 1.65, Method I), MS m/z 818 (M⁺+l).

Compound 29 Example 29

Step 29a: Preparation of N-tert-Butyl-l-propyl-cyclopropylsulfonamide

compound 29a

Step 29a) This compound was prepared in 70% (42.2 g) form N-butyl-3- chloropropane sulfonamide (59 g, 276 mmol) and propyl bromide (552 mmol) according to the procedure of Steps 3Ib-3Ic (Example 2) described in the synthesis of N-tert-butyl-(l-methyl) cyclopropylsulfonamide. The compound was used as crude: 1H NMR (300 MHz, CHLOROFORM-D) D ppm 0.82 (m, 2 H), 0.92 (t, 7=7.32 Hz, 3 H), 1.35 (s, 9 H), 1.82 (m, 2 H), 3.90 (s, 1 H).

Step 29b: Preparation 1-propyl-cvclopropylsulfonamide

compound 29b

Step 29b) This compound was made from Compound 29a in 80% yield (25.15 g) from N-tert-butyl-(l -propyl) cyclopropylsulfonamide (42.2 g, 193 mmol) according to the procedure of Steps 3Id (Example 2) described in the synthesis of 1-methylcyclopropylsulfonamide. The compound was recrystallized from EtOAc/hexanes as a white solid: 1H NMR CHLOROFORM-D) δ ppm 0.85 (m, 2 H), 0.94 (t, 7=7.32 Hz, 3 H), 1.36 (m, 2 H), 1.47 (m, 2 H), 1.87 (m, 2 H), 4.42 (s, 2 H).

Step 29c: Preparation of compound 29, Example 29, BOCNH-P3(L-t-BuGlv)- P2r(4_-)-(2-phenyl-7-methoxyquinoline-4-oxo)-S-proline]-Pl(l_..2S Vinyl Acca)- CONHSO₂(l-propyl-cyclopropan-l-yl) or alternate designation. Compound 29, example 29, (1-14-(7-Methoxy-2-phenyl-quinolin-4-yloxy -2- r 1 -( 1 -propyl- cvcloρropanesulfonylaminocarbonyl)-2-vinyl-cvclopropylcarbamoyl]- pyrrolidine-1 -carbonyl )-2,2-dimethyl-propyl)-carbamic acid tert-butyl ester

Step 29c) This compound was prepared in 62% yield (0.190 g) from tripeptide acid (0.250 g, 0.36 mmol) of the product of step 2e (Example 2) in analogous fashion to the procedure of Step 27c of Example 27 except that 1- propyl-cyclopropanesulfonic acid amide was used in place of 1- trimethylsilanylcyclopropanesulfonamide: 1H NMR (methanol-α ) Dppm 0.87 (m, 5 H), 1.05 (s, 9 H), 1.28 (s, 9 H), 1.45 (m, 5 H), 1.80 (m, 3 H), 2.16 (m, 1 H), 2.43 (m, 1 H), 2.69 (dd, 7=15.00, 8.05 Hz, 1 H), 3.95 (s, 3 H), 4.13 (m, 1 H), 4.26 (d, 7=8.78 Hz, 1 H), 4.53 (m, 2 H), 5.07 (d, 7=10.98 Hz, 1 H), 5.24 (d, 7=16.83 Hz, 1 H), 5.57 (s, 1 H), 5.75 (m, 1 H), 7.07 (dd, 7=8.97, 2.01 Hz, 1 H), 7.26 (s, 1 H), 7.39 (d, 7=2.20 Hz, 1 H), 7.52 (m, 3 H), 8.05 (m, 3 H). HRMS m/z (M-HV calcd for C ₄H₅₆N₅SO₉: 830.3799 found: 830.3816. LC (retention time: 1.83, Method H), MS m/z 833 (M⁺+l).

Compound 30 Example 30

Step 30a: Preparation 1-butyl-cyclopropanesulfonamide- tert-butylcarbamate

compound 30a

Step 30a) This compound, 1-butyl-cyclopropanesulfonamide- tert- butylcarbamate, was obtained in 89% yield (1.12 g) from 1.0 g (4.5 mmol) of cyclopropanesulfonamide-tert-butylcarbamate according to the procedure described in the synthesis of 1-methoxymethylcyclopropylsulfonylamine tert- butylcarbamate (Step 15IId) except 1.1 equivalents of butyl iodide was used as electrophile. The compound was purified by flash chromatography over SiO₂ using EtOAc/Hexanes (0% to 50%) as the eluent: 1H NMR (CDC1₃) D ppm 0.91 (m, 5 H), 1.31 (m, 2 H), 1.40 (m, 2 H), 1.50 (s, 9 H), 1.62 ,(m, 2 H), 1.86 (m, 2 H), 6.77 (s, 1 H); ¹³C NMR (CDC1₃) D ppm 12.36, 13.93, 22.80, 28.06, 28.48, 31.33, 40.65, 83.92, 149.25. Step 30b: Preparation of l-butyl-cyclopropanesulfonamide ^NH o compound 30b

Step 30b) A mixture of 1-butyl-cyclopropylsulfonylamine tert- butylcarbamate (1.2 g, 4.3 mmol) and TFA (2 mL, 26 mmol) was stirred at rt overnite. The solvent was removed in vacuo and the residue was chromatographed over SiO₂ eluting with EtOAC/Hexanes (0% to 50%) to afford 1-butyl-cyclopropanesulfonic acid amide, as a white solid (0.69 g, 90%): 1H NMR (methanol-d₄) D ppm 0.83 (m, 2 H), 0.92 (t, 7=7.32 Hz, 2 H), 1.24 (m, 2 H), 1.34 (m, 2 H), 1.47 (m, 2 H), 1.87 (m, 2 H); ^!CNMR (methanol-d₄) D ppm 12.09, 14.25, 23.93, 29.82, 32.38, 41.92.

Step 30c: Preparation of compound 30, Example 30. BOCNH-P3(L-t- BuGlv)-P2r(4_,)-(2-phenyl-7-methoxyQuinoline-4-oxo)-S-proline]-Pl(l_.,2S Vinyl Acca)-CONHSO2(l-butyl-cvclopropan-l-yl) or alternate designation, Compound 30, example 30, { l-r2-ri-Q -Butyl- cvclopropanesulfonylaminocarbonyl)-2-vinyl-cvclopropylcarbamoyl]-4-(7- methoxy-2-phenyl-quinolin-4-yloxy)-pyrrolidine-l-carbonyn-2,2-dimethyl- propyl I -carbamic acid tert-butyl ester

Step 30c) This compound was prepared in 30% yield (22.1 g) from tripeptide acid (0.060 g, 0.09 mmol)) of the product of step 2e (Example 2) in analogous fashion to the procedure Step 27c of Example 27 except that 1 -butyl - cyclopropanesulfonamide (Step 30b) was used in place of 1-trimethylsilanyl- cyclopropanesulfonamide and purified by PTLC (MeOH CH₂Cl ) and preparative HPLC (solvent B: 35% to 85%): 1H NMR (methanol- -) D ppm 0.83 (m, 5 H), 1.03 (s, 9 H), 1.27 (s, 9 H), 1.34 (m, 7 H), 1.82 (m, 3 H), 2.14 (m, 1 H), 2.44 (m, 1 H), 2.68 (dd, 7=12.99, 7.14 Hz, 1 H), 3.92 (s, 3 H), 4.06 (m, 1 H), 4.24 (s, 1 H), 4.53 (m, 2 H), 5.02 (d, 7=10.61 Hz, 1 H), 5.20 (d, 7=16.83 Hz, 1 H), 5.51 (s, 1 H), 5.92 (m, 1 H), 7.04 (d, 7=8.78 Hz, 1 H), 7.21 (s, 1 H), 7.36 (s, 1 H), 7.50 (m, 3 H), 8.04 (m, 3 H). LC-MS (retention time: 1.80, Method I), MS m/z 846 (M⁺+l).

Compound 31 Example 31

Step 31a: Preparation of l-iso-butyl- cyclopropanesulfonamide- tert- butylcarbamate

0-.

^<L ^H / LDA, iso-butyl iodide ^^^~*~/ °, - ^S _Λ II i O ' . \ . Δ o o compound 31a

Step 31a) To a solution of N,N-diisopropylamine (1.1 ml, 9.54 mmol) dissolved in THF (10 mL) cooled to -78 °C, was added ra-BuLi (1.6 M in hexane, 5.9 mL, 9.54 mmol). The mixture was stirred for 1 h, and a THF (10 mL) solution of cyclopropylsulfonylamine tert-butyl carbamate (1.0 g, 4.52 mmol) was added dropwise, the generated solution was stirred for 1 h. To this solution was added neat iso-butyl iodide (0.57 mL, 5.0 mmol). The reaction mixture was allowed slowly to warm up overnite. The reaction mixture was poured into cold pH 4.0 buffer and the pH was adjusted to <4 and extracted with EtOAc (3x). The combined extracts were dried (MgSO₄), concentrated. The residue was chromatographed over SiO₂ eluting with EtOAC/Hexanes (0% to 50%) to afford the product in 69% yield (0.87 g) as a white solid: 1H NMR (CDC1₃) D ppm 0.92 (m, 2 H), 0.95 (d, 7=6.71 Hz, 6 H), 1.49 (s, 9 H), 1.69 (m, 2 H), 1.71 (s, 2 H), 1.95 (m, 1 H), 6.80 (s, 1 H).

Step 31b: Preparation of l-tso-butyl-cyclopropanesulfonamide

° NH₂

TX compound 31 b

Step 31b) This compound, 1-isobutyl-cyclopropanesulfonic acid amide, was obtained in 69% yield (0.40 g) from 0.61 g (2.2 mmole) of 1-wo-butyl- cyclopropanesulfonamide-tert-butylcarbamate, according to the procedure described in the synthesis of 1-butyl-cyclopropanesulfonamide (Step 30b, Example 30) to provide the product as a white solid: 1H NMR (CDC1₃) D ppm 0.83 (m, 2 H), 0.96 (d, 7=6.71 Hz, 6 H), 1.39 (m, 2 H), 1.72 (d, 7=7.32 Hz, 2 H), 2.01 (m, 1 H), 4.51 (s, 2 H); 1 ^l3",C NMR (CDC1₃) D ppm 12.94, 23.40, 27.34, 40.32, 42.60.

Step 31c: Preparation of compound 31, Example 31, BOCNH-P3(L-t-BuGlv)- P2r(4_,)-(2-phenyl-7-methoxyquinoline-4-oxo)-S-proline]-Pl(l_,,2S Vinyl Acca)- CONHSO^Q-Z-'C'-butyl-cyclopropan-l-yl) or alternate designation. Compound 31, example 31, { l-r2-ri-(l-Isobutyl-cvclopropanesulfonylaminocarbonyl)-2-vinyl- cycloprop ylcarbamovπ -4-(7-methoxy-2-phenyl-quinolin-4-yloxy)-pyrrolidine- 1 - carbonyl]-2,2-dimethyl-propyl|-carbamic acid tert-butyl ester

Step 31c) Compound 31 was prepared in 48% yield (0.0352 g) from tripeptide acid (0.060 g, 0.09 mmol)) of the product of step 2e (Example 2) in analogous fashion to the procedure of Step 27c (Example 27) except that 1- isobutyl-cyclopropanesulfonamide (step 31b) was used in place of 1- trimethylsilanyl-cyclopropanesulfonamide and purified by PTLC plates from Analtech (catalog # 2053) using MeOH/CH₂Cl₂ as eluent (50% to 0% to 5%) and EM Plates (catalog #5744-7) using MeOH CH₂Cl₂ as eluent (MeOH/CH₂Cl₂: 1% to 2.5%) to provide the product as a white foam: 1H NMR (methanol-d₄) D ppm 0.87 (m, 2 H), 0.95 (d, 7=6.71 Hz, 6 H), 1.05 (s, 9 H), 1.29 (m, 9 H), 1.50 (m, 4 H), 1.80 (m, 1 H), 2.06 (m, 3 H), 2.44 (m, 1 H), 2.68 (dd, 7=13.58, 7.17 Hz, 1 H), 3.94 (s, 3 H), 4.14 (m, 1 H), 4.26 (m, 1 H), 4.53 (m, 2 H), 5.04 (m, 1 H), 5.23 (m, 1 H), 5.55 (s, 1 H), 5.77 (m, 1 H), 7.06 (dd, 7=9.16, 2.14 Hz, 1 H), 7.24 (s, 1 H), 7.38 (d, 7=2.14 Hz, 1 H), 7.51 (m, 3 H), 8.07 (m, 3 H). LC-MS (retention time: 1.79, Method I), MS m/z 846 (M⁺+l).

Compound 32 Example 32

Step 32a: Preparation of l-cyclobutylmethyl-cyclopropanesulfonamide- tert-butylc arbamate

Step 32a) This compound, 1-cyclobutylmethyl-cyclopropanesulfonamide- tert-butylcarbamate, was obtained in 55% yield (0.72 g) from l.Og (4.52 mmol) of cyclopropanesulfonamide-tert-butylcarbamate according to the procedure described in the synthesis of 1-butylcyclopropanesulfonamide (Step 30a) except that 1.10 equivalents of cyclobutylmethyl iodide was used as electrophile: 1H NMR (CDC1₃) □ ppm 0.89 (m, 2 H), 1.49 (s, 9 H), 1.55 (m, 2 H), 1.64 (m, 2 H), 1.82 (m, 2 H), 2.02 (d, 7=7.32 Hz, 2 H), 2.07 (m, 2 H), 2.37 (m, 1 H); ¹³C NMR (CDCI₃) D ppm 11.29, 18.75, 27.96, 29.14, 32.84, 37.29, 39.44, 83.78, 149.31.

Step 32b: Preparation of (l-cyclobutylmethyl-cyclopropane) sulfonamide

^NHa compound 32b

Step 32b) This compound, 1-cyclobutylmethyl-cyclopropanesulfonic acid amide, was obtained in 99% yield (0.136 g) from 0.21 g (0.76 mmole) of 1- cyclobutylmethyl - cyclopropanesulfonamide-tert-butylcarbamate, according to the procedure described in the synthesis of 1-butyl-cyclopropanesulfonamide (Step 30b, Example 30) to provide the product as a white solid: 1H NMR (Methanol-d₄) D ppm 0.82 (m, 2 H), 1.18 (m, 2 H), 1.68 (m, 2 H), 1.80 (m, 1 H), 1.89 (m, 1 H), 2.04 (d, 7=7.32 Hz, 2 H), 2.08 (m, 2 H), 2.51 (dd, 7=15.87, 7.93 Hz, 1 H); ¹³C NMR (Methanol-d₄) D ppm 11.12, 19.67, 30.20, 34.52, 38.48, 40.82.

Step 32c: Preparation of compound 32, Example 32, BOCNH-P3(L-t-BuGlv)-

P2r(4R)-(2-phenyl-7-methoχyquinoline-4-oxo)-S-proline]-Pl(l_-,2S Vinyl Acca)-

CONHSO^d-cyclobutylmethylcyclopropan-l-yl) or alternate designation.

Compound 32, example 32, ( l-Ω-ri-Q-Cvclobutylmethyl- cvclopropanesulfonylaminocarbonyl)-2-vinyl-cyclopropylcarbamoyl]-4-(7- methoxy-2-phenyl-quinolin-4-yloxy)-pyrrolidine-l-carbonvn-2,2-dimethyl- propyl) -carbamic acid tert-butyl ester

Step 32c) Compound 32 was prepared in 34% yield (0.0255 g) from tripeptide acid product (0.060 g, 0.09 mmol) of step 2e (Example 2) in analogous fashion to the procedure of Step 27c of Example 27 except that 1- Cyclobutylmethyl-cyclopropanesulfonic acid amide was used in place of 1- trimethylsilanylcyclopropanesulfonarnide and purified by preparative HPLC (solvent B: 35% to 85%) to afford the product as a foam: 1H NMR (methanol-d ) D ppm 0.70 (m, 2 H), 1.04 (s, 9 H), 1.28 (s, 9 H), 1.33 (m, 3 H), 1.70 (m, 5 H), 2.04 (m, 5 H), 2.38 (m, 2 H), 2.69 (dd, 7=13.54, 6.95 Hz, 1 H), 3.93 (s, 3 H), 4.08 (m, 1 H), 4.24 (s, 1 H), 4.53 (m, 2 H), 5.02 (d, 7=10.98 Hz, 1 H), 5.20 (d, 7=17.20 Hz, 1 H), 5.54 (s, 1 H), 5.99 (m, 1 H), 7.07 (m, 1 H), 7.23 (s, 1 H), 7.37 (d, 7=1.83 Hz, 1 H), 7.49 (m, 3 H), 8.05 (m, 3 H). LC-MS (retention time: 1.91, Method D), MS m/z 858(M++1). Compound 33 Example 33

Preparation of {l-[2-[l-(l-non-9-enyl- cyclopropanesulfonylaminocarbonyl)-2-vinyl-cyclopropylcarbamoyl]-4-(7- methoxy-2-phenyl-quinolin-4-yloxy)-pyrrolidine-l-carbonyl]-2,2-dimethyl- propyl}-carbamic acid tert-butyl ester

Step 33a: Preparation of l-dec-9-enyl-cyclopropanesulfonamide- tert- butylcarbamate

Step 33a) To a solution of diisopropyl-amine (2.5 ml) dissolved in THF (30 mL) cooled to -78 °C, was added n-BuLi (10.6 mL, 17 mmol, 1.6 M in hexane). The mixture was stirred for 1 h, and a THF (10 mL) solution of cyclopropylsulfonylamine tert-butyl carbamate (1.5 g, 6.78 mmol) was added dropwise. After the reaction mixture was stirred for 1 h, neat l-dec-9-enyl iodide (1.42 mL, 7.46 mmol) was added. The reaction mixture was allowed slowly to warm to rt overnite. The reaction mixture was poured into cold pH 4.0 buffer and the pH was adjusted to <4 and was then extracted with EtOAc (2x100 mL). The combined extracts were dried (MgSO₄), concentrated and purified by flash chromatograph over SiO₂ using EtOAc Hexanes (0% to 80%) as the eluent to afford 1.41 g (58%) yield of compound 33a as a white solid and 0.22 g (13%) of compound 33b as an amber solid. Compound 33a: 1H NMR (CDC1₃) D ppm 0.87 (m, 2 H), 1.44 (s, 9 H), 1.43 (m, 17 H), 2.01 (m, 2 H), 4.92 (d, 7=10.38 Hz, 1 H), 4.98 (dd, 7=17.24, 1.68 Hz, 1 H); compound 33b: 1H NMR (CDC1₃) D ppm 0.85 (m, 3 H), 1.27 (s, 8 H), 1.35 (m, 6 H), 1.87 (m, 2 H), 2.02 (m, 2 H), 4.46 (s, 2 H), 4.92 (dd, 7=9.61, 1.68 Hz, 1 H), 5.80 (m, 1 H).

Step 33b: Preparation of 1- dec-9-enyl -cyclopropanesulfonamide

o o

^ "NH₂ Compound 33b

Step 33b) Compound 33b was also obtained in the following method.l- Dec-9-enyl-cyclopropanesulfonamide- tert-butylcarbamate, 0.94 g (2.6 mmole) was added into a HCl /dioxane solution (30 mL, 120 mmol). The reaction mixture was stirred for 6 h at rt. The solvent was removed in vacuo and the residue was chromatographed over SiO₂ using EtOAc/hexanes (0% to 50%) as the eluent to afford 0.51 g (75%) of compound 33b as a white solid.

Step 33c: Preparation of compound 33, Example 33, BOCNH-P3(L-t-BuGly)-

P2r(4R)-(2-phenyl-7-methoxyquinoline-4-oxo)-S-proline1-Pl(l_.,2S Vinyl Acca)-

CONHSθ2ri-(l-dec-9-enyl)cyclopropan-l-yl] or alternate designation.

Compound 33, example 33, { j l-r2-ri-(l-dec-9-enyl- cvclopropanesulfonylaminocarbonyl)-2-vinyl-cyclopropylcarbamoyl]-4-(7- methoxy-2-phenyl-quinolin-4-yloxy)-pyrrolidine-l-arbonyl]-2,2-dimethyl- propyl) -carbamic acid tert-butyl ester

Step 33c) Compound 33 was prepared in 63% yield (0.170 g) from tripeptide acid (0.200 g, 0.29 mmol) of the product of step 2e (Example 2) in analogous fashion to the procedure of Step 27c (Example 27) except that l-dec-9- enyl-cyclopropanesulfonic acid amide was used in place of 1- trimethylsilanylcyclopropanesulfonamide and purified over PTLC plates from Analtech (catalog # 2050) using MeOH CH₂Cl₂ as eluent (1% to 5%) as a white foam: 1H NMR (methajιol-d₄) Dppm 1.07 (s, 9 H), 1.72 (m, 27 H), 1.84 (m, 3 H), 2.04 (m, 4 H), 2.59 (m, 1 H), 2.72 (m, 1 H), 3.95 (s, 3 H), 4.14 (m, 1 H), 4.28 (s, 1 H), 4.58 (m, 1 H), 4.89 (s, 3 H), 4.95 (m, 3 H), 5.20 (d, 7=17.09 Hz, 1 H), 5.51 (m, 2 H), 5.78 (m, 1 H), 5.98 (m, 1 H), 7.10 (m, 1 H), 7.25 (s, 1 H), 7.39 (d, 7=2.44 Hz, 1 H), 7.53 (m, 3 H). HRMS m/z (M-H)^" calcd for C₅₁H₆₈N₅SO₉: 926.4738 found: 926.4750. LC-MS (retention time: 2.10, Method F).

Compound 34 Example 34

compound 3₄ Step 34a: Preparation of l-non-8-enyl -cyclopropanesulfonamide- tert- butylcarbamate

compound3₄a compound 3₄b

Step 34a) These compounds, l-non-8-enyl-cyclopropanesulfonamide- tert-butylcarbamate (compound 33a) in 50% yield (1.17 g), and - non-8-enyl - cyclopropanesulfonic acid amide (33b) in 25% (0.41 g) were obtained from 1.5g (6.78 mmol) of cyclopropanesulfonamide-tert-butylcarbamate according to the procedure of Step 33a (Example 33) described in the synthesis of preparation of l-dec-9-enyl-cyclopropanesulfonamide-tert-butylcarbamate except 1.10 equivalents of l-non-8-enyl iodide was used as electrophile. Compound 34a: 1H NMR D ppm 0.91 (m, 2 H), 1.34 (m, 12 H), 1.49 (s, 7 H), 1.60 (m, 2 H), 1.84 (m, 2 H), 2.02 (q, 7=7.02 Hz, 2 H), 4.91 (m, 1 H), 4.97 (m, 1 H), 5.78 (m, 1 H), 7.07 (s, 1 H); ¹³C NMR (CDC1₃) D ppm 12.30, 26.27, 28.01, 28.84, 28.98, 29.24, 29.58, 31.53, 33.73, 40.62, 83.83, 114.25, 139.07, 149.34; compound 33b: 1H 5 NMR (CDC1₃) D ppm 0.85 (m, 2 H), 1.36 (m, 13 H), 1.87 (m, 2 H), 2.02 (m, 2 H), 4.45 (s, 2 H), 4.92 (m, 1 H), 4.98 (m, 1 H).

Step 34b: Preparation of 1- non-8-enyl -cyclopropanesulfonamide

o o

HW^S ~NH,

]_ 0 compound 3₄b

Step 33b) This compound, 1-non -8-enyl -cyclopropanesulfonic acid amide, was also obtained in 60% yield (0.193 g) from 0.451 g (1.31 mmole) of l-non-8-enyl - cyclopropanesulfonamide-tert-butylcarbamate, according to the 15 procedure of Step 33b (Example 33) described in the synthesis of l-dec-9-enyl- cyclopropanesulfonamide as a white solid.

Step 34c: Preparation of compound 34. Example 34, BQCNH-P3(L-t-BuGly)- P2 r(4_,)-r2-phenyl-7-methoxyquinoline-4-oxo)-S-ρroline1 -P 1 ( 1__,2S Vinyl Acca)- 20 CONHSO^ri-d-non-δ-envDcyclopropan-l-yll or alternate designation.

Compound 34, example 34, (l-|4-(7-Methoxy-2-phenyl-quinolin-4-yloxy)-2-ri-

(l-non-8-enyl-cvclopropanesulfonylaminocarbonyl)-2-vinyl- cyclopropylcarbamoyl]-pyrrolidine-l-carbonyl|-2,2-dimethyl-propyl)-carbamic acid tert-butyl ester

2 5 compound 3₄ Step 34c) Compound 34 was prepared in 61% (0.1619 g) yield from tripeptide acid product (200 g) of step 2e (Example 2) in analogous fashion to the procedure of Step 27c (Example 27) except that l-non-8-enyl- cyclopropanesulfonamide was used in place of 1-tirmethylsilanyl- cyclopropanesulfonamide: 1H NMR (methanol- _t) Dppm 0.71 (m, 2 H), 1.04 (s, 9 H), 1.28 (m, 22 H), 1.85 (m, 5 H), 2.09 (m, 1 H), 2.53 (s, 1 H), 2.72 (m, 1 H), 3.94 (m, 3 H), 4.10 (m, 1 H), 4.24 (s, 1 H), 4.53 (m, 2 H), 4.95 (m, 3 H), 5.18 (m, 1 H), 5.54 (s, 1 H), 5.72 (m, 1 H), 5.96 (s, 1 H), 7.05 (m, 1 H), 7.24 (s, 1 H), 7.38 (m, 1 H), 7.51 (m, 3 H), 8.08 (m, 3 H). HRMS m/z (M-H)^" calcd for CsoHeeNsSOc-: 912.4581 found: 912.4564. LC-MS (retention time: 2.03 Method F).

Compound 35 Example 35

Step 35a: Preparation of 1- (2-methoxy-ethyl)-cyclopropanesulfonamide- tert- butylcarbamate

compound 31a

Step 35a) This compound, 1- (2-methoxy-ethyl)- cyclopropanesulfonamide- tert-butylcarbamate, was obtained in 96% yield (1.55 g) from 1.28 g (6.78 mmol) of cyclopropanesulfonamide-tert-butylcarbamate according to the procedure described in the synthesis of 1 -methoxymethyl - cyclopropylsulfonylamine tert-butylcarbamate (Step 15IId) except 1.10 equivalents of 2-methoxy-ethyl bromide was used as electrophile. The compound was taken directly into the next reaction without purification: 1H NMR (CDC1₃) D ppm 1.00 (m, 2 H), 1.50 (s, 9 H), 1.66 (m, 2 H), 2.14 (t, 7=6.22 Hz, 2 H), 3.34 (s, 3 H), 3.57 (t, 7=6.40 Hz, 2 H), 7.55 (s, 1 H).

Step 35b: Preparation of 1 of 1- (2-methoxy-ethyl)-cyclopropanesulfonic acid amide

-,^-^ .--NH₂ compound 35b

Step 35b) This compound, 1 of 1- (2-methoxy-ethyl-cyclopropanesulfonic acid amide, was obtained in 45% yield (0.364 g) from 1.25 g (5.55 mmole) of 1- cyclobutylmethyl - cyclopropanesulfonamide-tert-butylcarbamate, according to the procedure described in the synthesis of 1-butyl-cyclopropanesulfonic acid amide (Step 30d, Example 30) but chromatographed over SiO₂ eluting with EtOAC/Hexanes (15% to 60%) and followed by recrystalizing from minimum amount of MeOH/CH₂Cl₂/hexanes: 1H NMR (CDC1₃) D ppm 0.88 (m, 2 H), 1.41 (m, 2 H), 2.11 (t, 7=5.67 Hz, 2 H), 3.34 (s, 3 H), 3.59 (t, 7=5.67 Hz, 2 H), 5.21 (s,

2 H); ¹³C NMR (CDC1₃) D ppm 12.82, 32.64, 40.37, 58.46, 70.56.

Step 35c: Preparation of compound 35, Example 35, BOCNH-P3(L-t-BuGlv)-

P2r(4_-)-(2-phenyl-7-methoxyquinoline-4-oxo)-S-proline1-Pl(l--,2S Vinyl Acca)-

CONHSθ2(l-(2-methoxyethyl)-cyclopropan-l-yl) or alternate designation.

Compound 35, example 35, U-r2-{ l-ri-(2-Methoxy-ethyl)- cvclopropanesulfonylan_inocarbonyl]-2-vinyl-cyclopropylcarbamoyl}-4-(7- methoxy-2-phenyl-quinolin-4-yloxy)-pyrrolidine-l-carbonyl]-2,2-dimethyl- propyl } -carbamic acid tert-butyl ester

Step 35c) Compound 35 was prepared in 71% (0.1103 g) yield from tripeptide acid (0.125 g, 0.18 mmol) of the product of step 2e (Example 2) in analogous fashion to the procedure of Step 27c (Example 27) except that 1- (2- methoxy-ethyl)-cyclopropanesulfonamide (compound 35b, Example 35) was used in place of 1-trimetmethylsilanylcyclopropanesulfonamide: 1H NMR (methanol- -) D ppm 0.96 (m, 2 H), 1.04 (s, 9 H), 1.28 (s, 9 H), 1.42 (m, 3 H), 1.81 (dd, 7=7.68, 5.12 Hz, 1 H), 2.09 (m, 3 H), 2.38 (m, 1 H), 2.68 (dd, 7=13.91, 6.95 Hz, 1 H), 3.25 (s, 3 H), 3.53 (m, 2 H), 3.93 (s, 3 H), 4.12 (m, 1 H), 4.25 (m, 1 H), 4.53 (m, 2 H), 5.07 (d, 7=10.61 Hz, 1 H), 5.24 (d, 7=16.83 Hz, 1 H), 5.53 (s, 1 H), 5.76 (m, 1 H), 7.06 (d, 7=9.15 Hz, 1 H), 7.23 (s, 1 H), 7.38 (s, 1 H), 7.53 (m, 3 H), 8.07 (m, 3 H). LC-MS (retention time: 1.64, Method B), MS m/z 848 (MM).

Compound 36 Example 36

Step 36a: Preparation of 1- (2-benzyloxy-ethyl)-cyclopropanesulfonamide- tert- butylcarbamate

compound 31a

Step 36a) This compound, 1- (2-Benzyloxy-ethyl)- cyclopropanesulfonamide- tert-butylcarbamate, was obtained in 47% yield (1.15 g) from 1.5 g (6.78 mmol) of cyclopropanesulfonamide-tert-butylcarbamate according to the procedure described in the synthesis of 1- methoxymethylcyclopropylsulfonylamine tert-butylcarbamate (Step 15IId) except 1.10 equivalents of (2-Bromo-ethoxy)-benzene was used as electrophile: 1H NMR (CHLOROFORM-D) D ppm 1.05 (s, 2 H), 1.48 (m, 11 H), 2.16 (t, 7=6.59 Hz, 2 H), 3.69 (t, 7=6.77 Hz, 2 H), 4.48 (s, 2 H), 7.32 (m, 5 H).

Step 36b: Preparation of l-(2-Benzyloxy-ethyl) -cyclopropanesulfonic acid amide

compound 36b

Step 36b) This compound, l-(2-Benzyloxy-ethyl -cyclopropanesulfonic acid amide, was obtained in 85% yield (0.702 g) from 1.15 g (3.24 mmole) of 1- cyclobutylmethyl - cyclopropanesulfonamide-tert-butylcarbamate, according to the procedure described in the synthesis of 1-butyl-cyclopropanesulfonic acid amide (Step 30b, Example 30) and the compound was purified over Biotage 40M using EtOAc/Hexanes (0% to 60%) as eluent: 1H NMR (Methanol-d₄) D ppm 0.94 (m, 2 H), 1.26 (m, 2 H), 2.18 (t, 7=6.56 Hz, 2 H), 3.72 (t, 7=6.56 Hz, 2 H), 4.49 (s, 2 H), 7.27 (m, 1 H), 7.32 (m, 4 H)); ¹³C NMR (Methanol-d ) D ppm 12.42, 32.79, 69.31, 74.02, 128.72, 128.92, 129.39, 139.56. 1H NMR (methanol-cU) D ppm 0.94 (m, 2 H), 1.26 (m, 2 H), 2.18 (t, 7=6.56 Hz, 2 H), 3.72 (t, 7=6.56 Hz, 2 H), 4.49 (s, 2 H), 7.27 (m, 1 H), 7.32 (m, 4 H).

Step 36c: Preparation of Compound 36, example 36. BOCNH-P3(L-t-BuGlv)- P2r(4/?)-(2-phenyl-7-methoxyquinoline-4-oxo)-S-proline1-Pl QR,2S Vinyl Acca)- CONHSθ₂(l-(2-benzoxyethyl)-cyclopropan-l-yl) or alternate designation.

Compound 36, example 36, { 142-1 l-ri-(2-Benzyloxy-ethyl)- cyclopropanesulfonylaminocarbonyl1-2-vinyl-cvclopropylcarbamoyl|-4-(7- methoxy-2-phenyl-quinolin-4-yloxy)-pyrrolidine-l-carbonyl1-2,2-dimethyl- propyll-carbamic acid tert-butyl ester

Step 36c) Compound 36 was prepared in 66% (0.1031 g) yield from tripeptide acid (0.120 g, 0.17 mmol) of the product of step 2e (Example 2) in analogous fashion to the procedure of Step 27c of Example 27 except that 1- (2- benzyloxy-ethyl)-cyclopropanesulfonamide (compound 36b, Example 36) was used in place of 1-trimethylsilanyl-cyclopropanesulfonamide and purified by preparative HPLC (solvent B: 30% to 100%) to provide the product as a thick oil which solidified upon storage: 1H NMR (methanol-d₄) D ppm 0.91 (m, 2 H), 1.06 (s, 9 H), 1.30 (s, 9 H), 1.38 (m, 3 H), 1.82 (m, 1 H), 2.20 (m, 3 H), 2.52 (m, 1 H), 2.72 (dd, 7=14.19, 7.17 Hz, 1 H), 3.68 (t, 7=6.56 Hz, 2 H), 3.97 (m, 3 H), 4.12 (m, 1 H), 4.27 (s, 1 H), 4.42 (d, 7=7.63 Hz, 2 H), 4.56 (m, 2 H), 5.01 (m, 1 H), 5.22 (d, 7=16.79 Hz, 1 H), 5.53 (m, 1 H), 5.93 (m, 1 H), 7.10 (m, 1 H), 7.26 (m, 6 H), 7.41 (m, 1 H), 7.53 (m, 3 H), 8.09 (m, 3 H). MS m/z 924(M⁺+1), MS m/z 922(M^"-1): HPLC (retention time: 1.88, Method D).

Compound 37 Example 37

Step 37a: Preparation of 1- o-propoxymethylcyclopropanesulfonarnide- tert- butylcarbamate

Step 37a) This compound, l-zsø-propoxymethyl- cyclopropanesulfonamide- tert-butylcarbamate, was obtained 79% (0.98 g) from 1.0 g (4.52 mmol) of cyclopropanesulfonamide-tert-butylcarbamate according to the procedure described in the synthesis of 1-methoxymethylcyclo- propylsulfonylamine tert-butylcarbamate (Step 15IId) except 1.10 equivalents of 2-bromomethoxylpropane was used as electrophile as a white solid and furthered to net step.

Step 37b: Preparation of l-t_o-propoxymethylcyclopropanesulfonamide

compound 37b

Step 37b) This compound, 1- ■sopropoxymethyl -cyclopropanesulfonic acid amide, was obtained in 98% yield (0.62 g) from 0.96 g (0.58 mmole) of 1- z^'sø-propoxymethylcyclopropanesulfonamide- tert-butylcarbamate, according to the procedure described in the synthesis of 1-butyl-cyclopropanesulfonic acid amide (Step 30b, Example 30) as a white solid: 1H NMR (Methanol-d-) D ppm 0.98 (dd, 7=7.02, 4.88 Hz, 2 H), 1.16 (d, 7=6.10 Hz, 6 H), 1.30 (m, 2 H), 3.66 (m, 1 H), 3.76 (s, 2 H). Step 37c: Preparation of Compound 37, BOCNH-P3(L-t-BuGlv)-P2r(4R)-(2- phenyl-7-meτhoxyquinoline-4-oxo)-S-proline]-Pl(lR,2S Vinyl Acca)- CONHSO2(l-^o-propoxyethyl)-cyclopropan-l-yl) or alternate designation.

Compound 37, example 37 j l-r2-ri-(l-Isopropoxymethyl- cyclopropanesulfonylaminocarbonyl)-2-vinyl-cvclopropylcarbamoyl]-4-(7- methoxy-2-phenyl-quinolin-4-yloxy)-pyrrolidine-l-carbonyl]-2,2-dimethyl- propyl I -carbamic acid tert-butyl ester

Step 37c) Compound 37 was prepared in 52% yield (0.065 g) from tripeptide acid product (0.100 g, 0.15 mmol)) of step 2e (Example 2) in analogous fashion to the procedure of Step 27c of Example 27 except that 1-iso- propoxymethyl-cyclopropanesulfonamide was used in place of 1- trimethylsilanyl-cyclopropanesulfonamide and purified over 20X40 cM 1000 D Analtech PTLC plates (MeOH/CH₂Cl₂: 5%) to afford the desired product as a white foam: 1H NMR (methanol-d₄) Dppm 1.03 (m, 8 H), 1.04 (s, 9 H), 1.28 (s, 9 H), 1.33 (m, 3 H), 1.78 (m, 1 H), 2.16 (m, 1 H), 2.50 (m, 1 H), 2.72 (m, 1 H), 3.54 (m, 1 H), 3.82 (m, 2 H), 3.93 (d, 7=4.58 Hz, 3 H), 4.10 (m, 1 H), 4.25 (m, 1 H), 4.54 (m, 2 H), 5.01 (dd, 7=20.45, 9.77 Hz, 1 H), 5.21 (m, 1 H), 5.51 (m, 1 H), 5.92 (m, 1 H), 7.05 (dd, 7=9.16, 2.14 Hz, 1 H), 7.22 (m, 1 H), 7.38 (m, 1 H), 7.49 (m, 3 H), 8.05 (m, 3 H). LC-MS (retention time: 1.81, Method L), MS m/z 862 (M⁺+1). Compound 38 Example 38

compound 38

Step 38a: Preparation of 1- chloro- cyclopropanesulfonamide- tert- butylcarbamate

compound 38a

step 38a) To a solution of cyclopropylsulfonylamine tert-butyl carbamate (1.0 g, 4.52 mmol) dissolved in THF (10 mL) cooled to -78 °C, was added 7 -BuLi (6.4 mL, 10.2 mmol, 1.6 M in hexane) and the reaction mixture was stirred for 1 h. To this solution was added a THF (10 mL) solution of NCS (0.86 g, 6.34 mmol). After stirred for 5 min, the bath was changed to ice bath and the mixture was stirred for 3 h at the temperature. The reaction mixture was diluted with ice water, the pH was adjusted to <4. The aqueous mixtire was extracted with EtOAc. The combined extracts were dried (MgSO ), concentrated and purified by flash chromatography over SiO₂ using EtOAc/hexanes (0% to 60%) as the eluent to afford 0.98 g (67%) of 1- chloro- cyclopropanesulfonamide- tert-butylcarbamate as a white solid: 1H NMR (CDC1₃) δ ppm 1.51 (m, 11 H), 2.01 (m, 2 H), 7.60 (s, I H).

Step 38b: Preparation of 1- chloro -cyclopropanesulfonamide

compound 38b Step 38b ) This compound, 1 -chloro -cyclopropanesulfonic acid amide, was obtained in 100% yield (0.09 g) from 0.148 g (0.58 mmole) of 1- chloro - cyclopropanesulfonamide-tert-butylcarbamate, according to the procedure described in the synthesis of 1-butyl-cyclopropanesulfonic acid amide (step 30b, Example 30) but without purification as a light brown solid: 1H NMR (Methanol- dø) D ppm 1.38 (m, 2 H), 1.70 (m, 2 H).

Step 38c: Preparation of Compound 38. example 38, BOCNH-P3(L-t-BuGlv)-

P2r(4_?)-(2-ρhenyl-7-methoxyquinoline-4-oxo)-S-proline]-Pl(lR.2S Vinyl AccaV

CONHS0₂(l-chlorocyclopropan-l-yl) or alternate designation. Compound 38, example 38, { l-[2-ri-(l-Chloro-cyclopropanesulfonylaminocarbonyl)-2-vinyl- cyclopropylcarbamoyl]-4-(7-methoxy-2-phenyl-quinolin-4-yloxy)-pyrrolidine-l- carbonyl]-2,2-dimethyl-propyl|-carbamic acid tert-butyl ester

compound 38

Step 38c) Compound 38 was prepared in 39% (0.0464 g) yield from tripeptide acid product (0.100 g, 0.15 mmol) of step 2e (Example 2) in analogous fashion to the procedure of Step 27c (Example 27) except that 1- chlorocyclopropanesulfonic acid amide was used in place of 1-trimethylsilanyl- cyclopropanesulfonamide and purified by preparative HPLC (solvent B: 30% to 100%) as a white foam: 1H NMR (methanol-d₄) D ppm 1.07 (s, 9 H), 1.22 (s, 9 H), 1.43 (m, 2 H), 1.46 (dd, 7=9.61, 5.65 Hz, 1 H), 1.91 (dd, 7=8.09, 5.65 Hz, 1 H), 1.96 (m, 1 H), 2.05 (m, 1 H), 2.30 (q, 7=8.85 Hz, 1 H), 2.47 (m, 1 H), 2.81 (dd, 7=14.04, 7.02 Hz, 1 H), 4.08 (s, 3 H), 4.17 (m, 2 H), 4.67 (dd, 7=10.22, 7.17 Hz, 1 H), 4.72 (d, 7=12.21 Hz, 1 H), 5.17 (d, 7=10.38 Hz, 1 H), 5.33 (d, 7=17.09 Hz, 1 H), 5.73 (m, 1 H), 5.87 (s, 1 H), 7.42 (dd, 7=9.31, 2.29 Hz, 1 H), 7.57 (d, 7=2.14 Hz, 1 H), 7.69 (s, 1 H), 7.79 (m, 3 H), 8.11 (d, 7=7.02 Hz, 2 H), 8.38 (m, 1 H). LC-MS (retention time: 1.60, Method H), MS m/z 824 (M⁺+l).

Compound 39 Example 39

compound 39

Step 39a: Preparation of 1- iodo -cyclopropanesulfonamide

V ° ° ' - — ^ l_a -~ ^H2> ° ^ ° ' compound 39a Step 39a) This compound, 1-iodo-cyclopropanesulfonic acid amide, was obtained in 78% (0.87 g) yield from 1.0 g (4.52 mmol) of cyclopropanesulfonamide-tert-butylcarbamate according to the procedure described in the synthesis of 1- chloro- cyclopropanesulfonamide- tert- butylcarbamate (Step 38a, Example 38) except 1.4 equivalent iodine was used as electrophile and purified by flash chromatograph (EtOAc/hexanes: 0% to 60%) to provide the product as a pale brown solid: 1H NMR (CDC1₃) D ppm 1.37 (m, 2 H), 1.78 (m, 2 H), 4.75 (s. 2 H).

Step 39b: Preparation Compound 39, BOCNH-P3(L-t-BuGlv)-P2r(4R)-(2- phenyl-7-meτhoxyquinoline-4-oxo)-S-proline1-Pl (1R,2S Vinyl Acca)-

CONHSO2(l-iodocyclopropan-l-yl) or alternate designation. Compound 39, example 39, I l-r2-ri-(lTodo-cyclopropanesulfonylaminocarbonyl)-2-vinyl- cyclopropylcarbamoyl]-4-(7-methoxy-2-phenyl-quinolin-4-yloxy)-pyrrolidine-l- carbonyl]-2,2-dimethyl -propyl} -carbamic acid tert-butyl ester

compound 39

Step 39b) Compound 39 was prepared in 65% (0.1077 g) yield from tripeptide acid product (0.125 g, 0.18 mmol) of step 2e (Example 2) in analogous fashion to the procedure of Step 27c of Example 27 except that 1-iodo- cyclopropanesulfonamide was used in place of 1-trimethylsilanyl- cyclopropanesulfonamide and purified by repeatedly PTLC to provide the product as a foam: 1H NMR (methanol-d₄) D ppm 1.05 (s, 9 H), 1.12 (m, 2 H), 1.27 (s, 9 H), 1.33 (m, 2 H), 1.76 (m, 2 H), 1.99 (m, 1 H), 2.66 (m, 1 H), 2.77 (m, 1 H), 3.94 (s, 3 H), 4.14 (m, 2 H), 4.53 (m, 2 H), 4.97 (m, 1 H), 5.15 (d, 7=17.09 Hz, 1 H), 5.55 (s, 1 H), 5.96 (m, 1 H), 7.06 (dd, 7=9.00, 2.29 Hz, 1 H), 7.26 (s, 1 H), 7.38 (m, 1 H), 7.51 (m, 3 H), 8.06 (m, 3 H). HRMS m/z (M+H)⁺ calcd for iK-c-INsSOc-: 914.2296 found: 914.2301. HPLC (retention time: 1.65, Method I). Compound 40 Example 40

Step 40a: Preparation of 1- (4-floro-benzyl)-cyclopropanesulfonamide- tert- butylcarbamate

Step 40a) This compound, 1- (4-floro-benzyl)- cyclopropanesulfonamide- tert-butylcarbamate, was obtained from 1.0 g (4.52 mmol) of cyclopropanesulfonamide-tert-butylcarbamate according to the procedure described in the synthesis of 1-methoxymethylcyclo-propylsulfonylamine tert- butylcarbamate (Step 15IId) except 1.2 equivalents of 4-floro-benzyl bromide was used as electrophile. The crude product was directly used in next step. Step 40b: Preparation of l-(4-floro-benzy) -cyclopropanesulfonamide

compound ₄0b

Step 40b) This compound, 1 -(4-floro-benzyl) -cyclopropanesulfonamide, was obtained in 25% yield (0.26 g) in two steps from crude product of step 40a according to the procedure described in the synthesis of 1-butyl- cyclopropanesulfonic acid amide (Step 30a) and purified by Biotage 40 L column using EtOAc/hexanes (5% to 100%) as the eluent to provide the product as a white solid: 1H NMR (CDC1₃) D ppm 0.83 (m, 2 H), 1.39 (m, 2 H), 3.23 (s, 2 H), 4.16 (s, 2 H), 7.02 (m, 2 H); ¹³C NMR (CDC1₃) D ppm 11.00, 35.99, 41.76, 76.75, 115.60, 115.77, 131.30, 131.37, 132.06, 132.09, 161.10, 163.06.

Step 40c: Preparation of compound 40. Example 40, BOCNH-P3(L-t-BuGlv)-

P2r(4__)-(2-phenyl-7-methoxyquinoline-4-oxo)-S-ρroline]-Pl(lR.2S Vinyl Acca)-

CONHSO₂ri-(4-fluorobenzyl)-clopropan-l-yl) or alternate designation.

Compound 40, example 40, I l-f2-{ l-[T-(4-Fruoro-benzyl)- cvclopropanesulfonylaminocarbonyn-2-vinyl-cyclopropylcarbamoyl|-4-(7- methoxy-2-phenyl-quinolin-4-yloxy)-pyrrolidine-l-carbonyl]-2,2-dimethyl- propyl I -carbamic acid tert-butyl ester

Step 40c) Compound 40 was prepared in 41% (32.0) yield from tripeptide acid product (0.060 g, 0.09 mmol)) of step 2e (Example 2) in analogous fashion to the procedure of Step 27c of Example 27 except that l-(4-fluoro-benzyl)- cyclopropanesulfonamide was used in place of 1-trimethylsilanyl- cyclopropanesulfonamide and purified by preparative HPLC (solvent B: 30% to 100%): 1H NMR (methanol-c^) D ppm 0.91 (m, 2 H), 0.97 (s, 9 H), 1.24 (s, 9 H), 1.47 (m, 3 H), 1.86 (m, 1 H), 2.26 (m, 1 H), 2.35 (m, 1 H), 2.71 (dd, 7=13.73, 6.71 Hz, 1 H), 3.24 (d, 7=14.04 Hz, 1 H), 3.33 (d, 7=12.21 Hz, 1 H), 3.97 (s, 3 H), 4.08 (m, 1 H), 4.21 (m, 1 H), 4.59 (m, 2 H), 5.15 (d, 7=8.24 Hz, 1 H), 5.32 (d, 7=17.09 Hz, 1 H), 5.63 (s, 1 H), 5.77 (m, 1 H), 6.99 (d, 7=4.88 Hz, 2 H), 7.16 (m, 3 H), 7.35 (s, 1 H), 7.43 (d, 7=2.14 Hz, 1 H), 7.57 (m, 3 H), 8.03 (d, 7=3.05 Hz, 2 H), 8.17 (d, 7=9.15 Hz, 1 H). LC-MS (retention time: 1.83, Method L), MS m/z 898 (M⁺+1). Compound 41 Example 41

Step 41a: Preparation of 1- (2-floro-benzyl)-cyclopropanesulfonamide- tert- butylcarbamate

Step 41a) This compound, 1- (2-floro-benzyl)- cyclopropanesulfonamide- tert-butylcarbamate, was obtained from 1.0 g (4.52 mmol) of cyclopropanesulfonamide-tert-butylcarbamate according to the procedure described in the synthesis of 1-methoxymethylcyclp-propylsulfonylamine tert- butylcarbamate (Step 15IId) except 1.1 equivalents of 2-floro-benzyl chloride was used as electrophile. The crude product was directly used in next step.

Step 41b: Preparation of l-(2-floro-benzy) -cyclopropanesulfonamide

compound ₄1b

Step 41b) This compound, 1 -(2-floro-benzyl) -cyclopropanesulfonamide, was obtained in 36% yield (0.41 g) in two steps from crude product of step step 41a according to the procedure described in the synthesis of 1-butyl- cyclopropanesulfonic acid amide (Step 30b) and purified by Biotage 40L column using EtOAc (5% to 100%) as eluent: 1H NMR (CDC1₃) D ppm 0.83 (m, 2 H), 1.39 (m, 2 H), 3.23 (s, 2 H), 4.16 (s, 2 H), 7.02 (m, 2 H). Step 41c: Preparation of compound 41, Example 41, BOCNH-P3(L-t-BuGlvV

P2r(4R)-(2-phenyl-7-methoxyquinoline-4-oxo)-S-proline]-PlQR,2S Vinyl AccaV

CONHSθ2ri-(2-fluorobenzyl)-clopropan-l-yl) or alternate designation.

Compound 41, example 41, { 1-12-f l-ri-(2-Fluoro-benzyl)- cyclopropanesulfonylaminocarbonyll-2-vinyl-cyclopropylcarbamoyl}-4-(7- methoxy-2-phenyl-quinolin-4-yloxy)-pyrrolidine-l-carbonyl]-2,2-dimethyl- propyl} -carbamic acid tert-butyl ester

Step 41c) Compound 41 was prepared in 47% (0.037 g) yield from tripeptide acid product (0.060 g, 0.09 mmol) of step 2e (Example 2) in analogous fashion to the procedure of Step 27c of Example 27 except that l-(2-Fluoro- benzyl)-cyclopropanesulfonamide (41b) was used in place of 1-trimethylsilanyl- cyclopropanesulfonamide and purified by preparative HPLC (solvent B: 30% to 100%): 1H NMR (methanol-d₄) D ppm 0.94 (m, 2 H), 0.98 (s, 9 H), 1.23 (s, 9 H), 1.40 (m, 3 H), 1.87 (m, 1 H), 2.27 (m, 1 H), 2.40 (s, 1 H), 2.75 (dd, 7=13.17, 6.59 Hz, 1 H), 3.39 (s, 2 H), 3.99 (s, 3 H), 4.09 (m, 1 H), 4.19 (s, 1 H), 4.61 (m, 2 H), 5.15 (m, 1 H), 5.31 (d, 7=17.57 Hz, 1 H), 5.70 (s, 1 H), 5.77 (s, 1 H), 7.06 (m, 2 H), 7.24 (m, 3 H), 7.43 (s, 1 H), 7.48 (d, 7=2.20 Hz, 1 H), 7.62 (m, 3 H), 8.04 (m, 2 H), 8.22 (d, 7=9.15 Hz, 1 H). LC-MS (retention time: 1.76, Method H), MS m/z 898 (M⁺+l).

Compound 42 Example 42

Step 42a: Preparation of 1- (4-methoxy-benzyl)-cyclopropanesulfonamide- tert- butylcarbamate

compound ₄2a

Step 42a) This compound, 1- (4-methoxy-benzyl)- cyclopropanesulfonamide- tert-butylcarbamate, was obtained 1.2 g (78%) from 1.0 g (4.52 mmol) of cyclopropanesulfonamide-tert-butylcarbamate according to the procedure described in the synthesis of 1-methoxymethylcyclo- propylsulfonylamine tert-butylcarbamate (Step 15IId) except 1.1 equivalents of 4-methoxy-benzyl chloride was used as electrophile: ^lH NMR (Methanol-d*) D ppm 0.78 (m, 2 H), 1.46 (s, 9 H), 1.47 (m, 2 H), 3.20 (s, 2 H), 3.76 (s, 3 H), 6.87 (m, 2 H), 7.09 (m, 2 H). Step 42b: Preparation of l-(4-methoxybenzyl) -cyclopropanesulfonamide

"Ox NH₂ o o compound ₄2b

Step 42b) This compound, 1 -(4-methoxy-benzyl) - cyclopropanesulfonamide, was obtained in 89% yield (0.63 g) in two steps from 1.0 g (2.93 mmol) of l-(4-methoxy-benzyl)-cyclopropanesulfonamide- tert- butylcarbamate according to the procedure described in the synthesis of 1-butylcyclopropanesulfonamide (Step 30b, Example 30) as a white solid: 1H NMR (CDCI₃) D ppm 0.86 (m, 2 H), 1.38 (m, 2 H), 3.18 (s, 2 H), 3.78 (s, 3 H), 4.11 (s, 2 H), 6.85 (m, 2 H), 7.18 (d, 7=8.55 Hz, 2 H); ¹³C NMR (CDC1₃) D ppm 11.07, 36.18, 42.00, 55.24, 114.20, 128.31, 130.76, 158.88.

Step 42c: Preparation of Compound 42. BOCNH-P3(L-t-BuGly)-P2r(4J-)-(2- phenyl-7-methoxyquinoline-4-oxo)-S-proline]-Pl (1R.2S Vinyl Acca)-

CONHSO2ri-(4-methoxybenzyl)-clopropan-l-yl) or alternate designation.

Compound 42, example 42, I l-f2-{ l-|T-(4-Methoxy-benzyl)- cyclopropanesulf onylaminocarbonyl] -2-vinyl-cyclopropylcarbamoyl I -4-(7- methoxy-2-phenyl-quinolin-4-yloxy)-pyrrolidine-l-carbonvn-2,2-dimethyl- propyl) -carbamic acid tert-butyl ester

Step 42c) Compound 42 was prepared in 25% (0.033 g) yield from tripeptide acid product (0.100 g, 0.15 mmol) of step 2e (Example 2) in analogous fashion to the procedure of Step 27c of Example 27 except that l-(4-methoxy- benzyl)-cyclopropanesulfonamide (compond 42b was used in place of 1- trimethylsilanyl-cyclopropanesulfonamide and purified by PTLC (MeOH7CH₂Cl₂: 2% to 5%) and preparative HPLC (solvent B: 35 to 100%): 1H NMR (methanol-d₄) D ppm 0.94 (m, 2 H), 0.98 (s, 9 H), 1.24 (s, 9 H), 1.39 (m, 3 H), 1.88 (m, 1 H), 2.36 (m, 2 H), 2.73 (dd, 7=13.36, 7.14 Hz, 1 H), 3.23 (m, 2 H), 3.74 (s, 3 H), 3.98 (s, 3 H), 4.10 (m, 1 H), 4.20 (s, 1 H), 4.60 (m, 2 H), 5.16 (d, 7=9.15 Hz, 1 H), 5.33 (d, 7=17.20 Hz, 1 H), 5.67 (s, 1 H), 5.79 (s, 1 H), 6.82 (d, 7=6.59 Hz, 2 H), 7.04 (d, 7=8.78 Hz, 2 H), 7.20 (dd, 7=9.15, 2.20 Hz, 1 H), 7.40 (s, 1 H), 7.45 (d, 7=2.56 Hz, 1 H), 7.61 (m, 3 H), 8.04 (d, 7=3.66 Hz, 2 H), 8.20 (d, 7=9.15 Hz, 1 H). MS m/z 908 ( T-1), LC-MS (retention time: 1.53, Method H).

Compound 43 Example 43

compound ₄3

Step 43a: Preparation of 1- 1 -(1 -hydroxy- 1-methylethvD- cyclopropanesulfonamide- tert-butylcarbamate

Step 43a) Compound 43a, l-(l-hydroxy-l-methylethyl)- cyclopropanesulfonamide- tert-butylcarbamate, was obtained in 49% (1.23 g) from 2.0 g (9.04 mmol) of cyclopropanesulfonamide-tert-butylcarbamate according to the procedure described in the synthesis of 1-methoxymethylcyclo- propylsulfonylamine tert-butylcarbamate (Step 15IId) except 1.1 equivalents of 2-acetone was used as electrophile and purified by Biotage 40M column using EtOAc/hexanes (0% to 60%) as the eluent: 1H NMR (CDC1₃) D ppm 1.13 (m, 2 H), 1.40 (s, 6 H), 1.48 (s, 9 H), 1.68 (m, 2 H), 2.59 (m, 1 H), 7.42 (s, 1 H); ¹³C NMR (CDC1₃) D ppm 10.94, 27.96, 28.49, 48.46, 83.91, 149.35.

Step 43b: Preparation of l-(2-floro-benzy) -cyclopropanesulfonic acid amide

-δ .-^NH₂

compound 3b Step 43b) This compound, 1-isopropenyl -cyclopropanesulfonamide, was obtained in 94% yield (0.36 g) from 0.6 g (2.15 mmol) of 1-(1 -hydroxy- 1-methylethyl)- cyclopropanesulfonamide- tert-butylcarbamate according to the procedure described in the synthesis of 1-butyl-cyclopropanesulfonic acid amide (Step 30b) and purified by Redisep 35 g column using EtOAc/hexanes (5% to 100% ) as the eluent: 1H NMR (Methanol- *) D ppm 1.00 (m, 2 H), 1.42 (m, 2 H), 1.97 (s, 3 H), 5.27 (d, 7=6.59 Hz, 2 H).

Step 43c: Preparation of compound 43, Example 43, BOCNH-P3(L-t-BuGlv)-

P2r(4_-)-(2-ρhenyl-7-methoxyquinoline-4-oxo)-S-proline]-Pl(l__,2S Vinyl Acca)-

CONΗSθ2(l-z'- -propenylclopropan-l-yl) or alternate designation. Compound

43, example 43, { l-r2-ri-(l-Isopropenyl-cyclopropanesulfonylaminocarbonyl)-

2-vinyl-cvclopropylcarbamoyl]-4-(7-methoxy-2-phenyl-quinolin-4-yloxy)- pyrrolidine-l-carbonyl1-2,2-dimethyl-propyl)-carbamic acid tert-butyl ester

compound ₄3

Step 43c) Compound 43 was obtained in 30% (0.0215 g) yield from tripeptide acid product (0.060 g, 0.09 mmol) of step 2e (Example 2) in analogous fashion to the procedure of Step 27c of Example 27 except that 1-isopropenyl- cyclopropanesulfonamide was used in place of 1-trimethylsilanyl- cyclopropanesulfonamide: 1H NMR (methanol-d₄) D ppm 0.96 (m, 2 H), 1.03 (s, 9 H), 1.27 (s, 9 H), 1.37 (dd, 7=9.33, 4.94 Hz, 1 H), 1.58 (m, 2 H), 1.77 (m, 1 H), 1.94 (s, 3 H), 2.14 (m, 1 H), 2.42 (m, 1 H), 2.68 (dd, 7=13.54, 7.32 Hz, 1 H), 3.93 (s, 3 H), 4.06 (m, 1 H), 4.24 (s, 1 H), 4.53 (m, 2 H), 5.14 (m, 4 H), 5.52 (s, 1 H), 5.90 (m, 1 H), 7.06 (d, 7=8.78 Hz, 1 H), 7.22 (s, 1 H), 7.37 (d, 7=2.20 Hz, 1 H), 7.50 (m, 3 H), 8.06 (m, 3 H). LC-MS (retention time: 1.74, Method I), MS m/z 830(M⁺+1).

Compound 44 Example 44

compound ₄₄

Step 44a: Preparation of 1 -/■so-butenylcvclopropanesulfonamide- tert- butylcarbamate

Step 44a) This compound, 1 -(2-Methyl-allyl)-cyclopropanesulfonamide- tert-butylcarbamate, was obtained in 95% (1.18 g) from 1.0 g (4.52 mmol) of cyclopropanesulfonamide-tert-butylcarbamate according to the procedure described in the synthesis of 1-methoxymethylcyclo-propylsulfonylamine tert- butylcarbamate (Step 15IId) except 1.1 equivalents of iso-butyl bromide was used as electrophile: 1H NMR (CDC1₃) D ppm 0.93 (m, 2 H), 1.49 (s, 9 H), 1.73 (m, 2 H), 1.78 (d, 7=7.93 Hz, 3 H), 2.58 (s, 2 H), 4.87 (m, 1 H), 4.88 (m, 1 H), 6.77 (s, I H).

Step 44b: Preparation of l-^o-butenylclopropanesulfonamide

compound 44b1 compound ₄₄b2 Step 44b) A 1/1 mixtur of compound 44bl and compound 44b2 (0.3 lg ) was obtained from 1.0 g (3.6 mmol) of 1 -zso-butenylcyclopropanesulfonamide- tert-butylcarbamate (compound 44a) by fellowing the procedure described in the synthesis of 1-butyl-cyclopropanesulfonic acid amide (Step 30b) as a white solid: 1H NMR (Methanol-d₄) D ppm 0.97 (m, 2 H), 1.09 (m, 1 H), 1.35 (m, 2 H), 1.40 (s, 6 H), 1.49 (m, 2 H), 1.80 (s, 3 H), 1.88 (s, 3 H), 2.25 (s, 2 H), 5.49 (s, 1 H).

Step 44c: Preparation of compound 44. Example 44, BOCNH-P3(L-t-BuGlv)-

P2r(4R)-(2-phenyl-7-methoχyquinoline-4-oxo)-S-proline1-Pl(l_,,2S Vinyl Acca -

CONHSO2ri-(2-methyl-propen-3-yl)-clopropan-l-yl) or alternate designation.

Compound 44, example 44, ri-(4-(7-Methoxy-2-phenyl-quinolin-4-yloxy)-2-{ 1- ri-(2-methyl-propenyl)-cvclopropanesulfonylaminocarbonyl]-2-vinyl- cvclopropylcarbamoyl|-pyrrolidine-l-carbonyl)-2,2-dimethyl-propyl1-carbamic acid tert-butyl ester

compound ₄₄

Step 44c) Compound 44 was prepared in 28% (0.0346 g) yield from tripeptide acid product (0.100 g, 0.09 mmol) of step 2e (Example 2) in analogous fashion to the procedure of Step 27c of Example 27 except that l-(2-methyl- propenyl)-cyclopropanesulfonamide (compound 44b) was used in place of 1- trimethylsilanyl-cyclopropanesulfonamide and purified by preparative HPLC (solvent B: 40-85%): 1H NMR (methanol-d₄) D ppm 0.85 (m, 2 H), 1.04 (s, 9 H), 1.28 (s, 9 H), 1.58 (m, 10 H), 2.10 (m, 1 H), 2.47 (m, 1 H), 3.03 (m, 1 H), 3.93 (s, 3 H), 4.08 (m, 1 H), 4.24 (s, 1 H), 4.55 (m, 2 H), 5.00 (m, 1 H), 5.21 (d, 7=17.57 Hz, 1 H), 5.37 (s, 1 H), 5.53 (s, 1 H), 5.89 (m, 1 H), 7.05 (dd, 7=9.15, 2.20 Hz, 1 H), 7.23 (s, 1 H), 7.37 (d, 7=2.20 Hz, 1 H), 7.49 (m, 3 H), 8.07 (m, 3 H). LC-MS (retention time: 1.82, Method L), MS m/z 844 (MM). Compound 45 Example 45

Step 45a: Preparation of 1- Pent-2-ynyl-cyclopropanesulfonamide- tert- butylcarbamate

Step 45a ) This compound, 1- Pent-2-ynyl-cyclopropanesulfonamide- tert-butylcarbamate, was obtained 79% (1.03 g) from 1.0 g (4.52 mmol) of cyclopropanesulfonamide-tert-butylcarbamate according to the procedure described in the synthesis o l-methoxymethylcyclo-propylsulfonylamine tert- butylcarbamate (Step 15IId) except 1.1 equivalents of l-bromo-pent-2-yne was used as electrophile: 1H NMR (CDC1₃) D ppm 1.10 (t, 7=7.48 Hz, 3 H), 1.15 (m, 2 H), 1.50 (s, 9 H), 1.62 (m, 2 H), 2.14 (m, 2 H), 2.90 (t, 7=2.44 Hz, 2 H), 6.91 (s, 1 H).

Step 45b: Preparation of 1- Pent-2-ynyl -cyclopropanesulfonamide

-e^NH-. O O compound 5b Step 45b) This compound, 1- Pent-2-ynyl -cyclopropanesulfonic acid amide, was obtained in 100% yield (0.72 g) from 1.1 g (3.83 mmole) of 1- Pent- 2-ynyl-cyclopropanesulfonamide- tert-butylcarbamate, according to the procedure described in the synthesis of l-butyl-cyclopropanesulfonic acid amide (Step 29ϋe) as a white solid: 1H NMR (Methanol-d-) D ppm 1.06 (m, 2 H), 1.09 (t, 7=7.48 Hz, 3 H), 1.23 (m, 2 H), 2.14 (m, 2 H), 2.94 (t, 7=2.44 Hz, 2 H).

Step 45c: Preparation of compound 45, Example 45, BOCNH-P3(L-t-BuGly)- P2r(4_-)-(2-phenyl-7-methoxyquinoline-4-oxo)-S-proline]-Pl(lR,2S Vinyl Acca)-

CONHSO2ri-(l-pent-2-ynyl)-clopropan-l-yl) or alternate designation. Compound 45, example 45, (l-{4-(7-Methoxy-2-phenyl-quinolin-4-yloxy)-2-ri-

(l-pent-2-ynyl-cvclopropanesulfonylaminocarbonyl)-2-vinyl- cyclopropylcarbamoyl1-pyrrolidine-l-carbonyl}-2,2-dimethyl-propyl)-carbamic acid tert-butyl ester

Step 45c) Compound 45 was prepared in 31% (0.0382 g)yield from tripeptide acid product (0.100 g, 0.15 mmol) of step 2e (Example 2) in analogous fashion to the procedure of Step 27c of Example 27 except that l-Pent-2-ynyl- cyclopropanesulfonic acid amide was used in place of 1-trimethylsilanyl- cyclopropanesulfonamide and purified by preparative HPLC (solvent B: 40- 100%): 1H NMR (methanol-d-) D ppm 0.97 (m, 5 H), 1.04 (s, 9 H), 1.26 (s, 9 H), 1.30 (m, 3 H), 1.83 (m, 1 H), 2.03 (m, 3 H), 2.50 (m, 1 H), 2.73 (m, 1 H), 2.99 (s, 2 H), 3.92 (s, 3 H), 4.08 (m, 1 H), 4.25 (m, 1 H), 4.56 (m, 2 H), 5.01 (m, 1 H), 5.20 (d, 7=17.09 Hz, 1 H), 5.52 (s, 1 H), 5.91 (m, 1 H), 7.05 (m, 1 H), 7.20 (m, 1 H), 7.37 (m, 1 H), 7.50 (m, 3 H), 8.07 (m, 3 H). LC-MS (retention time: 1.86, Method L), MS m/z 856 (M^+l).

Compound 46 Example 46

compound ₄6

Step 46a: Preparation of l-(5-Phenyl-oxazol-4-ylmethyl)- cyclopropanesulfonamide- tert-butylcarbamate

y==N V7 H

BuLi s—r^^Sss X =N ^Pl- ° ° O I

V ° ° °v .Br compound ₄6a

Ph

Step 46a) This compound, l-(5-ρhenyl-oxazol-4-ylmethyl)- cyclopropanesulfonamide- tert-butylcarbamate, was obtained 27% (0.461 g) from 1.0 g (4.52 mmol) of cyclopropanesulfonamide-tert-butylcarbamate according to the procedure described in the synthesis of 1-methoxymethylcyclo- propylsulfonylamine tert-butylcarbamate (Step 15IId) except 1.1 equivalents of 5-bromomethyl-3-phenyl-isoxazole was used as electrophile: 1H NMR (CDC1₃) δ ppm 1.06 (m, 2 H), 1.48 (s, 9 H), 1.66 (m, 2 H), 3.51 (s, 2 H), 7.41 (m, 4 H), 7.55 (m, 1 H), 7.63 (d, 7=6.95 Hz, 1 H), 7.85 (s, 1 H).

Step 46b: Preparation of l-(5-Phenyl-oxazol-4-ylmethyl)- cyclopropanesulfonamide

compound ₄6b

Step 46b) This compound, l-(5-phenyl-oxazol-4-ylmethyl)- cyclopropanesulfonic acid amide, was obtained in 54% yield (0.126g) from 0.32 g (3.83 mmole) of 1- Pent-2-ynyl-cyclopropanesulfonamide- tert-butylcarbamate, according to the procedure described in the synthesis of l-butyl- cyclopropanesulfonic acid amide (Step 30a, Example 30) but without purification: 1H NMR (Methanol-d ) D ppm 0.79 (m, 2 H), 1.26 (m, 2 H), 3.59 (s, 2 H), 7.37 (m, 2 H), 7.50 (m, 2 H), 7.72 (d, 7=6.95 Hz, 1 H), 8.17 (s, 1 H).

Step 46c: Preparation of compound 46, Example 46, BOCNH-P3(L-t-BuGlv)- P2r(4_?)-(2-phenyl-7-methoxyαuinoline-4-oxo)-S-ρroline1-Pl(l__,2S Vinyl AccaV

CONHSθ2-ri-(5-phenyl-oxazol-4-ylmethyl)-clopropan-l-vn or alternate designation. Compound 46, example 46, rri-(4-(7-Methoxy-2-phenyl-quinolin-4- ylo y)-2- { 1 - f 1 -(5 -phen yl-oxazol-4- ylmethyl)- cvclopropanesulfonylaminocarbonyl]-2-vinyl-vclopropylcarbamoyl)-pyrrolidine- l-carbonyl)-2,2-dimethyl-propyl]-carbamic acid tert-butyl ester

compund ₄6

Step 46c) Compound 46 was prepared in 18% (0.0255 g) yield from tripeptide acid product (0.080 g, 0.12 mmol) of step 2e (Example 2) in analogous fashion to the procedure of Step 27c of Example 27 except that l-(4-phenyl- isoxazol-5-ylmethyl)-cyclopropanesulfonamide of the product of Step 46b (Example 46) was used in place of 1-trimethylsilanyl-cyclopropanesulfonamide and purified by preparative HPLC (solvent B: 40-90%): 1H NMR (methanol-d-) D ppm 1.04 (s, 9 H), 1.32 (s, 9 H), 1.41 (m, 4 H), 1.68 (m, 1 H), 1.84 (dd, 7=7.32, 4.88 Hz, 1 H), 2.06 (m, 1 H), 2.60 (m, 1 H), 2.72 (m, 1 H), 3.57 (d, 7=14.65 Hz, 1 H), 3.62 (m, 1 H). 4.17 (m, 3 H), 4.23 (dd, 7=5.49, 3.05 Hz, 1 H), 4.28 (s, 1 H), 4.51 (d, 7=11.60 Hz, 1 H), 4.56 (t, 7=8.55 Hz, 1 H), 4.97 (d, 7=11.29 Hz, 1 H), 5.18 (d, 7=17.09 Hz, 1 H), 5.54 (s, 1 H), 6.05 (m, 1 H), 7.06 (dd, 7=9.00, 1.98 Hz, 1 H), 7.27 (m, 2 H), 7.41 (m, 3 H), 7.49 (m, 3 H), 7.68 (m, 3 H), 8.01 (m, 3 H). MS m/z 946 (M^"-l) HPLC (retention time: 1.96, Method M).

Compound 47 Example 47

compound ₄7

Step 47a: Preparation of 1- (4-pyridyl)-cyclopropanesulfonamide

step 47a) To a solution of cyclopropylsulfonylamine tert-butyl carbamate

(105 g, 4.52 mmol) in THF (9 mL) cooled to -78 °C, was added π-BuLi (6.2 mL, 9.2 mmol, 1.6 M in hexane). The mixture was stirred for 1 h at -78 °C, and 0.55 mL (0.5 mmol) of fresh 4-(bromomethyl)pyridine was injected in one portion. The fresh 4-(bromomethyl)-pyridine was made from 4-(bromomethyl)pyridine hydrobromide by tributing between aqueous sodium bicarbonate and ether, ether layer was quickly separated, dried (MgSO₄), removed solvent in vacuo, and immediately used to the reaction. The reaction mixture was stirred for 5 min at - 78 °C, changed the bath into ice water, and stirred for another 1 h. The reaction mixture was diluted with pH 4.0 buffer, adjusted pH to 4, and extracted with EtOAc. The combined extractions were dried (MgSO₄), concentrated, and purified by pre-HPLC to afford a mixture (only 0.42 g) with 1- (4-pyridyl)- cyclopropanesulfonamide- tert-butylcarbamate and the mixture was used in next step. Step 47b: Preparation of 1- (4-pyridyl)-cyclopropanesulfonamide

compound ₄₇b

Step 47b ) This compound, l-Pyridin-2-ylmethyl)-cyclopropanesulfonic acid amide, was obtained in 13% yield (0.12 g) two steps from the mixture of 47 according to the procedure described in the synthesis of 1-butylcyclopropanesulfonamide (Step 30b) and purified by prep-HPLC (solvent B: 0- 80%) as a white solid: 1H NMR (Methanol-d₄) D ppm 0.90 (m, 2 H), 1.38 (m, 2 H), 3.38 (s, 2 H), 7.55 (d, 7=6.22 Hz, 2 H), 8.50 (d, 7=4.39 Hz, 2 H).

Step 47c: Preparation of compound 47, Example 47, BOCNH-P3(L-t-BuGlv)-

P2r(4_?)-(2-phenyl-7-methoxyquinoline-4-oxo)-S-proline1-Pl(l_.,2S Vinyl Acca)-

CONHSθ2-ri-(l-pyridin-4-ylmethyl) -clopropan-l-yl] or alternate designation, Compound 47, example 47, (l-{4-(7-Methoxy-2-phenyl-quinolin-4-yloxy)-2-ri-

( 1 -p yridin-4- ylmeth yl-c yclopropanesulf onylaminocarbon yl)-2- vinyl- cyclopropylcarbamoyl1-pyrrolidine-l-carbonyl|-2,2-dimethyl-propyl)-carbamic acid tert-butyl ester

compound ₄7

Step 47c) Compound 47 was prepared in 58 % (0.0739 g) yield from tripeptide acid product (0.120 g, 0.17 mmol) of step 2e (Example 2) in analogous fashion to the procedure of Step 27c of Example 27 except that l-pyridin-4- ylmethyl cyclopropanesulfonamide (compound 47b, Example 47) was used in place of 1-trimethylsilanyl-cyclopropanesulfonamide and purified by preparative HPLC (solvent B: 0-85%): 1H NMR (methanol-d-) D ppm 2.30 (m, 1 H), 2.39 (m, 1 H), 2.76 (dd, 7=13.43, 6.71 Hz, 1 H), 3.37 (m, 2 H), 4.01 (s, 3 H), 4.12 (d, 7=9.46 Hz, 1 H), 4.23 (s, 1 H), 4.65 (m, 2 H), 5.19 (d, 7=8.85 Hz, 1 H), 5.35 (d, 7=16.79 Hz, 1 H), 5.67 (s, 1 H), 5.77 (s, 1 H), 6.94 (s, 1 H), 7.21 (d, 7=9.16 Hz, 1 H), 7.41 (s, 3 H), 7.47 (s, 1 H), 7.62 (s, 3 H), 8.07 (s, 2 H), 8.22 (d, 7=9.16 Hz, 1 H), 8.48 (s, 2 H). MS m z 881 (M⁺+l), MS m/z 799 (M^'-l). LC-MS (retention time: 1.39, Method H), MS m/z 881 (M⁺+l).

Compound 48 Example 48

compound ₄8

Step 48a: Preparation of l-Pyridin-2-ylmethyl -cyclopropanesulfonamide- tert- butylcarbamate

step 48a) This umpure compound , l-Pyridin-2-ylmethyl- cyclopropanesulfonamide- tert-butylcarbamate, was obtained 0.61 g from 1.0 g (4.52 mmol) cyclopropanesulfonamide- tert-butylcarbamate, according to the procedure described in the synthesis of l-pyridin-4-ylmethyl- cyclopropanesulfonamide- tert-butylcarbamate (step 47a). The umpure product was used in next step. Step 48b: Preparation of l-pyridin-2-ylmethyl-cyclopropanesulfonamide

-■_o-NH. O O compound 48b

Step 48b) This compound, l-(pyridin-2-ylmethyl)- cyclopropanesulfonamide- tert-butylcarbamate, was obtained in 18% yield (0.171 g) in two steps from umpure product of Step 48a according to the procedure described in the synthesis of l-pyridin-4-ylmethyl-cyclopropanesulfonamide- tert-butylcarbamate (Step 47b) and purified by preparative HPLC (solvent B: 0 to 80%) as a white solid as a white solid: 1H NMR (Methanol-d₄) D ppm 1.19 (m, 2 H), 1.48 (m, 2 H), 3.60 (s, 2 H), 7.89 (t, 7=6.77 Hz, 1 H), 8.09 (d, 7=8.42 Hz, 1 H), 8.46 (t, 7=7.87 Hz, 1 H), 8.71 (d, 7=5.86 Hz, 1 H).

Step 48c: Preparation of compound 48, Example 48, BOCNH-P3(L-t-BuGlv)-

P2 r(4__)-(2-phenyl-7-methoxyquinoline-4-oxo)-S-proline1 -P 1 ( 1R.2S Vinyl Acca)-

CONHSθ2-ri-(l-pyridin-2-ylmethyl) -clopropan-l-yl] or alternate designation.

Compound 48, example 48, (l-{4-(7-Methoxy-2-phenyl-quinolin-4-yloxy)-2-[^"l-

(l-pyridin-2-ylmethyl-cvclopropanesulfonylaminocarbonyl)-2-vinyl- cvclopropylcarbamoyl1-pyπOlidine-l-carbonyl}-2,2-dimethyl-propyl)-carbamic acid tert-butyl ester

compound ₄8

Step 48c) Compound 48 was prepared in 67% (0.086 g) yield from tripeptide acid product (0.120 g, 0.17 mmol) of step 2e (Example 2) in analogous fashion to the procedure of Step 27c of Example 27 except that l-pyridin-2- ylmethyl cyclopropanesulfonamide (Compound 48b) was used in place of 1- trimethylsilanyl-cyclopropanesulfonamide preparative HPLC (solvent 0 to 85%): 1H NMR (methanol-d₄) D ppm 0.97 (s, 9 H), 0.99 (m, 2 H), 1.22 (s, 9 H), 1.48 (m, 3 H), 1.85 (m, 1 H), 2.27 (q, 7=8.90 Hz, I H), 2.41 (m, 1 H), 2.76 (dd, 7=13.54, 6.95 Hz, 1 H), 3.39 (d, 7=13.91 Hz, 1 H), 3.50 (m, 1 H), 3.99 (s, 3 H), 4.09 (d, 7=12.08 Hz, 1 H), 4.18 (s, 1 H), 4.62 (m, 2 H), 5.14 (d, 7=10.25 Hz, 1 H), 5.31 (d, 7=16.83 Hz, 1 H), 5.76 (m, 2 H), 7.25 (dd, 7=9.15, 2.20 Hz, 1 H), 7.31 (dd, 7=7.68, 5.12 Hz, 1 H), 7.46 (m, 3 H), 7.64 (m, 3 H), 7.78 (m, 1 H), 8.05 (m, 2 H), 8.24 (d, 7=9.15 Hz, 1 H), 8.44 (d, 7=4.03 Hz, 1 H). MS m/z 881 (M⁺+1), MS m/z 799 (M^'-l). LC-MS (retention time: 1.43, Method H), MS m/z 881 (M⁺+1).

Compound 49 Example 49

compound ₄9 Step 49a: Preparation of l-Pyridin-3-ylmethyl cyclopropanesulfonamide- tert- butylcarbamate

Step 49a) To a solution of cyclopropylsulfonylamine tert-butyl carbamate (105 g, 4.52 mmol) in THF (9 mL) cooled to -78 °C, was added n-BuLi (6.2 mL, 9.2 mmol, 1.6 M in hexane). The mixture was stirred for 1 h at -78 °C, and fresh ether solution (2 mL) of 3-(bromomethyl)pyridine was injected in one portion. The fresh 3-(bromomethyl)pyridine was made from 1.5 g (5.9 mmol) of 3- (bromomethyl)pyridine hydrobromide tributed between aqueous sodium bicarbonate and ether. The ether layer was quickly separated, dried (MgSO₄), and concentrated in vacuo till about 2 mL liquid left. The reaction mixture was stirred for 4 min, changed the bath into ice water, and stirred for 1 h. The reaction mixture was diluted with pH 4.0 buffer, adjusted pH to 4, and extracted with EtOAc. The extraction was dried (MgSO₄), concentrated, and purified by prep-

1

HPLC (sovent B: 0 to 80%) to afford 0.61 g mixture with 1- (3-pyridyl)- cyclopropanesulfonamide- tert-butylcarbamate, and the mixture was used in next step.

Step 49b: Preparation of l-(pyridin-2-ylmethyl)-cyclopropanesulfonamide

compound 9b

Step 49b) This compound, l-(Pyridin-2-ylmethyl)-cyclopropanesulfonic acid amide, was obtained in 11% yield (0.107 g, two steps) from 0.5 g of impure l-(pyridin-3-ylmethyl)-)-cyclopropanesulfonamide- tert-butylcarbamate according to the procedure described in the synthesis of l-(Pyridin-4-ylmethyl)- cyclopropanesulfonic acid amide (Step 48b, Example 48): 1H NMR (Methanol- U) D ppm 1.11 (m, 2 H), 1.46 (m, 2 H), 3.44 (s, 2 H), 7.94 (dd, 7=8.09, 5.65 Hz, 1 H), 8.53 (d, 7=8.24 Hz, 1 H), 8.71 (d, 7=5.19 Hz, 1 H), 8.82 (s, 1 H).

Step 49c: Preparation of compound 49, Example 49, BOCNH-P3(L-t-BuGly)-

P2 r(4R)-(2-phenyl-7-methoxyquinoline-4-oxo)-S-proline] -PI ( 1R,2S Vinyl Acca)-

CONHSθ2-Fl-(l-pyridin-3-ylmethyl) -clopropan-1-yl] or alternate designation.

Compound 49, example 49, (l-{4-(7-Methoxy-2-phenyl-quinolin-4-yloxy)-2-f 1-

( 1 -pyridin-3-ylmethyl-cyclopropanesulf ^onylaminocarbonyl)-2-vinyl- cvclopropylcarbamoyl1-pyιτolidine-l-carbonyl|-2,2-dimethyl-propyl)-carbarnic acid tert-butyl

compound ₄9 Step 49c) Compound 49 was prepared in 14% (0.0127 g)yield from tripeptide acid product (0.080 g, 0.12 mmol)of step 2e (Example 2) in analogous fashion to the procedure of Step 27c of Example 27 except that l-pyridin-3- ylmethyl-cyclopropanesulfonamide was used in place of 1-trimethylsilanyl- cyclopropanesulfonamide and purified by preparative HPLC (solvent B: 0 to 85%): 1H NMR (methanol-d-) D ppm 0.97 (s, 9 D 1.20 (s, 9 D 1.31 (m, 4 D 1.58 (m, 1 01.91 (dd, 7=8.24, 5.49 Hz, 1 D2.29 (m, 1 D2.41 (m, 1 D2.77 (dd, 7=14.19, 6.87 Hz, 1 D3.30 (m, 1 D3.39 (m, 1 D4.03 (s, 3 D4.ll (dd, 7=12.05, 2.90 Hz, 1 Q4.17 (s, 1 D4.65 (m, 2 D5.18 (m, 1 D5.34 (d, 7=17.09 Hz, 1 D5.75 (m, 2 D6.92 (s, 1 D7.32 (m, 1 D7.46 (s, 1 D7.49 (s, 1 D7.56 (s, 1 D .71 (m, 3 D7.86 (d, 7=6.41 Hz, 1 D8.06 (dd, 7=7.78, 1.68 Hz, 2 D8.30 (d, 7=8.85 Hz, 1 D8.49 (s, 1 H). LC-MS (retention time: 1.49, Method I), MS m/z 881 (M⁺+l).

Compound 50 Example 50

Step 50a: Preparation of l-(3,5-Dimethyl-isoxazol-4-ylmethyl)- cyclopropanesulfonamide- tert-butylcarbamate

Step 50a) This compound, l-(3,5-Dimethyl-isoxazol-4-ylmethyl)- cyclopropanesulfonamide- tert-butylcarbamate, was obtained 45% (0.672 g) from 1.0 g (4.52 mmol) of cyclopropanesulfonamide-tert-butylcarbamate according to the procedure described in the synthesis of 1-methoxymethylcyclo- propylsulfonylamine tert-butylcarbamate (Step 15IId) except 1.1 equivalents of 4-chloromethyl-3,5-dimethyl-isoxazole was used as electrophile and purified over Biotage 40L using EtOAc/Hexanes (5% to 100%) as the eluent: 1H NMR (CDC1₃) 5 D ppm 0.66 (m, 2 H), 1.50 (s, 9 H), 1.64 (m, 2 H), 2.20 (s, 3 H), 2.32 (s, 3 H), 3.07 (s, 2 H), 6.80 (s, 1 H).

Step 50b: Preparation of l-(3,5-Dimethyl-isoxazol-4-ylmethyl)- cyclopropanesulfonic acid amide 1

^*J_ Q compound 50b

Step 50b) Compound 50b, l-(3,5-Dimethyl-isoxazol-4-ylmethyl)- cyclopropanesulfonic acid amide, was obtained in 24% yield (0.083 g) from 0.48 g ( of l-(3,5-Dimethyl-isoxazol-4-ylmethyl)-cyclopropanesulfonamide- tert- 15 butylcarbamate according to the procedure described in the synthesis of 1-

(Pyridin-4-ylmethyl)-cyclopropanesulfonic acid amide (Step 47b, example 47): 1H NMR (Methanol-d₄) D ppm 0.47 (m, 2 H), 1.18 (m, 2 H), 2.14 (s, 3 H), 2.26 (s, 3 H), 3.06 (s, 2 H), 4.73 (s, 2 H).

Step 50c: Preparation of compound 50, Example 50, BOCNH-P3(L-t-BuGlvV

P2r(4_,)-(2-phenyl-7-methoxyquinoline-4-oxo)-S-proline]-Pl(l-.,2S Vinyl AccaV

CONHSθ₂-ri-(3,5-Dimethyl-isoxazol-4-ylmethyl)-clopropan-l-yl] or alternate designation. Compound 50, example 50, { l-r2-(l-ri-(3,5-Dimethyl-isoxazol-4- ylmethyl)-cyclopropanesulfonylaminocarbonyl]-2-vinyl-cyclopropylcarbamoyli-

4-(7-methoxy-2-phenyl-quinolin-4-yloxy)-pyrrolidine-l-carbonyl]-2,2-dimethyl- propyll -carbamic acid tert-butyl ester

Step 50c) Compound 50 was prepared in 32% (0.0254 g) yield from tripeptide acid product (θ'.060 g) of step 2e (Example 2) in analogous fashion to the procedure of Step 27c of Example 27 except that l-(3,5-dimethyl-isoxazol-4- ylmethyl)-cyclopropanesulfonamide (Compound 50b, Example 50) was used in place of 1-trimethylsilanyl-cyclopropanesulfonamide and purified by preparative HPLC (solvent B: 40 to 85%): 1H NMR (methanol-d₄) D ppm 0.60 (m, 2 H),

0.95 (s, 9 H), 1.19 (s, 9 H), 1.43 (m, 2 H), 1.61 (m, 1 H), 1.90 (dd, 7=8.1, 5.3 Hz, 1 H), 2.19 (s, 3 H), 2.28 (m, 1 H), 2.32 (s, 3 H), 2.38 (m, 1 H), 2.77 (dd, 7=13.9, 7.2 Hz, 1 H), 3.07 (d, 7=14.7 Hz, 1 H), 3.15 (m, 1 H), 4.03 (s, 3 H), 4.10 (m, 1 H), 4.16 (s, 1 H), 4.65 (m, 2 H), 5.15 (m, 1 H), 5.33 (m, 1 H), 5.74 (m, 2 H), 7.34 (dd, 7=9.2, 2.14 Hz, 1 H), 7.50 (d, 7=2 Hz, 1 H), 7.57 (s, 1 H), 7.70 (m, 3 D8.06 (m, 2 H), 8.31 (m, 1 H). LC-MS (retention time: 1.69, Method I) MS m/z 899 (M÷+l). Compound 51 Example 51

Step 51a: Preparation of l-(5-Methyl-isoxazol-3-ylmethyl)- cyclopropanesulfonamide- tert-butylcarbamate

Step 51a) This compound, l-(5-methyl-isoxazol-3-ylmethyl)- cyclopropanesulfonamide- tert-butylcarbamate, was obtained 34% (0.486 g) from 1.0 g (4.52 mmol) of cyclopropanesulfonamide-tert-butylcarbamate according to the procedure described in the synthesis of -(3,5-Dimethyl-isoxazol- 4-ylmethyl)-cyclopropanesulfonamide- tert-butylcarbamate (Step 50a) except 1.1 equivalents of 3-Chloromethyl-5-methyl-isoxazolewas used as electrophile: 1H NMR (CDC1₃) D ppm 1.04 (m, 2 H), 1.45 (s, 9 H), 1.71 (m, 2 H), 2.37 (s, 3 H), 3.23 (s, 2 H), 5.98 (s, 1 H), 7.65 (s, 1 H).

Step 51b Preparation of compound l-(5-Methyl-isoxazol-3-ylmethyl)- cyclopropanesulfonic acid amide

compound 51b

Step 51b) This compound l-(5-methyl-isoxazol-3-ylmethyl)- cyclopropanesulfonic acid amide, was obtained in 24% yield (0.0813 g) from 0.48 g ( of l-(3,5-Dimethyl-isoxazol-4-ylmethyl)-cyclopropanesulfonamide- tert- butylcarbamate according to the procedure described in the synthesis of 1- butylcyclopropanesulfonic acid amide (Step 20b): 1H NMR (Methanol-d-) D ppm 0.89 (m, 2 H), 1.33 (m, 2 H), 2.38 (s, 3 H), 3.26 (s, 2 H), 6.16 (s, 1 H).

Step 51c: Preparation of compound 51, Example 51, BOCNH-P3(L-t-BuGly)- P2r(4-,)-(2-phenyl-7-methoxyquinoline-4-oxo)-S-proline]-Pl(l_-,2S Vinyl AccaV

CONHSO2~r 1 -(5-methyl-isoxazol-3-ylmethyl)-clopropan- 1 -yl] or alternate designation. Compound 51, example 51, lT-(4-(7-Methoxy-2-phenyl-quinolin-4- yloxy)-2-{ l-ri-(5-methyl-isoxazol-3-ylmethyl)- cyclopropanesulfonylaminocarbonyl]-2-vinyl-cyclopropylcarbamoyl)- pyrrolidine-l-carbonyl)-2,2-dimethyl-propyl]-carbamic acid tert-butyl ester

Step 51c) Compound 51 was prepared in 7% (0.0058 g)- yield from tripeptide acid product (0.060 g) of step 2e (Example 2) in analogous fashion to the procedure of Step 27c of Example 27 except that l-(5-Methyl-isoxazol-3- ylmethyl)-cyclopropanesulfonamide was used in place of 1-trimethylsilanyl- cyclopropanesulfonamide and purified by preparative HPLC (solvent B: 30 tol00%): 1H NMR (methanol-d₄) D ppm 0.89 (m, 2 H), 1.02 (s, 9 H), 1.28 (s, 9 H), 1.26 (m, 2 H), 1.60 (m, 1 H), 1.78 (m, 1 H), 2.12 (m, 1 H), 2.31 (s, 3 H), 2.50 (m, 1 H), 2.76 (m, 1 H), 3.28 (m, 2 H), 3.94 (m, 3 H), 4.10 (m, 1 H), 4.24 (s, 1 H), 4.54 (m, 2 H), 5.02 (s, 1 H), 5.20 (d, 7=16.79 Hz, 1 H), 5.55 (s, 1 H), 5.91 (m, 1 H), 6.10 (s, 1 H), 7.06 (d, 7=8.85 Hz, 1 H), 7.24 (s, 1 H), 7.39 (m, 1 H), 7.50 (m, 3 H), 8.05 (m, 3 H). LC-MS (retention time: 1.69, Method I), MS m/z 885 (M⁺+l). Compound 52 Example 52

compound 52

Step 52a: Preparation of compound 52a, example 52a, BOCNH-P3(L-val)-

P2r(4_,)-(2-phenyl-7-methoxyquinoline-4-oxo)-S-proline1-Pl(l__,2S Vinyl Acca)-

Carboxylic acid ethyl ester or alternate designation Compound 52a, example 52a, l-iri-(2-tert-Butoxycarbonylamino-3-methyl-butyryl)-4-(7-methoxy-2-phenyl- quinolin-4-yloxy)-pyrrolidine-2-carbonyl]-amino}-2-vinyl- cyclopropanecarboxylic acid ethyl ester

compund 52a

Step 52a) To a suspension of the product of Step 2c (Example 2), the HCl salt of (1R,2S) vinyl Acca PI isomer of 2-(l-Ethoxycarbonyl-2- vinylcyclopropylcarbamoyl)-4-(7-methoxy-2-phenyl-quinolin-4- yloxy)pyrrolidine-l-carboxylic acid ethyl ester (1.2 g; 1.99 mmol), N-BOC-L- valine (0.65 g, 2.39 mmol), ΝMM (1.0 g, 9.97 mmol) in DMF (12 mL) was added HATU (1.0 g, 2.59 mmol). After being stirred for overnite, the reaction mixture was diluted with EtOAc (200 mL), washed with pH 4.0 buffer (2x), saturated aqueous ΝaHCO₃ (30 mL), brine (30mL), dried (MgSO ), purified by a Biotage 40 M column (eluted with 15% to 60% EtOAc in Hexanes) to supply the titled product as a white solid (0.98 g, 70%). 1H NMR (methanol-d-) D ppm 0.95 (m, 6 H), 1.23 (m, 12 H), 1.42 ( , 1 H), 1.71 (dd, 7=8.05, 5.49 Hz, 1 H), 1.97 (m, 1 H), 2.22 (m, 1 H), 2.42 (m, 1 H), 2.73 (m, 1 H), 3.95 (s, 3 H), 4.10 (m, 4 H), 4.60 (m, 2 H), 5.09 (dd, 7=10.43, 1.65 Hz, 1 H), 5.26 (dd, 7=17.02, 1.65 Hz, 1 H), 5.57 (s, 1 H), 5.76 (m, 1 H), 7.10 (dd, 7=8.97, 2.38 Hz, 1 H), 7.25 (s, 1 H), 7.39 (d, 7=2.56 Hz, 1 H), 7.54 (m, 3 H), 8.07 (m, 3 H).

Step 52b: Preparation of Compound 52b, example 52b.BOCNH-P3(L-vaD-

P2r(4R)-(2-phenyl-7-methoxyouinoline-4-oxo)-S-proline1-Pl(lR,2S Vinyl Acca -

Carboxylic acid or alternate designation. Compound 52b, example 52b, l-(ri-(2- tert-Butoxycarbonylamino-3-methyl-butyryl)-4-(7-methoxy-2-phenyl-quinolin-4- yloxy)-pyrrolidine-2-carbonyl1-amino}-2-vinyl-cyclopropanecarboxylic acid

compound 52b

Step 52b) Compound 52b was prepared in 96% (0.90 g) yield from compound 52a product of step 52a (Example 52) in analogous fashion to the procedure of Example 2, Step 2e as a pale yellow foam: IH NMR (methanol-d-) D ppm 0.93 (m, 6 H), 1.23 (s, 9 H), 1.42 (m, 1 H), 1.69 (dd, 7=8.05, 5.49 Hz, 1 H), 1.97 (m, 1 H), 2.21 (m, 1 H), 2.47 (m, 1 H), 2.75 (m, 1 H), 3.95 (s, 3 H), 4.03 (m, 2 H), 4.60 (m, 2 H), 5.08 (d, 7=10.25 Hz, 1 H), 5.26 (d, 7=17.20 Hz, 1 H), 5.57 (s, 1 H), 5.83 (m, 1 H), 7.11 (dd, 7=8.97, 2.38 Hz, 1 H), 7.27 (s, 1 H), 7.40 (d, 7=2.20 Hz, 1 H), 7.54 (m, 3 H), 8.06 (m, 3 H).

Step 52c: Preparation of compound 52. Example 52, BOCNH-P3(L-f-ValV

P2r(4_,)-(2-phenyl-7-methoxyquinoline-4-oxo)-S-proline1-PUl-.,2S Vinyl AccaV

CONHSO2-(l-cvclopropylmethylclopropan-l-yl) or alternate designation.

Compound 52, example 52, ll-r2-ri-(l-Cyclopropylmethyl- cvclopropanesulfonylaminocarbonyl)-2-vinyl-cyclopropylcarbamovn-4-(7- methoxy-2-phenyl-quinolin-4-yloxy)-pyrrolidine-l-carbonyl1-2-methyl-propyll- carbamic acid tert-butyl ester

compoun 52

Step 52c) Compound 52 was prepared in 26% (0.0447 g, ) yield from the tripeptide acid product (0.140 g, 0.21 mmol) of step 52b (Example 52) in analogous fashion to the procedure of Step 27c of Example 27 but that valine tripeptide acid product (Step 52b) was used in place of tripeptide acid product of step 2e (Example 2) and 1-cyclopropylmethyl-cyclopropane sulfonamide in place of 1-trimethylsilanyl-cyclopropanesulfonamide. The reaction mixture was purified by PTLC (MeOHyCH₂Cl₂): 1H NMR (methanol-d₄) 1H NMR (methanol- d-) D ppm 0.05 (m, 2 H), 0.44 (m, 2 H), 0.68 (m, 1 H), 0.95 (dd, 7=17.70, 6.41 Hz, 6 H), 1.09 (m, 2 H), 1.24 (s, 9 H), 1.39 (dd, 7=9.31, 5.34 Hz, 1 H), 1.50 (m, 2 H), 1.83 (m, 3 H), 2.14 (m, 2 H), 2.37 (t, 7=10.53 Hz, 1 H), 2.62 (dd, 7=13.58, 6.56 Hz, 1 H), 3.93 (s, 3 H), 4.07 (m, 2 H), 4.54 (m, 2 H), 5.07 (d, 7=10.38 Hz, 1 H), 5.26 (d, 7=17.09 Hz, 1 H), 5.53 (s, 1 H), 5.76 (m, 1 H), 7.07 (dd, 7=9.16, 2.14 Hz, 1 H), 7.21 (s, 1 H), 7.37 (d, 7=2.14 Hz, 1 H), 7.50 (m, 3 H), 8.05 (m, 3 H). calcd for C₄₄H₅₆N₅SO₉: found: . LC-MS (retention time: 1.68, Method I), MS m/z 830 (M⁺+1). Compound 53 Example 53

Step 53: Preparation of compound 53, Example 53, BOCNH-P3(L-t- Val)-P2[(4R)-(2-phenyl-7-methoxyquinoline-4-oxo)-5-proline]-Pl(lR,25 Vinyl Acca)-CONHSO₂-[l-(2-methoxyethyl)-clopropan-l-yI] or alternate designation, Compound 53, example 54, {l-[2-{l-[l-(2-Methoxy-ethyl)- cyclopropanesulfonylaminocarbonyl]-2-vinyl-cyclopropylcarbamoyl}-4-(7- methoxy-2-phenyl-quinolin-4-yloxy)-pyrrolidine-l-carbonyl]-2-methyl- propyl}-carbamic acid tert-butyl ester

Step 53) Compound 53 was prepared in 61% (0.1063 g) yield from the tripeptide acid product (0.140 g, 0.21 mmol) of step 52b (Example 52) in analogous fashion to the procedure of Step 52c except that l-(2-methoxy-ethyl)- cyclopropanesulfonamide was used in place of 1- cyclopropylmethylcyclopropanesulfonamide: 1H NMR (methanol-d₄) D ppm 0.84 (d, 7=6.10 Hz, 6 H), 1.02 (m, 11 H), 1.32 (m, 3 H), 1.97 (m, 2 H), 2.11 (m, 2 H), 2.21 (m, 2 H), 2.58 (dd, 7=12.97, 5.04 Hz, 1 H), 3.31 (s, 3 H), 3.69 (t, 7=7.17 Hz, 2 H), 3.94 (m, 1 H), 3.95 (s, 3 H), 4.08 (m, 1 H), 4.22 (d, 7=8.85 Hz, 1 H),

4.57 (m, 1 H), 4.96 (d, 7=10.68 Hz, 1 H), 5.12 (d, 7=17.09 Hz, 1 H), 5.44 (s, 1 H), 6.01 (m, 1 H), 6.70 (d, 7=7.63 Hz, 1 H), 7.14 (s, 1 H), 7.36 (dd, 7=9.77, 2.75 Hz, 1 H), 7.50 (m, 3 H), 7.77 (d, 7=7.32 Hz, 1 H), 8.03 (d, 7=7.02 Hz, 2 H), . LC-MS (retention time: 1.56, Method I), MS m/z 834 (M⁺+1).

Compound 54 Example 54

Step 54: Preparation of compound 54, Example 54, BOCNH-P3(L-t- Val)-P2[(4R)-(2-phenyl-7-methoxyquinoline-4-oxo)-5-proline]-Pl(lR,2S Vinyl Acca)-CONHSO₂-(l-methoxymethylclopropan-l-yl) or alternate designation, Compound 54, example 55, {l-[2-[l-(l-Methoxymethyl- cyclopropanesulfonylaminocarbonyl)-2-vinyl-cyclopropylcarbamoyl]-4-(7- methoxy-2-phenyl-quinolin-4-yloxy)-pyrrolidine-l-carbonyl]-2-methyl- propyl}-carbamic acid tert-butyl ester

compound 5₄

Step 54) Compound 54 was prepared in 25% (0.0404 g) yield from the tripeptide acid product (0.140 g, 0.21 mmol) of step 52b (Example 52) in analogous fashion to the procedure of Step 52c (Example 52) except that l-(2- methoxy-ethyl)-cyclopropanesulfonamide was used in place of 1- cyclopropylmethyl-cyclopropanesulfonamide and : 1H NMR (Solvent methanol- cU) D ppm 0.94 (m, 8 H), 1.25 (s, 9 H), 1.40 (m, 3 H), 1.81 (dd, 7=7.68, 5.49 Hz, 1 H), 2.08 (m, 2 H), 2.45 (t, 7=10.25 Hz, 1 H), 2.67 (m, 1 H), 3.30 (s, 3 H), 3.66 (d, 7=10.98 Hz, 1 H), 3.75 (d, 7=10.98 Hz, 1 H), 3.93 (s, 3 H), 4.09 (m, 2 H), 4.56 (m, 2 H), 5.04 (d, 7=10.61 Hz, 1 H), 5.23 (d, 7=17.20 Hz, 1 H), 5.53 (s, 1 H), 5.83 (m, 1 H), 7.07 (m, 1 H), 7.22 (s, 1 H), 7.37 (s, 1 H), 7.51 (m, 3 H), 8.07 (m, 3 H). LC-MS (retention time: 1.53, Method I), MS m/z 820 (M⁺+l).

Compound 55 Example 55

compound 55 Step 55a: preparation bis HCl salt of l-(2-Amino-3,3-dimethyl-butyryl)-4-(7- methoxy-2-phenyl-quinolin-4-yloxy)-pyrrolidine-2-carboxylic acid Tl-d-benzyl- cyclopropanesulfonylaminocarbonyl)-2-vinyl-cvclopropyl]-amide

Scheme 1

HCI/dioxane

compound 55a

Step 55a) This bis HCl salt was prepared in 100% (0.678 g) yield from compound 5 (0.700 g, 0.795 mmol) in analogous fashion to the procedure of example 25 step 15g: 1H NMR (methanol-d-) D ppm 0.64 (m, 2 H), 1.12 (s, 9 H), 1.17 (m, 4 H), 1.45 (m, 3 H), 1.94 (dd, 7=8.05, 5.49 Hz, 1 H), 2.34 (m, 1 H), 2.44 (m, 1 H), 2.82 (dd, 7=14.64, 6.95 Hz, 1 H), 3.24 (d, 7=13.54 Hz, 1 H), 3.35 (m, 1 H), 4.19 (m, 1 H), 4.52 (d, 7=12.44 Hz, 1 H), 4.75 (dd, 7=10.25, 6.95 Hz, 1 H), 5.21 (d, 7=10.25 Hz, 1 H), 5.37 (d, 7=17.20 Hz, 1 H), 5.77 (m, 1 H), 5.84 (s, 1 H), 7.15 (m, 2 H), 7.26 (m, 4 H), 7.43 (dd, 7=9.33, 2.38 Hz, 1 H), 7.56 (m, 2 H), 7.69 (m, 3 H), 8.11 (dd, 7=7.68, 1.83 Hz, 2 H), 8.40 (d, 7=9.51 Hz, 1 H). LC-MS (retention time: 2.06, Method K), MS m/z 780 (M⁺+l).

Step 55b: Preparation of compound 55 Example 55, N-cyclopentoxycarbonyl-

NH-P3(L-t-BuGlv)-P2r(4R)-(2-phenyl-7-methoχyquinoline-4-oxo)-S-proline1-

PK1R.2S Vinyl Acca)-CONHSO?Q-benzylcvclopropan-l-yl) or alternate designation. Compound 55, example 55, { l-r2-|^"l-(l-Benzyl- cvclopropanesulfonylaminocarbonyl)-2-vinyl-cyclopropylcarbamovn-4-(7- methoxy-2-phenyl-quinolin-4-yloxy)-pyrrolidine-l-carbonyl]-2,2-dimethyl- propyl} -carbamic acid cyclopentyl ester

compound 55a compound 55

Step 55b) Compound 55 was prepared in 95% (0.124 g) yield from the bis HCl salt (0.125 g, 0.15 mmol) of the product of Step 55a (Example 55) in analogous fashion to the procedure of Example 25 step 25h in preparation of Compound 12 and purified by preparative HPLC (solvent B: 45% to 85%): 1H NMR (methanol-d₄) D ppm 0.63 (s, 2 H), 0.96 (s, 9 H), 1.50 (m, 12 H), 2.32 (m, 2 H), 2.73 (dd, 7=13.54, 7.32 Hz, 1 H), 3.30 (m, 2 H), 3.99 (s, 3 H), 4.09 (m, 1 H), 4.24 (m, 1 H), 4.60 (m, 3 H), 5.18 (d, 7=10.98 Hz, 1 H), 5.34 (d, 7=17.20 Hz, 1 H), 5.68 (s, 1 H), 5.79 (m, 1 H), 7.14 (m, 2 H), 7.23 (m, 4 H), 7.44 (m, 2 H), 7.61 (m, 3 H), 8.06 (m, 2 H), 8.18 (d, 7=9.15 Hz, 1 H). calcd for C₄₄H₅₆N₅SO₉: LC-MS (retention time: 3.40, Method J), MS m/z 892 (MM)

Compound 56 Example 56

compound 56

Step 56: Preparation of compound 56 Example 56, N- tetrahydro- pyran-4-yloxy carbonyl-NH-P3(L-^-BuGly)-P2[(4R)-(2-phenyl-7- methoxyquinoline-4-oxo)-5-proline]-Pl(lR,25 Vinyl Acca)-CONHSO₂(l- benzylcyclopropan-1-yl) or alternate designation, Compound 56, example 56, {l-[2-[l-(l-Benzyl-cyclopropanesulfonylaminocarbonyI)-2-vinyl- cyclopropylcarbamoyl]-4-(7-methoxy-2-phenyl-quinolin-4-yloxy)- pyrrolidine-l-carbonyl]-2,2-dimethyl-propyl}-carbamic acid tetrahydro- pyran-4-yI ester

compound 55a compound 56

Step 56) Compound 56 was prepared in 46% (0.072 g) yield from the bis

HCl salt (0.150 g, 0.18 mmol) of the product of Step 55a (Example 55) in analogous fashion to the procedure of step 55b (Example 55) in preparation of Compound 55 except that tetrahydro-pyran-4-yl chloroformate was used in place of cyclopentyl chloroformate: 1H NMR (methanol-d ) D ppm 0.65 (m, 2 H), 0.96 (s, 9 H), 1.02 (m, 1 H), 1.44 (m, 6 H), 1.74 (m, 1 H), 1.93 (dd, 7=8.05, 5.49 Hz, 1 H), 2.34 (m, 2 H), 2.74 (dd, 7=13.36, 6.77 Hz, 1 H), 3.34 (m, 2 H), 3.77 (m, 2 H), 4.00 (s, 3 H), 4.08 (m, 1 H), 4.27 (m, 3 H), 4.63 (m, 2 H), 5.19 (d, 7=10.25 Hz, 1 H), 5.35 (d, 7=16.83 Hz, 1 H), 5.74 (m, 2 H), 7.14 (m, 2 H), 7.27 (m, 4 H), 7.46 (m, 2 H), 7.63 (m, 3 H), 8.07 (m, 2 H), 8.19 (d, 7=9.15 Hz, 1 H). MS /z 908 (MM), MS m/z 906 (M-l). HPLC (retention time: 3.08, Method J).

Compound 57 Example 57

compound 57

Step 57: Preparation of {l-[2-[l-(l-Benzyl- cyclopropanesulfonylaminocarbonyl)-2-vinyl-cyclopropylcarbamoyl]-4-(7- methoxy-2-phenyl-quinolin-4-yloxy)-pyrrolidine-l-carbonyl]-2,2-dimethyl- propyl}-carbamic acid tetrahydro-furan-3-yl ester

compound 55a compound 57

Step 57) Compound 57 was prepared in 95% (0.085 g) yield from the bis HCl salt (0.125 g , 0.12 mmol) of Compound 55a (Step 55a) in analogous fashion to the procedure of Example 55 (Step 55b) in preparation of compound 55 except that (S)- tetrahydro-furan-3-yl chloroformate was used in place of cyclopentyl chloroformate purified by preparative HPLC (solvent B: 45% to 85%): 1H NMR (CDC1₃) D ppm 1.02 (s, 9 H), 1.40 (dd, 7=8.97, 5.67 Hz, 1 H), 1.60 (m, 4 H), 1.91 (m, 2 H), 2.03 (m, 2 H), 2.60 (m, 2 H), 3.19 (d, 7=13.91 Hz, 1 H), 3.31 (d, 7=13.91 Hz, 1 H), 3.82 (m, 3 H), 3.95 (s, 3 H), 4.02 (dd, 7=11.34, 3.66 Hz, 1 H), 4.29 (d, 7=9.15 Hz, 1 H), 4.49 (m, 2 H), 5.05 (m, 1 H), 5.21 (d, 7=11.34 Hz, 1 H), 5.29 (d, 7=16.47 Hz, 1 H), 5.38 (m, 1 H), 5.45 (d, 7=9.51 Hz, 1 H), 5.78 (m, 1 H), 7.01 (s, 1 H), 7.07 (dd, 7=9.15, 2.56 Hz, 1 H), 7.12 (m, 2 H), 7.24 (m, 3 H), 7.50 (m, 4 H), 8.03 (m, 3 H). LC-MS (retention time: 3.08, Method J), MS m/z 894 (MM).

Compound 58 Example 58

compound 58

Step 58: Preparation of l-[2-(2-Cyclopropyl-acetylamino)-3,3- dimethyl-butyryl]-4-(7-methoxy-2-phenyl-quinolin-4-yloxy)-pyrrolidine-2- carboxylic acid [l-(l-benzyI-cyclopropanesulfonylaminocarbonyl)-2-vinyl- cyclopropyl] -amide

compound 55a compound 58

Step 58) Compound 58 was prepared in 71% (0.0903 g) yield from the bis HCl salt (0.125 g, 0.15 mmol) of the product of Step 55a (Example 55) in analogous fashion to the procedure of Example 26 step 26h in preparation of compound 13 and purified by preparative HPLC (solvent B: 45% 85%): 1H NMR (methanol-d-) □ ppm 0.44 (m, 2 H), 0.63 (m, 2 H), 0.86 (m, 1 H), 0.99 (s, 9 H), 1.04 (m, 2 H), 1.45 (m, 3 H), 1.92 (dd, 7=8.05, 5.49 Hz, 1 H), 2.01 (d, 7=6.95 Hz, 2 H), 2.32 (m, 2 H), 2.69 (dd, 7=13.72, 7.14 Hz, 1 H), 3.31 (m, 2 H), 3.97 (s, 3 H), 4.13 (dd, 7=12.08, 3.29 Hz, 1 H), 4.57 (m, 3 H), 5.17 (m, 1 H), 5.34 (d, 7=16.83 Hz, 1 H), 5.63 (s, 1 H), 5.78 (m, 1 H), 7.15 (m, 3 H), 7.28 (m, 4 H), 7.42 (d, 7=2.56 Hz, 1 H), 7.56 (m, 3 H), 8.07 (t, 7=8.23 Hz, 3 H). LC-MS (retention time: 3.25, Method J), MS m/z 862 (MM).

Compound 59 Example 59

compound 59

Step 59: Preparation of l-[3,3-Dimethyl-2-(2-tetrahydro-pyran-4-yl- acetylamino)-butyryl]-4-(7-methoxy-2-phenyl-quinolin-4-yloxy)-pyrrolidine- 2-carboxylic acid [l-(l-benzyl-cyclopropanesulfonylaminocarbonyl)-2-vinyl- cyclopropyl] -amide

compound 55a

Step 59) Compound 59 was prepared in 81% (0.1084 g) yield from the bis HCl salt (0.125 g, 0.15 mmol) of product of Step 55a (Example 55) in analogous fashion to the procedure of Example 26 step 26h in preparation of compound 13 except that copmound 55a was used in place of the Bis HCl salt product of Step 26g, and purified by preparative HPLC (solvent B: 45 to 85%): 1H NMR (methanol-d-) D ppm 0.63 (m, 2 H), 0.98 (s, 9 H), 1.22 (m, 2 H), 1.47 ( , 6 H), 1.92 (m, 4 H), 2.31 (m, 2 H), 2.68 (dd, 7=13.17, 6.59 Hz, 1 H), 2.67 (m, 1 H), 3.27 (m, 2 H), 3.80 (m, 2 H), 3.97 (s, 3 H), 4.11 (dd, 7=11.53, 3.11 Hz, 1 H), 4.56 (m, 3 H), 5.18 (d, 7=10.25 Hz, 1 H), 5.34 (d, 7=16.83 Hz, 1 H), 5.59 (s, 1 H), 5.77 (m, 1 H), 7.15 (m, 3 H), 7.27 (m, 4 H), 7.42 (d, 7=2.20 Hz, 1 H), 7.56 (m, 3 H), 8.07 (m, 3 H). HPLC (retention time: 3.11, Method J).MS m/z 906 (MM), 904 (M^"-l), .

Compound 60 Example 60

compound 60

Step 60: Preparation of l-{3,3-Dimethyl-2-[(tetrahydro-pyran-4- carbonyl)-amino]-butyryl}-4-(7-methoxy-2-phenyl-quinolin-4-yloxy)- pyrrolidine-2-carboxylic acid [l-(l-benzyl- cyclopropanesulfonylaminocarbonyl)-2-vinyl-cyclopropyl]-amide

compound 55a

Step 60) Compound 60 was prepared in 82% (0.084 g) yield from the bis HCl salt (0.100 g, 0.18 mmol) of Step 55a (Example 55) in analogous fashion to the procedure of step 59 (Example 59) in preparation of compound 59 except that Tetrahydro-pyran-4-carboxylic acid was used in place of cyclopropyl acetic acid: 1H NMR (methanol-d-) D ppm 4.00 (q, 7=7.12 Hz, 2 H), 4.04 (s, 3 H), 4.13 (dd, 7=12.05, 2.90 Hz, 1 H), 4.25 (m, 1 H), 4.60 (m, 2 H), 5.18 (m, 1 H), 5.34 (d, 7=17.09 Hz, 1 H), 5.76 (m, 2 H), 7.14 (m, 2 H), 7.25 (m, 3 H), 7.37 (m, 1 H), 7.51 (d, 7=2.14 Hz, 1 H), 7.53 (s, 1 H), 7.70 (m, 3 H), 8.05 (m, 2 H), 8.33 (d, 7=9.16 Hz, 1 H). LC-MS (retention time: 3.06, Method J), MS m/z 893 (MM).

Compound 61 Example 61

61

Step 61 : Preparation of 1- [2-(3-Ethyl-ureido)-3,3-dimethyl-butyryl]-

4-(7-methoxy-2-phenyl-quinolin-4-yIoxy)-pyrrolidine-2-carboxylic acid [1-(1- benzyl-cyclopropanesulfonylaminocarbonyl)-2-vinyl-cyclopropyl]-amide

compound 55a compound 61 step 61) A mixture of the bis HCl salt (0.100 g, 0.117 mmol) of compound 55a of Example 55 (Step55a), ethyl isocyanate (26 μL, 0.32 mmol), and triethyl amine (82 μL, 0.585 mmol) in CH₂C1₂ was stirred for 16 h at rt, removed the solvent in vacuo. The product was attained by preparative HPLC (solvent B: 40 to 85%) as a white foam: 1H NMR (methanol-d₄) D ppm 0.63 (m, 2 H), 0.92 (m, 3 H), 0.95 (s, 9 H), 1.28 (s, 1 H), 1.43 (m, 3 H), 1.93 (dd, 7=8.24, 5.49 Hz, 1 H), 2.29 (q, 7=8.85 Hz, 1 H), 2.41 (m, 1 H), 2.78 (m, 2 H), 2.87 (m₅ 1 H), 3.27 (d, 7=13.43 Hz, 1 H), 3.34 (d, 7=13.42 Hz, 1 H), 4.05 (s, 3 H), 4.11 (dd, 7=12.36, 3.20 Hz, 1 H), 4.28 (s, 1 H), 4.65 (m, 2 H), 5.18 (dd, 7=10.38, 1.53 Hz,

1 H), 5.35 (d, 7=17.09 Hz, 1 H), 5.75 (m, 1 H), 5.82 (s, 1 H), 7.13 (d, 7=7.02 Hz,

2 H), 7.26 (m, 3 H), 7.38 (dd, 7=9.46, 2.44 Hz, 1 H), 7.53 (d, 7=2.14 Hz, 1 H), 7.60 (s, 1 H), 7.74 (m, 3 H), 8.07 (m, 2 H), 8.35 (d, 7=9.16 Hz, 1 H). LC-MS (retention time: 3.09, Method J), MS m/z 851 (MM).

Compound 62 Example 62

compound 62 Step 62: Preparation of l-[2-(3-tert-Butyl-ureido)-3,3-dimethyl- butyryl]-4-(7-methoxy-2-phenyl-quinolin-4-yloxy)-pyrrolidine-2-carboxylic acid [l-(l-benzyl-cyclopropanesulfonylaminocarbonyl)-2-vinyl-cyclopropyl]- amide

compound 55a compound 62

Step 62) Compound 62 was prepared in 46% (0.072 g) yield from the bis HCl salt (0.100 g, 0.117 mmol) of Compound 55a of Step 55a (Example 55), in analogous fashion to the procedure of Example 61 step 61 in preparation of compound 48 except that tert-butyl isocyanate was used in place of ethyl isocyanate: 1H NMR (methanol-d-) D ppm 0.62 (m, 2 H), 0.96 (s, 9 H), 1.11 (s, 9 H), 1.30 (m, 1 H), 1.45 (m, 3 H), 1.91 (dd, 7=8.09, 5.34 Hz, 1 H), 2.28 (q, 7=8.75 Hz, 1 H), 2.37 (m, 1 H), 2.72 (dd, 7=14.34, 6.71 Hz, 1 H), 3.27 (d, 7=13.43 Hz, 1 H), 3.33 (d, 7=13.42 Hz, 1 H), 4.00 (s, 3 H), 4.10 (dd, 7=12.21, 3.36 Hz, 1 H), 4.26 (s, 1 H), 4.59 (dd, 7=10.22, 7.17 Hz, 1 H), 4.65 (d, 7=12.21 Hz, 1 H), 5.17 (d, 7=10.38 Hz, 1 H), 5.33 (d, 7=17.09 Hz, 1 H), 5.74 (m, 2 H), 7.13 (m, 2 H), 7.25 (m, 4 H), 7.45 (s, 1 H), 7.46 (d, 7=2.44 Hz, 1 H), 7.64 (m, 3 H), 8.06 (m, 2 H), 8.26 (d, 7=9.46 Hz, 1 H). LC-MS (retention time: 3.26, Method J), MS m/z 879 (MM).

Compound 63 Example 63

compound 63

Schemel

Low Rf Isomer

compound 63c

Step 63a: Preparation of N-Boc- 4-(7-Chloro-quinolin-4-yloxy)-proline methyl ester To a suspension of N-Boc- s-L^-Hydroxyproline methyl ester (10 g, 40.7mmol) and 7-chloroquinolin-4-ol (8.73 g, 49.0 mmol) in THF (200 mL) cooled to 0 °C was added PPh₃ (12.82 g, 48.9 mmol) and DIAD. (8.80 g, 42.13 mmol). The mixture was slowly allowed to warm to rt overnite, stirred at total of 30 h. The mixture was dissolved in EtOAc (800 mL), washed with IN aqueous HCl, 5% aqueous ₂CO₃ (3X100 mL), brine (2x100 mL) and dried (MgSO₄), and concentrated. The residue was purified several times over a Biotage 65M (MeOH CH₂Cl₂: 0 to 10%) to afford cumulatively 10.57 g (68%) of the desired product as a glass: 1H ΝMR (CDC1₃) 6 1.40 (s, 9H), 2.33-2.42 (m, IH), 2.61-2.72 (m, IH), 3.75 (s, 3H), 3.91 (m, 2H), 4.45-4.59 (m, IH), 5.13 (m, IH), 6.61-6.64 (m, IH), 7.41 (dd, 7=9, 2 Hz, IH), 7.98 (d, 7=2 Hz, IH), 8.03 (d, 7=9 Hz, IH), 8.67-8.71 (m, IH). LC-MS (retention time: 1.39, method D), MS m e 407 (MM) .

Step 63b: Preparation of N-Boc- 4-(7-Chloro-quinolin-4-yloxy)-proline

To a solution of the product (10.57 g, 26.0 mmol) of Step 63a of Example 63 {BOC-N-P2[(4R)-(7-chloroquinoline-4-oxo) proline methyl ester} dissolved in MeOH (800 mL) cooled to 0 °C was added an aqueous IN ΝaOH solution (44.5 mL, 44.5 mmol). The mixture was warmed to rt after 6 h, stirred overnite, and the pH adjusted to pH 7 using 1.0 Ν aqueous HCl. The solution was concentrated until only the water layer remained, the pH adjusted to 4 using 6Ν aqueous HCl and the mixture was partitioned repeatedly with EtOAc (3x500 mL). The combined organic layers were dried (MgSO ) and concentrated to afford 10.16 g (100%) of the as a white solid. 1H NMR (DMSO-d₆) δ 1.32, 1.34 (two s (rotamers) 9H), 2.31-2.40 (m, IH), 2.58-2.69 (m, IH), 3.65-3.81 (m, 2H), 4.33- 4.40 (m, IH), 5.34 (m, IH) 7.10-7.11 (m, IH), 7.57 (d, 7=9 Hz, IH), 7.98 (s, IH), 8.09-8.14 (m, IH), 8.75 (d, 7=5 Hz, IH), 12.88 (brs, IH). ¹³C NMR (DMSO- d_) δ 27.82,, 35.84, 51.52, 57.75, 76.03, 79.33, 102.95, 119.54, 123.86, 126.34, 127.24, 134.49, 149.32, 152.88, 153.25, 159.08, 173.74. LC-MS (retention time: 1.48, method D), MS m e 393 (MM) Step 63c: Preparation of BOC-NH-P2r(4_-)-(7-chloroquinoline-4-oxo)-S-proline]-

P1(1R,2S vinyl accaVCOOEt

To a solution of the product (5.11 g, 13 mmol) of Step 63b of Example 633 {Boc-4(R)-(7-chloroquinoline-4-oxo) proline}, the HCl salt (3.48 g, 18.2 mmol) of vinyl Acca (existing as a 1:1 mixture of diastereoisomers (1R,2S11S,2R where cyclopropyl carboxyethyl group is syn to vinyl moiety) and NMM (7.1 mL 65 mmol) in DMF (30 mL) was added HATU (6.92 g, 18.2 mmol). The mixture was stirred for 3 days. The reaction mixture was diluted with EtOAc (180 mL) and was partitioned with pH 4.0 buffer (3x100 mL). The organic layer was washed with saturated aqueous NaHCO₃ (2x50mL), water (2x50mL), and brine (2x50mL). The organic solution was dried (MgSO₄) and concentrated. The residue was purified over a Biotage 40M column (EtOAc/hexanes: 50% to 100%) to afford 2.88 g of the product existing as a diastereomeric mixture. This mixture was partially separated using a Biotage 65M column (MeOH-EtOAc: 0% to 9%) to afford BOC-NH-P2[(4R)-(7-chloroquinoline-4-oxo)-S-proline]-Pl(l_?,2S vinyl acca PI moiety)-COOEt as the initial eluted high Rf isomer (1.20 g, 17.4%). 1H NMR (CDCl₃/Methanol-d₄) δ 1.16 (t, 7=7 Hz, 3H), 1.35 (s, 9H), 1.37-1.43 (m, IH), 1.76-1.84 (m, IH), 2.06-2.11 (m, IH), 2.35-2.45 (m, IH), 2.63 (m, IH), 3.72-3.93 (m, 2H), 4.02-4.15 (m, IH), 4.33-4.40 (m, IH), 5.06 (d, 7=9 Hz, IH),

5.16 (m, IH), 5.24 (d, 7=17 Hz, IH), 5.63-5.70 (m, IH), 6.74 (m, IH), 7.39 (dd, 7=9, 2 Hz, IH), 7.74-7.78 (m, IH), 7.89 (d, 7=2 Hz,l H), 7.97 (d, 7=9 Hz ,1H), 8.60 (d, 7=5 Hz, IH). 1H NMR (methanol-d₄, 60/40 Rotomers) D 1.24 (t, 7=7 Hz, 3H), 1.39, 1.43 (2s, 9H, ratio 4:6), 1.71-1.74 (m, 0.4H), 178-1.81 (m, 0.6H). 2.18-2.23 (m, IH), 2.65-2.69 (m, 0.4H), 2.71-2.76 (m, 0.6H), 3.88-3.96 (m, 2H), 4.11-4.18 (m, 2H), 4.39-4.45 (m, IH), 5.09-5.13 (m, IH), 5.28-5.33 (m, IH), 5.37 (m, IH), 5.73-5.81 (m, IH), 7.05 (d, 7=5 Hz, IH), 7.53 (d, 7=8.9 Hz, IH), 7.92 (s, IH), 8.12 (d, 7=8.9 Hz, IH), 8.70 (d, 7=5 Hz, IH). LC-MS (retention time: 1.54, method A) MS m/z 530 (MM). The rest of the material (-1.66 g, 24%) was mixed fractions greatly enriched in the lower Rf isomer. Step 63d: Preparation of (L)-2-Cyclopentyloxycarbonylamino-3,3-dimethyl- butyric acid

Scheme 2

compound 63d

To a solution of L-tert-leucine (2 g, 15.25 mmol) dissolved in CH₃CN (50 mL) was added TMSCN (7.06 mL, 56.41 mmol) and stirred for 15 min. The reaction mixture was heated to 75 °C for 30 min. Cyclopentyl chloroformate (2.83 g, 19.06 mmol) was added to the reaction mixture and the reaction mixture was heated at 80 °C overnite, concentrated in vacuo. The residue was treated with MeOH (40 mL), stirred for 10 min, and concentrated in vacuo. The residue was adjusted pH to 8.5, and extracted with Et₂O (2x200mL). The aqueous layer was acidified to pH 3 and extracted with CH₂C1₂ (2x200mL). The combined extract was dried (MgSO₄), and concentrated in vacuo. The residue was recrystallized from minimal amount of Et₂O/hexanes to afford the product 3.48 g (94%): 1H NMR (methanol-d-) D ppm 1.00 (s, 9 H), 1.59 (m, 2 H), 1.73 (m, 4 H), 1.84 (dd, 7=5.95, 3.20 Hz, 2 H), 3.98 (s, 1 H), 5.02 (m, 1 H).

Scheme 3

compound 63f

step 63e: Preparation of Bis HCl salt of NH₂-P2r(4_,)-(7-chloroquinoline-4-oxo)- S-proline1-Pl(l_-,2S vinyl accaVCOOEt

The product (0.65 g, 1.22 mmol) of step 63c of Example 63 {BOC-P2 [(4R)-(7- chloroquinoline-4-oxo)-S-proline]-Pl(l__,2S Vinyl Acca-CO₂Et} was dissolved in 4N HCl/dioxane (4.5ml, 18 mmol) and stirred for 1 h at rt. The reaction mixture was concentrated and the crude product was directly used in next step: LC-MS (retention time: 0.94, method A) LC-MS m z 430 (MM).

Step 63f : Preparation of compound 63f, example 63f, N-Cyclopentyloxycarbonyl

- NH-P3(L-val)-P2r(4--)-f2-ρhenyl-7-methoxyquinoline-4-oxo)-S-proline1-

P1(1_-,2S Vinyl Acca)-Carboxylic acid ethyl ester or alternate designation

Compound 63f, example 63f, l-{ r4-(7-Chloro-quinolin-4-yloxy)-l-(2- cyclopentyloxycarbonylamino-3,3-dimethyl-butyryl)-pyrrolidine-2-carbonyl1- amino}-2-vinyl-cyclopropanecarboxylic acid ethyl ester

Step 63f) To a solution of the product (0.530 g, 1.04 mmol) of Step 63e of

Example 63 {HCl salt of P2[(4R)-7-chloroquinoline-4-oxo)-S-proline]-Pl(lR,2S Vinyl Acca) COOEt, the product (0.328 g, 1.35 mmol) of Step 63d of Example 63 {(L)-2-Cyclopentyloxycarbonylanιino-3,3-dimethyl-butyric acid}, HOBT (0.146 g, 1.08 mmol), and diisopropylethylamine (0.755 mL, 4.32 mmol) in CH₂C1₂ (7 mL) was added HBTU (0.512 g, 1.35 mmol). The reaction mixture was stirred for overnite and partitioned between CH₂C1₂ and pH 4.0 buffer. The CH₂C1₂ layer was washed with water, saturated NaHCO₃ (aq.), dried (MgSO₄), concentrated. The residue was purified over a Biotage 40M column (EtOAc/Hexanes: 35 to 100%) to afford the product 0.640 g, (92%): 1H NMR (methanol-d₄) δ ppm 1.02 (s, 9 H), 1.26 (m, 4 H), 1.56 (m, 10 H), 2.19 (q, 7=8.75 Hz, 1 H), 2.41 (m, 1 H), 2.70 (dd, 7=14.19, 8.09 Hz, 1 H), 4.01 (dd, 7=11.90, 3.05 Hz, 1 H), 4.13 (m, 2 H), 4.20 (s, 1 H), 4.53 (m, 1 H), 4.62 (m, 1 H), 5.09 (d, 7=10.38 Hz, 1 H), 5.26 (d, 7=17.09 Hz, 1 H), 5.47 (m, 1 H), 5.77 (m, 1 H), 7.07 (d, 7=5.49 Hz, 1 H), 7.47 (m, 1 H), 7.94 (m, 1 H), 8.20 (d, 7=8.85 Hz, 1 H), 8.72 (d, 7=5.49 Hz, 1 H). LC-MS (retention time:1.71, Method B), MS m/z 655 (MM).

Step 63g: Preparation of Compound 63g, example 63g, N-

Cyclopentyloxycarbonyl - NH-P3(L-val)-P2r(4_-)-(2-phenyl-7-methoxyquinoline-

4-oxo)-S-proline]-Pl(l-_,2S Vinyl Acca)-Carboxylic acid ethyl ester or alternate designation Compound 63 , example 63 , l-{ r4-(7-Chloro-quinolin-4-yloxy)-l-

(2-cvclopentyloxycarbonylamino-3,3-dimethyl-butyryl)-pyrrolidine-2-carbonyl1- amino } -2-vinyl-cvclopropanecarboxylic acid

Step 63g) Compound 63g was obtained in 69% (0.424 g) yield from Compound 63f (0.636 g, 0.97 mmol) in analogous fashion to the procedure of step 2e Example 2 as a white solid: IH NMR (methanol-d ) D ppm 1.02 (s, 9 H), 1.57 (m, 11 H), 2.14 (q, 7=9.03 Hz, 1 H), 2.46 (m, 1 H), 2.68 (m, 1 H), 4.02 (dd, 7=11.89, 3.11 Hz, 1 H), 4.19 (m, 1 H), 4.50 (d, 7=26.35 Hz, 1 H), 4.64 (t, 7=8.42 Hz, 1 H), 5.04 (m, 1 H), 5.24 (d, 7=17.20 Hz, 1 H), 5.44 (s, 1 H), 5.87 (m, 1 H), 7.05 (d, 7=5.12 Hz, 1 H), 7.48 (m, 1 H), 7.92 (m, 1 H), 8.18 (d, 7=8.78 Hz, 1 H),

8.71 (d, 7=5.49 Hz, 1 H). LC-MS (retention time: 2.32, Method A), MS m/z 627 (MM). Step 63h: Preparation of (l-{4-(7-Chloro-quinolin-4-yloxy)-2-ri-(l-methyl- cyclopropanesulfonylaminocarbonyl)-2-vinyl-cvclopropylcarbamoyl1- pyrrolidine-1 -carbonyl) -2,2-dimethyl-propyl)-carbamic acid cyclopentyl ester

Step 63h) Compound 63 was prepared in 14% yield (0.0095 g) from the tripeptide acid (0.058 g, 0.13 mmol) of compound 63g of the product of Step 63g (Example 63) in analogous fashion to the procedure of Step 27c of Example 27 in the synthesis of compound 27 and purified by PTLC: 1H NMR (DMSO-D6) δ ppm 0.77 (m, 2 H), 1.02 (s, 9 H), 1.52 (m, 14 H), 1.85 (m, 1 H), 2.15 (m, 1 H), 2.46 (m, 1 H), 2.67 (m, 1 H), 4.06 (m, 1 H), 4.21 (m, 1 H), 4.55 (m, 3 H), 5.04 (m, 1 H), 5.23 (m, 1 H), 5.47 (m, 1 H), 5.85 (m, 1 H), 7.08 (d, 7=5.49 Hz, 1 H), , 7.47 (d, 7=8.85 Hz, 1 H), 7.93 (s, 1 H), 8.20 (t, 7=8.09 Hz, 1 H), 8.72 (d, 7=5.49 Hz, 1 H). LC-MS (retention time: 1.57, Method I), MS m/z 1 A (MM).

Compound 64 Example 64

Preparation of (l-{4-(7-Chloro-quinolin-4-yloxy)-2-[l-(l-propyl- cyclopropanesulfonylaminocarbonyl)-2-vinyl-cyclopropylcarbamoyl]- pyrrolidine-l-carbonyl}-2,2-dimethyl-propyI)-carbamic acid cyclopentyl ester

Step 64) Compound was prepared in 45% yield (0.032 g) from the chloro-P2 tripeptide acid (0.058 g, 0.13 mmol) of Compound 63g (step 63g, Example 63) in analogous fashion to the procedure of Step 27c of Example 27 in the synthesis of 'compound 27 and purified by PTLC: 1H NMR (met_a_oi-_4) □ ppm 0.78 (m, 2 H), 0.89 (t, 7=7.02 Hz, 3 H), 1.02 (s, 9 H), 1.57 (m, 16 H), 2.12 (m, 1 H), 2.49 (m, 1 H), 2.68 (dd, 7=13.73, 7.02 Hz, 1 H), 4.08 (m, 1 H), 4.22 (s, 1 H), 4.56 (m, 3 H), 5.01 (dd, 7=25.18, 9.61 Hz, 1 H), 5.21 (d, 7=17.09 Hz, 1 H), 5.47 (s, 1 H), 5.89 (m, 1 H), 7.08 (d, 7=5.19 Hz, 1 H), 7.46 (d, 7=7.93 Hz, 1 H), 7.92 (s, 1 H), 8.19 (d, 7=8.24 Hz, 1 H), 8.72 (d, 7=5.19 Hz, 1 H). LC-MS (retention time: 1.64, Method D), MS m/z 772 (MM).

Compound 65 Example 65

compound 65

Preparation {l-[2-[l-(l-Butyl-cyclopropanesulfonyIaminocarbonyl)-2- vinyl-cyclopropylcarbamoyl]-4-(7-chloro-quinolin-4-yloxy)-pyrrolidine-l- carbonyl]-2,2-dimethyI-propyl}-carbamic acid cyclopentyl ester

compound 65

Step 65) Compound 65 was prepared in 37% yield (0.0271 g) from the chloro-P2 tripeptide acid (0.058 g, 0.13 mmol) of compound 63g (step 63g, Example 63) in analogous fashion to the procedure of Step 27c of Example 27 in the synthesis of compound 1 and purified by PTLC: 1H NMR (methanol-d ) δ ppm 0.90 (m, 5 H), 1.02 (s, 9 H), 1.60 (m, 18 H), 2.15 (m, 1 H), 2.48 (m, 1 H), 2.67 (dd, 7=14.04, 7.02 Hz, 1 H), 4.05 (m, 1 H), 4.22 (s, 1 H), 4.49 (d, 7=11.90 Hz, 1 H), 4.57 (m, 2 H), 5.03 (m, 1 H), 5.23 (d, 7=17.09 Hz, 1 H), 5.47 (s, 1 H), 5.83 (m, 1 H), 7.09 (m, 1 H), 7.46 (d, 7=8.85 Hz, 1 H), 7.92 (s, 1 H), 8.19 (m, 1 H), 8.72 (d, 7=5.19 Hz, 1 H). LC-MS (retention time: 1.87, Method D), MS m/z 786 (MM).

Compound 66 Example 66

Preparation of (l-{4-(7-ChIoro-quinoIin-4-yloxy)-2-[l-(l- cyclopropylmethyl-cyclopropanesulfonylaminocarbonyl)-2- vinyl- cyclopropylcarbamoyl]-pyrrolidine-l-carbonyl}-2,2-dimethyl-propyl)- carba ic acid cyclopentyl ester

Step 66) Compound 66 was prepared in 54% yield (0.1016 g) from the chloro-P2 tripeptide acid (0.150 g, 0.24 mmol) of compound 63g (step 63g) in analogous fashion to the procedure of Example 63 (step 63h) in the synthesis of compound 50 and purified by PTLC: 1H NMR (methanol-d₄) D ppm 0.04 (m, 2 H), 0.42 (m, 2 H), 0.70 (m, 1 H), 1.02 (s, 9 H), 1.57 (m, 16 H), 2.10 (m, 1 H),

2.48 (s, 1 H), 2.68 (dd, 7=13.73, 7.32 Hz, 1 H), 4.06 (m, 1 H), 4.22 (s, 1 H), 4.49 (d, 7=11.90 Hz, 1 H), 4.57 (m, 2 H), 5.00 (dd, 7=23.19, 10.99 Hz, 1 H), 5.20 (d, 7=17.09 Hz, 1 H), 5.46 (m, 1 H), 5.93 (m, 1 H), 7.08 (d, 7=5.49 Hz, 1 H), 7.46 (d, 7=8.55 Hz, 1 H), 7.92 (s, 1 H), 8.19 (d, 7=8.85 Hz, 1 H), 8.72 (d, 7=5.19 Hz, 1 H). LC-MS (retention time: 1.76, Method I), MS m/z 784 (MM).

Compound 67 Example 67

compound 67

Preparation {l-[2-[l-(l-Allyl-cycIopropanesuIfonylaminocarbonyl)-2- vinyl-cyclopropylcarbamoyl]-4-(7-chIoro-quinolin-4-yloxy)-pyrrolidine-l- carbonyl]-2,2-dimethyI-propyl}-carbamic acid cyclopentyl ester

compound 63g compound 67

Step 67) Compound was prepared in 16% yield (0.0051 g) from the chloro-P2 tripeptide acid (0.026 g, 0.04 mmol) of compound 63g (step 63g) in analogous fashion to the procedure of Example 63 step 63h in the synthesis of compound 63 and purified by PTLC: 1H NMR (methanol-d₄) D ppm 0.87 (m, 2 H), 1.02 (s, 9 H), 1.51 (m, 14 H), 1.99 (dd, 7=24.72, 15.87 Hz, 1 H), 2.65 (m, 3 H), 4.16 (s, 1 H), 4.22 (s, 1 H), 4.49 (m, 1 H), 4.57 (m, 1 H), 4.99 (m, 3 H), 5.17 ' (m, 1 H), 5.47 (m, 1 H), 5.78 (m, 2 H), 7.10 (d, 7=5.49 Hz, 1 H), 7.47 (m, 1 H), 7.93 (m, 1 H), 8.21 (m, 1 H), 8.72 (d, 7=5.49 Hz, 1 H). LC-MS (retention time: 1.72, Method I), MS m/z 770 (MM).

Compound 68 Example 68

compound 68 Scheme 1 step 68a

Step 68a: Preparation of Cyclopropanecarboxylic acid (2-acetyl-5-methoxy- phenvD-amide

Step 68a) A solution of 2-amino-4-methoxylacetophenone (4.45 g, 26.94 mmol) at 0 °C dissolved in CH₂C1₂ (100 mL) was treated with cyclopropanecarbonyl chloride (3.1 mL, 33.68 mmol) diisopropylethylamine (19 mL, 107.8 mmol), DMAP (0.780 g, 6.4 mmol). The reaction mixture was stirred at rt overnite and concentrated in vacuo. The residue dissolved in CH₂C1₂ (500 mL) was washed with aqueous 1 N HCl, water, NaHCO₃ (aq.), and dried (MgSO₄). The solvent was removed in vacuo and the solid residue was treated with EtOAc/hexanes (1/1) to provide the product (5.35 g, 85%): 1H NMR (methanol-d₄) D ppm 0.94 (m, 4 H), 1.69 (m, 7=3.97 Hz, 1 H), 2.60 (s, 3 H), 3.84 (s, 3 H), 6.69 (d, 7=7.93 Hz, 1 H), 7.98 (d, 7=8.85 Hz, 1 H), 8.23 (s, 1 H). Step 68b: Preparation of 2-Cyclopropyl-7-methoxy-quinolin-4-ol

Step 68b) A solution of product (5.35 g, 22.72 mmol) of step 1 example 376 {cyclopropanecarboxylic acid (2-acetyl-5-methoxy-phenyl)-amide} and tert- BuOK (5.45 g, 48.6 mmol) in tert-butanol (130 g) was refluxed for 6 h. The reaction mixture was cooled, poured into ice cold buffer and adjusted to pH 7, filtered. The solid collection was recrystallized from MeOH/Et₂O to provide the product (1 g, 20%): 1H NMR (methanol-d-) δ ppm 0.96 (m, 2 H), 1.15 (m, 2 H), 1.94 (m, 1 H), 3.87 (s, 3 H), 5.86 (m, 1 H), 6.93 (m, 2 H), 8.04 (d, 7=8.85 Hz, 1 H).

Step 68c: Preparation of Boc-(4R)-(2-cvclopropyl-7-methoxy-quinoline-4-oxo)-

S-proline methyl ester

Step 68c) To a solution of N-Boc-L-3-hydroxyproline (1.06 g, 4.32 mmol) and triphenylphosphine (2.27 g, 8.64 mmol) at 0 °C dissolved THF (25 mL) was added a solution of the product (0.93 g, 4.32 mmol) of Step 2 Example 376 {2- Cyclopropyl-7-methoxy-quinolin-4-ol} and DEAD (1.50 g, 8.64 mmol) in THF (25 mL) over 30 min. The reaction mixture was stirred overnite and concentrated. The residue was purified twice by a Biotage 40+M column (EtOAC/hexanes: 20 to 65%) to afford the product 1.74 g (90%): LC-MS (retention time: 2.56, Method J), MS m/z 443 (MM).

Step 68d: Preparation of Boc-(4R)-(2-cyclopropyl-7-methoxy-quinoline-4-oxo)-

S -proline,

Step 68d) To a suspension of (1.70 g, 3.86 mmol) of the product of Step 3 of Example 376 (Boc-(4R)-(2-cyclopropyl-7-methoxy-quinoline-4-oxo)-S-proline methyl ester} in THF(91 mL), CH₃OH (18.2 mL), and H₂O (27 mL) was added LiOH (0.73 g, 30 mmol). The reaction mixture was stirred for 16 h, adjusted to pH 6, the organic solvent was removed in vacuo. The residue was acidified to pH 4, and extracted with EtOAc (4x100 mL). The combined organic extract was dried (MgSO₄), and concentrated in vacuo to supply the product 1.64 g (100%): 1H NMR (methanol-d-) δ ppm 1.32 (m, 13 H), 2.37 (m, 2 H), 2.71 (m, 1 H), 3.86 (m, 1 H), 3.95 (s, 3 H), 4.14 (m, 1 H), 4.43 (m, 1 H), 5.41 (s, 1 H), 6.65 (s, 1 H), 7.19 (m, 1 H), 7.30 (m, 1 H), 8.02 (dd, 7=12.63, 9.33 Hz, 1 H).

Step 68e: Preparation of 4-(2-Cvclopropyl-7-methoxy-quinolin-4-yloxy)-2-(l- ethoxycarbonyl-2-vinyl-cyclopropylcarbamoyl)-pyrrolidine- 1 -carboxylic acid tert-butyl ester

Step 68e) The product (1.61 g, 2.79 mmol) of Step 4 of Example 376 {Boc- P2{ (4R)-[2- cyclopropyl-7-methoxylquinoline-4-oxo]-S-proline}-Pl(l_-,2S Vinyl Acca) COOEt} was dissolved in HCl/dioxane (15 mL; 60 mmol) and stirred for 3 h at rt. The reaction mixture was concentrated and azeotroped with dry THF to afford the product (1.58 g, 100%): LC-MS (retention time: 2.12, Method K), MS m/z 566 (MM).

Scheme 2

compound 68

Step 68f : preparation of Bis HCl salt

Step 68f) To a suspension of the product (1.58 g, 2.79 mmol) of Step 5 of Example 376 {Bis HCl salt of P2 { (4R)-[2- cyclopropyl-7-methoxylquinoline-4- oxo]-S-proline}-Pl(lR,2S Vinyl Acca) COOEt}, diisopropylethylamine (1.65 mL, 9.25 mmol), N-Boc-L-tert-leucine (0.775 g, 3.35 mmol), HOBT.H₂O (0.515 g, 3.36 mmol) in CH₂C1₂ (13 mL) was added HBTU (1.28 g, 3.36 mmol). The mixture was stirred for 14 h and partitioned between EtOAc and pH 4.0 buffer. The EtOAc layer was dried (MgSO₄), concentrated. The residue was purified over a Biotage 40+M column (EtOAc/hexanes: 20 to 100%, followed MeOH) and further purified by PTLC (MeOH/CH₂Cl₂ 2%) to afford the product 1.4 g (63%): 1H NMR (methanol-d₄) D ppm 1.04 (s, 9 H), 1.20 (m, 5 H), 1.28 (s, 9 H), 1.39 (m, 2 H), 1.69 (m, 1 H), 2.19 (m, 2 H), 2.36 (m, 1 H), 2.63 (dd, 7=13.54, 7.68 Hz, 1 H), 3.90 (s, 3 H), 4.08 (m, 4 H), 4.19 (d, 7=11.34 Hz, 1 H), 4.47 (d, 7=11.71 Hz, 1 H), 4.56 (t, 7=8.60 Hz, 1 H), 5.08 (m, 1 H), 5.24 (m, 1 H), 5.39 (s,

1 H), 5.78 (m, 1 H), 6.56 (s, 1 H), 6.96 (dd, 7=9.15, 2.20 Hz, 1 H), 7.21 (d, 7=2.56 Hz, 1 H), 7.97 (d, 7=9.15 Hz, 1 H). LC-MS (retention time: 2.34, Method K), MS m/z 679 (MM).

Step 68g: preparation of l-{ ri-(2-tert-Butoxycarbonylamino-3,3-dimethyl- butyryl)-4-(2-cvclopropyl-7-methoxy-quinolin-4-yloxy)-pyrrolidine-2-carbonyl]- amino }-2-vinyl-cvclopropanecarboxylic acid ethyl ester

Step 68g) To a suspension of the product of Step 6 of Example 376 (1.28 g, 1.89 mmol), Boc - NH-P3(L-tert-BuGly)-P2[(4R)-(2- cyclopropyl-7- methoxylquinoline-4-oxo)-S-proline]-Pl(l_.,2S Vinyl Acca)-COOEt, in THF(93 mL), CH₃OH (23 mL), and H₂O (45 mL) was added LiOH (0.491 g, 20.4 mmol). The reaction mixture was stirred for 18.5 h, adjusted to pH 4, removed the organic solvent in vacuo. The residue was extracted with EtOAc (5x lOOmL). Combined organic solvents were dried (MgSO₄), and concentrated in vacuo to afford the desired product 1.17 g (97% ): 1H NMR (methanol-d-) δ ppm 1.04 (s, 9 H), 1.24 (s, 9 H), 1.27 (m, 3 H), 1.42 (m, 2 H), 1.68 (dd, 7=8.05, 5.12 Hz, 1 H). 2.17 (m, 1 H), 2.33 (m, 1 H), 2.47 (m, 1 H), 2.66 (m, 1 H), 3.95 (s, 3 H), 4.09 (m,

2 H), 4.51 (d, 7=11.71 Hz, 1 H), 4.59 (t, 7=8.60 Hz, 1 H), 5.07 (m, 1 H), 5.26 (m, 1 H), 5.52 (s, 1 H), 5.85 (m, 1 H), 6.69 (s, 1 H), 7.10 (dd, 7=9.15, 2.20 Hz, 1 H), 7.27 (d, 7=2.20 Hz, 1 H), 8.10 (d, 7=9.15 Hz, 1 H). LC-MS (retention time: 2.21, Method K), MS m/z 651 (MM). Step 69h: Preparation of compound 69. Example 69. BOCNH-P3(L-t-BuGlv)- P2r(4_-)-(2-cyclopropyl-7-methoxyquinoline-4-oxo)-S-proline]-Pl(l__,2S Vinyl Acca)-CONHSO2(l-benzylclopropan-l-yl) or alternate designation. Compound

69, example 69, (l-|4-(2-Cvclopropyl-7-methoxy-quinolin-4-yloxy)-2-ri-(l- phenethyl-cvclopropanesulfonylaminocarbonyl)-2-vinyl-cyclopropylcarbamovn- pyrrolidine-1 -carbonyl }-2,2-dimethyl-propyl)-carbamic acid tert-butyl ester

compound 69h compound 69

Step 68h) Compound 69 was prepared in 41% yield (0.095 g) from the cyclopropyl-P2 tripeptide acid (0.160 g, 0.25 mmol) of the product of Step 68g (Example 68) in analogous fashion to the procedure of Step 27c (Example 27) in the synthesis of compound 27 and purified by preparative HPLC (solvent B: 45% to 85%): 1H NMR (methanol-d-) D ppm 0.65 (m, 2 H), 0.96 (s, 9 H), 1.18 (s, 9 H), 1.48 (m, 6 H), 1.92 (dd, 7=8.05, 5.49 Hz, 1 H), 2.37 (m, 3 H), 2.69 (dd, 7=14.09, 7.50 Hz, 1 H), 3.29 (m, 2 H), 4.01 (s, 3 H), 4.09 (m, 2 H), 4.59 (m, 2 H), 5.18 (m, 1 H), 5.35 (d, 7=17.20 Hz, 1 H), 5.67 (s, 1 H), 5.77 (m, 1 H), 6.83 (s, 1 H), 7.14 (m, 2 H), 7.31 (m, 6 H), 8.23 (d, 7=9.15 Hz, 1 H). LC-MS (retention time: 3.73, Method K), MS m/z 844 (MM).

Compound 69 Example 69

Compound 69, Example 69, BOCNH-P3(L-t-BuGly)-P2[(4R)-(2- cyclopropyl-7-methoxyquinoline-4-oxo)-S-proline]-Pl(lR,2S Vinyl Acca)- CONHSO₂[l-(l-pent-2-ynyl)-clopropan-l-yl) or alternate designation, Compound 69, example 69, (l-{4-(2-Cyclopropyl-7-methoxy-quinolin-4- yloxy)-2-[l-(l-pent-2-ynyl-cyclopropanesulfonylaminocarbonyl)-2-vinyl- cyclopropylcarbamoyl]-pyrrolidine-l-carbonyl}-2,2-dimethyl-propyl)- carbamic acid tert-butyl ester

Step 69) Compound 69 was prepared in 43% yield (0.086 g) from the cyclopropyl-P2 tripeptide acid (0.160 g, 0.25 mmol) of compound 69h of product of Step 69h (Example 69) in analogous fashion to the procedure of Example 46 in the synthesis of compound 33 and purified by preparative HPLC (solvent B: 30% to 100%): 1H NMR (methanol-d₄) D ppm 0.91 (m, 2 H), 1.01 (m, 3 H), 1.04 (s, 9 H), 1.15 (m, 5 H), 1.26 (m, 11 H), 1.80 (m, 1 H), 2.08 (m, 2 H), 2.22 (m, 1 H), 2.45 (m, 1 H), 2.99 (s, 2 H), 3.34 (s, 2 H), 3.90 (s, 3 H), 4.08 (m, 1 H), 4.23 (m, 1 H), 4.45 (d, 7=11.90 Hz, 1 H), 4.52 (m, 1 H), 5.04 (d, 7=10.38 Hz, 1 H), 5.20 (d, 7=17.09 Hz, 1 H), 5.42 (s, 1 H), 5.90 (m, 1 H), 6.57 (m, 1 H), 6.98 (dd, 7=9.00, 2.29 Hz, 1 H), 7.22 (d, 7=2.44 Hz, 1 H), 7.99 (d, 7=9.16 Hz, 1 H). LC-MS (retention time: 1.98, Method H), MS m/z 820 (MM). 169

Compound 70 Example 70

Compound 70, Example 70, BOCNH-P3( -t-BuGly)-P2[(4R)-(2- cyclopropyl-7-methoxyquinoline-4-oxo)-5-proline]-Pl(lR,25 Vinyl Acca)- CONHSO₂(l-cyclopropylmethylclopropan-l-yl) or alternate designation, Compound 70, example 70, (l-{4-(2-CyclopropyI-7-methoxy-quinolin-4- yIoxy)-2-[l-(l-cyclopropylmethyl-cyclopropanesulfonylaminocarbonyl)-2- vinyl-cyclopropylcarbamoyl]-pyrroIidine-l-carbonyl}-2,2-dimethyl-propyl)- carbamic acid tert-butyl ester

compound 68h

Step 70) Compound 70 was prepared in 43% yield (0.086 g) from the cyclopropyl-P2 tripeptide acid (0.160 g, 0.25 mmol) of compound 56h Step 69h in analogous fashion to the procedure of Step 27c of Example 27 in the synthesis of compound 1 except that 1-cyclopropylmethylcyclopropanesulfonamide was used in place of 1-trimethylsilanyl-cyclopropanesulfonamide: and purified by 170

preparative HPLC (solvent B: 45% to 85%): 1H NMR (methanol-d ) D ppm 0.06 (m, 2 H), 0.45 (m, 2 H), 0.67 (m, 1 H), 1.04 (s, 9 H), 1.28 (s, 9 H), 1.43 (m, 8 H), 1.87 (m, 4 H), 2.25 (m, 3 H), 2.60 (dd, 7=12.99, 6.77 Hz, 1 H), 3.91 (s, 3 H), 4.07 (dd, 7=12.08, 3.29 Hz, 1 H), 4.24 (d, 7=9.15 Hz, 1 H), 4.48 (m, 2 H), 5.09 (d, 7=10.25 Hz, 1 H), 5.26 (d, 7=17.20 Hz, 1 H), 5.45 (s, 1 H), 5.73 (m, 1 H), 6.60 (s, 1 H), 7.00 (dd, 7=9.15, 2.20 Hz, 1 H), 7.23 (d, 7=2.20 Hz, 1 H), 7.99 (d, 7=9.15 Hz, 1 H). LC-MS LC-MS (retention time: 3.16, Method L), MS m/z 808 (MM).

Compound 71 Example 71

compound 71

compound 71 e compound 71

Step 71a: P2 HN-r(4R)-(2-phenyl-7-methoxyquinoline-4-oxo)-S-proline methyl ester dihydrochloride

Step 71a) To a solution of 10 g (21.5 mmol) of N-Boc (4R)-(2-phenyl-7- methoxyquinoline-4-oxo)-S-proline, 4-(7-Methoxy-2-phenyl-quinolin-4-yloxy)- pyrrolidine-l,2-dicarboxylic acid 1-tert-butyl ester in 500 mL of MeOH cooled to -78 °C, was bubbled in gaseous HCl for 10 min. The mixture was warmed to rt, stirred overnite and concentrated in vacuo. The residue was azeotroped repeatedly with toluene and dioxane to afford 9.7 lg (100%) of the titled product as an offwhite solid. 1H NMR (DMSO-d₆) δ 2.56-2.66 (m, IH), 2.73-2.80 (m, IH), 3.67-3.86 (m, 2H), 3.79 (s, 3H), 3.97 (s, 3H), 4.76-4.82 (m, IH), 5.95 (m, IH), 7.42 (dd, 7=9, 2 Hz, IH), 7.65-7.72 (m, 4H), 8.23-8.27 (m, 2H), 8.51 (d, 7=9.2 Hz, IH), 9.68 (bs, IH), 11.4 (bs, IH); LC-MS (retention time: 0.94, method D), MS m/e 379 (MM). Step 71b: Preparation of P3 N-BOC (L-t-BuGly)-P2 r(4R)-(2-phenyl-7- methoxyquinoline-4-oxo)-S-prolirie)]-COOMe

Step 71b) To suspension of the product (3.90 g, 8.60 mmol) of Step 72a

(Example 72), [HΝ-(4_-)-(2-phenyl-7-methoxyquinoline-4-oxo)-S-proline) methyl ester, bis hydrochloride], 2.65g (11.47 mmmol) of N-BOC-L-tert-leucine (L- tBuGly), 3.48 g (34.40 mmol) of NMM in DMF (20mL) was added 3.62 g (9.52 mmol) of HATU at 0 °C. The reaction mixture was slowly allowed to warm to rt overnite, was stirred for 4 days, diluted with EtOAc (200 mL), washed with pH 4.0 buffer (3x40 mL), saturated aqueous NaHCO₃ (40 mL), dried (MgSO₄), and purified by a Biotage 40 M column (eluted with 15% to 70% EtOAc in Hexanes) to supply 4.16 g (81%) of l-(2-tert-Butoxycarbonylamino-3,3-dimethylbutyryl)- 4-(7-methoxy-2-phenylquinolin-4-yloxy)-pyrrolidine-2-carboxylic acid methyl ester, which is also named P3 N-BOC (L-tBuGly)-P2 [(4R)-(2-phenyl-7- methoxyquin-oline-4-oxo)-S-proline)]-COOMe, as a foam. 1H NMR (CDC1₃) δ 1.07 (s, 9H), 1.37 (s, 9H), 2.29-2.39 (m, IH), 2.78 (dd, 7=14, 8 Hz, IH), 3.96 (s, 3H), 4.06-4.1 l(m, IH), 4.31 (d, 7=10 Hz, IH), 4.54 (d, 7=11 Hz, IH), 4.72-4.77 (m, IH), 5.23 (d, 7=10 Hz, IH), 5.34 (m, IH), 6.96 (s, IH), 7.07 (dd, 7=9, 2 Hz, IH), 7.44-7.52 (m, 3H), 7.99-8.03 (m, 3H). LC-MS (retention time: 1.43, method A) MS m/e 592 (MM).

Step 71c: Preparation of P3 N-BOC (L-t-BuGlv)-P2 IY4_,)-(2-phenyl-7- methoxyquinoline-4-oxo)-S-proline)1-COOH

Step 71c) To a solution of l-(2-tert-butoxycarbonyl-amino-3,3- dimethylbutyryl)-4-(7-methoxy-2-phenyl-quinolin-4-yloxy)-pyrrolidine-2- carboxylic acid methyl ester (4.179 g, 7.06 mmol) in THF (318 mL), CH₃OH (42 mL), and H₂O (170 mL) was added LiOH (1.356 g, 56.5 mmol). The reaction mixture was stirred for one day, acidified to neutral pH, and concentrated in vacuo until only the aqueous layer remained. The resulting aqueous residue was acidified to pH 4.0 by addition of 1.0 Ν aqueous HCl and then saturated with solid ΝaCl. This aqueous mixture was extracted repeatedly with 80% EtOAc/THF (4X300 mL), the combined organic solvent dried (Mg₂SO₄), filtered, and concentrated in vacuo to supply 3.69 g (91%) of the titled product as a foam. 1H NMR (CDCI₃) δ 1.03 (s, 9H), 1.27 (s, 9H), 2.36-2.43 (m, IH), 2.78-2.83 (m, IH), 3.94 (s, 3H), 4.05 (d, 7=10 Hz, IH), 4.24 (d, 7=9 Hz, IH), 4.54 (d, 7=12 Hz, IH), 4.63-4.67 (m, IH), 5.52 (m, IH), 7.09 (dd, 7=9 Hz, IH), 7.20 (s, IH), 7.38 (s, IH), 7.51-7.55 (m, 3H), 7.99-8.00 (m, 3H), 8.09 (d, 7=9 Hz, IH). LC-MS (retention time: 1.44, Method A), MS m/z 578 (MM).

Step 7 Id: BOC P3-(L-tBuGlv)-P2 r(4R)-(2-ρhenyl-7-methoxyquinoline-4-oxo)-S- proline)] -P 1 -( 1 -aminoc yclopropane- 1 -)COOMe

Step 71d) A mixture of the product (2.0 g, 3.46 mmol) of Step 72c (Example 72), diisopropylethylamine (3 mL, 17.3 mmol), HOBT.H₂O (0.64 g, 4.15 mmol), and HBTU (1.58 g, 4.15 mmol) in CH C1₂ (35 mL) was stirred overnite. The reaction mixture was diluted with EtOAc (300 mL), Washed with pH 4.0 buffer (3x), ' aqueous NaHCO₃(2x), brine, dried (MgSO ), and concentrated. The residure was purified over Biotage 65M column (EtOAc/hexanes: 15% to 100%) to provide the product as a foam 1.97 g: 1H NMR IH NMR (CHLOROFORM-D) D ppm 1.02 (s, 9 H), 1.29 (m, 3 H), 1.29 (s, 9 H), 1.57 (m, 1 H), 2.40 (m, 1 H), 2.67 (dd, 7=13.91, 7.68 Hz, 1 H), 3.65 (s, 3 H), 3.89 (s, 3 H), 4.04 (m, 1 H), 4.21 (m, 1 H), 4.48 (d, 7=11.71 Hz, 1 H), 4.60 (t, 7=8.42 Hz, 1 H), 5.41 (s, 1 H), 7.00 (d, 7=8.78

Hz, 1 H), 7.14 (s, 1 H), 7.32 (s, 1 H), 7.50 (m, 3 H), 8.02 (m, 3 H). LC-MS (retention time: 1.49 method C), MS m/z 675 (MM).

Step 71e: BOC P3-(L-tBuGly)-P2 [Y4R)-(2-phenyl-7-methoxyquinoline-4-oxo)-S- proline)]-Pl-(l-aminocyclopropane-l-)COOH

Step 71e) To a suspension of the product (1.97 g, 2.92 mmol) of Step 72d (Example 72), { BOC P3-(L-tBuGly)-P2 [(4R)-(2-phenyl-7-methoxyquinoline-4- oxo)-S-proline)]-Pl-(l-aminocyclopropane-l-)COOMe}, in THF(75 mL), CH₃OH (18 mL), and H₂O (60 mL) was added LiOH (0.42 g, 18 mmol). The reaction mixture was stirred overnite, adjusted to pH 7, removed the organic solvents in vacuo. The aqueous residue was acidified to pH 4, and extracted with EtOAc(3x200 mL). Combined organic solvent was dried (MgSO₄), and concentrated in vacuo to afford the desired product (Compound 80g) 1.59 g (82%): 1H NMR (Methanol-d₄) D ppm 1.06 (s, 9 H), 1.30 (s, 9 H), 1.45 (m, 2 H), 1.60 (m, 1 H), 1.60 (m, 1 H), 2.53 (m, 1 H), 2.77 (dd, 7=13.43, 7.32 Hz, 1 H), 3.97 (s, 3 H), 4.09 (m, 1 H), 4.25 (d, 7=8.55 Hz, 1 H), 4.57 (d, 7=11.90 Hz, 1 H), 4.64 (t, 7=8.39 Hz, 1 H), 5.57 (m, 1 H), 7.10 (d, 7=8.55 Hz, 1 H), 7.29 (s, 1 H), 7.41 (s, 1 H), 7.57 (m, 3 H), 8.07 (d, 7=7.02 Hz, 2 H), 8.13 (d, 7=8.85 Hz, 1 H); LC-MS (retention time: 1.54, Method I), MS m/z 661 (MM).

Step 71f: Preparation ((l-{4-(7-Methoxy-2-phenyl-ouinolin-4-yloxy)-2-ri-(l- trimethylsilanyl-cyclopropanesulfonylaminocarbonvD-cvclopropylcarbamoyll- pyrrolidine-1 -carbonyl }-2.2-dimethyl-propyl)-carbamic acid tert-butyl ester

Step 71f) To a solution of the tripeptide acid (0.080 g, 0.12 mmol) of (0.080 g, 0.12 mmol) of the product of Step 71e (Example 71) in THF (2 mL) was added CDI (0.039 g, 0.24 mmol), and the resulting solution was heated at 72 °C for 60 min and allowed to cool down to rt. 1-Trimethylsilanylcyclopropylsulfonamide (0.027g, 0.14 mmol) and neat DBU (0.037 mL, 0.24 mmol) were added. The reaction mixture was stirred overnite, diluted with EtOAc (150 mL) and washed pH 4.0 buffer (2x30 mL), dried (Na₂SO₄/MgSO₄), concentrated. The residue was purified over 20X40 cM 1000D Analtech PTLC plates (MeOH CH₂Cl₂: 2 to 5%) to afford the desired product (Compound 71) 0.043 g (42%) as a foam: 1H NMR (CDC1₃) D ppm 0.12 (s, 9 H), 0.90 (m, 2 H), 0.99 (s, 9 H), 1.29 (d, 7=18.01 Hz, 9 H), 1.33 (m, 6 H), 2.42 (s, 1 H), 2.60 (s, 1 H), 3.91 (s, 3 H), 4.07 (s, 2 H), 4.26 (d, 7=8.85 Hz, 1 H), 4.46 (d, 7=11.29 Hz, 1 H), 5.35 (s, 1 H), 6.98 (s, 1 H), 7.01 (d, 7=10.68 Hz, 1 H), 7.36 (s, 1 H), 7.45 (m, 3 H), 7.94 (d, 7=7.32 Hz, 2 H), 7.99 (d, 7=9.16 Hz, 1 H). LC-MS (retention time: 1.77, Method E), MS m/z 836 (MM).

Compound 72 Example 72

Compound 72, Example 72, BOCNH-P3(L-.-BuGly)-P2[(4R)-(2-phenyl-7- methoxyquinoline-4-oxo)-5-proline]-Pl(cyclopropane)-CONHSO2(l- phenylcarbamoyl-cyclopropan-1-yl) or alternative destination Compound 72, Example 72, (l-{4-(7-Methoxy-2-phenyl-quinolin-4-yloxy)-2-[l-(l- phenylcarbamoyl-cyclopropanesulfonylaminocarbonyl)- cyclopropylcarbamoyI]-pyrrolidine-l-carbonyI}-2,2-dimethyl-propyl)- carbamic acid tert-butyl ester

Step72 ) Compound 72 was prepared in 73% yield (0.0785 g) from the tripeptide acid (0.080 g, 0.12 mmol) of the product of Step 71e (Example 71) in analogous fashion to the procedure of Step 71f (Example 71) in the synthesis of compound 71 except that 1-phenylcarbamoylcyclopropanesulfonamide (prepared in step 8Id) was used in place of 1-trimethylsilanylcyclopropanesulfonamide: 1H NMR (methanol-d₄) D ppm 1.01 (s, 11 H), 1.32 (s, 9 H), 1.34 (m, 4 H), 1.54 (m, 5 H), 2.38 (m, 1 H), 2.53 (m, 1 H), 3.66 (d, 7=9.46 Hz, 1 H), 4.20 (m, 1 H), 4.39 (d, 7=11.90 Hz, 1 H), 4.48 (t, 7=8.70 Hz, 1 H), 5.23 (s, 1 H), 6.95 (m, 1 H), 7.01 (dd, 7=9.00, 1.98 Hz, 1 H), 7.16 (m, 3 H), 7.37 (d, 7=2.14 Hz, 1 H), 7.52 (m, 6 H), 8.03 (d, 7=9.16 Hz, 1 H), 8.08 (d, 7=7.93 Hz, 2 H). HRMS m/z (M+H)⁺ calcd for C₄₆H₅₅N₆SOi₀: 83.3701 found: 883.3735. LC-MS (retention time: 1.58, Method F), MS m/z 883 (MM).

Compound 73 Example 73

Preparation of BOCNH-P3(L-^-BuGly)-P2[(4R)-(2-phenyl-7- methoxyquinoline-4-oxo)-5-proline]-Pl(cyclopropane)-CONHSO2(l- benzoyl-cyclopropan-1-yl) or alternative destination Compound 73, Example 73, ({l-[2-[l-(l-BenzoyI-cycIopropanesulfonylaminocarbonyl)- cyclopropylcarbamoyl]-4-(7-methoxy-2-phenyl-quinolin-4-yIoxy)- pyrrolidine-l-carbonyl]-2,2-dimethyl-propyl}-carbamic acid tert-butyl ester

Step 73) Compound 73 was prepared in 68% yield (0.071 g) from the cyclopropyl-P2 tripeptide acid (0.080 g, 0.12 mmol) of the product of Step 71e (Example 71) in analogous fashion to the procedure of Step 71f (Example 71) in the synthesis of compound 71 except that 1-benzoylcyclopropanesulfonamide (prepared in step 8Id) was used in place of 1- trimethylsilanylcyclopropanesulfonamide: 1H NMR (methanol-d₄) D ppm 1.00 (m, 2 H), 1.04 (s, 9 H), 1.32 (s, 9 H), 1.34 (m, 3 H), 1.71 (m, 3 H), 2.53 (m, 1 H), 2.71 (m, 1 H), 3.95 (s, 3 H), 3.99 (dd, 7=11.60, 2.44 Hz, 1 H), 4.27 (m, 1 H), 4.52 (d, 7=11.90 Hz, 1 H), 4.58 (t, 7=8.70 Hz, 1 H), 5.46 (s, 1 H), 7.07 (dd, 7=9.16,

10 2.14 Hz, 1 H), 7.24 (s, 1 H), 7.38 (m, 2 H), 7.51 (m, 5 H), 8.09 (m, 5 H). LC-MS (retention time: 1.66, Method I), MS m/z 868 (MM).

Compound 74 Example 74

2.5 compound 7₄

Preparation of BOCNH-P3(L-t-BuGly)-P2[(4__)-(2-phenyl-7- methoxyquinoline-4-oxo)-5-proline]-Pl(cyclopropane)-CONHSO₂(l-benzyl- cyclopropan-1-yl) or alternative destination Compound 74, Example 74, {1- [2-[l-(l-Benzyl-cyclopropanesulfonylaminocarbonyl)- 20 cyc_opropylcarbamoyl]-4-(7-methoxy-2-phenyl-quinolin-4-yloxy)- pyrrolidine-l-carbonyl]-2,2-dimethyl-propyl}-carbamic acid tert-butyl ester

compound 71 e compound 7₄ Step 74) Compound 74 was prepared in 29% yield (0.0298 g) from the cyclopropyl-P2 tripeptide acid (0.080 g, 0.12 mmol) of the product of Step 71e (Example 71) in analogous fashion to the procedure of Step 71f (Example 71) in the synthesis of compound 71 except that 1-benzylcyclopropanesulfonamide (prepared in step 7Id) was used in place of 1- trimethylsilanylcyclopropanesulfonamide: 1H NMR (CDC1₃) D ppm 0.95 (s, 9 H), 1.32 (s, 9 H), 1.57 (m, 6 H), 2.39 (m, 2 H), 2.55 (m, 1 H), 2.85 (m, 1 H), 3.37 (m, 2 H), 3.89 (s, 3 H), 4.03 (m, 2 H), 4.22 (d, 7=9.46 Hz, 1 H), 4.45 (m, 1 H), 5.32 (s, 1 H), 6.93 (s, 1 H), 6.98 (dd, 7=8.85, 1.83 Hz, 1 H), 7.36 (s, 1 H), 7.43 (m, 5 H), 7.85 (m, 1 H), 7.93 (m, 4 H), 8.10 (s, 1 H). HRMS m/z (M+H)⁺ calcd for C₄₆H₅₆N₅SO₉: 854.3799 found: 854.3813. LC-MS (retention time: 1.35, Method H), MS m/z 854 (MM).

Compound 75 Example 75

compound 75

Preparation of BOCNH-P3(L-t-BuGly)-P2[(4R)-(2-phenyl-7- methoxyquinoline-4-oxo)-5-proline]-Pl(cyclopropane)-CONHSO₂(l-allyl- cyclopropan-1-yl) or alternative destination Compound 75, Example 75, {1- [2-[l-(l-Allyl-cyclopropanesulfoήylaminocarbonyl)-cyclopropylcarbamoyl]- 4-(7-methoxy-2-phenyl-quinolin-4-yIoxy)-pyrrolidine-l-carbonyl]-2,2- dimethyl-propyl}-carbamic acid tert-butyl ester

compound 71 e

Step 75) Compound 75 was prepared in 40% yield (0.039 g) from the cyclopropyl-Pl tripeptide acid (0.080 g, 0.12 mmol) of the product of Step 71e (Example 71) in analogous fashion to the procedure of Step 71f (Example 71) in the synthesis of compound 71 except that 1-allylcyclopropanesulfonamide (prepared in Example 4) was used in place of 1- trimethylsilanylcyclopropanesulfonamide: 1H NMR (CDC1₃) D ppm 0.91 (m, 2 H), 0.99 (s, 9 H), 1.31 (s, 9 H), 1.34 (m, 7 H), 2.48 (s, 1 H), 2.59 (m, 2 H), 3.91 (s, 3 H), 4.01 (m, 1 H), 4.24 (s, 1 H), 4.44 (d, 7=11.29 Hz„ 1 H), 4.59 (s, 1 H), 4.92 (m, 2 H), 5.34 (s, 1 H), 5.61 (m, 1 H), 7.01 (m, 2 H), 7.36 (s, 1 H), 7.45 (m, 3 H), 7.94 (d, 7=7.02 Hz, 2 H), 7.98 (d, 7=8.85 Hz, 1 H). LC-MS (retention time: 1.63, Method I), MS m/z 804 (MM).

Compound 76 Example 76

Preparation of BOCNH-P3(L-*-BuGly)-P2[(4__)-(2-phenyl-7- methoxyquinoline-4-oxo)-S-proline]-Pl(cycIopropane)-CONHSθ2[l-(l- cyclohexenyl)-cyclopropan-l-yl] or alternative destination Compound 76, Example 76, {l-[2-[l-(l-Cyclohex-l-enyl- cycIopropanesulfonyIaminocarbonyl)-cyclopropylcarbamoyl]-4-(7-methoxy- 2-phenyl-quinolin-4-yloxy)-pyrrolidine-l-carbonyl]-2,2-dimethyl-propyl}- carbamic acid tert-butyl ester

compound 71 e

Step 76) Compound 76 was prepared in 36% yield (0.0368 g) from the cyclopropyl-Pl tripeptide acid (0.080 g, 0.12 mmol) of the product of Step 71e (Example 71) in analogous fashion to the procedure of Step 71f (Example 71) in the synthesis of compound 71 except that l-(l-cyclohexenyl)- cyclopropanesulfonamide (prepared in Example 5) was used in place of 1- trimethylsilanylcyclopropanesulfonamide: 1H NMR (CDC1₃) D ppm 0.92 (m, 2 H), 0.99 (s, 9 H), 1.00 (m, 2 H), 1.32 (s, 9 H), 1.46 (m, 8 H), 1.96 (s, 2 H), 2.13 (s, 2 H), 2.43 (m, 1 H), 2.59 (m, 1 H), 3.91 (s, 3 H), 4.01 (m, 1 H), 4.26 (d, 7=9.16 Hz, 1 H), 4.45 (d, 7=11.60 Hz, 1 H), 4.55 (s, 1 H), 5.36 (s, 1 H), 5.85 (s, 1 H), 7.03 (m, 2 H), 7.36 (m, 1 H), 7.45 (m, 3 H), 7.94 (d, 7=7.02 Hz, 2 H), 7.98 (d, 7=9.16 Hz, 1 H). HRMS m/z (M+H)⁺ calcd for C₄₅H₅₇N₅SO₉: 844.3955 found: 844.3978. LC-MS (retention time: 1.66, Method F), MS /z 844 (MM).

Compound 77 Example 77

compound 77 Preparation 4-[2-(4-Isopropyl-thiazol-2-yl)-7-methoxy-quinolin-4-yloxy]- pyrrolidine-l,2-dicarboxylic acid 1-tert-butyl ester Schem 1

Step 77b

Step 77d

Step 77a: Preparation of l-bromo-3-methyl-2-butanone

To a solution of 4.0 g (46.5 mmol) of 3-methyl-2-butanone (Aldrich) in 50 mL of MeOH was added dropwise a solution of 2.4 mL (46.5 mmol) of bromine over 40 min. The mixture was stirred 1.5h, diluted with 300 mL of pentane, washed with sat. aqueous NaHCO₃, dried (MgSO₄) and concentrated to afford 5.81 g of impure l-Bromo-3-methyl-butan-2-one which was taken directly into the step B. Step 77b: Preparation of 4-Isopropyl-thiazole-2-carboxylic acid ethyl ester

A neat solution of 5.58g (34 mmol) of l-Bromo-3-methyl-butan-2-one and 4.50g (34 mmol) of ethyl thioxamate (Aldrich) was heated at 70 °C over 18h and then cooled to room temperature. The mixture was partitioned between sat. aqueous NaHCO₃ and EtOAc, the EtOAc layer dried (MgSO ), concentrated and chromatographed over SiO₂ (eluted with 2% to 40% EtOAc/hexanes) to afford 3.4 g (48% overall) of 4-isopropylthiazole-2-carboxylic acid ethyl ester as an oil: IH NMR (500 MHz, CDC13) δ ppm 1.32 (d, J=7 Hz, 6 H), 1.42 (t, J=7.2 Hz, 3 H), 3.23 (m, 1 H), 4.46 (q, J=7.2 Hz, 2 H), 7.18 (s, 1 H).

Step 77c: 4-Isopropyl-thiazole-2-carboxylic acid

To a solution of 3.12 g (15.7 mmol) of 4-isopropylthiazole-2-carboxylic acid ethyl ester in 32 mL of 75% THF/MeOH, was added 110 mg (31.3 mmol) of LiOH in 8 mL of H₂O. The mixture was stirred overnite, the solution adjusted to pH 5 using IN aqueous HCl solution and concentrated in vacuo to afford 4- isopropylthiazole-2-carboxylic acid as a white solid (2.97g including salts) which was used directly in Step E: IH NMR (500 methanol-d δ ppm 1.29 (d, J=6.7 Hz, 6H), 3.20 (m, 1 H), 7.39 (m, 1 H).

Step 77d: 4-Isopropyl-thiazole-2-carboxylic acid (2-acetyl-5-methoxy- phenyl)-amide

To a suspension of 2.59g (15.7 mmol) of 2-amino-4-methoxybenzophenone

(product of step D) and 2.68 g (15.7 mmol) of 4-isopropylthiazole-2-carboxylic acid (product of step 77c) in 75 mL of pyridine cooled to -30 °C, was added 1.93 mL (23.5 mmol) of POCl₃ slowly dropwise over 5 min. The mixture was stirred 3 h, warmed to room temperature and was stirred overnite. The reaction mixture was poured into ice water, and extracted several times with EtOAc. The combined EtOAc extracts were dried (MgSO ), concentrated and chromatographed over SiO₂ (eluted with 0% to 15% MeOH/EtOAc) to afford 2.57g (51%) of 4-Methylthiazole-2-carboxylic acid (2-acetyl-5-methoxyphenyl)amide as a yellow solid: IH NMR (CDC1₃) δ ppm 1.41 (d, J=6.7 Hz, 6 H), 2.64 (s, 3 H), 3.24 (m, 1 H), 3.91 (s, 3 H), 6.67 (dd, J=9, 2.5 Hz, 1 H), 7.18 (s, 1 H), 7.86 (d, J=9 Hz, 1 H), 8.56 (d, J=2.5 Hz, 1 H), 13.48 (s, 1 H). Step 77e: 2-(4-Isopropyl-thiazol-2-yl)-7-methoxy-quinolin-4-ol

Step 77e) To a solution of 2.5g (7.85 mmol) of 4-methylthiazole-2-carboxylic acid (2-acetyl-5-methoxyphenyl)amide (product of step E) in 50 mL of THF, was added 19 mL (19 mmol) of IM KOtBu in THF. The mixture was heated to 70 °C for 3h, cooled to rt and stirred overnight. The mixture was concentrated, cold water added to form a suspension. The mixture was then acidified to pH 4, filtered and dried. The resulting solid was chromatographed over SiO₂ (eluted with 0% to 25% MeOH in CH₂C1₂) to afford 1.31 g (56%) of 2-(4-Isopropylthiazol-2-yl)-7-methoxyquinolin-4-ol as a beige solid: 1H NMR (DMSO-D₆) δ ppm 1.32 (d, J=6.6 Hz, 6 H), 3.14 (m, 1 H), 3.89 (s, 3 H), 7.06 (s, 1 H), 7.38 (s, 1 H), 7.51 (s, 1 H), 7.99 (d, J=9.2 Hz, 1 H), 11.77 (m, 1 H). LC-MS m/e 301 (retention time: 1.53, method A).

Step 77f: 4-Chloro-2-(4-isopropyl-thiazol-2-yl)-7-methoxy-quinoline

A suspension of 1.3g (4.3 mmol) of 2-(4-Isopropylthiazol-2-yl)-7- methoxyquinolin-4-ol, product of step F, in 60 mL of POCl₃ was heated to reflux for 2h. The solvent was removed in vacuo, the residue diluted with ice cold water and the mixture adjusted to pH 9 while cooling to 0 °C. This aqueous solution was extracted several times with EtOAc. The combined EtOAc extracts were washed once with brine, pH 4 buffer, dried (MgSO₄), and concentrated to afford 0.89 g (64%) of 4-Chloro-2-(4-isopropylthiazol-2-yl)-7-methoxyquinoline as a yellow solid: 1H NMR (500 MHz, CDC1₃) δ ppm 1.38 (d, J=7 Hz, 6 H), 3.19 (m, 1 H), 3.98 (s, 3 H), 7.06 (s, 1 H), 7.26 (m, 1 H), 7.47 (d, J=2 Hz, 1 H), 8.10 (d, J=9 Hz, 1 H), 8.31 (s, 1 H). LC-MS m/e 319 (retention time: 2.20, method A).

Scheme 2

compound 77 Step 77g: 4-r2-(4-Isopropyl-thiazol-2-yl)-7-methoxy-quinolin-4-yloxy]-proline

To a DMSO solution (10 mL) of (2S, 4R)-N-Boc-L-4-hydroxyproline (0.53 g, 2.3 mmol) was added t-BuOK (0.64 g, 5.7 mmol) portionwise. The generated mixture was stirred for 1.5 h then 4-Chloro-2-(4-isopropyl-thiazol-2- yl)-7-methoxy-quinoline (0.80 g, 2.5 mmol) from Step 77f (Example 77) was added. The reaction mixture was stirred for 1.5 day. The reaction mixture diluted with cold water and extracted with EtO Ac/Ether (1/4, 2x). The aqueous layer was acidified with 1.0 N aqueous HCl to pH 4, filtered. The solid was dried in dry box to provide the product in 70% yield (0.82 g) as a pale yellow solid: LC-MS (retention time: 1.46, Method I), MS m/z 514 (MM).

Step 77h: Preparation 4-r2-(4-Isopropyl-thiazol-2-yl)-7-methoxy-quinolin-4- yloxy]-2-ri-(l-propyl-cyclopropanesulfonylaminocarbonyl)-2-vinyl- cyclopropylcarbamoyl1-pyrrolidine-l-carboxylic acid tert-butyl ester

Step 77h) A slurry of Compound 77g (Example 77) (0.200 g, 0.39 mmol), diisopropylethylamine (0.27 mL, 1.95 mmol), HCl salt of 1-propyl- cyclopropanesulfonic acid [(1R, 2S)l-amino-2-vinyl-cyclopropanecarbonyl]- amide (0.144 g, 0.47 mmol), HATU (0.192 g, 0.51 mmol), and HOBT (0.063 g, 0.39 mmol) in CH₂C1₂ was stirred overnite and removed the solvent . the residue was purified by preparative HPLC (solvent B: 30 to 100) to afford the product as a light yellow solid: 1H NMR (methanol-d₄) D ppm 0.96 (m, 5 H), 1.42 (m, 6 H), 1.49 (s, 9 H), 1.47 (m, 5 H), 1.80 (m, 1 H), 1.88 (m, 2 H), 2.27 (q, 7=8.75 Hz, 1 H), 2.42 (m, 1 H), 2.66 (dd, 7=14.04, 6.71 Hz, 1 H), 3.22 (m, 1 H), 3.96 (dd, 7=14.34, 6.41 Hz, 5 H), 4.44 (dd, 7=9.92, 6.87 Hz, 1 H), 5.14 (d, 7=11.60 Hz, 1 H), 5.34 (m, 1 H), 5.50 (s, 1 H), 5.78 (m, 1 H), 7.20 (dd, 7=9.16, 2.14 Hz, 1 H), 7.36 (s, 1 H), 7.41 (d, 7=2.44 Hz, 1 H), 7.65 (s, 1 H), 8.03 (d, 7=9.16 Hz, 1 H). Step 77i: Preparation of { l-r2-ri-(l-Cyclopropylmethyl- cyclopropanesulfonylaminocarbonyl)-2-vinyl-cyclopropylcarbamoyl]-4-(7- methoxy-2-phenyl-quinolin-4-yloxy)-pyrrolidine-l-carbonyl]-2-methyl-propyl}- carbamic acid tert-butyl ester

Step 77i) A slurry of the compound 77h (0.287 g, 0.3 7 mmol) in 2 mL (8 mL) of 4M HCl/dioxane solution was stirred at for 2 h. The solvent was removed in vacuo and to the residue was added CH₂C1₂ (10 mL), diisopropylethylamine (0.26 mL), Boc-L-tert-leucine (0.104 g, 0.45 mmol), HOBt (0.061 g, 0.37 mmol), and HATU (0.185 g, 0.49 mmol). The reaction mixture was stirred overnite. Removed the solvent in vacuo and purified the residue by preparative HPLC (solvent B: 30% to 100%) to afford the product (Compund 77) as a light yellow foam: 1H NMR (methanol-d₄) D ppm 0.85 (m, 5 H), 1.04 (s, 9 H), 1.31 (m, 9 H), 1.33 (m, 5 H), 1.38 (d, 7=6.95 Hz, 6 H), 1.80 (m, 3 H), 2.08 (m, 1 H), 2.50 (m, 1 H), 2.72 (dd, 7=13.54, 7.32 Hz, 1 H), 3.18 (m, 1 H), 3.91 (s, 3 H), 4.13 (m, 1 H), 4.24 (s, 1 H), 4.54 (m, 2 H), 5.01 (d, 7=10.61 Hz, 1 H), 5.19 (d, 7=16.47 Hz, 1 H), 5.48 (s, 1 H), 5.93 (s, 1 H), 7.04 (dd, 7=9.15, 1.83 Hz, 1 H), 7.27 (s, 1 H), 7.32 (m, 1 H), 7.63 (s, 1 H), 8.04 (d, 7=9.15 Hz, 1 H).

Compound 78 Example 78

Scheme 1

step 78a: Preparation Pyridine-2-carboxylic acid (2-acetyl-5-methoxy-phenyl)- amide

, To a suspension of 2-picolic acid (3.73g, 30.3 mmol) and 2-amino-4- methoxybenzophenone (5.0 g, 30.3 mmol) at -30 °C dissolved in pyridine (150 mL) was added POCl₃ (3.7 mL, 45.4 mmol) in 5 min. the reaction mixture was

10 stirred for 3 hr at the temperature, and stirred at rt overnite. The reaction mixture was poured into cold water and extracted with EtOAc (3x). The combined extract was dried to provide the product (7.67 g, 93%): 1H NMR (methanol-d-.) δ ppm 2.65 (s, 3 H), 3.92 (s, 3 H), 6.78 (m, 1 H), 7.60 (m, 1 H), 8.00 (m, 1 H), 8.06 (m, 1 H), 8.21 (d, 7=7.63 Hz, 1 H), 8.59 (t, 7=2.29 Hz, 1 H), 8.76 (d, 7=3.97 Hz, 1 H).

15 LC-MS (retention time: 1.56, Method D), MS m/z 271 (MM). Step 78b: 7-Methoxy-2-pyridin-2-yl-quinolin-4-ol

To a suspension suspension of Pyridine-2-carboxylic acid (2-acetyl-5-methoxy- phenyl)-amide (2.90 g, 10.7 mmol) in THF (50 mL) was added t-BuOK/THF (IM, 24 mL, 24 mmol). The reaction mixture was heated at 70 °C for 3 h and stirred overnite. The solvent was removed the in vacuo. Cold water was added to the residue and adjusted pH to 4.6 with aqueous 1.0 N HCl, filtered. The solid residue was purified over a Biotage 65M column (MeOH/CH₂Cl₂: 0 to 15%) to provide the product (2.26 g, 84%): LC-MS (retention time: 1.19, Method D), MS m/z 253.(MM).

Step 78c: 4-Chloro-7-methoxy-2-pyridin-2-yl-quinoline

A mixture of 7-Methoxy-2-pyridin-2-yl-quinolin-4-ol (2.2 g, 8.71 mmol) in POCl₃ (92 mL) was refluxed for 3 h and then removed the solvent in vacuo. Ice water was added to the residue, adjusted the pH >10 with 1.0 N NaOH, and extrated with EtOAc (2x). The combined extract was washed with water, brine, dried (MgSO₄), removed solvent to supply the product as a yellow solid (89 %, 2.1 g): DMSO-D6) δ ppm 3.97 (s, 3 H), 7.40 (dd, 7=9.16, 2.44 Hz, 1 H), 7.53 (m, 1 H), 8.01 (m, 1 H), 8.09 (d, 7=9.16 Hz, 1 H), 8.46 (s, 1 H), 8.56 (d, 7=7.93 Hz, 1

H), 8.74 (d, 7=3.97 Hz, 1 H). LC-MS (retention time: 1.50, Method D), MS m/z 271 (MM).

Step 78d: Preparation of 4-(7-Methoxy-2-pyridin-2-yI-quinoIin-4-yIoxy)- pyrrolidine-l,2-dicarboxyIic acid 1-tert-butyl ester

To a solution of N-Boc-4-hydroxyproline (1.6 g, 6.7 mmol) in DMSO (20 mL) was added t-BuOK (1.9 g, 16.8 mmol). The generated mixture was stirred for 1.5 h and 4-Chloro-7-methoxy-2-pyridin-2-yl-quinoline (2.0 g, 7.4 mmol) and DMSO (10 mL) were added. The reaction mixture was stirred for 38 h, diluted with cold water and extracted with EtO Ac/ether (1/4, 2x). the aqueous layer was acidified to pH 4 and extracted with EtOAc/THF (5x). the combined extract was dried (Na₂SO /MgSO₄), removed the solvent in vacuo and the residue was purified by preparative HPLC (0-80% solvent B) to provide the product (1.6 g, 50%): LC-MS (retention time: 1.23, Method I), MS m/z 466 (MM). Step 78e: Preparation 2-ri-(l-Cyclopropylmethyl- cvclopropanesulfonylaminocarbonyl)-2-vinyl-cyclopropyIcarbamoyn-4-(7- methoxy-2-pyridin-2-yl-quinolin-4-yloxy)-pyrroIidine-l-carboxylic acid tert- butyl ester

Step 78e) To a mixture of the acid (0.33 g, 0.71 mmol) of the product of Step 78d (Example 78), diisopropylethylamine (0.5 mL, 3.6 mmol), TFA salt (0.205 g, 0.51 mmol) of 1-Cyclopropylmethyl-cyclopropanesulfonic acid (l-amino-2- vinyl-cyclopropanecarbonyl)-amide, and HOBt (0.1 g, 0.6 mmol) in CH₂C1₂ (8 mL) was added HATU (0.35 g, 0.92 mmol). The reaction mixture was stirred at rt overnite and diluted with EtOAc, washed with pH 4.0 buffer, dried (MgSO₄), removed the solvent in vacuo. The residue was purified by PTLC to provide the product in 59% (0.22 g) yield: 1H NMR (methanol-d₄) D ppm 0.64 (m, 1 H), 0.96 (m, 2 H), 1.33 (m, 8 H), 1.39 (m, 9 H), 1.90 (m, 2 H), 2.18 (m, 1 H), 2.54 (m, 1 H), 2.81 (m, 1 H), 4.01 (m, 5 H), 4.44 (d, 7=28.99 Hz, 1 H), 5.08 (m, 1 H), 5.31 (m, 1 H), 5.57 (s, 1 H), 6.03 (m, 1 H), 6.94 (s, 1 H), 7.27 (d, 7=8.24 Hz, 1 H), 7.64 (m, 1 H), 7.92 (m, 1 H), 8.14 (m, 2 H), 8.66 (s, 1 H), 8.74 (s, 1 H).

Step 78f: Preparation ( l-r2-ri-Q-Cvclopropylmethyl- ^; cvclopropanesulfonylaminocarbonyl)-2-vinyl-cvclopropylcarbamoyn-4-(7- methoxy-2-pyridin-2-yl-quinolin-4-yloxy)-pyrrolidine-l-carbonyl]-2.2-dimethyl- propyl} -carbamic acid tert-butyl ester

Step ) A slurry of the compound 78e (0.220 g, 0.3 mmol) of the product of Step 78e (Example 78) in 4M HCIJdioxane (2 mL, 8 mmol) was stirred at for 2 h, removed the solvent in vacuo. To the residue was added CH₂C1₂ (2 mL), diisopropylethylamine (0.2 mL), Boc-L-tert-leucine (0.083 g, 0.36 mmol), HOBt (0.046 g, 0.3 mmol), and HATU (0.172 g, 0.45 mmol). The reaction mixture was stirred at rt overnite and diluted with EtOAc, washed with pH 4.0 buffer, dried (MgSO ), removed the solvent in vacuo.purification from preparative HPLC (solvent B: 30% to 100%) to afford the product in 76% (0.192 g) yield of compound 64 as a yellow foam: 1H NMR (methanol-d-.) D ppm -0.05 (m, 1 H), 0.30 (m, 1 H), 0.66 (m, 1 H), 0.91 (m, 2 H), 1.05 (s, 9 H), 1.28 (s, 9 H), 1.67 (m, 8 H), 2.15 (m, 1 H), 2.58 (m, 1 H), 2.77 (m, 1 H), 3.96 (s, 3 H), 4.19 (d, 7=40.25 Hz, 2 H), 4.51 (d, 7=16.47 Hz, 2 H), 4.95 (m, 1 H), 5.15 (m, 1 H), 5.53 (s, 1 H), 5.89 (dd, 7=16.65, 9.33 Hz, 1 H), 7.09 (d, 7=8.42 Hz, 1 H), 7.43 (d, 7=1.83 Hz, 1 H), 7.50 (m, 1 H), 7.82 (s, 1 H), 7.99 (m, 1 H), 8.10 (d, 7=9.15 Hz, 1 H), 8.48 (d, 7=7.68 Hz, 1 H), 8.72 (s, 1 H).

Compound 79 Example 79

compound 79

Scheme 1

Step 79a: Preparation 2-ri-(l-Benzyl-cyclopropanesulfonylaminocarbonyl)-2- vinyl-cvclopropylcarbamoyl1-4-(7-methoxy-2-pyridin-2-yl-quinolin-4-yloxy)- pyrrolidine-1 -carboxylic acid tert-butyl ester

Step 79a ) Compound was prepared in 63% yield (0.207 g) from 0.20 g

(0.5 mmol) of the compound 78d of the acid product of step 78d in analogous fashion to the procedure of Step 78e in the synthesis of compound 78e and purified by preparative HPLC (solvent B: 30% to 100% to afford the product: ) and over 20X40 cM 1000 D Analtech PTLC plates (MeOH/CH₂Cl₂: 0 to 7%) to afford the product in 63 % (0.207g): LC-MS (retention time: 1.75, Method H), MS m/z 768 (MM).

Step 79b: Preparation (l-|4-(7-Methoxy-2-pyridin-2-yl-quinolin-4-yloxy)-2-ri- (l-phenethyl-cvclopropanesulfonylaminocarbonyl)-2-vinyl- cyclopropylcarbamoyl1-pyrrolidine-l-carbonyl}-2,2-dimethyl-propyl)-carbamic acid tert-butyl ester

Step 79b) Compound was prepared in 14% yield (0.042 g) from 0.263 g (0.34 mmol) of the compound 79a in analogous fashion to the procedure of Example in the synthesis of compound 78 (step 78 f) and purified by preparative HPLC (solvent B: 30% to 100%) and followed by PTLC (MeOH/CH₂Cl₂: 5%): 1H NMR (methanol-d-) D ppm 1.00 (s, 9 H), 1.26 (d, 7=19.76 Hz, 9 H), 1.29 (m, 5 H), 1.85 (s, 1 H), 2.15 (m, 1 H), 2.52 (s, 1 H), 2.75 (m, 1 H), 3.32 (m, 2 H), 3.94 (s, 3 H), 4.11 (m, 1 H), 4.24 (s, 1 H), 4.55 (m, 2 H), 5.05 (m, 1 H), 5.24 (d, 7=17.57 Hz, 1 H), 5.50 (s, 1 H), 5.89 (s, 1 H), 7.10 (m, 6 H), 7.43 (m, 2 H), 7.77 (s, 1 H), 7.96 (t, 7=7.68 Hz, 1 H), 8.07 (m, 1 H), 8.46 (d, 7=7.68 Hz, 1 H), 8.66 (s, 1 H); LC-MS (retention time: 1.67, Method H), MS m/z 845 (MM).

Compound 80 Example 80

Compound 8Q

Scheme 1

Step 80a:

A solution of (lR,2S)/(lS,2R)-l-amino-2-vinylcyclopropane carboxylic acid ethyl ester hydrochloride (2.54 g, 12 mmol) in CH₃CN (70 mL) was treated with a solution of diisopropylethylamine (9.5 mL, 67 mmol), [(4R)-(2- methoxycarbonyl-7-methoxylquinoline-4-oxo)-S-proline] (5.9 g, 13.2 mmol), and TBTU (3.89 g, 12.21 mmol) in CH₃CN (50 mL). The reaction mixture was stirred for 14 h and concentrated. The residue dissolved in EtOAc was repeatedly washed with NaHCO₃ (aq.), brine, dried (MgSO ), and concentrated. The residue was purified over Biotage 65M column (EtOAc/hexane: 45 to 100%) to provide the high Rf stereo isomer (Boc-P2[(4R)-(2- methoxycarbonyl-7- methoxylquinoline-4-oxo)-S-proline]-Pl(l__,2S Vinyl Acca) Acid ethyl ester 2.0 g (52%) as a white solid: 1H NMR (methanol-d4) δ ppm 1.24 (t, 7=7.02 Hz, 3 H), 1.38 (m, 11 H), 1.76 (m, 1 H), 2.21 (m, 1 H), 2.45 (m, 1 H), 2.71 (m, 1 H), 3.92 (m, 2 H), 3.96 (s, 3 H), 4.03 (s, 3 H), 4.16 (q, 7=7.22 Hz, 2 H), 4.42 (m, 1 H), 5.10 (m, 1 H), 5.30 (m, 1 H), 5.44 (s, 1 H), 5.77 (m, 1 H), 7.27 (d, 7=9.16 Hz, 1 H), 7.48 (s, 1 H), 7.52 (s, 1 H), 8.05 (s, 1 H). Scheme 2

Hi Rf isomer

compound 80g

Step 80b:

A solution of the high Rf product (3.16g, 5.40 mmol) of Step 1 of Example 370 {Boc-P2[(4_.)-(2- methoxycarbonyl-7-methoxylquinoline-4-oxo)-S- proline]-Pl(li?,2S Vinyl Acca) COOEt} at 0 °C dissolved in MeOH/THF (1/1, 13.2 mL) was treated with aqueous 1.0 N NaOH (5.5 mL, 5.5 mmol), stirred for 1 h, neutralized by the addition of AcOH. The solvent was removed in vacuo. The residue was redissolved in THF/CH₂C1₂ (1/1, 150 mL), dried (MgSO₄) and concentrated in vacuo to provide the product which was directly used in next step: LC-MS (retention time: 1.53 Method D), MS m/z 570 (MM).

Step 80c: To a solution of the product (assumed at 5.4 mmol) of step 2 example 370 at 0°C dissolved in THF (35 mL) was added a solution of fresh made CH₂N₂ (30 mmol) in Et₂O (80 mL). The reaction mixture was stirred at the temperature for 0.5 h, and stirred at rt for 18.5 h. After bubbling nitrogen for 1 h to the reaction mixture, the solution was removed in vacuo. The residue redissolved in EtOAc (1 L) was washed with saturated NaHCO (aq.), (2x200 mL), brine (100 mL), and dried (MgSO₄). The solvent was removed in vacuo to afford the product 3.10 g (97% two steps): LC-MS (retention time: 3.06, Method J), MS m/z 594 (MM).

Step 80d:

To a solution of the product (3.03g, 5.10 mmol) of step 3 of example 370 {Boc- P2[(4_?)-(2- diazoacetyl-7-methoxylquinoline-4-oxo)-S-ρroline]-Pl(l_?,2S Vinyl Acca) COOEt} at 0°C dissolved in THF (110 mL) was added 2 mL of 48% HBr. The mixture was stirred for 1 h, partitioned between EtOAc (500 mL) and saturated NaHCO₃ (aq.) (100 mL). The EtO AC layer was separated, dried (MgSO₄). The solvent was removed to afford the product (3.12g, 95%): LC-MS (retention time: 1.56 Method D). MS m/z 648 (MM), MS m/z 646 (M^"-l).

Step 80e:

The product (1.0 g, 1.54 mmol) of step 4 of example 370 {Boc-P2[(4R)-(2- bromoacetyl-7-methoxylquinoline-4-oxo)-S-proline] -P 1 (1__,2S Vinyl Acca) COOEt} was treated with isopropylthiourea (0.365 g, 3.09 mmol) in isopropyl alcohol (57 mL) for 2 h, and then the solvent was removed. The residue dissolved in aqueous 1.0 N HCl (30 mL) and EtO AC (200 mL) was adjusted pH to 7 by addition of 1.0 N NaOH (aq.). The aqueous layer was extracted with EtOAc (2x100 mL) and the combined extract was dried (MgSO₄), concentrated. The residue was purified by over Biotage 40+M column (EtOAc/hexanes: 30 to

100%) to afford the product 0.870 g, (84%) and ready for the next step.

Step 80f: The product (0.250 g, 0.375 mmol) of step 5 of example 370 {Boc- P2{(4_?)-[2- (2-isopropylaminothiazol-4-yl)-7-methoxylquinoline-4-oxo]-S- proline}-Pl(lR,2S Vinyl Acca) COOEt} was treated with 4N HCl/dioxane (2.5 mL, 10 mmol) for 2.5 h and concentrated in vacuo. To the residue was added N- methylmorpholine (0.206 mL, 1.875 mmol) in DMF (3 mL), N-Boc-L-tert- leucine (0.117 g, 0.506 mmol), and HATU (0.192 g, 0.506 mmol). The mixture was stirred ovenite and partitioned between EtOAc and pH 4.0 buffer. The EtOAc layer was washed with water, NaHCO (aq.), dried (MgSO₄), concentrated. The residue was purified over a Biotage 40M column (MeOH/CH₂Cl₂: 0 to 8%) to afford the product 0.289 g (99%): LC-MS (retention time: 2.53, Method K), MS m/z 779 (MM).

Step 80g: To a suspension of the product of Step 6 (0.274 g, 0.352 mmol) of Example 370 {BOCNH-P3(L-t-BuGly)- {[2- (2-isoρropylaminothiazol-4-yl)-7- methoxylquinoline-4-oxo]-S-proline} -P1(1_?,2S Vinyl Acca)-COOEt} in THFQ0.6 mL), CH₃OH (2.6 mL), and H₂O (5.3 mL) was added LiOH (0.068 g, 2.86 mmol). The reaction mixture was stirred for 24, adjusted to pH 6, removed the organic solvents in vacuo. The aqueous residue was acidified to pH 4, and extracted with CH₂C1₂ repeatedly. Combined organic solvent was dried (MgSO ), and concentrated in vacuo to afford the desired product (Compound 80g) 0.255 g (95%): LC-MS (retention time: 2.58, Method K), MS m/z 751 (MM).

Preparation (l-{2-[l-(l -Cyclopropylmethyl- cyclopropanesulfonylaminocarbonyl)-2-vinyl-cyclopropylcarbamoyl]-4-[2-(2- isopropylamino-thiazol-4-yl)-7-methoxy-quinolin-4-yloxy]-pyrrolidine-l- carbonyl}-2,2-dimethyl-propyl)-carbamic acid tert-butyl ester

Step 80h:

Scheme 3

compound 80

Step 80h) The compound 80 was prepared in 2.4% yield (0.0018 g) from (0.060 g, 0.081 mmol) of the compound 67 g the product of Example 80 Step 80g in analogous fashion to the procedure of Step 27c (Example 27) in the synthesis of compound 27 and combination purification by PTLC and Isco 35g column: MS m/z 908 (MM), MS /z 906 (M^"-l); LC-MS (retention time: 1.77, Method E),

Compound 81 Example 81

compund 81

Step 81a: preparation of l-ethoxylcarbonyl-cyclopropanyl chloroformate

Step 81) A THF solution (50 mL) of 1-hydroxy-cyclopropanecarboxylic acid ethyl ester (5g, 38.4 mmol) and pyridine (3.3 mL, 41 mmol) was added dropwise a phosgen/toleune solution (25 mL, 47.5 mmol) at 0 °C in 5-10 min. the reaction mixture was allowed slowly warm up overnite. The solid was filtered off and the filtration was concentrated in vacuo. The residue was dissolved in hexane, refiltered, and concentrated in vacuo to afford.7.4g (100%) the product. The product was dissolved in CH₂C1₂ (100 mL) as a stack solution: 1H NMR (300 MHz, CHLOROFORM-D) D ppm 1.25 (t, 7=7.14 Hz, 3 H), 1.37 (m, 2 H), 1.57 (m, 2 H), 4.21 (q, 7=6.95 Hz, 2 H); (ppm) 13.97, 15.75, 62.07, 62.13, 150.54, 168.71.

Step 81b:

compound 81 compound 55a

Step 81b) Compound 56 was prepared in 46% (0.086 g) yield from the bis HCl salt (0.100 g, 0.18 mmol) of the product of Step 55a (Example 55) in analogous fashion to the procedure of step 55b (Example 55) in preparation of Compound 55 except that 1-ethoxylcarbonyl-cyclopropanyl chloroformate was used in place of cyclopentyl chloroformate and Triethyl amine was used as the base. The product was purified by preparative HPLC (solvent B: 40% to 85%): MS m/z 934 (M^"-l); HPLC (retention time: 3.22, Method J),

1HNMR (500 MHz, Solvent) δ ppm 0.90 (m, 2 H), 1.03 (s, 9 H), 1.14 (m, 4 H), 1.30 (m, 3 H), 1.48 (m, 3 H), 1.95 (dd, 7=8.09, 5.34 Hz, 1 H), 2.32 (q, 7=8.85 Hz, 1 H), 2.44 (m, 1 H), 2.78 (dd, 7=14.04, 7.02 Hz, 1 H), 3.30 (d, 7=13.43 Hz, 1 H), 3.37 (d; 7=13.43 Hz, 1 H), 4.03 (q, 7=7.12 Hz, 2 H), 4.07 (s, 3 H), 4.16 (dd, 7=12.05, 3.20 Hz, 1 H), 4.28 (m, 1 H), 4.64 (dd, 7=10.22, 6.87 Hz, 2 H), 5.21 (m, 1 H), 5.37 (d, 7=17.09 Hz, 1 H), 5.79 (m, 2 H), 7.17 (m, 2 H), 7.28 (m, 3 H), 7.40 (m, 1 H), 7.55 (m, 2 H), 7.72 (m, 3 H), 8.09 (d, 7=6.41 Hz, 2 H), 8.36 (d, 7=9.16 Hz, 1 H). Section C Example 100: Preparation of Compound 100

Compound 100

Scheme 1

Step 1:

As described above

Step 2:

As described above.

Step 3: A solution of l(R)-tert-butoxycarbonylamino-2(S)-vinyl-cyclopropanecarboxylic acid (4.45 g, 19.6 mmol) and l,l'-carbonyldiimidazole (3.97 g, 24.5 mmol) in dry THF (60 mL) was heated to boiling under reflux for 90 min. Upon cooling to rt, the mixture was treated sequentially with the product from Example 100, Step 2 (5.17 g, 24.5 mmol) and l,8-diazabicyclo[5.4.0]undec-7-ene (6.26 g, 41.1 mmol). The resulting mixture was stirred at rt for 72h, and was then concentrated in vacuo to a viscous brown oil. The residue was dissolved in ethyl acetate (300 mL) and was washed with IN HCl (3 x 75 mL) and then with brine (75 mL). The organic was dried over anhydrous magnesium sulfate, filtered, and concentrated. Purification by flash silica gel chromatography (DCM, then 1% MeOH in DCM) gave 8.4 g (quantitative yield) of the desired product as an off-white solid: MS m/z 443 ((M+Na)+).

Step 4: The product from Example 100, Step 3 (8.4 g, 19.6 mmol) was dissolved in a mixture of TFA (75 mL) and DCM (75 mL) and the resulting solution was stirred for 2.5 h at rt. Concentration in vacuo to an oily residue, followed by addition of IN HCl in Et₂O (35 mL) gave a white solid which was isolated by filtration and dried in vacuo to give 6.30 g (90.2% yield) of the desired product as an off-white powder: 1H NMR (CD₃OD) δ 0.66-0.83 (m, 2 H), 1.41-1.50 (m, 1 H), 1.60 (ddd, J=10.89, 6.31, 4.76 Hz, 1 H), 1.71 (dd, J=10.06, 7.87 Hz, 1 H), 2.17 (t, J=7.87 Hz, 1 H), 2.35-2.47 (m, 1 H), 3.33 (s, 2 H), 5.37 (d, J=10.25 Hz, 1 H), 5.48 (d, J=17.20 Hz, 1 H), 5.78 (ddd, J=17.11, 10.15, 7.50 Hz, 1 H), 7.13-7.20 (m, 2 H), 7.24-7.35 (m, 3 H); MS m/z 321 (MH+), 343 ((M+Na)+).

Scheme 2

Step 5: The product of Example 100, Step 4 (3.00 g, 8.41 mmol) was combined with 4(R)-(7-Methoxy-2-phenyl-quinolin-4-yloxy)-pyrrolidine-l,2(S)-dicarboxylic acid 1-tert-butyl ester (3.90 g, 8.41 mmol), HATU (3.84 g, 10.1 mmol), DIPEA (3.26 g, 25.2 mmol) and DMF (75 mL) and the resulting solution was stirred at rt for 4.5 h. The mixture was concentrated in vacuo to a residue and was then redissolved in ethyl acetate (250 mL) and washed successively with pH = 4 buffer (4 x 75 mL), water (50 mL) and brine (75 mL). The organic was dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. Purification by flash silica gel chromatography (step gradient: DCM, then 1% MeOH in DCM, then 2% MeOH in DCM) gave the product as 6.08 g (94.3% yield) of a beige solid: 1H NMR (CD₃OD) δ 0.57-0.64 (m, 2 H), 1.41 (s, 9 H), 1.44-1.54 (m, 3 H), 1.90 (dd, J=7.93, 5.49 Hz, 1 H), 2.36 (ddd, 1=13.89, 9.77, 4.12 Hz, 1 H), 2.62 (dd, J=13.89, 6.87 Hz, 1 H), 2.80 (s, 2 H), 3.28-3.35 (m, 1 H), 3.89-3.91 (m, 2 H), 3.95 (s, 3 H), 4.43 (dd, J=9.61, 6.87 Hz, 1 H), 5.16 (d, J=10.07 Hz, 1 H), 5.34 (d, J=17.09 Hz, 1 H), 5.52 (s, 1 H), 5.74-5.82 (m, 1 H), 7.14-7.29 (m, 8 H), 7.41 (d, J=2.14 Hz, 1 H), 7.52-7.57 (m, 3 H), 7.97-8.06 (m, 2 H); MS m/z 767 (MH+).

Step 6:

The product of Example 100, Step 5 (4.50 g, 5.87 mmol) was combined with DCM (75 mL) and TFA (50 mL) and the resulting solution was stirred for 30 min at rt. Solvent was removed in vacuo to give a brown oil. The residue was dissolved in 1,2-dichloroethane and the mixture was again concentrated in vacuo to give a glassy solid. The solid was taken up in DCM (30 mL) and to the resulting solution was added IN HCl in ether (50 mL) in dropwise fashion with rapid stirring. The slightly purple solid that precipitated from solution was isolated by filtration and dried under high vacuum. Total recovery of the desired product was 4.08 g (98.8% yield): 1H NMR (CD₃OD) δ 0.60-0.66 (m, 2 H), 1.38-

1.42 (m, 2 H), 1.48-1.52 (m, 1 H), 1.99 (dd, J=7.93, 5.49 Hz, 1 H), 2.44 (q, J=8.85 Hz, 1 H), 2.57 (ddd, J=14.80, 10.68, 4.43 Hz, 1 H), 2.81 (s, 1 H), 3.13 (dd, J=14.65, 7.32 Hz, 1 H), 3.99 (d, J=2.14 Hz, 2 H), 4.08 (s, 3 H), 4.84-4.89 (m, 2 H), 5.22 (dd, J=10.38, 1.22 Hz, 1 H), 5.39 (dd, J=17.09, 1.22 Hz, 1 H), 5.70 (ddd, J=17.09, 10.22, 8.70 Hz, 1 H), 6.00 (s, 1 H), 7.14 (d, J=7.02 Hz, 2 H), 7.22-7.25

(m, 1 H), 7.29 (t, J=7.32 Hz, 2 H), 7.50 (dd, J=9.16, 2.44 Hz, 1 H), 7.59 (d, J=2.44 Hz, 1 H), 7.64 (s, 1 H), 7.71-7.79 (m, 3 H), 8.09-8.10 (m, 2 H), 8.54 (d, 1=9.16 Hz, 1 H),: MS m/z 667 (MH+).

Step 7: The product of Example 100, Step 6 (2.00 g, 2.84 mmol) was combined with N- Boc- L-tert-leucine (0.658 g, 2.84 mmol), HATU (1.30 g, 3.41 mmol), DIPEA (1.11 g, 8.53 mmol) and DMF (30 mL) and the resulting solution was stined at rt for 18 h. The mixture was concentrated in vacuo to a residue and was then redissolved in ethyl acetate (150 mL) and washed successively with pH = 4 buffer (3 x 75 mL) and brine (50 mL). The organic was dried over anhydrous

, magnesium sulfate, filtered and concentrated in vacuo. Purification by flash silica gel chromatography (gradient: DCM, to 3% MeOH in DCM) gave 2.23 g (89.2% yield) of the desired product as a beige solid: 1H NMR (CD₃OD) δ 0.62- 0.66 (m, 2 H), 0.98 (s, 9 H), 1.01-1.06 (m, 2 H), 1.25 (s, 9 H), 1.43-1.47 (m, 3 H), 1.92 (dd, J=8.09, 5.34 Hz, 1 H), 2.28 (q, J=8.85 Hz, 1 H), 2.34-2.39 (m, 1 H),

2.72 (dd, J=14.19, 7.17 Hz, 1 H), 3.99 (s, 3 H), 4.08-4.11 (m, 1 H), 4.21-4.23 (m, 1 H), 4.57-4.61 (m, 2 H), 5.18 (d, J=10.07 Hz, 1 H), 5.34 (d, J=17.40 Hz, 1 H), 5.66 (s, 1 H), 5.77 (ddd, J=17.40, 9.77, 9.46 Hz, 1 H), 7.14-7.30 (m, 6 H), 7.38 (s, 1 H), 7.44 (d, J=2.14 Hz, 1 H), 7.60-7.61 (m, 3 H), 8.05 (dd, J=7.32, 2.14 Hz, 2 H), 8.18 (d, J=9.16 Hz, 1 H); MS m/z 881 (MH+).

Scheme 3

Compound 100

Step 8:

A solution of the product from Example 100, Step 7 (1.50g, 1.70 mmol) in DCM (50 mL) and trifluoroacetic acid (50 mL) was stirred for 3 h at rt. The mixture was concentrated in vacuo to a viscous residue, and was then dissolved in 1,2- dichloroethane and again concentrated in vacuo to give the desired bis- trifluoroacetic acid salt product as an off-white glassy solid (quantitative). The material was used directly in the next step without purification. 1H NMR (CD3OD) δ 0.64-0.72 (m, 2 H), 1.12 (s, 9 H), 1.42-1.56 (m, 4 H), 1.94 (dd, J=8.05, 5.49 Hz, 1 H), 2.33 (q, J=8.90 Hz, 1 H), 2.41-2.50 (m, 1 H), 2.81 (s, 2 H), 4.06 (s, 3 H), 4.16-4.21 (m, 2 H), 4.48 (d, J=12.44 Hz, 1 H), 4.75 (dd, J=10.43, 7.14 Hz, 1 H), 5.21 (dd, J=10.25, 1.46 Hz, 1 H), 5.33-5.39 (m, 1 H), 5.77 (ddd, J=17.20, 10.25, 8.78 Hz, 1 H), 5.87 (d, J=2.93 Hz, 1 H), 7.14 (dd, J=7.68, 1.46 Hz, 2 H), 7.24-7.30 (m, 3 H), 7.46 (dd, J=9.33, 2.38 Hz, 1 H), 7.57 (d, J=2.56 Hz,

1 H), 7.61 (s, 1 H), 7.69-7.77 (m, 3 H), 8.06-8.09 (m, 2 H), 8.33 (d, J=9.15 Hz, 1 H),

Step 9:

To a solution of the product from Example 100, Step 8 (123 mg, 0.122 mmol) in

1,2-dichloroethane (3 mL) was added -tolyl chloroformate (27.0 mg, 0.158 mmol) and NN-diisopropylethylamine (78.7 mg, 0.609 mmol). The mixture was agitated at rt for 72 h. The reaction mixture was washed with pH = 4 buffer solution (3 x 3 mL), and the washes were back-extracted with 1,2-dichloroethane (3 mL). The organic phases were combined and concentrated in vacuo. The crude product was then dissolved in MeOH and purified by reverse phase preparative HPLC to give Compound 100 as an off-white solid (68.1 mg, 61.2% yield): 1H ΝMR (CD₃OD) δ 0.61-0.67 (m, 2 H), 1.06 (s, 9 H), 1.42-1.50 (m, 3 H), 1.91 (dd, 7=7.93, 5.49 Hz, 1 H), 2.24-2.36 (m, 2 H), 2.33 (s, 3 H), 2.68-2.72 (m, 1 H), 3.95 (s, 3 H), 4.09 (dd, 7=11.75, 3.20 Hz, 1 H), 4.37 (s, 1 H), 4.52-4.59 (m, 2 H), 5.17 (d, 7=10.99 Hz, 1 H), 5.33 (d, 7=16.79 Hz, 1 H), 5.54 (s, 1 H), 5.77 (ddd, 7=17.24, 9.61, 9.46 Hz, 1 H), 6.83 (d, 7=8.55 Hz, 3 H), 7.10 (d, 7=8.24 Hz,

2 H), 7.15 (d, 7=7.02 Hz, 2 H), 7.21-7.24 (m, 2 H), 7.28 (t, 7=7.17 Hz, 2 H), 7.37 (d, 7=2.44 Hz, 1 H), 7.48-7.53 (m, 3 H), 7.97-8.06 (m, 3 H); MS m/z 914 (MH+), m/z 912 (M-l).

Example 101: Preparation of Compound 101

Compound 101

Compound 101 was prepared by following Step 9 of Example 100 except that phenyl chloroformate was used in place of p-tolyl chloroformate.

Step 9:

Modifications: 25 mg (0.16 mmol) phenyl chloroformate used, 59.5 mg product obtained as a white solid (54.3% yield): 1H NMR (CD₃OD) δ 0.61-0.67 (m, 2 H), 1.06 (s, 9 H), 1.09-1.14 (m, 1 H), 1.41-1.51 (m, 3 H), 1.92 (dd, 7=7.93, 5.49 Hz, 1 H), 2.27 (q, 7=8.85 Hz, 1 H), 2.30-2.36 (m, 1 H), 2.68-2.72 (m, 1 H), 3.94 (s, 3 H), 3.94-3.98 (m, 1 H), 4.10 (dd, 7=11.90, 3.05 Hz, 1 H), 4.38 (s, 1 H), 4.53 (d, 7=11.90 Hz, 1 H), 4.58 (dd, 7=10.07, 7.32 Hz, 1 H), 5.17 (d, 7=10.99 Hz, 1 H), 5.33 (d, 7=17.09 Hz, 1 H), 5.55 (s, 1 H), 5.77 (ddd, 7=17.09, 9.77, 9.46 Hz, 1 H), 6.88 (dd, 7=9.00, 2.29 Hz, 1 H), 6.96 (d, 7=7.63 Hz, 2 H), 7.14-7.24 (m, 5 H), 7.27-7.32 (m, 4 H), 7.37 (d, 7=2.14 Hz, 1 H), 7.47-7.53 (m, 3 H), 8.00 (d, 7=6.71 Hz, 2 H), 8.05 (d, 7=9.16 Hz, 1 H); MS m/z 900 (MH+), m/z 898 (M-l).

Example 102: Preparation of Compound 102

Compound 102

Compound 102 was prepared by following Step 9 of Example 100 except that 4- fluorophenyl chloroformate was used in place of p-tolyl chloroformate.

Step 9:

Modifications: 28 mg (0.16 mmol) 4-fluorophenyl chloroformate used, 78.7 mg product obtained as an off-white solid (70.4% yield): 1H NMR (CD₃OD) δ 0.61-

0.67 (m, 2 H), 1.05 (s, 9 H), 1.10-1.13 (m, 1 H), 1.42-1.50 (m, 3 H), 1.92 (dd, 7=7.93, 5.49 Hz, 1 H), 2.25-2.37 (m, 2 H), 2.68-2.72 (m, 1 H), 3.95 (s, 3 H), 4.09 (dd, 7=11.90, 3.05 Hz, 1 H), 4.35 (s, 1 H), 4.52 (d, 7=11.60 Hz, 1 H), 4.60 (dd, 7=10.07, 7.02 Hz, 1 H), 5.18 (d, 7=10.68 Hz, 1 H), 5.34 (d, 7=17.09 Hz, 1 H), 5.55 (s, 1 H), 5.77 (ddd, 7=17.09, 9.77, 9.46 Hz, 1 H), 6.90-6.92 (m, 3 H), 7.00 (t, 7=8.55 Hz, 2 H), 7.15 (d, 7=7.02 Hz, 2 H), 7.23-7.30 (m, 4 H), 7.38 (d, 7=2.44 Hz, 1 H), 7.48-7.53 (m, 3 H), 8.00-8.05 (m, 3 H); MS m/z 918 (MH+), m/z 916 (M-l).

Example 103: Preparation of Compound 103

Compound 103

Compound 103 was prepared by following Step 9 of Example 100 except that 4- methoxyphenyl chloroformate was used in place of p-tolyl chloroformate.

Step 9:

Modifications: 29 mg (0.16 mmol) 4-methoxyphenyl chloroformate used, 79.8 mg product obtained as an off-white solid (70.5% yield): 1H NMR (CD₃OD) δ

0.61-0.67 (m, 2 H), 1.05 (s, 9 H), 1.08-1.13 (m, 1 H), 1.41-1.48 (m, 3 H), 1.92 (dd, 7=7.63, 5.49 Hz, 1 H), 2.24-2.35 (m, 2 H), 2.65-2.71 (m, 1 H), 3.78 (d,

7=3.05 Hz, 4 H), 3.94 (s, 3 H), 4.08-4.10 (m, 1 H), 4.36 (s, 1 H), 4.53 (d, 7=12.21 Hz, 1 H), 4.56-4.60 (m, 1 H), 5.17 (d, 7=10.38 Hz, 1 H), 5.33 (d, 7=17.09 Hz, 1 H), 5.54 (s, 1 H), 5.73-5.81 (m, 1 H), 6.81-6.89 (m, 5 H), 7.15 (d, 7=7.32 Hz, 2 H), 7.22-7.24 (m, 2 H), 7.28 (t, 7=7.17 Hz, 2 H), 7.38 (d, 7=2.44 Hz, 1 H), 7.48- 7.53 (m, 3 H), 8.00-8.06 (m, 3 H); MS m z 930 (MH+), m/z 928 (M-l).

Example 104: Preparation of Compound 104

Compound 104

Compound 104 was prepared by following Step 9 of Example 100 except that chloroformic acid 2-methoxyethyl ester was used in place of -tolyl chloroformate.

Step 9:

Modifications: 22 mg (0.16 mmol) chloroformic acid 2-methoxyethyl ester used,

76.5 mg product obtained as an off-white solid (71.2% yield): 1H NMR (CD₃OD) δ 0.60-0.66 (m, 2 H), 0.98 (s, 9 H), 1.00-1.05 (m, 1 H), 1.41-1.50 (m, 3

H), 1.91 (dd, 7=7.93, 5.49 Hz, 1 H), 2.27 (q, 7=8.65 Hz, 1 H), 2.31-2.36 (m, 1 H),

2.67-2.71 (m, 1 H), 3.42-3.46 (m, 2 H), 3.78 (s, 1 H), 3.88-3.91 (m, 1 H), 3.96 (s,

3 H), 3.97-3.99 (m, 1 H), 4.08 (dd, 7=11.75, 2.90 Hz, 1 H), 4.29-4.31 (m, 1 H),

4.52 (d, 7=11.90 Hz, 1 H). 4.57 (dd, 7=9.77, 7.32 Hz, 1 H), 5.17 (d, 7=10.38 Hz, 1 H), 5.33 (d, 7=17.09 Hz, 1 H), 5.57 (s, 1 H), 5.77 (dt, 7=17.17, 9.58 Hz, 1 H),

7.13-7.15 (m, 3 H), 7.22-7.30 (m, 4 H), 7.41 (d, 7=2.14 Hz, 1 H), 7.49-7.56 (m, 3

H), 8.05-8.09 (m, 3 H), MS m/z 882 (MH+), m/z 880 (M-l).

Example 105: Preparation of Compound 105

Compound 105

Compound 105 was prepared by following Step 9 of Example 100 except that neopentyl chloroformate was used in place of -tolyl chloroformate.

Step 9:

Modifications: 24 mg (0.16 mmol) neopentyl chloroformate used, 81.4 mg product obtained as an off-white solid (74.8% yield): 1H NMR (CD₃OD) δ 0.55

(s, 1 H), 0.61-0.67 (m, 2 H), 0.84 (s, 9 H), 0.98 (s, 9 H), 1.00-1.05 (m, 1 H), 1.43- 1.47 (m, 3 H), 1.91 (dd, 7=7.93, 5.49 Hz, 1 H), 2.27 (q, 7=8.85 Hz, 1 H), 2.31- 2.37 (m, 1 H), 2.69 (dd, 7=13.12, 7.63 Hz, 1 H), 3.40 (d, 7=10.38 Hz, 1 H), 3.57 (d, 7=10.38 Hz, 1 H), 3.95 (s, 3 H), 4.09 (dd, 7=11.90, 2.44 Hz, 1 H), 4.30 (s, 1 H), 4.52 (d, 7=11.60 Hz, 1 H), 4.58 (dd, 7=10.22, 7.17 Hz, 1 H), 5.18 (d, 7=10.68 Hz, 1 H), 5.34 (d, 7=17.09 Hz, 1 H), 5.57 (s, 1 H), 5.78 (ddd, 7=17.32, 9.77, 9.54 Hz, 1 H), 7.09 (dd, 7=9.16, 2.14 Hz, 1 H), 7.14 (d, 7=6.71 Hz, 2 H), 7.22-7.30 (m, 4 H), 7.41 (d, 7=2.14 Hz, 1 H), 7.49-7.56 (m, 3 H), 8.07 (t, 7=8.85 Hz, 3 H); MS m/z 894 (MH+), m/z 892 (M-l).

Example 106: Preparation of Compound 106

Compound 106

Compound 106 was prepared by following Step 9 of Example 100 except that 2- fluoroethyl chloroformate was used in place of p-tolyl chloroformate.

Step 9:

Modifications: 20 mg (0.16 mmol) 2-fluoroethyl chloroformate used, 72.3 mg product obtained as an off-white solid (68.3% yield): 1H NMR (CD₃OD) δ 0.62-

0.66 (m, 2 H), 0.99 (s, 9 H), 1.01-1.05 (m, 1 H), 1.42-1.50 (m, 3 H), 1.90-1.92

(m, 1 H), 2.24-2.30 (m, 1 H), 2.33-2.36 (m, 1 H), 2.67-2.71 (m, 1 H), 3.96 (s, 3

H), 4.00-4.10 (m, 3 H), 4.31 (s, 1 H), 4.37-4.53 (m, 3 H), 4.56-4.59 (m, 1 H), 5.17

(d, 7=10.38 Hz, 1 H), 5.33 (d, 7=17.40 Hz, 1 H), 5.58 (s, 1 H), 5.74-5.81 (m, 1

H), 7.12-7.15 (m, 3 H), 7.22-7.30 (m, 4 H), 7.41 (s, 1 H), 7.49-7.56 (m, 3 H),

8.05-8.09 (m, 3 H); MS m/z 870 (MH+), m z 868 (M-l).

Example 107: Preparation of Compound 107

Compound 107

Compound 107 was prepared by following Step 9 of Example 100 except that 2- methoxyphenyl chloroformate was used in place of p-tolyl chloroformate.

Step 9:

Modifications: 29 mg (0.16 mmol) 2-methoxyphenyl chloroformate used, 82.0 mg product obtained as an off-white solid (72.4% yield): 1H NMR (CD₃OD) δ

0.64 (s, 2 H), 1.07 (s, 9 H), 1.14 (s, 1 H), 1.42-1.50 (m, 3 H), 1.90-1.93 (m, 1 H), 2.26-2.36 (m, 2 H), 2.65-2.71 (m, 1 H), 3.68 (s, 3 H), 3.95 (s, 3 H), 4.12 (d,

7=10.38 Hz, 1 H), 4.40 (s, 1 H), 4.46 (d, 7=11.90 Hz, 1 H), 4.57-4.60 (m, 1 H), 5.17 (d, 7=10.07 Hz, 1 H), 5.33 (d, 7=17.09 Hz, 1 H), 5.53 (s, 1 H), 5.74-5.81 (m, 1 H), 6.89-6.93 (m, 3 H), 7.00 (d, 7=7.93 Hz, 1 H), 7.16 (t, 7=7.63 Hz, 3 H), 7.21- 7.25 (m, 2 H), 7.29 (t, 7=7.02 Hz, 2 H), 7.37 (s, 1 H), 7.50 (d, 7=7.32 Hz, 3 H), 7.99-8.05 (m, 3 H); MS m/z 930 (MH+), m/z 928 (M-l).

Example 108: Preparation of Compound 108

Compound 108

Compound 108 was prepared by following Step 9 of Example 100 except that 3- trifluoromethylphenyl chloroformate was used in place of -tolyl chloroformate.

Step 9:

Modifications: 36 mg (0.16 mmol) 3-trifluoromethylphenyl chloroformate used,

57.3 mg product obtained as an off-white solid (48.6% yield): MS m/z 968

(MH+), m/z 966 (M-l).

Example 109: Preparation of Compound 109

Compound 109 Compound 109 was prepared by following Step 9 of Example 100 except that 2- (-)-( __)-menthyl chloroformate was used in place of p-tolyl chloroformate.

Step 9:

Modifications: 35 mg (0.19 mmol) (-)-(iRj-menthyl chloroformate used, 79.8 mg product obtained as an off-white solid (68.1% yield): MS m/z 962 (MH+), m/z 960 (M-l).

Example 110: Preparation of Compound 110

Compound 110

Scheme 1

Product from Example 100, Step 8 Compound 110 Step 1:

A mixture of the product from Example 100, Step 8 (123 mg, 0.122 mmol), tert- butyl acetic acid (18.3 mg, 0.158 mmol), HATU (60 mg, 0.16 mmol) and N- methylmorpholine (49 mg, 0.49 mmol) in 1,2-dichloroethane was stirred for 24 h at rt. The reaction mixture was washed with pH = 4 buffer solution (3 x 3 mL), and the washes were back-extracted with 1,2-dichloroethane (3 mL). The organic phases were combined and concentrated in vacuo. The crude product was then dissolved in MeOH and purified by reverse phase preparative HPLC to give the title compound (Compound 110) as a white solid (45.0 mg, 42.1% yield): 1H ΝMR (CD₃OD) δ 0.65 (s, 2 H), 0.84 (s, 9 H), 0.99 (s, 9 H), 1.04-1.06 (m, 1 H), 1.43-1.48 (m, 3 H), 1.91 (dd, J=7.32, 5.80 Hz, 1 H), 1.98 (s, 2 H), 2.27 (q, J=8.85 Hz, 1 H), 2.31-2.36 (m, 1 H), 2.65-2.69 (m, 1 H), 3.96 (s, 3 H), 4.13 (dd, J=11.60, 2.75 Hz, 1 H), 4.48 (d, J=11.90 Hz, 1 H), 4.55 (dd, 1=10.38, 7.02 Hz, 1 H), 4.64 (d, J=9.16 Hz, 1 H), 5.17 (d, J=10.38 Hz, 1 H), 5.34 (d, J=17.09 Hz, 1 H), 5.58 (s, 1 H), 5.78 (ddd, J=17.24, 9.61, 9.46 Hz, 1 H), 7.09-7.15 (m, 3 H), 7.22-7.30 (m, 4 H), 7.41 (d, J=1.22 Hz, 1 H), 7.48-7.55 (m, 3 H), 7.79 (d, J=8.55 Hz, 1 H), 8.05 (d, J=8.24 Hz, 3 H); MS m/z 878 (MH+), m/z 876 (M-l).

Example 111: Preparation of Compound 111

Compound 111

Compound 111 was prepared by following Step 1 of Example 110 except that methoxyacetic acid was used in place of tert-butyl acetic acid. Step 1:

Modifications: 14 mg (0.16 mmol) methoxyacetic acid used, 75.6 mg product obtained as an off-white solid (72.9 % yield): 1H NMR (CD₃OD) δ 0.62-0.67 (m,

2 H), 1.00 (s, 9 H), 1.02-1.06 (m, 1 H), 1.43-1.48 (m, 3 H), 1.91 (dd, J=7.93, 5.49

Hz, 1 H), 2.27 (q, J=8.85 Hz, 1 H), 2.35 (ddd, J=13.89, 10.38, 4.12 Hz, 1 H),

2.65-2.72 (m, 1 H), 3.36 (s, 3 H), 3.69 (d, J=15.26 Hz, 1 H), 3.84 (d, J=15.26 Hz,

1 H), 3.96 (s, 3 H), 4.13 (dd, J=11.90, 3.36 Hz, 1 H), 4.43 (d, J=11.90 Hz, 1 H),

4.58 (dd, 1=10.38, 7.02 Hz, 1 H), 4.65 (s, 1 H), 5.18 (dd, J=10.38, 1.22 Hz, 1 H),

5.34 (d, J=17.09 Hz, 1 H), 5.59 (s, 1 H), 5.78 (dt, J=17.09, 9.61 Hz, 1 H), 7.12-

7.15 (m, 3 H), 7.22-7.30 (m, 4 H), 7.41 (d, J=2.44 Hz, 1 H), 7.49-7.56 (m, 3 H),

8.02 (d, J=9.16 Hz, 1 H), 8.05 (d, J=7.32 Hz, 2 H); MS m/z 852 (MH+), m z 850

(M-l).

Example 112: Preparation of Compound 112

Compound 112

Compound 112 was prepared by following Step 1 of Example 110 except that methoxypropionic acid was used in place of tert-butyl acetic acid.

Step 1:

Modifications: 17 mg (0.16 mmol) methoxypropionic acid used, 66.6 mg product obtained as an off-white solid (63.2 % yield): 1H NMR (CD₃OD) δ 0.61-0.67 (m, 2 H), 1.00 (s, 9 H), 1.01-1.07 (m, 2 H), 1.42-1.48 (m, 3 H), 1.91 (dd, 7=8.09, 5.34 Hz, 1 H), 2.24-2.37 (m, 3 H), 2.43 (ddd, 7=14.95, 7.32, 5.49 Hz, 1 H), 2.65-2.69 (m, 1 H), 3.26 (s, 3 H), 3.46-3.55 (m, 2 H), 3.78 (s, 1 H), 3.96 (s, 3 H), 4.13 (dd, 7=11.90, 3.36 Hz, 1 H), 4.46 (d, 7=11.60 Hz, 1 H), 4.56 (dd, 7=10.07, 7.02 Hz, 1 H), 4.62-4.64 (m, 1 H), 5.17 (dd, 7=10.22, 1.68 Hz, 1 H), 5.33 (dd, 7=17.09, 1.22 Hz, 1 H), 5.58 (s, 1 H), 5.78 (ddd, 7=17.09, 10.22, 9.00 Hz, 1 H), 7.13-7.15 (m, 3 H), 7.22-7.30 (m, 4 H), 7.41 (d, 7=2.14 Hz, 1 H), 7.48-7.56 (m, 3 H), 8.05-8.07 (m, 3 H); MS m/z 866 (MH+), m/z 864 (M-l).

Example 113: Preparation of Compound 113

Compound 113

Compound 113 was prepared by following Step 1 of Example 110 except that S)-l,4-benzodioxane-2-carboxylic acid was used in place of tert-butyl acetic acid.

Step 1:

Modifications: 29 mg (0.16 mmol) (S)~l,4-benzodioxane-2-carboxylic acid used, 70.4 mg product obtained as a yellow glassy solid (61.4% yield): 1H NMR

(CD₃OD) δ 0.61-0.67 (m, 2 H), 0.77 (s, 9 H), 0.79-0.82 (m, 1 H), 1.45-1.51 (m, 3

H), 1.91 (dd, 7=8.09, 5.34 Hz, 1 H), 2.27 (q, 7=8.85 Hz, 1 H), 2.35 (ddd, 7=13.81,

10.45, 3.81 Hz, 1 H), 2.65-2.71 (m, 1 H), 3.93 (s, 3 H), 4.10 (dd, 7=12.21, 3.36

Hz, 1 H), 4.16 (dd, 7=11.60, 2.75 Hz, 1 H), 4.32 (dd, 7=11.44, 4.12 Hz, 1 H), 4.41 (d, 7=11.60 Hz, 1 H), 4.51-4.52 (m, 1 H), 4.58 (s, 1 H), 4.61 (dd, 7=10.38, 7.02 ^' Hz, 1 H), 5.18 (d, 7=11.60 Hz, 1 H), 5.34 (dd, 7=17.24, 1.07 Hz, 1 H), 5.59 (s, 1 H), 5.80 (ddd, 7=17.24, 9.77, 9.61 Hz, 1 H), 6.80-6.90 (m, 3 H), 7.03 (dd, 7=7.63, 2.14 Hz, 1 H), 7.13-7.15 (m, 3 H), 7.21-7.29 (m, 4 H), 7.40 (d, 7=2.44 Hz, 1 H), 7.49-7.56 (m, 3 H), 8.03 (d, 7=9.16 Hz, 1 H), 8.06 (d, 7=6.71 Hz, 2 H); MS m/z 942 (MH+), m/z 940 (M-l). Section D

Example 119: Preparation of Compound 119

Compound 119

Scheme 1.

Stepl.

To a solution of lR-tert-butoxycarbonylamino-2S-vinyl-cyclopropanecarboxylic acid (2.1 g, 9.24 mmol) in THF (26 mL) was added CDI (1.87 g, 11.6 mmol) and was heated to 78 °C for 45 min. After let cool to rt, the reaction mixture was treated with Example 16 (2.11 g, 12.01 mmol) and DBU (2.95 g, 19.4 mmol). After stirring at rt for 14 h, the reaction was diluted with EtOAc (50 mL) and washed with 4x50 mL IN HCl. The combined aqueous layer was extracted with 3x50 mL EtOAc. The combined organic layer was with brine, dried over MgSO4 and concentrated to a light brown solid product (3.48 g, 98%). The product was used as crude. 1H NMR (500 MHz, CD3OD, 500 MHz) δ 0.07 (q, 7=4.88 Hz, 2 H) 0.44-0.48 (m, 2 H) 0.68-0.72 (m, 1 H) 1.14 (s, 2 H) 1.28 (dd, 7=9.46, 5.19 Hz, 1 H) 1.43 (d, 7=7.02 Hz, 1 H) 1.46 (s', 9 H) 1.49-1.53 (m, 2 H) 1.81 (dd, 7=7.78, 5.34 Hz, 1 H) 1.86 (s, 2 H) 2.16-2.20 (m, 1 H) 5.08 (dd, 7=10.38, 1.22 Hz, 1 H) 5.27 (dd, 7=17.24, 1.37 Hz, 1 H) 5.51-5.55 (m, 1 H).

Step 2.

To a solution of the product from step 1 of Example 119 (3.75 g, 9.75 mmol) in DCM (15 mL) was added TFA (15 mL) and was stirring rt for 20 min. Solvent was concentrated under vacuum to give viscous brown oil in quantitative yield. The product was used as crude: MS m/z 285 (MH⁺).

Step 3:

To a solution mixture of 4R-(7-methoxy-2-phenyl-quinolin-4-yloxy)proline from step lc of Example 1 (0.167 g, 0.359 mmol), DIEA (0.140 g, 1.08 mmol) and the product from step 2 of Example 119 (0.143 g, 0.359 mmol) in DCM (4 mL) was added HATU (0.178 g, 0.467 mmol). After stirring at rt for 14 h, the reaction was washed with 5% aqueous NaHCO₃ (5 mL) and the aqueous layer was extracted with 2x25 mL DCM. The combined organic layer was washed with 5% aqueous citric acid (5 mL), dried over MgSO₄ and concentrated. The resulting brown viscous oil was purified by flash column chromatography to give light brown viscous oil (0.215 g, 82% yield): MS m z 731 (MH⁴).

Step 4: To a solution of the product from step 10 ofExample 119 (0.157 g, 0.215 mmol) in DCM (1.5 mL) was treated with TFA (1.5 mL) and stirred at rt for 10 mins. The reaction was concentrated and dried under vacuum to give a red viscous oil product, which was used without further purification. : MS m/z 731 (MH^1").

Step 5: To a solution mixture of the product from step 4 of Example 119 (1.03 g, 1.38 mmol) DIEA (0.716g, 5.53 mmol) and Boc-L-tert Leu-OH (0.667 g, 2.07 mmol) in DCM (14 mL) was added HATU (0.789g, 2.07 mmol). After stirring at rt for 3 h, the reaction was diluted with DCM (25 mL) washed with 5% aqueous NaHCO₃ (10 mL). Th aqueous layer was extracted with DCM (50 mL). The combined organic layer was washed with 5% aqueous citric acid (15 mL), dried over MgSO₄ and concentrated. The resulting brown viscous oil was purified by flash column chromatography (SiO2, 95:5 DCM:MeOH) to give Compound 8, Example 20 as a light brown solid (0.980 g, 84%) yield): MS m/z 844 (Mtf)

Step 6:

The product from step 5 of Example 119 (1.1 g, 1.30 mmol) in DCM (1.5 mL) was treated with a 50% solution of TFA (5 mL) in DCM and stirred at rt for 15 mins. The reaction was concentrated and dried under vacuum to give a brown viscous, which was redisolved in DCM (2 mL) and treated with IN HCl (5 mL) in Et₂O. Solvent was concentrated and the residue was treated with IN HCl one more time. The reaction was then concentrated and dried under vacuum to give a light brown foamy solid in quantitative yield : MS m/z 744 (MH⁺).

Scheme 3.

Compound 119

Product from step 6 of Example 119

Step 7:

To a solution mixture of the product from step 6 of Example 119 (0.062 g, 0.076 mmol) DIEA (0.040 g, 0.31 mmol) and S-(+)-α-methoxy phenylacetic acid

(0.019 g, 0.095 mmol) in DCM (2 mL) was added HATU (0.044 g, 0.114 mmol). After stirring at rt for 3 h, the reaction was diluted with DCM (5 mL) washed with 5% aqueous NaHCO₃ (3 mL). Th aqueous layer was extracted with DCM (5 mL). The combined organic layer was washed with 5% aqueous citric acid (3 mL), dried over MgSO₄ and concentrated. The resulting brown viscous oil was purified by flash column chromatography (SiO2, 95:5 DCM:MeOH) to give as a light brown solid (0.051 g, 75% yield): 1H NMR (500 MHz, CD₃OD) δ 0.08- 0.12 (m, 3 H) 0.46-0.50 (m, 2 H) 0.70-0.74 (m, 1 H) 0.94 (dd, 7=8.85, 4.27 Hz, 1 H) 0.96-0.98 (m, 2 H) 1.01 (s, 9 H) 1.04 (s, 2 H) 1.12-1.14 (m, 1 H) 1.15-1.17 (m, 1 H) 1.23-1.27 (m, 1 H) 1.44 (dd, 7=9.46, 5.49 Hz, 1 H) 1.49-1.53 (m, 1 H) 1.61 (m, 1 H) 1.81 (dd, 7=14.80, 7.17 Hz, 1 H) 1.85 (dd, 7=7.93, 2.44 Hz, 1 H) 1.89 (dd, 7=13.73, 6.71 Hz, 1 H) 1.93 (dd, 7=13.50, 6.77 Hz, 1 H) 2.23 (q, 7=8.95 Hz, 1 H) 2.33-2.37 (m, 1 H) 2.66-2.70 (m, 1 H) 3.25 (s, 3 H) 3.25-3.29 (m, 2 H) 3.33- 3.37 (m, 2 H) 3.98 (s, 3 H) 4.13 (dd, 7=12.05, 3.51 Hz, 1 H) 4.37 (s, 1 H) 4.57 (d, 7=10.68 Hz, 1 H) 4.59 (d, 7=9.77 Hz, 1 H) 5.12 (dd, 7=10.38, 1.53 Hz, 1 H) 5.29 (dd, 7=17.24, 1.37 Hz, 1 H) 5.61 (s, 1 H) 5.72-5.76 (m, 1 H) 7.30 (d, 7=9.77 Hz, 3 H) 7.32 (d, 7=1.83 Hz, 2 H) 7.45 (d, 7=2.44 Hz, 1 H) 7.84 (d, 7=9.46 Hz, 1 H) 8.03 (d, 7=9.16 Hz, 1 H) 8.06 (s, 1 H) 8.07 (d, 7=1.53 Hz, 1 H), MS m/z 892 (MH⁺). Example 120: Preparation of Compound 120

Scheme 1.

Step 1:

To a solution mixture of Boc-tert-Leu-OH (20.0 g, 86.5 mmol) and K₂CO₃ (13.15 g, 95.1 mmol) in DMF (100 mL) was added benzyl bromide (15.53 g, 90.8 mmol). After stirring at rt 72 h, the reaction was diluted with EtOAc (500 mL). The resulting white precipitation was filtered and washed with EtOAc. The liquid filtrated was washed with 1x400 ml and 3x150 mL H O, brine (100 mL), dried over MgSO₄ and concentrated to give a quantitative yield of a clear, colorless thick oil (28.03g): MS m/z 322 (MH^1").

Step 2:

To a solution of the product from step 3 of Example 120 (27.8g, 86.5 mmol) in

1,4-dioxane (100 mL) was added 4N HCl in 1,4-dioxane (215 mL) and stirred at rt for 1 h. The reaction was concentrated and dried under vacuum to give a slightly yellow waxy solid (25.62 g, 100% yield) : MS m/z 222 (MH*).

Step 3: To a solution of phosgene (20% in Toluene, 5.2 mL, 10.0 mmol) in DCM (30 mL) was added dropwise a solution mixture of the product from step 2 of Example 120 (0.516 g, 2.0 mmol) and DIEA (0.544 g, 4.2 mmol) in DCM (10 mL). After stirring at rt for 1 h, the reaction mixture was concentrated and dried under vacuum for lh. The excess phosgene was slowly quenched in the roto-vap trap that contained IN NaOH at -78 °C.

The resulting solid product from above was dissolved in DCM (20 mL) and was treated N-methyl-tert-butyl amine (0.349, 4.00 mmol) . After stirring at rt for 2 h, the reaction mixture was diluted with DCM (30 mL) and washed 3x25 mL with 5% aqueous citric acid, brine. The organic layer was then dried over MgSO₄ and concentrated and dried under vacuum to give a light yellow solid (0.600 g, 90%). 1H NMR (500 MHz, CHLOROFORM-D) δ 0.98 (d, 7=3.66 Hz, 6 H) 1.41 (s, 9 H) 1.53 (s, 1 H) 2.86 (s, 3 H) 4.26 (s, 1 H) 5.10 (d, 7=12.21 Hz, 1 H) 5.21 (d, 7=12.20 Hz, 1 H) 7.30-7.37 (m, 5 H)

Step 4:

To a solution of the product from step 3 of Example 120 (0.595 g, 1.78 mmol) in MeOH (5 mL) was added Pearlman catalyst (0.120 g) and stirred at rt under a H₂ (g) atmosphere for 3 h. The catalyst was removed by vacuum filtration and washed with MeOH. It was then concentrated to give a yellow solid (0.400g, 92% yield): MS m/z 245 (MH^").

Step 5:

To a solution mixture of the product from step 4 of Example 119 (0.106 g, 0.142 mmol), DIEA (0.074 g, 0.569 mmol) and the product from step 4 of Example 120 (0.045 g, 0.185 mmol) in DCM (2 mL) was added HATU (0.082 g, 0.213 mmol). After stirring at rt for 14 h, the reaction was diluted with DCM (15 mL) washed with 5% aqueous NaHCO₃ (3 mL), 5% aqueous citric acid (3 mL), brine, dried over MgSO₄ and concentrated. The resulting brown viscous oil was purified by flash column chromatography (SiO₂, 97:3 DCM:MeOH) to give a yellow solid (0.051 g, 75% yield): ¹HNMR(CD₃OD, 500 MHz) δ 0.05-0.09 (m, 3 H) 0.46-0.50 (m, 3 H) 0.66-0.70 (m, 1 H) 0.99 (s, 3 H) 1.04 (t, 7=4.73 Hz, 3 H) 1.07 (s, 9 H) 1.10-1.14 (m, 3 H) 1.18-1.24 (m, 2 H) 1.25 (s, 9 H) 1.28-1.32 (m, 1 H) 1.37 (s, 3 H) 1.42-1.46 (m, 3 H) 1.56-1.60 (m, 1 H) 1.78 (dd, 7=14.80, 7.48 Hz, 1 H) 1.83 (dd, 7=8.09, 5.34 Hz, 1 H) 1.89 (d, 7=7.02 Hz, 1 H) 1.92 (dd, 7=14.65, 6.41 Hz, 1 H) 2.19 (dd, 7=17.90, 9.30 Hz, 1 H) 2.32-2.36 (m, 1 H) 2.64 (dd, 7=13.74, 7.02 Hz, 1 H) 2.87 (s, 3 H) 2.93 (s, 1 H) 3.70 (s, 1 H) 4.14 (dd, 7=11.29, 3.00 Hz, 1 H) 4.42 (s, 1 H) 4.53 (dd, 7=10.83, 6.56 Hz, 1 H) 4.57 (d, 7=12.82 Hz, 1 H) 5.10 (d, 7=10.38 Hz, 1 H) 5.27 (d, 7=17.40 Hz, 1 H) 5.60 (s, 1 H) 5.73-5.77 (m, 1 H) 7.08 (dd, 7=9.16, 2.44 Hz, 1 H) 7.27 (s, 1 H) 7.41 (d, 7=2.44 Hz, 1 H) 7.50-7.54 (m, 3 H) 8.05 (s, 1 H) 8.07 (d, 7=1.53 Hz, 1 H) 8.09 (d, 7=9.16 Hz, I H); MS m/z 656 (MH-). Section E

Example 200, Preparation of Compound 200 ( 1 - { 4-(7-Methoxy-2-phenyl-quinolin-4-yloxy)-2- [ 1 -(1 -propyl- cyclopropane-sulfonylaminocarbonyl)-spiro[2.2]pent-l-ylcarbamoyl]- pyrrolidine- 1 -carbonyl }-2,2-dimethyl-propyl)-carbamic acid tert-butyl ester, shown below, was prepared as described in Steps 200a-e.

Step 200a. Preparation of spiro[2.2]pentane-l,l-dicarboxylic acid dimethyl ester, shown below.

To a cooled (0°C) mixture of methylenecyclopropane (3.89 g, 72 mmol)(prepared according to P. Binger US Patent Serial No. 5,723,714) and Rh₂(OAc) (3.18g, 7.2 mmol) in anhydrous CH₂C1₂ (40 mL), was added dimethyl diazomalonate (11.38 g, 72 mmol). At the top of the flask was installed a cold finger kept at - 78°C. The green reaction mixture was warmed to rt at which time bubbling due to N₂ evolution was evident. An exotherm caused mild reflux for 15 minutes. The reaction was stirred for another 4 h. The mixture was concentrated in vacuo and purified by flash chromatography (eluting with 10:1 hexane Et₂O to 5:1 hexane Et₂O) to give 10.5 g (79%) of the dimethyl ester as a yellow oil. ^H NMR (300 MHz, CDC1₃) δ 3.73 (s, 6 H), 1.92 (s, 2 H), 1.04 (d, 4 H, 7=3 Hz).

Step 200b: Spiro[2.2]pentane-l,l-dicarboxylic acid methyl ester, shown below, was prepared as follows.

To the mixture of spiro[2.2]pentane-l,l-dicarboxylic acid dimethyl ester 800 mg (4.3 mmol) in 8 mL of MeOH and 2 mL of water was added KOH (240 mg, 4.3 mmol). This solution was stirred at rt for 2 days. It was then acidified with dilute HCl to pH 3 and extracted two times with ether. The combined organic phases were dried (MgSO₄) and concentrated to yield 600 mg (82%) of spiro[2.2]pentane-l,l-dicarboxylic acid methyl ester as a white solid. ^H NMR (300 MHz, CDCI3) δ 3.82 (s, 6 H), 2.35 (d, 1 H, 7=3 Hz), 2.26 (d, 1 H, 7=3 Hz),

1.20 (m, 1 H), 1.15 (m, 1 H), 1.11 (m, 1 H), 1.05 (m, 1 H). LRMS: MS m/z 169 (M⁺-l).

Step 200c: l-Amino-spiro[2.2]pentane-l-carboxylic acid methyl ester hydrochloride salt, shown below, was prepared as follows.

To a mixture of spiro[2.2]pentane-l,l-dicarboxylic acid methyl ester (400 mg, 2.30 mmol) in 3 mL of anhydrous t-BuOH was added 700 mg (2.50 mmol) of DPPA and 278 mg (2.70 mmol) of Et₃N. The mixture was heated at reflux for 21 h and then partitioned between H₂O and ether. The ether phase was dried over magnesium sulfate, filtered and concentrated in vacuo to yield an oil. To this oil was added 3 mL of a 4 M HCl/dioxane solution. This acidic solution was stirred at rt for 2 h and then concentrated in vacuo. The residue was triturated with ether to give 82 mg (20 %) of l-amino-spiro[2.2]pentane-l-carboxylic acid methyl ester hydrochloride salt as a white solid. ^XH NMR (300 MHz, CDCI3) δ 9.19 (br s, 3 H), 3.81 (s, 3 H), 2.16, (d, 7=5.5 Hz, 1 H), 2.01 (d, 7=5.5 Hz, 1 H), 1.49 (m, 1 H), 1.24, (m, 1 H), 1.12 (m, 2 H). LRMS of free amine: MS m/z 142 (MM)

Step 200d: l-{ [l-(2-tert-Butoxycarbonylamino-3,3-dimethyl-butyryl)-4- (7-methoxy-2-phenyl-quinolin-4-yloxy)-pyrrolidine-2-carbonyl]-amino}- spiro[2.2]pentane-l-carboxylic acid, shown below, was prepared from the product of Step 203c using the general method illustrated in Scheme I and detailed in Example 2.

Step 200e: l-{[l-(2-tert-Butoxycarbonylamino-3,3-dimethyl-butyryl)-4-

(7-methoxy-2-phenyl-quinolin-4-yloxy)-pyrrolidine-2-carbonyl]-amino}- spiro[2.2]pentane-l-carboxylic acid (200 mg, 0.29 mmol) was slurried in 10 mL of THF. CDI (62 mg, 0.38 mmol) was added, and the mixture was refluxed for 1 h. The mixture was cooled to rt, 1-propyl-cyclopropanesulfonic acid amide (62 mg, 0.38 mmol) was added followed by DBU (58 mg, 0.38 mmol). The reaction mixture was stirred for 18 h, concentrated in vacuo, and purified by flash chromatography (hexane/ethyl acetate gradient) to give 50 mg (21%) of the titled compound, (l-{4-(7-methoxy-2-phenyl-quinolin- 4-yloxy)-2-[l-(l-propyl-cyclopropane-sulfonylaminocarbonyl)-spiro[2.2]pent-l- ylcarbamoyl]-pyrrolidine-l-carbonyl }-2,2-dimethyl-propyl)-carbamic acid tert- butyl ester, as a mixture of diastereoisomers (racemic at PI). LC-MS (retention time: 3.21, similar to the general LC/MS methods A-G: YMC Xterra MS C18 S7 3.0 x 50 mm, gradient time 4 min, flow rate 4 mL/min, hold time 1 min), MS m/z 832 (M⁺+1). Example 201 Preparation of Compound 201 { 1 -[2-[ 1 -( 1 -Benzyl -cyclopropanesulfonylaminocarbonyl)-spiro [2.2]pent- 1- ylcarbamoyl]-4-(7-methoxy-2-phenyl-quinolin-4-yloxy)-pyrrolidine-l-carbonyl]- 2,2-dimethyl-propyl} -carbamic acid tert-butyl ester, shown below, was prepared as described for Example 200

Compound 201

except that 1-benzyl-cyclopropanesulfonic acid amide (see example 7) was used.

This procedure provided 192 mg (75%) of the titled compound as an off-white glassy foam (mixture of diastereoisomers; racemic at PI).

LC-MS (retention time: 3.36, similar to the general LC/MS methods A-G: Xterra

ODS S7 3.0 x 50 mm, gradient time 4 min, flow rate 4 mL/min, hold time 1 min),

MS m/z 880 (MM).

Example 202. Preparation of Compound 202 { l-[2-[l-(l-Cyclopropylmethyl-cyclopropanesulfonylaminocarbonyl)- spiro[2.2]pent-l-ylcarbamoyl]-4-(7-methoxy-2-phenyl-quinolin-4-yloxy)- pynolidine-l-carbonyl]-2,2-dimethyl-propyl}-carbamic acid tert-butyl ester, shown below, was prepared as described for Example 200

Compound 202

except that 1-cyclopropylmethyl-cyclopropanesulfonic acid amide was used. This procedure (0.218 mmol scale) provided 50 mg (27%) of the titled compound as an off-white solid (mixture of diastereoisomers; racemic at PI). LC-MS, MS m/z 844 (MM).

Example 203, Preparation of Compound 203

Compound 203 The title compound was prepared as described in Steps 203a-c.

Step 203a: Synthesis of N-Boc-(lR,2S)-l-amino-2- cyclopropylcyclopropane carboxylic acid ethyl ester

A solution of N-Boc-(l_-,2S)-l-amino-2-vinylcyclopropane carboxylic acid (255 mg, 1.0 mmol) in ether (10 mL) was treated with palladium acetate (5 mg, 0.022 mmol). The orange/red solution was placed under an atmosphere of Ν₂. An excess of diazomethane in ether was added dropwise over the course of 1 h. The resulting solution was stirred at rt for 18 h. The excess diazomethane was removed using a stream of nitrogen. The resulting solution was concentrated by rotary evaporation to give the crude product. Flash chromatography (10% EtOAc/hexane) provided 210 mg (78%) of N-Boc-(lR,2S)-l-amino-2- cyclopropylcyclopropane carboxylic acid ethyl ester as a colorless oil. LC-MS (retention time: 2.13, similar to method A except: gradient time 3 min, Xterra MS C18 S7 3.0 x 50mm column), MS m/e 270 (MM).

Step 203b: The title compound was prepared from N-Boc-(lR,2S)-l- amino-2-cyclopropylcyclopropane carboxylic acid ethyl ester using methods illustrated in Scheme I and detailed in the examples above. MS (electrospray, ES+) m/z 847 (MM).

Step 203c: Alternatively, the title compound may be prepared by cyclopropanation of the vinyl cyclopropane moiety present in (1R,2S) PI isomer of l-{[l-2-tert-butoxycarbonylamino-3,3-dimethyl-butyryl)-4-(7-methoxy-2- phenylquinolin-4-yloxy)p-pyrrolidine-2-carbonyl] amino } -2-vinyl- cyclopropanecarboxylic acid ethyl ester followed by conversion to the desired acylsulfonamide derivative using methods described herein.

Example 204, Preparation of Compound 204

Compound 204

The title compound was prepared from N-Boc-(l_.,2S)-l-amino-2- cyclopropylcyclopropane carboxylic acid ethyl ester using methods illustrated in Scheme I and detailed in the examples above. MS (electrospray, ES-) m/z 892 (M-H)^".

Example 205, Preparation of Compound 205

Compound 205

The title compound was prepared from N-Boc-(lR,2S)-l-amino-2- cyclopropylcyclopropane carboxylic acid ethyl ester using methods illustrated in Scheme I and detailed in the examples above. MS (electrospray, ES+) m/z 858 (MM).

Example 206 Preparation of additional PI Intermediates for incorporation in compounds of Formula I.

The PI intermediates described in this section can be used to prepare compounds of Formula I by the methods described herein.

1. Resolution of N-Boc-(lR,2S)/(lS,2R)-l-amino-2-vinylcyclopropane carboxylic acid ethyl ester

Resolution A

To an aqueous solution of sodium phosphate buffer (0.1 M, 4.25 liter ("L"), pH 8) housed in a 12 Liter jacked reactor, maintained at 39°C, and stirred at 300 rpm was added 511 grams of Acalase 2.4L (about 425 mL) (Novozymes North America Inc.). When the temperature of the mixture reached 39°C, the pH was adjusted to 8.0 by the addition of a 50% NaOH in water. A solution of the racemic N-Boc-(lR,2S)/(lS,2_-)-l-amino-2-vinylcyclopropane carboxylic acid ethyl ester (85g) in 850 mL of DMSO was then added over a period of 40 min. The reaction temperature was then maintained at 40°C for 24.5h during which time the pH of the mixture was adjusted to 8.0 at the 1.5h and 19.5h time points using 50% ΝaOH in water. After 24.5h, the enantio-excess of the ester was determined to be 97.2%, and the reaction was cooled to room temperature (26°C) and stirred overnight (16h) after which the enantio-excess of the ester was determined to be 100%. The pH of the reaction mixture was then adjusted to 8.5 with 50% NaOH and the resulting mixture was extracted with MTBE (2 x 2 L). The combined MTBE extract was then washed with 5% NaHCO₃ (3 x 100 mL), water (3 x 100 mL), and evaporated in vacuo to give the enantiomerically pure N- Boc-(lR,2S)/-l-amino-2-vinylcyclopropane carboxylic acid ethyl ester as light yellow solid (42.55 g; purity: 97% @ 210 nm, containing no acid; 100% enantiomeric excess ("ee").

The aqueous layer from the extraction process was then acidified to pH 2 with 50% H₂SO₄ and extracted with MTBE (2 x 2 L). The MTBE extract was washed with water (3 x 100 mL) and evaporated to give the acid as light yellow solid (42.74 g; purity: 99% @ 210 nm, containing no ester).

1 R, 2S-ester 1 S,2R-acid

Resolution B

To 0.5 mL 100 mM Heps»Na buffer (pH 8.5) in a well of a 24 well plate (capacity: 10 ml/well), 0.1 mL of Savinase 16.0L (protease from Bacillus clausii) (Novozymes North America Inc.) and a solution of the racemic N-Boc- (l_-,2S)/(lS,2_?)-l-amino-2-vinylcyclopropane carboxylic acid ethyl ester (10 mg) in 0.1 mL of DMSO were added. The plate was sealed and incubated at 250 rpm at 40°C. After 18h, enantio-excess of the ester was determined to be 44.3% as following: 0.1 mL of the reaction mixture was removed and mixed well with 1 mL ethanol; after centrifugation, 10 microliter ("μl") of the supernatant was analyzed with the chiral HPLC. To the remaining reaction mixture, 0.1 mL of DMSO was added, and the plate was incubated for additional 3 days at 250 rpm at 40°C, after which four mL of ethanol was added to the well. After centrifugation, 10 μl of the supernatant was analyzed with the chiral HPLC and enantio-excess of the ester was determined to be 100%. Resolution C

To 0.5 ml 100 mM Heps»Na buffer (pH 8.5) in a well of a 24 well plate (capacity: 10 mL/well), 0.1 ml of Esperase 8.0L, (protease from Bacillus halodurans) (Novozymes North America Inc.) and a solution of the racemic N- Boc-(l_-,2S)/(lS,2_-)-l-amino-2-vinylcyclopropane carboxylic acid ethyl ester (10 mg) in 0.1 mL of DMSO were added. The plate was sealed and incubated at 250 rpm at 40°C. After 18 hour, enantio-excess of the ester was determined to be 39.6% as following: 0.1 mL of the reaction mixture was removed and mixed well with 1 mL ethanol; after cenrifugation, 10 μl of the supernatant was analyzed with the chiral HPLC. To the remaining reaction mixture, 0.1 mL of DMSO was added, and the plate was incubated for additional 3 days at 250 rpm at 40°C, after which four mL of ethanol was added to the well. After centrifugation, 10 μl of the supernatant was analyzed with the chiral HPLC and enantio-excess of the ester was determined to be 100%.

Samples analysis was carried out in the following manner:

1) Sample preparation: About 0.5 ml of the reaction mixture was mixed well with 10 volume of EtOH. After centrifugation, 10 μl of the supernatant was injected onto HPLC column.

2) Conversion determination:

Column: YMC ODS A, 4.6 x 50 mm, S-5 μm Solvent: A, 1 mM HCl in water; B, MeCΝ

Gradient: 30% B for 1 min; 30%) to 45% B over 0.5 min; 45% B for 1.5 min; 45% to 30% B over 0.5 min. Flow rate: 2 ml/min UV Detection: 210 nm Retention time: acid, 1.2 min; ester, 2.8 min.

3) Enantio-excess determination for the ester: Column: CHIRACEL OD-RH, 4.6 x 150 mm, S-5 μm Mobile phase: MeCN/50 mM HClO₄ in water (67/33) Flow rate: 0.75 ml/min. UV Detection: 210 nm. Retention time:

(IS, 2R) isomer as acid: 5.2 min; Rcaemate: 18.5 min and 20.0 min; (1R, 2S) isomer as ester: 18.5 min.

2. Preparation of 1-aminocyclobutanecarboxylic acid methyl ester-hydrochloride

1-aminocyclobutanecarboxylic acid (100 mg, 0.869 mmol)(Tocris) was dissolved in 10 mL of MeOH, HCl gas was bubbled in for 2h. The reaction mixture was stirred for 18 h, and then concentrated in vacuo to give 144 mg of a yellow oil. Trituration with 10 mL of ether provided 100 mg of the titled product as a white solid. 1H NMR (CDCI₃) δ 2.10-2.25 (m, IH), 2.28-2.42 (m, IH), 2.64-

2.82 (m, 4H), 3.87 (s, 3H), 9.21 (br s, 3H).

3. Preparation of racemic (1R,2R)/(1S,2S) l-Amino-2- ethylcyclopropanecarboxylic acid tert-butyl ester, shown below.

ethyl syn to carboxy

Step 1: Preparation of 2-Ethylcyclopropane-l,l-dicarboxylic acid di-tert-butyl ester, shown below.

To a suspension of benzyltriethylammonium chloride (21.0 g, 92.2 mmol) in a 50% aqueous NaOH solution (92.4 g in 185 mL H₂O) was added 1 ,2- dibromobutane (30.0 g, 138.9 mmol) and di-tert-butylmalonate (20.0 g, 92.5 mmol). The reaction mixture was vigorously stirred 18 h at rt, a mixture of ice and water was then added. The crude product was extracted with CH₂C1₂ (3x) and sequentially washed with water (3x), brine and the organic extracts combined. The organic layer was dried (MgSO₄), filtered and concentrated in vacuo. The resulting residue was flash chromatographed (100 g SiO₂, 3% Et₂O in hexane) to afford the titled product (18.3 g, 67.8 mmol, 73% yield) which was used directly in the next reaction.

Step 2: Preparation of racemic 2-Ethylcyclopropane-l,l-dicarboxylic acid tert- butyl ester, shown below.

The product of Step 1 (18.3 g, 67.8 mmol) was added to a suspension of potassium tert-butoxide (33.55 g, 299.0 mmol) in dry ether (500 mL) at 0 °C, followed by H₂0 (1.35 mL, 75.0 mmol) and was vigorously stirred overnight at rt. The reaction mixture was poured in a mixture of ice and water and washed with ether (3x). The aqueous layer was acidified with a 10% aq. citric acid solution at 0°C and extracted with EtOAc (3x). The combined organic layers were washed ' with water (2x), brine, dried (MgSO ) and concentrated in vacuo to afford the titled product as a pale yellow oil (10 g, 46.8 mmol, 69% yield). Step 3: Preparation of (IR,2R)1(1S,2S) 2-Ethyl-l-(2- trimethylsilanylethoxycarbonylamino)cyclopropane-carboxylic acid tert-butyl ester, shown below.

To a suspension, of the product of Step 2 (10 g, 46.8 mmol) and 3 g of freshly activated 4 A molecular sieves in dry benzene (160 mL), was added Et₃N (7.50 mL, 53.8 mmol) and DPPA (11 mL, 10.21 mmol). The reaction mixture was refluxed for 3.5 h, 2-trimethylsilyl-ethanol (13.5 mL, 94.2 mmol) was then added, 5 and the reaction mixture was refluxed overnite. The reaction mixture was filtered, diluted with Et₂O, washed with a 10% aqueous citric acid solution, water, saturated aqueous NaHCO₃, water (2x), brine (2X), dried (MgSO₄) and concentrated in vacuo. The residue was suspended with lOg of Aldrich polyisocyanate scavenger resin in 120 mL of CH₂C1₂, stirred at rt overnite and 10 filtered to afford the titled product (8 g, 24.3 mmol; 52%) as a pale yellow oil: 1H NMR (CDC1₃) δ 0.03 (s, 9H), 0.97 (m, 5H), 1.20 (bm, IH), 1.45 (s, 9H), 1.40- 1.70 (m, 4H), 4.16 (m, 2H), 5.30 (bs, IH). Step 4: Preparation of racemic (1R,2R)1(1S,2S) l-Amino-2- ethylcyclopropanecarboxylic acid tert-butyl ester, shown below.

•_j_5 ethyl syn to carboxy

To the product of Step 3 (3 g, 9 mmol) was added a 1.0 M TBAF solution in THF (9.3 mL, 9.3 mmol) and the mixture heated to reflux for 1.5 h, cooled to rt and then diluted with 500 ml of EtOAc. The solution was successively washed with water (2x100 mL), brine (2x100 mL), dried (MgSO₄), concentrated in vacuo to

20 provide the title intermediate

4. Preparation of l-Amino-spiro[2.3]hexane-l-carboxylic acid methyl ester hydrochloride salt

25 Step 1 Preparation of [2,3]hexane-l,l-dicarboxylic acid dimethyl ester, shown below.

To a mixture of methylene-cyclobutane (1.5 g, 22 mmol) and Rh₂(OAc)₄ (125 mg, 0.27 mmol) in anhydrous CH₂C1₂ (15 mL) was added 3.2 g (20 mmol) of dimethyl diazomalonate (prepared according to J. Lee et al. Synth. Comm., 1995, 25, 1511-1515) at 0°C over a period of 6 h. The reaction mixture was then warmed to rt and stirred for another 2 h. The mixture was concentrated and purified by flash chromatography (eluting with 10:1 hexane/Et₂O to 5:1 hexane/Et₂O) to give 3.2 g (72%) of [2,3]hexane- 1,1 -dicarboxylic acid dimethyl ester as a yellow oil. !H NMR (300 MHz, CDCI3) δ 3.78 (s, 6 H), 2.36 (m, 2 H), 2.09 (m, 3 H), 1.90 (m, 1 H), 1.67 (s, 2 H). LC-MS: MS m/z 199 (MM).

Step 2: Preparation of spiro[2,3]hexane-l,l-dicarboxylic acid methyl ester, shown below.

To the mixture of spiro [2,3]hexane-l,l-dicarboxylic acid dimethyl ester (200 mg, 1.0 mmol) in 2 mL of MeOH and 0.5 mL of water was added KOH (78 mg, 1.4 mmol). This solution was stirred at rt for 2 days. It was then acidified with dilute HCl and extracted two times with ether. The combined organic phases were dried (MgSO₄) and concentrated to yield 135 mg (73%) of 2 as a white solid. *H NMR (300 MHz, CDCI3) δ 3.78 (s, 3 H), 2.36-1.90 (m, 8 H). LC-MS:

MS m/z 185 (MM)

Step 3: Preparation of the titled product, l-amino-spiro[2.3]hexane-l-carboxylic acid methyl ester hydrochloride salt. To a mixture of spiro[2,3]hexane-l,l-dicarboxylic acid methyl ester (660 mg, 3.58 mmol) in 3 mL of anhydrous t-BuOH was added 1.08 g (3.92 mmol) of DPPA and 440 mg (4.35 mmol) of Et₃N. The mixture was heated at reflux for 21 h and then partitioned between H₂O and ether. The ether phase was dried over magnesium sulfate, filtered and concentrated in vacuo to yield an oil. To this oil was added 3 mL of a 4 M HCl/dioxane solution. This acidic solution was stirred at rt for 2 h and then concentrated in vacuo. The residue was triturated with ether to give 400 mg (58 %) of desried prodict as a white solid. !H NMR (300 MHz, d6-DMSO) δ 8.96 (br s, 3 H), 3.71 (s, 3 H), 2.41 (m, 1 H), 2.12 (m, 4 H), 1.93 (m, 1 H), 1.56 (q, 2 H, 7=8 Hz). LC-MS of free amine: MS m/z 156 (MM).

5. Preparation of l-Amino-spiro[2.4]heptane-l-carboxylic acid methyl ester hydrochloride salt, shown below, was prepared as follows.

Step 1: Spiro[2.4]heptane-l,l-dicarboxylic acid dimethyl ester, shown below, was prepared as follows.

Using the same procedure described in the preparation of 1-Amino- spiro[2.3]hexane-l-carboxylic acid methyl ester hydrochloride salt 1.14g (13.9 mmol) of methylenecyclopentane and 2.0 g (12.6 mmol) of dimethyl diazomalonate were reacted to yield 1.8 g (67%) of the dimethyl ester. H NMR (300 MHz, CDCI3) δ 3.73 (s, 6 H), 1.80 (m, 2 H), 1.70 (m, 4 H), 1.60 (m, 4 H). LC-MS: MS m/z 213 (MM).

Step 2: Preparation of Spiro[2.4]heptane-l,l-dicarboxylic acid methyl ester, shown below, was prepared as follows.

Using the same procedure described in the preparation of 1-Amino- spiro[2.3]hexane-l-carboxylic acid methyl ester hydrochloride salt

1.7 g (8.0 mmol) of the produc of Step 1 and 493 mg (8.8 mmol) of KOH gave

1.5 g (94%) of spiro[2.4]heptane-l,l-dicarboxylic acid methyl ester. 1H NMR (300 MHz, CDCI3) δ 3.80 (s, 3 H), 2.06 (d, 1 H, 7=5 Hz), 1.99 (d, 1 H, 7=5 Hz), 1.80-1.66 (m, 8 H). LC-MS: MS m/z 199 (MM).

Step 3: Preparation of l-Amino-spiro[2.4]heptane-l-carboxylic acid methyl ester hydrochloride salt, shown below, was prepared as follows.

Using the same procedure described above in preparation of 1-Amino- spiro[2.3]hexane-l-carboxylic acid methyl ester hydrochloride salt, 500 mg (2.5 mmol) of the product of Step 2, 705 mg (2.5 mmol) of DPPA and 255 mg (2.5 mmol) of Et₃N gave 180 mg (35%) of this hydrochloride salt. 1H NMR (300 MHz, d6-DMSO) δ 8.90 (br s, 3 H), 3.74 (s, 3 H), 1.84 (m, 1 H), 1.69 (m, 4 H), 1.58 (m, 4 H), 1.46 (d, 1 H, 7=6 Hz). LC-MS of free amine: MS m/z 170 (MM).

6. Preparation of 5-Amino-spiro[2.3]hexane-5-carboxylic acid ethyl ester, shown below, was prepared as follows.

Spiro[2.3]hexan-4-one (500 mg, 5 mmol), which was prepared from bicyclopropylidene (A. Meijere et al. Org. Syn. 2000, 78, 142-151) according to A. Meijere et al. J. Org. Chem. 1988, 53, 152-161, was combined with ammonium carbamate (1.17 g, 15 mmol) and_potassium cyanide (812 mg, 12.5 mmol) in 50 mL of EtOH and 50 mL of water. The mixture was heated at 55 °C for 2 days. Then NaOH (7 g, 175 mmol) was added and the solution was heated under reflux overnight. The mixture was then chilled to 0 °C, acidified to pH 1 with concentrated HCl, and concentrated in vacuo. EtOH was added to the crude amino acid mixture and then concentrated to dryness (5x) so as to remove residual water. The residue dissolved in 100 mL of EtOH was cooled to 0 °C. It was then treated with 1 mL of SOCl₂ and refluxed for 3 days. The solids were removed by_filtration, and the filtrate was concentrated in vacuo to give the crude product. The crude product was partitioned between 3 N NaOH, NaCI and EtOAc. The organic phase was dried over potassium carbonate and concentrated. The residue was purified using column chromatography on C18 silica gel (eluting with MeOH/H₂O) to yield 180 mg (21%) of 15 as an oil. !H NMR (300 MHz, CDCI3) δ 8.20 (br s, 2 H), 4.27 (s, 2 H), 2.80 (s, 1 H), 2.54 (s, 1 H), 2.34 (m, 2

H), 1.31 (s, 3 H), 1.02 (s, 1 H), 0.66 (m, 3 H). ¹ C NMR (300 MHz, CDCI3) δ 170.2(s), 63.0(s), 62.8 (s), 26.1 (s), 26.0 (s), 24.9 (s), 13.9 (s), 11.4 (s), 10.9 (s). LC-MS: MS m/z 170 (MM).

Example 207

Biological Studies Recombinant HCV NS3/4A protease complex FRET peptide assay

The purpose of this in vitro assay was to measure the inhibition of HCV NS3 protease complexes, derived from the BMS, H77C or J416S strains, as described below, by compounds of the present invention. This assay provides an indication of how effective compounds of the present invention would be in inhibiting HCV proteolytic activity.

Serum from an HCV-infected patient was obtained from Dr. T. Wright, San Francisco Hospital. An engineered full-length cDNA (compliment deoxyribonucleic acid) template of the HCV genome (BMS strain) was constructed from DNA fragments obtained by reverse transcription-PCR (RT- PCR) of serum RNA (ribonucleic acid) and using primers selected on the basis of homology between other genotype la strains. From the determination of the entire genome sequence, a genotype la was assigned to the HCV isolate according to the classification of Simmonds et al. (See P Simmonds, KA Rose, S Graham, SW Chan, F McOmish, BC Dow, EA Follett, PL Yap and H Marsden, J. Clin. Microbiol., 31(6), 1493-1503 (1993)). The amino acid sequence of the nonstructural region, NS2-5B, was shown to be >97% identical to HCV genotype la (H77C) and 87% identical to genotype lb (J4L6S). The infectious clones, H77C (la genotype) and J4L6S (lb genotype) were obtained from R. Purcell (NTH) and the sequences are published in Genbank (AAB67036, see Yanagi,M., Purcell,R.H., Emerson,S.U. and BukhJ. Proc. Natl. Acad. Sci. U.S.A. 94(16),8738-8743 (1997); AF054247, see Yanagi,M., St Claire,M., Shapiro,M., Emerson,S.U., Purcell,R.H. and BukhJ, Virology 244 (1), 161-172. (1998)). The BMS, H77C and J4L6S strains were used for production of recombinant NS3/4A protease complexes. DNA encoding the recombinant HCV NS3/4A protease complex (amino acids 1027 to 1711) for these strains were manipulated as described by P. Gallinari et al. (see Gallinari P, Paolini C, Brennan D, Nardi C, Steinkuhler C, De Francesco R. Biochemistry. 38(17):5620- 32, (1999)). Briefly, a three-lysine solubilizing tail was added at the 3'-end of the NS4A coding region. The cysteine in the PI position of the NS4A-NS4B cleavage site (amino acid 1711) was changed to a glycine to avoid the proteolytic cleavage of the lysine tag. Furthermore, a cysteine to serine mutation was introduced by PCR at amino acid position 1454 to prevent the autolytic cleavage in the NS3 helicase domain. The variant DNA fragment was cloned in the pET21b bacterial expression vector (Novagen)and the NS3/4A complex was expressed in Escherichia. coli strain BL21 (DE3) (Invitrogen) following the protocol described by P. Gallinari et al. (see Gallinari P, Brennan D, Nardi C, Brunetti M, Tomei L, Steinkuhler C, De Francesco R., J Virol. 72(8):6758-69 (1998)) with modifications. Briefly, NS3/4A expression was induced with 0.5mM Isopropyl β-D-1-thiogalactopyranoside (IPTG) for 22hr at 20°C. A typical fermentation (10L) yielded approximately 80g of wet cell paste. The cells were resuspended in lysis buffer (lOmL/g) consisting of 25mM N-(2- Hydroxyethyl)Piperazine-N'-(2-Ethane Sulfonic acid) (HEPES), pH7.5, 20% glycerol, 500mM Sodium Chloride (NaCI), 0.5% Triton-XlOO, lug/ml lysozyme, 5mM Magnesium Chloride (MgCl₂), lug/ml Dnasel, 5mM β-Mercaptoethanol

(βME), Protease inhibitor - Ethylenediamine Tetraacetic acid (EDTA) free (Roche), homogenized and incubated for 20 mins at 4°C. The homogenate was sonicated and clarified by ultra-centrifugation at 235000g for lhr at 4°C. Imidazole was added to the supernatant to a final concentration of 15mM and the pH adjusted to 8.0. The crude protein extract was loaded on a Nickel - Nitrilotriacetic acid (Ni-NTA) column pre-equilibrated with buffer B (25mM HEPES, pH8.0, 20%) glycerol, 500mM NaCI, 0.5% Triton-XlOO, 15mM imidazole, 5mM βME). The sample was loaded at a flow rate of lmL/min. The column was washed with 15 column volumes of buffer C (same as buffer B except with 0.2% Triton-XlOO). The protein was eluted with 5 column volumes of buffer D (same as buffer C except with 200mM Imidazole). NS3/4A protease complex-containing fractions were pooled and loaded on a desalting column Superdex-S200 pre-equilibrated with buffer D (25mM HEPES, pH7.5, 20%) glycerol, 300mM NaCI, 0.2%) Triton-XlOO, lOmM βME). Sample was loaded at a flow rate of lmL/min. NS3/4A protease complex- containing fractions were pooled and concentrated to approximately 0.5mg/ml. The purity of the NS3/4A protease complexes, derived from the BMS, H77C and J4L6S strains, were judged to be greater than 90% by SDS-PAGE and mass spectrometry analyses.

The enzyme was stored at -80°C, thawed on ice and diluted prior to use in assay buffer. The substrate used for the NS3/4A protease assay was RET SI (Resonance Energy Transfer Depsipeptide Substrate; AnaSpec, Inc. cat #

22991)(FRET peptide), described by Taliani et al. in Anal. Biochem. 240(2):60- 67 (1996). The sequence of this peptide is loosely based on the NS4A/NS4B natural cleavage site except there is an ester linkage rather than an amide bond at the cleavage site. The peptide substrate was incubated with one of the three recombinant NS3/4A complexes, in the absence or presence of a compound of the present invention, and the formation of fluorescent reaction product was followed in real time using a Cytofluor Series 4000.

The reagents were as follow: HEPES and Glycerol (Ultrapure) were obtained from GIBCO-BRL. Dimethyl Sulfoxide (DMSO) was obtained from Sigma. β-Mercaptoethanol was obtained from Bio Rad. ,

Assay buffer: 50mM HEPES, pH7.5; 0.15M NaCI; 0.1% Triton; 15% Glycerol; lOmM βME. Substrate: 2 μM final concentration (from a 2mM stock solution in DMSO stored at -20°C). HCV NS3/4A type la (lb), 2-3 nM final concentration (from a 5μM stock solution in 25mM HEPES, pH7.5, 20% glycerol, 300mM NaCI, 0.2% Triton-XlOO, lOmM βME). For compounds with potencies approaching the assay limit, the assay was made more sensitive by adding 50 μg/ml Bovine Serum Albumin (Sigma) to the assay buffer and reducing the end protease concentration to 300 pM.

The assay was performed in a 96-well polystyrene black plate from Falcon. Each well contained 25μl NS3/4A protease complex in assay buffer, 50μl of a compound of the present invention in 10% DMSO/assay buffer and 25μl substrate in assay buffer. A control (no compound) was also prepared on the same assay plate. The enzyme complex was mixed with compound or control solution for 1 min before initiating the enzymatic reaction by the addition of substrate. The assay plate was read immediately using the Cytofluor Series 4000 (Perspective Biosystems). The instrument was set to read an emission of 340nm and excitation of 490nm at 25°C. Reactions were generally followed for approximately 15 minutes.

The percent inhibition was calculated with the following equation:

100 - [(δF_inh/δF_con)xl00]

where δF is the change in fluorescence over the linear range of the curve. A nonlinear curve fit was applied to the inhibition-concentration data, and the 50% effective concentration (IC₅₀) was calculated by the use of Excel Xl-fit software using the equation, y=A+((B-A)/(l+((C/x)^ΛD))).

All of the compounds tested were found to have IC50s of 1.3 μM or less. Further, compounds of the present invention, which were tested against more than one type of NS3/4A complex, were found to have similar inhibitory properties though the compounds uniformly demonstrated greater potency against the lb strains as compared to the la strains. Specificity Assays

The specificity assays were performed to demonstrate the selectivity of the compounds of the present invention in inhibiting HCV NS3/4A protease as compared to other serine or cysteine proteases. The specificities of compounds of the present invention were determined against a variety of serine proteases: human sputum elastase (HS), porcine pancreatic elastase (PPE) and human pancreatic chymotrypsin and one cysteine protease: human liver cathepsin B. In all cases a 96-well plate format protocol using colorimetric p-nitroaniline (pNA) substrate specific for each enzyme was used as described previously (Patent WO 00/09543) with some modifications to the serine protease assays. All enzymes were purchased from Sigma while the substrates were from Bachem.

Each assay included a 2hr enzyme-inhibitor pre-incubation at room temperature followed by addition of substrate and hydrolysis to -30% conversion as measured on a Spectramax Pro microplate reader. Compound concentrations varied from 100 to 0.4 μM depending on their potency.

The final conditions for each assay were as follows:

50mM Tris(hydroxymethyl)aminomethane hydrochloride (Tris-HCl) pH8,

0.5M Sodium Sulfate (Na₂SO₄), 50mM NaCI, O.lmM EDTA, 3% DMSO, 0.01% Tween-20 with:

133 μM succ-AAA-pNA and 20nM HS or 8nM PPE; 100 μM succ-AAPF- pNA and 250pM Chymotrypsin.

lOOmM NaHPO₄ (Sodium Hydrogen Phosphate) pH 6, O.lmM EDTA, 3% DMSO, ImM TCEP (Tris(2-carboxyethyl)phosphine hydrochloride), 0.01%) Tween-20, 30μM Z-FR-pNA and 5nM Cathepsin B (enzyme stock activated in buffer containing 20mM TCEP before use).

The percentage of inhibition was calculated using the formula: [l-((UV_inh-UV_blank)/(UV_ctl-UV_bι_ank))] x 100

A non-linear curve fit was applied to the inhibition-concentration data, and the 50% effective concentration (IC₅₀) was calculated by the use of Excel XI- fit software.

HCV Replicon Cell-based Assay

An HCV replicon whole cell system was established as described by Lohmann V, Korner F, Koch J, Herian U, Theilmann L, Bartenschlager R., Science 285(5424): 110-3 (1999). This system enabled us to evaluate the effects of our HCV Protease compounds on HCV RNA replication. Briefly, using the HCV strain IB sequence described in the Lohmann paper (Assession number:AJ238799), an HCV cDNA was generated encoding the 5' internal ribosome entry site (IRES), the neomycin resistance gene, the EMCV (encephalomyocarditis viurs)-_RES and the HCV nonstructural proteins, NS3- NS5B, and 3' non-translated region (NTR). In vitro transcripts of the cDNA were transfected into the human hepatoma cell line, Huh7. Selection for cells constitutively expressing the HCV replicon was achieved in the presence of the selectable marker, neomycin (G418). Resulting cell lines were characterized for positive and negative strand RNA production and protein production over time. Huh7 cells, constitutively expressing the HCV replicon, were grown in Dulbecco's Modified Eagle Media (DMEM) containing 10% Fetal calf serum (FCS) and lmg/ml G418 (Gibco-BRL). Cells were seeded the night before (1.5 x 10⁴ cells/well) in 96-well tissue-culture sterile plates. Compound and no compound controls were prepared in DMEM containing 4% FCS, 1 : 100

Penicillin / Streptomysin, 1:100 L-glutamine and 5% DMSO in the dilution plate (0.5% DMSO final concentration in the assay). Compound / DMSO mixes were added to the cells and incubated for 4 days at 37°C. After 4 days, plates were rinsed thoroughly with Phosphate-Buffered Saline (PBS) (3 times 150μl). The cells were lysed with 25μl of a lysis assay reagent containing the FRET peptide

(RET SI, as described for the in vitro enzyme assay). The lysis assay reagent was made from 5X cell Luciferase cell culture lysis reagent(Promega #E153A) diluted to IX with distilled water, NaCI added to 150 mM final, the FRET peptide diluted to 10 μM final from a 2 mM stock in 100% DMSO. The plate was then placed into the Cytofluor 4000 instrument which had been set to 340nm excitation / 490 emission, automatic mode for 21 cycles and the plate read in a kinetic mode. EC₅₀ determinations were carried out as described for the IC₅₀ determinations.

As a secondary assay, EC₅₀ determinations from the replicon FRET assay were confirmed in a quantitative RNA assay. Cells were lyzed using the Rneasy kit (Qiagen). Purified total RNA was normalized using RiboGreen (Jones LJ, Yue ST, Cheung CY, Singer VL, Anal. Chem., 265(2):368-74 (1998)) and relative quantitation of HCV RNA expression assessed using the Taqman procedure (Kolykhalov AA, Mihalik K, Feinstone SM, Rice CM, Journal of Virology 74, 2046-2051 (2000)) and the Platinum Quantitative RT-PCR Thermoscript One-Step kit (Invitrogen cat # 11731-015). Briefly, RNA made to a volume of 5μl (< lng) was added to a 20μl Ready-Mix containing the following: 1.25X Thermoscript reaction mix (containing Magnesium Sulfate and 2-deoxynucleoside 5'-triphosphates (dNTPs)), 3mM dNTPs, 200nM forward primer (sequence: 5'-gggagagccatagtggtctgc-3'), 600nM reverse primer (5 - cccaaatctccaggcattga-3'), lOOnM probe (5'-6-FAM-cggaattgccaggacgaccgg-BHQ- 1-3'XFAM: Fluorescein-aminohexyl amidite; BHQ: Black Hole Quencher), lμM Rox reference dye (Invitrogen cat # 12223-012) and Thermoscript Plus Platinum Taq polymerase mixture. All primers were designed with ABI Prism 7700 software and obtained from Biosearch Technologies, Novato, CA. Samples containing known concentrations of HCV RNA transcript were run as standards.

Using the following cycling protocol (50°C, 30 min; 95°C, 5 min; 40 cycles of 95°C, 15 sec, 60°C, 1 min), HCV RNA expression was quantitated as described in the Perkin Elmer manual using the ABI Prism 7700 Sequence Detector.

The luciferase reporter assay was also used to confirm compound potency in the replicon. Utilization of a replicon luciferase reporter assay was first described by Krieger et al (Krieger N, Lohmann V, and Bartenschlager R, J. Virol. 75(10):4614-4624 (2001)). The replicon construct described for our FRET assay was modified by replacing the resistance gene neomycin with the Blasticidin-resistance gene fused to the N-terminus of the humanized form of Renilla luciferase (restriction sites Ascl / Pmel used for the subcloning). The adaptive mutation at position 1179 (serine to isoleucine) was also introduced (Blight KJ, Kolykhalov, AA, Rice, CM, Science 290(5498): 1972-1974). The luciferase reporter assay was set up by seeding huh7 cells the night before at a density of 2 x 10^ cells per T75 flask. Cells were washed the next day with 7.5ml Opti-MEM. Following the Invitrogen protocol, 40 μl DMRIE-C was vortexed with 5 ml Opti-MEM before adding 5 μg HCV reporter replicon RNA. The mix was added to the washed huh7 cells and left for 4 hours at 37°C. In the mean time, serial compound dilutions and no compound controls were prepared in DMEM containing 10% FCS and 5% DMSO in the dilution plate (0.5% DMSO final concentration in the assay). Compound / DMSO mixes were added to each well of a 24-well plate. After 4 hours, the transfection mix was aspirated, and cells washed with 5ml of Opti-MEM before trypsinization. Trypsinized cells were resuspended in 10% DMEM and seeded at 2 x 10⁴ cells/well in the 24-well plates containing compound or no compound controls. Plates were incubated for 4 days. After 4 days, media was removed and cells washed with PBS. lOOμl lx Renilla Luciferase Lysis Buffer (Promega) was immediately added to each well and the plates either frozen at -80°C for later analysis, or assayed after 15 mins of lysis. Lysate (40μl) from each well was transferred to a 96-well black plate (clear bottom) followed by 200 μl lx Renilla Luciferase assay substrate. Plates were read immediately on a Packard TopCount NXT using a luminescence program.

The percentage inhibition was calculated using the formula below:

% control = average luciferase signal in experimental wells (+ compound) average luciferase signal in DMSO control wells (- compound)

The values were graphed and analyzed using XLFit to obtain the EC₅o value. Biological Examples

Representative compounds of the invention were assessed in the HCV replicon cell assay and/or in several of the outlined specificity assays. For example, Compound 1 was found to have an IC₅₀ of 1.8 nM against the NS3/4A BMS strain in the enzyme assay. Similar potency values were obtained with the published H77C (IC₅₀ of 1.2 nM) and J4L6S (IC₅₀ of 1.1 nM) strains. The EC₅₀ value in the replicon assay was 13.9 nM.

In the specificity assays, the same compound was found to have the following activity: HS = 43 μM; PPE > 100 μM; Chymotrypsin > 100 μM; Cathepsin B > 100 μM. These results indicate this family of compounds are highly specific for. the NS3 protease and many of these members inhibit HCV replicon replication.

The compounds of the current invention were tested using the assays described above and found to have activities in the following ranges:

IC₅₀ Activity Ranges (NS3/4A BMS Strain): A is 5 - 50 micromolar (μM); B is

0.5 - 5 μM; C is 0.05 - 0.5 μM, D is < 0.05 μM ^'

EC₅₀ Activity Ranges: A is 5 - 50 micromolar (μM); B is 0.5 - 5 μM; C is 0.05 -

0.5 μM, D is < 0.05 μM

The structures of compounds used in the tests can be found from the Patent compound number shown in the Actvity Table below.

In accordance with the present invention, preferred compound have a biological activity (EC₅₀) of 5 μM or less, more preferably 0.5 μM or less and most preferably 0.05 μM or less.

Example 208 In accord with the present invention the following compounds can be made using the methods and intermediates described herein. It should be understood that this list of compounds in no way limits the invention as described.

254

Although the invention has been described with respect to specific aspects, those skilled in the art will recognize that other aspects, not specifically described herein, are intended to be included within the scope of the claims that follow.

Claims

1. A compound having the formula

wherein:

(m) R is trialkylsilane; halo; C_3-7 cycloalkyl, C _-7 cycloalkenyl; C_6-10 aryl; C_7-14 alkylaryl; C_6-10 aryloxy; C_7-1 alkylaryloxy; C_8-15 alkylarylester; Het; or C_1-8 alkyl optionally substituted with C_1-6 alkoxy, hydroxy, halo, C_2-10 alkenyl, C_2-10 alkynyl, C_3-7 cycloalkyl, C_4-7 cycloalkenyl, C_6-10 aryl, C_7-14 alkylaryl, C_6-10 aryloxy, C_7-14 alkylaryloxy, C_8-1s alkylarylester or Het; o — C-R₈ wherein R₈ is C_3-7 cycloalkyl, C_4-7 cycloalkenyl; C_6-1o aryl; C_7-14 alkylaryl; C_6-10 aryloxy; C_7-14 alkylaryloxy; C_8-15 alkylarylester; Het; or C_1-8 alkyl optionally substituted with C_1-6 alkoxy, hydroxy, halo, C_2-10 alkenyl, C_2-10 alkynyl, C _-7 cycloalkyl,

C_4-7 cycloalkenyl, C_6-10 aryl, C_7-14 alkylaryl, C_6-1o aryloxy, C _-1 alkylaryloxy, C_8-15 alkylarylester or Het; o — C-OR9 wherein R₉ is C_3-7 cycloalkyl, C_4-7 cycloalkenyl; C_6-10 aryl; C_7-14 alkylaryl; C_6-10 aryloxy; C_7-14 alkylaryloxy; C_8-15 alkylarylester; Het; or C_1-8 alkyl optionally substituted with C_1-6 alkoxy, hydroxy, halo, C_2-10 alkenyl, C _-1o alkynyl, C_3-7 cycloalkyl, C_4-7 cycloalkenyl, C_6-10 aryl, C_7-1 alkylaryl, C₆.₁₀ aryloxy, C _-14 alkylaryloxy, C_8-1s alkylarylester or Het; o — C-NR10R-11 , wherein R₁₀ and Rπ are each independently C_3-7 cycloalkyl, C _-7 cycloalkenyl; C_6-1o aryl; C _-1 alkylaryl; C_6-1o aryloxy; C_7-1 alkylaryloxy; C_8-15 alkylarylester; Het; or C_1-8 alkyl optionally substituted with C_1-6 alkoxy, hydroxy, halo, C_2-10 alkenyl, C_2-10 alkynyl, C_3-7 cycloalkyl, C _-7 cycloalkenyl, C_6-10 aryl,

C₇.₁₄ alkylaryl, C_6-10 aryloxy, C_7-14 alkylaryloxy, C_8-15 alkylarylester or Het; -SO₂R₁₂ wherein R₁₂ is C_3- cycloalkyl, C_4-7 cycloalkenyl; C_6-ιo aryl; C_7-14 alkylaryl; C_6-10 aryloxy; C_7-14 alkylaryloxy; C₈-ιs alkylarylester; Het; or C_1-8 alkyl optionally substituted with C_1-6 alkoxy, hydroxy, halo, C_2-1o alkenyl, C2-₁₀ alkynyl, C_3-7 cycloalkyl, C_4-7 cycloalkenyl, C_6-10 aryl, C_7-14 alkylaryl, C_6-1o aryloxy, C_7-1 alkylaryloxy, C_8-15 alkylarylester or Het; o or — OCR-13 wherein R₁ is C_3-7 cycloalkyl, C_4- cycloalkenyl; C_6-10 aryl; C_7-14 alkylaryl; C_6-10 aryloxy; C_7-14 alkylaryloxy; C_8-15 alkylarylester; Het; or C_1-8 alkyl optionally substituted with C_1-6 alkoxy, hydroxy, halo, C_2-1o alkenyl, C_2-1o alkynyl, C_3-7 cycloalkyl, C _-7 cycloalkenyl, C_6-10 aryl, C _-14 alkylaryl, C_6-10 aryloxy, C_7-14 alkylaryloxy, C_8-1s alkylarylester or Het; (n) R₂ is C_1-6 alkyl, C _-6 alkenyl or C_3-7 cycloalkyl, each optionally substituted from one to three times with halogen; or R₂ is H; or R₂ together with the carbon to which it is attached forms a 3, 4 or 5 membered ring;

(o) R₃ is C_1-8 alkyl optionally substituted with halo, cyano, amino, C_1-6 dialkylamino, C_6-10 aryl, C _-14 alkylaryl, C_1-6 alkoxy, carboxy, hydroxy, aryloxy, C_7-1 alkylaryloxy, C_2-6 alkylester, C_8-15 alkylarylester; C_3-1 alkenyl, C_3-7 cycloalkyl, or C _-10 alkylcycloalkyl, wherein the cycloalkyl or alkylcycloalkyl are optionally substituted with hydroxy, C_1-6 alkyl, C_2-6 alkenyl or C_1-6 alkoxy; or R₃ together with the carbon atom to which it is attached forms a C_3-7 cycloalkyl group optionally substituted with C_2-6 alkenyl;

(p) R₆ is H, C_1-6 alkyl, C_3-7 cycloalkyl, C_1-6 alkoxy, C_3- cycloalkoxy, halo-C*-₆ alkyl, CF₃, mono-or di- halo-C_1-6 alkoxy, cyano, halo, thioalkyl, hydroxy, alkanoyl, NO₂, SH, , amino, C_1-6 alkylamino, di (C--₆) alkylamino, di

alkylamide, carboxyl, (C*-₆) carboxyester, C_1-6 alkylsulfone, C_1-6 alkylsulfoxide, C_1-6 alkylsulfonamide or di (C*-₆) alkyl(alkoxy)amine; (q) R is H, C e alkyl, C_3-7 cycloalkyl, C_6-10 aryl, C_7-1 alkylaryl; C_6-1o aryloxy; C_7-14 alkylaryloxy; C_8-15 alkylarylester or Het;

(r) m is 1 or 2;

(s) n is 1 or 2;

(t) p is 1, 2 or 3; (u) Y is H, phenyl substituted with nitro, pyridyl substituted with nitro, or C_1- alkyl optionally substituted with cyano, OH or C_3-7 cycloalkyl; provided that if R or R₅ is H then Yis H;

(v) B is H, C_1-6 alkyl, R₄-(C=O)-, R₄θ(C=O)-, R₄-N(R₅)-C(=O)-, R₄-N(R₅)-C(=S)-, R₄SO₂-, or R₄-N(R₅)-SO₂-; (w) R₄ is (i) C_1-10 alkyl optionally substituted with phenyl, carboxyl,

C_1-6 alkanoyl, 1-3 halogen, hydroxy, -OC(O)C_1-6 alkyl, C_1-6 alkoxy, amino optionally substituted with C_1-6 alkyl, amido, or (lower alkyl) amido; (ii) C_3- cycloalkyl, C_3-7 cycloalkoxy, or C_4-10 alkylcycloalklyl, each optionally substituted with hydroxy, carboxyl, (C_1-6 alkoxy)carbonyl, amino optionally substituted with

C_1-6 alkyl, amido, or (lower alkyl) amido; (iii) C_6-10 aryl or C_7-ι₆ arylalkyl, each optionally substituted with C_1-6 alkyl, halogen, nitro, hydroxy, amido, (lower alkyl) amido, or amino optionally substituted with C_1-6 alkyl; (iv) Het; (v) bicyclo(l.l.l)pentane; or (vi) -C(O)OC_1-6 alkyl, C_2-6alkenyl or C_2-6 alkynyl; and.

(x) R₅ is H; C_1-6 alkyl optionally substituted with 1-3 halogens; or C_1-6 alkoxy provided R₄ is C_MO alkyl; or a pharmaceutically acceptable salt, solvate or prodrug thereof.

2. The compound of Claim 1 wherein R* is C_1-8 alkyl optionally substituted with C_1-6 alkoxy, hydroxy, halo, C_2-10 alkenyl, C_2-ιo alkynyl, C_3-6 cycloalkyl, C_4- cycloalkenyl, C_6-1o aryl, C_7-14 alkylaryl, C_6-10 aryloxy, C_7- ₁₄ alkylaryloxy, C_8-15 alkylarylester or Het.

3. The compound of Claim 2 wherein Ri is C_1-8 alkyl optionally substituted with C_1-6 alkoxy, hydroxy, halo, C_2-1o alkenyl, C_2-1o alkynyl, C_3-6 cycloalkyl, C_4-7 cycloalkenyl, C_6-10 aryl, C_7-14 alkylaryl, C_6-10 aryloxy, C_7- ₁₄ alkylaryloxy, or C_8-15 alkylarylester.

4. The compound of Claim 1 wherin R₂ is C_1-6 alkyl, C_2-6 alkenyl or C_3-7 cycloalkyl.

5. The compound of Claim 4 wherein R₂ is C_2-6 alkenyl.

6. The compound of Claim 5 wherein R₂ is vinyl.

7. The compound of Claim 1 wherein R₃ is C_1-8 alkyl optionally substituted with C₆aryl, C_1-6 alkoxy, carboxy, hydroxy, aryloxy, C_7-14 alkylaryloxy, C_2-6 alkylester, C_8-15 alkylarylester; C_3-12 alkenyl, C_3-7 cycloalkyl, or C_4-10 alkylcycloalkyl.

8. The compound of Claim 7 wherein R₃ is C_1-8 alkyl optionally substituted with C_1-6 alkoxy; or C _-7 cycloalkyl.

9. The compound of Claim 8 wherein R₃ is t-butyl.

10. The compound of Claim 1 wherein Y is H.

11. The compound of Claim 1 wherein B is H, C_1-6 alkyl, R -(C=O)-, R₄θ(C=O)-, R₄-N(R₅)-C(=O)-, R₄-N(R₅)-C(=S)-, R₄SO₂-, or R₄-N(R₅)-SO₂-.

12. The compound of Claim 11 wherein B is R₄-(C=O)-, R₄O(C=O)-, or R₄-N(R₅)-C(=O)-.

13. The compound of Claim 12 wherein B is R₄O(C=O)- and R is C_1-6 alkyl.

14. The compound of Claim 1 wherein R₄ is (i) C_1-10 alkyl optionally substituted with phenyl, carboxyl, C_1-6 alkanoyl, 1-3 halogen, hydroxy, C-_-6 alkoxy; (ii) C_3-7 cycloalkyl, C_3-7 cycloalkoxy, or C_4-10 alkylcycloalklyl; or (iii) C₆- ₁₀ aryl or C _-16 arylalkyl, each optionally substituted with C_1-6 alkyl or halogen.

15. The compound of Claim 14 wherein R₄ is (i) C_1-10 alkyl optionally substituted with 1-3 halogen or C_1-6 alkoxy; or (ii) C_3- cycloalkyl or Gno alkylcycloalkyl.

16. The compound of Claim 15 wherein R₄ is t-butyl.

17. The compound of Claim 1 wherein R₅ is H or C_1-6 alkyl optionally substituted with 1-3 halogens.

18. The compound of Claim 17 wherein R₅ is H.

19. The compound of Claim 1 wherein R₆ is C_1-6 alkyl, C_3-7 cycloalkyl, or C_1-6 alkoxy.

20. The compound of Claim 19 wherein R₆ is C_1-6 alkoxy.

21. The compound of Claim 20 wherein R₇ is C₆ aryl or a 5-7 membered monocyclic heterocycle.

22. A method of treating an HCV infection in a patient, comprising administering to the patient a therapeutically effective amount of the compound of claim 1 or a pharmaceutically acceptable salt, solvate or prodrug thereof.

23. A method of inhibiting HCV NS3 protease comprising administering to a patient in need thereof a therapeutically effective amount of the compound of claim 1 or a pharmaceutically acceptable salt, solvate or prodrug. thereof.

24. A composition comprising the compound of claim 1 or a pharmaceutically acceptable salt, solvate or prodrug thereof and a pharmaceutically acceptable carrier.

25. The composition of claim 24 further comprising an additional immunomodulatory agent.

26. The composition of claim 25 wherein the additional immunomodulatory agent is selected from the group consisting of -, β-, and δ- interferons.

27. The composition of claim 24 further comprising an antiviral agent.

28. The composition of claim 27 wherein the antiviral agent is selected from the group consisting of ribavirin and amantadine.

29. The composition of claim 24 further comprising an inhibitor of HCV protease other than the compound of claim 1.

30. The composition of claim 29 further comprising an inhibitor of a target in the HCV life cycle other than HCV NS3 protease.

31. The composition of claim 30 wherein the other target is selected from the group consisting of helicase, polymerase, metalloprotease and mixtures thereof.

32. Use of the composition of claim 24 for the manufacture of a medicament for treating a hepatitis C viral infection in a patient.