The invention relates to 2-amino- and 2-oxypurinone compounds useful in treating disorders that are mediated by adenosine receptor function, including neurodegenerative diseases and inflammation.
Adenosine is a modulator of multiple physiological functions, including cardiovascular, neurological, respiratory and renal functions. Adenosine mediates its effects through specific G-protein coupled membrane receptors. Four adenosine receptors have been identified, A1, A2a, A2b and A3 receptors.
Adenosine 2a (A2a) receptor antagonists are useful in the treatment of Parkinson's disease have been disclosed in U.S. Pat. No. 6,875,772 and U.S. Pat. No. 6,787,541. A2a antagonists have also been shown to be useful for the treatment of restless leg syndrome (as outlined in WO 2004019949). These disclosures are incorporated herein by reference as they relate to utility.
In one aspect the present invention provides compounds according to formula I useful as adenosine 2a receptor antagonists:
In these compounds
R1 is selected from lower alkyl, lower alkyloxyalkyl, arylalkyl aryl, substituted aryl and substituted arylalkyl;
X is selected from NR2a and O;
R2 is selected from H, C1-C20 hydrocarbon, C1-C20acyl, heterocyclyl (other than 2-pyridinyl and 1-imidazolyl), heterocyclylalkyl, substituted alkyl, substituted aryl, substituted heterocyclyl, substituted arylalkyl and substituted heterocyclylalkyl;
R2A is selected from H and C1-C10 hydrocarbon;
or R2 and R2A together form a 5-7 membered heterocycle or substituted 5-7 membered heterocycle; and
R3 is selected from H, lower alkyl, arylalkyl, heterocyclyl, substituted heterocyclyl, heterocyclylalkyl and substituted arylalkyl; with the provisos that
(i) at least one of R1, R2 and R3 must provide an aryl or heteroaryl moeity;
(ii) when R3 is H, R1 must be other than lower alkyl;
(iii) when X is NR2A, R2Ais H, and R1 is phenyl or tolyl, then R2 must be other than phenyl and tolyl; and
(iv) R2 is not p-chlorophenethyl.
In another aspect, the invention relates to pharmaceutical compositions comprising a therapeutically effective amount of at least one compound of general formula I, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.
The compounds and pharmaceutical compositions described herein are useful in methods for preventing and treating a condition for which an antagonist of adenosine 2a receptor is indicated.
In a third aspect, the invention relates to a method for treating a disease by antagonizing a response mediated by adenosine 2a receptors. The method comprises bringing into contact with adenosine receptor at least one compound of general formula I or a pharmaceutically acceptable salt thereof.
In yet another aspect the present invention relates to a method of treating disease mediated by adenosine receptors in a subject in need thereof comprising administering to the subject a therapeutically effective amount of at least one compound of general formula I or a pharmaceutically acceptable salt thereof.
The compounds of the present invention are useful in preventing and treating diseases and disorders mediated by adenosine receptors, including neurological diseases and disorders.
The compounds of the present invention are useful in effecting neuroprotection and as such the present invention provides a method of neuroprotection in a subject in need thereof comprising administering to the subject a therapeutically effective amount of at least one compound of general formula I or a pharmaceutically acceptable salt thereof.
Other indications in which the adenosine antagonists are useful include central nervous system disorders, neurodegenerative diseases, cardiovascular disorders, and diabetes.
The compounds of the present invention are useful in stand alone treatments or in combination with one or more of (1) an agent useful in the treatment of Parkinson's disease, i.e. L-dopa, caffeine or other dopaminergic receptor agonist (2) an agent useful in the treatment of movement disorders, (3) an agent useful in the treatment of depression.
Throughout this specification the substituents are defined when introduced and retain their definitions.
It has now been found that compounds of general formula I are potent antagonists of adenosine 2a (A2a) receptor:
In one embodiment, R2 is selected from C1-C20 hydrocarbon, heterocyclyl, heterocyclylalkyl, substituted alkyl, substituted aryl, substituted heterocyclyl, substituted arylalkyl and substituted heterocyclylalkyl, and R3 is selected from H, lower alkyl arylalkyl and substituted arylalkyl with the proviso that when X is NR2A, and R2A is H, then R2 must be other than aryl, heteroaryl and substituted aryl.
Two subgenera may be identified based on the value of X. In one subgenus X is NR2a and 2-aminopurinone derivatives arise; in the second case, X is oxygen and a subgenus of 2-oxypurinones arise, having chemical formulae II and III, respectively, as set forth below:
In specific embodiments of genus II, at least two of R1, R2 and R3 provide aryl or heteroaryl moieties. In other words, two of R1, R2 and R3 are residues that contain a benzene ring or a heteroaryl ring somewhere within the substituent. Examples of such residues found among the examples below include thienylethyl (a heteroarylalkyl residue), 2,4-difluorobenzyl (a substituted arylalkyl) and m-tolyl (substituted aryl). Not among the examples below, but still residues that provide an aryl or heteroaryl moiety are phenylcyclopropyl (a C1-C20 hydrocarbon) and phenylpyrrolidinyl (a substituted heterocyclyl).
In some embodiments R2a is H or CH3.
In some embodiments R1 is phenyl or substituted phenyl and R3 is benzyl or substituted benzyl. The phenyl and benzyl may be unsubstituted or substituted with one to three substituents chosen from halogen, C1-C4alkoxy (e.g. methoxy), C1-C4alkyl (e.g. methyl and ethyl), —OH, —CN, fluoro(C1-C4)alkoxy (e.g. trifluoromethoxy), fluoro(C1-C4)alkyl (e.g. trifluoromethyl) and methylenedioxy.
In some embodiments R1 is C1-C3alkoxyphenyl, methylenedioxyphenyl, trifluoromethoxyphenyl or fluorophenyl.
In some embodiments R2 is chosen from:
(i) (C1-C6)alkyl;
(ii) (C1-C6)alkyl substituted with halogen, methoxy, —NHC(═O)CH3, —N(alkyl)2, —OH or —CN;
wherein n is 1, 2 or 3 and R30 is chosen from H, methoxy, methyl and halogen; and
wherein Het is heteroaryl or saturated heterocycle;
n is 1, 2 or 3 and R31 is chosen from H and methyl. C1-C20 hydrocarbon. In some embodiments R2 and R2a together form a 5-7 membered ring.
Examples of embodiments of R2 according to the foregoing systematic subdivisions include cyclopropyl, thienylethyl, pyridinylmethyl, pyridinylethyl, methyl, ethyl, 2-hydroxyethyl, isopropyl, propyl, piperidinylethyl, halophenethyl, imidazolylpropyl, H, phenethyl, 3-methoxypropyl, acetylaminoethyl, cyclobutyl, methoxyethyl, isobutyl, cyclopentyl, cyanoethyl 3-cyanopropyl, piperidinyl, halobenzyl, morpholinoethyl, dimethylaminoethyl, neopentyl, methoxybenzyl, N-methylpiperidin-4-yl, benzyl and pyrrolidin-3-yl.
In a second aspect the present invention provides a pharmaceutical composition comprising a pharmaceutically acceptable carrier and a therapeutically effective amount of at least one compound according to formula I.
Although the compounds of the invention are selective A2a antagonists, some of them may exhibit sufficient residual affinity for other classes of adenosine receptors to be useful to treat conditions associated with additional adenosine receptors. As a result, the present invention also provides a method of treating a disorder associated with the A2a receptor and one or more of A1, A2b or A3 receptors.
In a third aspect the present invention provides a method of treating a disorder, which is mediated by adenosine 2a (A2a) receptor function, which comprises administering to a subject in need of such treatment a therapeutically effective amount of a compound of formula I. The disorder is selected from the group consisting of central nervous system and peripheral nervous system diseases; neurodegenerative diseases; cardiovascular diseases; cognitive disorders; CNS injury; renal ischemia; acute and chronic pain; affective disorders; cognitive disorders; central nervous system injury; cerebral ischemia; myocardial ischemia; muscle ischemia; sleep disorders; eye disorders and diabetic neuropathy. CNS and PNS are movement disorders.
The method may be used to treat a movement disorder consisting of a disorder of the basal ganglia which results in dyskinesias Huntington's disease, multiple system atrophy, progressive supernuclear palsy, essential tremor, myoclonus, corticobasal degeneration, Wilson's disease, progressive pallidal atrophy, Dopa-responsive dystoma-Parkinsonism, spasticity, Alzheimer's disease and Parkinson's disease. An example of a movement disorder is Parkinson's disease.
In one embodiment, the compounds of the invention may be used for neuroprotection in a subject at risk of neural ischemia. In another embodiment, the compounds of the invention may be used for treating injuries to the central nervous system. In another embodiment, the compounds of the invention may be used for treating restless leg syndrome.
All of the compounds falling within the foregoing parent genera and their subgenera are useful as adenosine receptor antagonists.
For convenience and clarity certain terms employed in the specification, examples and claims are described below.
Alkyl is intended to include linear, branched, or cyclic hydrocarbon structures and combinations thereof. Lower alkyl refers to alkyl groups of from 1 to 6 carbon atoms. Examples of lower alkyl groups include methyl, ethyl, propyl, isopropyl, butyl, s- and t-butyl and the like. Preferred alkyl groups are those of C20 or below. Cycloalkyl is a subset of alkyl and includes cyclic hydrocarbon groups of from 3 to 8 carbon atoms. Examples of cycloalkyl groups include c-propyl, c-butyl, c-pentyl, norbornyl and the like.
C1 to C20 hydrocarbon includes alkyl, cycloalkyl, alkenyl, alkynyl, aryl, arylalkyl and combinations thereof. Examples include benzyl, phenethyl, cyclohexylmethyl, camphoryl adamantly, phenylcyclopropyl, and naphthylethyl.
Alkoxy or alkoxyl refers to groups of from 1 to 8 carbon atoms of a straight, branched, cyclic configuration and combinations thereof attached to the parent structure through an oxygen. Examples include methoxy, ethoxy, propoxy, isopropoxy, cyclopropyloxy, cyclohexyloxy and the like. Lower-alkoxy refers to groups containing one to four carbons. For the purpose of this application, alkoxy and lower alkoxy include methylenedioxy and ethylenedioxy.
Alkoxyalkyl refers to ether groups of from 3 to 8 atoms of a straight, branched, cyclic configuration and combinations thereof attached to the parent structure through an alkyl. Examples include methoxymethyl, methoxyethyl, ethoxypropyl, and the like.
Alkoxyaryl refers to alkoxy substituents attached to an aryl, wherein the aryl is attached to the parent structure.
Acyl refers to groups of from 1 to 10 carbon atoms of a straight, branched, cyclic configuration, saturated, unsaturated and aromatic and combinations thereof, attached to the parent structure through a carbonyl functionality. One or more carbons in the acyl residue may be replaced by nitrogen, oxygen or sulfur as long as the point of attachment to the parent remains at the carbonyl. Examples include formyl, acetyl, benzoyl, propionyl, isobutyryl, t-butoxycarbonyl, benzyloxycarbonyl and the like. Lower-acyl refers to groups containing one to four carbons.
Aryl and heteroaryl mean a 5- or 6-membered aromatic or heteroaromatic ring containing 0-3 heteroatoms selected from O, N, or S; a bicyclic 9- or 10-membered aromatic or heteroaromatic ring system containing 0-3 heteroatoms selected from O, N, or S; or a tricyclic 13- or 14-membered aromatic or heteroaromatic ring system containing 0-3 heteroatoms selected from O, N, or S. The aromatic 6- to 14-membered carbocyclic rings include, e.g., benzene and naphthalene, and according to the invention benzoxalane and residues in which one or more rings are aromatic, but not all need be. The 5- to 10-membered aromatic heterocyclic rings include, e.g., imidazole, pyridine, indole, thiophene, benzopyranone, thiazole, furan, benzimidazole, quinoline, isoquinoline, quinoxaline, pyrimidine, pyrazine, tetrazole and pyrazole.
Arylalkyl refers to a substituent in which an aryl residue is attached to the parent structure through alkyl. Examples are benzyl, phenethyl and the like. Heteroarylalkyl refers to a substituent in which a heteroaryl residue is attached to the parent structure through alkyl. Examples include, e.g., pyridinylmethyl, pyrimidinylethyl and the like.
Heterocycle means a cycloalkyl or aryl residue in which from one to three carbons is replaced by a heteroatom selected from the group consisting of N, O and S. The nitrogen and sulfur heteroatoms may optionally be oxidized, and the nitrogen heteroatom may optionally be quaternized. Examples of heterocycles include pyrrolidine, pyrazole, pyrrole, indole, quinoline, isoquinoline, tetrahydroisoquinoline, benzofuran, benzodioxan, benzodioxole (commonly referred to as methylenedioxyphenyl when occurring as a substituent), tetrazole, morpholine, thiazole, pyridine, pyridazine, pyrimidine, thiophene, furan, oxazole, oxazoline, isoxazole, dioxane, tetrahydrofuran and the like. It is to be noted that heteroaryl is a subset of heterocycle in which the heterocycle is aromatic. Examples of heterocyclyl residues additionally include piperazinyl 2-oxopiperazinyl, 2-oxopiperidinyl, 2-oxo-pyrrolidinyl, 2-oxoazepinyl, azepinyl, 4-piperidinyl, pyrazolidinyl, imidazolyl imidazolinyl, imidazolidinyl, pyrazinyl, oxazolidinyl, isoxazolidinyl, thiazolidinyl, isothiazolyl, quinuclidinyl, isothiazolidinyl, benzimidazolyl, thiadiazolyl, benzopyranyl, benzothiazolyl, tetrahydrofuryl, tetrahydropyranyl, thienyl, benzothienyl, thiamorpholinyl, thiamorpholinylsulfoxide, thiamorpholinylsulfone, oxadiazolyl, triazolyl and tetrahydroquinolinyl.
An oxygen heterocycle is a heterocycle containing at least one oxygen in the ring; it may contain additional oxygens, as well as other heteroatoms. A sulphur heterocycle is a heterocycle containing at least one sulphur in the ring; it may contain additional sulphurs, as well as other heteroatoms. Oxygen heteroaryl is a subset of oxygen heterocycle; examples include furan and oxazole. Sulphur heteroaryl is a subset of sulphur heterocycle; examples include thiophene and thiazine. A nitrogen heterocycle is a heterocycle containing at least one nitrogen in the ring; it may contain additional nitrogens, as well as other heteroatoms. Examples include piperidine, piperazine, morpholine, pyrrolidine and thiomorpholine. Nitrogen heteroaryl is a subset of nitrogen heterocycle; examples include pyridine, pyrrole and thiazole.
Substituted alkyl, aryl, cycloalkyl, heterocyclyl etc. refer to alkyl aryl, cycloalkyl, or heterocyclyl wherein up to three H atoms in each residue are replaced with acyl, halogen, haloalkyl, alkyl, hydroxy, loweralkoxy, carboxy, carboalkoxy (also referred to as alkoxycarbonyl), carboxamido (also referred to as alkylaminocarbonyl), cyano, carbonyl (oxo), nitro, amino, alkylamino, dialkylamino, mercapto, alkylthio, sulfoxide, sulfone, acylamino, amidino, phenyl, benzyl, heteroaryl, phenoxy, benzyloxy, or heteroaryloxy. For the purpose of this application, “substituted” includes the (difluoromethylene)dioxy and dialkylaminoalkoxy substituents, which are exemplified below.
The terms “halogen” and “halo” refer to fluorine, chlorine, bromine or iodine.
Some of the compounds described herein may contain one or more asymmetric centers and may thus give rise to enantiomers, diastereomers, and other stereoisomeric forms that may be defined, in terms of absolute stereochemistry, as (R)- or (S)-. The present invention is meant to include all such possible isomers, as well as, their racemic and optically pure forms. Optically active (R)- and (S)-isomers may be prepared using chiral synthons or chiral reagents, or resolved using conventional techniques. When the compounds described herein contain olefinic double bonds or other centers of geometric asymmetry, and unless specified otherwise, it is intended that the compounds include both E and Z geometric isomers. Likewise, all tautomeric forms are also intended to be included. The configuration of any carbon-carbon double bond appearing herein is selected for convenience only and is not intended to designate a particular configuration; thus a carbon-carbon double bond depicted arbitrarily herein as trans may be Z, E or a mixture of the two in any proportion.
The graphic representations of racemic, ambiscalemic and scalemic or enantiomerically pure compounds used herein are taken from Maehr J. Chem. Ed. 62, 114-120 (1985): solid and broken wedges are used to denote the absolute configuration of a chiral element; wavy lines indicate disavowal of any stereochemical implication which the bond it represents could generate; solid and broken bold lines are geometric descriptors indicating the relative configuration shown but denoting racemic character, and wedge outlines and dotted or broken lines denote enantiomerically pure compounds of indeterminate absolute configuration.
It will be recognized that the compounds of this invention can exist in radiolabeled form, i.e., the compounds may contain one or more atoms containing an atomic mass or mass number different from the atomic mass or mass number usually found in nature. Radioisotopes of hydrogen, carbon, phosphorous, fluorine, chlorine and iodine include 3H, 14C, 35S, 18F, 36Cl and 125I, respectively. Compounds that contain those radioisotopes and/or other radioisotopes of other atoms are within the scope of this invention. Tritiated, i.e. 3H, and carbon-14, i.e., 14C, radioisotopes are particularly preferred for their ease in preparation and detectability. Radiolabeled compounds of this invention can generally be prepared by methods well known to those skilled in the art. Conveniently, such radiolabeled compounds can be prepared by carrying out the procedures disclosed in the Examples by substituting a readily available radiolabeled reagent for a non-radiolabeled reagent. Because of the high affinity for the A2a receptor, radiolabeled compounds of the invention are useful for A2a receptor assays.
Terminology related to “protecting”, “deprotecting” and “protected” functionalities occurs throughout this application. Such terminology is well understood by persons of skill in the art and is used in the context of processes that involve sequential treatment with a series of reagents. In that context, a protecting group refers to a group which is used to mask a functionality during a process step in which it would otherwise react, but in which reaction is undesirable. The protecting group prevents reaction at that step, but may be subsequently removed to expose the original functionality. The removal or “deprotection” occurs after the completion of the reaction or reactions in which the functionality would interfere. Thus, when a sequence of reagents is specified, as it is in the processes of the invention, the person of ordinary skill can readily envision those groups that would be suitable as “protecting groups”. Suitable groups for that purpose are discussed in standard textbooks in the field of chemistry, such as Protective Groups in Organic Synthesis by T. W. Greene [John Wiley & Sons, New York, 1991], which is incorporated herein by reference.
A comprehensive list of abbreviations utilized by organic chemists appears in the first issue of each volume of the Journal of Organic Chemistry. The list, which is typically presented in a table entitled “Standard List of Abbreviations”, is incorporated herein by reference.
In general, the compounds of the present invention may be prepared by the methods illustrated in the general reaction schemes as, for example, described below, or by modifications thereof, using readily available starting materials, reagents and conventional synthesis procedures. In these reactions, it is also possible to make use of variants that are in themselves known, but are not mentioned here. The starting materials, for example in the case of suitably substituted benzimidazole ring compounds, are either commercially available, synthesized as described in the examples or may be obtained by the methods well known to persons of skill in the art.
The present invention further provides pharmaceutical compositions comprising as active agents, the compounds described herein.
As used herein a “pharmaceutical composition” refers to a preparation of one or more of the compounds described herein, or physiologically acceptable salts or solvents thereof, with other chemical components such as physiologically suitable carriers and excipients.
Pharmaceutical compositions for use in accordance with the present invention thus may be formulated in conventional manner using one or more physiologically acceptable carriers comprising excipients and auxiliaries, which facilitate processing of the active compounds into preparations which, can be used pharmaceutically. Proper formulation is dependent upon the route of administration chosen.
Compounds that antagonize the adenosine receptor can be formulated as pharmaceutical compositions and administered to a mammalian subject, such as a human patient in a variety of forms adapted to the chosen route of administration, i.e., orally or parenterally, by intravenous, intramuscular, topical, transdermal or subcutaneous routes.
For oral administration, the compounds can be formulated readily by combining the active compounds with pharmaceutically acceptable carriers well known in the art. Such carriers enable the compounds of the invention to be formulated as tablets, pills, dragees, capsules, liquids, gels, syrups, slurries, suspensions, and the like, for oral ingestion by a patient. Pharmacological preparations for oral use can be made using a solid excipient, optionally grinding the resulting mixture, and processing the mixture of granules, after adding suitable auxiliaries if desired, to obtain tablets or dragee cores. Suitable excipients are, in particular, fillers such as sugars, including lactose, sucrose, mannitol, or sorbitol; cellulose preparations such as, for example, maize starch, wheat starch, rice starch, potato starch, gelatin, gum tragacanth, methyl cellulose, hydroxypropylmethyl-cellulose, sodium carbomethylcellulose; and/or physiologically acceptable polymers such as polyvinylpyrrolidone (PVP). If desired, disintegrating agents may be added, such as cross-linked polyvinyl pyrrolidone, agar or alginic acid or a salt thereof such as sodium alginate.
In addition, enteric coating may be useful as it is may be desirable to prevent exposure of the compounds of the invention to the gastric environment. Pharmaceutical compositions, which can be used orally, include push-fit capsules made of gelatin as well as soft, sealed capsules made of gelatin and a plasticizer, such as glycerol or sorbitol. The push-fit capsules may contain the active ingredients in admixture with filler such as lactose, binders such as starches, lubricants such as talc or magnesium stearate and, optionally, stabilizers.
In soft capsules, the active compounds may be dissolved or suspended in suitable liquids, such as fatty oils, liquid paraffin, or liquid polyethylene glycols. In addition, stabilizers may be added. All formulations for oral administration should be in dosages suitable for the chosen route of administration.
For injection, the compounds of the invention may be formulated in aqueous solutions, preferably in physiologically compatible buffers such as Hank's or Ringer's solution or physiological saline buffer. For transmucosal and transdermal administration, penetrants appropriate to the barrier to be permeated may be used in the composition. Such penetrants, including for example DMSO or polyethylene glycol, are known in the art.
For administration by inhalation, the compounds for use according to the present invention are conveniently delivered in the form of an aerosol spray presentation from a pressurized pack or a nebulizer with the use of a suitable propellant, e.g., dichlorodifluoromethane, trichlorofluoromethane, dichloro-tetrafluoroethane or carbon dioxide. In the case of a pressurized aerosol, the dosage unit may be determined by providing a valve to deliver a metered amount. Capsules and cartridges of, e.g., gelatin for use in an inhaler or insufflator may be formulated containing a powder mix of the compound and a suitable powder base such as lactose or starch.
Pharmaceutical compositions for parenteral administration include aqueous solutions of the active ingredients in water-soluble form. Additionally, suspensions of the active compounds may be prepared as appropriate oily injection suspensions. Suitable lipophilic solvents or vehicles include fatty oils such as sesame oil, or synthetic fatty acids esters such as ethyl oleate, triglycerides or liposomes. Aqueous injection suspensions may contain substances, which increase the viscosity of the suspension, such as sodium carboxymethyl cellulose, sorbitol or dextran. Optionally, the suspension may also contain suitable stabilizers or agents, which increase the solubility of the compounds, to allow for the preparation of highly concentrated solutions.
The compounds of the present invention may also be formulated in rectal compositions such as suppositories or retention enemas, using, e.g., conventional, suppository bases such as cocoa butter or other glycerides.
Depending on the severity and responsiveness of the condition to be treated, dosing can also be a single administration of a slow release composition, with course of treatment lasting from several days to several weeks or until cure is effected or diminution of the disease state is achieved. The amount of a composition to be administered will, of course, be dependent on many factors including the subject being treated, the severity of the affliction, the manner of administration, the judgment of the prescribing physician. The compounds of the invention may be administered orally or via injection at a dose from 0.001 to 2500 mg/kg per day. The dose range for adult humans is generally from 0.005 mg to 10 g/day. Tablets or other forms of presentation provided in discrete units may conveniently contain an amount of compound of the invention which is effective at such dosage or as a multiple of the same, for instance, units containing 5 mg to 500 mg, usually around 10 mg to 200 mg. The precise amount of compound administered to a patient will be the responsibility of the attendant physician. However, the dose employed will depend on a number of factors, including the age and sex of the patient, the precise disorder being treated, and its severity. Also, the route of administration may vary depending on the condition and its severity.
As used herein, and as would be understood by the person of skill in the art, the recitation of “a compound” is intended to include salts, solvates and inclusion complexes of that compound. The term “solvate” refers to a compound of Formula I in the solid state, wherein molecules of a suitable solvent are incorporated in the crystal lattice. A suitable solvent for therapeutic administration is physiologically tolerable at the dosage administered. Examples of suitable solvents for therapeutic administration are ethanol and water. When water is the solvent, the solvate is referred to as a hydrate. In general, solvates are formed by dissolving the compound in the appropriate solvent and isolating the solvate by cooling or using an antisolvent. The solvate is typically dried or azeotroped under ambient conditions. Inclusion complexes are described in Remington: The Science and Practice of Pharmacy 19th Ed. (1995) volume 1, page 176-177, which is incorporated herein by reference. The most commonly employed inclusion complexes are those with cyclodextrins, and all cyclodextrin complexes, natural and synthetic, are specifically encompassed within the claims.
The term “pharmaceutically acceptable salt” refers to salts prepared from pharmaceutically acceptable non-toxic acids or bases including inorganic acids and bases and organic acids and bases. When the compounds of the present invention are basic, salts may be prepared from pharmaceutically acceptable non-toxic acids including inorganic and organic acids. Suitable pharmaceutically acceptable acid addition salts for the compounds of the present invention include acetic, benzenesulfonic (besylate), benzoic, camphorsulfonic, citric, ethenesulfonic, fumaric, gluconic, glutamic, hydrobromic, hydrochloric, isethionic, lactic, maleic, malic, mandelic, methanesulfonic, mucic, nitric, pamoic, pantothenic, phosphoric, succinic, sulfuric, tartaric acid, p-toluenesulfonic, and the like. When the compounds contain an acidic side chain, suitable pharmaceutically acceptable base addition salts for the compounds of the present invention include metallic salts made from aluminum, calcium, lithium, magnesium, potassium, sodium and zinc or organic salts made from lysine, N,N′-dibenzylethylenediamine, chloroprocaine, choline, diethanolamine, ethylenediamine, meglumine (N-methylglucamine) and procaine.
The term “preventing” as used herein refers to administering a medicament beforehand to forestall or obtund an attack. The person of ordinary skill in the medical art (to which the present method claims are directed) recognizes that the term “prevent” is not an absolute term. In the medical art it is understood to refer to the prophylactic administration of a drug to substantially diminish the likelihood or seriousness of a condition, and this is the sense intended herein.
It should be understood that in addition to the ingredients particularly mentioned above, the formulations of this invention may include other agents conventional in the art having regard to the type of formulation in question, for example those suitable for oral administration may include flavoring agents.
The compositions may be presented in a packaging device or dispenser, which may contain one or more unit dosage forms containing the active ingredient. Examples of a packaging device include metal or plastic foil, such as a blister pack and a nebulizer for inhalation. The packaging device or dispenser may be accompanied by instructions for administration. Compositions comprising a compound of the present invention formulated in a compatible pharmaceutical carrier may also be placed in an appropriate container and labeled for treatment of an indicated condition.
The compounds of the present invention are useful in inhibiting the activity of A2a receptors or in inhibiting A2a receptor-mediated activity and are useful in treating complications arising therefrom.
According to the present invention, the A2a receptor antagonists may be administered prophylactically, for example prior to onset of an acute condition, or they may be administered after onset of the condition, or at both times.
The following examples will further describe the invention, and are used for the purposes of illustration only, and should not be considered as limiting the invention being disclosed.
The following abbreviations and terms have the indicated meaning throughout:
Compounds of formula I were synthesized by means of conventional organic synthesis executable by those skilled in the art. The illustration of examples, but not the limitation, of the synthesis of compounds of formula I is detailed in schemes 1-4, herein below:
Compounds of formula I (type I-5) were synthesized in five steps from commercially available 2,4-dichloro-5-nitropyrimidine (Scheme 1). Initial N-arylation of a primary amine (R1—NH2) with 2,4-dichloro-5-nitropyrimidine provides a mixture (typically a 10:1 ratio) of regioisomers which can be readily separated by flash chromatography. The predominant regioisomer (I-1, corresponding to amino substitution at the C-4 position) was further functionalized at C-2 with a primary or secondary amine (R2—NH—R2a) followed by nitro reduction to provide I-3. Purinone formation is achieved using carbonyl diimidazole and further functionalization of the purinone nucleus to afford I-5 was achieved using alkyl halides in the presence of base. Analogous compounds of formula I can be synthesized using similar experimental procedures.
Alternatively, compounds of formula I (type I-5) can be synthesized by reductive alkylation of I-3 with an aldehyde or ketone followed by cyclization to the purinone with carbonyl diimidazole (Scheme 2). Analogous compounds of formula I can be synthesized using similar experimental procedures.
Compounds of formula I (type I-5) can also be synthesized employing a modified synthetic route from I-1 (Scheme 3). Reduction of the nitro group of 1-1 provides I-6, which is subsequently cyclized to the 2-chloropurinone with carbonyl diimidazole to provide I-7. Functionalization of the purinone nucleus to afford I-8 was achieved using alkyl halides in the presence of base. Final displacement of the 2-chloro group of I-8 is conducted under either thermal or microwave assisted conditions using a primary or secondary amine (R2—NH—R2a) to provide I-5. Arylation of 2,4-dimethoxy benzyl amine with I-8 followed by acid mediated cleavage of the dimethoxybenzyl group provides compounds of formula I where R2═R2a═H. Analogous compounds of formula I can be synthesized using similar experimental procedures.
Compounds of formula I (type I-10) which incorporate an aryl substituent at the R3 position were synthesized from I-3 (Scheme 4). Buchwald coupling of an aryl halide to I-3 provides I-9. Purinone formation is achieved by heating with carbonyl diimidazole followed by the application of hydrolytic conditions to generate I-10. Analogous compounds of formula I can be synthesized using similar experimental procedures.
To 2.1 g (11.0 mmol, 1.0 eq.) of 2,4-dichloro-5-nitropyrimidine in 20 mL of THF at −78° C. under an argon atmosphere was added 3.8 mL (22 mmol, 2.0 eq.) of N,N-diisopropylethylamine and 1.2 mL (11.0 mmol, 1.0 eq.) of m-anisidine. The reaction mixture was stirred for 30 min at −78° C. and then allowed to warm to room temperature and stirred for an additional 3 h. The solvent was removed in vacuo and the residue partitioned between 100 mL of EtOAc and 50 mL of water. The organic solution was washed with 50 mL of saturated brine, dried (Na2SO4) and the solvent removed in vacuo. The product was purified by flash chromatography eluting with 80% CH2Cl2/hexanes to provide 1.9 g (6.8 mmol, 62%) of 2-chloro-N-(3-methoxyphenyl)-5-nitropyrimidin-4-amine (I-1) as a yellow solid. δH (300 MHz, CDCl3) 3.85 (s, 3H), 6.82 (m, 1H), 7.14 (m, 1H), 7.35 (m, 2H), 9.18 (s, 1H), 10.21 (bs, 1H); (ESI) 281.1, [M+H]+.
To a solution of 0.25 g (0.89 mmol, 1.0 eq.) of 2-chloro-N-(3-methoxyphenyl)-5-nitropyrimidin-4-amine (I-1) in 5 mL of THF was added 0.25 mL (1.78 mmol, 2.0 eq.) of triethylamine and 75 μL (1.07 mmol, 1.2 eq.) of cyclopropylamine. The mixture was stirred for at room temperature for 1 h and a solution of 1.5 g (˜7.3 mmol, ˜85% tech. grade, ˜8 eq) of sodium hydrosulfite and 0.75 g (8.9 mmol, ˜10 eq.) of sodium hydrogen carbonate in 10 mL of water was added. The mixture was diluted with 5 mL of THF and 5 mL of MeOH and the mixture stirred vigorously at room temperature for 1 h. The mixture was diluted with 35 mL of EtOAc and 15 mL of sat. NaHCO3 (aq) and the layers separated. The organic phase was washed with 10 mL of sat. brine, dried (Na2SO4) and the solvent removed in vacuo to provide 0.22 g of N2-cyclopropyl-N4-(3-methoxyphenyl)pyrimidine-2,4,5-triamine (I-3). δH (300 MHz, CDCl3) 0.53 (m, 2H), 0.80 (m, 2H), 2.73 (m, 1H), 3.82 (s, 3H), 5.15 (bs, 1H), 6.60 (m, 1H), 7.21 (m, 2H), 7.58 (m, 2H), 7.74 (s, 1H); m/z (ESI) found 272.1 [M+H]+.
To a solution of 86 mg (0.32 mmol, 1.0 eq.) of N2-cyclopropyl-N4-(3-methoxyphenyl)pyrimidine-2,4,5-triamine (I-3) in 3 mL of CH2Cl2 was added 115 mg (0.71 mmol, 2.2 eq.) of carbonyl diimidazole. The reaction mixture was stirred at room temperature for 16 h. The mixture was diluted with 20 mL of chloroform and 10 mL of sat. NaHCO3 (aq) and the layers separated. The organic phase was dried (Na2SO4) and the solvent removed in vacuo to provide 75 mg (0.25 mmol, 78%) of 2-(cyclopropylamino)-9-(3-methoxyphenyl)-7H-purin-8(9H)-one (1-4) as an off-white solid. δH (300 MHz, d6DMSO) 0.42 (m, 2H), 0.75 (m, 2H), 2.53 (m, 1H), 3.70 (s, 3H), 7.00 (m, 3H), 7.37 (m, 1H), 7.82 (s, 1H), 11.72 (bs, 1H), 7.74 (s, 1H); (ESI) 298.1 [M+H]+.
To a suspension of 50 mg (0.17 mmol, 1 eq.) of 2-(cyclopropylamino)-9-(3-methoxyphenyl)-7H-purin-8(9H)-one (14) and 150 mg (2.2 mmol/g, 0.33 mmol) of polystyrene bound 2-tert-butylimino-2-diethylamino-1,3-dimethyl-1,3,2-diazaphosphorinane (Polystyrene bound BEMP) in 6 mL of acetonitrile was added 60 μL (0.5 mmol, 3 eq.) of benzyl bromide and the mixture stirred vigorously at room temperature for 30 min. The resin was removed by filtration and washed with 3 mL of CH2Cl2. The solvent was removed in vacuo and the residue purified by flash chromatography (50% EtOAc/hexanes to EtOAc) to provide 48 mg (0.12 mmol, 73%) of 7-benzyl-2-(cyclopropylamino)-9-(3-methoxyphenyl)-7H-purin-8(9H)-one (I-5) as a white solid. δH (300 MHz, CDCl3) 0.20 (m, 2H), 0.72 (m, 2H), 2.65 (m, 1H), 3.82 (s, 3H), 5.00 (s, 2H), 5.14 (s, 1H), 6.91 (m, 1H), 7.30 (m, 8H), 7.72 (s, 1H); (ESI) 388.2 [M+H]+.
To a solution of 25 mg (0.09 mmol, 1.0 eq.) of N2-cyclopropyl-N4-(4-methoxyphenyl)pyrimidine-2,4,5-triamine (I-3) in 2 mL of THF was added 100 μL (1.0 mmol, ˜10 eq.) of benzaldehyde. The reaction mixture was stirred at room temperature for 2 h. The mixture was diluted with 2 mL of methanol and 120 mg (3.2 mmol, 35 eq.) of sodium borohydride was added. The mixture was stirred at room temperature for 30 min and 5 mL of acetone added. The mixture was stirred at room temperature for an additional 30 min and the solvent removed in vacuo. The residue was redissolved in 20 mL of EtOAc and washed with 10 mL of sat. NaHCO3 and 10 mL of sat. brine. The organic phase was dried (Na2SO4) and the solvent removed in vacuo. The residue was redissolved in 2 mL of CH2Ch and 150 mg (0.92 mmol, 10 eq.) of carbonyl diimidazole added. The mixture was stirred at room temperature for 16 h. The mixture was diluted with 10 mL of CH2Cl2 and washed with 10 mL of sat. NaHCO3. The organic phase was dried (Na2SO4) and the solvent removed in vacuo. The residue was purified by flash chromatography (50-80% EtOAc/hexanes) to provide 10.5 mg (27 μmol 30% from I-3) of 7-benzyl-2-(cyclopropylamino)-9-(4-methoxyphenyl)-7H-purin-8(9H)-one (I-5) as a white solid. (δH, 300 MHz, CDCl3) 0.46 (m, 2H), 0.75 (m, 2H), 2.67 (m, 1H), 3.85 (s, 3H), 5.04 (s, 2H), 5.13 (bs, 1H), 7.11 (d, 2H), 7.37 (m, 5H), 7.57 (d, 2H), 7.72 (s, 1H); ESI, 388.1 [M+H].
To a solution of 4.3 g (15.4 mmol, 1.0 eq.) of 2-chloro-N-(3-methoxyphenyl)-5-nitro pyrimidin-4-amine (I-1) in 100 mL of THF was added a solution of 13.3 g (76.8 mmol ˜85% tech. grade, ˜5 eq) of sodium hydrosulfite and 8.14 g (76.8 μmmol 5 eq.) of sodium hydrogen carbonate in 100 mL of water. The mixture was stirred vigorously at room temperature for 1 h. The mixture was diluted with 100 mL of EtOAc and the layers separated. The organic phase was dried (Na2SO4) and the solvent removed in vacuo. The residue was redissolved in 50 mL of CH2Cl2 and 13 g (80 mmol, ˜5 eq.) of carbonyl diimidazole was added. The reaction mixture was stirred at room temperature for 16 h. The mixture was diluted with 50 mL of chloroform and 50 mL of sat. NaHCO3 (aq) and the layers separated. The organic phase was dried (Na2SO4) and the solvent removed in vacuo. The residue was purified by flash chromatography (eluting with a linear gradient of 20-100% EtOAc/hexanes) to provide 2.7 g (9.78 mmol. 64%) of 2-(cyclopropylamino)-9-(3-methoxyphenyl)-7H-purin-8(9H)-one (1-7) as an off-white solid.
To a suspension of 28 mg (0.10 mmol, 1 eq.) of 2-chloro-9-(3-methoxyphenyl)-7H-purin-8(9H)-one (1-3) and 150 mg (2.2 mmol/g, 0.33 mmol) of polystyrene bound 2-tert-butylimino-2-diethylamino-1,3-dimethyl-1,3,2-diazaphosphorinane (polystyrene bound BEMP) in 6 mL of acetonitrile was added 36 μL (0.30 mmol, 3 eq.) of 2-fluorobenzyl bromide and the mixture stirred vigorously at room temperature for 30 min. The resin was removed by filtration and washed with 3 mL of CH2Cl2. The solvent was removed in vacuo and the residue was triturated with 5:1 v/v hexanes/EtOAc 3 times to provide 36 mg (0.093 mmol, 92%) of 7-(2-fluorobenzyl)-2-chloro-9-(3-methoxyphenyl) 7H-purin-8(9H)-one (1-8) as a white solid.
To a solution of 10 mg (26 μmol, 1 eq.) of 7-(2-fluorobenzyl)-2-chloro-9-(3-methoxyphenyl)-7H-purin-8(9H)-one (14) in 0.5 mL of DMA was added 26 μL (0.26 nmol, 10 eq.) of 3-aminomethlypyridine and the mixture subjected to microwave irradiation maintaining an internal reaction temperature of 180° C. for 20 min. The solvent was removed in vacuo and the residue was purified by semi-preparative hplc to provide 6.7 mg (14 mmol, 54%) m/z (ESI) found 457.1, [M+H]+.
To a solution of 10 mg (26 umol, 1 eq.) of 7-(2-fluorobenzyl)-2-chloro-9-(3-methoxyphenyl)-7H-purin-8(9H)-one (14) in 0.5 mL of DMA was added 40 μL (0.26 mmol 10 eq.) of 2,4-dimethoxybenzyl amine and the mixture subjected to microwave irradiation maintaining an internal reaction temperature of 180° C. for 20 min. The mixture was diluted with 1 mL of 1 M HCl and 5 mL of EtOAc. The layers were separated and the aqueous phase extracted with 3×5 mL of EtOAc. The combined organic extracts were dried (Na2SO4) and the solvent was removed in vacuo. The residue was purified by flash chromatography, eluting with 50% EtOAc/hexanes to provide 6 mg of 2-(2,4-dimethoxybenzylamino)-7-(2-fluorobenzyl)-9-(3-methoxyphenyl)-7H-purin-8(9H)-one (1-6) which was subsequently treated with 1 mL of 50% v/v TFA/CH2Cl2 and 50 μL oftriethylsilane. The mixture was stirred at room temperature for 2 h and the solvent removed in vacuo. The residue was purified by flash chromatography eluting with 50% EtOAc/hexanes to provide 2 mg (5.2 mmol, 20% from I-8) of 7-(2-fluorobenzyl)-2-amino-9-(3-methoxyphenyl)-7H-purin-8(9H)-one. OH (300 MHz, CDCl3) 3.85 (s, 3H), 5.08 (s, 2H), 7.1 (m, 5H), 7.38 (m, 1H), 7.45 (m, 2H), 7.60 (s, 1H); m/z (ESI) found 366.2, [M+H]+
To a mixture of 2 mg (4.3 mmol, 0.02 eq.) of 2-(2′-di-tert-butylphosphine) biphenylpalladium(II) acetate and 26 mg (0.27 mmol, 1.4 eq.) of sodium tert-butoxide in 1 mL of toluene under an argon atmosphere was added 52 mg (0.19 mmol) of N2-cyclopropyl-N4-(3-methoxyphenyl)pyrimidine-2,4,5-triamine. A portion of 24 μL (0.19 mmol, 1 eq.) of 3-bromoanisole was added and the mixture was stirred at 80° C. for 18 h. The volatiles were removed in vacuo and the residue purified by flash chromatography eluting with 50% EtOAc/hexane to provide 26 mg (69 μmol) of N2-cyclopropyl-N4,N5-bis(3-methoxyphenyl)pyrimidine-2,4,5-triamine (I-9) as a white solid. ESI, 378.2 [M+H].
To a solution of 12 mg (32 Mmol, 1 eq.) of N2-cyclopropyl-N4,N5-bis(3-methoxyphenyl)pyrimidine-2,4,5-triamine (I-9) in 2 mL of dichloromethane in a sealed tube reaction vessel was added 52 mg (0.32 mmol, 10 eq.) of carbonyldiimidazole. The reaction vessel was sealed and heated at 60° C. for 18 h. The mixture was allowed to cool to room temperature and then washed with water. The organic phase was dried (Na2SO4) and the solvent removed in vacuo. The residue was redissolved in 2 mL of 20% H2O/THF and 0.05 mL of trifluoroacetic acid added. The mixture was heated at 50° C. for 16 h. The mixture was allowed to cool to room temperature and was extracted with 3×2 mL of EtOAc. The combined organic extracts were dried (Na2SO4) and the solvent removed in vacuo. The residue was purified by flash chromatography (50% EtOAc/hexanes) to provide 6 mg (15 μmol, 50%) of 2-(cyclopropylamino)-7,9-bis(3-methoxyphenyl)-7H-purin-8(9H)-one (I-10). (δH, 300 MHz, CDCl3) 0.53 (m, 2H), 0.80 (m, 2H), 2.75 (m, 1H), 3.86 (s, 6H), 5.30 (m, 1H), 6.95 (m, 2H), 7.17 (m, 2H), 7.32 (m, 2H), 7.44 (m, 2H), 8.13 (s, 1H); ESI, 404.2 [M+H].
Method A: Waters Millenium 2690/996PDA separations system employing a Phenomonex Luna 3u C8 50×4.6 mm analytical column. The aqueous acetonitrile based solvent gradient involves;
0-1 min—Isocratic 10% of (0.1% TFA/acetonitrile); 1 min-7 min—Linear gradient of 10-90% of (0.1% TFA/acetonitrile): 7 min-9 min—Isocratic 90% of (0.1% TFA/acetonitrile); 9 min-10 min—Linear gradient of 90-10% of (0.1% TFA/acetonitrile); 10 min-12 min—Isocratic 10% of (0.1% TFA/acetonitrile). Flow rate=1 mL/min.
Method B: Waters Millenium 2690/996PDA separations system employing a Phenomenex Columbus 5u C18 column 50×4.60 mm analytical column. The aqueous acetonitrile-based solvent gradient involves;
0-0.5 min—Isocratic 10% of (0.05% TFA/acetonitrile); 0.5 min-5.5 min—Linear gradient of 10-90% of (0.05% TFA/acetonitrile): 5.5 min-7.5 min—Isocratic 90% of (0.05% TFA/acetonitrile); 7.5 min-8 min—Linear gradient of 90-10% of (0.05% TFA/acetonitrile); 8 min-10 min—Isocratic 10% of (0.05% TFAlacetonitrile). Flow rate=0.4 mL/min.
Method C: Waters Millenium 600/996PDA separations system employing a Waters Sunfire 5u C18 column 100×4.60 mm analytical column. The aqueous acetonitrile based solvent gradient involves;
0 min-5.5 min—Linear gradient of 20-90% of (0.05% TFA/acetonitrile): 5.5 min-7.0 min—Isocratic 90% of (0.05% TFA/acetonitrile); 7.0 min-8 min—Linear gradient of 90-20% of (9.05% TFA/acetonitrile); 8 min-10 min—Isocratic 20% of (0.05% TFA/acetonitrile). Flow rate=1.0 mL/min
Mass Spectroscopy was conducted using a Thermo-electron LCQ classic or an Applied Biosciences PE Sciex API150ex. Liquid Chromatography Mass Spectroscopy was conducted using a Waters Millenium 2690/996PDA linked Thermo-electron LCQ classic.
1H NMR spectroscopy was conducted using a Varian 300 MHz Gemini 2000 and a Bruker 300 MHz AVANCE 300 FTNMR.
Membranes prepared from HEK-293 cells that express human A2a (0.04 mg/mL final, PerkinElmer Life and Analytical Sciences, Boston, Mass.) were mixed with yttrium oxide wheatgerm-agglutinin (WGA)-coated SPA beads (4 mg/mL final, Amersham Biosciences, Piscataway, N.J.) and adenosine deaminase (0.01 mg/mL final) in assay buffer (Dulbecco's phosphate-buffered saline containing 10 mM MgCl2) for 15 minutes at 4° C. This mixture (10 μL) was added with continuous agitation to the test compounds (10 μL) prepared in 2.5% DMSO orto 2.5% DMSO (1% final) in 384-well assay plates (Corning #3710).
Binding was initiated with the addition of 5 L of [3H]-SCH 58261 (2 nM final, Amersham Biosciences) immediately followed by centrifugation at 1000 rpm for 2 min. The assay plates were incubated in the dark, overnight at room temperature and the signal was detected using a ViewLux CCD Imager (PerkinElmer). Compounds were tested at 11 different concentrations ranging from 0.1 nM to 10 μM. Nonspecific binding was determined in the presence of 10 μM CGS 15943. Assays were performed in duplicate and compounds were tested at least twice. The data were fit to a one-site competition binding model for IC50 determination using the program GraphPad Prism (GraphPad Software, Inc., San Diego, Calif.) and Ki values were calculated using the Cheng-Prusoff equation (Cheng, Y, Prusoff, W. H. Biochem. Pharmacol. 1973, 22, 3099).
As described in Matasi et al. (Bioorg. Med. Chem. Lett 2005, 15, 1333), membranes (10 μg) prepared from CHO (Chinese Hamster Ovary) cells that express human A1 were mixed with 1 nM (final) [3H]-DPCPX in 200 μL assay buffer (2.7 mM KCl, 1.1 mM KH2PO4, 137 mM NaCl, 7.6 mM Na2HPO4, 10 mM MgCl2, 0.04% methyl cellulose, 20 μg/mL adenosine deaminase) containing 4% DMSO with or without test compounds. Reactions were carried out for 60 min at room temperature and were terminated by rapid filtration over GF/B filters. Filters were washed seven times with 1 mL cold distilled H2O, air dried, and radioactivity retained on filters were counted in a Packard TopCount® NXT microplate scintillation counter (Global Medical Instrumentation, Inc., Ramsey, Minn.). Compounds were tested at 10 different concentrations ranging from 0.1 nM to 10 μM. Non-specific binding was determined in the presence of 10 μM NECA (5′-(N-ethylcarboxamido)adenosine). Assays were preformed in duplicate and compounds were tested two times. Data were fit to a one-site competition binding model for IC50 determination using the program GraphPad Prism (GraphPad Software, Inc., San Diego, Calif.) and Ki values were calculated using the Cheng-Prusoff equation (Cheng, Y, Prusoff, W. H. Biochem. Pharmacol. 1973, 22, 3099).
Representative species are shown below in Table 1. Compounds exhibited Ki values for A2a≦10 μM.
(δH, 300 MHz, CD3OD) 3.81 (s, 3H), 4.72 (s, 2H), 5.20 (s, 2H), 7.03 (m, 5H), 7.44 (m, 2H), 7.94 (m, 2H), 8.45 (d, 1H), 8.72 (m, 2H); ESI, 475.2 [M+H].
(δH, 300 MHz, CDCl3) 1.56 (d, 3H) 3.85 (s, 3H), 4.90 (m, 1H), 5.10 (q, 2H), 6.97 (m, 4H), 7.04 (m, 1H), 7.21 (m, 1H), 7.25 (m, 4H), 7.40 (m, 3H); ESI, 488.1 [M+H].
(δH, 300 MHz, CD3OD) 1.21 (t, 3H), 3.31 (q, 2H), 3.82 (s, 3H), 5.19 (s, 2H), 7.08 (m, 3H), 7.15 (m, 2H), 7.46 (m, 2H), 7.93 (m, 1H), 7.81 (s, 1H); ESI, 412 [M+H].
(δH, 300 MHz, CDCl3) 3.50 (q, 2H), 3.77 (t, 2H), 3.85 (s, 3H), 5.16 (s, 2H), 5.35 (bt, 1H), 6.96 (m, 3H), 7.21 (m, 1H), 7.26 (m, 1H), 7.33 (m, 1H), 7.40 (m, 1H), 7.79 (s, 1H); ESI, 428.2 [M+H].
(δH, 300 MHz, CD3OD) 3.81 (s, 3H), 4.71 (s, 2H), 5.20 (s, 2H), 7.02 (m, 5H), 7.40 (m, 2H), 7.70 (m, 1H), 7.78 (d, 1H), 7.89 (s, 1H), 8.26 (m, 1H), 8.58 (d, 1H); ESI, 475.2 [M+H].
(δH, 300 MHz, CD3OD) 2.81 (s, 6H), 3.30 (m, 2H), 3.74 (m, 2H), 3.83 (s, 3H), 5.21 (s, 2H), 7.06 (m, 3H), 7.16 (m, 2H), 7.46 (r, 2H), 7.95 (s, 1H); ESI, 455.1 [M+H].
(δH, 300 MHz, CDCl3) 0.44 (m, 2H), 0.73 (m, 2H), 2.65 (m, 1H), 3.82 (s, 3H), 5.09 (bd, 1H), 5.24 (s, 2H), 6.90 (m, 1H), 7.04 (m, 1H), 7.26 (m, 4H), 7.38 (m, 1H), 7.76 (s, 1H); ESI, 440.1 [M+H].
(δH, 300 MHz, (CD3)2SO) 2.94 (m, 2H), 3.48 (m, 2H), 3.86 (s, 3H), 7.05 (m, 2H), 7.28 (m, 2H), 7.31 (m, 4H), 7.34 (m, 1H), 7.51 (m, 1H), 7.97 (s, 1H), 11.08 (s, 1H); ESI, 380 [M+H].
(δH, 300 MHz, CDCl3) 1.42 (d, 6H), 3.80 (s, 3H), 3.72 (s, 3H), 4.58 (d, 2H), 4.60 (m, 1H), 4.90 (s, 2H), 5.20 (bt, 1H), 6.90 (m, 2H), 7.10 (m, 2H), 7.25 (m, 3H), 7.68 (s, 1H); ESI, 422.1 [M+H].
(δH, 300 MHz, CDCl3) 0.53 (m, 2H), 0.80 (m, 2H), 2.75 (m, 1H), 3.86 (s, 6H), 5.30 (m, 1H), 6.95 (m, 2H), 7.17 (m, 2H), 7.32 (m, 2H), 7.44 (m, 2H), 8.13 (s, 1H); ESI, 404 [M+H].
(δH, 300 MHz, CD3OD) 1.8 (m, 4H), 2.8 (1,4H), 3.1 (m, 1H), 3.45 (d, 1H), 3.8 (d, 1H), 3.85 (s, 3H), 4.1 (m, 1H), 5.2 (s, 2H), 7.0 (t, 3H), 7.15 (m, 2H), 7.45 (m, 2H), 7.9 (m, 1H); ESI, 481 [M+H].
(δH, 300 MHz, CDCl3) 2.94 (m, 3H), 3.85 (s, 3H), 3.92 (s, 3H), 3.85 (m, 1H) 5.18 (s, 2H) 6.93 (m, 3H), 7.31 (m, 3H), 7.39 (m, 2H), 7.87 (s, 1H); ESL 392 [M+H].
(δH, 300 MHz, CDCl3) 1.36 (d, 6H), 3.60 (s, 3H), 3.72 (s, 3H), 4.40 (d, 2H), 4.50 (m, 1H), 4.80 (s, 2H), 5.00 (bt, 1H), 6.64 (dd, 1H), 6.75 (m, 4H), 7.12 (m, 3H), 7.54 (s, 1H); ESI, 434.1 [M+H].
(δH, 300 MHz, CDCl3) 3.09 (t, 2H), 3.63 (q, 2H), 3.84 (s, 3H), 3.90 (s, 3H), 5.08 (s, 2H), 6.81 (d, 1H), 6.93 (m, 4H), 7.13 (dd, 1H), 7.31 (m, 3H), 7.40 (m, 2H), 7.85 (s, 1H); ESI, 488.1 [M+H].
(δH, 300 MHz, CD3OD) 0.93 (d, 6H), 1.84 (sept, 1H), 3.17 (t, 2H), 3.85 (s, 3H), 4.94 (bt, 1H), 5.16 (s, 2H), 6.94 (m, 3H), 7.29 (m, 3H), 7.40 (m, 1H), 7.82 (s, 1H); ESI, 440.2 [M+H].
(δH, 300 MHz, CD3OD) 1.26 (d, 6H), 3.83 (s, 3H), 3.99 (sept, 1H), 5.20 (s, 2H), 7.06 (m, 3H), 7.17 (m, 2H), 7.44 (m, 2H), 7.80 (s, 1H); ESI, 426.2 [M+H].
(δH, 300 MHz, CD3OD) 1.3 (m, 2H), 1.55 (m, 3H), 1.9 (m, 2H), 2.85 (m, 2H), 3.25 (m, 2H), 3.4 (m, 2H), 3.8 (s, 3H), 5.2 (s, 2H), 7.05 (m, 3H), 7.15 (m, 2H), 7.45 (m, 2H), 7.8 (s, 1H); ESI, 495 [M+H].
(δH, 300 MHz, CDCl3) 3.80 (s, 3H), 5.20 (s, 2H), 7.0 (m, 3H), 7.2 (m, 4H), 7.4 (m, 2H), 7.55 (m, 1H), 7.7 (s, 1H); ESI, 494 [M+H].
(δH, 300 MHz, CD3OD) 0.25 (m, 2H), 0.50 (m, 2H), 1.05 (m, 1H), 3.20 (d, 2H), 3.80 (s, 3H), 5.20 (s, 2H), 7.05 (m, 3H), 7.15 (m, 2H), 7.45 (m, 2H), 7.8 (s, 1H); ESL 438 [M+H].
(δH, 300 MHz, CDCl3) 2.92 (m, 2H), 3.61 (m, 2H), 3.85 (s, 3H), 3.92 (s, 3H) 5.18 (s, 2H) 6.94 (m, 2H), 7.12 (m, 1H), 7.32 (m, 2H), 7.39 (m, 1H), 7.51 (m, 2H), 7.87 (s, 1H); ESL 500 [M+H].
(δH, 300 MHz, CDCl3) 0.42 (m, 2H), 0.74 (m, 2H), 2.70 (m, 1H), 3.82 (s, 3H), 5.15 (s, 2H), 5.17 (bd, 1H), 6.94 (m, 1H), 7.02-7.36 (m, 5H), 7.40 (m, 1H), 7.93 (s, 1H); ESI, 424.1 [M+H].
(δH, 300 MHz, CDCl3) 0.61 (m, 2H), 0.67 (m, 2H), 2.76 (m, 1H), 3.84 (s, 3H), 5.18 (s, 2H), 7.00 (m, 1H), 7.20-7.40 (m, 6H), 7.45 (m, 2H); ESI, 422.1 [M+H].
(δH, 300 MHz, CD3OD) 1.75 (m, 2H), 2.25 (m, 2H), 2.85 (s, 3H), 3.07 (m, 2H), 3.53 (m, 2H), 3.83 (s, 3H), 3.94 (m, 1H), 5.20 (s, 2H), 7.04 (m, 3H), 7.14 (m, 2H), 7.45 (m, 2H), 7.91 (s, 1H); ESL 481 [M+H].
(δH, 300 MHz, CDCl 3) 3.9 (s, 3H), 5.2 (s, 2H), 6.95 (m, 4H), 7.15 (m, 3H), 7.3 (m, 2H), 7.45 (m, 1H), 7.75 (s, 1H), 7.85 (s, 1H); ESI, 494 [M+H].
(δH, 300 MHz, CDCl3) 2.3 (s, 3H), 3.8 (s, 3H), 5.2 (s, 2H), 6.9 (d, 2H), 7.0 (m, 3H), 7.15 (m, 1H), 7.3 (m, 1H), 7.45 (m, 5H), 7.7 (s, 1H); ESI, 474 [M+H].
(δH, 300 MHz, d6-DMSO) 0.37 (m, 2H), 0.57 (m, 2H), 2.57 (m, 1H), 5.03 (s, 2H), 6.11 (s, 2H), 7.06 (m, 2H), 7.11 (m, 1H), 7.21 (s, 1H), 7.37 (m, 5H), 7.95 (s, 1H); ESI, 402.2 [M+H].
(δH, 300 MHz, CDCl3) 0.61 (m, 2H), 0.80 (m, 2H), 2.78 (m, 1H), 3.83 (s, 3H), 3.90 (s, 3H), 5.00 (s, 2H), 6.88 (m, 1H), 7.00 (, 2H), 7.12 (m, 1H), 7.23 (m, 2H), 7.43 (m, 1H), 7.75 (s, 1H); ESI, 436.1 [M+H].
(δH, 300 MHz, CDCl3) 1.56 (d, 3H), 3.85 (s, 3H), 4.90 (m, 1H), 5.10 (q, 2H), 6.97 (m, 4H), 7.04 (m, 1H), 7.21 (m, 1H), 7.25 (m, 4H), 7.40 (m, 3H); ESI, 488.1 [M+H].
(δH, 300 MHz, CD3OD) 3.85 (s, 3H), 5.2 (s, 2H), 6.7 (t, 1H), 7.0 (m, 3H), 7.1 (m, 1H), 7.2 (m, 1H), 7.4 (m, 4H), 7.65 (m, 1H), 7.9 (m, 1H); ESI, 478 [M+H].
(δH, 300 MHz, CD3OD) 3.18 (t, 2H), 3.74 (t, 2H), 3.83 (s, 3H), 5.20 (s, 2H), 7.07 (m, 3H), 7.17 (m, 2H), 7.46 (m, 2H), 7.82 (d, 2H), 7.88 (s, 1H), 8.59 (d, 2H); ESI, 489.0 [M+H].
(δH, 300 MHz, CD3OD) 0.93 (t, 3H), 1.61 (m, 2H), 3.03 (m, 2H), 3.83 (s, 3H), 5.19 (s, 2H), 7.06 (m, 3H), 7.16 (m, 2H), 7.43 (m, 2H), 7.80 (s, 1H); ESI, 426.1 [M+H].
(δH, 300 MHz, CDCl3) 3.8 (s, 3H), 5.2 (s, 2H), 6.95 (m, 4H), 7.1 (s, 1H), 7.3 (m, 5H), 7.55 (d, 2H), 7.9 (s, 1H); ESI, 460 [M+H].
(δH, 300 MHz, CD3OD) 1.43 (m, 1H), 1.70 (m, 5H), 2.83 (t, 2H), 3.27 (t, 2H), 3.51 (d, 2H), 3.76 (d, 2H), 3.80 (s, 31), 5.22 (s, 2H), 7.06 (m, 3H), 7.18 (m, 2H), 7.45 (m, 2H), 7.95 (s, 1H); ESI, 495.2 [M+H].
(δH, 300 MHz, CDCl3) 3.08 (t, 2H), 3.62 (q, 2H), 3.84 (s, 3H), 5.05 (t, 1H), 5.17 (s, 2H), 6.81 (dd, 1H), 6.95 (m, 4H), 7.12 (dd, 1H), 7.30 (m, 3H), 7.38 (q, 1H), 7.84 (s, 1H); ESI, 494 [M+H].
(δH, 300 MHz, CD3OD) 2.80-3.10 (m, 9H), 3.22 (m, 2H), 3.31 (m, 2H), 3.59 (m, 2H), 3.84 (s, 3H), 5.21 (s, 2H), 7.07 (m, 3H), 7.18 (m, 2H), 7.47 (m, 2H), 7.90 (s, 1H); ESI, 510.1 [M+H].
(δH, 300 MHz, CD3OD) 0.85 (m, 2H), 1.83 (m, 2H), 3.31 (s, 3H), 3.45 (m, 4H), 3.86 (s, 3H), 5.16 (s, 3H), 6.94 (m, 3H), 7.30 (m, 3H), 7.40 (m, 1H), 7.82 (s, 1H); ESI, 456.2 [M+H].
(δH, 300 MHz, CDCl3) 3.82 (s, 3H), 5.06 (s, 2H), 7.00-7.20 (m, 5H), 7.38 (m, 1H), 7.42 (m, 2H), 7.60 (s, 1H); ESL 366.2 [M+H].
(δH, 300 MHz, CDCl3) 0.46 (m, 2H), 0.75 (m, 2H), 2.67 (m, 1H), 3.85 (s, 3H), 5.04 (s, 2H), 5.13 (bs, 1H), 7.11 (d, 2H), 7.37 (m, 5H), 7.57 (d, 2H), 7.72 (s, 1H); ESI, 388.1 [M+H].
(δH, 300 MHz, CDCl3) 2.96 (t, 2H), 3.29 (s, 3H), 3.51 (q, 2H), 3.68 (s, 3H), 5.17 (bt, 1H), 6.67 (m, 1H), 6.78 (m, 2H), 6.98 (dd, 1H), 7.10 (m, 2H), 7.26 (t, 1H), 6.72 (s, 1H); ESI, 382.1 [M+H].
(δH, 300 MHz, CD3OD) 3.00 (t, 2H), 3.30 (t, 2H), 3.10 (s, 3H), 3.83 (s, 3H), 5.19 (s, 2H), 7.10 (m, 8H), 7.24 (m, 1H), 7.45 (m, 2H), 7.82 (s, 1H); ESI, 522.2 [M+H].
(δH, 300 MHz, CDCl3) 3.8 (s, 3H), 5.2 (s, 2H), 7.0 (m, 3H), 7.2 (m, 2H), 7.45 (m, 2H), 7.55 (m, 1H), 7.95 (s, 1H), 8.35 (m, 2H), 8.6 (m, 1H); ESI, 461 [M+H].
(δH, 300 MHz, CDCl3) 3.80 (s, 3H), 3.88 (s, 3H), 5.06 (s, 2H), 6.84-7.04 (m, 6H), 7.25-7.38 (m, 4H) 7.46 (m, 1H), 7.57 (m, 2H), 7.80 (s, 1H); ESI, 454.2 [M+H].
(δH, 300 MHz, CD3OD) 1.3 (m, 1H), 1.9 (m, 3H), 2.2 (m, 1H), 2.8 (m, 5H), 3.25 (m, 1H), 3.45 (m, 3H), 3.75 (s, 3H), 5.2 (s, 2H), 7.05 (t, 3H), 7.2 (m, 2H), 7.45 (m, 2H), 7.9 (s, 1H); ESI, 495 [M+H].
(δH, 300 MHz, CDCl3) 0.61 (m, 2H), 0.79 (m, 2H), 2.78 (m, 1H), 3.77 (s, 3H), 3.84 (s, 3H), 5.00 (s, 2H), 6.83 (m, 1H), 6.92 (m, 1H), 7.00 (m, 2H), 7.20 (m, 2H), 7.42 (m, 1H), 7.62 (s, 1H), 9.60 (bs, 1H); ESI, 436.2 [M+H].
(δH, 300 MHz, CDCl3) 0.43 (m, 2H), 0.77 (m, 2H), 2.68 (m, 1H), 3.85 (s, 3H), 5.09 (s, 1H), 5.30 (s, 2H), 6.98 (m, 1H), 7.23-7.58 (m, 6H), 7.62 (s, 1H), 7.77 (d, 1H); ESI, 456.1 [M+H].
(δH, 300 MHz, CD3OD) 0.93 (s, 9H), 3.21 (s, 2H), 3.84 (s, 3H), 5.20 (s, 2H), 7.06 (m, 3H), 7.15 (m, 2H), 7.44 (m, 2H), 7.82 (s, 1H); ESI, 454.2 [M+H].
(δH, 300 MHz, CD3OD) 0.40 (m, 2H), 0.62 (m, 2H), 2.55 (m, 1H), 3.78 (s, 3H), 5.00 (s, 2H), 6.91 (dd, 1H), 7.02 (m, 2H), 7.18 (m, 2H), 7.36 (m, 3H), 7.72 (s, 1H); ESI, 406.1 [M+H].
(δH, 300 MHz, CD3OD) 0.40 (m, 2H), 0.62 (m, 2H), 2.55 (m, 1H), 3.78 (s, 3H), 5.02 (s, 2H), 6.90 (dd, 1H), 6.98 (m, 1H), 7.15 (m, 4H), 7.32 (m, 2H), 7.72 (s, 1H); ESI, 406.2 [M+H].
(δH, 300 MHz, CDCl3) 0.48 (m, 2H), 0.75 (m, 2H), 2.70 (m, 1H), 3.40 (s, 3H), 3.82 (s, 3H), 5.13 (bs, 1H), 6.90 (m, 1H), 7.24 (m, 2H), 7.36 (m, 1H), 7.91 (s, 1H), 8.70 (bs, 1H); ESI, 312.2 [M+H].
(δH, 300 MHz, d6-DMSO) 0.39 (m, 2H), 0.58 (m, 2H), 2.60 (m, 1H), 3.85 (s, 3H), 4.97 (s, 2H), 6.11 (s, 2H), 6.92 (m, 1H), 7.05 (m, 4H), 7.18 (m, 2H), 7.31 (m, 1H), 7.85 (s, 1H); ESI, 438.1 [M+H].
(δH, 300 MHz, CD3OD) 2.85 (t, 2H), 3.54 (t, 2H), 3.80 (s, 3H), 5.18 (s, 2H), 6.90 (m, 3H), 7.06 (m, 3H), 7.16 (m, 3H), 7.43 (m, 2H), 7.82 (s, 1H); ESI, 506.2 [M+H].
(δH, 300 MHz, CD3OD) 2.33 (s, 3H), 3.84 (s, 3H), 5.24 (s, 2H), 7.08 (m, 3H), 7.22 (m, 4H), 7.35 (d, 2H), 7.46 (m, 2H), 7.86 (s, 1H); ESI, 474.2 [M+H].
(δH, 300 MHz, d6-DMSO) 0.40 (m, 2H), 0.57 (m, 2H), 2.59 (m, 1H), 3.77 (s, 6H), 3.85 (s, 3H), 4.88 (s, 2H), 6.56 (m, 1H), 6.88 (m, 2H), 6.93 (m, 1H), 7.05 (d, 1H), 7.13 (bd, 1H), 7.19 (d, 1H), 7.31 (m, 1H), 7.87 (s, 1H); ESI, 448.2 [M+H].
(δH, 300 MHz, CD3OD) 2.83 (t, 2H), 3.54 (t, 2H), 3.83 (s, 3H), 5.20 (s, 2H), 6.93 (t, 2H), 7.14 (m, 7H), 7.45 (m, 2H), 7.83 (s, 1H); ESI, 506 [M+H].
(δH, 300 MHz, CDCl3) 0.45 (m, 2H), 0.75 (m, 2H), 2.67 (m, 1H), 3.82 (s, 3H), 5.13 (s, 3H), 6.92 (m, 1H), 7.22-7.43 (m, 7H), 7.74 (s, 1H); ESI, 472.2 [M+H].
(δH, 300 MHz, CDCl3) 1.74 (m, 2H), 1.90 (m, 3H), 2.63 (t, 2H), 2.74 (s, 3H), 3.29 (m, 2H), 3.57 (d, 2H), 3.84 (s, 3H), 5.14 (s, 2H), 6.98 (m, 3H), 7.18 (m, 2H), 7.37 (m, 1H), 7.44 (m, 1H), 7.62 (s, 1H); ESI, 495.1 [M+H].
(δH, 300 MHz, CDCl3) 3.10 (t, 2H), 3.65 (q, 2H), 3.85 (s, 3H), 5.10 (m, 1H), 6.83 (m, 1H), 6.95 (m, 2H), 7.14 (m, 1H), 7.26 (m, 2H), 7.44 (m, 1H), 7.96 (s, 1H), 8.70 (bs, 1H); ESI, 368.1 [M+H].
(δH, 300 MHz, d6-DMSO) 0.39 (m, 2H), 0.58 (m, 2H), 2.60 (m, 1H), 5.15 (s, 2H), 6.11 (s, 2H), 7.06 (m, 2H), 7.20 (m, 4H), 7.41 (s, 1H), 7.97 (s, 1H); ESI, 438.1 [M+H].
(δH, 300 MHz, CD3OD) 3.77 (s, 3H), 4.50 (s, 2H), 5.18 (s, 2H), 7.06 (m, 4H), 7.12 (m, 1H), 7.24 (m, 5H), 7.44 (m, 2H), 7.84 (s, 1H); ESI, 474.2 [M+H].
(δH, 300 MHz, CDCl3) 1.13 (m, 3H), 1.85 (m, 2H), 2.95 (m, 2H), 3.63 (m, 2H), 3.85 (m, 5H), 5.18 (m, 1H) 6.95 (m, 1H), 7.05 (in 2H), 7.19 (m, 2H), 7.39 (m, 2H), 7.43 (m, 1H), 7.87 (s, 1H); ESI, 422 [M+H].
(δH, 300 MHz, CDCl3) 0.46 (m, 2H), 0.74 (m, 2H), 2.68 (m, 1H), 3.85 (s, 3H), 3.86 (s, 6H), 5.13 (s, 2H), 6.56 (d, 2H), 6.92 (m, 1H), 7.28 (m, 3H), 7.40 (m, 1H), 7.74 (s, 1H); ESI, 448.1 [M+H].
(δH, 300 MHz, CD3OD) 3.05 (t, 2H), 3.65 (t, 2H), 3.8 (s, 3H), 5.2 (s, 2H), 7.05 (m, 3H), 7.15 (m, 2H), 7.45 (m, 2H), 7.8 (m, 1H), 8.35 (d, 1H), 8.6 (s, 2H); ESL 489 [M+H].
(δH, 300 MHz, CDCl3) 1.96 (m, 4H), 3.49 (m, 4H), 3.80 (s, 3H), 3.88 (s, 3H), 5.02 (s, 2H), 6.82 (m, 1H), 6.94 (m, 3H), 7.25 (m, 2H), 7.42 (m, 2H), 7.74 (s, 1H); ESI, 432.2 [M+H].
(δH, 300 MHz, CDCl3) 0.45 (m, 2H), 0.72 (m, 2H), 2.65 (m, 1H), 3.82 (s, 3H), 5.02 (s, 2H), 5.12 (bs, 1H), 6.91 (m, 1H), 7.36 (m, 8H), 7.71 (s, 1H); ESI, 388.2 [M+H].
(δH, 300 MHz, CDCl3) 2.65 (m, 2H), 3.45 (m, 2H), 3.71 (s, 3H), 4.88 (m, 1H) 4.92 (s, 2H), 6.89 (m, 5H), 7.03 (m, 3H), 7.28 (m, 3H), 7.38 (m, 1H), 7.57 (s, 1H); ESI, 488 [M+H].
(δH, 300 MHz, CDCl3) 1.54 (d, 3H), 3.87 (s, 3H), 4.88 (m, 1H), 5.10 (q, 2H), 7.00 (m, 7H), 7.25 (m, 2H), 7.41 (m, 3H); ESI, 506.1 [M+H].
(δH, 300 MHz, CD3OD) 1.35-1.97 (m, 8H), 2.83 (dt, 1H), 3.03 (m, 1H), 3.23 (m, 1H), 3.47 (m, 2H), 3.83 (s, 3H), 5.20 (s, 2H), 7.05 (m, 3H), 7.16 (m, 2H), 7.46 (m, 2H), 7.88 (s, 1H); ESI, 495.2 [M+H].
(δH, 300 MHz, CDCl3) 0.65 (m, 2H), 0.76 (m, 2H), 1.86 (s, 3H), 2.74 (m, 1H), 3.88 (s, 3H), 5.87 (q, 1H), 7.03 (dd, 1H), 7.10 (bs, 1H), 7.25-7.50 (m, 8H); ESI, 402.1 [M+H].
(δH, 300 MHz, CD3OD) 2.24 (m, 1H), 2.50 (m, 1H), 3.60-3.90 (m, 7H), 4.04 (m, 1H), 5.21 (s, 2H), 7.02 (m, 3H), 7.19 (m, 2H), 7.44 (m, 2H), 7.92 (s, 1H); ESI, 453.2 [M+H].
(δH, 300 MHz, CDCl3) 1.54 (d, 3H), 3.87 (s, 3H), 4.88 (m, 1H), 5.10 (q, 2H), 7.00 (m, 7H), 7.25 (m, 2H), 7.41 (m, 3H); ESI, 506.1 [M+H].
(δH, 300 MHz, CDCl3) 0.44 (m, 2H), 0.72 (m, 2H), 2.65 (m, 1H), 3.78 (s, 3H), 3.86 (s, 3H), 5.00 (s, 2H), 5.10 (s, 1H), 6.84 (dd, 1H), 6.93 (m, 3H), 7.27 (m, 3H), 7.32 (m, 1H), 7.74 (s, 1H); ESI, 418.1 [M+H].
(δH, 300 MHz, CD3OD) 1.78 (m, 2H), 2.03 (m, 2H), 2.33 (m, 2H), 3.83 (s, 3H), 4.19 (i, 1H), 5.19 (s, 2H), 7.04 (m, 3H), 7.15 (m, 2H), 7.44 (m, 2H), 7.77 (s, 1H); ESI, 438.2 [M+H].
(δH, 300 MHz, CD3OD) 2.73 (t, 2H), 3.62 (t, 2H), 3.82 (s, 3H), 5.21 (s, 2H), 7.04 (m, 3H), 7.17 (t, 2H), 7.43 (m, 2H), 7.91 (s, 1H); ESI, 437.1 [M+H].
(δH, 300 MHz, CDCl3) 3.06 (t, 2H), 3.62 (q, 2H), 3.84 (s, 3H), 5.03 (s, 2H), 6.76 (d, 1H), 6.90 (m, 3H), 7.04 (dd, 1H), 7.15 (m, 3H), 7.25 (m, 1H), 7.42 (m, 2H), 7.98 (s, 1H), 9.53 (bs, 1H); ESI, 474.1 [M+H]
(δH, 300 MHz, CD3OD) 1.88 (m, 2H), 2.20 (m, 2H), 3.14 (m, 2H), 3.38 (m, 1H), 3.59 (m, 1H), 3.98 (s, 3H), 4.24 (m, 1H), 5.32 (s, 2H), 7.20 (m, 1H), 7.33 (m, 4H), 7.50-7.68 (m, 3H), 8.04 (s, 1H); ESL 449.1 [M+H].
(δH, 300 MHz, CD3OD) 1.95 (m, 2H), 3.05 (t, 2H), 3.20 (s, 3H), 3.38 (t, 2H), 3.56 (t, 2H), 3.87 (t, 2H), 6.82 (m, 1H), 6.87 (m, 1H), 7.14 (dd, 1H), 7.71 (s, 1H); ESI, 334.1 [M+H].
(δH, 400 MHz, CD3OD) 1.45 (t, 2H), 1.85 (m, 4H), 2.0 (m, 1H), 2.2 (m, 1H), 2.27 (m, 3H), 2.95 (m, 2H), 3.20 (m, 1H), 3.45 (m, 2H), 3.85 (s, 3H), 5.2 (s, 2H), 7.05 (m, 3H), 7.15 (m, 2H), 7.45 (m, 2H), 7.9 (s, 1H); ESI, 509 [M+H].
(δH, 300 MHz, CDCl3) 0.87 (m, 1H), 1.50-1.90 (m, 7H), 2.65 (m, 2H), 2.76 (s, 3H) 3.46 (m, 2H), 3.57 (m, 2H), 3.85 (s, 3H), 5.14 (s, 2H), 7.00 (m, 3H), 7.13 (m, 2H), 7.38 (m, 1H), 9.95 (bs, 1H), 11.45 (bs, 1H); ESI, 509.1 [M+H].
(δH, 300 MHz, CD3OD) 1.50 (m, 2H), 1.75 (m, 1H), 2.00 (m, 1H), 2.96 (m, 1H), 3.05 (m, 1H), 3.15 (m, 1H), 3.82 (s, 3H), 4.14 (dt, 1H), 4.35 (dd, 1H), 5.19 (s, 2H), 6.97 (dd, 1H), 7.04 (m, 2H), 7.19 (m, 2H), 7.42 (m, 2H), 7.90 (s, 1H); ESI, 467.1 [M+H].
(δH, 300 MHz, CD3OD) 3.1 (t, 2H), 3.3 (m, 8H), 3.7 (t, 2H), 3.85 (s, 3H), 5.2 (s, 2H), 7.05 (m, 3H), 7.15 (m, 2H), 7.45 (m, 2H), 7.9 (s, 1H); ESI, 496 [M+H].
(δH, 300 MHz, CD3OD) 3.83 (s, 3H), 4.77 (s, 2H), 5.18 (s, 2H), 6.88 (bs, 1H), 7.00 (m, 2H), 7.04 (m, 2H), 7.35 (m, 1H), 7.43 (m, 1H), 7.92 (m, 3H), 8.70 (d, 2H); ESI, 475.2 [M+H].
(δH, 300 MHz, d6-DMSO) 0.34 (m, 2H), 0.54 (m, 2H), 2.56 (m, 1H), 3.72 (s, 3H), 3.83 (s, 3H), 3.86 (s, 3H), 4.97 (s, 2H), 6.63 (dd, 1H), 6.74 (d, 1H), 6.94 (m, 1H), 7.11 (m, 2H), 7.30 (m, 2H), 7.80 (s, 1H); ESI, 448.1 [M+H].
(δH, 300 MHz, CD3OD) 3.8 (s, 3H), 5.2 (s, 2H), 7.05 (m, 3H), 7.25 (m, 2H), 7.45 (m, 2H), 7.75 (m, 2H), 8.1 (s, 1H), 8.2 (m, 1H); EST, 461 [M+H].
(δH, 300 MHz, CDCl3) 0.42 (m, 2H), 0.72 (m, 2H), 2.65 (m, 1H), 3.78 (s, 3H), 3.84 (s, 3H), 4.98 (s, 2H), 5.10 (s, 1H), 6.87 (d, 2H), 6.92 (m, 1H), 7.30 (m, 4H), 7.38 (m, 1H), 7.73 (s, 1H); ESI, 418.1 [M+H].
(δH, 300 MHz, CDCl3) 0.46 (m, 2H), 0.74 (m, 2H), 2.67 (m, 1H), 3.82 (s, 3H), 3.88 (s, 3H), 5.07 (s, 2H), 5.12 (bs, 1H), 6.90 (m, 3H), 7.28 (m, 3H), 7.37 (m, 2H), 7.88 (s, 1H); ESI, 418.1 [M+H].
(δH, 300 MHz, CD3OD) 2.85 (t, 2H), 3.55 (t, 2H), 3.83 (s, 3H), 5.20 (s, 2H), 7.05-7.21 (m, 10H), 7.44 (m, 2H), 7.81 (s, 1H); ESI, 488.2 [M+H].
(δH, 300 MHz, CDCl3) 1.39 (m, 3H), 2.95 (m, 2H), 3.63 (m, 2H), 3.85 (s, 3H), 3.95 (m, 2H) 5.18 (m, 1H) 6.95 (m, 1H), 7.05 (m, 2H), 7.19 (m, 2H), 7.39 (m, 2H), 7.43 (m, 1H), 7.89 (s, 1H); ESI, 408 [M+H].
(δH, 300 MHz, CD3OD) 2.10 (m, 2H), 3.35 (t, 2H), 3.74 (s, 3H), 4.21 (t, 2H) 5.13 (s, 2H), 6.98 (m, 4H), 7.08 (m, 2H), 7.40 (m, 3H), 7.82 (s, 1H), 8.83 (s, 1H); ESI, 492 [M+H].
(δH, 300 MHz, d6-DMSO) 0.34 (m, 2H), 0.53 (m, 2H), 2.55 (m, 1H), 3.72 (s, 3H), 3.83 (s, 3H), 5.03 (s, 2H), 6.63 (dd, 1H), 6.74 (d, 1H), 7.08 (bd, 1H), 7.34 (m, 6H), 7.92 (s, 1H); ESI, 418.2 [M+H].
(δH, 300 MHz, d6-DMSO) 0.39 (m, 2H), 0.58 (m, 2H), 2.58 (m, 1H), 3.78 (s, 6H), 5.04 (s, 2H), 6.57 (m, 1H), 6.89 (m, 2H), 7.15 (bd, 1H), 7.36 (m, 5H), 7.97 (s, 1H); ESI, 418.2 [M+H].
(δH, 300 MHz, CD3OD) 1.85 (m, 3H), 1.85 (m, 3H), 2.85 (t, 2H), 3.30 (m, 2H), 3.55 (m, 2H), 3.8 (s, 3H), 5.2 (s, 2H), 7.05 (m, 3H), 7.15 (m, 2H), 7.45 (m, 2H), 7.9 (s, 1H); ESI, 481 [M+H].
(δH, 300 MHz, CD3OD) 2.84 (t, 2H), 3.55 (t, 2H), 3.82 (s, 3H), 5.19 (s, 2H), 7.04-7.18 (m, 9H), 7.45 (m, 2H), 7.81 (s, 1H); ESI, 522.2 [M+H].
(δH, 300 MHz, CDCl3/CD3OD) 0.49 (m, 2H), 0.75 (m, 2H), 2.63 (m, 1H), 3.86 (s, 3H), 5.09 (s, 2H), 6.85 (m, 2H), 6.96 (d, 1H), 7.22 (m, 2H), 7.34 (d, 1H), 7.42 (m, 3H), 8.05 (s, 1H); ESI, 404 [M+H].
(δH, 300 MHz, d6-DMSO) 0.34 (m, 2H), 0.53 (m, 2H), 2.55 (m, 1H), 3.74 (s, 3H), 3.86 (s, 3H), 4.98 (s, 2H), 6.94 (m, 1H), 7.10 (m, 2H), 7.13 (m, 1H), 7.22 (d, 1H), 7.31 (m, 1H), 7.40 (d, 1H), 7.48 (m, 1H), 7.83 (s, 1H); ESI, 418.1 [M+H].
(δH, 300 MHz, CD3OD) 0.48 (m, 2H), 0.75 (m, 2H), 2.38 (s, 3H), 2.68 (m, 1H), 3.86 (s, 3H), 5.08 (s, 2H), 5.11 (m, 1H), 6.95 (m, 1H), 7.23 (m, 3H), 7.31 (m, 3H), 7.40 (q, 1H), 7.60 (s, 1H); ESI, 402.1 [M+H].
(δH, 300 MHz, CDCl3) 0.475 (m, 2H), 0.76 (m, 2H), 2.68 (m, 1H), 3.85 (s, 3H), 3.88 (s, 3H), 5.141 (s, 2H), 5.144 (m, 1H), 6.72 (m, 2H), 6.90 (m, 1H), 7.28 (m, 3H), 7.36 (q, 1H), 7.83 (s, 1H); ESI, 436.1 [M+H].
(δH, 300 MHz, CDCl3) 3.81 (s, 3H), 5.18 (s, 2H), 7.00 (m, 5H), 7.20 (m 2H), 7.41 (m, 2H), 7.56 (m, 2H), 7.63 (s, 1H), 11.86 (bs, 1H); ESI, 478 [M+H].
(δH, 300 MHz, CD3OD) 3.20 (t, 2H), 3.75 (t, 2H), 3.89 (s, 3H), 5.22 (s, 2H), 6.88 (d, 1H), 7.08 (m, 1H), 7.40-7.80 (m, 6H), 7.62 (m, 3H), 7.88 (s, 1H); ESI, 476.1 [M+H]
(δH, 300 MHz, d6-DMSO) 0.33 (m, 2H), 0.52 (m, 2H), 2.55 (m, 1H), 3.74 (s, 3H), 5.04 (s, 2H), 7.09 (d, 2H), 7.22 (m, 1H), 7.28-7.52 (m, 6H), 7.94 (s, 1H); ESI, 388.2 [M+H].
(δH, 300 MHz, CDCl3) 3.25 (s, 6H), 3.85 (s, 3H), 2.95 (s, 3H), 5.15 (s, 2H), 6.96 (m, 3H), 7.18 (r, 2H), 7.34 (m, 1H), 7.45 (m, 2H), 8.21 (s, 1H); ESI, 406 [M+H].
(δH, 300 MHz, CDCl3) 0.42 (m, 2H), 0.67 (m, 2H), 2.63 (m, 1H), 3.80 (s, 3H), 5.10 (bd, 1H), 5.18 (s, 2H), 6.90 (m, 3H), 7.26 (m, 3H), 7.38 (m, 1H), 7.89 (s, 1H); ESI, 424.1 [M+H].
(δH, 300 MHz, CDCl3) 3.76 (s, 3H), 3.79 (s, 3H), 5.07 (s, 2H), 6.82-6.96 (m, 4H), 7.12 (m, 2H), 7.30-7.42 (m, 7H) 7.74 (s, 1H); ESI, 455.1 [M+H].
(δH, 300 MHz, CDCl3) 0.98 (m, 1H), 1.50 (m, 2H), 1.60-2.25 (m, 5H), 2.40 (m, 1H), 2.46 (s, 3H), 3.42 (m, 4H), 3.82 (s, 3H), 5.10 (q, 2H), 6.98 (m, 3H), 7.16 (m, 2H), 7.38 (m, 3H), 10.08 (bs, 1H); ESI, 509.1 [M+H].
(δH, 300 MHz, CDCl3) 2.3 (s, 3H), 3.7 (s, 3H), 5.2 (s, 2H), 6.95 (m, 1H), 7.0 (m, 2H), 7.1 (m, 4H), 7.2 (m, 1H), 7.35 (m, 2H), 7.55 (d, 1H), 7.7 (s, 1H); ESI, 474 [M+H].
(δH, 300 MHz, CD3OD) 2.90 (t, 2H), 3.58 (t, 2H), 3.80 (s, 3H), 5.17 (s, 2H), 6.90-7.16 (m, 9H), 7.45 (m, 2H), 7.82 (s, 1H); ESI, 506.2 [M+H].
(δH, 300 MHz, CD3OD) 3.8 (s, 3H), 4.0 (q, 2H), 5.2 (s, 2H), 7.05 (m, 3H), 7.15 (m, 2H), 7.45 (m, 2H), 7.9 (s, 1H); ESI, 466 [M+H].
(δH, 300 MHz, CDCl3) 1.36 (d, 6H), 3.72 (s, 3H), 4.41 (d, 2H), 4.55 (m, 1H), 4.82 (s, 2H), 5.07 (bs, 1H), 6.75 (m, 3H), 7.16 (m, 6H), 7.53 (s, 1H); ESI, 404.2 [M+H].
(δH, 300 MHz, CD3OD) 1.59 (m, 4H), 1.72 (m, 2H), 1.98 (m, 2H), 3.82 (s, 3H), 4.08 (m, 1H), 5.19 (s, 2H), 7.03 (m, 3H), 7.08 (m, 2H), 7.46 (m, 2H), 7.79 (s, 1H); ESI, 452.1 [M+H]
(δH, 300 MHz, CDCl3) 1.23 (m, 1H), 1.40 (m, 1H), 2.04 (m, 1H), 2.92 (m, 1H), 3.71 (s, 3H), 5.15 (q, 2H), 6.97 (m, 5H), 7.10 (m, 6H), 7.38 (m, 1H), 7.53 (s, 1H); ESI, 500.2 [M+H].
(δH, 300 MHz, CD3OD) 3.20 (t, 2H), 3.76 (t, 2H), 3.84 (s, 3H), 5.18 (s, 2H), 7.06 (m, 3H), 7.15 (m, 2H), 7.55 (m, 2H), 7.65 (m, 2H), 7.82 (s, 1H), 8.13 (m, 1H), 8.43 (d, 1H); ESI, 489.1 [M+H].
(δH, 300 MHz, CD3OD) 2.92 (d, 3H), 3.85 (s, 3H), 4.86 (s, 1H), 5.17 (s, 2H), 6.93 (m, 3H), 7.35 (m, 4H), 7.85 (s, 1H); ESI, 398 [M+H].
(δH, 300 MHz, CDCl3) (δH, 300 MHz, CDCl3) 0.65 (m, 2H), 0.80 (m, 2H), 2.75 (m, 1H), 3.08 (t, 2H), 3.87 (s, 3H), 4.10 (m, 2H), 7.01 (m, 2H), 7.20 (m, 4H), 7.32 (m, 3H), 7.45 (m, 1H); EST, 404.2 [M+H].
(δH, 300 MHz, CDCl3) 0.47 (m, 2H), 0.78 (m, 2H), 2.67 (m, 1H), 3.82 (s, 3H), 5.14 (s, 1H), 5.28 (s, 2H), 6.93 (m, 1H), 7.29 (m, 2H), 7.40 (m, 2H), 7.50 (m, 1H), 7.57 (m, 1H), 7.70 (m, 1H), 7.80 (s, 1H); EST, 413.2 [M+H].
(δH, 300 MHz, d6-DMSO) 0.38 (m, 2H), 0.57 (m, 2H), 2.59 (m, 1H), 5.10 (s, 2H), 6.11 (s, 2H), 7.02 (m, 2H), 7.14 (m, 4H), 7.48 (s, 1H), 7.90 (s, 1H); ESI, 438.2 [M+H].
(δH, 300 MHz, CD3OD) 1.3 (m, 2H), 1.9 (m, 3H), 2.9 (m, 2H), 3.3 (m, 4H), 3.8 (s, 3H), 5.2 (s, 2H), 7.05 (m, 3H), 7.2 (m, 2H), 7.45 (m, 2H), 7.8 (s, 1H); ESI, 481 [M+H].
This application claims benefit from U.S. Provisional Application 60/719,015, filed on Sep. 21, 2005, the entire contents of which is incorporated herein by reference.
Number | Date | Country | |
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60719015 | Sep 2005 | US |