Patent Application
20080255060
The present invention relates to novel semi-synthetic macrolides having antimicrobial activity, in particular antibacterial activity. More particularly, the invention relates to 14- and 15-membered macrolides substituted at the 4″ position, to processes for their preparation, to compositions containing them and to their use in medicine.
Macrolide antibacterial agents are known to be useful in the treatment or prevention of bacterial infections. However, the emergence of macrolide-resistant bacterial strains has resulted in the need to develop new macrolide compounds. For example, EP 0 895 999 describes derivatives modified at the 4″ position of the macrolide ring having antibacterial activity.
According to the present invention, we have now found novel 14- and 15-membered macrolides substituted at the 4″ position which also have antimicrobial activity.
Thus, the present invention provides compounds of general formula (I)
wherein
A is a bivalent radical selected from —C(O)—, —C(O)NH—, —NHC(O)—, —N(R7)—CH2—, —CH2—N(R7)—, —CH(N8R9)— and —C(═NR10)—;
R1 is —OC(O)(CH2)dXR11;
R2 is hydrogen or a hydroxyl protecting group;
R3 is hydrogen, C1-4alkyl, or C3-6alkenyl optionally substituted by 9 to 10 membered fused bicyclic heteroaryl;
R4 is hydroxy, C2-6alkenyloxy optionally substituted by 9 to 10 membered fused bicyclic heteroaryl, or C1-6alkoxy optionally substituted by C1-6alkoxy or —O(CH2)eNR7R12,
R5 is hydroxy, or
R4 and R5 taken together with the intervening atoms form a cyclic group having the following structure:
wherein Y is a bivalent radical selected from —CH2—, —CH(CN)—, —O—, —N(R13)— and —CH(SR13)—;
R6 is hydrogen or fluorine;
R7 is hydrogen or C1-6alkyl;
R8 and R9 are each independently hydrogen, C1-6alkyl, —C(═NR10)NR14R15 or —C(O)R14, or
R8 and R9 together form ═CH(CR14R15)faryl, ═CH(CR14R15)fheterocyclyl, ═CR14R15 or ═C(R14)C(O)OR14, wherein the alkyl, aryl and heterocyclyl groups are optionally substituted by up to three groups independently selected from R16;
R10 is —OR17, C1-6alkyl, —(CH2)garyl, —(CH2)gheterocyclyl or —(CH2)hO(CH2)iOR7, wherein each R10 group is optionally substituted by up to three groups independently selected from R16;
R11 is a heterocyclic group having the following structure:
R12 is hydrogen or C1-6alkyl;
R13 is hydrogen or C1-4alkyl substituted by a group selected from optionally substituted phenyl, optionally substituted 5 or 6 membered heteroaryl and optionally substituted 9 to 10 membered fused bicyclic heteroaryl;
R14 and R15 are each independently hydrogen or C1-6alkyl;
R16 is halogen, cyano, nitro, trifluoromethyl, azido, —C(O)R21, —C(O)OR21, —OC(O)R21, —OC(O)OR21, —NR22C(O)R23, —C(O)NR22R23, —NR22R23, hydroxy, C1-6alkyl, —S(O)kC1-6alkyl, C1-6alkoxy, —(CH2)maryl or —(CH2)mheteroaryl, wherein the alkoxy group is optionally substituted by up to three groups independently selected from —NR14R15, halogen and —OR14, and the aryl and heteroaryl groups are optionally substituted by up to five groups independently selected from halogen, cyano, nitro, trifluoromethyl, azido, —C(O)R24, —C(O)OR24, —OC(O)OR24, —NR25C(O)R26, —C(O)NR25R26, —NR25R26, hydroxy, C1-6alkyl and C1-6alkoxy;
R17 is hydrogen, C1-6alkyl, C3-7cycloalkyl, C3-6alkenyl or a 5 or 6 membered heterocyclic group, wherein the alkyl, cycloalkyl, alkenyl and heterocyclic groups are optionally substituted by up to three substituents independently selected from optionally substituted 5 or 6 membered heterocyclic group, optionally substituted 5 or 6 membered heteroaryl, —OR27, —S(O)nR27, —NR27R28, —CONR27R28, halogen and cyano;
R18 is hydrogen, —C(O)OR29, —C(O)NHR29, —C(O)CH2NO2, or —C(O)CH2SO2R7;
R19 is hydrogen, C1-4alkyl optionally substituted by hydroxy, cyano, NH2, —NH(C1-4alkyl) or —N(C1-4alkyl)2; C2-4alkenyl optionally substituted by hydroxy, cyano, NH2, —NH(C1-4alkyl) or —N(C1-4alkyl)2; C1-4alkoxy, C3-7cycloalkyl, —NH2, —NH(C1-4alkyl) or —N(C1-4alkyl)2; (C1-4alkyl)OC(O)N(C1-4alkyl) or optionally substituted phenyl or benzyl;
R20 is halogen, C1-4alkyl, C1-4thioalkyl, C1-4alkoxy, —NH2, —NH(C1-4alkyl) or —N(C1-4alkyl)2;
R21 is hydrogen, C1-10alkyl, —(CH2)paryl or —(CH2)pheteroaryl;
R22 and R23 are each independently hydrogen, —OR14, C1-6alkyl, —(CH2)qaryl or —(CH2)qheterocyclyl;
R24 is hydrogen, C1-10alkyl, —(CH2)raryl or —(CH2)rheteroaryl;
R25 and R26 are each independently hydrogen, —OR14, C1-6alkyl, ‘3(CH2)saryl or —(CH2)sheterocyclyl;
R27 and R28 are each independently hydrogen, C1-4alkyl or C1-4alkoxyC1-4alkyl;
R29 is hydrogen or C1-6alkyl optionally substituted by up to three groups independently selected from halogen, C1-4alkoxy, —OC(O)C1-6alkyl and —OC(O)OC1-6alkyl, —(CH2)qheterocyclyl, —(CH2)qheteroaryl, —(CH2)qaryl, or —(CH2)qC3-7cycloalkyl;
R30 is hydrogen, C1-4alkyl, C3-7cycloalkyl, optionally substituted phenyl or benzyl, acetyl or benzoyl;
R31 is hydrogen or R20, or R31 and R19 are linked to form the bivalent radical —O(CH2)2—, —(CH2)t—; —NR7(CH2)a—, —OCH2NR7—, —SCH2NR7—, —CH2NR7CH2—, —CH2OCH2—, —CH2SCH2—, —(CH2)aNR7—;
R32 is hydrogen, or R32 and R19 are linked to form the bivalent radical selected from the group, —S(CH2)b—, and —N(R7)(CH2)b—, —O(CH2)b—;
R33 is C1-8alkyl, C2-6alkenyl or C2-6alkynyl;
X is —U(CH2)VB(CH2)VD-, —U(CH2)VB(CH2)VD(CH2)VE-, —U(CH2)VB—R33—, or
U(CH2)VB(CH2)vD-R33—;
or X is a group selected from:
U, B, D and E are independently divalent radicals selected from —N(R30)—, —O—, —S(O)Z—, —N(R30)C(O)—, —C(O)N(R30)— and —N[C(O)R30]—;
W is —C(R31)— or a nitrogen atom;
a is 1 or 2
b is an integer from 1 to 3;
d is an integer from 1 to 5;
e is an integer from 2 to 4;
f, g, h, m, p, q, r and s are each independently integers from 0 to 4;
i is an integer from 1 to 6;
j, k, n and z are each independently integers from 0 to 2;
t is 2 or 3;
v is an integer from 1 to 8 independently selected for each occurance;
and pharmaceutically acceptable derivatives thereof.
The term “pharmaceutically acceptable” as used herein means a compound which is suitable for pharmaceutical use. Salts and solvates of compounds of the invention which are suitable for use in medicine are those wherein the counterion or associated solvent is pharmaceutically acceptable. However, salts and solvates having non-pharmaceutically acceptable counterions or associated solvents are within the scope of the present invention, for example, for use as intermediates in the preparation of other compounds of the invention and their pharmaceutically acceptable salts and solvates.
The term “pharmaceutically acceptable derivative” as used herein means any pharmaceutically acceptable salt, solvate or prodrug, e.g. ester, of a compound of the invention, which upon administration to the recipient is capable of providing (directly or indirectly) a compound of the invention, or an active metabolite or residue thereof. Such derivatives are recognizable to those skilled in the art, without undue experimentation. Nevertheless, reference is made to the teaching of Burger's Medicinal Chemistry and Drug Discovery, 5th Edition, Vol 1: Principles and Practice, which is incorporated herein by reference to the extent of teaching such derivatives. Preferred pharmaceutically acceptable derivatives are salts, solvates, esters, carbamates and phosphate esters. Particularly preferred pharmaceutically acceptable derivatives are salts, solvates and esters. Most preferred pharmaceutically acceptable derivatives are salts and esters.
The compounds of the present invention may be in the form of and/or may be administered as a pharmaceutically acceptable salt. For a review on suitable salts see Berge et al., J. Pharm. Sci., 1977, 66, 1-19.
Typically, a pharmaceutical acceptable salt may be readily prepared by using a desired acid or base as appropriate. The salt may precipitate from solution and be collected by filtration or may be recovered by evaporation of the solvent. For example, an aqueous solution of an acid such as hydrochloric acid may be added to an aqueous suspension of a compound of formula (I) and the resulting mixture evaporated to dryness (lyophilised) to obtain the acid addition salt as a solid. Alternatively, a compound of formula (I) may be dissolved in a suitable solvent, for example an alcohol such as isopropanol, and the acid may be added in the same solvent or another suitable solvent. The resulting acid addition salt may then be precipitated directly, or by addition of a less polar solvent such as diisopropyl ether or hexane, and isolated by filtration.
Suitable addition salts are formed from inorganic or organic acids which form non-toxic salts and examples are hydrochloride, hydrobromide, hydroiodide, sulphate, bisulphate, nitrate, phosphate, hydrogen phosphate, acetate, trifluoroacetate, maleate, malate, fumarate, lactate, tartrate, citrate, formate, gluconate, succinate, pyruvate, oxalate, oxaloacetate, trifluoroacetate, saccharate, benzoate, alkyl or aryl sulphonates (eg methanesulphonate, ethanesulphonate, benzenesulphonate or p-toluenesulphonate) and isethionate. Representative examples include trifluoroacetate and formate salts, for example the bis or tris trifluoroacetate salts and the mono or diformate salts, in particular the tris or bis trifluoroacetate salt and the monoformate salt.
Pharmaceutically acceptable base salts include ammonium salts, alkali metal salts such as those of sodium and potassium, alkaline earth metal salts such as those of calcium and magnesium and salts with organic bases, including salts of primary, secondary and tertiary amines, such as isopropylamine, diethylamine, ethanolamine, trimethylamine, dicyclohexyl amine and N-methyl-D-glucamine.
Compounds of the invention may have both a basic and an acidic centre may therefore be in the form of zwitterions.
Those skilled in the art of organic chemistry will appreciate that many organic compounds can form complexes with solvents in which they are reacted or from which they are precipitated or crystallized. These complexes are known as “solvates”. For example, a complex with water is known as a “hydrate”. Solvates of the compound of the invention are within the scope of the invention. The salts of the compound of formula (I) may form solvates (e.g. hydrates) and the invention also includes all such solvates.
The term “prodrug” as used herein means a compound which is converted within the body, e.g. by hydrolysis in the blood, into its active form that has medical effects. Pharmaceutically acceptable prodrugs are described in T. Higuchi and V. Stella, “Prodrugs as Novel Delivery Systems”, Vol. 14 of the A.C.S. Symposium Series, Edward B. Roche, ed., “Bioreversible Carriers in Drug Design”, American Pharmaceutical Association and Pergamon Press, 1987, and in D. Fleisher, S. Ramon and H. Barbra “Improved oral drug delivery: solubility limitations overcome by the use of prodrugs”, Advanced Drug Delivery Reviews (1996) 19(2) 115-130, each of which are incorporated herein by reference.
Prodrugs are any covalently bonded carriers that release a compound of structure (I) in vivo when such prodrug is administered to a patient. Prodrugs are generally prepared by modifying functional groups in a way such that the modification is cleaved, either by routine manipulation or in vivo, yielding the parent compound. Prodrugs include, for example, compounds of this invention wherein hydroxy, amine or sulfhydryl groups are bonded to any group that, when administered to a patient, cleaves to form the hydroxy, amine or sulfhydryl groups. Thus, representative examples of prodrugs include (but are not limited to) acetate, formate and benzoate derivatives of alcohol, sulfhydryl and amine functional groups of the compounds of structure (I). Further, in the case of a carboxylic acid (—COOH), esters may be employed, such as methyl esters, ethyl esters, and the like. Esters may be active in their own right and/or be hydrolysable under in vivo conditions in the human body. Suitable pharmaceutically acceptable in vivo hydrolysable ester groups include those which break down readily in the human body to leave the parent acid or its salt.
References hereinafter to a compound according to the invention include both compounds of formula (I) and their pharmaceutically acceptable derivatives.
With regard to stereoisomers, the compounds of structure (I) have more than one asymmetric carbon atom. In the general formula (I) as drawn, the solid wedge shaped bond indicates that the bond is above the plane of the paper. The broken bond indicates that the bond is below the plane of the paper.
It will be appreciated that the substituents on the macrolide may also have one or more asymmetric carbon atoms. Thus, the compounds of structure (I) may occur as individual enantiomers or diastereomers. All such isomeric forms are included within the present invention, including mixtures thereof.
Where a compound of the invention contains an alkenyl group, cis (Z) and trans (E) isomerism may also occur. The present invention includes the individual stereoisomers of the compound of the invention and, where appropriate, the individual tautomeric forms thereof, together with mixtures thereof.
Separation of diastereoisomers or cis and trans isomers may be achieved by conventional techniques, e.g. by fractional crystallisation, chromatography or HPLC. A stereoisomeric mixture of the agent may also be prepared from a corresponding optically pure intermediate or by resolution, such as HPLC of the corresponding mixture using a suitable chiral support or by fractional crystallisation of the diastereoisomeric salts formed by reaction of the corresponding mixture with a suitable optically active acid or base, as appropriate.
The compounds of structure (I) may be in crystalline or amorphous form. Furthermore, some of the crystalline forms of the compounds of structure (I) may exist as polymorphs, which are included in the present invention.
Compounds wherein R2 represents a hydroxyl protecting group are in general intermediates for the preparation of other compounds of formula (I).
When the group OR2 is a protected hydroxyl group this is conveniently an ether or an acyloxy group. Examples of particularly suitable ether groups include those in which R2 is a trialkylsilyl (i.e. trimethylsilyl). When the group OR2 represents an acyloxy group, then examples of suitable groups R2 include acetyl or benzoyl.
R6 is hydrogen or fluorine. However, it will be appreciated that when A is —C(O)NH— or —CH2—N(R7)—, R6 is hydrogen.
When R11 is a heterocyclic group having the following structure:
said heterocyclic is linked in the 6 or 7 position to the X group as above defined. When present, the R20 group or groups may be attached at any position on the ring. In one embodiment, an R20 group is attached at the 6 or 7 position.
When R11 is a heterocyclic group having the following structure:
wherein W is —C(R31)— where R31 is R20 or R31 and R19 are linked to form the bivalent radical —O(CH2)2—, —(CH2)t—; —NR7(CH2)a—, —OCH2NR7—, —SCH2NR7—, —CH2NR7CH2—, —CH2OCH2—, —CH2SCH2—, —(CH2)aNR7—, said heterocyclic is linked in the (ii) or (iii) position to the X group as above defined.
When R11 is a heterocyclic group having the following structure:
said heterocyclic is linked in the 6 or 7 position to the X group as defined above.
When R11 is a heterocyclic group having the following structure:
said heterocyclic is linked in the 7 or 8 position to the X group as above defied.
When R11 is a heterocyclic group having the following structure:
wherein W is —C(R31)— where R31 is R20 or R31 and R19 are linked to form the bivalent radical —O(CH2)2—, —(CH2)t—; —NR7(CH2)a—, —OCH2NR7—, —SCH2NR7—, —CH2NR7CH2—, —CH2OCH2—, —CH2SCH2—, —(CH2)aNR7—, said heterocyclic is linked in the (i), (ii) or (iii) position to the X group as above defined. In one embodiment, the heterocyclic is linked to the (i) position. In another embodiment, the heterocyclic is linked in the (ii) or (iii) position.
When R11 is a heterocyclic group having the following structure:
said heterocyclic is linked in the 2 or 3 position to the X group as above defined. In one embodiment, the heterocyclic is linked in the 2 or 3 position. In another embodiment, the heterocyclic is linked in the 4 position.
The term “alkyl” as used herein as a group or a part of a group refers to a straight or branched hydrocarbon chain containing the specified number of carbon atoms. For example, C1-10alkyl means a straight or branched alkyl containing at least 1, and at most 10, carbon atoms. Examples of “alkyl” as used herein include, but are not limited to, methyl, ethyl, n-propyl, n-butyl, n-pentyl, isobutyl, isopropyl, t-butyl, hexyl, heptyl, octyl, nonyl and decyl. A C1-4alkyl group is preferred, for example methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl or t-butyl.
The term “C3-7cycloalkyl” group as used herein refers to a non-aromatic monocyclic hydrocarbon ring of 3 to 7 carbon atoms such as, for example, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl or cycloheptyl.
The term “alkoxy” as used herein refers to a straight or branched chain alkoxy group containing the specified number of carbon atoms. For example, C1-6alkoxy means a straight or branched alkoxy containing at least 1, and at most 6, carbon atoms. Examples of “alkoxy” as used herein include, but are not limited to, methoxy, ethoxy, propoxy, prop-2-oxy, butoxy, but-2-oxy, 2-methylprop-1-oxy, 2-methylprop-2-oxy, pentoxy and hexyloxy. A C1-4alkoxy group is preferred, for example methoxy, ethoxy, propoxy, prop-2-oxy, butoxy, but-2-oxy or 2-methylprop-2-oxy.
The term “alkenyl” as used herein as a group or a part of a group refers to a straight or branched hydrocarbon chain containing the specified number of carbon atoms and containing at least one double bond. For example, the term “C2-6alkenyl” means a straight or branched alkenyl containing at least 2, and at most 6, carbon atoms and containing at least one double bond. Examples of “alkenyl” as used herein include, but are not limited to, ethenyl, 2-propenyl, 3-butenyl, 2-butenyl, 2-pentenyl, 3-pentenyl, 3-methyl-2-butenyl, 3-methylbut-2-enyl, 3-hexenyl and 1,1-dimethylbut-2-enyl. It will be appreciated that in groups of the form —O—C2-6alkenyl, the double bond is preferably not adjacent to the oxygen.
The term “alkynyl” as used herein as a group or a part of a group refers to a straight or branched hydrocarbon chain containing the specified number of carbon atoms and containing at least one triple bond. For example, the term “C2-6alkynyl” means a straight or branched alkynyl containing at least 2, and at most 6, carbon atoms and containing at least one triple bond. Examples of “alkynyl” as used herein include, but are not limited to, ethynyl, 2-propynyl, 3-butynyl, 2-butynyl, 2-pentynyl, 3-pentynyl, 3-methyl-2-butynyl, 3-methylbut-2-ynyl, 3-hexynyl and 1,1-dimethylbut-2-ynyl. It will be appreciated that in groups of the form —O—C2-6alkynyl, the triple bond is preferably not adjacent to the oxygen.
The term “aryl” as used herein refers to an aromatic carbocyclic moiety such as phenyl, biphenyl or naphthyl.
The term “heteroaryl” as used herein, unless otherwise defined, refers to an aromatic heterocycle of 5 to 10 members, having at least one heteroatom selected from nitrogen, oxygen and sulfur, and containing at least 1 carbon atom, including both mono and bicyclic ring systems. Examples of heteroaryl rings include, but are not limited to, furanyl, thiophenyl, pyrrolyl, pyrazolyl, imidazolyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, triazolyl, oxadiazolyl, tetrazolyl, thiadiazolyl, pyridyl, pyridazinyl, pyrazinyl, pyrimidinyl, triazinyl, quinolinyl, isoquinolinyl, 1,2,3,4-tetrahydroisoquinolinyl, benzofuranyl, benzimidazolyl, benzothienyl, benzoxazolyl, 1,3-benzodioxazolyl, indolyl, benzothiazolyl, furylpyridine, oxazolopyridyl and benzothiophenyl.
The term “5 or 6 membered heteroaryl” as used herein as a group or a part of a group refers to a monocyclic 5 or 6 membered aromatic heterocycle containing at least one heteroatom independently selected from oxygen, nitrogen and sulfur. Examples include, but are not limited to, furanyl, thiophenyl, pyrrolyl, pyrazolyl, imidazolyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, triazolyl, oxadiazolyl, tetrazolyl, pyridyl, pyridazinyl, pyrazinyl, pyrimidinyl and triazinyl.
The term “9 to 10 membered fused bicyclic heteroaryl” as used herein as a group or a part of a group refers to quinolinyl, isoquinolinyl, 1,2,3,4-tetrahydroisoquinolinyl, benzofuranyl, benzimidazolyl, benzothienyl, benzoxazolyl, 1,3-benzodioxazolyl, indolyl, benzothiazolyl, furylpyridine, oxazolopyridyl or benzothiophenyl.
The term “heterocyclyl” as used herein, unless otherwise defined, refers to a monocyclic or bicyclic three- to ten-membered saturated or non-aromatic, unsaturated hydrocarbon ring containing at least one heteroatom selected from oxygen, nitrogen and sulfur. Preferably, the heterocyclyl ring has five or six ring atoms. Examples of heterocyclyl groups include, but are not limited to, pyrrolidinyl, tetrahydrofuranyl, tetrahydrothiophenyl, imidazolidinyl, pyrazolidinyl, piperidyl, piperazinyl, morpholino, tetrahydropyranyl and thiomorpholino.
The term “5 or 6 membered heterocyclic group” as used herein as a group or part of a group refers to a monocyclic 5 or 6 membered saturated hydrocarbon ring containing at least one heteroatom independently selected from oxygen, nitrogen and sulfur. Examples of such heterocyclyl groups include, but are not limited to, pyrrolidinyl, tetrahydrofuranyl, tetrahydrothiophenyl, imidazolidinyl, pyrazolidinyl, piperidyl, piperazinyl, morpholino, tetrahydropyranyl and thiomorpholino.
The term “halogen” refers to a fluorine, chlorine, bromine or iodine atom.
The terms “optionally substituted phenyl”, “optionally substituted phenyl or benzyl”, “optionally substituted 5 or 6 membered heteroaryl”, “optionally substituted 9 to 10 membered fused bicyclic heteroaryl” or “optionally substituted 5 or 6 membered heterocyclic group” as used herein refer to a group which is substituted by 1 to 3 groups selected from halogen, C1-4alkyl, C1-4alkoxy, hydroxy, nitro, cyano, amino, C1-4alkylamino or diC1-4alkylamino, phenyl and 5 or 6 membered heteroaryl.
In one embodiment, A is —C(O)—, —C(O)NH—, —NHC(O)—, —N(R7)—CH2—, —CH2—N(R7)— or —CH(NR8R9)—. In another embodiment, A is —C(O)—, —C(O)NH—, —NHC(O)—, —CH2—N(R7)—, —CH(NR8R9)— or —C(═NR10)—. In a further embodiment, A is —C(O)—, —C(O)NH—, —NHC(O)—, —CH2—NR7— or —CH(NR8R9)—. Representative examples of A include —C(O)— and —N(R7)—CH2—. In one preferred embodiment, A is —N(R7)—CH2—.
A representative example of R2 is hydrogen.
Representative examples of R3 include hydrogen and C1-4alkyl, in particular hydrogen and methyl.
In one embodiment, R4 is hydroxy or C1-6alkoxy, in particular hydroxy or methoxy. In a preferred embodiment, R4 is hydroxy. In another embodiment, R5 is hydroxy. Alternatively, R4 and R5 taken together with the intervening atoms form a cyclic group having the following structure:
wherein Y is a bivalent radical selected from —O— and —N(R13)—.
A representative example of R6 is hydrogen.
A representative example of R7 is C1-6alkyl, for example C1-4alkyl, in particular methyl.
Representative examples of R11 include heterocyclic groups having the following structures:
wherein the heterocyclic is linked in the 6 or 7 position to the X group as above defined, and heterocyclic groups having the following structure:
wherein W is —C(R31)— and R31 and R19 are linked to form the bivalent radical —(CH2)t—, and the heterocylic is linked in the (ii) or (iii) position to the X group as above defined. In one preferred embodiment, R11 is a heterocyclic group having the following structure:
A representative example of R13 is hydrogen.
In one embodiment, R18 is —C(O)OR29, —C(O)NHR29, —C(O)CH2NO2. or —C(O)CH2SO2R7.
A representative example of R18 is —C(O)OR29. In one preferred embodiment, R18 is —C(O)OR29 wherein R29 is hydrogen.
Representative examples of R19 include C1-4alkyl, in particular ethyl, and C3-7cycloalkyl, in particular cyclopropyl.
In one embodiment, R20 is halogen, in particular chlorine or fluorine, or methoxy.
In one embodiment, R30 is hydrogen or C1-4alkyl. A representative example of R30 is hydrogen or methyl.
A representative example of R31 is hydrogen, or R31 and R19 are linked to form the bivalent radical —(CH2)t—.
A representative example of X is —U(CH2)VB(CH2)vD-, —U(CH2)VB(CH2)vD(CH2)vE-, —U(CH2)VB—R33—, or U(CH2)vB(CH2)vD-R33—.
Representative examples of U, B, D and E include the divalent radicals —N(R30)—, —O—, —S(O)Z—, —N(R30)C(O)— and —C(O)N(R30)—.
A representative example of R33 is C1-8 alkyl or C2-6 alkynyl. In one preferred embodiment, R33 is propyl.
A representative example of d is 1 to 4, for example 2 to 4. A particularly preferred example of d is 2.
A representative example of v is 1 to 4, for example 2 or 3. A particularly preferred example is when each v independently is 2.
In one embodiment, X is —U(CH2)VB(CH2)vD- or —U(CH2)VB—R33— wherein U is —O—, B is —O—, and D is —N—. Particularly preferred X groups are O(CH2)2O(CH2)2N— and —O(CH2)2O—(CH2)3—
In one embodiment, j is 0 to 2. A representative example of j is 0 or 1.
A representative example of t is 3.
A representative example of z is 0.
Particularly preferred compounds of the invention are:
4″-O-(3-{4-[3-(3-Ethoxycarbonyl-1-ethyl-4-oxo-1,4-dihydro-quinolin-6-yl)-prop-2-ynyl]-piperazin-1-yl}-propionyl)-azithromycin,
4″-O-(3-{4-[3-(3-Ethoxycarbonyl-1-ethyl-4-oxo-1,4-dihydro-quinolin-6-yl)-propyl]-piperazin-1-yl}-propionyl)-azithromycin,
4−-O-(3-{4-[3-(3-Ethoxycarbonyl-1-ethyl-4-oxo-1,4-dihydro-quinolin-6-yl)-prop-2-ynyl]-piperazin-1-yl}-propionyl)-6-O-methyl-erythromycin A,
4″-O-(3-{4-[3-(3-Ethoxycarbonyl-1-ethyl-4-oxo-1,4-dihydro-quinolin-6-yl)-prop-2-ynyl]-piperazin-1-yl}-propionyl)-11-O-methyl-azithromycin,
4″-O-(3-{4-[3-(3-Ethoxycarbonyl-1-ethyl-4-oxo-1,4-dihydro-quinolin-6-yl)-propyl]-piperazin-1-yl}-propionyl)-11-O-methyl-azithromycin,
4″-O-(3-{2-[2-(3-Carboxy-7-chloro-1-cyclopropyl-4-oxo-1,4-dihydro-quinolin-6-ylamino)-ethoxy]-ethoxy}-propionyl)-roxythromycin,
4″-O-(3-{2-[2-(3-Carboxy-7-chloro-1-cyclopropyl-4-oxo-1,4-dihydro-quinolin-6-ylamino)-ethoxy]-ethoxy}-propionyl)-6-O-methyl-erythromycin A,
4″-O-(3-{2-[2-(3-Carboxy-7-chloro-1-cyclopropyl-4-oxo-1,4-dihydro-quinolin-6-ylamino)-ethoxy]-ethoxy}-propionyl)-azithromycin,
4″-O-(3-{2-[2-(3-carboxy-7-chloro-1-cyclopropyl-4-oxo-1,4-dihydro-quinolin-6-ylamino)-ethoxy]-ethoxy}-propionyl)-11-O-methyl-azithromycin,
4″-O-(3-{2-[2-(3-Carboxy-1-cyclopropyl-4-oxo-1,4-dihydro-quinolin-6-ylamino)-ethoxy]-ethoxy}-propionyl)-azithromycin,
4″-O-(2-{3-[2-(3-Carboxy-7-chloro-1-cyclopropyl-4-oxo-1,4-dihydro-quinolin-6-yloxy)-ethoxy]-propionylamino}-acetyl)-azithromycin 11,12-cyclic carbonate,
4″-O-(2-{3-[2-(3-Carboxy-7-chloro-1-cyclopropyl-4-oxo-1,4-dihydro-quinolin-6-ylamino)-ethoxy]-propionylamino}-acetyl)-azithromycin 11,12-cyclic carbonate,
4″-O-(2-{3-[2-(3-Carboxy-6-fluoro-1-cyclopropyl-8-methoxy-4-oxo-1,4-dihydro-quinolin-7-ylamino)-ethoxy]-propionylamino}-acetyl)-azithromycin 11,12-cyclic carbonate,
4″-O-[2-(3-{2-[2-(3-Carboxy-6-fluoro-1-cyclopropyl-4-oxo-1,4-dihydro-quinolin-7-ylamino)-ethoxy]-ethoxy}-propionylamino)-acetyl]-azithromycin 11,12-cyclic carbonate,
4″-O-[2-(3-{2-[2-(3-Carboxy-7-chloro-1-cyclopropyl-4-oxo-1,4-dihydro-quinolin-6-ylamino)-ethoxy]-ethoxy}-propionylamino)-acetyl]-azithromycin 11,12-cyclic carbonate,
4″-O-[2-(3-{2-[2-(3-Carboxy-7-chloro-1-cyclopropyl-4-oxo-1,4-dihydro-quinolin-6-ylamino)-ethoxy]-ethoxy}-propionylamino)-acetyl]-azithromycin,
4″-O-{2-[3-({2-[3-(6-Ethoxycarbonyl-7-oxo-2,3-dihydro-1H,7H-pyrido[3,2,1-ij]quinolin-9-yl)-prop-2-ynylamino]-ethyl}-propyl-amino)-propionylamino]-acetyl}-azithromycin,
4″O-{2-[3-({2-[3-(6-Ethoxycarbonyl-7-oxo-2,3-dihydro-1H,7H-pyrido[3,2,1-ij]quinolin-9-yl)-propylamino]-ethyl}-propyl-amino)-propionylamino]-acetyl}-azithromycin,
4″-O-(3-{2-[2-(3-Carboxy-7-chloro-1-cyclopropyl-4-oxo-1,4-dihydro-quinolin-6-ylamino)-ethoxy]-ethoxy}-propionyl)-9(E)-ethoxyimino-erythromycin A,
4″-O-[3-(2-{2-[2-(3-Carboxy-7-chloro-1-cyclopropyl-4-oxo-1,4-dihydro-quinolin-6-ylamino)-ethoxy]-ethoxy}-ethylamino)-propionyl]-6-O-methyl-erythromycin A,
4″-O-[3-(2-{2-[2-(3-Carboxy-6-fluoro-1-cyclopropyl-4-oxo-1,4-dihydro-quinolin-7-ylamino)-ethoxy]-ethoxy}-ethylamino)-propionyl]-6-O-methyl-erythromycin A,
4″-O-(3-{2-[2-(3-Carboxy-7-chloro-1-cyclopropyl-4-oxo-1,4-dihydro-quinolin-6-ylamino)-ethoxy]-ethylamino}-propionyl)-6-O-methyl-erythromycin A,
4″-O-(3-{2-[2-(3-Carboxy-6-fluoro-1-cyclopropyl-4-oxo-1,4-dihydro-quinolin-7-ylamino)-ethoxy]-ethylamino}-propionyl)-6-O-methyl-erythromycin A,
4″-O-(3-{2-[2-(10-Carboxy-9-oxo-3,4-dihydro-2H,9H-1-oxa-4a-aza-phenanthren-6-ylamino)-ethoxy]-ethoxy}-propionyl)-azithromycin,
11-O-Methyl-4″-O-(3-{2-[3-(3-Carboxy-1-ethyl-4-oxo-1,4-dihydro-quinolin-6-yl)-prop-2-ynyloxy]-ethylamino}-propionyl)-azithromycin,
11-O-Methyl-4″-O-(3-{2-[3-(3-Carboxy-1-ethyl-4-oxo-1,4-dihydro-quinolin-6-yl)-propoxy]-ethylamino}-propionyl)-azithromycin, and
4″-O-(3-{2-[2-(3-Carboxy-6-fluoro-1-cyclopropyl-4-oxo-1,4-dihydro-quinolin-7-ylamino)-ethoxy]-ethoxy}-propionyl)-azithromycin A, or pharmaceutically acceptable derivatives thereof.
Further particularly preferred compounds of the invention are:
4″-O-(3-{2-[2-(3-Carboxy-7-chloro-1-cyclopropyl-4-oxo-1,4-dihydro-quinolin-6-ylamino)-ethoxy]-ethoxy}-propionyl)-6-O-methyl-erythromycin A 11,12-cyclic carbamate,
4″-O-(3-{2-[2-(3-Carboxy-6-fluoro-1-cyclopropyl-4-oxo-1,4-dihydro-quinolin-7-ylamino)-ethoxy]-ethoxy}-propionyl)-6-O-methyl-erythromycin A,
4″-O-(3-{2-[2-(3-Carboxy-7-chloro-1-ethyl-4-oxo-1,4-dihydro-quinoline-6-ylamino)-ethoxy]-ethoxy}-propionyl)-azithromycin,
4″-O-(3-{2-[2-(3-Carboxy-6-fluoro-1-ethyl-4-oxo-1,4-dihydro-quinoline-7-ylamino)-ethoxy]-ethoxy}-propionyl)-azithromycin,
4″-O-(3-{2-[2-(3-Carboxy-1-ethyl-4-oxo-quinoline-6-ylamino)-ethoxy]-ethoxy}-propionyl)-azithromycin,
4″-O-(3-{2-[2-(3-carboxy-7-chloro-1-isopropyl-4-oxo-1,4-dihydro-quinoline-6ethoxy]-ethoxy}-propionyl)-azithromycin,
4″-O-(3-{2-[2-(6-Carboxy-7-oxo-2,3-dihydro-1H,7H-pyrido[3,2,1-ij]quinolin-9-ylamino)-ethoxy]-ethoxy}-propionyl)-azithromycin,
4″-O-(3-{2-[2-(6-Carboxy-7-oxo-2,3-dihydro-1H,7H-pyrido[3,2,1-ij]quinolin-ethoxy]-ethoxy}-propionyl)-6-O-methyl-erythromycin A,
4″-O-(3-{2-[2-(3-Carboxy-7-chloro-1-cyclopropyl-4-oxo-1,4-dihydro-quinolin-6-ylamino)-ethoxy]-ethoxy}-propionyl)-6-O-propyl-erythromycin A,
4″-O-(3-{2-[2-(3-Carboxy-1-cyclopropyl-4-oxo-1,4-dihydro-quinolin-7-yloxy)-ethoxy]-ethoxy}-propionyl)-azithromycin,
4″-O-(3-{2-[3-(3-carboxy-1-ethyl-4-oxo-1,4-dihydro-quinolin-6-yl)-prop-2-ynyloxy]-ethylamino}-propionyl)-6-O-methyl-erythromycin A,
4″-O-(3-{2-[3-(3-Carboxy-1-ethyl-4-oxo-1,4-dihydro-quinolin-6-yl)-propoxy-ethylamino}-propionyl)-6-O-methyl-erythromycin A,
4″-O-(3-{2-[2-(3-Carboxy-1-cyclopropyl-4-oxo-1,4-dihydro-quinolin-7-yloxy)-ethoxy]-ethoxy}-propionyl)-6-O-methyl-erythromycin A,
4″-O-(3-{2-[2-(3-Carboxy-1-cyclopropyl-4-oxo-1,4-dihydro-quinolin-7-yloxy)-ethoxy]-ethoxy}-propionyl)-9-ethyloximino-6-O-methyl-erythromycin A,
4″-O-[3-(2-{2-[2-(3-Carboxy-7-chloro-1-cyclopropyl-4-oxo-1,4-dihydro-quinolin-6-ylamino)-ethoxy]-ethoxy}-ethylamino)-propionyl]-9-(1-isopropoxy-cyclohexyl)oximino-erythromycin A,
4″-O-(3-{2-[2-(3-Carboxy-7-chloro-1-cyclopropyl-4-oxo-1,4-dihydro-quinolin-6-ylamino)-ethoxy]-ethoxy}-propionyl)-9-(1-isopropoxy-cyclohexyl)oximino-erythromycin A,
4″-O-(3-{2-[2-(3-Carboxy-1-cyclopropyl-4-oxo-1,4-dihydro-quinolin-7-yloxy)-ethoxy]-ethoxy}-propionyl)-9-(1-isopropoxy-cyclohexyl)oximino-erythromycin A,
4″-O-(3-{2-[2-(3-Carboxy-7-chloro-1-cyclopropyl-4-oxo-1,4-dihydro-quinolin-6-ylamino)-ethoxy]-ethoxy}-propionyl)-9-oxime erythromycin A,
4″-O-(3-{2-[2-(3-Carboxy-1-cyclopropyl-4-oxo-1,4-dihydro-quinolin-7-yloxy)-ethoxy]-ethoxy}-propionyl)-9-oxime erythromycin A,
4″-O-[3-(2-{2-[2-(3-Carboxy-7-chloro-1-cyclopropyl-4-oxo-1,4-dihydro-quinolin-6-ylamino)-ethoxy]-ethoxy}-ethylamino)-propionyl]-9-oxime erythromycin A,
4″-O-(3-{2-[2-(3-Carboxy-1-cyclopropyl-7-methoxy-4-oxo-1,4-dihydro-quinolin-6-ylamino)-ethoxy]-ethoxy}-propionyl)-azithromycin,
4″-O-(3-{2-[2-(3-Carboxy-1-cyclopropyl-7-dimethylamino-4-oxo-1,4-dihydro-quinolin-6-ylamino)-ethoxy]-ethoxy}-propionyl)azithromycin,
4″-O-(3-{2-[3-(3-carboxy-1-ethyl-4-oxo-1,4-dihydro-quinolin-6-yl)-propoxy]-ethoxy}-propionyl)-azithromycin,
4″-O-(3-{2-[3-(3-carboxy-1-ethyl-4-oxo-1,4-dihydro-quinolin-6-yl)-propoxy]-ethoxy}-propionyl)-6-O-methyl erythromycin A,
9-Ethyloximino-4″-O-(3-{2-[3-(3-carboxy-1-ethyl-4-oxo-1,4-dihydro-quinolin-6-yl)-propoxy]-ethoxy}-propionyl)-erythromycin A,
4″-O-(3-{2-[3-(3-Carboxy-1-ethyl-4-oxo-1,4-dihydro-quinolin -6-yl)-propoxy]-ethoxy}-propionyl)-6-O-methyl-8a-aza-8a-homoerythromycin A,
4″-O-(3-{2-[3-(3-Carboxy-1-ethyl-4-oxo-1,4-dihydro-quinolin-6-yl)-propoxy]-ethoxy}-propionyl)-roxythromycin,
4″-O-(3-{2-[2-(3-Carboxy-7-chloro-1-cyclopropyl-4-oxo-1,4-dihydro-quinolin-6-yloxy)-ethoxy]-ethoxy}-propionyl)-azithromycin,
4″-O-(3-{2-[3-(3-Carboxy-1-ethyl-4-oxo-1,4-dihydro-quinolin-6-yl)-propoxy]-ethoxy}-propionyl)-6-O-methyl-11-desoxy-11-(R)-methylamino-erythromycin A 11,12-carbamate,
4″-O-(3-{2-[3-(3-Carboxy-1-cyclopropyl-4-oxo-1,4-dihydro-quinolin-6-yl)-propoxy]-ethoxy}-propionyl)-azithromycin,
4″-O-(3-{2-[3-(3-Carboxy-4-oxo-1,4-dihydro-quinolin-6-yl)-propoxy]-ethoxy}-propionyl)-azithromycin,
4″-O-(3-{2-[3-(3-Carboxy-4-oxo-1-propyl-1,4-dihydro-quinolin-6-yl)-propoxy]-ethoxy}-propionyl)-azithromycin,
4″-O-[3-(2-{2-[2-(3-Carboxy-7-chloro-1-cyclopropyl-4-oxo-1,4-dihydro-quinolin-6-ylamino)-ethoxy]-ethoxy}-ethylamino)-propionyl]-azithromycin,
4″-O-[3-(2-{2-[2-(3-Carboxy-6-fluoro-1-cyclopropyl-4-oxo-1,4-dihydro-quinolin-7-ylamino)-ethoxy]-ethoxy}-ethylamino)-propionyl]-azithromycin,
4″-O-(3-{2-[2-(3-Carboxy-7-chloro-1-cyclopropyl-4-oxo-1,4-dihydro-quinolin-6-ylamino)-ethoxy]-ethylamino}-propionyl)-azithromycin,
4″-O-(3-{2-[2-(3-Carboxy-6-fluoro-1-cyclopropyl-4-oxo-1,4-dihydro-quinolin-7-ylamino)-ethoxy]-ethylamino}-propionyl)-azithromycin,
4″-O-[3-(2-{2-[3-(3-Carboxy-1-ethyl-4-oxo-1,4-dihydro-quinolin-6-yl)-prop-2-yloxy]-ethoxy}-ethylamino)-propionyl]-azithromycin,
4″-O-[3-(2-{2-[2-(3-Carboxy-7-chloro-1-cyclopropyl-4-oxo-1,4-dihydro-quinolin-6-ylamino)-ethoxy]-ethoxy}-ethylamino)-propionyl]-6-O-methyl erythromycin A,
4″-O-(3-{2-[2-(3-Carboxy-7-chloro-1-cyclopropyl-4-oxo-1,4-dihydro-quinolin-6-ylamino)-ethoxy]-ethoxy}-propionyl)-6-O-methyl-8a-aza-8a-homoerythromycin A,
4″-O-[3-(2-{2-[2-(3-Carboxy-7-chloro-1-cyclopropyl-4-oxo-1,4-dihydro-quinolin-6-ylamino)-ethoxy]-ethoxy}-ethylamino)-propionyl]-azithromycin,
4″-O-[3-(2-{[2-(3-Carboxy-7-chloro-1-cyclopropyl-4-oxo-1,4-dihydro-quinolin-6-ylamino)-ethyl]-methyl-amino}-ethoxy)-propionyl]-azithromycin,
4″-O-(3-{2-[2-(3-Carboxy-1-cyclopropyl-4-oxo-1,4-dihydro-quinolin-6-yloxy)-ethoxy]-ethoxy}-propionyl)-azithromycin,
4″-O-(3-{2-[2-(3-Carboxy-7-chloro-4-oxo-1,4-dihydro-quinolin-6-yloxy)-ethoxy]-ethoxy}-propionyl)-azithromycin,
4″-O-(3-{2-[2-(3-Carboxy-7-chloro-4-oxo-1,4-dihydro-quinolin-6-ylamino)-ethoxy]-ethoxy}-propionyl)-azithromycin,
4″-O-{[6-({2-[(2-Aminoethyl)(methyl)amino]ethyl}thio)-1-ethyl-4-oxo-1,4-dihydro-3-quinolinecarboxylic acid]propionyl}-6-O-methylerythromycin A,
4″-O-{[6-({2-[(2-Aminoethyl)(methyl)amino]ethyl}thio)-1-ethyl-4-oxo-1,4-dihydro-3-quinolinecarboxylic acid]propionyl}-azithromycin,
4″-O-{[6-({2-[(2-Aminoethyl)oxy]ethyl}oxy)-1-ethyl-4-oxo-1,4-dihydro-3-quinolinecarboxylic acid]propionyl}-6-O-methylerythromycin A,
4″-O-{[6-({2-[(2-Aminoethyl)oxy]ethyl}oxy)-1-ethyl-4-oxo-1,4-dihydro-3-quinolinecarboxylic acid]propionyl}-O-(9E)-methoxymethyloximino erythromycin A,
4″-O-{[6-({2-[(2-Aminoethyl)oxy]ethyl}oxy)-1-ethyl-4-oxo-1,4-dihydro-3-quinolinecarboxylic acid]propionyl}-O-(9E)-hydroximino erythromycin A,
4″-O-{[1-Ethyl-6-(3-{[2-Aminoethyl]oxy}propyl)-4-oxo-1,4-dihydro-3-quinolinecarboxylic acid]]propionyl}-O-(9E)-hydroximino erythromycin A,
4″-O-{[1-Ethyl-6-(3-{[2-(methylamino)ethyl]oxy}propyl)-4-oxo-1,4-dihydro-3-quinolinecarboxylic acid]]propionyl}-O-(9E)-hydroximino erythromycin A, and
4″-O-{[6-({2-[(2-aminoethyl)oxy]ethyl}oxy)-1-ethyl-4-oxo-1,4-dihydro-3-quinolinecarboxylic acid]propionyl}-6-O-methylerythromycin A,
or pharmaceutically acceptable derivatives thereof.
Compounds according to the invention also exhibit a broad spectrum of antimicrobial activity, in particular antibacterial activity, against a wide range of clinical pathogenic microorganisms. Using a standard microtiter broth serial dilution test, compounds of the invention have been found to exhibit useful levels of activity against a wide range of pathogenic microorganisims. In particular, the compounds of the invention may be active against strains of Staphylococcus aureus, Streptopococcus pneumoniae, Moraxella catarrhalis, Streptococcus pyogenes, Haemophilus influenzae, Enterococcus faecalis, Chlamydia pneumoniae, Mycoplasma pneumoniae and Legionella pneumophila. The compounds of the invention may also be active against resistant strains, for example erythromycin resistant strains. In particular, the compounds of the invention may be active against erythromycin resistant strains of Streptococcus pneumoniae, Streptococcus pyogenes and Staphylococcus aureus.
The compounds of the invention may therefore be used for treating a variety of diseases caused by pathogenic microorganisms, in particular bacteria, in human beings and animals. It will be appreciated that reference to treatment includes acute treatment or prophylaxis as well as the alleviation of established symptoms.
Thus, according to another aspect of the present invention we provide a compound of formula (I) or a pharmaceutically acceptable derivative thereof for use in therapy.
According to a further aspect of the invention we provide a compound of formula (I) or a pharmaceutically acceptable derivative thereof for use in the therapy or prophylaxis of systemic or topical microbial infections in a human or animal subject.
According to a further aspect of the invention we provide the use of a compound of formula (I) or a pharmaceutically acceptable derivative thereof in the manufacture of a medicament for use in the treatment or prophylaxis of systemic or topical microbial infections in a human or animal body.
According to a yet further aspect of the invention we provide a method of treatment of the human or non-human animal body to combat microbial infections comprising administration to a body in need of such treatment of an effective amount of a compound of formula (I) or a pharmaceutically acceptable derivative thereof.
While it is possible that, for use in therapy, a compound of the invention may be administered as the raw chemical it is preferable to present the active ingredient as a pharmaceutical formulation eg when the agent is in admixture with a suitable pharmaceutical excipient, diluent or carrier selected with regard to the intended route of administration and standard pharmaceutical practice.
Accordingly, in one aspect, the present invention provides a pharmaceutical composition or formulation comprising at least one compound of the invention or a pharmaceutically acceptable derivative thereof in association with a pharmaceutically acceptable excipient, diluent and/or carrier. The excipient, diluent and/or carrier must be “acceptable” in the sense of being compatible with the other ingredients of the formulation and not deleterious to the recipient thereof.
In another aspect, the invention provides a pharmaceutical composition comprising, as active ingredient, at least one compound of the invention or a pharmaceutically acceptable derivative thereof in association with a pharmaceutically acceptable excipient, diluent and/or carrier for use in therapy, and in particular, in the treatment of human or animal subjects suffering from a condition susceptible to amelioration by an antimicrobial compound. In another aspect, the invention provides a pharmaceutical composition comprising a therapeutically effective amount of the compounds of the present invention and a pharmaceutically acceptable excipient, diluent and/or carrier (including combinations thereof).
There is further provided by the present invention a process of preparing a pharmaceutical composition, which process comprises mixing at least one compound of the invention or a pharmaceutically acceptable derivative thereof, together with a pharmaceutically acceptable excipient, diluent and/or carrier.
The compounds of the invention may be formulated for administration in any convenient way for use in human or veterinary medicine and the invention therefore includes within its scope pharmaceutical compositions comprising a compound of the invention adapted for use in human or veterinary medicine. Such compositions may be presented for use in a conventional manner with the aid of one or more suitable excipients, diluents and/or carriers. Acceptable excipients, diluents and carriers for therapetic use are well known in the pharmaceutical art, and are described, for example, in Remington's Pharmaceutical Sciences, Mack Publishing Co. (A. R. Gennaro edit. 1985). The choice of pharmaceutical excipient, diluent and/or carrier can be selected with regard to the intended route of administration and standard pharmaceutical practice. The pharmaceutical compositions may comprise as—or in addition to—the excipient, diluent and/or carrier any suitable binder(s), lubricant(s), suspending agent(s), coating agent(s), solubilising agent(s).
Preservatives, stabilisers, dyes and even flavouring agents may be provided in the pharmaceutical composition. Examples of preservatives include sodium benzoate, sorbic acid and esters of p-hydroxybenzoic acid. Antioxidants and suspending agents may be also used.
For some embodiments, the agents of the present invention may also be used in combination with a cyclodextrin. Cyclodextrins are known to form inclusion and non-inclusion complexes with drug molecules. Formation of a drug-cyclodextrin complex may modify the solubility, dissolution rate, bioavailability and/or stability property of a drug molecule. Drug-cyclodextrin complexes are generally useful for most dosage forms and administration routes. As an alternative to direct complexation with the drug the cyclodextrin may be used as an auxiliary additive, e.g. as a carrier, diluent or solubiliser. Alpha-, beta- and gamma-cyclodextrins are most commonly used and suitable examples are described in WO 91/11172, WO 94/02518 and WO 98/55148.
The compounds of the invention may be milled using known milling procedures such as wet milling to obtain a particle size appropriate for tablet formation and for other formulation types. Finely divided (nanoparticulate) preparations of the compounds of the invention may be prepared by processes known in the art, for example see International Patent Application No. WO 02/00196 (SmithKline Beecham).
The routes for administration (delivery) include, but are not limited to, one or more of: oral (e.g. as a tablet, capsule, or as an ingestable solution), topical, mucosal (e.g. as a nasal spray or aerosol for inhalation), nasal, parenteral (e.g. by an injectable form), gastrointestinal, intraspinal, intraperitoneal, intramuscular, intravenous, intrauterine, intraocular, intradermal, intracranial, intratracheal, intravaginal, intracerebroventricular, intracerebral, subcutaneous, ophthalmic (including intravitreal or intracameral), transdermal, rectal, buccal, epidural and sublingual.
There may be different composition/formulation requirements depending on the different delivery systems. By way of example, the pharmaceutical composition of the present invention may be formulated to be delivered using a mini-pump or by a mucosal route, for example, as a nasal spray or aerosol for inhalation or ingestable solution, or parenterally in which the composition is formulated by an injectable form, for delivery, by, for example, an intravenous, intramuscular or subcutaneous route. Alternatively, the formulation may be designed to be delivered by both routes.
Where the agent is to be delivered mucosally through the gastrointestinal mucosa, it should be able to remain stable during transit though the gastrointestinal tract; for example, it should be resistant to proteolytic degradation, stable at acid pH and resistant to the detergent effects of bile.
Where appropriate, the pharmaceutical compositions can be administered by inhalation, in the form of a suppository or pessary, topically in the form of a lotion, solution, cream, ointment or dusting powder, by use of a skin patch, orally in the form of tablets containing excipients such as starch or lactose, or in capsules or ovules either alone or in admixture with excipients, or in the form of elixirs, solutions or suspensions containing flavouring or colouring agents, or they can be injected parenterally, for example intravenously, intramuscularly or subcutaneously. For parenteral administration, the compositions may be best used in the form of a sterile aqueous solution, which may contain other substances, for example enough salts or monosaccharides to make the solution isotonic with blood. For buccal or sublingual administration the compositions may be administered in the form of tablets or lozenges, which can be formulated in a conventional manner.
It is to be understood that not all of the compounds need be administered by the same route. Likewise, if the composition comprises more than one active component, then those components may be administered by different routes.
The compositions of the invention include those in a form especially formulated for parenteral, oral, buccal, rectal, topical, implant, ophthalmic, nasal or genito-urinary use. For some applications, the agents of the present invention are delivered systemically (such as orally, buccally, sublingually), more preferably orally. Hence, preferably the agent is in a form that is suitable for oral delivery.
If the compound of the present invention is administered parenterally, then examples of such administration include one or more of: intravenously, intraarterially, intraperitoneally, intrathecally, intraventricularly, intraurethrally, intrasternally, intracranially, intramuscularly or subcutaneously administering the agent; and/or by using infusion techniques.
For parenteral administration, the compound is best used in the form of a sterile aqueous solution which may contain other substances, for example, enough salts or glucose to make the solution isotonic with blood. The aqueous solutions should be suitably buffered (preferably to a pH of from 3 to 9), if necessary. The preparation of suitable parenteral formulations under sterile conditions is readily accomplished by standard pharmaceutical techniques well-known to those skilled in the art.
The compounds according to the invention may be formulated for use in human or veterinary medicine by injection (e.g. by intravenous bolus injection or infusion or via intramuscular, subcutaneous or intrathecal routes) and may be presented in unit dose form, in ampoules, or other unit-dose containers, or in multi-dose containers, if necessary with an added preservative. The compositions for injection may be in the form of suspensions, solutions, or emulsions, in oily or aqueous vehicles, and may contain formulatory agents such as suspending, stabilising, solubilising and/or dispersing agents. Alternatively the active ingredient may be in sterile powder form for reconstitution with a suitable vehicle, e.g. sterile, pyrogen-free water, before use.
The compounds of the invention can be administered (e.g. orally or topically) in the form of tablets, capsules, ovules, elixirs, solutions or suspensions, which may contain flavouring or colouring agents, for immediate-, delayed-, modified-, sustained-, pulsed-or controlled-release applications.
The compounds of the invention may also be presented for human or veterinary use in a form suitable for oral or buccal administration, for example in the form of solutions, gels, syrups, mouth washes or suspensions, or a dry powder for constitution with water or other suitable vehicle before use, optionally with flavouring and colouring agents. Solid compositions such as tablets, capsules, lozenges, pastilles, pills, boluses, powder, pastes, granules, bullets or premix preparations may also be used. Solid and liquid compositions for oral use may be prepared according to methods well known in the art. Such compositions may also contain one or more pharmaceutically acceptable carriers and excipients which may be in solid or liquid form.
The tablets may contain excipients such as microcrystalline cellulose, lactose, sodium citrate, calcium carbonate, dibasic calcium phosphate and glycine, disintegrants such as starch (preferably corn, potato or tapioca starch), sodium starch glycollate, croscarmellose sodium and certain complex silicates, and granulation binders such as polyvinylpyrrolidone, hydroxypropylmethylcellulose (HPMC), hydroxypropylcellulose (HPC), sucrose, gelatin and acacia.
Additionally, lubricating agents such as magnesium stearate, stearic acid, glyceryl behenate and talc may be included.
Solid compositions of a similar type may also be employed as fillers in gelatin capsules. Preferred excipients in this regard include lactose, starch, a cellulose, milk sugar or high molecular weight polyethylene glycols. For aqueous suspensions and/or elixirs, the agent may be combined with various sweetening or flavouring agents, colouring matter or dyes, with emulsifying and/or suspending agents and with diluents such as water, ethanol, propylene glycol and glycerin, and combinations thereof.
The compounds of the invention may also be administered orally in veterinary medicine in the form of a liquid drench such as a solution, suspension or dispersion of the active ingredient together with a pharmaceutically acceptable carrier or excipient.
The compounds of the invention may also, for example, be formulated as suppositories e.g. containing conventional suppository bases for use in human or veterinary medicine or as pessaries e.g. containing conventional pessary bases.
The compounds according to the invention may be formulated for topical administration, for use in human and veterinary medicine, in the form of ointments, creams, gels, hydrogels, lotions, solutions, shampoos, powders (including spray or dusting powders), pessaries, tampons, sprays, dips, aerosols, drops (e.g. eye ear or nose drops) or pour-ons.
For application topically to the skin, the agent of the present invention can be formulated as a suitable ointment containing the active compound suspended or dissolved in, for example, a mixture with one or more of the following: mineral oil, liquid petrolatum, white petrolatum, propylene glycol, polyoxyethylene polyoxypropylene compound, emulsifying wax and water.
Alternatively, it can be formulated as a suitable lotion or cream, suspended or dissolved in, for example, a mixture of one or more of the following: mineral oil, sorbitan monostearate, a polyethylene glycol, liquid paraffin, polysorbate 60, cetyl esters wax, cetearyl alcohol, 2-octyldodecanol, benzyl alcohol and water.
The compounds may also be dermally or transdermally administered, for example, by use of a skin patch.
For ophthalmic use, the compounds can be formulated as micronised suspensions in isotonic, pH adjusted, sterile saline, or, preferably, as solutions in isotonic, pH adjusted, sterile saline, optionally in combination with a preservative such as a benzylalkonium chloride. Alternatively, they may be formulated in an ointment such as petrolatum.
As indicated, the compound of the present invention can be administered intranasally or by inhalation and is conveniently delivered in the form of a dry powder inhaler or an aerosol spray presentation from a pressurised container, pump, spray or nebuliser with the use of a suitable propellant, e.g. dichlorodifluoromethane, trichlorofluoromethane, dichlorotetrafluoroethane, a hydrofluoroalkane such as 1,1,1,2-tetrafluoroethane (HFA 134AT″″) or 1,1,1,2,3,3,3-heptafluoropropane (HFA 227EA), carbon dioxide or other suitable gas. In the case of a pressurised aerosol, the dosage unit may be determined by providing a valve to deliver a metered amount. The pressurised container, pump, spray or nebuliser may contain a solution or suspension of the active compound, e.g. using a mixture of ethanol and the propellant as the solvent, which may additionally contain a lubricant, e.g. sorbitan trioleate.
Capsules and cartridges (made, for example, from gelatin) for use in an inhaler or insufflator may be formulated to contain a powder mix of the compound and a suitable powder base such as lactose or starch.
For topical administration by inhalation the compounds according to the invention may be delivered for use in human or veterinary medicine via a nebuliser.
The compounds of the invention may also be used in combination with other therapeutic agents. The invention thus provides, in a further aspect, a combination comprising a compound of the invention or a pharmaceutically acceptable derivative thereof together with a further therapeutic agent.
When a compound of the invention or a pharmaceutically acceptable derivative thereof is used in combination with a second therapeutic agent active against the same disease state the dose of each compound may differ from that when the compound is used alone. Appropriate doses will be readily appreciated by those skilled in the art. It will be appreciated that the amount of a compound of the invention required for use in treatment will vary with the nature of the condition being treated and the age and the condition of the patient and will be ultimately at the discretion of the attendant physician or veterinarian. The compounds of the present invention may for example be used for topical administration with other active ingredients such as corticosteroids or antifungals as appropriate.
The combinations referred to above may conveniently be presented for use in the form of a pharmaceutical formulation and thus pharmaceutical formulations comprising a combination as defined above together with a pharmaceutically acceptable carrier or excipient comprise a further aspect of the invention. The individual components of such combinations may be administered either sequentially or simultaneously in separate or combined pharmaceutical formulations by any convenient route.
When administration is sequential, either the compound of the invention or the second therapeutic agent may be administered first. When administration is simultaneous, the combination may be administered either in the same or different pharmaceutical composition.
When combined in the same formulation it will be appreciated that the two compounds must be stable and compatible with each other and the other components of the formulation. When formulated separately they may be provided in any convenient formulation, conveniently in such manner as are known for such compounds in the art.
The compositions may contain from 0.01-99% of the active material. For topical administration, for example, the composition will generally contain from 0.01-10%, more preferably 0.01-1% of the active material.
Typically, a physician will determine the actual dosage which will be most suitable for an individual subject. The specific dose level and frequency of dosage for any particular individual may be varied and will depend upon a variety of factors including the activity of the specific compound employed, the metabolic stability and length of action of that compound, the age, body weight, general health, sex, diet, mode and time of administration, rate of excretion, drug combination, the severity of the particular condition, and the individual undergoing therapy.
For oral and parenteral administration to humans, the daily dosage level of the agent may be in single or divided doses.
For systemic administration the daily dose as employed for adult human treatment it will range from 2-100 mg/kg body weight, preferably 5-60 mg/kg body weight, which may be administered in 1 to 4 daily doses, for example, depending on the route of administration and the condition of the patient. When the composition comprises dosage units, each unit will preferably contain 200 mg to 1 g of active ingredient. The duration of treatment will be dictated by the rate of response rather than by arbitrary numbers of days.
Compounds of general formula (I) and salts thereof may be prepared by the general methods outlined hereinafter, said methods constituting a further aspect of the invention. In the following description, the groups R1 to R33, A, B, D, E, X, Y, U, W a, b, d, e, f, g, h, i, j, k, m, n, p, q, r, s, t, v and z have the meaning defined for the compounds of formula (1) unless otherwise stated.
The group XaR11a is XR11 as defined for formula (I) or a group convertible to XR11. Conversion of a group XaR11a to a XR11 group typically arises if a protecting group is needed during the reactions described below. A comprehensive discussion of the ways in which such groups may be protected and methods for cleaving the resulting protected derivatives is given by for example T. W. Greene and P. G. M Wuts in Protective Groups in Organic Synthesis 2nd ed., John Wiley & Son, Inc 1991 and by P. J. Kocienski in Protecting Groups, Georg Thieme Verlag 1994 which are incorporated herein by reference. Examples of suitable amino protecting groups include acyl type protecting groups (e.g. formyl, trifluoroacetyl and acetyl), aromatic urethane type protecting groups (e.g. benzyloxycarbonyl (Cbz) and substituted Cbz, and 9-fluorenylmethoxycarbonyl (Fmoc)), aliphatic urethane protecting groups (e.g. t-butyloxycarbonyl (Boc), isopropyloxycarbonyl and cyclohexyloxycarbonyl) and alkyl type protecting groups (e.g. benzyl, trityl and chlorotrityl). Examples of suitable oxygen protecting groups may include for example alkyl silyl groups, such as trimethylsilyl or tert-butyldimethylsilyl; alkyl ethers such as tetrahydropyranyl or tert-butyl; or esters such as acetate. Hydroxy groups may be protected by reaction of for example acetic anhydride, benzoic anhydride or a trialkylsilyl chloride in an aprotic solvent. Examples of aprotic solvents are dichloromethane, N,N-dimethylformamide, dimethylsulfoxide, tetrahydrofuran and the like.
Compounds of formula (I) wherein d is an integer from 1 to 5, may be prepared by reaction of a 4″ hydroxy compound of formula (II) wherein R2 is a hydroxy protecting group with a suitable activated and protected derivative of the carboxylic acid (III), followed where necessary by subsequent removal of the hydroxyl protecting group R2 and conversion of the XaR11a group to XR11.
Suitable activated derivatives of the carboxyl group include the corresponding acyl halide, mixed anhydride or activated ester such as a thioester. The reaction is preferably carried out in a suitable aprotic solvent such as a halohydrocarbon (e.g. dichloromethane) or N,N-dimethylformamide optionally in the presence of a tertiary organic base such as dimethylaminopyridine or triethylamine or in the presence of inorganic base (eg sodium hydroxide) and at a temperature within the range of 0° to 120° C. The compounds of formula (II) and (III) may also be reacted in the presence of a carbodiimide such as dicyclohexylcarbodiimide (DCC).
In a further embodiment of the invention, compounds of formula (I) wherein d is an integer from 1 to 5 and U is —N(R30)—, may be prepared by reaction of compounds of formula (V),
wherein d is an integer from 1 to 5 and L is a suitable leaving group, with XaR11a (IV) in which U is —N(R30)—. The reaction is preferably carried out in a solvent such as a halohydrocarbon (e.g. dichloromethane), an ether (e.g. tetrahydrofuran or dimethoxyethane), acetonitrile or ethyl acetate and the like, dimethylsulfoxide, N,N-dimethylformamide or 1-methyl-pyrrolidone and in the presence of a base, followed, if desired, by removal of the hydroxyl protecting group R2 and conversion of the XaR11a group to XR11. Examples of the bases which may be used include organic bases such as diisopropylethylamine, triethylamine and 1,8-diazabicyclo[5.4.0]undec-7-ene, and inorganic bases such as potassium hydroxide, cesium hydroxide, tetraalkylammonium hydroxide, sodium hydride, potassium hydride and the like. Suitable leaving groups for this reaction include halides (e.g. chloride, bromide or iodide) and sulfonyloxy groups (e.g. tosyloxy or methanesulfonyloxy).
Compounds of formula (V) may be prepared by reaction of a compound of formula (II), wherein R2 is a hydroxyl protecting group, with a suitable activated derivative of the carboxylic acid HOC(O)(CH2)dL (VI), wherein L is a suitable leaving group as above defined. Suitable activated derivatives of the carboxyl group are those defined above for carboxylic acid (III). The reaction is carried out using the conditions described above for the reaction of a compound of formula (II) with carboxylic acid (III).
In a preferred embodiment of the invention, compounds of formula (I) wherein d is 2 and U is —N(R30)—, may be prepared by Michael reaction of a compound of formula (VII) wherein R2 is optionally a hydroxy protecting group
with a compound of formula XaR11a (IV). The reaction is suitably carried out in a solvent such as dimethylsulfoxide, N,N-dimethylformamide, 1-methyl-pyrrolidone, a halohydrocarbon (e.g. dichloromethane), an ether (e.g. tetrahydrofuran or dimethoxyethane), acetonitrile or alcohol (e.g methanol or isopropanol) and the like, and in the presence of a base, followed, if desired, by removal of hydroxyl protecting group R2 and conversion of the XaR11a group to XR11.
Compound of formula R11aL (VIII), wherein L is a suitable leaving group such as chlorine, fluorine or bromine, and R31 and R19 are linked to form the bivalent radical —O(CH2)2—, —(CH2)t—; —NR7(CH2)a—, —OCH2NR7—, —SCH2NR7—, —CH2NR7CH2—, —CH2OCH2—, —CH2SCH2— or —(CH2)aNR7— are known compounds or they may be prepared by analogous methods to those known in the art. Thus, they can be prepared according to the procedures described in US 2002/0025959 A1.
Compounds of formula (III) wherein X is —U(CH2)VB(CH2)vD-, —U(CH2)VB—R33—, or X is a group selected from:
may be prepared by reaction of XaR11a (V), wherein X has the meaning defined above with R34OC(O)CH═CH2 (VII) wherein R34 is carboxyl protecting group, followed by removal of R34. Suitable R34 carboxyl protecting group include t-butyl, allyl or benzyl.
Compounds of formula (III) may also be prepared by reaction of XaR11a (V) with acrylonitrile followed by hydrolysis of the nitrile to the acid.
Compounds of formula (IV) wherein X is —U(CH2)VB(CH2)vD- in which D is —N(R30)—, —O— or —S—, or wherein X is —U(CH2)VB(CH2)vD(CH2)vE- in which E is —N(R30)—, —O— or —S— or X is a group selected from:
may be prepared by reaction of a compound of formula R11aL (VIII), wherein L is a suitable leaving group such as chlorine, fluorine or bromine, with a compound of formula —U(CH2)VB(CH2)D- (IX) in which D is —N(R30)—, —O— or —S—, or with compound of formula —U(CH2)VB(CH2)vD(CH2)vE- (X) in which E is —N(R30)—, —O— or —S— or with piperazine or with imidazolidin or with 1H-octahydro-pyrrolo[3,4-b]pyridine.
Compound of formula R11aL (VIII), wherein L is a suitable leaving group such as chlorine, fluorine or bromine, and R32 and R19 are linked to form the bivalent radical selected from the group —S(CH2)b—, —N(R7)(CH2)b— or —O(CH2)b— are known compounds or they may be prepared by analogous methods to those known in the art. Thus, they can be prepared according to the procedures described in Arch. Pharm. Pharm. Med. Chem. 330, 63 (1997).
Compounds of formula (I) may be converted into other compounds of formula (I). Thus compounds of formula (I) wherein B is —S(O)z— and z is 1 or 2 may be prepared by oxidation of the corresponding compound of formula (I) wherein z is 0. The oxidation is preferably carried out using a peracid, e.g. peroxybenzoic acid, followed by treatment with a phosphine, such as triphenylphosphine. The reaction is suitably carried out in an organic solvent such as methylene chloride. Compounds of formula (I) wherein U or B is —N(R30)— and R30 is C1-4alkyl can be prepared from compounds wherein R30 is hydrogen by reductive alkylation.
Compounds of formula (II) wherein A is —C(O)NH— or —NHC(O)—, R4 or R5 are hydroxy, R3 is hydrogen and R6 is hydrogen are known compounds or they may be prepared by analogous methods to those known in the art. Thus they can be prepared according to the procedures described in EP 507595 and EP 503932.
Compounds of formula (II), wherein A is —C(O)NH— or —NHC(O)—, R4 or R5 are hydroxy and R3 is C1-4alkyl or C3-6alkenyl optionally substituted by 9 to 10 membered fused bicyclic heteroaryl and R6 is hydrogen are known compounds or they may be prepared by analogous methods to those known in the art. Thus they can be prepared according to the procedures described in WO 9951616 and WO 0063223.
Compounds of formula (II), wherein A is —C(O)NH—, R4 and R5 taken together with the intervening atoms form a cyclic group having the following structure:
R3 is C1-4alkyl, or C3-6alkenyl optionally substituted by 9 to 10 membered fused bicyclic heteroaryl and R6 is hydrogen are known compounds or they may be prepared by analogous methods to those known in the art. Thus they can be prepared according to the procedures described in U.S. Pat. No. 6,262,030.
Compounds of formula (II), wherein A is —C(O)—, —C(O)NH—, —NHC(O)—, —N(R7)—CH2—, —CH2—N(R7)—or —CH(NR8R9)—, R4 or R5 are hydroxy or R4 and R5 taken together with the intervening atoms form a cyclic group having the following structure:
wherein Y is a bivalent radical selected from —O— and —N(R13)—, and R3 is C1-4alkyl, or C3-6alkenyl optionally substituted by 9 to 10 membered fused bicyclic heteroaryl are known compounds or they may be prepared by analogous methods to those known in the art. Thus they can be prepared according to the procedures described in EP 307177, EP 248279, WO 0078773, WO 9742204.
Compounds of formula (II), wherein A is —C(O)NH—, —NHC(O)—, —N(CH3)—CH2— or —CH2—N(CH3)—, R4 or R5 are hydroxy or R4 and R5 taken together with the intervening atoms form a cyclic group having the following structure:
and R6 is hydrogen are known compounds or they may be prepared by analogous methods to those known in the art. Thus they can be prepared according to the procedures described in EP 508699 and J. Chem. Res. Synop (1988 pages 152-153), U.S. Pat. No. 6,262,030.
Compounds of formula (II), wherein A is —C(═NR10)—, R4 or R5 are hydroxy or R4 and R5 taken together with the intervening atoms form a cyclic group having the following structure:
and R6 is hydrogen, are known compounds or they may be prepared by analogous methods to those known in the art. Thus they can be prepared according to the procedures described in EP 284203.
Compounds of formula (II), wherein A is —C(O)—, R4 and R5 taken together with the intervening atoms form a cyclic group having the following structure:
R6 is hydrogen and R3 is C1-4 alkyl may be prepared by decarboxylation of a compound of formula (XI), wherein R35 is hydroxy protecting group followed, if required, by removal of the protecting group R2 or R35.
The decarboxylation may be carried out in the presence of a lithium salt such as lithium chloride, preferably in an organic solvent such as dimethylsulfoxide.
Compounds of formula (II), wherein A is —C(O)—, R4 and R5 taken together with the intervening atoms form a cyclic group having the following structure:
and R3 is C1-4 alkyl may be prepared according to the procedures described in WO 02/50091 and WO 02/50092.
The following abbreviations are used in the text: DBU for 1,8-diazabicyclo[5.4.0]undec-7-ene, DCM for dichloromethane, DMAP for 4-dimethylaminopyridine, DMF for N,N-dimethylformamide, DMSO for dimethyl sulfoxide, EDAC.HCl for 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride, EtOAc for ethyl acetate, KO-t-Bu for potassium tert-butoxide, MeOH for methanol, TEA for triethylamine and THF for tetrahydrofuran, MIBK for methyl iso-buthyl ketone.
All references contained in this application are herein incorporated by reference in their entireties.
In order that the invention may be more fully understood the following examples are given by way of illustration only.
2′-O-Acetyl-6-O methyl-erythromycin A may be prepared by the procedure described by W. R. Baker et al. in J. Org. Chem. 1988, 53, 2340, 2′-O-acetyl-azithromycin and 2′-O-acetyl-azithromycin-11,12-carbonate may be prepared by the procedures described by S. Djokic et al. in J. Chem. Res. (S) 1988, 152 and 11-O-methyl-azithromycin may be prepared by the procedure described by G. Kobrehel et al. in J. Antibiotics 1992, 45, 527-532. 9(E)-Ethoxyimino-erythromycin A may be prepared by the procedures described in EP 1 167 375. 6-O-Ethyl erythromycin A, 6-O-propyl erythromycin A and 9-(1-isopropoxy-cyclohexyl)oximino-erythromycin A may be prepared by procedure described in U.S. Pat. No. 4,990,602 and Bioorg. Med. Chem. Lett. 2000, 10, 815-819. 6-O-Methyl-8a-aza-8a-homoerythromycin A may be prepared by procedure described in U.S. Pat. No. 6,110,965. 8,9-Anhydro-9-deoxo-erythromycin A 6,9-cyclic ether may be prepared by procedure described in Experientia 1971, 27, 362. 2′-O-Acetyl-O-(9E)-acetylhydroximino erythromycin A may be prepared by procedure described in WO2004/039822. 4″-O-Propenoyl-azithromycin may be prepared by procedure described in WO03/042228. 7-[2-(2-Carboxy-ethoxy)-ethylamino]-6-fluoro-1-cyclopropyl-8-methoxy-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid my be prepared according to the procedure described in WO2004/101585. 1-Cyclopropyl-6-iodo-4-oxo-1,4-dihydro-qunoline-3-carboxylic acid ethyl ester, 7-chloro-1-isopropyl-6-fluoro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid and 7-chloro-1-tert-butyl-6-fluoro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid may be prepared by the procedure described in J. Med. Chem., 1995, 38, 973. 1-Ethyl-6-iodo-4-oxo-1,4-dihydro-qunoline-3-carboxylic acid ethyl ester my be prepared by procedure described in Aust. J. Chem., 1973, 26, 907. Ethyl 1-ethyl-6-hydroxy-4-oxo-1,4-dihydro-3-quinolinecarboxylate may be prepared by the procedure described in GB1433774.
Synthesis of Intermediate 1a was done by standard procedure starting from 2,4-dichloroacetophenone, diethylcarbonate (25 eq) and NaH (2 eq ) at 80° C. for 60 minutes. MS (ES+) m/z: [MH]+=262
To a mixture of Intermediate 1a (15.7 g) and Cs2CO3 (2.5 eq) in THF (230 mL) was added CS2 (4.6 eq) with stirring at −10° C. After 5 minutes CH3I (2.5 eq) was added in one portion and reaction was stirred at room temperature overnight. The reaction was diluted with ether (50 mL) and filtered. Filtrate was concentrated in vacuo.
MS (ES+) m/z: [MH]+=366
A mixture of Intermediate 1b (18.08 g), 3-amino-1-propanole (1.2 eq) and K2CO3 (2.4 eq) in dioxane (500 mL) was stirred at room temperature for 1 hour and refluxed overnight. The reaction mixture was filtrated and filtrate was concentrated to dryness under reduced pressure. The crude product was precipitated from MeOH affording the title compound (2.6 g).
MS (ES+) m/z: [MH]+=308
To a solution of Intermediate 1c (1.4 g) in THF (15 mL) solution of NaOH (4.6 eq) in water (15 mL) was added and the reaction mixture was stirred at 80° C. overnight. THF was evaporated, HCl (0.6 M) was added to reach pH value about 4 and extracted with 3×10 mL of DCM. The organic layers were washed with brine, dried over Na2SO4, filtered and DCM was evaporated under reduced pressure affording the title compound (1:16 g).
MS (ES+) m/z: [MH]+=280
Intermediate 1d (1 g) was diluted in 5 mL of methyl-pyrrolidone, 1.8 mL (5 eq) of 2-(2-aminoetoxy)ethanol was added and stirred at 110° C. for 24 hours. To the reaction mixture was added EtOAc, pH adjusted to 6 and extracted with 3×15 mL of H20 The organic layers were washed with brine, dried over Na2SO4, filtered and EtOAc was evaporated under reduced pressure affording the title compound (600 mg).
MS (ES+) m/z: [MH]+=349
Intermediate 1e (600 mg) was diluted in 7.4 mL of C3H3N, 0.515 mL of DBU was added and the mixture stirred at 80° C. for 24 hours. C3H3N was evaporated under reduced pressure, residue dissolved in EtOAc, pH was adjusted to 3 and extracted with 3×15 mL of H2O. EtOAc was evaporated under reduced pressure affording 650 mg of cyano derivative. The cyano derivative was dissolved in 40 mL of H2O/H2SO4 (2:1) and stirred for 24 h at 75° C. affording the title compound.
MS (ES+) m/z: [MH]+=421
A mixture of 7-chloro-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid (1 g, 3.55 mmol) and of 1,1-carbonyldiimidazole (2.88 g, 17.75 mmol) in 15 ml CCl3 was heated to reflux over the night the mixture was cooled and the solvent was removed under reduced pressure. To the resudue a small amount of diethyl ether was added and the resulting solid was collected by filtration and washed with diethyl ether to give a imidazolide intermediate in a quantitative yield.
To the mixture of NaH (0.26 g, 0.0108 mol, 60% disperse oil) and of nitromethane (0.58 ml 0.0108 mol) in 20 ml of anhydrous THF a solution of imidazolide intermediate (0.9 g, 0.289 mmol) in 20 ml of anhydrous THF was added dropwise and heated to reflux for 18 h. The mixture was cooled and 20 ml of H2O was slowly added and neutralized by HCl, and then extracted with CH2Cl2. The organic layer was washed with H2O and brine, dried by anhydrous Na2SO4 and evaporated. The product was precipitated and filtrated off yielding 0.4 g of title compound. (90.6% pure compound according to LC-MS).
MS (ES+) m/z: [MH]+=325.1
A mixture of 1-cyclopropyl-6,7-difluoro-8-methoxy-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid (1 g, 3.38 mmol) and 1,1-carbonyldiimidazole (2.19 g, 13.54 mmol) in 15 ml CCl3 was heated to reflux over the night. The mixture was cooled and the solvent was removed under reduced pressure. To the resudue a small amount of diethyl ether was added and the resulting solid was collected by filtration and washed with diethyl ether to give a imidazolide intermediate in a quantitative yield.
To the mixture of NaH (0.28 g, 0.0116 mmol, 60% disperse oil) and nitromethane (0.62 ml, 0.01158 mol) in 20 ml of anhydrous THF a solution of imidazolide intermediate (1 g, 2.89 mmol) in 20 ml of anhydrous THF was added dropwise and heated to reflux for 18 h. The mixture was cooled and 20 ml of H2O was slowly added and neutralized by HCl, and then extracted with CH2Cl2. The organic layer was washed with H2O and brine, dried by anhydrous Na2SO4 and evaporated. The product was precipitated and filtrated off yielding 0.56 g of title product. (93.46% pure compound according to LG-MS).
MS (ES+) m/z: [MH]+=339.1
To a solution of Intermediate 3 (250 mg) in DMSO (15 ml) ethanolamine (0.425 ml) was added and the reaction mixture was stirred at 90° C. for 1.5 hours. pH Value of mixture was adjusted to 4.5 and product was precipitated. After filtration, 190 mg of 1-cyclopropyl-6-fluoro-7-(2-hydroxy-ethylamino)-8-methoxy-4-oxo-1,4-dihydro-quinoline-3-(2-nitroacetyl) was obtained. A solution of 1-cyclopropyl-6-fluoro-7-(2-hydroxy-ethylamino)-8-methoxy-4-oxo-1,4-dihydro-quinoline-3-(2-nitroacetyl) (180 mg) in acrylonitrile and DBU was stirred at 80° C. under N2 for 5 hours. CH3CN was evaporated under reduced pressure yielding oily title product.
To the degassed solution of piperazine-1-carboxylic acid tert-butyl ester (1.0 g, 5.37 mmol) in acetonitrile (10 ml) were added Na2CO3 (1.708 g, 16.11 mmol ) and mixture was stirred for 20 min. The suspension was heated to 50° C. and 3-bromo-propyne (0.9 mL, 8.055 mmol) was added. The solvent was evaporated and the residue was extracted with Et-Ac and water (2×50 mL). Organic layer was washed with NaCl and NaHCO3 (2×50 ml). The organic layer was dried over K2CO3 and evaporated in vacuum yielding (0.70 g) oil title intermediate.
MS (ES+) m/z: [MH]+=225.1
1-Ethyl-6-iodo-4-oxo-1,4-dihydro-qunoline-3-carboxylic acid ethyl ester (0.7 g, 3.125 mmol), copper (I) iodide (42.47 mg, 0.223 mmol) and triethylamine (10.809 mL, 78.05 mmol) were suspended in dry acetonitrile (20 ml). The suspension was heated to 50° C. and N2 bubbled through. After 20 min, dichlorobis (triphenylposphine) palladium (II) (46.96 mg, 0.0669 mmol) and Intermediate 5a (0.7 g 3.125 mmol) were added and dark red suspension was heated at 50° C. for 3 hours. The solvent was evaporated and the residue was extracted with EtOAc and water (2×50 mL). Organic layer was washed with NaCl and NaHCO3 (2×50 mL), dried over K2CO3 and evaporated in vacuum yielding (1.24 g) oil red title product.
MS (ES+) m/z: [ME]+=468.3
To the solution of Intermediate 5b (1.2 g, 2.57 mmol) in DCM (1.2 mL) was added CF3COOH (1.2 mL) and mixture was stirred at room temp. for 48 h. To the reaction mixture was added water (pH=1.2) and layers were separated (pH=9.6). The organic layer was dried over K2CO3 and evaporated in vacuum yielding (1.7 g) oil red title product.
MS (ES+) m/z: [MH]+=368.3
To a mixture of 7-chloro-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid (10 g, 0.035 mol) in 1-methyl-2-pirolidone (70 mL) 2-(2-amino-ethoxy)-ethanol (18 mL, 0.18 mol, 5 eq.) was added, the reaction mixture was stirred at 110° C. for 24 hours. Then was diluted with water (200 mL) and CH2Cl2 (60 mL) and pH was adjusted to 10. The aqueous layer was extracted with CH2Cl2 (5×50 mL) and then pH was adjusted to 6.7. After 10 minutes first product precipitated. Filtrated off yielding 2.7 g of crude 7-chloro-1-cyclopropyl-6-[2-(2-hydroxy-ethoxy)-ethylamino]-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid. (according to LC-MS 100% pure Intermediate 6B) Over night second product precipitated. Filtrated off yielding 7.7 g of yellow product (according to LC-MS a mixture of Intermediate 6A and Intermediate 6B in a 1:1 ratio).
Intermediate 6B (2 g, 5.45 mmol) was diluted in 25 mL of acrylonitrile, DBU (2.0 mL) was added and stirred at 80° C. for 24 hours. Acrylonitrile was evaporated under reduced pressure, residue was dissolved in DCM, pH was adjusted to pH 3 and extracted with 3×20 mL H2O.
The organic layers were washed with brine, dried over Na2SO4, filtered and DCM was evaporated under reduced pressure affording 1.9 g of 6-{2-[2-(2-cyano-ethoxy)ethoxy]ethylamino}-1-cyclopropyl-7-chloro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid. This product was dissolved in 40 mL of mixture H2O/H2SO4 (1:1) and stirred for 24 hours at 75° C. The obtained precipitate was filtered and dried under reduced pressure for 1 h affording 1.7 g of title product.
A mixture of 1-cyclopropyl-6-fluoro-7-chloro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid (2 g, 0.0071 mol) and 1,1′-carbonyldiimidazole (5.76 g, 0.035 mol) in 15 mL CHCl3 was heated to reflux for 17 hours. The solvent was removed by reduced pressure. To the residue ether was added and then stirred at room temperature for 30 min. The solid was filtered and dried affording 1.64 g of 3-imidazolide derivative. Imidazolide derivative (1 g, 0.003 mol) was dissolved in 40 mL acetonitrile, then methanesulphonylacetone (2 g, 0.015 mol) and K2CO3 were added and the mixture was heated to reflux for 21 hours. The solvent was removed under reduced pressure and 120 mL of H2O was added. The solution was acidified by 2N HCl (pH ˜3) and extracted with EtOAc. The organic layer was dried and concentrated to give a crude solid product. The crude product was purified by column chromatography (DCM-EtOH—NH4OH=90:9:1.5) to give pure product 1-cyclopropyl-6-fluoro-7-chloro-4-oxo-1,4-dihydro-3-[(2-methanesulfonyl)acetyl]-quinoline.
MS (ES+) m/z: [MH]+=358.1
1H NMR (500 MHz, DMSO) □ 8.58, 8.37, 8.13, 5.22, 3.78, 3.13, 1.31 and 1.16
To a stirring solution of ethanolamine (1.96 mL, 32.7 mmol) in dioxane (40 mL) and water (20 mL) saturated solution of NaHCO3 (20 mL) was added. The solution was cooled in ice bath and di-t-butyl dicarbonate (8.0 g) was added portionwise. After 1 hour TLC showed no starting material. EtOAc (50 mL) and water (20 mL) were added, organic layer was separated and evaporated yielding 4.20 g of the oily title compound.
To a stirring solution of Intermediate 9a (1.16 g) in THF (30 mL) at room temperature t-butylammonium iodide (0.15 g), sodium iodide (0.15 g) and propargyl bromide (80% in toluene, 1.20 mL) were added. KOH (0.40 g) was added portionwise during 30 minutes and the suspension was stirred at room temperature for 24 hours. The solvent was evaporated, EtOAc (30 mL) and water (30 mL) were added, organic layer was washed with 10% Na2S2O5 solution and evaporated yielding 1.21 g of the title compound.
CuI (55 mg) and triethylamine (14.06 mL) were added into a solution of 1-ethyl-6-iodo-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid (1.0 g) in MeCN (20 mL). The mixture has been stirring at room temperature for 20 minutes. Pd(PPh3)2Cl2 (61 mg) and Intermediate 9b (0.70 g) were added and the mixture has been stirring at 50° C. for 4 hours. The solvents were evaporated, EtOAc (30 mL) and water (30 mL) were added, organic layer was washed with water (30 mL) and brine (30 ml) and evaporated yielding 1.0 g of the title compound.
MS (ES+) m/z: [MH]+=415.24
Trifluoroacetic acid (0.386 mL) was added into solution of Intermediate 9c (0.42 g) in MeCN (5 mL) at room temperature. The solution has been stirring at room temperature for 48 hours and evaporated yielding 0.80 g of the title compound.
To the solution of 1-Oxo-6,7-dihydro-1H,5H-pyrido[3,2,1-ij]quinoline-2-carboxylic acid ethyl ester (7.5 g, 29 mmol) in glacial acetic acid (120 mL) was added brome (1.6 ml, 32 mmol). The mixture was stirred over night at room temperature, and new portion of brome (1.6 mL, 32 mmol) was added. After 24 h, reaction mixture was diluted with 100 mL of H2O and pH was adjusted to 2.9. Precipitate was filtered and dried. The crude product was precipitated from CH2Cl2/Diisoprophylether and dried in vacuum drier yielding 13.07 g of the crude title product.
MS (ES+) m/z: [MH]+=338.0
Tris(dibenzylideneacetone)dipalladium chloroform complex (50 mg, 0.05 mmol), rac-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (100 mg, 0.16 mmol), Intermediate 10a (3 g, 8.9 mmol) and benzophenone imine (1.2 ml) were diluted in THF (45 ml). The air of atmosphere was replaced with N2, and Cs2CO3 (2.5 g) was added. The mixture was stirred under reflux. Another two portions of Tris(dibenzylideneacetone)dipalladium chloroform complex (50 mg, 0.05 mmol), rac-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (100 mg, 0.16 mmol), benzophenone imine (1.2 ml) and Cs2CO3 (2.5 g) was added every 2.5 h. The mixture was stirred under reflux over night and then cooled to room temperature and filtered. HPLC/MS indicated the presents of product 10b.
MS (ES+) m/z: [MH]+=437.3
To the mixture of Intermediate 10b 5% HCl was added dropwise until appearance of precipitate. Precipitate was filtered and dried in vacuum drier yielding 2 g of the crude title product.
MS (ES+) m/z: [MH]+=273.2
13C-NMR(125 MHz, DMSO) δ: 13.81, 19.90, 25.57, 51.37, 59.24, 108.39, 115.66, 124.99, 128.06, 129.06, 129.91, 130.51, 133.95, 147.54, 163.98, 171.63.
To the solution of Intermediate 10c (200 mg, 0.73 mmol) in MeOH (75 mL), benzyloxyacetaldehide (110 mg, 0.73 mmol), NaBH3CN (137 mg, 2.2 mmol) and AcOH (250 μl) was added. Reaction mixture was stirred for 20 minutes and evaporated in vacuum. Oil product was purified by column chromatography in system CH2Cl2-(MeOH—NH4OH=9:1.5)=9:(1.5) yielding 159 mg of the title product.
MS (ES+) m/z: [MH]+=407.2
To the solution of Intermediate 10d (159 mg, 0.39 mmol) in EtOH (41.6 mL) cyclohexene (12.8 mL) and 10% Pd/C (243 mg) were added. The mixture was stirred under reflux over night, filtered through celite and evaporated in vacuum yielding 80 mg of the title product.
To a solution of 2″-O-Acetyl azithromycin-11,12-cyclic carbonate (8.16 g, 9.8 mmol) in CH2Cl2 (50 mL) were added DMAP (0.61 g, 5 mmol), N-(9-Fluorenylmethoxy-carbonyl) glycine (Fmoc Gly, 4.46 g, 15 mmol), and 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (EDC HCl, 3.83 g, 20 mmol). The mixture was stirred overnight at room temperature. The solvent was evaporated and the crude product dissolved in 200 mL of methanol. The mixture was stirred under reflux overnight at 65° C. and then concentrated under reduced pressure. After column chromatography in system (CH2Cl2-MeOH—NH4OH=90:9:0.5) and rechromatography in the same system, 480 mg of title compound was afforded.
MS (ES+) m/z: [MH]+=833.5
13C-NMR(125 MHz, CDCl3) δ: 5.55, 10.45, 10.84, 14.19, 14.83, 17.82, 21.34, 21.58, 22.03, 22.15, 22.69, 26.27, 26.89, 29.15, 29.69, 34.40, 34.93, 35.26, 39.27, 40.39, 41.99, 42.92, 43.23, 43.92, 45.25, 49.50, 49.60, 61.26, 62.86, 65.39, 67.68, 68.18, 68.30, 68.93, 70.76, 73.02, 73.35, 74.30, 76.29, 76.82, 77.07, 77.33, 77.90, 78.07, 79.54, 85.12, 85.96, 95.27, 102.90, 106.59, 147.48, 153.36, 154.93, 158.06, 171.09, 174.23, 177.18
Using the similar procedure to that described in Intermediate 11, Intermediate 12 was prepared starting from 2′-O-Acetyl azithromycin.
MS (ES+) m/z: [MH]+=806.5
13C-NMR(125 MHz, CDCl3) δ: 7.45, 9.12, 11.27, 14.12, 14.69, 15.50, 16.24, 17.89, 21.29, 21.39, 21.79, 21.99, 22.66, 26.55, 26.78, 27.54, 28.98, 29.70, 31.59, 35.04, 35.29, 36.35, 38.42, 40.38, 42.00, 42.28, 43.76, 44.42, 45.15, 45.32, 49.48, 62.45, 62.88, 65.61, 67.87, 70.15, 70.98, 72.94, 73.60, 73.83, 74.31, 76.79, 77.05, 77.30, 77.45, 77.87, 79.52, 80.15, 83.16, 94.73, 102.34, 174.12, 178.81
Mixture of 50 mL diethylene glycole and 50 mL DMSO was prepared and heated on 70° C. Into mixture 8 g of KO-t-Bu portionwise was added. Then, 5 g of fluoro-chloro quinolonic acid (17.8 mmol) was added portionwise. The temperature was increased to 105° C. After 5 hours, the 25 mL of H2O was added and the mixture was extracted with 2×20 mL of DCM. Water layer was adjusted to pH 4. The obtained precipitate was filtered off and dried under reduced pressure affording 500 mg of 7-chloro-1-cyclopropyl-6-[2-(2-hydroxy-ethoxy)-ethoxy]-4-oxo-1,4-dihydro-quinolone-3-carboxylic acid.
7-Chloro-1-cyclopropyl-6-[2-(2-hydroxy-ethoxy)-ethoxy]-4-oxo-1,4-dihydro-quinolone-3-carboxylic acid (500 mg) was dissolved in 12.5 mL of acrylonitrile, then 1 mL of DBU was added and the mixture stirred for 24 hours at 80° C. Acrylonitrile was evaporated under reduced pressure, residue was dissolved in 300 mL of 2-propanol and the pH of the mixture was adjusted to pH 3.5. The precipitate was obtained after 12 hours, filtered off and washed with water (pH 3.5). The precipitate was dissolved in 20 mL H2O:H2SO4 (1:1) and stirred for 24 hours at room temperature. The obtained precipitate was filtered off and dried under reduced pressure affording 300 mg of the title compound.
2″-O-Ac 11-O-Methyl-azithromycin was dissolved in toluene under N2 atmosphere and TEA (3 eqv) and 3-Chloropropionyl-chloride (1 eqv) were added. Reaction mixture was stirred 5 minutes and then the same amount of TEA and 3-Chloropropionyl-chloride was added. After 10 minutes the reaction was finished, extracted with Na2HCO3 and toluene. The organic layer was washed with H2O and brine, dried by anhydrous Na2SO4 and evaporated.
A solution of Intermediate 14a in MeOH was stirred at room temperature for 48 hours. The solvent was evaporated under reduced pressure affording the title compound.
To the degassed solution of piperazine-1-carboxylic acid tert-butyl ester (0.5 g, 2.69 mmol) in acetonitrile (5 mL) was added Na2CO3 (0.854 g, 8.05 mmol ) and mixture was stirred for 20 min. The suspension was heated to 50° C. and 3-bromo-propyne (448.65 μl, 4.03 mmol) was added. The solvent was evaporated and the residue was extracted with EtOAc and water. Organic layer was washed with NaCl and NaHCO3 (2×20 ml), dried over K2CO3 and evaporated in vacuum yielding 0.45 g of the title product as yellowish oil.
MS (ES+) m/z: [MH]+=247.2
Intermediate 17 (0.2 g, 0.524 mmol), copper (I) iodide (9.98 mg, 0.0524 mmol) and triethylamine (2.54 ml, 18.34 mmol) were suspended in dry acetonitrile (10 mL). The suspension was heated to 50° C. and N2 bubbled through. After 20 min, dichlorobis (triphenylposphine) palladium (II) (11.03 mg, 0.0157 mmol) and Intermediate 15a (0.164 g 0.733 mmol) were added and dark red suspension was heated for 3 hours at 50° C. The solvent was evaporated and the residue was extracted with EtOAc and water (2×20 ml). Organic layer was washed with NaCl and NaHCO3 (2×20 ml), dried over K2CO3 and evaporated in vacuum yielding 0.34 g of the title product as red oil.
To the solution of Intermediate 15b (0.34 g, 0.71 mmol) in DCM (3.4 mL) was added CF3COOH (3.4 mL) and mixture was stirred. for 48 hours at room temp. To the reaction mixture was added water (pH 1.2) and layers were separated (pH 9.6). The organic layer was dried over K2CO3 and evaporated in vacuum yielding 0.22 g of the title product as red oil.
MS (ES+) m/z: [MH]+=380.2
1-Oxo-6,7-dihydro-1H,5H-pyrido[3,2,1-ij]quinoline-2-carboxylic acid ethyl ester (1.0 g) was placed in round bottom flask and to that, mixture of H2SO4/HNO3 (1:1) was added and stirred for 3 hours at 0° C. The reaction mixture was poured on ice and precipitate was filtered off affording 900 mg of title product (LC/MS: 95%).
Intermediate 16a (9oo mg) was diluted in 35 mL of acetic acid and to this mixture 800 mg of 10% Pd/C was added and stirred for 15 h at room temperature and at 30 Ba. The reaction mixture was filtered to remove catalyst and then acetic acid was evaporated under reduced pressure affording 700 mg of the title product. (LC/S: 95%).
To a 0° C. cooled trifluoromethansulfonic acid (3 mL, 33.31 mmol) 1-Oxo-6,7-dihydro-1H,5H-pyrido[3,2,1-ij]quinoline-2-carboxylic acid ethyl ester (1.53 g, 5.95 mmol) was added and to that solution N-Iodosuccinimide (1.6 g, 714 mmol) was added. The mixture was allowed to warm from 0° C. to room temperature while stirring. Reaction mixture was poured in ice and precipitate was filtered off affording 1 g of the title product (LC/MS: 57%).
A Pyrex tube was charged with sodium tert-butoxide (1.4 mmol), Pd2(dba)3 (0.00125 mmol), and BINAP (0.00375 mmol). The Pyrex tube was fitted with a septum and after the air atmosphere was replaced with argon, toluene (4 mL), 1-ethyl-6-iodo-4-oxo-1,4-dihydro-qunoline-3-carboxylic acid ethyl ester (1.0 mmol), and benzophenone imine (1.2 mmol) were added by syringe. The reaction was sealed and heated to 80° C. with stirring until starting material was consumed as judged by GC analysis. The reaction mixture was cooled to room temperature, diluted with ether (40 mL), filtered, and concentrated. The crude reaction mixture was then recrystallized from MeOH to furnish the desired product in 90% yield.
Method A: Transamination with Hydroxylamine
To a solution of the imine adduct in MeOH (0.1 M) at RT was added NaOAc (2.4 eq) and hydroxylamine hydrochloride (1.8 eq). Oxime formation was usually complete in 15 to 30 minutes. The solution was then partitioned between 0.1 M NaOH and CH2Cl2. The organic layer was dried over anhydrous Na2SO4 and concentrated in vacuo. The product was purified by chromatography on silica gel.
Method B: Hydrogenolysis
A solution of the imine adduct, ammonium formate (15 eq) and 5% Pd/C (10 mol %) were heated to 60° C. in MeOH (0.2 M in imine). After 2 hours reduction was usually complete. The solution was cooled to room temperature and diluted with CH2Cl2 (5× volume of MeOH) to be passed through a plug of celite. The organic solution was washed with 0.1 M NaOH, dried over anhydrous Na2SO4 and concentrated in vacuo. The product was purified by chromatography on silica gel.
Method C: Acidic Hydrolysis
To a solution of the imine adduct in THF (0.3 M) was added aqueous 2.0 M HCl (added 5% by volume of THF). After 5-20 minutes hydrolysis was complete and the reaction mixture was partitioned between 0.5 M HCl and 2:1 hexane/EtOAc. The aqueous layer was separated and made alkaline. The product aniline was extracted with CH2Cl2, dried over anhydrous Na2SO4 and concentrated in vacuo.
To a solution of 2′-O-acetyl-6-O-methyl-erythromycin A (1.1 g) in DCM (20 mL) pyridine (1.7 mL) and acryloyl chloride (1.1 mL) were added at 0° C. After 2 hours a further addition of pyridine (1.7 mL) and of acryloyl chloride (1.1 mL) was performed. The reaction mixture was quenched with a saturated solution of NH4Cl (10 mL) and extracted with DCM (3×20 mL). The organic phase was washed with a saturated solution of NaHCO3 (10 mL), water (10 mL), dried over Na2SO4, filtered and evaporated under reduced pressure. The crude product was purified by flash-chromatography (DCM-MeOH—NH3 95:5:0.5) affording the title compound (470 mg).
MS (ES+) m/z: [MH]+=844
Intermediate 19 (1.82 g) was dissolved in MeOH (100 mL) and stirred at 60° C. for 4 hours, then at room temperature for 16 hours. The solvent was evaporated under reduced pressure and the crude product was purified by flash chromatography (eluent: MeOH-DCM-NH4OH 5:90:0.5) affording the title compound (1.4 g).
MS (ES+) m/z: [MH]+=802
1H-NMR (500 MHz) δ: 6.44 (d, 1H), 6.13 (dd, 1H), 5.89 (d, 1H), 5.07 (d, 1H), 5.00 (d, 1H), 4.75 (d, 1H), 4.60 (d, 1H), 4.38 (m, 1H), 3.97 (s, 1H), 3.80-3.73 (m, 2H), 3.66 (d, 1H), 3.46 (s, 1H), 3.32 (s, 3H), 3.21-3.18 (m, 2H), 3.04 (s, 3 H), 3.00 (m, 1H), 2.92 (m, 1H), 2.56 (m, 2H), 2.43 (d, 1H), 2.31 (s, 6H).
13C-NMR (75 MHz) δ: 221.0; 175.7; 165.8; 131.5; 128.0; 102.1; 96.0; 80.5, 78.8, 78.3; 78.0; 76.6; 74.3, 72.7; 71.1; 69.1; 67.8; 65.3; 63.2: 50.7; 49.5; 45.3; 44.9; 40.3; 39.2; 38.8; 37.2; 35.2; 28.9; 21.7, 21.1; 19.7, 18.3, 18.0, 15.9; 12.3; 10.6; 9.1.
A solution of 2′-O-acetyl-azithromycin-11,12-carbonate (10.9 g) in toluene (300 mL) was stirred at room temperature under argon atmosphere. To this solution TEA (12.66 mL) and 3-chloro-propionyl chloride (1.94 mL) were added in two portions over a period of 10 minutes. After 20 minutes the solution was diluted with a saturated aqueous solution of NaHCO3 (300 mL) and extracted with toluene (4×80 mL). The collected organic phase was dried, filtered and concentrated under reduced pressure affording the title compound (11.0 g).
MS (ES+) m/z: [MH]+=872
A solution of Intermediate 21 (11.0 g) in MeOH (200 mL) was stirred at room temperature for 48 hours. The solvent was evaporated under reduced pressure affording the title compound (9.81 g).
MS (ES+) m/z: [MH]+=829.1
1H-NMR (500 MHz,) δ: 6.45 (d, 1H), 6.17 (dd, 1H), 5.87 (d, 1H), 5.11 (d, 1H), 4.88 (dd, 1H), 4.77 (d, 1H), 4.53 (d, 1H), 4.47-4.40 (m, 3H), 3.72 (m, 1H), 3.60 (d, 1H), 3.33 (s, 3H), 3.25 (dd, 1H), 2.87-2.85 (m, 2H), 2.58 (m, 1H), 2.44-2.38 (m, 2H), 2.32 (s, 6H), 2.21 (s, 3H), 2.06 (m, 1H), 2.00 (m, 1H), 1.92 (m, 1H), 1.84 (m, 1H), 170-1.56 (m, 4H), 1.45 (s, 3H), 1.40 (dd, 1H), 1.29 (s, 3H), 1.25 (m, 1H), 1.22 (d, 3H), 1.18 (d, 6H), 1.12 (s, 3H), 108-1.06 (2d, 6H), 0.93 (m, 6H).
To the solution of dioxane (40 mL), H2O (20 mL) and NaOH (20 mL; 1 M) was added 2-(2-aminoetoxy)ethanol. The reaction mixture was cooled to 0° C. and di-t-Bu dicarbonate (4.8 g) was added. The mixture was stirred for 30 min at 0° C., and then the stirring was continued for 2 hours at room temperature. In next 3 hours two portion of di-t-Bu dicarbonate (2×0.22 g) were added. The mixture was stirred over night at room temperature and then concentrated (20-30 mL). EtOAc (60 mL) was added to the solution and pH was adjusted to 2.5. Aqueous layer was extracted with EtOAc (3×20 mL). Organic layers was washed with H2O (3×30 mL), dried over K2CO3 and evaporated in vacuum to give 3.7 g of the title product as oil.
To a mixture of DMSO (5 mL) and ethyleneglycol (6 mL), KOtBu (1.6 g, 14.23 mmol) was added portionwise over 10 min, and then heated to 90° C. To the mixture, 7-chloro-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid (1.0 g) was added portionwise over 20 min, the temperature was increased to 105° C. and the mixture was stirred for 6 h. Water (30 mL) was added to the reaction solution and the pH of the solution was adjusted to pH=5. The resulting solution was left in the refrigerator overnight. The precipitate obtained was filtered, washed with cold water, and dried affording a 2:1 mixture of Intermediate 24A and Intermediate 24B (1.0 g).
Part of the crude product (700 mg) was dissolved in EtOH (15 mL) by heating to the reflux. The resulting solution was cooled to 30° C. and a first precipitation occurred. The precipitate was filtered, washed with cold EtOH and dried under reduced pressure. Intermediate 24A (204 mg) was obtained as a white solid;
1H-NMR (500 MHz, DMSO-d6) δ: 15.06 (s, 1H), 8.71 (s, 1H), 8.40 (s, 1H), 7.86 (s, 1H), 4.97 (t, 1H), 4.25 (t, 2H), 3.87 (m, 1H), 3.82 (q, 2H), 1.32 (m, 2H), 1.20 (m, 2H); 13C-NMR (75 MHz, DMSO-d6) δ: 176.61, 165.67, 152.47, 147.54, 135.34, 129.48, 124.95, 120.02, 106.90, 106.66, 71.22, 59.15, 35.99, 7.46;
To a suspension of Intermediate 24A (2 g) in acrylonitrile (40 mL) was added DBU (2.3 mL). The reaction mixture was stirred at 80° C. for 24 h. The acrylonitrile was evaporated under reduced pressure. Isopropanol (30 mL) was added to the residue and the pH of the solution was adjusted to pH=5 by adding 2M HCl, during which the product precipitated. The precipitate was filtered, washed with water, and dried affording Intermediate 25 (1.7 g) as a white solid.
MS (ES+) m/z: [MH]+=377.0
1H-NMR (500 MHz, DMSO-d6) δ: 8.68 (s, 1H), 8.38 (s, 1H), 7.84 (s, 1H), 4.38 (t, 2H), 3.91 (t, 2H), 3.86 (m, 1H), 3.75 (t, 2H), 2.79 (t, 2H), 1.32 (m, 2H), 1.20 (m, 2H); 13C-NMR (75 MHz, DMSO-d6) δ: 176.63, 165.65, 152.18, 147.61, 135.50, 129.44, 124.97, 120.04, 119.11, 106.96, 106.80, 69.02, 68.30, 65.49, 35.99, 18.06, 7.46;
A solution of Intermediate 25 (1.10 g) in a mixture of conc. H2SO4 (10 mL) and H2O (20 mL) was stirred at 75° C. for 24 h. The pH of the reaction mixture was adjusted to 10.2 with 40% NaOH, during which the product precipitated. The precipitate was filtered, washed with water, and dried affording Intermediate 26 (0.8 g) as a white solid.
MS (ES+) m/z: [MH]+=396.0
1H-NMR (300 MHz, DMSO-d6) δ: 15.0 (s, 1H), 11.8 (s, 1H), 8.69 (s, 1H), 8.38 (s, 1H), 7.85 (s, 1H), 4.35 (m, 2H), 3.91-3.82 (m, 3H), 3.74 (dt, 2H), 2.49 (m, 2H), 1.31 (m, 2H), 1.19 (m, 2H);
Using the similar procedure to that described in Intermediate 7, starting from a mixture of Intermediate 6A and Intermediate 6B, Intermediate 27 was prepared as a mixture of Intermediate 27A and Intermediate 27B in a 1:1 ratio.
A mixture of 7-chloro-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid (5 g, 0.018 mol), 2,2′-(ethylenedioxy)bis-(ethylamine) (26 mL, 0.18 mol, 10 eq.) in 1-methyl-2-pyrrolidone was heated at 110° C. for 24 hours. Reaction mixture was diluted with water (70 mL) pH was adjusted to 11 and extracted with CH2Cl2 (9×40 mL). Water layer was then acified to pH 6.8 with H2SO4, extracted with CH2Cl2 (50 mL) and evaporated. 2-Propanol was added (200 mL) and stirred at 82° C. for 30 minutes. The reaction mixture was then filtered and 2-propanol was evaporated in vacuum yielding 8 g of oily product, according to LC-MS 50% of chloro derivative (A) and 30% of fluoro derivative. Product was purified by column chromatography (eluent CH2Cl2-2-propanol=1:1) yielding pure chloro derivative (A).
MS (ES+) m/z: [MH]+=409.9 (A)
MS (ES+) m/z: [MH]+=393.4 (B)
To the solution of (2-amino-ethylamino)-acetic acid tert-butyl ester (1.0 mL, 6.32 mmol) in i-PrOH (50 mL) was added acrylic acid tert-butyl ester (309.1 μL, 2.11 mmol). The suspension was heated for 48 hours at 60° C. The solvent was evaporated and product was purificated by column chromatography (DCM-MeOH—NH3=90:3:0.5) yielded the title product as colorless oil (0.45 mg).
MS (ES+) m/z: [MH]+=289.2
To the solution of Intermediate 29a (0.45 mg, 1.56 mmol) in chloroform (20 mL) were added HCOOH (0.218 mL, 5.78 mmol) and HCHO (0.24 mL, 8.69 mmol) and stirred at room temperature for 2 hours. To the reaction mixture was added water (pH 1.3) and layers were separated (pH 2.5). The organic layer was dried over K2CO3 and evaporated in vacuum yielding 034 g of oil colorless product.
MS (ES+) m/z: [MH]+=301.2
To a solution of 7-chloro-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid (0.55 g, 1.95 mmol) in 1-methyl-2-pyrrolidone (40 mL) bis-(2-aminoethyl)-ether dihydrochlorid (2.1 g, 11.9 mmol, 6 eq.) and DBU (3.49 mL, 23.4 mmol, 12 eq.) added and the reaction mixture was stirred at 110° C. for 18 hours. The reaction mixture was then diluted with water (70 mL), pH was adjusted to 11 and extracted with CH2Cl2 (9×40 mL). Water layer was then acified with H2SO4 to pH 6.8, extracted with 50 mL of CH2Cl2 and then evaporated in vacuum. Crude product was diluted in 2-propanol (60 mL), stirred at 82° C. for 20 minutes and filtrated. Precipitate was pure salt (Na2SO4). 2-Propanol was evaporated in vacuum and product was purified by column chromatography (fraction, eluent: CH2Cl2-MeOH-NH3—CH3CN=4:4:2:1) yielding 0.5 g of title compounds as a mixture of chloro and fluoro derivatives in ratio 3:1
MS (ES+) m/z: [MH]+=365.8 (A) (75%)
MS (ES+) m/z: [MH]+=349.4 (B) (25%)
Starting from 7-chloro-1-ethyl-6-fluoro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid (2.5 g, 9.27 mmol) using the procedure of Intermediate 6, the mixture of Intermediates A and B (1.0 g) was obtained
According to HPLC/MS product contains Intermediate A and Intermediate B in a ratio 1:1
Mixture of Intermediates 31A and 31 B (600 mg, 1.13 mmol) was dissolved in 10% NaOH solution (5 mL) and cooled to 0° C. and then acrylonitrile (370 μL, 5.65 mmol) was added portionwise and stirred at R.T. for 2 h. To reaction mixture water (50 mL) was added and extracted with MIBK (3×50 mL). H2O layer was filtered with charcoal and pH was adjusted to pH 4. The obtained precipitate was filtered and dried affording 600 mg of product.
According to HPLC/MS product contains Intermediates (A):(B) in a ratio 1:1
Mixture of Intermediates 32A and 32 B (600 mg, 1.47 mmol) was dissolved in H2SO4/H2O=1/1.5 (15 mL) and stirred at 70° C. for 24 h. Reaction mixture was poured on cold water, precipitate was filtered and dried affording 400 mg of product.
According to HPLC/MS product contains Intermediates (A):(B) in a ratio 1:1
To a mixture of 7-chloro-1-isopropyl-6-fluoro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid (3 g, 10.57 mmol) in 1-methyl-2-pirolidone (30 mL) 2-(2-amino-ethoxy)-ethanol (5.3 mL, 52.85 mmol, 5 eq.) was added, the reaction mixture was stirred at 110° C. for 24 hours. Then was diluted with water (50 mL) and extracted with CH2Cl2 (3×150 mL). After separation water layer was acidified to pH 4 and left overnight at 4° C. The obtained precipitate was filtered off and dried under reduced pressure for 1 h affording 974 mg of title product.
HPLC/MS (ES) m/z: [MH]+=370.1
To the solution of Intermediate 34a (1.82 g, 4.94 mmol) in MIBK (50 mL) 40% aqueos solution of NaOH (1.03 mL, 14.8 mmol) was added and then acrylonitrile (6.5 mL, 98.7 mmol) was added portionwise and stirred at 0-10° C. for 2 h. Than DBU (2 mL) was added and stirred at R.T. for 1 h. The reaction mixture was then diluted with cold MIBK (20 mL) and H2O (20 mL), extracted with H2O (2×15 mL). The combined water layers were filtrated with charcoal and pH was adjusted to pH 5. The precipitate was filtered and dried under reduced pressure yielding 1.2 g of the title product.
HPLC/MS (ES) m/z: [MH]+=422.78.
The Intermediate 34b (1.2 mg, 2.85 mmol) was dissolved in H2SO4:H2O=1:1.5 (50 mL) and stirred at 70° C. for 48 h. Than reaction mixture was poured on cold water. The obtained precipitate was filtered off and dried under reduced pressure affording 1 g of the title compound.
HPLC/MS (ES) m/z: [MH]+=441.85.
THF (40 ml) was cooled to 0° C. under N2 atmosphere for 30 minutes and in this solution 2-allyloxyethanol (3.14 mL, 29.4 mmol) and NaH (1.1 g, 27.5 mmol) were added. The reaction mixture was heated to 35° C. and after 45 minutes, this mixture was cooled to 0° C. and benzyl bromide (5.24 ml, 44.1 mmol) was added. Reaction mixture was stirred at RT overnight and then extracted with EtOAc/H2O. The combined organic layers were dried over anhydrous Na2SO4 and evaporated under vacuum.
The crude product was purified via flash chromatography (hexane:acetone=6:1) giving (2-allyloxy-ethoxymethyl)-benzene.
To the solution of (2-allyloxy-ethoxymethyl)-benzene (2 g, 10.4 mmol) in THF:H2O=1:1 (50 ml), cooled to 0° C., OsO4 (0.127 g; 2.5% solution in THF) and NaIO4 (12.83 g suspended in 50 ml of H2O) were added. The reaction mixture was stirred at RT for 3 h, filtered and then extracted with EtOAc/H2O. The combined organic layers were dried over anhydrous Na2SO4 and evaporated under vacuum giving 2.08 g of the title intermediate.
To the solution of Intermediate 10c (400 mg, 1.47 mmol) in MeOH (150 mL), Intermediate 35a (285 mg, 1.47 mmol), NaBH3CN (273 mg, 2.2 mmol) and AcOH (300 μl) were added. Reaction mixture was stirred at RT over night, filtered and evaporated in vacuum. Oil product was purified by column chromatography (eluent CH2Cl2:MeOH:NH4OH=90:15::1.5 yielding 850 mg of the title product.
MS (ES+) m/z: [MH]+=451.19.
To the solution of Intermediate 35b (850 mg, 1.89 mmol) in MeOH (30 mL) 10% Pd/C (425 mg) and acetic acid (100 μL) were added. The mixture was stirred under pressure of 5 bar on R.T. for 48 hours. The reaction mixture was filtered through celite and evaporated in vacuum yielding 685 mg of crude product. After purification by spe-chromatography 306 mg (assay 97.7%) of the title product was obtained.
1H-NMR(500 MHz, DMSO-d6) δ: 1.27 (t, 3H), 2.05 (k, 2H), 2.9 (t, 2H), 3.26 (q, 2H), 3.46 (m, 2H), 3.51 (m, 2H), 3.58 (t, 2H), 4.2 (m,4H), 4.6 (t, 1H), 5.9 (t, 1H), 6.9 (s, 1H), 7.13 (s, 1H), 8.35 (s, 1H).
13C-NMR(300 MHz, DMSO-d6) δ: 14.30, 20.96, 26.16, 42.65, 51.7, 59.17, 60.15, 68.60, 72.17, 102.39, 106.95, 118.47, 127.58, 128.94, 129.73, 145.05, 145.89, 165.02, 172.41.
Using the similar procedure to that described in Intermediate 34b, starting from Intermediate 35c, 274 mg (assay 91%) of Intermediate 35d was obtained.
1H-NMR(500 MHz, DMSO-d6) δ: 2.11 (k, 2H), 2.73 (t, 2H), 2.9 (t, 2H), 3.3 (m, 2H), 3.58 (m, 8H), 4.39 (t,2H), 6.34 (t, 1H), 7.1 (s, 1H), 7.14 (s, 1H), 8.65 (s, 1H), 15.95 (s, 1H).
13C-NMR(300 MHz, DMSO-d6) δ: 17.99, 20.72, 26.17, 42.43, 52.64, 65.21, 68.66, 69.53, 65.56, 100.19, 105.43, 119.20, 120.44, 126.94, 128.48, 129.96, 143.83, 146.82, 166.86, 176.47.
Using the similar procedure to that described in Intermediate 34c, starting from Intermediate 35d, Intermediate 35e (342 mg) was obtained.
1H-NMR(500 MHz, DMSO-d6) δ: 2.09 (m, 2H), 2.42 (t, 2H), 2.97 (t, 2H), 3.29 (q, 2H), 3.52 (m, 4H), 3.58 (m, 4H), 4.40 (t, 2H), 6.35 (t, 1H), 7.13 (s, 1H), 7.21 (s, 1H), 8.64 (s, 1H), 12.20 (s, 1H), 15.90 (s, 1H).
13C-NMR(300 MHz, DMSO-d6) δ: 20.70, 26.16, 34.61, 42.41, 52.62, 66.14, 68.56, 69.52, 69.54, 100.12, 105.40, 120.43, 126.90, 128.44, 129.94, 143.79, 146.79, 166.88, 172.55, 176.44.
7-Chloro-1-cyclopropyl-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid ethyl ester (1.50 g) was suspended in THF (15 ml) at room temperature. NaOH (411 mg, 2 eq) solution in water (15 ml) was added and the mixture was stirred at 80° C. for 24 hours. THF was evaporated and the solution was acidified to pH 5 using HCl. The obtained precipitate was filtrated off and dried under reduced pressure yielding 1.18 g of the titled Intermediate 36a.
Using the similar procedure to that described for Intermediate 13, starting from Intermediate 36a 180 mg of the title compound was obtained.
HPLC/MS (ES+) m/z [MH]+=416.19
Using the similar procedure to that described in Intermediate 19, starting from 2′-O-acetyl-9-(1-isopropoxy-cyclohexyl)oximino-erythromycin A (0.50 g) titled Intermediate 37 (0.48 g) was obtained.
Sodium (2.5 g, 0.1086 mole) was added portion wise to methanol (60 mL) followed with addition of Intermediate 6B (7.00 g, 0.019 mole) at R.T. Reaction mixture was heated in sealed tube for 100 hours at 130° C. Mixture was evaporated in vacuum to dryness, solid residue was dissolved in water (50 mL) and acidified with acetic acid to pH about 5.5. After cooling in ice bath yellow crystals precipitated, The precipitate was filtrated, washed with water and dried in vacuum yielding 5.9 g of the titled compound.
HPLC/MS (ES+) m/z [MH]+=362.
Using the similar procedure to that described in Intermediate 32, starting from Intermediate 38a afforded Intermediate 38b (3.18 g).
HPLC/MS (ES+) m/z [MH]+=415.
Using the similar procedure to that described in Intermediate 33, starting from Intermediate 38b afforded Intermediate 38c (2.34 g).
HPLC/MS (ES+) m/z [MH]+=434.5.
To a solution of Intermediate 6B (2.58 g) in n-butanol (40 mL) 40% water solution of dimethylamine (7 mL) was added and heated in sealed tube for 75 hours at 140° C. After cooling the reaction mixture was evaporated at reduced pressure to dryness and ethanol (20 mL) was added. After keeping in refrigerator over night precipitate occured. The precipitate was filtered off and washed with ethanol yielding the title product (2.05 g)
HPLC/MS (ES+) m/z [MH]+=375.
Using the similar procedure to that described in Intermediate 32, starting from Intermediate 39a afforded Intermediate 39b (1.75 g).
HPLC/MS (ES+) m/z [MH]+=429.
Using the similar procedure to that described in Intermediate 33, starting from Intermediate 39b afforded Intermediate 39c (1.33 g).
HPLC/MS (ES+) m/z [MH]+=444.7.
THF (120 ml) was cooled to 0° C. under N2 atmosphere and to this solution 2-benzyloxyethanol (25 mL, 0.154 mol) and NaH (60% min.oil, 7.4 g, 0.184 mol) were added. The reaction mixture was heated at 35° C. for 45 minutes, cooled to 0° C., and than 3-bromo-propyne (27.44 mL, 0.308 mol) was added. Reaction mixture was stirred at RT overnight and then partitioned between EtOAc/H2O. The combined organic layer was dried over anh. Na2SO4, evaporated in vacuo to yield 24.8 g of the title product.
HPLC/MS(ES+) m/z [MH]+=190.48.
Starting from 1,4-Dihydro-1-ethyl-6-iodo-4-oxo-quinoline-3-carboxylic acid ethyl ester (7.5 g, 0.02 mol) using the procedure of Intermediate 36a the title compound was obtained (7.3 g).
LC/MS(ES+) m/z [MH]+=344.2
To solution of Intermediate 41 (10.6 g, 0.03 mol) in MeCN:H2O=1:1 (250 mL), CuI (0.571 g, 0.003 mol) was added and stirred for 20 minutes at 50° C. Then solution of Pd(OPh3)2Cl2 (1.05 g, 0.0014 mol) and Intermediate 40 (10.26 g, 0.0015 mol) in MeCN:H2O=1:1 (40 mL) were added to the reaction mixture and stirred at 50° C. overnight. Organic solvents were evaporated and water (500 mL) was added to the residue, pH was adjusted to 12 and water layer was extracted with diizopropyl-ether (3×150 mL). Charcoal was added to water layer, then stirred for 15 minutes and filtrated over Celite. After pH was adjusted to 6 product precipitated. The precipitate was filtrated off yielding 10.1 g of the title product.
LC/MS(ES+) m/z [MH]+=406.3
1H-NMR (300 MHz, CDCl3) δ: 8.78 (s, 1H); 8.57 (d, 1H); 7.83 (dd, 1H); 7.57 (d, 1H); 7.38-7.27 (m, 5H); 4.60 (s, 2H); 4.48 (s,2H); 4.39 (q, 2H); 3.82-3.80 (m, 2H); 3.72-3.69 (m, 2H); 1.59 (t, 3H)
13C-NMR (75 MHz, CDCl3) δ: 177.79; 166.76; 148.14; 138.51; 138; 136.67; 130.67; 128.39; 126.49; 121.046; 116.53; 109.36; 87.87; 84.27; 73.36; 69.49; 69.49; 59.12; 49.8; 14.66
Hydrogenation of Intermediate 42 a (10 g, 0.025 mol) in MeOH (120 mL) with addition of 10% Pd/C (3 g) at 5 bar for 48 hours yilded the titled product (6.45 g).
LC/MS(ES+) m/z [MH]+=320.29
1H-NMR (300 MHz, DMSO) δ: 9.02 (s, 1H); 8.19 (s, 1H); 7.98 (d, 1H); 7.84 (d, 1H); 4.62 (q, 2H); 3.51 (t, 2H); 3.43-3.39 (m,4H); 2.86 (t, 2H); 1.95-1.85 (m, 2H); 1.43 (t, 3H)
13C-NMR (75 MHz, DMSO) δ: 177.62; 166.34; 148.69; 140.52; 137.54; 135.14; 125.65; 124.73; 118.24; 108; 72.18; 69.38; 60.37; 49.10; 31.21; 30.85; 14.76
Using the similar procedure to that described in Intermediate 32, starting from Intermediate 42b (6.4 g, 0.02 mol) Intermediate 42c (7.2 g) was obtained.
LC/MS(ES+) m/z [MH]+=373.2
1H-NMR (300 MHz, DMSO-d6) δ: 8.57 (s, 1H); 8.09 (d, 1H); 7.68 (d, 1H); 7.59 (dd, 1H); 4.34 (q, 2H); 3.62 (t, 2H); 3.57-3.59 (m, 2H); 3.49-3.51 (m, 2H); 3.42 (t, 2H); 2.76 (t, 2H); 2.75 (t, 2H), 1.34 (t, 3H).
13C-NMR (75 MHz, DMSO-d6) δ: 175.38; 167.18; 146.69; 137.15; 136.97; 132.59; 128.09; 125.08; 119.24; 116.53; 110; 69.55; 69.32; 69.29; 65.19; 47.32; 31.01; 30.75; 14.42
Using the similar procedure to that described in Intermediate 33, starting from Intermediate 42c (7.2 g, 0.019 mol) Intermediate 42d (4.2 g) was obtained.
LC/MS(ES+) m/z [MH]+=392.2
1H-NMR (300 MHz, DMSO-d6) δ: 9.02 (s, 1H); 8.18 (d, 1H); 7.98 (s, 1H); 7.85 (dd, 1H); 4.60 (q, 2H); 3.47-3.53 (ov, 4H); 3.62 (m, 2H); 3.41 (t, 2H); 2.85 (t, 2H); 2.45 (t, 2H), 1.87 (m, 2H), 1.43 (t, 3H).
13C-NMR (75 MHz, DMSO-d6) δ: 177.41; 172.51; 166.09; 148.43; 140.26; 137.32; 134.94; 125.40; 124.51; 117.99; 107.42; 69.54; 69.34; 69.15; 66.15; 48.87; 34.66; 30.96; 30.52; 14.52.
Using the similar procedure to that described in Intermediate 41, starting from 1-cyclopropyl-6-iodo-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid ethyl ester (2.6 g, 6.8 mmol) Intermediate 43 (2.3 g) was obtained.
LC/MS(ES+) m/z [MH]+=355.93.
Using the similar procedure to that described in Intermediate 42a, using Intermediate 43 (2.3 g, 6.5 mmol) and Intermediate 40 (2.47 g, 13 mmol) Intermediate 44a (2.1 g) was obtained.
LC/MS(ES+) m/z [MH]+=418.2
Using the similar procedure to that described in Intermediate 42b, starting from Intermediate 44a (2.1 g, 5 mmol) Intermediate 44b (1.5 g) was obtained.
LC/MS(ES+) m/z [MH]+=332.08
Using the similar procedure to that described in Intermediate 32, starting from Intermediate 44b (1.34 g, 4 mmol) Intermediate 44c (1.83 g) was obtained.
LC/MS(ES+) m/z [MH]+=385.03
Using the similar procedure to that described in Intermediate 33, starting from Intermediate 44c (1.33 g, 3.5 mmol) Intermediate 44d (0.64 g) was obtained.
LC/MS(ES+) m/z [MH]+=404.11
Using the similar procedure to that described in Intermediate 41, starting from 6-iodo-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid ethyl ester (317 mg, 0.85 mmol) Intermediate 45 (224 mg) was obtained.
LC/MS(ES+) m/z [MH]+=315.97.
Using the similar procedure to that described in Intermediate 42a, using Intermediate 45 (6 g, 0.02 mol) and Intermediate 40 (7.6 g, 0.04 mol) Intermediate 46a (2.2 g) was obtained.
LC/MS(ES+) m/z [MH]+=378.12.
Using the similar procedure to that described in Intermediate 42b, starting from Intermediate 46a (2 g, 5 mmol) Intermediate 46b (1 g) was obtained.
LC/MS(ES+) m/z [MH]+=292.01.
Using the similar procedure to that described in Intermediate 32, starting from Intermediate 46b (0.933 g, 3.2 mmol) Intermediate 46c (970 mg) was obtained.
LC/MS(ES+) m/z [MH]+=345.09.
Using the similar procedure to that described in Intermediate 33, starting from Intermediate 46c (970 mg, 2.8 mmol) Intermediate 46d (0.95 g) was obtained.
LC/MS(ES+) m/z [MH]+=364.09.
In the solution of 6-iodo-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid ethyl ester (4 g, 0.0117 mol) and K2CO3 (3.22 g, 0.023 mol) in DMF (40 mL), allyl-bromide (1.48 mL, 0.0176 mol) was added and stirred at 65° C. for 1 hour. Reaction mixture was diluted with water (50 mL) and the Intermediate 47a was precipitated yielding 3.3 g the title product.
LC/MS(ES+) m/z [MH]+=383.98
1H-NMR (300 MHz, DMSO-d6) δ: 8.71 (s, 1H); 8.49 (d, 1H); 8.04 (dd, 1H); 7.53 (d, 1H); 6.00-6.07 (m, 1H); 5.11 (dd, 1H); 5.24 (dd, 1H); 5.03 (d, 2H); 4.23 (q, 2H); 1.29 (t, 3H)
13C-NMR (75 MHz, DMSO-d6) δ: 171.60; 164.42; 149.94; 140.71; 138.68; 134.87; 132.65; 129.93; 120.30; 118.06; 110.82; 90.36; 60.02; 54.69; 14.44.
Using the similar procedure to that described in Intermediate 36a, starting from Intermediate 47a (3.3 g, 8.6 mmol) Intermediate 47b (2.7 g) was obtained.
LC/MS(ES+) m/z [MH]+=355.92.
Using the similar procedure to that described in Intermediate 42a, using Intermediate 47b (2.7 g, 76 mmol) and Intermediate 40 (2.9 g, 15.2 mmol) Intermediate 48a (2.7 g) was obtained.
LC/MS(ES+) m/z [MH]+=418.12.
Using the similar procedure to that described in Intermediate 42b, starting from Intermediate 48a (1.1 g, 2.6 mmol) Intermediate 48b (740 mg) was obtained.
LC/MS(ES+) m/z [MH]+=334.10.
Using the similar procedure to that described in Intermediate 32, starting from Intermediate 48b (740 mg, 2.2 mmol) Intermediate 48c (900 mg) was obtained.
LC/MS(ES+) m/z [MH]+=387.16.
Using the similar procedure to that described in Intermediate 33, starting from Intermediate 48c (900 mg, 2.3 mmol) Intermediate 48d (950 mg) was obtained.
LC/MS(ES+) m/z [MH]+=406.16.
Using the similar procedure to that described in Intermediate 9b, starting from Intermediate 23 (2.87 g, 14 mmol) Intermediate 49a (3 g) was obtained.
Using the similar procedure to that described in Intermediate 9c, starting from 1-ethyl-6-iodo-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid (2 g, 5.8 mmol) and Intermediate 49a (1.7 g, 6.9 mmol) Intermediate 49b (3.9 g) was obtained.
LC/MS(ES+) m/z [MH]+=458.5.
Using the similar procedure to that described in Intermediate 9d, starting from Intermediate 49b (3.9 g, 8.5 mmol) crude Intermediate 49c was obtained. After purification by column chromatography (eluent: DCM:MeOH:NH3=90:15:1.5) the title product was obtained (0.9 g)
LC/MS(ES+) m/z [MH]+=359.
Using a similar procedure as described in Intermediates 6A and 6B starting from 7-chloro-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid (8.65 g, 30.8 mmol) and 2-(2-aminoethylamino)ethanol (5 eqv.) mixture of (8.5 g) chloro and fluoro derivative was obtained.
To the mixture of Intermediates 50A and B (2.23 g) in CHCl3 (40 mL) formaldehyde (2 eq, 355 μL) and formic acid (3.7 eq, 892 μL) were added and heated in a screw cap vial at 60° C. for 4 hours. The solvent was evaporated, to the residue water (30 mL) and ethyl acetate (30 mL) were added, pH adjusted to 9 and water layer washed with ethyl acetate. Than pH of water layer was adjusted to pH 6-7 with 1N HCl yielding Intermediate 51A (389 mg) as a yellow precipitate. LC-MS [ES+] m/z: 380.
1H-NMR (300 MHz, DMSO-d6) δ: 8.6; 8.3; 7.4; 6.3; 5.2;3.8; 3.7; 3.6; 3.3; 3.1; 2.7; 1.3;1.2.
13C-NMR (75 MHz, DMSO-d6) δ: 176.7; 166.3; 146.1; 142.6; 132.7; 126.9; 125.6; 119.4; 106.5; 103.2;57.8;53.9;40.8;36.0.
Intermediate 51B was isolated from a mother liquor as a yellow solid (1.657 g).
Using the similar procedure to that described in Intermediate 32, starting from Intermediate 51a (2.68 g, 7 mmol) Intermediate 52a (1.76 mg) was obtained.
LC/MS(ES+) m/z [MH]+=433.
Using the similar procedure to that described in Intermediate 33, starting from Intermediate 52a (1.7 g, 4 mmol) the title compound (730 mg) was obtained.
LC/MS(ES+) m/z [MH]+=452.
1H-NMR (500 MHz, DMSO-d6) δ: 8.6; 8.3; 7.5; 6.2; 3.8; 3.7; 3.6; 2.9; 2.8; 1.3; 1.2.
To a solution of diethylene glycol (19 ml, 0.2 mol, 20 eq.) and DMSO (15 ml) slowly KO-t-Bu (4.5 g, 0.4 mol, 4 eq.) was added. The reaction mixture was warmed up to 90° C. and 1-tert.-butyl-7-chloro-6-fluoro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid (3 g, 0.01 mol) was added slowly. The mixture was then stirred at 105° C. for 6 hours and then left over night at R.T. Than water (70 ml) was added, pH was adjusted to 3.5 and placed into refrigerator, the product precipitated. The precipitate was filtered off yielding 1.1 g of the title product.
LC/MS(ES+) m/z [MH]+=383.8.
Using the similar procedure to that described in Intermediate 32, starting from Intermediate 53 (1 g, 2.6 mmol) Intermediate 54a (780 mg) was obtained.
LC/MS(ES+) m/z [MH]+=436.9.
Using the similar procedure to that described in Intermediate 33, starting from Intermediate 54a (700 mg, 1.5 mmol) the title compound (430 mg) was obtained.
LC/MS(ES+) m/z [MH]+=399.8.
To a mixture of 1-tert.-butyl-7-chloro-6-fluoro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid (3 g, 10 mmol) in 1-methyl-2-pyrrolidone (20 ml) 2-(2-amino-ethoxy)-ethanol (5 ml, 50 mmol, 5 eq) was added and the reaction mixture was stirred at 110° C. for 24 hours. The reaction mixture was diluted with H2O (20 ml) and CH2Cl2 (50 ml) and pH was adjusted to 13. The aqueous layer was extracted with CH2Cl2 (2×30 ml) and pH was adjusted to 3.5. After 5 minutes in the refrigerator precipitation occurred. The precipitate was filtered off yielding 1.83 g of the title compounds (according to LC-MS a mixture of Intermediate 55A and Intermediate 55B in a ratio 2:1). The filtrate was left at 5° C. for 1 hour giving additional amount (0.75 g ) of the Intermediate 55A and Intermediate 55B in a ratio 1:1.
LC/MS(ES+) m/z [MH]+=382.8 (Intermediate 55A)
LC/MS(ES+) m/z [MH]+=366.4 (Intermediate 55B)
Using the similar procedure to that described in Intermediate 32, starting from a mixture of Intermediate 55A and Intermediate 55B (1.5 g, 3.9 mmol) a mixture of Intermediate 56A and Intermediate 56B (1.3 g) was obtained in a ratio 2:1.
LC/MS(ES+) m/z [MH]+=435.9 (Intermediate 56A)
LC/MS(ES+) m/z [MH]+=419.5 (Intermediate 56B)
Using the similar procedure to that described in Intermediate 33, starting from a mixture of Intermediate 56A and Intermediate 56B (1.3 g, 2.98 mmol) a mixture of Intermediate 56C and Intermediate 56D (850 mg) was obtained in a ratio 3:1.
LC/MS(ES+) m/z [MH]+=398.8 (Intermediate 56C)
LC/MS(ES+) m/z [MH]+=382.3 (Intermediate 56D)
A mixture of potassium carbonate (10.4 g, 74.7 mmol) and 6-bromoquinolone-3-carboxylic acid (10.0 g, 37.3 mmol) in dimethylformamide (100 mL) was heated to 40° C. under argon for 10 minutes, iodoethane (12 mL, 150 mmol) was then added. After 14 h the mixture was cooled and the DMF evaporated. The residue was treated with water (40 mL), cooled to 5° C. and filtered under vacuum. The resultant cream-coloured solid was dried under vacuum to yield the title compound (11.2 g).
1H-NMR (D6-DMSO) δ: 1.41(3H, t, J=7.12 Hz); 1.54(3H, J=7.24 Hz); 4.24(2H, q, J=7.24 Hz); 4.40(2H, q, J=7.12 Hz); 7.34(1H, d, J=9 Hz); 7.76(1H, d×d, J=2.4 & 9 Hz); 8.65(1H, d, J=2.4 Hz), 8.49(1H, s).
A mixture of 1,1-dimethylethyl (2-oxoethyl)carbamate (5.0 g, 30 mmol), potassium carbonate (4.0 g, 30 mmol) and Intermediate 57a (5.0 g, 1.5 mmol) in DMSO (50 mL) was heated at 90° C. After 16 h the reaction was cooled and poured into water (200 mL), the organic material extracted into dichloromethane (2×50 mL). The combined organic layers were dried and evaporated to yield a brown solid. Chromatography over silica gel eluting with dichloromethane containing an increasing concentration of methanol/ammonium hydroxide gave the title compound as a white solid.
ESMS m/z [MH]+=421.2.
A solution of Intermediate 57b (1.04 g, 2.47 mmol) in trifluoroacetic acid (25 mL) was stirred at room temperature. After 15 minutes the excess trifluoroacetic acid was evaporated to yield the title compound as a light brown solid (1.32 g).
ESMS m/z [MH]+=321.2.
A mixture of Intermediate 57c (1.00, 2.47 mmol), 1,1-dimethylethyl (2-oxoethyl)carbamate (0.47 g, 2.96 mmol) and sodium acetate (0.51 g, 6.8 mmol) in 1% acetic acid in methanol (20 mL) was allowed to stir for 10 mins at room temperature before sodium cyanoborohydride (0.31 g, 4.94 mmol) was added. After 20 h an additional batch (0.18 g, 1.13 mmol) of the aldehyde was added. After 3 days the reaction evaporated and the residue chromatographed over silica gel eluting with 0-10% [9:1 methanol/20 M ammonia] in dichloromethane to give the desired compound contaminated with the bis-alkylated product (0.80 g). Reverse phase chromatography over C18 silica eluting with 0.5% aqueous formic acid/0.5% formic acid acetonitrile gave title compound (0.42 g).
ESMS m/z [MH]+=464.1.
To a mixture of Intermediate 57d (0.356 g, 0.617 mmol) and potassium carbonate (0.13 g, 0.93 mmol) in dry DMF (8 mL) was added iodomethane (0.043 mL, 0.69 mmol). After stirring at room temperature for 48 h the solvent was evaporated and the residue chromatographed over silca gel eluting with 0-10% [9:1 methanol/20 M ammonia] in dichloromethane to give the title compound (0.147 g).
ESMS m/z [MH]+=478.2.
Intermediate 57e (0.132 g, 0.27 mmol) in dioxan (5 mL), water (1 mL) and 2M sodium hydroxide (1.3 mL) were stirred at room temperature. After 20 h solid carbon dioxide was added, pH 9, and the solvent evaporated to yield the title compound a white solid (0.104 g).
ESMS m/z [MH]+=450.2.
A solution of Intermediate 57f (0.104 g, 0.23 mmol) in trifluoroacetic acid (5 mL) was stirred at room temperature. After 15 mins the excess trifluoroacetic acid was evaporated and the resultant crude product subjected to reverse phase chromatography over C18 silica eluting with 1% aqueous trifluoroacetic acid/acetonitrile yield the title compound as a colourless gum (0.134 g)
ESMS m/z [MH]+=350.
A mixture of 9-fluoro-5-(RS)-methyl-1-oxo-6,7-dihydro-1H,5H-pyrido[3,2,1-ij]quinoline-2-carboxylic acid (0.13 g, 0.5 mmol) {2-[(2-aminoethyl)oxy]ethyl}amine (0.25 mL, 2.4 mmol) in N-methyl pyrrolidinone (0.25 mL) was subjected to microwave irradiation resulting in an internal temperature of 200° C. After 0.5 h the mixture was cooled and purified by mass directed autoprep eluting with formic acid/water/acetonitrile to yield the title compound as a yellow oil (0.146 g).
ESMS m/z [MH]+=346.4.
A mixture of ethyl 1-ethyl-6-hydroxy-4-oxo-1,4-dihydro-3-quinolinecarboxylate (0.261 g, 1.0 mmol), potassium carbonate (0.345 g, 2.5 mmol) and iodoethanol (0.078 mL, 1.0 mmol) in DMF (3 mL) was heated at 80° C. after which time a further portion of potassium carbonate (0.345 g) and iodoethanol (0.078 mL) was added. Heating was continued for 16 h. The mixture was cooled, concentrated and the residue chromatographed over silica gel eluting with with 0-20% methanol in ethyl acetate to give the title compound (0.144 g).
ESMS m/z [MH]+=262.2.
A suspension of Intermediate 59a (0.117 g, 0.38 mmol) in a mixture of dichloromethane (5 mL) and triethylamine (0.212 mL) was treated with methanesulfonyl chloride (0.065 mL, 0.845 mmol). After 1 h the mixture was concentrated to yield the crude methanesulfonate ester which was used without further purification.
ESMS m/z [MH]+=384.3.
Intermediate 59b (0.147 g, 0.38 mmol) was suspended in DMF (5 mL) and treated with sodium iodide (0.058 g, 0.384 mmol), 1,1-dimethylethyl (2-mercaptoethyl)carbamate (0.047 mL, 0.576 mmol) and potassium carbonate (0.0.265 g, 1.42 mmol). After 4.5 h at room temperature a further portion of 1,1-dimethylethyl (2-mercaptoethyl)carbamate (0.097 mL, 1.18 mmol), potassium carbonate (0.08 g, 0.57 mmol) and DMSO (5 mL) was added. After stirring overnight the mixture diluted with dichloromethane and filtered. The filtrate was evaporated and subjected to freeze-drying to remove the DMSO. The residue was purified by mass-directed autoprep eluting with formic acid/water/acetonitrile to yield the title compound (0.113 g).
ESMS m/z [MH]+=465.3.
To a solution of Intermediate 59c (0.113 g, 0.24 mmol) in THF (3 mL) was added 2M sodium hydroxide (0.134 mL, 0.26 mmol). After stirring at 50° C. for 18 h the mixture was cooled and treated with solid carbon dioxide. Evaporation yielded the title compound (0.130 g).
ESMS m/z [M+H]+=437.3.
To a solution of Intermediate 59d (0.130 g, 0.24 mmol) in dichloromethane (5 mL) was added trifluoroacetic acid (2 mL). After stirring for 0.5 h the mixture was concentrated to yield the title compound (0.11 g).
ESMS m/z [M+H]+=337.3.
A solution of 1-ethyl-6-iodo-4-oxo-1,4-dihydro-3-quinolinecarboxylic acid ethyl ester (4.95 g, 15.6 mmol) and copper iodide (0.03 g) in dry acetonitrile (120 mL) and triethylamine (76 mL) was deoxgenated by purging with argon for 20 mins. The resultant mixture was treated with bis-tri-phenylphosphino palladium dichloride (0.13 g) and 1,1-dimethylethyl [2-(propyloxy)ethyl]carbamate (4.05 g, 20.3 mmol). After 3 h the mixture was concentrated and the residue chromatographed over silica gel eluting with with 0-4% [9:1 methanol/20 M ammonia] in dichloromethane to give the title compound (6.71 g).
ESMS m/z [M+H]+=443.2.
A mixture of Intermediate 60a (6.76 g, 15.1 mmol) and 10% palladium charcoal (0.7 g) suspended in ethanol (250 mL) was hydrogenated at atmospheric pressure and room temperature. After 4 h the reaction was filtered and the solvent evaporated to give the title compound as a yellow foam (5.95 g).
ESMS m/z [M+H]+=447.2.
A solution of Intermediate 60b (1.07 g, 2.40 mmol) in dioxan (35 mL) and ethanol (10 mL) was treated with 1M sodium hydroxide (27 mL). After 4 h solid carbon dioxide was added the mixture was concentrated to yield the title compound as a white solid (1.0 g).
ESMS m/z [M+H]+=419.2.
A mixture of Intermediate 60c and trifluoroacetic acid was stirred at room temperature. After 0.5 h the solvent was evaporated and the residue subjected to reverse phase chromatography over C18 silica eluting with 1% trifluoroacetic acid/water/acetonitrile. The resultant oil was dissolved in methanol and precipitated with diethyl ether to yield the title compound as a white solid (0.43 g).
ESMS m/z [M+H]+=319.2.
To a stirred mixture of 1,4-dihydro-6-iodo-4-oxo-quinoline-3-carboxylic acid ethyl ester (8.55 g, 23.0 mmol), triethylamine (4.82 mL, 34.6 mmol), and 2-{[2-(ethenyloxy)ethyl]oxy}ethanol (6.29 mL, 46.1 mmol) in toluene (25 mL) was added 10% palladium on charcoal (0.245 g) and the mixture heated to 100° C. After 3 h the solvent was removed in vacuo to give a residue which was taken up in ethyl acetate and filtered through celite. The filtrate was washed with an aqueous solution of sodium dihydrogen phosphate, dried (Na2SO4), filtered, and concentrated in vacuo to give a mixture containing 1-ethyl-6-[2-({2-[(2-hydroxyethyl)oxy]ethyl}oxy)ethenyl]-4-oxo-1,4-dihydro-3-quinolinecarboxylic acid ethyl ester as a brown oil (12.13 g), ESMS m/z 376.3 [M+H]+ which was used without further purification. A solution of this material in ethyl acetate (50 mL), and dichloromethane (100 mL) was hydrogenated over 10% palladium on charcoal (2 g) at atmospheric pressure, with additional 10% palladium on charcoal (5 g) added during the course of the reaction. After 72 h the catalyst was removed by filtration, and the filtrate concentrated in vacuo to give a residue which was purified by flash chromatography (silica gel, 0-7% methanolic ammonia [2M] in dichloromethane) to give a mixture (4.21 g) which was taken up dichloromethane (140 mL) and hydrogenated over 10% palladium on charcoal (2 g) at atmospheric pressure for 14 h. Further 10% palladium on charcoal (2.6 g) was then added and the mixture hydrogenated at 45 p.s.i. for 29 h. The mixture was then filtered and concentrated in vacuo to give a residue which was purified by flash chromatography (silica gel, 0-6% methanolic ammonia [2M] in dichloromethane) to give a mixture which was taken up in ethyl acetate, washed with an aqueous solution of sodium dihydrogen phosphate, dried (Na2SO4), filtered, and concentrated in vacuo to give the title compound as a yellow/brown oil (2.15 g).
ESMS m/z [M+H]+=378.2.
A solution of Intermediate 61a (1.58 g, 4.17 mmol) in dichloromethane (30 mL) at 0° C. was treated with triethylamine (0.99 mL, 7.10 mmol), followed by methanesulfonyl chloride (0.42 mL, 5.43 mmol), and the mixture stirred for 2 h. Saturated sodium hydrogen carbonate solution (20 mL) was then added and the organic solvent removed in vacuo. The aqueous mixture was adjusted to pH 11 by the addition of an aqueous solution of sodium carbonate, then extracted with ethyl acetate. The organic layers were combined, dried (Na2SO4), filtered, and concentrated in vacuo to give the title compound as a pale yellow gum (2.04 g).
ESMS m/z [M+H]+=456.3.
A solution of Intermediate 61b (1.90 g, 4.17 mmol) in dichloromethane (20 mL) was treated with 1,1,3,3-tetramethylguanidinium azide (1.95 g, 12.3 mmol) and stirred at room temperature for 21 h, then at reflux for 27 h. Additional 1,1,3,3-tetramethylguanidinium azide (0.30 g, 1.90 mmol) was added, and the mixture heated at reflux for a further 8 h. The mixture was concentrated in vacuo to give a residue which was taken up in ethyl acetate, washed with water, dried (Na2SO4), filtered, and concentrated in vacuo to give a residue which was purified by flash chromatography (silica gel, 0-6% methanolic ammonia [2M] in dichloromethane) to give the title compound as a colourless gum (1.49 g).
ESMS m/z [M+H]+=403.3.
A solution of Intermediate 61c (1.47 g, 3.64 mmol) in 1,4-dioxane (20 mL) was treated with 2 N aqueous sodium hydroxide (3.64 mL). After 20 h the mixture was concentrated in vacuo to give a residue which was taken up in water, and treated with excess solid carbon dioxide. The resulting precipitate was removed by filtration and dried in vacuo to give the title compound as a cream solid (1.09 g).
ESMS m/z [M+H]+=375.2.
A solution of Intermediate 61d (1.07 g, 2.87 mmol) in tetrahydrofuran (30 mL) was treated with triphenylphosphine (1.50 g, 5.73 mmol) and stirred for 20 min. Water (2 mL) was added and stirring continued for 21 h. The solvent was then removed in vacuo to give a residue which was taken up in hydrochloric acid (2 N) and washed with ethyl acetate. The aqueous solution was concentrated in vacuo to give a residue which was taken up in water and the solution lyophilised to give the title compound as a cream solid (0.63 g).
ESMS m/z [M+H]+=349.3.
The title compound (1.0 g) was prepared according to procedure described for Intermediate 14 starting from 2′-O-acetyl-O-(9E)-acetylhydroximino erythromycin A.
ESMS m/z [M+H]+=803.5.
The title compound (1.43 g) was prepared according to procedure described for Intermediate 14 starting from 2′-O-acetyl-(9E)-methoxymethyloximino-erythromycin A.
ESMS m/z [M+H]+=877.7.
To the solution of 4″acriloyl-azitromycine (0.4916 g, 0.613 mmol) in acetonitrile (20 mL) were added Intermediate 5 (0.9 mg, 2,45 mmol), triethylamine (0.273 mL) and water (0.685 mL) and suspension was heated at 90° C. for 24 hours. The solvent was evaporated and the residue was extracted with DCM and water (2×50 mL). Organic layer was washed with NaCl and NaHCO3 (2×50 mL), dried over K2CO3 and evaporated in vacuum. The product was precipitated from EtOAc/n-hexane yielding product (0.35 g). Product (0.17 g) was purificated by column chromatography (DCM:MeOH:NH3=90:3:0.5) yielded the title product (0.05 g).
MS (ES+) m/z: [MH]+=1170.6
1H-NMR(500 MHz, CDCl3) δ: 8.57 (1H, Q), 8.53 (1H, Q), 7.68 (1H, Q), 7.41 (1H, Q), 5.21 (1H, H-1″), 4.70 (2H, H-13+H-4″), 4.56 (1H, H-1′), 4.38 (3H, Q+H-5″), 4.25(3H, Q+H-3), 3.82 (1H, H-5′), 3.68 (1H, H-11), 3.61 (1H, H-5), 3.53 (2H, CH2), 3.31 (3H, H-3″OMe), 3.25 (1H, H-2″), 2.71 (12H, H-2, H-10, CH2, 4×CH2-P), 2.54 (4H, H-9a, H-3′, CH2), 2.38 (1H, H-2″a), 2.31 (6H, 3′NMe2), 2.02 (3H, H-4, H-8, H-9b), 1.91 (1H, H-14a), 1.75 (1H, H-7a), 1.68 (1H, H-4′a), 1.62 (1H, H-2″b), 1.55 (3H, Q), 1.48 (1H, H-14b), 1.41 (3H, Q), 1.30 (3H, 6Me), 1.28 (1H, H-2′b), 1.25 (1H, H-7b), 1.19 (6H, 5′Me+2Me), 1.18 (3H, 5″Me), 1.14 (3H, 3″Me), 1.10 (3H, 12Me), 1.09 (3H, 10Me), 1.04 (3H, 4Me), 0.89 (6H, 8Me+14Me)
13C-NMR(75 MHz, CDCl3) δ: 178.99, 173.57, 172.02, 165.67, 148.56, 138.05, 135.40, 131.57, 129.16, 120.12, 115.69, 111.57, 102.35, 85.98, 84.13, 83.21, 78.81, 77.67, 77.48, 74.24, 73.65, 73.55, 73.06, 70.92, 70.11, 67.84, 65.70, 63.02, 62.57, 61.00, 53.46, 52.80, 52.11, 49.43, 48.93, 47.71, 45.23, 42.29, 42.20, 40.39, 36.23, 34.96, 32.50, 29.70, 29.01, 27.60, 26.80, 21.98, 21.89, 21.35, 21.31, 17.83, 16.22, 14.54, 14.50, 14.45, 11.29, 9.03, 7.34.
Hydrogenation of Example 1 (0.25 mg) in methanol (20 mL) with addition of 10% Pd/C (100 mg) at 5 bar for 20 hours yielded the title product.
MS (ES+) m/z: [MH]+=1174.8
13C-NMR(75 MHz, DMSO) δ: 177.61, 173.24, 172.11, 165.24, 164.40, 163.56, 158.99, 154.18, 148.98, 139.37, 137.31, 133.76, 129.03, 125.90, 116.94, 110.30, 102.61, 94.91, 83.91, 78.45, 77.97, 76.89, 75.46, 74.11, 73.18, 72.99, 71.03, 69.18, 67.28, 65.40, 62.73, 62.00, 53.13, 49.33, 48.72, 45.13, 72.28, 42.20, 40.86, 40.82, 36.29, 34.84, 32.99, 32.73, 30.69, 28.47, 27.98, 25.93, 22.61, 22.32, 21.48, 21.24, 18.29, 18.22, 15.16, 14.95, 14.85, 11.48, 9.50, 7.30.
Using the procedure of Example 1, Intermediate 5 and Intermediate 20 gave the title compound.
MS (ES+) m/z: [MH]+=1169.9
1H-NMR(500 MHz, CDCl3) δ: 8.58 (1H, Q), 8.48 ((1H, Q), 7.68(1H, Q), 7.39 (1H, Q), 5.07 (1H, H-13), 4.98 (1H, H-1″), 4.68 (1H, H-4″), 4.60 (1H, H-1′), 4.39 (2H, CH2-Q), 4.34 (1H, H-5″), 4.25 (2H, CH2-Q), 3.77 (1H, H-3), 3.76 (2H, H-5′+H-11), 3.65 (1H, H-5), 3.53 (2H, CH2), 3.30 (3H, 3″OMe), 3.22 (1H,H-2′), 3.03 (3H, 6OMe), 2.98 (1H, H-10), 2.91 (1H, H-2), 2.74 (10H, CH2+4×CH2—P), 2.57 (4H, CH2+H-8+H-3′), 2.40 (1H, H-2″a), 2.35 (6H, 3′NMe2), 1.94 (1H, H-4), 1.89 (1H, H-14a), 1.83 (1H, H-7a), 1.70 (1H, H-4′a), 1.65 (1H, H-2″b), 1.61 (1H, H-7b), 1.55 (3H, CH3-Q), 1.47 (1H, H-14b), 1.41 (3H, CH3-Q), 1.37 (3H, 6Me), 1.24 (1H, H-4′b), 1.20 (3H, 5′Me), 1.19 (3H, 2Me), 1.15 (3H, 5″Me), 1.13 (3H, 3″Me), 1.12 (6H, 8Me+10Me), 1.10 (3H, 4Me), 0.84 (3H, 15Me).
13C-NMR(75 MHz, CDCl3) δ: 175.11, 172.97, 171.32, 165.00, 147.97, 137.45, 134.76, 130.99, 128.55, 119.49, 115.07, 110.97, 101.38, 95.41, 85.34, 83.53, 79.901, 78.08, 77.67, 77.38, 76.02, 73.70, 72.21, 70.47, 68.51, 67.13, 64.78, 62.42,60.39,39.74, 38.61, 38.16, 36.62, 34.61, 31.93, 29.10, 21.25, 20.54, 20.45, 19.11, 17.78, 17.45, 15.38, 13.93, 13.84, 13.53, 11.77, 10.00, 8.58.
Using the procedure of Example 1, Intermediate 5 and Intermediate 14 gave the title compound.
MS (ES+) m/z: [MH]+=1156.5
1H-NMR(500 MHz, CDCl3) δ: 8.77 (1H, Q), 8.59 (1H, Q), 7.85 (1H, Q), 7.59 (1H, Q), 5.15 (1H, H-1″), 4.71 (1H, H-4″), 4.67 (1H, H-13), 4.60 (1H, H-1′), 4.40 (1H, H-5″), 4.39 (2H, CH2-Q), 4.37 (1H, H-3), 3.82 (1H, H-5′), 3.63 (1H, H-5), 3.58 (3H, 11OM), 3.55, (2H, CH2),3.40 (1H, H-11), 3.32 (3H, 3″OMe), 3.29 (1H, H-2′), 2.74 (1H, H-2), 2.68 (10H, CH2+4×CH2—P), 2.55 (3H, H-9a+CH2), 2.38 (1H, H-2″a), 2.07 (1H, H-9b), 2.02 (2H, H-4+H-8), 1.92 (1H, H-14a), 1.68 (1H, H-7a), 1.56 (3H, CH2-Q+H-2″a), 1.43 (1H, H-14b), 1.31 (1H, H-7b), 1.25 (3H, 6Me), 1.21 (6H, 2Me+5′Me), 1.15 (3H, 5″Me), 1.14 (3H, 3″Me), 1.11(3H, 12Me), 1.03 (6H, 4Me+10Me), 0.91(3H, 8Me), 0.87 (3H, 15Me).
13C-NMR(75 MHz, CDCl3) δ: 177.91, 177.88, 172.06, 166.80, 147.98, 138.35, 136.78, 130.64, 126.59, 121.57, 116.45, 109.39, 101.99, 94.79, 87.41, 85.01, 83.77,83.47, 78.96, 78.01, 77.87, 74.42, 73.26, 73.08, 71.09, 70.96, 67.57, 65.52, 62.81, 62.70, 62.13, 53.42, 52.81, 52.05, 49.80, 49.45, 47.64, 45.44, 42.78, 42.55, 35.94, 35.11, 32.48, 29.70, 27.67, 26.75, 22.23, 21.77, 21.70, 21.35, 17.75, 17.09, 14.70, 14.65, 11.30, 9.45, 7.25.
Using the procedure of Example 2, Example 4 gave the title compound.
MS (ES+) m/z: [MH]+=1161.5
1H-NMR(500 MHz, CDCl3) δ: 8.77 (1H, Q), 8.37 (1H, Q), 7.68 (1H, Q), 7.56 (1H, Q), 5.16 (1H, H-1″), 4.69 (2H, H-13+H-4″), 4.58 (1H, H-1′), 4.39 (4H, H-3+H-5″+CH2-Q), 3.79 (1H, H-5′), 3.61 (1H, H-5), 3.58 (3H, 11OMe), 3.40 (1H, H-11), 3.32 (4H, 3″OMe-H-2′), 2.83 (2H, CH2), 2.74 (3H, H-2+CH2), 2.68 (10H, 4×CH2—P+H-10+H-3′), 2.52 (3H, CH2+H-9a), 2.41 (1H, H-2″a), 2.36 (8H, 3′NMe2+CH2), 2.24 (3H, 9NMe), 2.07 (2H, H-8+H-9b), 2.00 (1H, H-4), 1.89 (3H, H-14a+CH2), 1.73 (2H, H-7a+H-4′a), 1.60(4H, CH3-Q+H-2″b), 1.47 (1H, H-14b), 1.28 (2H, H-7b+H-4′b), 1.26 (3H, 6Me), 1.20 (6H, 2Me+5′Me), 1.14 (3H, 5″Me), 1.13 (3H, 3″Me), 1.11 (3H, 12Me), 1.04 (6H, 4Me+10Me), 0.91 (3H, 8Me), 0.90 (3H, 15Me).
13C-NMR(75 MHz, CDCl3) δ: 178.39, 177.95, 172.04, 167.29, 147.44, 140.81, 137.49, 134.85, 126.66, 126.35, 116.31, 108.83, 102.23, 94.82, 85.06, 83.67, 78.97, 78.10, 77.88, 74.43, 73.22, 73.17, 71.08, 70.11, 67.51, 65.51, 62.83, 62.70, 62.15, 57.45, 53.48, 53.02, 52.81, 49.70, 49.45, 45.47, 42.77, 42.62, 40.45, 35.93, 35.14, 33.01, 32.54, 29.70, 28.18, 27.67, 26.75, 22.23, 21.78, 21.75, 21.36, 17.75, 17.12, 14.74, 14.67, 11.29, 9.37, 7.22.
Intermediate 7 (2.51 g, 5.7 mmol) was dissolved in 10 mL of DMF/4 Å, and cooled to 0° C. under N2 atmosphere. In this solution, EDAC×HCl (1.1 g, 5.7 mmol) was added and stirred for 5 min. Then, 2′-O-acetyl-roxythromycin (2.5 g, 2.84 mmol) diluted in 10 mL of DCM/4 Å, and DMAP (1.1 g, 8.55 mmol) was added and stirred for 24 h. In the reaction mixture 30 mL of EtOAc was added and it was extracted with 3×20 mL of H2O. The organic layers were washed with brine and evaporated affording 500 mg g of 2′-O-acetyl protected product which was dissolved in 100 mL MeOH and stirred at 40° C. for 24 h. MeOH was evaporated under reduced pressure. The residue was purified by column chromatography in (DCM-MeO—:NH3=90:5:0.5) yielded 250 mg of the title product.
MS (ES+) m/z: [MH]+=1258.84.
Using the procedure of Example 6, Intermediate 7 and 2′-O-acetyl-6-O-methyl-erythromycin A gave the title compound.
MS (ES+) m/z: [MH]+=1169.79.
Using the procedure of Example 6, Intermediate 7 (1.7 g, 3.87 mmol), 2′-O-acetyl-azithromycin (6.1 g, 7.72 mmol), EDAC×HCl (1.47 g, 7.72 mmol) and DMAP (943 mg, 7.72 mmol) gave the title compound (500 mg).
MS (ES+) m/z: [MH]+=1169.37.
1H-NMR (500 MHz, CDCl3) δ: 8.73 (s, 1H), 8.05 (s, 1H), 7.55 (s, 1H), 5.18 (d, 1H), 5.04 (t, 1H), 4.70 (d, 2H), 4.69 (d, 2H), 4.55 (d, 1H), 4.42 (m, 1H), 4.43 (d, 1H), 4.25 (s, 1H), 3.80 (m, 2H), 3.79(m, 2H), 3.78 (m, 2H), 3.76 (m, 2H), 3.68 (m, 2H), 3.60 (m, 2H), 3.57 (q, 3H), 3.52 (q, 2H), 3.37 (m,3H), 3.31 (m, 2H), 2.74 (m, 3H), 2.70 (m, 2H), 2.68(m, 2H), 2.63 (m, 3H), 2.55 (m, 2H), 2.45 (m, 2H), 2.35 (m, 2H), 2.31 (q, 2H), 2.08 (m, 1H), 2.07 (m, 2H), 2.05 (m, 2H), 1.91 (q, 1H), 1.78 (d, 2H), 1.76 (d, 2H), 1.74 (d, 1H), 1.62 (d, 1H), 1.39 (q, 2H), 1.28 (q, 2H), 1.26 (m, 2H), 1.20 (m, 3H), 1.21 (m, 2H), 1.12 (d, 3H), 1.11 (m, 3H), 1.10 (d, 4H), 1.08 (d, 2H), 1.04 (d, 2H), 0.91 (m, 3H).
13C-NMR(75 MHz, CDCl3) δ: 178.29, 176.95, 170.72, 166.70, 145.33, 142.39, 132.08, 127.03, 125.71, 117.48, 107.06, 104.03, 101.62, 94.05, 82.62, 78.35, 77.09, 76.87, 76.45, 76.02, 73.67, 73.05, 73.01, 72.36, 70.36, 69.88, 69.81, 69.47, 68.29, 67.16, 66.10, 65.00, 62.38, 61.95, 48.84, 44.57, 42.72, 41.61, 41.51, 39.83, 35.69, 34.76, 34.54, 34.36, 30.99, 28.85, 26.93, 26.18, 22.06, 21.38, 21.19, 20.71, 20.58, 17.19, 15.60, 13.96, 13.52, 10.69, 8.52, 7.52, 6.84,
Using the procedure of Example 6, Intermediate 7 and 2′-O-acetyl-11-O-methyl-azithromycin gave the title compound. Product was purified by column chromatography (eluent CH2Cl2-MeOH-NH3:90:15:1.5) and precipitated twice from EtOAc: n-hexane yielding 95.8% pure the title compound.
MS (ES+) m/z: [MH]+=1184.1.
To a solution of Example 9 (0.3 g, 0.25 mmol) in EtOAc (2.5 mL) acetic acid (0.032 mL, 0.56 mmol) was added under stirring in an ice bath. Addition of diisopropylether (15 mL) and n-hexane (30 mL) yielded 0.289g of precipitated acetate salt. (92.5% pure).
Example 8 (300 mg, 0.26 mmol) was dissolved in 20 mL of ethanol, 100 mg of 10% Pd/C was added and the mixture was stirred under H2 pressure (5 bar) for 15 hours.
Column chromatography in (DCM-MeOH-NH3=90:5:0.5) yielded 200 mg of the title compound.
MS (ES+) m/z: [MH]+=1136.38.
To the solution of Intermediate 26 (100 mg, 0.25 mmol) and HBTU (91.04 mg, 0.24 mmol) in DMF (720 μL) was added DIPEA (61.6 μL, 0.35 mmol). Reaction mixture was stirred for 20 min and Intermediate 11 (147.12 mg, 0.18 mmol) was added in portions through 2-3 min. Stirring was continued for 3 days at room temperature. Then, 10 mL of H2O was added and extracted with 3×40 mL of EtOAc. The organic layer was washed with NaHCO3 (3×20 mL) and NaCl (3×20 mL). The organic layer was dried over Na2SO4 and evaporated in vacuum. The crude product was purified via SPE chromatography in system (CH2Cl2-MeOH—NH4OH=90:9:0.5) giving 24.17 mg of the title compound (purity 96.3%).
MS (ES+) m/z: [MH]+=1210.6
13C-NMR(125 MHz, CD3OD) δ: 5.7, 8.6, 10.15, 14.56, 20.37, 22.32, 23.31, 23.82, 23.86, 27.46, 27.71, 30.59, 30.87, 31.86, 32.87, 33.19, 35.09, 35.99, 36.76, 37.58, 40.54, 42.15, 43.04, 43.72, 46.53, 48.64, 48.81, 48.98, 49.15, 49.32, 49.49, 49.66, 62.54, 64.21, 64.94, 66.52, 68.47, 68.64, 68.67, 70.35, 70.67, 71.79, 74.56, 75.35, 77.85, 79.26, 81.07, 84.90, 86.65, 88.10, 96.39, 102.29, 103.62, 109.16, 120.41, 128.38, 131.44, 136.96, 154.98, 171.30, 174.54, 177.93, 179.42.
Using the procedure of Example 12, Intermediate 11 and 6-[2-(2-carboxy-ethoxy)-ethylamino]-7-chloro-1-cyclopropyl-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid gave the title compound.
MS (ES+) m/z: [MH]+=1209.1
13C-NMR(75 MHz, CD3OD) δ: 3.59, 6.43, 7.91, 8.05, 9.01, 11.93, 12.45, 13.34, 16.44, 19.67, 20.21, 20.34, 21.20, 21.75, 25.33, 25.56, 28.48, 28.76, 29.76, 31.08, 32.95, 33.83, 34.92, 35.52, 38.43, 40.05, 40.96, 41.63, 42.39, 44.44, 46.18, 46.46, 46.74, 47.03, 47.31, 47.60, 47.88, 48.20, 52.82, 60.47, 62.08, 64.37, 66.11, 66.41, 66.57, 68.23, 69.69, 72.45, 73.22, 75.47, 77.11, 78.92, 82.76, 84.48, 85.93, 94.26, 101.06, 101.53, 103.12, 117.94, 152.84, 169.13, 172.53, 177.25.
Using the procedure of Example 12, Intermediate 11 and 7-[2-(2-carboxy-ethoxy)-ethylamino]-6-fluoro-1-cyclopropyl-8-methoxy-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid gave the title compound.
MS (ES+) m/z: [MH]+=1223.6
To the solution of Intermediate 27 (800 mg) and HBTU (650 mg) in DMF (5.2 mL) were added DIPEA (450 μL). Intermediate 11 (1.5 g) was diluted in DMF (3 mL) and added to the reaction mixture. Stirring was continued over 2 days at room temperature. Then, 50 mL of H2O was added and extracted with EtOAc (3×100 mL). The organic layer was washed with NaHCO3 (3×100 mL) and NaCl (3×100 mL). The organic layer was dried over Na2SO4 and evaporated in vacuum. The product (0.73 g) was purified via SPE chromatography in system (CH2Cl2-MeOH—NH4OH=100:6:0.1) and 102 mg of title compound was isolated (purity 93.5%) as a mixture of fluoro and chloro derivatives in a ratio 25.5:74.5.
MS (ES+) m/z [MH2]2+=618.9 for (A)
MS (ES+) m/z [MH2]2+=626.9 for (B)
Using the procedure of Example 15, Intermediate 7 and Intermediate 12 gave the title compound.
MS (ES+) m/z: [MH]+=1226.4.
To the solution of 4″-O-acryloyl-azitromycin (116.29 mg, 0.613 mmol) in acetonitrile (20 mL) Intermediate 15 (0.22 g, 0.58 mmol), triethylamine (0.065 mL) and water (0.162 mL) were added and suspension was heated to 85° C. for 24 hours. The solvent was evaporated and the residue was extracted with DCM and water (2×20 mL). Organic layer was washed with NaCl and NaHCO3 (2×20 mL), dried over K2CO3 and evaporated in vacuum. The product was precipitated from EtOA/n-hexane yielding the crude product (0.35 g). Product (0.17 g) was purified by column chromatography (DCM-MeOH—NH3=90:3:0.5) yielded the title product (0.036 g).
MS (ES+) m/z: [MH]+=1182.5
1H-NMR(500 MHz, CDCl3) δ: 8.37 (1H, Q), 8.30 (1H, Q), 7.45 (1H, Q), 5.16 (1H, H-1″), 4.70 (1H, H-4″), 4.57 (1H, H-1′), 4.41 (1H, H-5″), 4.38 (2H, CH2-Q), 4.26 (1H, H-3), 4.17 (2H, CH2-Q), 3.80 (1H, H-5′), 3.69 (1H, H-11), 3.63 (1H, H-5), 3.52 (2H, CH2), 3.31 (3H, 3″OMe), 3.25 (1H, H-2′), 3.02 (2H, CH2-Q), 2.76 (1H, H-2), 2.72 (11H, CH2+4×CH2—P+H-10), 2.54 (4H, CH2+H-3′+H-9a), 2.37 (1H, H-2″a), 2.24 (2H, CH2-Q), 2.04 (2H, H-8+H-9b), 1.89 (1H, H-14a), 1.75 (1H, H-7a), 1.67 (1H, H-4′a), 1.61 (1H, H-2″b), 1.49 (1H, H-14b), 1.40 (3H, CH3-Q), 1.30 (3H, 6Me), 1.26 (2H, H-7b+H-4′b), 1.21 (3H, 5′Me), 1.20 (3H, 2Me), 1.16 (3H, 5″Me), 1.13 (3H, 3″Me), 1.10 (3H, 12Me), 1.09 (3H, 10 Me), 1.05 (3H, 4Me), 0.91 (3H, 8Me), 0.88 )3H, 15Me).
13C-NMR(75 MHz, CDCl3) δ: 178.89, 173.73, 172.01, 165.68, 147.81, 135.98134.50, 129.04, 128.77, 126.91, 119.64, 110.80, 102.33, 94.67, 85.51, 84.40, 83.25, 78.83, 77.73, 77.47, 74.27, 73.81, 73.61, 73.05, 70.94, 70.11, 67.83, 65.67, 62.98, 62.50, 60.89, 53.46, 52.80, 52.73, 52.07, 49.42, 47.70, 45.15, 42.24, 42.23, 40.39, 36.30, 35.01, 32.51, 28.98, 27.56, 26.79, 26.45, 22.00, 21.88, 21.32, 21.27, 21.19, 17.86, 16.20, 14.44, 14.12, 11.28, 9.10, 7.43
Hydrogenation of Example 17 (0.04 g) in methanol (10 mL) with addition of 10% Pd/C (20 mg) at 5 bar for 20 hours affording the title product (0.03 g).
MS (ES+) m/z: [MH]+=1187.6
In 4 mL of dry DMF was dissolved 1.5 g of Intermediate 27 (1 eq) and cooled on ice bath. To the solution was added EDC HCl (1.09 g; 1.5 eq) and the reaction mixture was stirred at 0° C. for 30 min under the flow of N2. Than was added a solution of 2′-O-acetyl-(9E)-ethoxyimino erythromycin A (2.48 g; 0.8 eq) in 4 mL of DMF and after 1 hour DMAP (2×463 mg; 2 eq). The resulting mixture was stirred over the weekend, during which time the reaction mixture was allowed to worm to ambient temperature. By extraction with water and DCM the layers are separated. The water layer was extracted two times with DCM. Organic layers were collected, dried on Na2SO4, filtered off and organic solvent evaporated. The foamy residue (260 mg) was dissolved in MeOH (20 mL) and solution was stirred over the night with heating at 60° C. The methanol was evaporated under vacuum and the foamy residue was purified by column chromatography on silica gel with DCM-MeOH—NH4OH=90:5:0.5 as eluent. Collected fractions with chloro derivative were precipitated from EtOAC/hexane.
MS (ES+) m/z: [MH]+=1197
To a solution of Intermediate 19 (0.26 mg) in CH3CN (10 mL), H2O (2 mL) and Et3N (0.3 mL) was added Intermediate 28 (0.25 mg, mixture (A) and (B) and the resulting mixture was heated at 70° C. for 17 hours. To the reaction solution was added EtOAc (50 mL) and water (50 mL), pH was adjusted to 10 and the layers were separated. The aqueous phase was washed with EtOAc (50 mL). The combined organic layers were concentrated under reduced pressure and the residue was purified on silica gel using: DCM-MeOH—NH4OH=90:9:1.5 affording the title_compound_(315 mg) as an mixture of two derivatives, 7-chloro and 6-fluoro in ratio 2:1 determined by 1H NMR.
MS (ES+) m/z: [MH]+=1195 (6-fluoro derivative)
MS (ES+) m/z: [MH]+=1211 (7-chloro derivative)
To a solution of Intermediate 20 (50 mg, 0.06 mmol), and Intermediate 30 (50 mg, 0.14 mmol, 2 eq.) in CH3CN/H2O=10/1 (11 ml), Et3N (0.25 mL, 0.18 mmol, 3 eq.) was added and the reaction mixture was stirred at 70° C. for 48 hours. Solvents were evaporated, 30 mL of EtOAc was added and extracted with aq. NaHCO3 (30 mL). Organic layer was evaporated and product was purified by column chromatography (eluent: CH2Cl2-MeOH—NH3=90:15:1.5) yielding 18 mg of the title compounds as a mixture chloro and fluoro derivatives.
MS (ES+) m/z: [MH]+=1151.4 (6-fluoro derivative)
MS (ES+) m/z: [MH]+=1167.8 (7-chloro derivative
Intermediate 1f (470 mg, 1.12 mmol) was dissolved in DMF/4 Å (6 mL), and cooled to 0° C. under N2 atmosphere. In this solution, EDAC×HCl (2 eq) was added and stirred for 5 min. Then, 2′-O-acetyl-azithromycin (1.3 g, 1.68 mmol) in 2.5 mL DCM/4 Å, and DMAP (3 eq) were added and stirred for 3 days. Water and EtOAc were added and the layers were separated. The water layer was extracted two times with EtOAc. The combined organic layers were dried over K2CO3 and evaporated yielding crude 2′-O-acetyl-protected product in a mixture with starting compounds. Obtained product was dissolved in MeOH (60 mL) and the solution was stirred for 24 hours at 55° C. The methanol was evaporated under vacuo and the residue was precipitated form EtOAc:n-hexane yielding 310 mg of the title compound.
MS (ES+) m/z: [MH]+=1152
Into a solution of Intermediate 9 (0.3 g) in MeCN (3 mL) and H2O (1 mL) triethylamine (0.525 mL) was added. The solution has been stirring at room temperature for 20 minutes. Intermediate 14b (0.145 g) solution in MeCN (7 mL) was added and the mixture has been stirring at room temperature for 20 hours. The solvents were evaporated, DCM (10 mL) and H2O (10 mL) were added, pH was adjusted to 9.2 by 2M NaOH and organic layer was separated and evaporated. The product was purified by column chromatography in system DCM-MeOH—NH3=90:13:1.8 and precipitated from EtOAc/n-hexane yielding 18 mg of the title compound.
MS (ES+) m/z: [MH]+=1131.57
Example 23 (15 mg) was dissolved in MeOH (20 mL) at room temperature and hydrogenated at 4 bar pressure in the presence of 10% Pd/C (15 mg) for 5 hours. The mixture was filtrated, evaporated and the product was precipitated from EtOAc/n-hexane yielding 2 mg of the title compound.
MS (ES+) m/z: [MH]+=1135.6
Using the procedure of Example 6 Intermediate 27A (600 mg, 1.19 mmol) and 2′-O-acetyl-azithromycin (1.4 g, 1.8 mmol) gave 200 mg of the title compound.
MS (ES+) m/z: [MH]+=1153.4
Using the procedure of Example 6, Intermediate 7 (0.3 g, 0.68 mmol) and 2′-O-acetyl-6-O-methyl-erythromycin A 11,12-cyclic carbamate (1.1 g, 1.36 mmol) gave the crude product. Column chromatography (eluent: DCM:MeOH:NH3=90:5:0.5 yielded 200 mg of the title compound.
MS (ES+) m/z: [MH]+=1194.85
Using the procedure of Example 6, Intermediate 27A (500 mg, 1.19 mmol) and 2′-O-acetyl-6-O-methyl-erythromycin A (1.87 g, 2.37 mmol) gave the crude product. Column chromatography in (eluent: DCM-MeOH—NH3=90:5:0.5) yielded 300 mg of the title compound.
MS (ES+) m/z: [MH]+=1153.35
Example 8 (200 mg, 0.17 mmol) was dissolved in DCM (5 mL), and to that solution NaHCO3 (67 mg, 0.79 mmol) and propionic acid anhydride (0.27 ml, 0.207 mmol) were added and stirred at R.T. overnight. To the reaction mixture H2O (15 mL) was added and extracted with DCM (2×10 mL). Organic layers were separated, washed with brine and solvent was evaporated under pressure affording 150 mg of the title compound
MS (ES+) m/z: [MH]+=1126.87
Using the procedure of Example 6, mixture of Intermediates 33A and 33B (400 mg, 0.9 mmol) and 2′-O-acetyl-azithromycin (1.4 g, 1.8 mmol) gave the mixture of chloro (A) and fluoro (B) compounds (700 mg).
According to HPLC/MS product contains (A):(B)=1:1
HPLC/MS (ES) m/z: [MH]+=1158.84 (Example 29A)
[MH]+=1142.42 (Example 29B)
Column chromatography (eluent: DCM-MeOH—NH3=90:5:0.5) yielded 300 mg of the title compound (A) and 250 mg of the title compound (B).
Using the procedure of Example 11, Example 29A (100 mg, 0.086 mmol) yielded 90 mg of the title compound.
HPLC/MS (ES) m/z: [MH]+=1124.5
Using the procedure of Example 6, Intermediate 34 (600 mg, 1.36 mmol) and 2′-O-acetyl-azythromycin (1.79 g, 2.26 mmol) gave the title compound. Product was purified by precipitation from EtOAc: n-hexane yielding 700 mg og the title compound.
HPLC/MS (ES) m/z: [MH]+=1172.9
Using the procedure of Example 6, Intermediate 35 (150 mg, 0.37 mmol) and 2′-O-acetyl-azythromycin (295 mg, 0.39 mmol) gave the title compound. Product was purified by precipitation from EtOAc: n-hexane yielding 104.5 mg of the title compound.
1H-NMR (500 MHz, DMSO-d6) δ: 0.80 (t, 3H), 0.84 (d, 3H), 0.94 (q, 6H), 1.01 (m, 6H), 1.08 (d, 7H), 1.14 (s, 3H), 1.25 (m, 2H), 1.37 (m, 1H), 1.51 (d, 1H), 1.58 (d, 1H), 1.64 (q, 1H), 1.77 (q, 1H), 1.87 (m, 1H), 1.90 (m, 1H), 2.10 (m, 3H), 2.19 (s, 3H), 2.21 (s, 6H), 2.30 (d, 1H), 2.35 (d, 1H), 2.39 (m, 1H), 2.50 (m, 2H), 2.67 (m, 2H), 2.97 (t, 2H), 3.4 (t, 1H), 3.22 (s, 3H), 3.27 (q, 2H), 3.43 (s, 1H), 3.46 (d, 1H), 3.52 (m, 4H), 3.58 (m, 2H), 3.66 (m, 3H), 4.18 (t, 1H), 4.33 (k, 1H), 4.39 (t, 2H), 4.43 (d, 1H), 4.55 (d, 1H), 4.74 (q, 1H), 4.91 (d, 1H), 6.31 (t, 1H), 7.09 (s, 1H), 7.14 (s, 1H), 8.65 (s, 1H).
13C-NMR (500 MHz, DMSO-d6) δ: 6.67, 8.86, 10.88, 14.55, 17.64, 20.47, 20.74, 20.89, 21.43, 21.54, 22.1, 26.00, 26.20, 27.36, 30.09, 34.22, 34.91, 35.67, 39.95, 41.60, 41.68, 42.44, 44.53, 48.80, 51.21, 52.64, 61.34, 62.15, 64.78, 66.09, 66.76, 68.66, 69.58, 70.47, 72.40, 73.52, 74.90, 76.30, 77.37, 78.02, 82.66, 94.29, 100.22, 102.02, 105.46, 120.43, 126.97, 128.47, 129.91, 143.82, 146.81, 166.87, 170.92, 176.49, 177.3.
Using the procedure of Example 6, Intermediate 35 (200 mg) and 2′-O-acetyl-6-O-methyl-erythromycin A (391 mg) gave the title compound. Product was purified by precipitation from EtOAc: n-hexane yielding 150 mg of the title compound.
1H-NMR (500 MHz, DMSO-d6) δ: 0.75 (t, 3H), 1.04 (m, 12H), 1.06 (m, 3H), 1.09 (m, 4H), 1.13 (d, 3H), 1.26 (s, 3H), 1.43 (m, 3H), 1.46 (m, 1H), 1.58 (m, 1H), 1.67 (d, 1H), 1.74 (d, 2H), 1.85 (m, 2H), 1.87 (m, 1H), 2.11 (m, 2H), 2.20 (s, 6H), 2.35 (m, 1H), 2.39 (m, 1H), 2.50 (m, 2H), 2.60 (m, 1H), 2.82 (m, 1H), 2.92 (s, 3H), 2.97 (m, 3H), 3.04 (t, 1H), 3.21 (s, 3H), 3.27 (q, 2H), 3.52 (m, 4H), 3.53 (m, 1H), 3.56 (m, 2H), 3.59 (m, 1H), 3.62 (m, 1H), 3.66 (m, 2H), 4.28 (k, 1H), 4.43 (d, 1H), 4.56 (d, 1H), 4.85 (d, 1H), 5.05 (d, 1H), 6.28 (m, 1H), 7.8 (s, 1H), 7.14 (s, 1H), 8.63 (s, 1H).
13C-NMR (500 MHz, DMSO-d6): 8.90, 10.40, 11.85, 15.89, 16.93, 17.62, 18.05, 19.77, 20.26, 20.63, 20.77, 21.52, 26.21, 30.14, 34.25, 34.90, 37.93, 40.26, 42.47, 43.62, 44.25, 48.86, 50.10, 52.56, 62.40, 64.51, 66.07, 66.82, 68.66, 68.85, 69.58, 70.60, 72.07, 74.10, 75.91, 77.03, 77.75, 77.83, 79.20, 95.44, 100.29, 101.88, 120.34, 127.11, 128.48, 129.81, 143.90, 146.71, 166.91, 170.87, 175.02, 176.40, 218.63.
Using the procedure of Example 6, Intermediate 7 (100 mg) and 2′-O-acetyl-6-O-propylerythromycin A (378 mg, 2 eq) gave the title compound. Product was purified by column chromatography (eluent CH2Cl2-MeOH—NH3=90:13:1.3) yielding the title compound (1 mg).
MS (ES+) m/z [MH2]2+=599.10.
Using the procedure of Example 6, Intermediate 36 (180 mg) and 2′-O-acetyl-azithromycin (702 mg, 2 eq) gave the title compound. Product was precipitated from EtOAc: n-hexane yielding the title compound (100 mg).
MS (ES+) m/z [MH2]2+=569.00
Using the procedure of Example 23, Intermediate 9 (300 mg) and Intermediate 20 (150 mg, 0.5 eq) gave the title compound. Product was purified by column chromatography (eluent CH2Cl2-MeOH—NH3=90:13:1.3) and precipitated from EtOAc: n-hexane yielding 95% pure title compound (63 mg).
MS (ES+) m/z [MH]+=1117.2.
Using the procedure of Example 24, Example 36 (50 mg) gave the title compound. Product was precipitated from EtOAc: n-hexane yielding 80% pure title compound (24 mg).
MS (ES+) m/z [MH]+=1121.2.
Using the procedure of Example 6, Intermediate 36 (100 mg, 0.25 mmol) and 2′-O-acetyl-6-O-methyl-erythromycin A (400 mg, 2 eq) gave the title compound. Product was purified by column chromatography (eluent CH2Cl2-MeOH—NH3=90:13:1.7) and precipitated from EtOAc: n-hexane yielding 70% pure title compound (5 mg).
MS (ES+) m/z [MH]+=1135.56.
Using the procedure of Example 6, Intermediate 36 (100 mg, 0.25 mmol) and 2′-O-acetyl-9-ethyloximino-6-O-methyl-erythromycin A (400 mg, 2 eq) gave the title compound. Product was purified by column chromatography (eluent CH2Cl2-MeOH—NH3=90:13:1.7) and precipitated from EtOAc: n-hexane yielding 94% pure title compound (10 mg).
MS (ES+) m/z [MH2]2+=590.12.
To the solution of Intermediate 28A (58 mg, 0.14 mmol) in acetonitrile (1.5 mL) and water (0.5 mL) trethylamine (50 μl, 2.5 eq) was added and the mixture was stirred at R.T. for 20 minutes. Than Intermediate 37 (70 mg, 0.07 mmol) solution in acetonitrile (3 mL) was added and the reaction mixture was stirred at 70° C. for 20 hours. The solvents were evaporated and to residue CH2Cl2 (5 mL) was added, filtrated and the filtrate was evaporated once again. The oily residue (105 mg) was dissolved in MeOH (6 mL) and the solution was stirred at 50° C. for 20 hours. MeOH was evaporated and the product was precipitated first from CH2Cl2/n-hexane (76 mg) and from CH2Cl2/di-i-propyl ether/n-hexane yielding 75% pure the title compound (69 mg).
MS (ES+) m/z [MH2]2+=677.30
Using the procedure of Example 6, Intermediate 7 (471 mg, 0.76 mmol) and 2′-O-acetyl-9-(1-isopropoxy-cyclohexyl)oximino-erythromycin A (350 mg, 0.38 mmol) gave the title compound. Product was purified by column chromatography (eluent CH2Cl2-MeOH—NH3=90:13:1.7) and precipitated from EtOAc: di-i-propyl ether: n-hexane yielding 90% pure title compound (58 mg).
MS (ES+) m/z [MH]+=1310.54.
Using the procedure of Example 6, Intermediate 36 (131 mg, 0.32 mmol) and 2′-O-acetyl-9-(1-isopropoxy-cyclohexyl)oximino-erythromycin A (150 mg, 0.16 mmol) gave the title compound. Product was precipitated from CH2Cl2: di-i-propyl ether: n-hexane yielding 70% pure title compound (88 mg).
MS (ES+) m/z [MH2]2+=1276.64.
To the solution of Example 41 (22 mg, 0.017 mmol) in EtOH (1 mL), water (2 mL) and HCOOH (10 μL) were added and the solution was stirred for 20 hours at R.T. After that EtOH was evaporated, CH2Cl2 (2 mL) added and pH was adjusted to 9.5. Than, organic layer was separated and evaporated giving oily residue. The pure product was precipitated from CH2Cl2: di-i-propyl ether yielding 5 mg of the title compound (91% Area by LC-MS).
MS (ES+) m/z [MH]+=1170.2.
To the solution of Example 43 (166 mg) in CH2Cl2 (1 mL) at R.T. acetic acid (16 μl, 2 eq) was added and the product was precipitated by addition of di-i-propyl ether (10 mL) yielding 148 mg of the title product.
Using the procedure of Example 43 from Example 42 (46 mg, 0.036 mmol) after precipitation from CH2Cl2: di-i-propyl ether the title compound (5 mg) was obtained as a mixture of E and Z isomers. According to HPLC/MS product contains E and Z isomer.
HPLC/MS (ES) m/z: [MH]+=1137.3.
Using the procedure of Example 43 from Example 40 (60 mg, 0.043 mmol) after precipitation from CH2Cl2: di-i-propyl ether the title compound (17 mg) was obtained as a 70% pure product.
MS (ES+) m/z [MH]+=1213.3.
Using the procedure of Example 6, Intermediate 38 (1.1 g) and 2′-O-acetyl-azithromycin (2.0 g, 3 mmol) gave the title compound. Product was precipitated from EtAc: n-hexane yielding the title compound (230 mg).
MS (ES+) m/z [MH2]2+=583.4.
Using the procedure of Example 6, Intermediate 39 and 2′-O-acetyl-azithromycin (2.5 g, 3 mmol) gave the title compound. Product was precipitated from EtAc: n-hexane yielding the title compound (231 mg).
MS (ES+) m/z [MH2]2+=589.4.
Using the procedure of Example 6, Intermediate 42 (3.75 g, 0.0096 mol), 2′-O-acetyl-azithromycin (9.11 g, 0.012 mol), EDAC×HCl (3.67 g, 0.019 mol)) and DMAP (2.35 g, 0.019 mol) gave the title compound. Product was purified by column chromatography (eluent CH2Cl2-MeOH—NH3=90:9:1.5) and precipitated from EtOAc: n-hexane yielding the title compound (7 g).
LC/MS(ES+) m/z [MH]+=1122.6
1H-NMR (300 MHz, DMSO) δ: 9.03 (s, 1H); 8.18(d, 1H); 7.98(d, 1H); 7.83 (dd, 1H); 4.91 (d, 1H); 4.73 (dd, 1H); 4.59 (t, 2H); 4.55 (d, 1H); 4.43 (d, 1H); 4.33 (m, 1H); 4.17(dd, 1H); 3.66 (m, 1H); 3.64 (m, 2H); 3.50 (ov, 2H), 3.47 (ov, 1H); 3.45 (ov, 1H); 3.43 (ov, 2H); 3.38(t, 2H); 3.22 (s, 3H); 3.05 (dd, 1H); 2.81(t, 2H); 2.67 (ov, 1H); 2.67 (ov, 1H); 2.59(m, 2H); 2.40 (m, 1H); 2.35 (dd, 1H); 2.31 (d, 1H); 2.21 (s, 3H); 2.18 (s, 3H); 2.11 (t, 1H); 1.88 (ov, 1H); 1.85 (ov, 2H); 1.85 (ov, 1H); 1.78 (m, 1H); 1.66 (dd, 1H); 1.59 (m, 1H); 1.51(d, 1H); 1.42 (t, 3H); 1.37 (m, 1H); 1.27 (dd, 1H); 1.12 (s, 3H); 1.1 (s, 3H); 1.09 (ov, 1H); 1.08 (d, 3H); 1.07 (dd, 3H); 1.03 (d, 3H); 1.01 (s, 3H); 0.96 (d, 3H); 0.94 (d, 3H); 0.84 (d, 3H); 0.79 (t, 3H)
13C-NMR (75 MHz, DMSO) δ: 177.44; 177.03; 170.92; 166.09; 148.46; 140.23; 137.35; 134.89; 125.45; 124.55; 118.03; 107.47; 102.02; 94.30; 82.66; 78.01; 77.34; 76.29; 74.87; 73.52; 72.40; 72.04; 70.45; 69.37; 69.66; 69.23; 68.61; 66.75; 66.09; 64.78; 62.16; 61.39; 48.79; 44.53; 41.59; 40.23; 35.66; 34.94; 34.24; 31.10; 30.99; 30.56; 27.31; 25.98; 22.00; 21.56; 20.88; 20.49; 17.64; 14.54; 10.88; 8.86; 6.67; 4.89.
To a solution of Example 49 (150 mg, 0.134 mmol) in EtOAc (10 mL) acetic acid (0.017 mL, 0.29 mmol) was added under stirring at R.T. Precipitate occurred after addition of n-hexane (100 mL), it was filtered off yielding the titled product (135 mg).
Using the procedure of Example 6, Intermediate 42 and 2′-O-acetyl-6-O-methyl erythromycin A gave the title compound. Product was precipitated from EtOAc: n-hexane yielding the title compound (112 mg).
LC/MS(ES+) m/z [MH]+=1122.1.
Using the procedure of Example 6, Intermediate 42 and 2′-O-acetyl-9-ethyloximinoerythromycin A gave the title compound. Product was precipitated from EtOAc: n-hexane yielding the title compound (106 mg).
LC/MS(ES+) m/z [MH]+=1151.1.
Using the procedure of Example 6, Intermediate 42d and 2′-O-acetyl-6-O-methyl-8a-aza-8a-homoerythromycin A gave the title compound. Product was precipitated from EtOAc: n-hexane yielding the title compound (60 mg).
LC/MS(ES+) m/z [MH]+=1136.1.
Using the procedure of Example 6, Intermediate 42 and 2′-O-acetyl-roxythromycin gave the title compound. Product was precipitated from EtOAc: n-hexane yielding the title compound (105.5 mg).
LC/MS(ES+) m/z [MH]+=1210.68.
Using the procedure of Example 6, Intermediate 13 and 2′-O-acetyl-azithromycin gave the title compound. Product was purified by column chromatography (eluent: CH2Cl2: MeOH:NH3=90:9:0.5) yielding the title compound (61 mg).
LC/MS(ES+) m/z [MH]+=1169.9.
Using the procedure of Example 6, Intermediate 42 and 2′-O-acetyl-6-O-methyl-11-desoxy-11-R)-methylamino-erythromycin A 11,12-carbamate reacted according to procedure in J. Org. Chem., 1988, 53(10), 2340-5 gave the title compound. Product was precipitated from EtOAc: n-hexane yielding the title compound (181 mg).
LC/MS(ES+) m/z [MH]+=1161.3.
Using the procedure of Example 6, Intermediate 44 (0.612 g, 1.5 mmol), and 2′-O-acetyl-azithromycin (1.4 g, 1.8 mmol), EDAC×HCl (0.574 g, 3 mmol) and DMAP (0.367 g, 3 mmol) gave the title compound. Product was purified by column chromatography (eluent CH2Cl2-MeOH—NH3=90:9:1.5) and precipitated from EtOAc: n-hexane yielding the title compound (640 mg).
LC/MS(ES+) m/z [MH]+=1134.35.
1H-NMR (300 MHz, DMSO) δ: 8.73 (s, 1H); 8.22 (d, 1H); 8.16 (d, 1H); 7.87 (dd, 1H); 4.91 (d, 1H); 4.74 (dd, 1H); 4.56 (d, 1H); 4.43 (d, 1H); 4.34 (m, 1H); 4.17 (dd, 1H); 3.84 (m, 1H); 3.69 (m, 1H); 3.66 (m, 2H); 3.47 (d, 1H); 3.43 (m, 1H); 3.38 (t, 2H); 3.33-3.37 (ov, 4H); 3.23 (s, 3H); 3.04 (t, 1H); 2.83 (t, 2H); 2.67 (m, 1H); 2.58 (t, 2H); 2.40 (m, 1H); 2.38 (d, 1H); 2.33 (d, 1H); 2.21 (s, 6H); 2.19 (s, 3H); 2.11 (t, 1H); 1.89 (m, 1H); 1.83-1.86 (ov, 3H); 1.78 (m, 1H); 1.67 (dd, 1H); 1.59 (m, 1H); 1.51 (s, 1H); 1.36 (m, 1H); 1.32 (m, 2H); 1.25 (m, 1H); 1.18 (m, 2H); 1.13 (s, 3H); 1.09 (d, 3H); 1.08 (d, 3H); 1.07-1.09 (ov, 1H); 1.03 (d, 3H); 1.01 (s, 6H); 0.95 (d, 3H); 0.94 (d, 3H); 0.85 (dd, 3H); 0.79 (t, 3H).
13C-NMR (75 MHz, DMSO) δ: 177.72; 177.04; 170.93; 165.92; 147.97; 140.43; 139.36; 134.81; 124.92; 124.29; 118.42; 107.14; 102.04; 94.32; 82.69; 78.03; 77.39; 76.32; 74.91; 73.54; 72.43; 70.45; 69.67; 69.39; 69.24; 68.64; 66.77; 66.10; 64.81; 62.18; 61.39; 48.82; 44.55; 41.69; 41.61; 40.27; 35.79; 35.68; 34.96; 34.26; 31.05; 30.65; 30.15; 27.35; 26.01; 22.02; 21.58; 20.51; 20.19; 17.67; 17.64; 14.59; 10.89; 8.89; 7.48; 6.68.
Using the procedure of Example 6, Intermediate 46 and 2′-O-acetyl-azithromycin gave the title compound. Product was precipitated from EtOAc: n-hexane yielding the title compound (170 mg).
LC/MS(ES+) m/z [MH]+=1094.70.
Using the procedure of Example 6, Intermediate 48 and 2′-O-acetyl-azithromycin gave the title compound. Product was precipitated from EtOAc: n-hexane yielding the title compound (400 mg).
LC/MS(ES+) m/z [MH]+=1136.42.
1H-NMR (300 MHz, DMSO-d6) δ: 9.02 (s, 1H); 8.18 (d, 1H); 7.98 (d, 1H); 7.82 (dd,1H); 4.95 (d, 1H); 4.75 (dd, 1H); 4.56 (t, 2H); 4.53 (d, 1H); 4.43 (d, 1H); 4.34 (m, 1H); 4.17 (d, 1H); 3.69 (m, 1H); 3.66 (t, 2h); 3.53-3.45 (ov, 4H); 3.47 (ov, 1H); 3.45 (ov, 1H); 3.38 (ov, 2H); 3.22 (s, 3H); 3.05 (dd, 1H); 2.81 (t, 2H); 2.67 (m, 2H); 2.58 (t, 2H); 2.41 (m, 1H); 2.34 (dbr, 1H); 2.28 (d, 1H); 2.22 (s, 3H); 2.19 (s, 3H); 2.12 (tbr, 1H); 1.88 (ov, 1H); 1.86-1.80 (ov, 2H); 1.83 (ov, 1H); 1.77 (m, 1H); 1.67 (dd, 1H); 1.61 (m, 1H); 1.52 (d, 1H); 1.38 (m, 1H); 1.27 (ddbr, 1H); 1.12 (s, 3H); 1.09 (d, 6H); 1.05 (ov, 1H); 1.02 (d, 3H); 1.01 (s, 6H); 0.85 (d, 3H); 0.95 (d, 6H); 0.92 (t, 3H); 0.80 (t, 3H);
13C-NMR (75 MHz, DMSO-d6) δ: 177.64; 177.24; 171.13; 166.34; 149.02; 140.46; 137.76; 135.06; 125.63; 124.73; 118.38; 107.42; 102.21; 94.51; 82.86; 78.21; 77.57; 76.49; 75.06; 73.73; 72.62; 70.62; 70.62; 69.87; 69.58; 69.45; 68.80; 66.30; 65.00; 32.37; 61.65; 55.03; 49.01; 44.74; 41.8; 41.5; 40.42; 35.88; 35.15; 34.44; 31.21; 30.78; 30.32; 27.51; 26.18; 22.20; 21.76; 21.4; 21.09; 20.7; 17.86; 17.78; 14.78; 11.09; 10.65; 9.07; 6.89.
Using the procedure of Example 1, Intermediate 14 and mixture of Intermediates 28A and 28B gave the title compounds (85 mg) as a mixture of chloro and fluoro derivatives in a ratio 3:1.
LC/MS(ES+) m/z [MH]+=1212.9 (Example 60A)
LC/MS(ES+) m/z [MH]+=1196.4 (Example 60B)
Using the procedure of Example 1, Intermediate 14 and mixture of Intermediates 30A and 30B gave the title compounds (81 mg) as a mixture of chloro and fluoro derivatives in a ratio 3:2.
LC/MS(ES+) m/z [MH]+=1168.4 (Example 61A)
LC/MS(ES+) m/z [MH]+=1152.5 (Example 61B)
Using the procedure of Example 1, Intermediate 14 and Intermediates 49 gave the title compound (3 mg).
LC/MS(ES+) m/z [MH]+=1161.4.
Using the procedure of Example 1, Intermediate 20 and Intermediates 28A gave the title compound (49 mg).
LC/MS(ES+) m/z [MH]+=1211.9.
Using the procedure of Example 6, Intermediate 7 and 2′-O-acetyl-6-O-methyl-8a-aza-8a-homoerythromycin A gave the title compound. Product was precipitated from EtOAc: n-hexane yielding the title compound (85 mg).
LC/MS(ES+) m/z [MH]+=1183.8.
Using the procedure of Example 1, Intermediate 14 and Intermediates 28A gave the title compound (152 mg).
LC/MS(ES+) m/z [MH]+=1212.9.
Using the procedure of Example 6, Intermediate 52 and 2′-O-acetyl-azithromycin gave the title compound. Product was precipitated from EtOAc: n-hexane yielding the title compound (50 mg).
LC/MS(ES+) m/z [MH]+=1182.9.
Example 55 (80 mg, 0.068 mmol) was dissolved in 30 mL of methanol, 40 mg of 10% Pd/C was added and the mixture was stirred under H2 pressure (5 bar) for 6 hours. The reaction mixture was filtrated and solvent evaporated in vacuum. Crude product was diluted in isopropylacetate
(8 mL) and extracted with aqueous NaHCO3 (2×5 mL). Organic layer was evaporated in vacuum and crude product precipitated from EtOAc:n-hexane yielding 68 mg of the title product.
LC/MS(ES+) m/z [MH]+=1136.6.
13C-NMR(75 MHz, CDCl3) δ: 178.9, 178.0, 171.4, 167.2, 157.3, 146.7, 135.8, 127.4, 125.0, 118.9, 108.1, 106.7, 102.3, 94.7, 83.2, 79.0, 77.8, 77.5, 74.3, 73.8, 73.6, 72.9, 71.0, 70.8, 70.6, 70.1, 69.5, 68.2, 67.9, 66.7, 65.6, 63.0, 62.5, 49.4, 45.2, 42.2, 42.1, 40.4, 36.3, 35.5, 35.2, 35.0, 29.0, 27.5, 26.8, 22.0, 21.9, 21.3, 21.2, 17.8, 16.2, 14.6, 11.3, 9.1, 8.3, 7.5,
Using the procedure of Example 6, Intermediate 54 and 2′-O-acetyl-azithromycin gave the title compound. Product was purified by column chromatography (eluent: CH2Cl2:MeOH:NH3=90:9:1.5) yielding the title compound (92 mg).
LC/MS(ES+) m/z [MH]+=1130.8.
Using the procedure of Example 6, 2′-O-acetyl-azithromycin and mixture of Intermediate 56C and Intermediate 56D gave a mixture of chloro and fluoro compounds (670 mg). Purification by column chromatography (eluent: CH2Cl2:MeOH:NH3=90:9:1.5) yield 150 mg of the title compound.
LC/MS(ES+) m/z [MH]+=1129.8.
Using the procedure of Example 1, Intermediate 20 and Intermediate 57 gave the title compound in 43% yield.
ESMS m/z [MH]+=1151.7.
Using the procedure of Example 1, 4″-O-propenoyl-azithromycin and Intermediate 57 gave the title compound in 20% yield.
ESMS m/z [MH]+=1152.8.
Using the procedure of Example 1, Intermediate 20 and Intermediate 59 gave the title compound in 62% yield.
ESMS m/z [MH]+=1138.9.
Using the procedure of Example 1, Intermediate 63 and Intermediate 59 gave the title compound in 44% yield.
ESMS m/z [MH]+=1184.2.
Using the procedure of Example 1, Intermediate 62 and Intermediate 59 gave the title compound in 48% yield.
ESMS m/z [MH]+=1140.2.
Using the procedure of Example 1, Intermediate 60 and Intermediate 62 gave the title compound in 52% yield.
ESMS m/z [MH]+=1122.0.
A solution of Example 75 (0.032 g, 0.049 mmol) dissolved in a mixture of chloroform (0.7 mL), 37% aqueous formaldehyde (7 uL) and formic acid (7 uL) was stirred at 60° C. After 4 h the mixture was cooled, evaporated and the residue subjected to chromatography over silica gel eluting with with 0-10% [9:1 methanol/20 M ammonia] in dichloromethane gave the title compound in 58% yield.
ESMS m/z [MH]+=1137.0.
Using the procedure of Example 1, Intermediate 61 and Intermediate 20 gave the title compound.
ESMS m/z [MH]+=1115.2.
Biological Data
The MIC (μg/ml) of test compounds against various organisms was determined including: S. aureus Smith ATCC 0329, S. pneumoniae 0541, S. pyogenes 0542, E. faecalis ATCC 0004, H. influenzae ATCC 0529, M. catarrhalis ATCC 0324.
Examples 3-8, 11, 14, 19, 20, 23, 24, 26, 27, 30-33, 35-38, 48, 49, 51, 55-57, 59, 62, 64 and 65 have an MIC ≦1 μg/ml against S. aureus Smith ATCC 0329, S. pneumoniae 0541, S. pyogenes 0542 and E. faecalis ATCC 0004.
Examples 3, 4, 8, 11, 14, 15, 19, 23, 24, 26, 27, 30-33, 35-38, 48, 49, 51, 55-57, 59, 62, 64 and 65 have an MIC ≦2 μg/ml against H. influenzae ATCC 0529 and M. catarrhalis ATCC 0324.
Examples 6, 8, 11, 19, 20, 30-33, 37, 49, 51, 52, 55-57, 59, 64 and 65 have an MIC ≦0.25 μg/ml against erythromycin resistant strains of Streptococcus pneumoniae and Streptococcus pyogenes.
The application of which this description and claims forms part may be used as a basis for priority in respect of any subsequent application. The claims of such subsequent application may be directed to any feature or combination of features described herein. They may take the form of product, composition, process, or use claims and may include, by way of example and without limitation, the following claims:
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/IB2005/001186 | 5/2/2005 | WO | 00 | 1/30/2007 |
| Number | Date | Country | |
|---|---|---|---|
| 60569402 | May 2004 | US | |
| 60581118 | Jun 2004 | US |
