Patent Application
20090137545
The present invention relates to compounds of general formula I
wherein A, B, D, Y, R1, R2, R3, R4 and R5 are as defined hereinbelow, the enantiomers, diastereomers, mixtures thereof and the salts thereof, particularly the physiologically acceptable salts thereof with organic or inorganic acids or bases, which have valuable properties, the preparation thereof, the pharmaceutical compositions containing the pharmacologically effective compounds, the preparation thereof and the use thereof.
In the above general formula I in a first embodiment
A second embodiment of the present invention comprises the compounds of the above general formula I, wherein
A third embodiment of the present invention comprises the compounds of the above general formula I, wherein
the enantiomers, the diastereomers, the mixtures and the salts thereof, particularly the physiologically acceptable salts thereof with organic or inorganic acids or bases.
A fourth embodiment of the present invention comprises the compounds of the above general formula I, wherein
the enantiomers, the diastereomers, the mixtures and the salts thereof, particularly the physiologically acceptable salts thereof with organic or inorganic acids or bases.
A fifth embodiment of the present invention comprises the compounds of the above general formula I, wherein
the enantiomers, the diastereomers, the mixtures and the salts thereof, particularly the physiologically acceptable salts thereof with organic or inorganic acids or bases.
A sixth embodiment of the present invention comprises the compounds of the above general formula I, wherein
the enantiomers, the diastereomers, the mixtures and the salts thereof, particularly the physiologically acceptable salts thereof with organic or inorganic acids or bases.
A seventh embodiment of the present invention comprises the compounds of the above general formula I, wherein A, B, D, Y, R2, R3, R4 and R5 are defined as hereinbefore under the first to sixth embodiments and
the enantiomers, the diastereomers, the mixtures and the salts thereof, particularly the physiologically acceptable salts thereof with organic or inorganic acids or bases.
An eighth embodiment of the present invention comprises the compounds of the above general formula I, wherein A, B, D, Y, R2, R3, R4 and R5 are defined as hereinbefore under the first to sixth embodiments and
the enantiomers, the diastereomers, the mixtures and the salts thereof, particularly the physiologically acceptable salts thereof with organic or inorganic acids or bases.
A ninth embodiment of the present invention comprises the compounds of the above general formula I, wherein A, B, R1, R3, R4 and R5 are defined as hereinbefore under the first to eighth embodiments and
A tenth embodiment of the present invention comprises the compounds of the above general formula I, wherein
The following are mentioned as examples of most particularly preferred compounds of the above general formula I:
the enantiomers, the diastereomers, the mixtures and the salts thereof, particularly the physiologically acceptable salts thereof with organic or inorganic acids or bases.
Unless otherwise stated, all the substituents are independent of one another. If for example there are a plurality of C1-6-alkyl groups as substituents in one group, in the case of three C1-6-alkyl substituents, independently of one another, one may represent methyl, one n-propyl and one tert-butyl.
Within the scope of this application, in the definition of possible substituents, these may also be represented in the form of a structural formula. If present, an asterisk (*) in the structural formula of the substituent is to be understood as being the linking point to the rest of the molecule.
The subject-matter of this invention also includes the compounds according to the invention, including the salts thereof, wherein one or more hydrogen atoms, for example one, two, three, four or five hydrogen atoms, are replaced by deuterium.
By the term “C1-2-alkyl” (including those which are part of other groups) are meant alkyl groups with 1 to 2 carbon atoms, by the term “C1-3-alkyl” are meant branched and unbranched alkyl groups with 1 to 3 carbon atoms, by the term “C1-4-alkyl” are meant branched and unbranched alkyl groups with 1 to 4 carbon atoms, by the term “C1-5-alkyl” are meant branched and unbranched alkyl groups with 1 to 5 carbon atoms, by the term “C1-6-alkyl” are meant branched and unbranched alkyl groups with 1 to 6 carbon atoms and by the term “C1-8-alkyl” are meant branched and unbranched alkyl groups with 1 to 8 carbon atoms. Examples include: methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, iso-pentyl, neo-pentyl, hexyl, heptyl and octyl. The following abbreviations may optionally also be used for the above-mentioned groups: Me, Et, n-Pr, i-Pr, n-Bu, i-Bu, t-Bu, etc. Unless stated otherwise, the definitions propyl, butyl, pentyl, hexyl, heptyl and octyl include all the possible isomeric forms of the groups in question. Thus, for example, propyl includes n-propyl and iso-propyl, butyl includes iso-butyl, sec-butyl and tert-butyl etc.
Moreover, the terms mentioned above also include those groups wherein each methylene group may be substituted by up to two fluorine atoms and each methyl group may be substituted by up to three fluorine atoms.
By the term “C1-2-alkylene” are meant branched and unbranched alkylene groups with 1 or 2 carbon atoms, by the term “C1-3-alkylene” (including those which are part of other groups) are meant branched and unbranched alkylene groups with 1 to 3 carbon atoms, by the term “C1-4-alkylene” are meant branched and unbranched alkylene groups with 1 to 4 carbon atoms, by the term “C1-6-alkylene” are meant branched and unbranched alkylene groups with 1 to 6 carbon atoms and by the term “C2-4-alkylene” are meant branched and unbranched alkylene groups with 2 to 4 carbon atoms. Examples include: methylene, ethylene, ethane-1,1-diyl, propylene, propane-2,2-diyl, 1-methylethylene, butylene, 1-methylpropylene, 1,1-dimethylethylene, 1,2-dimethylethylene. Unless stated otherwise, the definitions propylene and butylene include all the possible isomeric forms with the same number of carbons. Thus, for example, propyl also includes 1-methylethylene and butylene includes 1-methylpropylene, 1,1-dimethylethylene, 1,2-dimethylethylene.
In addition, the terms mentioned above also include those groups wherein each methylene group may be substituted by up to two fluorine atoms.
By the term “C3-5-cycloalkyl” are meant cyclic alkyl groups with 3 to 5 carbon atoms, by the term “C3-6-cycloalkyl” are meant cyclic alkyl groups with 3 to 6 carbon atoms and by the term “C3-7-cycloalkyl” (including those which are part of other groups) are meant cyclic alkyl groups with 3 to 7 carbon atoms. Examples include: cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl or cycloheptyl. Unless otherwise stated, the cyclic alkyl groups may be substituted by one or more groups selected from among methyl, ethyl, iso-propyl, tert-butyl, hydroxy, fluorine, chlorine, bromine and iodine.
By the term “C3-6-cycloalkylene” (including those which are part of other groups) are meant cyclic alkylene groups with 3 to 6 carbon atoms, by the term “C3-7-cycloalkylene” are meant cyclic alkylene groups with 3 to 7 carbon atoms and by the term “C4-6-cycloalkylene” are meant cyclic alkylene groups with 4 to 6 carbon atoms. Examples include: cyclopropylene, cyclobutylene, cyclopentylene, cyclohexylene or cycloheptylene. Unless otherwise stated, the cyclic alkylene groups may be substituted by one or more groups selected from among methyl, ethyl, iso-propyl, tert-butyl, hydroxy, fluorine, chlorine, bromine and iodine. A C4- or a C5-cycloalkylene group may be linked to the remainder of the molecule in the 1,2 position or in the 1,3 position, preferably in the 1,3 position. A C6- or a C7-cycloalkylene group may be linked to the remainder of the molecule in the 1,2 position, in the 1,3 position or in the 1,4 position, preferably in the 1,3 position.
By the term “C5-7-cycloalkenylene” (including those which are part of other groups) are meant cyclic alkenyl groups with 5 to 7 carbon atoms, which contain an unsaturated bond and which are fused to a phenyl ring via this unsaturated bond. Examples include: cyclopentenyl, cyclohexenyl or cycloheptenyl:
Unless otherwise stated, the cyclic alkenyl groups may be substituted by one or more groups selected from among methyl, ethyl, iso-propyl, tert-butyl, hydroxy, fluorine, chlorine, bromine and iodine.
By the term “saturated heterocyclic rings” are meant four, five, six or seven membered heterocyclic rings which may contain one, two or three heteroatoms selected from among oxygen, sulphur and nitrogen. The ring may be attached to the molecule through a carbon atom and/or—if present—through a nitrogen atom or also through two carbon atoms or through two nitrogen atoms. Although it is encompassed by the term “heterocyclic rings”, the term “heterocyclic non-aromatic rings” denotes five, six or seven membered saturated rings. Examples include:
By the term “saturated diaza-heterocycles” are meant six or seven membered heterocyclic rings which contain two nitrogen atoms. The ring is linked to the remainder of the molecule through both nitrogen atoms. Examples include:
By the term “saturated aza-heterobicycles” are meant eight, nine or ten membered heterobicyclic rings which contain a nitrogen atom. The ring is linked to the remainder of the molecule through a carbon atom and the nitrogen atom. Examples include:
By the term “saturated diaza-heterobicycles” are meant eight, nine or ten membered heterobicyclic rings which contain two nitrogen atoms. The ring is linked to the remainder of the molecule through both nitrogen atoms. Examples include:
By the term “unsaturated heterocyclic rings” are meant five-, six- or seven-membered, mono- or diunsaturated heterocyclic rings which may contain one, two or three heteroatoms, selected from among oxygen, sulphur and nitrogen and condensed through the unsaturated bonds with one or two phenyl rings. The heterocyclic ring may be linked to the molecule through a carbon atom and/or—if present—through a nitrogen atom or through two carbon atoms or through two nitrogen atoms. Examples include:
By the term “saturated diaza-spirocycles” are meant nine-, ten- or eleven-membered spirocyclic rings which contain two nitrogen atoms. The spirocyclic group is linked to the remainder of the molecule through the two nitrogen atoms. Examples include:
By the term “aryl” (including those which are part of other groups) are meant aromatic ring systems with 6 or 10 carbon atoms. Examples of these are phenyl, 1-naphthyl or 2-naphthyl; preferred aryl groups are phenyl and 1-naphthyl; the particularly preferred aryl group is phenyl. Unless otherwise stated, the aromatic groups may be substituted by one or more groups selected from among methyl, ethyl, n-propyl, iso-propyl, tert-butyl, hydroxy, methoxy, trifluoromethoxy, fluorine, chlorine, bromine and iodine, while the groups may be identical or different.
By the term “heteroaryl” are meant five- or six-membered heterocyclic aromatic groups or 9-11 membered bicyclic heteroaryl rings, which may contain one, two or three heteroatoms, selected from among oxygen, sulphur and nitrogen, and additionally contain sufficient conjugated double bonds to form an aromatic system. Examples of five- or six-membered heterocyclic aromatic groups are as follows:
Unless otherwise stated, the heteroaryls mentioned previously may be substituted by one or more groups selected from among methyl, ethyl, n-propyl, iso-propyl, tert-butyl, hydroxy, methoxy, trifluoromethoxy, fluorine, chlorine, bromine and iodine, while the groups may be identical or different.
Bicyclic heteroaryl rings may preferably be substituted in the phenyl group.
By the term “arylene” (including those which are part of other groups) are meant aromatic ring systems with 6 or 10 carbon atoms. Examples include: phenylene, 1-naphthylene or 2-naphthylene, the preferred arylene group being phenylene. Unless otherwise stated, the aromatic groups may be substituted by one or more groups selected from among methyl, ethyl, n-propyl, iso-propyl, tert-butyl, hydroxy, methoxy, trifluoromethoxy, fluorine, chlorine, bromine and iodine.
These aromatic ring systems are linked to the rest of the molecule at two places independently of one another through a carbon atom in each case.
By the term “heteroarylene” are meant five- or six-membered heterocyclic aromatic groups or 9-11 membered bicyclic heteroaryl rings which may contain one, two or three heteroatoms selected from among oxygen, sulphur and nitrogen, and additionally sufficient conjugated double bonds to form an aromatic system. These heterocyclic aromatic groups are linked at two points independently of one another either through carbon and/or nitrogen.
The following are examples of five- or six-membered heterocyclic aromatic groups:
Unless otherwise stated, the heteroaromatic groups may be substituted by one or more groups selected from among methyl, ethyl, n-propyl, iso-propyl, tert-butyl, hydroxy, methoxy, trifluoromethoxy, fluorine, chlorine, bromine and iodine. Preferably, the substituents in the above-mentioned 5-10 membered bicyclic heteroaryl rings are in the phenyl ring.
If they contain suitable basic functions, for example amino groups, compounds of general formula I may be converted, particularly for pharmaceutical use, into the physiologically acceptable salts thereof with inorganic or organic acids. Examples of inorganic acids for this purpose include hydrobromic acid, phosphoric acid, nitric acid, hydrochloric acid, sulphuric acid, methanesulphonic acid, ethanesulphonic acid, benzenesulphonic acid or p-toluenesulphonic acid, while organic acids that may be used include malic acid, succinic acid, acetic acid, fumaric acid, maleic acid, mandelic acid, lactic acid, tartaric acid or citric acid. In addition, any tertiary amino groups present in the molecule may be quaternised. Alkyl halides are used for the reaction. According to the invention methyl iodide is preferably used for the quaternisation.
In addition, the compounds of general formula I, if they contain suitable carboxylic acid functions, may if desired be converted into the addition salts thereof with inorganic or organic bases. Examples of inorganic bases include alkali or alkaline earth metal hydroxides, e.g. sodium hydroxide or potassium hydroxide, or carbonates, ammonia, zinc or ammonium hydroxides; examples of organic amines include diethylamine, triethylamine, ethanolamine, diethanolamine, triethanolamine, cyclohexylamine or dicyclohexylamine.
The compounds according to the invention may be present as racemates, provided that they have only one chiral element, but may also be obtained as pure enantiomers, i.e. in the (R) or (S) form.
However, the application also includes the individual diastereomeric pairs of antipodes or mixtures thereof, which are obtained if there is more than one chiral element in the compounds of general formula I, as well as the individual optically active enantiomers of which the above-mentioned racemates are made up. The invention relates to the compounds in question, optionally in the form of the individual optical isomers, mixtures of the individual enantiomers or racemates, in the form of the tautomers as well as in the form of the free bases or the corresponding acid addition salts with pharmacologically acceptable acids—such as for example acid addition salts with hydrohalic acids—for example hydrochloric or hydrobromic acid—or organic acids—such as for example oxalic, fumaric, diglycolic or methanesulphonic acid.
According to the invention the compounds of general formula I are obtained by methods known per se, for example by the following methods:
The linking of carboxylic acids of general formula III shown in Scheme 1 wherein all the groups are as hereinbefore defined, with amines of general formula IV, wherein all the groups are as hereinbefore defined, forming carboxylic acid amides of general formula Ia, wherein all the groups are as hereinbefore defined, may be carried out using conventional methods of amide formation.
The coupling is preferably carried out using methods known from peptide chemistry (cf. e.g. Houben-Weyl, Methoden der Organischen Chemie, Vol. 15/2), for example using carbodiimides such as e.g. dicyclohexylcarbodiimide (DCC), diisopropyl carbodiimide (DIC) or ethyl-(3-dimethylaminopropyl)-carbodiimide, O-(1H-benzotriazol-1-yl)-N,N-N′,N′-tetramethyluronium hexafluorophosphate (HBTU) or tetrafluoroborate (TBTU) or 1H-benzotriazol-1-yl-oxy-tris-(dimethylamino)-phosphonium hexafluorophosphate (BOP). By adding 1-hydroxybenzotriazole (HOBt) or 3-hydroxy-4-oxo-3,4-dihydro-1,2,3-benzotriazine (HOObt) the reaction speed can be increased. The couplings are normally carried out with equimolar amounts of the coupling components as well as the coupling reagent in solvents such as dichloromethane, tetrahydrofuran, acetonitrile, dimethyl formamide (DMF), dimethyl acetamide (DMA), N-methylpyrrolidone (NMP) or mixtures thereof and at temperatures between −30° C. and +30° C., preferably −20° C. and +25° C. If necessary, N-ethyl-diisopropylamine (Hünig base) is preferably used as an additional auxiliary base.
An alternative method of attachment consists in converting a carboxylic acid of general formula III, wherein all the groups are as hereinbefore defined, into a carboxylic acid chloride of general formula V, wherein all the groups are as hereinbefore defined, and subsequent reaction with an amine of general formula IV, wherein all the groups are as hereinbefore defined. The synthesis of a carboxylic acid chloride of general formula V is carried out using methods known from the literature (see e.g. Houben-Weyl, Methoden der Organischen Chemie, vol. E5/1).
The carboxylic acids of general formula III used as starting materials, wherein all the groups are as hereinbefore defined, is obtained using methods known per se from the literature, for example by the methods of synthesis shown in Schemes 2 to 7.
The sulphonic acid chlorides of general formula VI, wherein R1 is as hereinbefore defined, are either known from the literature or commercially obtainable. They are reacted under standard reaction conditions with an amine of general formulae H2N—R2, VIIIa or VIIIb to obtain sulphonic acid amides of general formulae VII, X or XI, wherein R1 and R2 are hereinbefore defined and n denotes a number 1, 2, 3 or 4 and R6 denotes a C1-6-alkyl group. The reaction is optionally carried out in the presence of a base such as triethylamine, DIPEA or pyridine and an inert solvent such as dichloromethane or tetrahydrofuran at a temperature of 0° C. to 100° C. with a typical reaction time of one to 24 hours.
The reaction of the sulphonic acid amides of general formula VII with a halide of general formula IX, wherein Hal1 denotes chlorine or bromine, is carried out using methods known from the literature, for example with the aid of a base such as potassium or sodium carbonate in dimethylformamide or tetrahydrofuran at 0° C. to 100° C.
The hydrolysis of the carboxylic acid esters of general formula XI, wherein R1 and R2 are as hereinbefore defined, n denotes a number 1, 2, 3 or 4 and R6 denotes a C1-3-alkyl group, to obtain carboxylic acids of general formula XII, wherein R1 and R2 are as hereinbefore defined and n denotes a number 1, 2, 3 or 4 and R6 denotes a C1-3-alkyl group, is carried out under known conditions, for example with lithium or sodium carbonate and water in methanol and/or tetrahydrofuran.
The preparation of sulphonic acid amides of general formula XIV is carried out as described under Scheme 2.
The alkylation of the hydroxyl function of the sulphonic acid amides of general formula XIV, wherein R1 and R2 are as hereinbefore defined with the proviso that R2 does not denote a hydrogen atom, and n denotes a number 1, 2, 3 or 4 and R6 denotes a C1-3-alkyl group, is carried out under reaction conditions known from the literature, for example under 2-phase conditions using a phase transfer catalyst in the presence of a strong inorganic base such as sodium hydroxide solution or potassium hydroxide solution and in an inert solvent such as toluene at 0° C. to 100° C.
The cleaving of the tert-butylester of general formula XVI, wherein R1 and R2 are as hereinbefore defined, n denotes a number 1, 2, 3 or 4 and R6 denotes a C1-3-alkyl group and R7 denotes a hydrogen atom or a C1-3-alkyl group, is carried out using methods known from the literature (see e.g. Philip J. Kocieński, Protecting Groups, 3rd Edition, 2005, published by Georg Thieme).
The sulphonation of the hydroxyl function of a compound of general formula XIV, wherein R1 and R2 are as hereinbefore defined, with the proviso that R2 does not denote a hydrogen atom, and n denotes a number 1, 2, 3 or 4 and R6 denotes a C1-3-alkyl group, with a sulphonic acid chloride of general formula R8SO2Cl, wherein R8 denotes a C1-3-alkyl group or a phenyl group optionally substituted by a C1-3-alkyl group, to form compounds of general formula XVIII, wherein all the groups are as hereinbefore defined, is carried out under standard reaction conditions, typically in the presence of a base such as DMAP and/or pyridine and an inert solvent such as dichloromethane or THF at −5° C. to 35° C. A liquid base such as pyridine may be used as the base and solvent simultaneously.
The subsequent alkylation of the amines of general formula VII to form compounds of general formula XIX, wherein R1 and R2 are as hereinbefore defined, n denotes a number 1, 2, 3 or 4 and R6 denotes a C1-3-alkyl group and R6 denotes a C1-6-alkyl group, is conveniently carried out in a solvent such as toluene, chlorobenzene, dimethylformamide, dimethylsulphoxide (DMSO), dichloromethane, acetonitrile or pyridine, for example at temperatures between 0° C. and 150° C. and conveniently in the presence of bases such as pyridine, triethylamine, DIPEA, potassium carbonate, potassium-tert-butoxide or sodium methoxide, the alkylsulphonate serving as the leaving group.
The hydrolysis of the carboxylic acid esters of general formula XIX to form carboxylic acids of general formula XX is carried out as described under Scheme 2.
The Finkelstein reaction of compounds of general formula XVIII, wherein R1 and R2 are as hereinbefore defined, n denotes a number 1, 2, 3 or 4 and R6 denotes a C1-3-alkyl group and R8 denotes a C1-3-alkyl group or a phenyl group optionally substituted by a C1-3-alkyl group, to form halides of general formula XXI, wherein R1 and R2 are as hereinbefore defined and n denotes a number 1, 2, 3 or 4 and R6 denotes a C1-3-alkyl group, is carried out under known reaction conditions (see e.g. H. Finkelstein, Berichte der Deutschen Chemischen Gesellschaft 43, 1910, 1528).
The subsequent alkylation of the glycine ester is carried out as described under Scheme 4 (R2≠H).
The amino function in the compounds of general formula XXIII is protected by a conventional protective group PG by known methods. The selected protective group is one which can be cleaved under non-hydrogenolytic conditions. A preferred protective group is the Boc group. An overview of the chemistry of protective groups can be found in Theodora W. Greene and Peter G. M. Wuts, Protective Groups in Organic Synthesis, Second Edition, 1991, published by John Wiley and Sons, and in Philip J. Kocienski, Protecting Groups, 3rd Edition, 2005, published by Georg Thieme.
The cleaving of the carboxylic acid esters of general formula XXIII to form carboxylic acids of general formula XXIV is carried out as described under Scheme 2.
The alkylation of a thiol of general formula XXV, wherein n denotes a number 1, 2, 3 or 4 and R6 denotes a C1-6-alkyl group, to obtain compounds of general formula XXVI, wherein R1 and R2 are as hereinbefore defined, n denotes a number 1, 2, 3 or 4 and R6 denotes a C1-6-alkyl group, is conveniently carried out in a solvent such as toluene, chlorobenzene, DMF, DMSO, dichloromethane, acetonitrile or pyridine, for example at temperatures between 0° C. and 150° C. and conveniently in the presence of bases such as pyridine, triethylamine, DIPEA, potassium carbonate, potassium-tert-butoxide or sodium methoxide, while the alkylsulphonate serves as leaving group.
The hydrolysis of the carboxylic acid esters of general formula XXVI to form carboxylic acids of general formula XXVII, wherein all the groups are as hereinbefore defined, is carried out as described under Scheme 2.
The amide linking of carboxylic acids of general formula XII, wherein R1 and R2 are as hereinbefore defined and n denotes a number 1, 2, 3 or 4, and amino acids of general formula VIII, wherein R1 and R2 are as hereinbefore defined, n denotes a number 1, 2, 3 or 4 and R6 denotes a C1-6-alkyl group, to obtain carboxylic acid amides of general formula XXVIII, wherein R1 and R2 are as hereinbefore defined, n denotes a number 1, 2, 3 or 4 and R6 denotes a C1-6-alkyl group, is carried out as described under Scheme 1.
As mentioned under Scheme 2, the carboxylic acid ester of general formula XXVIII is cleaved to form carboxylic acid of general formula XXIX, wherein R1 and R2 are as hereinbefore defined and n denotes a number 1, 2, 3 or 4.
The amines of general formula IV used as starting materials are either commercially obtainable, or are obtained using methods known per se from the literature, for example by the methods of synthesis represented in Schemes 8 to 12, wherein R1.1 is as hereinbefore defined, Hal1 denotes a chlorine or bromine atom and Hal2 denotes a fluorine, chlorine or bromine atom or a group R9.
The reaction of an amine of general formula XXX, wherein R9 denotes a C1-3-alkyl group, with a halo-nitrobenzene of general formula XXXI, wherein R1.1 is as hereinbefore defined and Hal2 denotes a fluorine, chlorine or bromine atom or a group R9, is carried out using known methods, for example in a solvent such as tetrahydrofuran, dimethylformamide or dimethylsulphoxide and conveniently in the presence of a suitable base such as triethylamine or potassium carbonate, at a temperature of 20° C. to 160° C. If the amine of general formula XXX is liquid, the reaction may also be carried out without a solvent and additional base.
The reduction of the nitro group to form anilines of general formula XXXIII, wherein R1.1 is as hereinbefore defined and R9 denotes a C1-3-alkyl group, is carried out under standard reaction conditions (see e.g. Richard C. Larock, Comprehensive Organic Transformations, 1989, VCH), preferably under standard conditions of catalytic hydrogenolysis with a catalyst such as palladium on charcoal or Raney nickel in a solvent such as methanol or ethanol.
The reaction of compounds of general formulae XXX, wherein R9 denotes a C1-3-alkyl group, with a compound of general formula XXXIV, wherein R1.1 is as hereinbefore defined and Hal2 denotes a fluorine, chlorine or bromine atom or a group R9, to obtain compounds of general formula XXXV, wherein R1.1 is as hereinbefore defined and R9 denotes a C1-3-alkyl group, is carried out as described under Scheme 8.
The reduction of a nitrile of general formula XXXV to form an amine of general formula XXXVI, wherein R1.1 is as hereinbefore defined and R9 denotes a C1-3-alkyl group, may be carried out under standard conditions of catalytic hydrogenolysis with a catalyst such as for example Raney nickel in a solvent such as ammoniacal methanol or ethanol or with a reducing agent such as lithium aluminium hydride or sodium borohydride in a solvent such as tetrahydrofuran, optionally in the presence of aluminium chloride.
The formylation of an amine of general formula XXXVI to obtain a compound of general formula XXXVII, wherein R1.1 is as hereinbefore defined and R9 denotes a C1-3-alkyl group, is conveniently carried out in a solvent such as dichloromethane, for example at temperatures from 40° C. to 70° C. and in the presence of acetic anhydride and formic acid.
The carbamate formation to obtain compounds of general formula XXXVIII, wherein R1.1 is as hereinbefore defined, R6 denotes a C1-6-alkyl and R9 denotes a C1-3-alkyl group is carried out by known methods, for example with a chloroformic acid ester or Boc-anhydride in the presence of a base such as triethylamine or sodium hydroxide solution and a solvent such as THF or dioxane.
The reduction of the formyl or of the carbamate to obtain compounds of general formula XXXIX, wherein R1.1 is as hereinbefore defined and R9 denotes a C1-3-alkyl group, is carried out under standard reaction conditions, preferably with a reducing agent such as lithium aluminium hydride and in a solvent such as tetrahydrofuran at a temperature of 50° C. to 100° C.
The halogen-nitrogen exchange in compounds of general formulae XXX, wherein R9 denotes a C1-3-alkyl group, and XL, wherein R1.1 is as hereinbefore defined and Hal2 denotes a fluorine, chlorine or bromine atom or a group R9, for preparing compounds of general formula XLI, wherein R1.1 is as hereinbefore defined and R9 denotes a C1-3-alkyl group, is carried out as described under Scheme 8.
The reaction of benzaldehydes of general formula XLI, wherein R1.1 is as hereinbefore defined and R9 denotes a C1-3-alkyl group, with an amine of general formula H2NR2, wherein R2 is as hereinbefore defined, to obtain a compound of general formula XLII, wherein R1.1 and R2 are as hereinbefore defined and R9 denotes a C1-3-alkyl group, is a reductive amination. It is carried out by known methods, for example with a reducing agent such as sodium triacetoxyborohydride, sodium borohydride or sodium cyanoborohydride, conveniently in a solvent such as tetrahydrofuran or dichloromethane, optionally with the addition of acetic acid.
The reaction of an amine of general formula XXX, wherein R9 denotes a C1-3-alkyl group, with a halogen-nitropyridine of general formula XLIII, wherein R1.1 is as hereinbefore defined and Hal1 denotes a chlorine or bromine atom, is carried out by known methods, for example in a solvent such as tetrahydrofuran, dichloromethane, methanol or DMSO and conveniently in the presence of a suitable base such as triethylamine, sodium hydroxide solution or potassium carbonate and at a temperature of 20° C. to 100° C.
The subsequent reduction of the nitro group of a compound of general formula XLIV, wherein R1.1 is as hereinbefore defined and R9 denotes a C1-3-alkyl group, to obtain compounds of general formula XLV, wherein R1.1 is as hereinbefore defined and R9 denotes a C1-3-alkyl group, is carried out as described under Scheme 8.
The amide linking of carboxylic acids of general formula XLVI, wherein all the groups are as hereinbefore defined, and amines of general formula H2NR2, wherein R2 is as hereinbefore defined, to form carboxylic acid amides of general formula XLVII, wherein all the groups are as hereinbefore defined, is carried out as described under Scheme 1.
The reduction of carboxylic acid amides of general formula XLVII to obtain amines of general formula XLVIII, wherein all the groups are as hereinbefore defined, is carried out under standard reaction conditions, preferably in the presence of a reducing agent such as lithium aluminium hydride and a solvent such as tetrahydrofuran at 40° C. to 100° C.
Description of the Method of hBK1 Receptor Binding
CHO cells expressing the hBK1 receptor are cultivated in Dulbecco's modified medium. The medium from confluent cultures is removed and the cells are washed with PBS buffer, scraped off and isolated by centrifugation. The cells are then homogenized in suspension and the homogenate is centrifuged and resuspended. The protein content is determined and the membrane preparation obtained in this manner is then frozen at −80° C.
After thawing, 200 μl of the homogenate (50 to 100 μg of proteins/assay) are incubated at room temperature with 0.5 to 1.0 nM of kallidin (DesArg10, Leu9), [3,4-prolyl-3,43H(N)] and increasing concentrations of the test substance in a total volume of 250 μl for 60 minutes. The incubation is terminated by rapid filtration through GF/B glass fibre filters which had been pretreated with polyethyleneimine (0.3%). The protein-bound radioactivity is measured in a TopCount NXT. Non-specific binding is defined as radioactivity bound in the presence of 1.0 μM of kallidin (DesArg10, Leu9), [3,4-prolyl-3,43H(N)]. The concentration/binding curve is analysed using a computer-assisted nonlinear curve fitting. The Ki which corresponds to the test substance is determined using the data obtained in this manner.
To demonstrate that the compounds of general formula I with different structural elements show good to very good bradykinin-B1-receptor antagonistic effects, the following Table gives the Ki values obtained according to the test method described above. It is pointed out that the compounds were selected for their different structural elements and not in order to emphasis specific compounds:
By virtue of their pharmacological properties, the novel compounds and their physiologically acceptable salts are suitable for treating diseases and symptoms of diseases caused at least to some extent by stimulation of bradykinin-B1 receptors.
In view of their pharmacological effect the substances are suitable for the treatment of
(a) acute pain such as e.g. toothache, peri- and postoperative pain, traumatic pain, muscle pain, the pain caused by burns, sunburn, trigeminal neuralgia, pain caused by colic, as well as spasms of the gastro-intestinal tract or uterus;
(b) visceral pain such as e.g. chronic pelvic pain, gynaecological pain, pain before and during menstruation, pain caused by pancreatitis, peptic ulcers, interstitial cystitis, renal colic, angina pectoris, pain caused by irritable bowel, non-ulcerative dyspepsia and gastritis, non-cardiac thoracic pain and pain caused by myocardial ischaemia and cardiac infarct;
(c) neuropathic pain such as e.g. painful neuropathies, pain of diabetic neuropathy, AIDS-associated neuropathic pain, pain of lumbago, non-herpes-associated neuralgia, post-zoster neuralgia, nerve damage, cerebro-cranial trauma, pain of nerve damage caused by toxins or chemotherapy, phantom pain, pain of multiple sclerosis, nerve root tears and painful traumatically-caused damage to individual nerves;
(d) inflammatory/pain receptor-mediated pain in connection with diseases such as osteoarthritis, rheumatoid arthritis, rheumatic fever, tendo-synovitis, tendonitis, gout, vulvodynia, damage to and diseases of the muscles and fascia (muscle injury, fibromyalgia), osteoarthritis, juvenile arthritis, spondylitis, gout-arthritis, psoriasis-arthritis, fibromyalgia, myositis, migraine, dental disease, influenza and other virus infections such as colds, systemic lupus erythematodes,
(e) tumour pain associated with cancers such as lymphatid or myeloid leukaemia, Hodgkin's disease, non-Hodgkin's lymphomas, lymphogranulomatosis, lymphosarcomas, solid malignant tumours and extensive metastases;
(f) headache diseases such as e.g. headache of various origins, cluster headaches, migraine (with or without aura) and tension headaches.
The compounds are also suitable for treating
(g) inflammatory changes connected with diseases of the airways such as bronchial asthma, including allergic asthma (atopic and non-atopic) as well as bronchospasm on exertion, occupationally induced asthma, viral or bacterial exacerbation of an existing asthma and other non-allergically induced asthmatic diseases;
chronic obstructive pulmonary disease (COPD) including pulmonary emphysema, acute adult respiratory distress syndrome (ARDS), bronchitis, lung inflammation, allergic rhinitis (seasonal and all year round), vasomotor rhinitis and diseases caused by dust in the lungs such as aluminosis, anthracosis, asbestosis, chalicosis, siderosis, silicosis, tabacosis and byssinosis;
(h) inflammatory phenomena caused by sunburn and burns, oedema after burns trauma, cerebral oedema and angiooedema, intestinal complaints including Crohn's diseases and ulcerative colitis, irritable bowel syndrome, pancreatitis, nephritis, cystitis (interstitial cystitis), uveitis; inflammatory skin diseases (such as e.g. psoriasis and eczema), vascular diseases of the connective tissue, lupus, sprains and fractures;
(i) diabetes mellitus and its effects (such as e.g. diabetic vasculopathy, diabetic neuropathy, diabetic retinopathy) and diabetic symptoms in insulitis (e.g. hyperglycaemia, diuresis, proteinuria and increased renal excretion of nitrite and kallikrein);
(j) neurodegenerative diseases such as Parkinson's disease and Alzheimer's disease;
(k) sepsis and septic shock after bacterial infections or after trauma;
(l) syndromes that cause itching and allergic skin reactions;
(m) osteoporosis;
(n) epilepsy;
(o) damage to the central nervous system;
(p) wounds and tissue damage;
(q) inflammation of the gums;
(r) benign prostatic hyperplasia and hyperactive bladder;
(s) pruritus;
(t) vitiligo;
(u) disorders of the motility of respiratory, genito-urinary, gastro-intestinal or vascular regions and
(v) post-operative fever.
In addition to being suitable as human therapeutic agents, these substances are also useful in the veterinary treatment of domestic animals, exotic animals and farm animals.
For treating pain, it may be advantageous to combine the compounds according to the invention with stimulating substances such as caffeine or other pain-alleviating active compounds. If active compounds suitable for treating the cause of the pain are available, these can be combined with the compounds according to the invention. If, independently of the pain treatment, other medical treatments are also indicated, for example for high blood pressure or diabetes, the active compounds required can be combined with the compounds according to the invention.
The following compounds may be used for combination therapy, for example:
Non-steroidal antirheumatics (NSAR): COX-2 inhibitors such as propionic acid derivatives (alminoprofen, benoxaprofen, bucloxic acid, carprofen, fenhufen, fenoprofen, fiuprofen, fiulbiprofen, ibuprofen, indoprofen, ketoprofen, miroprofen, naproxen, oxaprozin, pirprofen, pranoprofen, suprofen, tiaprofenic acid, tioxaprofen), acetic acid derivatives (indomethacin, acemetacin, alcofenac, isoxepac, oxpinax, sulindac, tiopinac, tolmetin, zidometacin, zomepirac) fenamic derivatives (meclofenamic acid, mefenamic acid, tolfenamic acid), biphenyl-carboxylic acid derivatives, oxicams (isoxicam, meloxicam, piroxicam, sudoxicam and tenoxicam), salicylic acid derivatives (acetylsalicylic acid, sulphasalazin, why not also mesalazin, olsalazin, and pyrazolone (apazone, bezpiperylone, feprazone, mofebutazone, oxyphenbutazone, phenylbutazone, why not also propyphenazone and metamizol, and coxibs (celecoxib, valecoxib, rofecoxib, etoricoxib).
Opiate receptor agonists such as e.g. morphine, propoxyphen (Darvon), tramadol, buprenorphine.
Cannabinoid agonists such as e.g. GW-1000, KDS-2000, SAB-378, SP-104, NVP001-GW-843166, GW-842166X, PRS-211375.
Sodium channel blockers such as e.g. carbamazepine, mexiletin, lamotrigin, pregabalin, tectin, NW-1029, CGX-1002.
N-type calcium channel blockers such as e.g. ziconitide, NMED-160, SP1-860.
Serotonergic and noradrenergic modulators such as e.g. SR-57746, paroxetine, duloxetine, clonidine, amitriptyline, citalopram.
Corticosteroids such as e.g. betamethasone, budesonide, cortisone, dexamethasone, hydrocortisone, methylprednisolone, prednisolone, prednisone and triamcinolone.
Histamine H1-receptor antagonists such as e.g. bromopheniramine, chloropheniramine, dexchlorpheniramine, triprolidine, clemastine, diphenhydramine, diphenylpyraline, tripelennamine, hydroxyzine, methdilazine, promethazine, trimeprazine azatadine, cyproheptadine, antazoline, pheniramine, pyrilamine, astemizole, terfenadine, loratadine, cetirizine, desloratadine, fexofenadine, levocetirizine.
Histamine H2-receptor antagonists such as e.g. cimetidine, famotidine, and ranitidine.
Proton pump inhibitors such as e.g. omeprazole, pantoprazole, esomeprazole.
Leukotriene antagonists and 5-lipoxygenasehemmer such as e.g. zafirlukast, montelukast, pranlukast and zileuton.
Local anaesthetics such as e.g. ambroxol, lidocaine.
VR1 agonists and antagonists such as e.g. NGX-4010, WL-1002, ALGRX-4975, WL-10001, AMG-517.
Nicotine receptor agonists such as e.g. ABT-202, A-366833, ABT-594, BTG-102, A-85380, CGX1204.
P2X3-receptor antagonists such as e.g. A-317491, ISIS-13920, AZD-9056.
NGF agonists and antagonists such as e.g. RI-724, RI-1024, AMG-819, AMG-403, PPH 207.
NK1 and NK2 antagonists such as e.g. DA-5018, R-116301, CP-728663, ZD-2249.
NMDA antagonists such as e.g. NER-MD-11, CNS-5161, EAA-090, AZ-756, CNP-3381.
potassium channel modulators such as e.g. CL-888, ICA-69673, retigabin.
GABA modulators such as e.g. lacosamide.
Serotonergic and noradrenergic modulators such as e.g. SR-57746, paroxetine, duloxetine, clonidine, amitriptyline, citalopram, flibanserine.
Anti-migraine drugs such as e.g. sumatriptan, zolmitriptan, naratriptan, eletriptan.
The dosage necessary for obtaining a pain-alleviating effect is, in the case of intravenous administration, expediently from 0.01 to 3 mg/kg of body weight, preferably from 0.1 to 1 mg/kg, and, in the case of oral administration, from 0.1 to 8 mg/kg of body weight, preferably from 0.5 to 3 mg/kg, in each case 1 to 3 times per day. The compounds prepared according to the invention can be administered intravenously, subcutaneously, intramuscularly, intrarectally, intranasally, by inhalation, transdermally or orally, aerosol formulations being particularly suitable for inhalation. They can be incorporated into customary pharmaceutical preparations, such as tablets, coated tablets, capsules, powders, suspensions, solutions, metered-dose aerosols or suppositories, if appropriate together with one or more customary inert carriers and/or diluents, for example with maize starch, lactose, cane sugar, microcrystalline cellulose, magnesium stearate, polyvinylpyrrolidone, citric acid, tartaric acid, water, water/ethanol, water/glycerol, water/sorbitol, water/polyethylene glycol, propylene glycol, cetylstearyl alcohol, carboxymethylcellulose or fatty substances, such as hardened fat, or suitable mixtures thereof.
Generally, there are IR, 1H NMR and/or mass spectra for the compounds that were prepared. The ratios given for the eluants are in volume units of the solvents in question. For ammonia, the given volume units are based on a concentrated solution of ammonia in water.
Unless indicated otherwise, the acid, base and salt solutions used for working up the reaction solutions are aqueous systems having the stated concentrations.
For chromatographic purification, silica gel from Millipore (MATREX™, 35-70 μm) or Alox (E. Merck, Darmstadt, Alumina 90 standardized, 63-200 μm, article No. 1.01097.9050) are used.
In the descriptions of the experiments, the following abbreviations are used:
The following analytical HPLC methods were used:
The following microwave apparatus was used: Biotage EmrysOptimizer™
1a)
A mixture of 1.0 g (4.07 mmol) of 2,3-dichlorobenzenesulphonic acid chloride, 0.33 g (4.89 mmol) of methylamine hydrochloride, 2.73 ml (19.55 mmol) of triethylamine and 20 ml dichloromethane is stirred overnight at ambient temperature. The reaction mixture is then washed once with 1N HCl, saturated sodium hydrogen carbonate solution, water and saturated sodium chloride solution, dried on sodium sulphate and then evaporated to dryness.
C7H7Cl2NO2S (240.11)
[M+H]+=240/242/244
TLC: silica gel, petroleum ether/ethyl acetate 2:1, Rf value=0.50
1b)
A mixture of 0.9 g (3.75 mmol) of product from 1a and 20 ml DMF is taken and combined with 1.55 g (11.24 mmol) of potassium carbonate and 0.49 ml (4.50 mmol) of ethyl 3-bromopropionate. The reaction mixture is stirred overnight at ambient temperature and then mixed with water. It is extracted twice with ethyl acetate. The organic extracts are washed three times with water and once with saturated sodium chloride solution, dried on sodium sulphate and evaporated to dryness.
C11H13Cl2NO4S (326.20)
[M+H]+=326/328/330
TLC: silica gel, petroleum ether/ethyl acetate 2:1, Rf value=0.45
1c)
A mixture of 1.15 g (3.53 mmol) of product from 1b, 0.74 g (17.63 mmol) of lithium hydroxide monohydrate, 15 ml THF and 15 ml of water is stirred for one hour at ambient temperature. Then the THF is eliminated in vacuo and the residue is acidified with concentrated HCl. The reaction mixture is then extracted three times with ethyl acetate. The organic extracts are washed with saturated sodium chloride solution, dried on sodium sulphate and evaporated to dryness. The crude product is triturated with diethyl ether and suction filtered.
C10H11Cl2NO4S (312.17)
[M+H]+=310/312/314
TLC: silica gel, petroleum ether/ethyl acetate 2:1, Rf value=0.03
1d)
A mixture of 5.0 g (30.63 mmol) of 1-pyridin-4-yl-piperazine, 4.32 g (30.63 mmol) of 1-fluoro-4-nitrobenzene (Aldrich), 10.62 ml (76.59 mmol) of triethylamine and 100 ml DMF is heated for 50 min at reflux temperature and then evaporated to dryness. The crude product thus obtained is purified by column chromatography through silica gel (eluant: dichloromethane/ethanol/ammonia 12:1:0.1 to 10:1:0.1).
C15H16N4O2 (284.31)
[M+H]+=285
TLC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.52
1e)
A mixture of 4.95 g (17.41 mmol) of product from 1d, 0.6 g palladium on charcoal (10%), 120 ml dichloromethane and 20 ml of methanol is hydrogenated for five hours in the autoclave at ambient temperature. Then the mixture is suction filtered and the filter cake is decocted another six times with dichloromethane/methanol 1:1 and suction filtered again. The combined filtrates are evaporated to dryness in vacuo.
C15H18N4 (254.33)
[M+H]+=255
1f)
A mixture of 1.25 g (4.00 mmol) of product from 1c, 2.0 ml (14.34 mmol) of triethylamine, 1.28 g (4.00 mmol) of TBTU and 7 ml DMF is stirred for 45 min at ambient temperature. Then 1.0 g (3.93 mmol) of product from 1e is added and the mixture is stirred overnight at ambient temperature. Then the reaction mixture is poured into water and extracted with dichloromethane. The organic extracts are washed with water, dried on Na2SO4 and evaporated to dryness. The crude product thus obtained was purified by column chromatography through silica gel (eluant: dichloromethane with 5-20% methanol).
C25H27Cl2N5O3S (548.49)
[M+H]+=548/550/552
TLC: silica gel, dichloromethane/methanol 4:1, Rf value=0.65
2a)
A mixture of 0.5 g (2.17 mmol) of N-(1-benzylpiperidin-4-yl)-phthalimide (Bioorg. Med. Chem. Lett. 11, 2001, 2325-2330), 0.33 g (2.17 mmol) of 4-chloropyridine hydrochloride, 1.2 ml (8.69 mmol) of triethylamine and 2.4 ml of absolute ethanol is heated in the microwave to 150° C. for one hour. The reaction mixture is then diluted with ethanol, the precipitate formed is filtered off. The filtrates are evaporated to dryness and the crude product is purified by preparative HPLC.
C18H17N3O2×C2HF3O2 (421.37)
[M+H]+=308
HPLC (Method 1): retention time=2.07 min
2b)
A mixture of 0.3 g (0.71 mmol) of product from 2a, 0.09 g (1.42 mmol) of hydrazine hydrate 80% and 6 ml of absolute ethanol is refluxed for four hours. The reaction mixture is then cooled to 0° C., the precipitate formed is filtered off. The filtrates are evaporated to dryness.
C10H15N3 (177.25)
[M+H]+=178
2c)
Example 2 is prepared analogously to 1f from 0.22 g (0.71 mmol) of product from 1c, 0.24 g (1.35 mmol) of product from 2b, 0.3 ml (2.13 mmol) of triethylamine and 0.23 g (0.71 mmol) of TBTU in 5.5 ml DMF.
C20H24Cl2N4O3S (471.40)
[M+H]+=471/473/475
TLC: silica gel, dichloromethane/methanol 9:1, Rf value=0.2
3a)
A mixture of 0.99 g (4.00 mmol) of 4-methoxy-2,3,6-trimethyl-benzenesulphonyl chloride, 0.69 g (4.51 mmol) of β-alanine ethylester hydrochloride, 2.23 ml (15.98 mmol) of triethylamine and 20 ml dichloromethane is stirred overnight at ambient temperature. The reaction mixture is then washed with 0.5 M HCl, saturated sodium hydrogen carbonate solution, water and saturated sodium chloride solution, dried on sodium sulphate and evaporated to dryness in vacuo.
C15H23NO5S (329.41)
[M+H]+=330
TLC: silica gel, petroleum ether/ethyl acetate 2:1, Rf value=0.43
3b)
A mixture of 1.24 g (3.76 mmol) of product from 3a, 0.84 ml (13.55 mmol) of methyl iodide, 1.04 g (7.53 mmol) of anhydrous potassium carbonate and 10 ml DMF is stirred for five hours at ambient temperature. The reaction mixture is then evaporated to dryness in vacuo, the residue is taken up in ethyl acetate. It is washed with water, saturated sodium hydrogen carbonate solution and saturated sodium chloride solution, dried on sodium sulphate and evaporated to dryness in vacuo.
C16H25NO5S (343.44)
[M+H]+=344
TLC: silica gel, petroleum ether/ethyl acetate 2:1, Rf value=0.52
3c)
The acid is prepared analogously to 1c from 1.29 g (3.76 mmol) of product from 3b, 0.79 g (18.80 mmol) of lithium hydroxide monohydrate, 15 ml THF and 15 ml of water.
C14H21NO5S (315.39)
[M+H]+=316
TLC: silica gel, petroleum ether/ethyl acetate 2:1, Rf value=0.07
3d)
Example 3 is prepared analogously to 1f from 0.15 g (0.47 mmol) of product from 3c, 0.12 g (0.47 mmol) of product from 1e, 0.2 ml (1.43 mmol) of triethylamine and 0.15 g (0.48 mmol) of TBTU in 8 ml DMF.
C29H37N5O4S (551.70)
[M+H]+=552
TLC: silica gel, dichloromethane/methanol 9:1, Rf value=0.38
Example 4 is prepared analogously to 1f from 0.39 g (1.26 mmol) of product from 1c, 0.24 g (1.26 mmol) of 4-(4-methylpiperazin-1-yl)-aniline (J. Med. Chem. SIR 48, 7, 2005, 2371-2387), 0.35 ml (2.51 mmol) of triethylamine and 0.50 g (1.32 mmol) of HATU in 5 ml DMF.
C21H26CL2N4O3S (485.43)
[M+H]+=485/487/489
HPLC (Method 2): retention time=2.64 min
5a)
5a is prepared analogously to 1f from 0.39 g (1.26 mmol) of product from 1c, 0.24 g (1.26 mmol) of 4-(4-methylpiperazin-1-yl)-aniline (J. Med. Chem. SIR 48, 7, 2005, 2371-2387), 0.35 ml (2.51 mmol) of triethylamine and 0.50 g (1.32 mmol) of HATU in 5 ml DMF.
C25H32CL2N4O5S (571.52)
5b)
A mixture of 0.60 g (1.05 mmol) of product from 5a, 3 ml TFA and 3 ml dichloromethane is stirred for two hours at ambient temperature. The reaction mixture is evaporated to dryness and the crude product is purified by preparative HPLC.
C20H24Cl2N4O3S (471.40)
[M+H]+=471/473/475
HPLC (Method 2): retention time=2.58 min
Example 6 is prepared analogously to 1f from 0.22 g (0.71 mmol) of product from 1c, 0.12 g (0.78 mmol) of 3-(4-methylpiperazin-1-yl)-propylamine (Bioorg. Med. Chem. Lett. 13, 2003, 2131-2136), 0.30 ml (2.13 mmol) of triethylamine and 0.23 g (0.71 mmol) of TBTU in 5.5 ml THF.
C18H28Cl2N4O3S×2C2HF3O2 (679.46)
[M+H]+=451/453/455
HPLC (Method 5): retention time=1.37 min
Example 7 is prepared analogously to 1f from 0.22 g (0.71 mmol) of product from 1c, 0.14 g (0.71 mmol) of 4-(1-methylpiperidin-4-yl)-aniline (JW Pharmlab), 0.30 ml (2.13 mmol) of triethylamine and 0.23 g (0.71 mmol) of TBTU in 5.5 ml THF.
C22H27Cl2N3O3S×C2HF3O2 (598.46)
[M+H]+=484/486/488
HPLC (Method 5): retention time=1.57 min
8a)
8a is prepared analogously to 1d from 0.5 g (3.90 mmol) of 4-dimethylamino-piperidine (Alfa Aesar), 0.44 g (4.18 mmol) of 1-fluoro-4-nitrobenzene (Aldrich) and 1.33 ml (76.59 mmol) of triethylamine in 12 ml DMF.
C13H19N3O2 (249.31)
[M+H]+=250
8b)
A mixture of 1.66 g (6.67 mmol) of product from 8a, 0.17 g palladium on charcoal (5%) and 132 ml of ethanol is hydrogenated in the autoclave at ambient temperature. Then the catalyst is removed by suction filtering and the filtrate is evaporated to dryness in vacuo.
C13H21N3 (219.33)
[M+H]+=220
TLC: silica gel, dichloromethane/methanol 9:1, Rf value=0.1
8c)
Example 8 is prepared analogously to 1f from 0.22 g (0.71 mmol) of product from 1c, 0.16 g (0.71 mmol) of product from 8b, 0.30 ml (2.13 mmol) of triethylamine and 0.23 g (0.71 mmol) of TBTU in 5.5 ml THF.
C23H30Cl2N4O3S×2C2HF3O2 (741.53)
[M+H]+=513/515/517
HPLC (Method 5): retention time=1.46 min
9a)
13 ml acetic anhydride are taken and 8 ml formic acid are slowly added thereto. The reaction mixture is heated for 1.5 hours to 50° C. and then combined with 80 ml dichloromethane. While cooling with the ice bath 5.0 g (19.66 mmol) are then added. The mixture is stirred for one hour at ambient temperature and then evaporated to dryness. The residue is combined with semisaturated sodium hydrogen carbonate solution and extracted twice with dichloromethane. The organic extracts are washed with saturated sodium chloride solution, dried on sodium sulphate and evaporated to dryness. The crude product thus obtained is purified by column chromatography through silica gel (eluant: dichloromethane/methanol/ammonia 9:1:0.1).
C16H18N4O (282.34)
[M+H]+=283
9b)
At 60° C. a mixture of 10.63 ml lithium aluminium hydride 2 M in THF (21.25 mmol) and 50 ml THF is slowly combined with 3.0 g (10.63 mmol) of product from 9a. The reaction mixture is stirred for eight hours at 60° C. and four hours at ambient temperature. While cooling with the ice bath 20 ml of water are then added. The mixture is filtered through Celite and washed with THF and dichloromethane. The filtrate is evaporated to dryness. The residue is combined with dichloromethane, washed with water and 1 M sodium hydroxide solution, dried on sodium sulphate solution and evaporated to dryness. The crude product thus obtained is purified by column chromatography through silica gel (eluant: dichloromethane/methanol/ammonia 9:1:0.1).
C16H20N4 (268.36)
9c)
Example 9 is prepared analogously to 1f from 0.15 g (0.48 mmol) of product from 1c, 0.14 g (0.51 mmol) of product from 9b, 0.13 ml (0.96 mmol) of triethylamine and 0.19 g (0.51 mmol) of HATU in 5 ml DMF.
C26H29Cl2N5O3S (562.51)
[M+H]+=562/564/566
HPLC (Method 2): retention time=2.86 min
10a)
A mixture of 1.0 g (9.70 mmol) of N-methyl-β-alanine (Convertex), 24 ml dioxane, 12 ml of water and 2.68 g (19.38 mmol) of anhydrous potassium carbonate is combined with 2.33 g (10.66 mmol) of Boc-anhydride while cooling with an ice bath. The reaction mixture is stirred for three days at ambient temperature. Then the dioxane is eliminated in vacuo. The aqueous residue is extracted with ethyl acetate (ethyl acetate phases are discarded), then acidified slightly with 1 M hydrochloric acid and then extracted with dichloromethane. The organic dichloromethane extracts are washed with saturated sodium chloride solution, dried on sodium sulphate and evaporated to dryness.
C9H17NO4 (203.24)
[M+H]+=204
10b)
10b is prepared analogously to 1f from 1.85 g (9.10 mmol) of product from 10a, 2.32 g (9.10 mmol) of product from 1e, 3.81 ml (27.31 mmol) of triethylamine and 2.92 g (9.10 mmol) of TBTU in 80 ml DMF.
C24H33N5O3 (439.55)
[M+H]+=440
TLC: silica gel, dichloromethane/methanol 9:1, Rf value=0.49
10c)
A mixture of 3.20 g (7.28 mmol) of product from 10b, 20 ml TFA and 60 ml dichloromethane is stirred for 30 min at ambient temperature. Then the reaction mixture is evaporated to dryness in vacuo. The crude product thus obtained is purified by column chromatography through silica gel (eluant: dichloromethane/ethanol/ammonia 9:1:0.1 to 4:1:0.1).
C19H25N5O (339.43)
[M+H]+=340
TLC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.25
10d)
A mixture of 0.1 g (0.30 mmol) of product from 10c, 0.056 g (0.25 mmol) of 1-naphthylsulphonic acid chloride, 0.137 ml (0.98 mmol) of triethylamine and 5 ml dichloromethane is stirred overnight at ambient temperature. Then the reaction mixture is evaporated to dryness in vacuo. The crude product thus obtained is purified by column chromatography through silica gel (eluant: dichloromethane/ethanol/ammonia 12:1:0.1).
C29H31N5O3S (529.65)
[M+H]+=530
TLC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.44
Example 11 is prepared analogously to 10d from 0.10 g (0.30 mmol) of product from 10c, 0.052 g (0.25 mmol) of 2-chlorobenzenesulphonic acid chloride, 0.14 ml (98 mmol) of triethylamine in 5 ml dichloromethane.
C25H28ClN5O3S (514.04)
[M+H]+=514/516
TLC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.47
Example 12 is prepared analogously to 10d from 0.10 g (0.30 mmol) of product from 10c, 0.047 g (0.25 mmol) of p-toluenesulphonic acid chloride, 0.14 ml (98 mmol) of triethylamine in 5 ml dichloromethane.
C26H31N5O3S (493.62)
[M+H]+=494
TLC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.43
13a)
A mixture of 2.0 g (14.69 mmol) of 3,5-dimethylanisol and 20 ml dichloromethane is combined with 5.85 ml (88.0 mmol) of chlorosulphonic acid while cooling with an ice bath. The reaction mixture is then stirred for 20 min at ambient temperature and then poured onto 50 ml ice water. The mixture is extracted with 100 ml dichloromethane. The organic extracts are washed with 5% sodium hydrogen carbonate solution, dried on sodium sulphate and evaporated to dryness.
C9H11ClO3S (234.70)
[M+H]+=234/236
TLC: silica gel, petroleum ether/ethyl acetate 9:1, Rf value=0.46
13b)
Example 13 is prepared analogously to 10d from 0.10 g (0.30 mmol) of product from 10c, 0.058 g (0.25 mmol) of product from 13a, 0.14 ml (98 mmol) of triethylamine in 5 ml dichloromethane.
C28H35N5O4S (537.67)
[M+H]+=538
TLC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.62
Example 14 is prepared analogously to 10d from 0.10 g (0.30 mmol) of product from 10c, 0.047 g (0.25 mmol) of m-toluenesulphonic acid chloride, 0.14 ml (98 mmol) of triethylamine in 5 ml dichloromethane.
C26H31N5O3S (493.62)
[M+H]+=494
TLC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.47
Example 15 is prepared analogously to 10d from 0.10 g (0.30 mmol) of product from 10c, 0.047 g (0.25 mmol) of o-toluenesulphonic acid chloride, 0.14 ml (98 mmol) of triethylamine in 5 ml dichloromethane.
C26H31N5O3S (493.62)
[M+H]+=494
HPLC (Method 1): retention time=2.37 min
Example 16 is prepared analogously to 10d from 0.10 g (0.30 mmol) of product from 10c, 0.043 g (0.25 mmol) of benzenesulphonic acid chloride, 0.14 ml (98 mmol) of triethylamine in 5 ml dichloromethane.
C25H29N5O3S (479.60)
[M+H]+=480
HPLC (Method 1): retention time=2.40 min
17a)
A mixture of 1.03 g (6.28 mmol) of 1-(4-pyridyl)-piperazine (Girindus) and 50 ml dichloromethane is combined with 1.0 g (6.28 mmol) of tert-butyl-N-(2-oxoethyl)-carbamate (Aldrich). The reaction mixture is then stirred for 30 min at ambient temperature, then combined with 2.66 g (12.56 mmol) of sodium-triacetoxyborohydride while cooling with an ice bath and then stirred overnight at ambient temperature. Another 60 ml dichloromethane are added and the reaction mixture is washed with saturated sodium hydrogen carbonate solution and saturated sodium chloride solution. The organic phase is dried on sodium sulphate and evaporated to dryness. The crude product thus obtained is purified by column chromatography through silica gel (eluant: dichloromethane/ethanol/ammonia 14:1:0.1 to 10:1:0.1).
C16H26N4O2 (306.40)
[M+H]+=307
17b)
A mixture of 0.36 g (1.19 mmol) of product from 17a, 1.19 ml (15.50 mmol) of TFA and 2 ml dichloromethane is stirred for two hours at ambient temperature. Then the reaction mixture is evaporated to dryness in vacuo.
C11H18N4×2C2HF3O2 (434.33)
[M+H]+=207
HPLC (Method 2): retention time=0.98 min
17c)
Example 17 is prepared analogously to 1f from 0.22 g (0.71 mmol) of product from 1c, 0.34 g (0.78 mmol) of product from 17b, 0.50 ml (3.56 mmol) of triethylamine and 0.23 g (0.71 mmol) of TBTU in 5.5 ml THF.
C21H27Cl2N5O3S×2C2HF3O2 (728.49)
[M+H]+=500/502/504
HPLC (Method 2): retention time=3.14 min
18a)
18a is prepared analogously to 1f from 0.20 g (0.64 mmol) of product from 1c, 0.17 g (0.64 mmol) of tert-butyl 4-(4-aminobutyl)-piperazine-1-carboxylate (J. Med. Chem. 47, 2004, 4300-4315), 0.27 ml (1.92 mmol) of triethylamine and 0.21 g (0.64 mmol) of TBTU in 5 ml THF.
C23H36CL2N4O5S (551.53)
M+H]+=551/553/555
TLC: silica gel, dichloromethane/methanol 30:1, Rf value=0.1
18b)
A mixture of 0.29 g (0.53 mmol) of product from 18a, 0.53 ml TFA and 1 ml dichloromethane is stirred for two hours at ambient temperature. The reaction mixture is washed with saturated sodium hydrogen carbonate solution. After the phase separation the aqueous phase is extracted three times more with dichloromethane. The organic extracts are dried on sodium sulphate and evaporated to dryness in vacuo.
C18H28Cl2N4O3S (451.41)
[M+H]+=451/453/455
HPLC (Method 2): retention time=2.22 min
19a)
A mixture of 5.0 ml (45.13 mmol) of N-methylpiperazine and 0.73 g (6.00 mmol) of 4-fluorobenzonitrile (Aldrich) is heated for 12 hours to 80° C. Then it is evaporated to dryness and the residue is mixed with water. It is extracted three times with ethyl acetate. The organic extracts are dried on sodium sulphate and evaporated to dryness in vacuo.
C12H15N3 (201.27)
M+H]+=202
TLC: silica gel, dichloromethane/ethanol 95:5, Rf value=0.31
19b)
A mixture of 1.17 g (5.81 mmol) of product from 19a, 0.3 g Raney nickel and 50 ml of methanolic ammonia solution is hydrogenated at 50° C. in the autoclave. Then the catalyst is filtered off and the filtrate is evaporated to dryness in vacuo.
C12H19N3 (205.30)
M+H]+=206
19c)
Example 19 is prepared analogously to 1f from 0.16 g (0.50 mmol) of product from 1c, 0.10 g (0.50 mmol) of product from 19b, 0.14 ml (1.00 mmol) of triethylamine and 0.16 g (0.50 mmol) of TBTU in 3 ml DMF.
C22H28Cl2N4O3S×HCl (535.91)
[M+H]+=499/501/503
HPLC (Method 3): retention time=3.49 min
20a)
A mixture of 0.5 g (4.99 mmol) of N-methylpiperazine (Aldrich), 1.41 g (4.99 mmol) of N-(4-bromobutyl)-phthalimide (Fluka), 0.86 ml (4.99 mmol) of DIPEA and 9.3 ml acetonitrile is heated for 45 min in the microwave to 120° C. Then it is evaporated to dryness. The crude product thus obtained is purified by column chromatography through silica gel (eluant: dichloromethane/methanol 98:2).
C17H23N3O2 (301.38)
M+H]+=302
20b)
A mixture of 1.94 g (6.44 mmol) of product from 20a, 1.61 g (25.75 mmol) of hydrazine hydrate and 15 ml of absolute ethanol is heated for 5.5 hours in the autoclave to 120° C. The precipitate formed is filtered off. Then the filtrate is evaporated to dryness.
C9H21N3 (171.28)
20c)
Example 20 is prepared analogously to 1f from 0.50 g (1.61 mmol) of product from 1c, 0.55 g (3.22 mmol) of product from 20b, 0.67 ml (4.83 mmol) of triethylamine and 0.52 g (1.61 mmol) of TBTU in 30 ml DMF.
C19H30Cl2N4O3S×2HCl (538.36)
[M+H]+=465/467/469
HPLC (Method 1): retention time=2.15 min
21a)
A mixture of 2.06 g (12.62 mmol) of 1-pyridin-4-yl-piperazine (Girindus), 2.00 g (12.62 mmol) of 2-chloro-5-nitropyridine (Fluka) and 50 ml dichloromethane is stirred for 15 min at ambient temperature and then combined with 6.31 ml (12.62 mmol) of 2 M sodium hydroxide solution. The reaction mixture is stirred for 20 hours at ambient temperature and then combined with 300 ml dichloromethane and 100 ml 5% sodium hydrogen carbonate solution. After the phase separation the organic phase is dried on sodium sulphate and evaporated to dryness in vacuo. The crude product is stirred with 100 ml diethyl ether/ethanol 2:1, filtered off and dried.
C14H15N5O2 (285.30)
[M+H]+=286
TLC: silica gel, dichloromethane/ethanol 9:1, Rf value=0.10
21b)
A mixture of 1.75 g (6.13 mmol) of product from 21a, 0.4 g palladium on charcoal (10%), 100 ml dichloromethane and 50 ml of methanol is hydrogenated for five hours in the autoclave at ambient temperature. Then the catalyst is removed by suction filtering and the filtrate is evaporated to dryness in vacuo. The residue is stirred with 100 ml diethyl ether/ethanol 2:1 and suction filtered. The crude product thus obtained is purified by column chromatography through silica gel (eluant: dichloromethane/methanol/ammonia 95:5:0.5).
C14H17N5 (255.32)
[M+H]+=256
TLC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.37
21c)
Example 21 is prepared analogously to 1f from 0.11 g (0.35 mmol) of product from 1c, 0.089 g (0.35 mmol) of product from 21b, 0.098 ml (0.70 mmol) of triethylamine and 0.13 g (0.42 mmol) of TBTU in 15 ml THF.
C24H26Cl2N6O3S (549.47)
[M+H]+=549/551/553
HPLC (Method 4): retention time=2.7 min
22a)
22a is prepared analogously to 3a from 3.00 g (12.78 mmol) of product from 13a, 2.16 g (14.06 mmol) of β-alanine ethylester hydrochloride, 7.13 ml (51.13 mmol) of triethylamine in 70 ml dichloromethane.
C14H21NO5S (315.39)
[M+H]+=316
TLC: silica gel, petroleum ether/ethyl acetate 2:1, Rf value=0.23
22b)
22b is prepared analogously to 3b from 4.06 g (12.87 mmol) of product from 22a, 2.40 ml (38.62 mmol) of methyl iodide, 3.56 g (25.75 mmol) of potassium carbonate anhydrous in 40 ml DMF.
C15H23NO5S (329.41)
[M+H]+=330
TLC: silica gel, petroleum ether/ethyl acetate 2:1, Rf value=0.36
22c)
The acid is prepared analogously to 1c from 3.83 g (11.63 mmol) of product from 22b, 2.44 g (58.13 mmol) of lithium hydroxide monohydrate in 30 ml THF and 30 ml of water.
C13H19NO5S (301.36)
[M+H]+=302
TLC: silica gel, petroleum ether/ethyl acetate 1:1, Rf value=0.12
22d)
Example 22 is prepared analogously to 1f from 0.13 g (0.42 mmol) of product from 22c, 0.089 g (0.35 mmol) of product from 21b, 0.098 ml (0.70 mmol) of triethylamine and 0.13 g (0.42 mmol) of TBTU in 15 ml THF.
C27H34N6O4S (538.66)
[M+H]+=539
HPLC (Method 4): retention time=2.6 min
Example 23 is prepared analogously to 1f from 0.30 g (1.00 mmol) of product from 22c, 0.22 g (1.00 mmol) of product from 8b, 0.42 ml (2.99 mmol) of triethylamine and 0.32 g (1.00 mmol) of TBTU in 15 ml DMF.
C26H38N4O4S (502.67)
[M+H]+=503
HPLC (Method 1): retention time=2.47 min
Example 24 is prepared analogously to 1f from 0.25 g (0.80 mmol) of product from 3c, 0.18 g (0.80 mmol) of product from 8b, 0.33 ml (2.39 mmol) of triethylamine and 0.26 g (0.80 mmol) of TBTU in 10 ml DMF.
C27H40N4O4S (516.70)
[M+H]+=517
HPLC (Method 1): retention time=2.50 min
Example 25 is prepared analogously to 1f from 0.20 g (0.66 mmol) of product from 22c, 0.14 g (0.73 mmol) of 4-(1-methylpiperidin-4-yl)-aniline (JW Pharmlab), 0.28 ml (1.99 mmol) of triethylamine and 0.21 g (0.66 mmol) of TBTU in 50 ml THF.
C27H40N4O4S×C2HF3O2 (587.65)
[M+H]+=474
HPLC (Method 2): retention time=3.03 min
Example 26 is prepared analogously to 1f from 0.20 g (0.66 mmol) of product from 22c, 0.14 g (0.73 mmol) of 4-(4-methylpiperazin-1-yl)-aniline (J. Med. Chem. SIR 48, 7, 2005, 2371-2387), 0.28 ml (1.99 mmol) of triethylamine and 0.21 g (0.66 mmol) of TBTU in 5 ml THF.
C24H34N4O4S×C2HF3O2 (588.65)
[M+H]+=475
HPLC (Method 5): retention time=1.50 min
27a)
A mixture of 1.00 g (6.31 mmol) of 2-chloro-5-nitropyridine (Fluka), 1.32 ml (9.46 mmol) of triethylamine and 2 ml of methanol is taken and slowly combined with 1.13 g (8.83 mmol) of 4-dimethylamino-piperidine (Alfa Aesar). The reaction solution is then quenched with semisaturated sodium chloride, the precipitate formed is suction filtered and dried.
C12H18N4O2 (250.30)
27b)
27b is prepared analogously to 8b from 1.50 g (5.99 mmol) of product from 27a, 0.20 g palladium on charcoal (10%) and 15 ml of methanol.
C12H20N4 (220.31)
27c)
A mixture of 0.11 g (0.35 mmol) of product from 22c and 2.0 ml of thionyl chloride is stirred for two hours at ambient temperature. The reaction mixture is then evaporated to dryness in vacuo.
C13H18ClNO4S (319.81)
27d)
A mixture of 0.11 g (0.34 mmol) of product from 27c, 0.091 g (0.41 mmol) of product from 27b, 0.18 ml (1.03 mmol) of DIPEA and 45 ml THF is stirred for two hours at ambient temperature. The reaction mixture is then evaporated to dryness in vacuo. The crude product is purified by preparative HPLC. Then the hydrochloride is prepared using 4 M HCl in dioxane.
C25H37N5O4S×2HCl (576.58)
[M+H]+=504
HPLC (Method 2): retention time=2.73 min
28a)
A mixture of 1.50 g (6.84 mmol) of 1-(2-aminoethyl)-4-benzylpiperazine (Maybridge), 1.64 g (7.52 mmol) of Boc-anhydride and 30 ml dichloromethane is stirred for one hour at ambient temperature. Then the reaction solution is diluted with 100 ml dichloromethane and washed with 1 M sodium hydroxide solution and water. The organic phase is dried on sodium sulphate and evaporated to dryness in vacuo.
C18H29N3O2 (319.44)
HPLC (Method 4): retention time=2.6 min
28b)
A mixture of 2.10 g (6.57 mmol) of product from 28a, 0.25 g palladium on charcoal (10%) and 30 ml of methanol is hydrogenated for 15 hours at ambient temperature in the autoclave. Then the catalyst is removed by suction filtering and the filtrate is evaporated to dryness in vacuo.
C11H23N3O4 (229.32)
[M+H]+=230
TLC: silica gel, dichloromethane/ethanol 9:1, Rf value=0.08
28c)
A mixture of 1.18 g (6.32 mmol) of 4-bromo-2,6-dimethylpyridine (Acta Chem. Scand. Ser. B 42, 1988, 373-377), 1.45 g (6.32 mmol) of product from 28b and 2.2 ml DIPEA is heated for 50 min to 130° C. in the microwave. The reaction mixture is combined with ethyl acetate and semisaturated potassium carbonate solution and then the phases are separated. The organic phase is dried on sodium sulphate and evaporated to dryness in vacuo. The crude product thus obtained is purified by column chromatography through silica gel (eluant: dichloromethane/methanol/ammonia 95:5:0.5).
C18H30N4O2S (334.46)
[M+H]+=335
TLC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.37
28d)
A mixture of 1.61 g (4.81 mmol) of product from 28c, 3.70 ml TFA and 30 ml dichloromethane is stirred for six hours at ambient temperature. The reaction mixture is then diluted with dichloromethane and washed with 5% sodium hydrogen carbonate solution. The aqueous phase is extracted twice more with ethyl acetate. The combined organic phases are dried on sodium sulphate and evaporated to dryness in vacuo. The crude product thus obtained is purified by column chromatography through silica gel (eluant: dichloromethane/methanol/ammonia 90:10:1).
C13H22N4 (234.34)
[M+H]+=235
TLC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.10
28e)
Example 28 is prepared analogously to 1f from 0.11 g (0.35 mmol) of product from 22c, 0.082 g (0.35 mmol) of product from 28d, 0.098 ml (0.70 mmol) of triethylamine and 0.13 g (0.42 mmol) of TBTU in 7 ml THF and 1 ml DMF.
C26H39N5O4S (517.69)
[M+H]+=518
HPLC (Method 4): retention time=2.4 min
29a)
29a is prepared analogously to 28c from 0.12 g (0.80 mmol) of 4-chloropyridine hydrochloride (Aldrich), 0.20 g (0.80 mmol) of N-methyl-N-(2-piperidin-4-yl-ethyl)-benzamide (J. Med. Chem. 33, 1990, 1880-1887), 0.23 ml (1.68 mmol) of triethylamine in 5 ml of ethanol.
C20H25N3O (323.43)
[M+H]+=324
29b)
A mixture of 0.52 g (1.61 mmol) of product from 29a, 10 ml of 2 M potassium hydroxide solution and 10 ml of ethanol is refluxed for 30 hours. The reaction mixture is evaporated down by half in vacuo and then extracted with dichloromethane. The organic extracts are dried on sodium sulphate and evaporated to dryness in vacuo.
C13H21N3 (219.33)
[M+H]+=220
TLC: silica gel, dichloromethane/methanol/ammonia 8:2:0.01, Rf value=0.46
29c)
Example 29 is prepared analogously to 1f from 0.14 g (0.46 mmol) of product from 22c, 0.10 g (0.46 mmol) of product from 29b, 0.15 ml (1.09 mmol) of triethylamine and 0.16 g (0.50 mmol) of TBTU in 30 ml THF and 5 ml DMF.
C26H38N4O4S×HCl (539.13)
[M+H]+=503
TLC: silica gel, dichloromethane/methanol/ammonia 8:2:0.01, Rf value=0.41
30a)
A mixture of 3.25 g (26.60 mmol) of 3,5-dimethylphenol (Aldrich), 3.20 g (28.52 mmol) of potassium-tert-butoxide and 40 ml DMSO is stirred for one hour at ambient temperature. Then 3.80 g (27.34 mmol) of bromoethylmethylether (Aldrich) is added dropwise thereto and the mixture is stirred for another two hours at ambient temperature. The reaction mixture is poured onto water and extracted with diethyl ether. The organic extracts are washed with water and saturated sodium chloride solution, dried on sodium sulphate and evaporated to dryness in vacuo.
C11H16O2 (180.24)
[M+H]+=181
TLC: silica gel, petroleum ether/ethyl acetate 9:1, Rf value=0.31
30b)
30b is prepared analogously to 13a from 4.30 g (23.86 mmol) of product from 30a and 5.60 g (48.06 mmol) of chlorosulphonic acid in 100 ml dichloromethane.
C11H15ClO4S (278.75)
TLC: silica gel, petroleum ether/ethyl acetate 9:1, Rf value=0.06
30c)
30a is prepared analogously to 3a from 1.70 g (6.10 mmol) of product from 30b, 1.20 g (7.81 mmol) of β-alanine ethylester hydrochloride, 2.60 ml (18.65 mmol) of triethylamine in 30 ml dichloromethane.
C16H25NO6S (359.44)
[M+H]+=360
TLC: silica gel, dichloromethane/methanol 19:1, Rf value=0.51
30d)
30d is prepared analogously to 3b from 1.90 g (5.29 mmol) of product from 30c, 1.10 g (7.75 mmol) of methyl iodide, 1.50 g (10.85 mmol) of anhydrous potassium carbonate in 30 ml DMF.
C17H27NO6S (373.47)
[M+H]+=374
30e)
The acid is prepared analogously to 1c from 1.70 g (4.55 mmol) of product from 30d, 0.80 g (20.00 mmol) of sodium hydroxide in 30 ml of ethanol and 10 ml of water.
C15H23NO6S (345.41)
[M+H]+=346
30f)
Example 30 is prepared analogously to 1f from 0.14 g (0.39 mmol) of product from 30e, 0.10 g (0.39 mmol) of product from 21b, 0.10 ml (0.99 mmol) of triethylamine and 0.14 g (0.44 mmol) of TBTU in 30 ml THF and 5 ml DMF.
C29H38N6O5S (582.72)
[M+H]+=583
TLC: silica gel, dichloromethane/methanol/ammonia 8:2:0.01, Rf value=0.44
Example 31 is prepared analogously to 1f from 0.16 g (0.46 mmol) of product from 30e, 0.10 g (0.46 mmol) of product from 29b, 0.11 ml (1.09 mmol) of triethylamine and 0.16 g (0.50 mmol) of TBTU in 30 ml THF and 5 ml DMF.
C28H42N4O5S×HCl (583.18)
[M+H]+=547
TLC: silica gel, dichloromethane/methanol/ammonia 8:2:0.01, Rf value=0.52
32a)
A mixture of 3.00 g (18.81 mmol) of 2-chloro-5-nitropyrimidine (Apin), 3.07 g (18.81 mmol) of 1-(4-pyridyl)-piperazine (Girindus), 9.40 ml (18.81 mmol) of 2 M sodium hydroxide solution in 80 ml dichloromethane is stirred for 2.5 hours at ambient temperature. Then the reaction mixture is diluted with 100 ml dichloromethane and washed with 5% sodium hydrogen carbonate solution. The organic phase is dried on sodium sulphate and evaporated to dryness in vacuo.
The crude product is triturated with a mixture of 50 ml of water and 30 ml ethyl acetate, filtered off and dried.
C13H14N6O2 (286.29)
[M+H]+=287
HPLC (Method 4): retention time=2.6 min
32b)
32b is prepared analogously to 21b from 1.93 g (6.74 mmol) of product from 32a and 0.3 g palladium on charcoal (10%) in 60 ml dichloromethane and 30 ml of methanol.
C13H16N6 (256.31)
[M+H]+=257
TLC: silica gel, dichloromethane/methanol 8:2, Rf value=0.11
32c)
Example 32 is prepared analogously to 1f from 0.11 g (0.35 mmol) of product from 22c, 0.090 g (0.35 mmol) of product from 32b, 0.098 ml (0.70 mmol) of triethylamine and 0.13 g (0.42 mmol) of TBTU in 7 ml THF and 1 ml DMF.
C26H33N7O4S (539.65)
[M+H]+=540
HPLC (Method 4): retention time=2.9 min
33a)
A mixture of 0.68 g (2.91 mmol) of 4-(4-dimethylamino-piperidin-1-yl)-benzaldehyde (Tetrahedron 57, 2001, 4781-4785), 15 ml of 2 M ammonia in ethanol and 0.10 g Raney nickel is hydrogenated at ambient temperature in the autoclave. Then the catalyst is filtered off and the filtrate is evaporated to dryness in vacuo.
C14H23N3 (233.35)
33b)
Example 33 is prepared analogously to 27d from 0.27 g (0.84 mmol) of product from 27c, 0.63 g (2.68 mmol) of product from 33a, 0.22 ml (1.26 mmol) of DIPEA in 3 ml dichloromethane.
C27H40N4O4S×2HCl (589.62)
[M+H]+=517
HPLC (Method 5): retention time=1.46 min
34a)
A mixture of 4.97 ml (59.50 mmol) of pyrrolidine and 100 ml dichloromethane is slowly combined with 5.00 g (23.80 mmol) of (4-bromomethyl-phenyl)-acetonitrile (Tetrahedron 47, 1991, 3969-3980) while cooling with an ice bath. Then the reaction mixture is heated to ambient temperature, washed with water, dried on magnesium sulphate and evaporated to dryness in vacuo.
C13H16N2 (200.28)
[M+H]+=201
TLC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.58
34b)
A mixture of 4.70 g (23.47 mmol) of product from 34a, 0.5 g Raney nickel and 50 ml of methanolic ammonia solution is hydrogenated in the autoclave at 50° C. Then the catalyst is filtered off and the filtrate is evaporated to dryness in vacuo.
C13H20N2 (204.31)
[M+H]+=205
34c)
A mixture of 4.09 g (20.00 mmol) of product from 34b, 5.62 ml (40.00 mmol) of triethylamine and 100 ml dichloromethane is slowly combined with 2.17 ml (22.00 mmol) of ethyl chloroformate (Aldrich) while cooling with an ice bath. Then the mixture is stirred for five hours at ambient temperature. The reaction mixture is then quenched with water and extracted with MTB-ether. The organic extracts are washed twice with water, dried on magnesium sulphate and evaporated to dryness in vacuo. The crude product thus obtained is purified by column chromatography through silica gel (eluant: dichloromethane/methanol/ammonia 9:1:0.1).
C16H24N2O2 (276.37)
[M+H]+=277
34d)
A mixture of 3.60 g (13.03 mmol) of product from 34c and 25 ml THF is slowly combined with 51.05 ml (51.05 mmol) of 1 M lithium aluminium hydride in THF (Aldrich). Then the mixture is stirred for two hours at ambient temperature and two hours at 70° C. The reaction mixture is then quenched with water and 15% sodium hydroxide solution and stirred for another hour at ambient temperature. The precipitate formed is filtered off and the filtrate is evaporated to dryness in vacuo.
The crude product thus obtained is purified by column chromatography through silica gel (eluant: dichloromethane/methanol/ammonia 9:1:0.1).
C14H22N2 (218.34)
[M+H]+=219
34e)
Example 34 is prepared analogously to 1f from 0.11 g (0.35 mmol) of product from 22c, 0.076 g (0.35 mmol) of product from 34d, 0.098 ml (0.70 mmol) of triethylamine and 0.13 g (0.42 mmol) of TBTU in 7 ml THF and 1 ml DMF.
C27H39N3O4S (501.68)
[M+H]+=502
HPLC (Method 4): retention time=3.1 min
35a)
A mixture of 0.33 g (2.34 mmol) of 1-fluoro-4-nitrobenzene (Aldrich), 0.30 g (2.34 mmol) of 3-dimethylamino-piperidine (Chess), 0.46 ml (3.27 mmol) of triethylamine and 4 ml DMF is stirred for six hours at ambient temperature. The reaction mixture is then quenched with water and extracted with dichloromethane. The organic extracts are washed with saturated sodium chloride solution, dried on sodium sulphate and evaporated to dryness in vacuo.
C13H19N3O2 (249.31)
[M+H]+=250
TLC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.56
35b)
A mixture of 0.25 g (1.00 mmol) of product from 35a, 30 mg Raney nickel and 10 ml ethyl acetate is hydrogenated in the autoclave at ambient temperature. The catalyst is filtered off and the filtrate is evaporated to dryness in vacuo.
C13H21N3 (219.33)
TLC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.25
35c)
Example 35 is prepared analogously to 1f from 0.16 g (0.50 mmol) of product from 1c, 0.11 g (0.50 mmol) of product from 35b, 0.14 ml (1.00 mmol) of triethylamine and 0.16 g (0.50 mmol) of TBTU in 3 ml DMF.
C23H30Cl2N4O3S×HCl (539.14)
[M+H]+=513/515/517
HPLC (Method 1): retention time=2.43 min
36a)
A mixture of 2.50 g (13.35 mmol) of 3-piperazin-1-yl-benzonitrile (Tetrahedron 55, 1999, 13285-13300), 3.00 g (13.75 mmol) of Boc-anhydride, 2.40 ml (13.78 mmol) of DIPEA and 50 ml THF is stirred for four hours at ambient temperature and then evaporated to dryness in vacuo. The residue is taken up in water and extracted with diethyl ether. The organic extracts are dried on sodium sulphate and evaporated to dryness in vacuo.
C16H21N3O2 (287.36)
[M+Na]+=310
36b)
36b is prepared analogously to 34b from 4.40 g (15.31 mmol) of product from 36a, 0.7 g Raney nickel and 45 ml of methanolic ammonia solution.
C16H25N3O2 (291.39)
[M+H]+=292
36c)
36c is prepared analogously to 1f from 0.40 g (1.33 mmol) of product from 22c, 0.43 g (1.46 mmol) of product from 36b, 0.56 ml (3.98 mmol) of triethylamine and 0.43 g (1.33 mmol) of TBTU in 10 ml THF.
C29H42N4O6S (574.73)
M+H]+=575
TLC: silica gel, dichloromethane/methanol 9:1, Rf value=0.53
36d)
Example 36 is prepared analogously to 18b from 0.50 g (0.57 mmol) of product from 36c, 0.44 ml TFA in 5 ml dichloromethane.
C18H28Cl2N4O3S×C2HF3O2 (588.64)
[M+H]+=475
HPLC (Method 2): retention time=2.95 min
37a)
A mixture of 2.00 g (12.25 mmol) of 1-(4-pyridyl)-piperazine (Girindus), 1.65 g (14.70 mmol) of potassium-tert-butoxide and 50 ml DMSO is stirred for 30 min at ambient temperature and then combined with 2.25 g (12.25 mmol) of 1-benzylmethylamino-2-chloroethane (Chem. Pharm. Bull. 45, 1997, 996-1007). The reaction mixture is stirred overnight at ambient temperature and then poured onto ice water. It is extracted four times with dichloromethane. The organic extracts are dried on sodium sulphate and evaporated to dryness in vacuo. The crude product thus obtained is purified by column chromatography through silica gel (eluant: dichloromethane/methanol/ammonia 9:1:0.1).
C19H26N4 (310.44)
[M+H]+=311
TLC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.22
37b)
A mixture of 1.78 g (5.73 mmol) of product from 37a, 0.40 g palladium hydroxide and 50 ml of methanol is hydrogenated at 40° C. in the autoclave. The catalyst is filtered off and the filtrate is evaporated to dryness in vacuo. The crude product thus obtained is purified by column chromatography through silica gel (eluant: dichloromethane/methanol/ammonia 9:1:0.1).
C12H20N4 (220.31)
[M+H]+=221
TLC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.13
37c)
Example 37 is prepared analogously to 1f from 0.11 g (0.35 mmol) of product from 22c, 0.072 g (0.35 mmol) of product from 37b, 0.098 ml (0.70 mmol) of triethylamine and 0.13 g (0.42 mmol) of TBTU in 7 ml THF.
C25H37N5O4S×2HCl (576.58)
[M+H]+=504
HPLC (Method 4): retention time=2.5 min
38a)
A mixture of 4.44 g (33.29 mmol) of aluminium chloride (Merck) and 16 ml of dichloroethane is taken and 1.24 ml (17.44 mmol) of acetyl chloride (Aldrich) is slowly added while cooling with an ice bath. The mixture is stirred for 30 min at ambient temperature. Then 3.00 g (15.85 mmol) of 1-(1,2,4,5-tetrahydrobenzo[d]azepin-3-yl)-ethanone (J. Med. Chem. 46, 2003, 4952-4964) in 7 ml of dichloroethane slowly added to the reaction mixture. After two hours' stirring at ambient temperature the reaction mixture is poured onto a mixture of 6 M HCl and ice. After the phase separation the aqueous phase is extracted another three times with dichloromethane. The combined organic phases are washed with water, dried on sodium sulphate and evaporated to dryness in vacuo.
The crude product thus obtained is triturated with diethyl ether, filtered off and dried.
C14H17NO2 (231.29)
[M+H]+=232
38b)
A mixture of 2.86 g (12.37 mmol) of product from 38a and 79 ml 2.5 M sodium hydroxide solution is slowly combined at ambient temperature with 2.48 ml (48.23 mmol) of bromine. The reaction mixture is then stirred for one hour at ambient temperature. The precipitate formed is filtered off and the filtrate is extracted with MTB-ether. The aqueous phase is then mixed with concentrated HCl and a little sodium disulphite solution while cooling with an ice bath. The precipitate formed is filtered off and dried in the circulating air dryer at 30° C.
C13H15NO3 (233.26)
[M+H]+=234
38c)
A mixture of 2.12 g (9.09 mmol) of product from 38b and 20 ml 6 M HCl is heated for 3.5 days to 100° C. The reaction mixture is then cooled with a mixture of ice and ethanol. The precipitate formed is filtered off, washed with a little cooled acetone and diethyl ether and dried in the desiccator.
C11H13NO2×HCl (227.69)
[M+H]+=192
38d)
First 0.94 ml (17.83 mmol) of 50% sodium hydroxide solution, then 2.66 ml (35.66 mmol) of 37% formalin solution are slowly added to a mixture of 2.03 g (8.92 mmol) of product from 38c and 3.36 ml (89.16 mmol) of formic acid. The reaction mixture is heated for two hours to 70° C. and then evaporated to dryness in vacuo. The residue is combined with water and concentrated HCl and again evaporated to dryness. The crude product is triturated with a little ice-cold water, filtered off and dried in the circulating air dryer at 60° C.
C12H15NO2×HCl (241.71)
[M+H]+=206
38e)
38e is prepared analogously to 1f from 2.00 g (8.27 mmol) of product from 38d, 18.20 ml (9.10 mmol) of ammonia 0.5 M in dioxane (Aldrich), 3.46 ml (24.82 mmol) of triethylamine and 3.19 g (9.93 mmol) of TBTU in 30 ml THF.
C12H16N2O (204.27)
[M+H]+=205
HPLC (Method 2): retention time=1.54 min
38f)
A mixture of 5.20 ml (5.20 mmol) of lithium aluminium hydride 1 M in THF (Aldrich) and 18 ml THF is heated to 50° C. and slowly combined with 0.84 g (2.64 mmol) of product from 38e. The reaction mixture is then stirred for 30 min at 50° C. It is then cooled to −20° C. and the reaction mixture is quenched first with a mixture of water and THF, then with 2 M sodium hydroxide solution. It is stirred for one hour at ambient temperature. The precipitate formed is filtered off, the filtrate is evaporated to dryness in vacuo. The residue is taken up in dichloromethane and washed with saturated sodium hydrogen sulphate solution. The organic phase is dried on sodium sulphate and evaporated to dryness in vacuo.
C12H18N2 (190.28)
[M+H]+=191
HPLC (Method 2): retention time=2.21 min
38g)
Example 38 is prepared analogously to 1f from 0.19 g (0.63 mmol) of product from 22c, 0.12 g (0.63 mmol) of product from 38f, 0.26 ml (1.89 mmol) of triethylamine and 0.20 g (0.63 mmol) of TBTU in 5 ml THF.
C25H35N3O4S×C2HF3O2 (587.65)
[M+H]+=474
HPLC (Method 4): retention time=2.98 min
39a)
A mixture of 1.50 g (6.07 mmol) of benzyl 4-oxo-azepan-1-carboxylate (Tyger), 20 ml (40.00 mmol) of dimethylamine 2 M in THF (Aldrich) and 0.34 ml (6.07 mmol) of acetic acid is stirred for 20 min at ambient temperature and then combined with 3.82 g (18.00 mmol) of sodium triacetoxyborohydride (Aldrich). The mixture is stirred overnight at ambient temperature. The reaction mixture is then mixed with saturated sodium hydrogen carbonate solution and extracted with ethyl acetate. The organic extracts are washed with saturated sodium chloride solution, dried on sodium sulphate and evaporated to dryness in vacuo. The crude product thus obtained is purified by column chromatography through silica gel (eluant: dichloromethane/4-12% (methanol+10% ammonia)).
C16H24N2O2 (276.37)
[M+H]+=277
HPLC (Method 1): retention time=2.12 min
39b)
A mixture of 1.00 g (3.62 mmol) of product from 39a, 0.10 g palladium on charcoal (10%) and 30 ml of methanol is hydrogenated at ambient temperature in the autoclave. The catalyst is then filtered off, the filtrate is evaporated to dryness in vacuo.
C8H18N2 (142.24)
[M+H]+=143
TLC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.12
39c)
39c is prepared analogously to 1d from 0.56 g (4.37 mmol) of product from 39b, 0.64 g (4.50 mmol) of 4-fluoro-nitrobenzene (Aldrich), 0.65 ml (4.60 mmol) of triethylamine in 5 ml DMF.
C14H21N3O2 (263.34)
[M+H]+=264
TLC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.60
39d)
39d is prepared analogously to 8b from 0.94 g (3.55 mmol) of product from 39c and 0.10 g palladium on charcoal (10%) in 30 ml of methanol.
C14H23N3O2 (233.35)
TLC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.15
39e)
Example 39 is prepared analogously to 1f from 0.30 g (1.00 mmol) of product from 22c, 0.23 g (1.00 mmol) of product from 39d, 0.42 ml (3.00 mmol) of triethylamine and 0.32 g (1.00 mmol) of TBTU in 15 ml DMF.
C27H40N4O4S×HCl (553.16)
[M+H]+=517
TLC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.42
HPLC (Method 5): retention time=1.50 min
Example 40 is prepared analogously to 1f from 0.16 g (0.50 mmol) of product from 1c, 0.12 g (0.50 mmol) of product from 39d, 0.21 ml (1.50 mmol) of triethylamine and 0.16 g (0.50 mmol) of TBTU in 5 ml DMF.
C24H32Cl2N4O3S×HCl (563.97)
[M+H]+=527/529/531
TLC: silica gel, dichloromethane/methanol/ammonia 6:1:0.2, Rf value=0.48
HPLC (Method 5): retention time=1.53 min
41a)
41a is prepared analogously to 1d from 1.00 g (5.87 mmol) of diethyl-piperidin-4-ylmethyl-amine (Chem. Pharm. Bull. 42, 1994, 74-84), 0.83 g (5.87 mmol) of 4-fluoro-nitrobenzene (Aldrich), 1.14 ml (8.20 mmol) of triethylamine in 12 ml DMF.
C16H25N3O2 (291.39)
[M+H]+=292
TLC: silica gel, dichloromethane/ethanol 9:1, Rf value=0.5
41b)
A mixture of 0.40 g (1.37 mmol) of product from 41a, 0.10 g palladium on charcoal (10%) and 30 ml of methanol is hydrogenated at ambient temperature in the autoclave. The catalyst is then filtered off, the filtrate is evaporated to dryness in vacuo.
C16H27N3 (261.41)
TLC: silica gel, dichloromethane/ethanol 9:1, Rf value=0.1
41c)
Example 41 is prepared analogously to 1f from 0.40 g (1.34 mmol) of product from 22c, 0.35 g (1.34 mmol) of product from 41b, 0.47 ml (3.35 mmol) of triethylamine and 0.43 g (1.34 mmol) of TBTU in 7 ml THF and 1 ml DMF.
C29H44N4O4S×HCl (581.21)
[M+H]+=545
HPLC (Method 5): retention time=1.42 min
42a)
42a is prepared analogously to 1d from 1.88 g (12.00 mmol) of dimethyl-(2-piperidin-4-yl-ethyl)-amine (J. Med. Chem. 36, 1993, 162-165), 1.69 g (12.00 mmol) of 4-fluoro-nitrobenzene (Aldrich), 2.37 ml (17.00 mmol) of triethylamine in 15 ml DMF.
C15H23N3O2 (277.36)
[M+H]+=278
TLC: silica gel, dichloromethane/ethanol 9:1, Rf value=0.2
42b)
A mixture of 0.30 g (1.08 mmol) of product from 42a, 0.10 g palladium on charcoal (10%) and 30 ml of methanol is hydrogenated at ambient temperature in the autoclave. The catalyst is then filtered off, the filtrate is evaporated to dryness in vacuo.
C15H25N3 (247.38)
42c)
Example 42 is prepared analogously to 1f from 0.33 g (1.08 mmol) of product from 22c, 0.27 g (1.08 mmol) of product from 42b, 0.38 ml (2.70 mmol) of triethylamine and 0.35 g (1.08 mmol) of TBTU in 7 ml THF and 1 ml DMF.
C28H42N4O4S (530.72)
[M+H]+=531
HPLC (Method 5): retention time=1.41 min
A mixture of 0.15 g (0.25 mmol) of product from 36d, 0.025 ml (0.40 mmol) of methyl iodide (Aldrich), 0.10 ml (0.75 mmol) of potassium carbonate and 5 ml acetonitrile is stirred overnight at ambient temperature. The reaction mixture is then combined with 10% TFA, the product is separated off by preparative HPLC.
C25H36N4O4S×C2HF3O2 (602.67)
[M+H]+=489
HPLC (Method 2): retention time=2.99 min
44a)
A mixture of 0.72 g (4.61 mmol) of dimethyl-(2-piperidin-4-yl-ethyl)-amine (J. Med. Chem. 36, 1993, 162-165), 0.73 g (4.61 mmol) of 2-chloro-5-nitropyridine (Fluka), 1.30 g (9.41 mmol) of potassium carbonate and 100 ml THF is stirred at ambient temperature over the weekend. The precipitate is filtered off, the filtrate is evaporated to dryness in vacuo. The crude product thus obtained is purified by column chromatography through silica gel (eluant: dichloromethane/methanol 19:1 to 4:1).
C14H22N4O2 (278.35)
[M+H]+=279
44b)
A mixture of 0.26 g (0.93 mmol) of product from 44a, 0.05 g palladium on charcoal (10%) and 30 ml of methanol is hydrogenated at ambient temperature in the autoclave. The catalyst is then filtered off, the filtrate is evaporated to dryness in vacuo.
C14H24N4 (248.37)
[M+H]+=249
44c)
Example 44 is prepared analogously to 1f from 0.12 g (0.40 mmol) of product from 22c, 0.10 g (0.40 mmol) of product from 44b, 0.069 ml (0.50 mmol) of triethylamine and 0.14 g (0.44 mmol) of TBTU in 40 ml THF and 5 ml DMF.
C27H41N5O4S×2HCl (604.63)
[M+H]+=532
HPLC (Method 5): retention time=1.40 min
45a)
45a is prepared analogously to 44a from 1.00 g (5.87 mmol) of diethyl-piperidin-4-ylmethyl-amine (Chem. Pharm. Bull. 42, 1994, 74-84), 0.93 g (5.87 mmol) of 2-chloro-5-nitropyridine (Fluka) and 1.70 g (12.30 mmol) of potassium carbonate in 100 ml THF.
C15H24N4O2 (292.38)
[M+H]+=293
45b)
A mixture of 0.20 g (0.68 mmol) of product from 45a, 0.03 g palladium on charcoal (10%) and 30 ml of methanol is hydrogenated at ambient temperature in the autoclave. The catalyst is then filtered off, the filtrate is evaporated to dryness in vacuo.
C15H26N4 (262.39)
[M+H]+=263
45c)
Example 45 is prepared analogously to 1f from 0.16 g (0.53 mmol) of product from 22c, 0.14 g (0.53 mmol) of product from 45b, 0.096 ml (0.69 mmol) of triethylamine and 0.19 g (0.58 mmol) of TBTU in 40 ml THF and 5 ml DMF.
C28H43N5O4S×2HCl (618.66)
[M+H]+=546
HPLC (Method 5): retention time=1.40 min
46a)
46a is prepared analogously to 1d from 3.00 g (15.21 mmol) of 2-piperazin-1-yl-1-pyrrolidin-1-yl-ethanone (Chess), 2.15 g (15.21 mmol) of 1-fluoro-4-nitrobenzene (Aldrich) and 3.07 ml (22.00 mmol) of triethylamine in 25 ml DMF.
C16H22N4O3 (318.37)
[M+H]+=319
TLC: silica gel, dichloromethane/ethanol 9:1, Rf value=0.4
46b)
A mixture of 3.00 g (9.42 mmol) of product from 46a, 0.30 g palladium on charcoal (10%) and 200 ml of methanol is hydrogenated at ambient temperature in the autoclave. The catalyst is then filtered off, the filtrate is evaporated to dryness in vacuo.
C16H24N4O (288.39)
TLC: silica gel, dichloromethane/ethanol 9:1, Rf value=0.42
46c)
30.00 ml (30.00 mmol) of lithium aluminium hydride 1 M in THF (Aldrich) is placed in 50 ml THF and at ambient temperature combined with a mixture of 2.70 g (9.36 mmol) of product from 46b and 20 ml THF. The reaction mixture is then stirred for three hours at ambient temperature and then combined with 20% sodium hydroxide solution while cooling with an ice bath. The precipitate formed is filtered off, the filtrate is evaporated to dryness in vacuo.
C16H26N4 (274.40)
46d)
Example 46 is prepared analogously to 1f from 0.30 g (1.00 mmol) of product from 22c, 0.27 g (1.00 mmol) of product from 46c, 0.35 ml (2.50 mmol) of triethylamine and 0.32 g (1.00 mmol) of TBTU in 7 ml THF and 1 ml DMF.
C29H43N5O4S×HCl (594.21)
[M+H]+=558
HPLC (Method 5): retention time=1.43 min
Example 47 is prepared analogously to 1f from 0.20 g (0.66 mmol) of product from 22c, 0.14 g (0.66 mmol) of 4-(4-methyl-piperazin-1-ylmethyl)-phenylamine (Med. Chem. Res. 9, 1999, 149-161), 0.28 ml (1.99 mmol) of triethylamine and 0.21 g (0.66 mmol) of TBTU in 5 ml THF.
C25H36N4O4S (488.64)
[M+H]+=489
HPLC (Method 5): retention time=1.42 min
48a)
48a is prepared analogously to 1f from 0.24 g (1.45 mmol) of 4-nitrobenzoic acid (Aldrich), 0.19 g (1.45 mmol) of 4-dimethylamino-piperidine (Alfa Aesar), 0.21 ml (1.52 mmol) of triethylamine and 0.49 g (1.52 mmol) of TBTU in 8 ml DMF.
C14H19N3O3×C2HF3O2 (391.34)
[M+H]+=278
HPLC (Method 2): retention time=2.29 min
48b)
A mixture of 0.36 g (0.92 mmol) of product from 48a, 0.092 g palladium on charcoal (10%) and 5 ml of methanol is hydrogenated at ambient temperature in the autoclave. The catalyst is then filtered off, the filtrate is evaporated to dryness in vacuo.
C14H21N3O×C2HF3O2 (361.36)
[M+H]+=248
HPLC (Method 2): retention time=0.66 min
48c)
Example 48 is prepared analogously to 1f from 0.15 g (0.50 mmol) of product from 22c, 0.18 g (0.50 mmol) of product from 48b, 0.21 ml (1.49 mmol) of triethylamine and 0.16 g (0.50 mmol) of TBTU in 3 ml THF.
C27H38N4O5S×C2HF3O2 (644.70)
[M+H]+=531
HPLC (Method 5): retention time=1.48 min
Example 49 is prepared analogously to 1f from 0.15 g (0.50 mmol) of product from 22c, 0.11 g (0.50 mmol) of (4-aminophenyl)-(4-methylpiperazin-1-yl)-methanone (J. Org. Chem. 24, 1959, 459-463), 0.21 ml (1.49 mmol) of triethylamine and 0.16 g (0.50 mmol) of TBTU in 3 ml THF.
C25H34N4O5S×C2HF3O2 (616.65)
[M+H]+=503
HPLC (Method 5): retention time=1.47 min
50a)
50a is prepared analogously to 1f from 0.60 g (4.34 mmol) of 5-amino-pyridine-2-carboxylic acid (Pharm. Acta Helv. 44, 1969, 637-643), 0.56 g (4.34 mmol) of 4-dimethylamino-piperidine (Alfa Aesar), 0.64 ml (4.56 mmol) of triethylamine and 1.46 g (4.56 mmol) of TBTU in 24 ml DMF.
C13H20N4O×2C2HF3O2 (476.37)
HPLC (Method 2): retention time=0.65 min
50b)
A mixture of 0.64 g (1.99 mmol) of product from 27c, 1.90 g (2.39 mmol) of product from 50a, 0.08 g (0.33 mmol) of DMAP and 16 ml chlorobenzene is heated to 15° C. for 39 hours. The reaction mixture is then evaporated to dryness in vacuo. The product is obtained by preparative HPLC.
C26H37N5O5S×C2HF3O2 (645.69)
[M+H]+=532
HPLC (Method 5): retention time=1.44 min
51a)
A mixture of 0.26 g (1.11 mmol) of product from 39d, 0.27 g (1.22 mmol) of Boc-anhydride, 0.17 ml (1.22 mmol) of triethylamine and 15 ml dichloromethane is stirred overnight at ambient temperature. Then the reaction mixture is diluted with dichloromethane, washed with saturated sodium hydrogen carbonate solution and saturated sodium chloride solution, dried on sodium sulphate and evaporated to dryness in vacuo.
C19H31N3O2 (333.47)
[M+H]+=334
HPLC (Method 1): retention time=2.40 min
51b)
0.13 g (3.40 mmol) of lithium aluminium hydride are placed in 5 ml THF, heated to 60° C. and combined with 0.38 g (1.14 mmol) of product from 51a in 5 ml THF. The reaction mixture is then refluxed for four hours and stirred overnight at ambient temperature. Then the reaction mixture is quenched with water and 1 M sodium hydroxide solution. The precipitate formed is filtered off through Celite, the filtrate is evaporated to dryness in vacuo.
C15H25N3 (247.38)
TLC: silica gel, dichloromethane/methanol/ammonia 4:1:0.2, Rf value=0.68
51c)
Example 51 is prepared analogously to 1f from 0.15 g (0.50 mmol) of product from 22c, 0.12 g (0.50 mmol) of product from 51b, 0.21 ml (1.50 mmol) of triethylamine and 0.18 g (0.55 mmol) of TBTU in 8 ml DMF.
C28H42N4O4S×HCl (567.18)
[M+H]+=531
HPLC (Method 1): retention time=2.5 min
52a)
0.70 ml (7.36 mmol) of acetic anhydride are placed under a nitrogen atmosphere and slowly combined with 0.42 ml (9.06 mmol) of formic acid while cooling with an ice bath. The reaction mixture is heated for two hours to 50-60° C. and then combined with 0.50 g (2.28 mmol) of product from 8b in 7 ml dichloromethane while cooling with an ice bath. After 20 minutes' stirring at ambient temperature the reaction mixture is evaporated to dryness in vacuo. The crude product thus obtained is purified by column chromatography through silica gel (eluant: dichloromethane/methanol/ammonia 9:1:0.1).
C14H21N3O (247.34)
[M+H]+=248
HPLC (Method 5): retention time=0.50 min
52b)
52b is prepared analogously to 51b from 0.17 g (4.51 mmol) of lithium aluminium hydride and 0.58 g (2.34 mmol) of product from 52a in 10 ml THF.
C14H23N3 (233.35)
TLC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.5
52c)
Example 52 is prepared analogously to 1f from 0.21 g (0.68 mmol) of product from 22c, 0.24 g (0.68 mmol) of product from 52b, 0.28 ml (2.04 mmol) of triethylamine and 0.22 g (0.68 mmol) of TBTU in 4 ml THF.
C27H40N4O4S×C2HF3O2 (630.72)
[M+H]+=517
HPLC (Method 5): retention time=1.50 min
53a)
53a is prepared analogously to 3a from 4.50 g (19.17 mmol) of product from 13a, 1.69 g (21.10 mmol) of N-methylaminoethanol (BASF), 6.68 ml (47.90 mmol) of triethylamine in 150 ml dichloromethane.
C12H19NO4S (273.35)
[M+H]+=274
TLC: silica gel, dichloromethane/ethanol 19:1, Rf value=0.43
53b)
First 100 ml 35% sodium hydroxide solution, then 4.18 ml (28.26 mmol) of tert-butyl bromoacetate in 20 ml of toluene are added to a mixture of 5.15 g (18.84 mmol) of product from 53a, 1.75 g (6.60 mmol) of tetrabutylammonium chloride (Fluka) and 80 ml of toluene at 0° C. The reaction mixture is then stirred for 1.5 hours at ambient temperature, then diluted with diethyl ether. After the phase separation the organic phase is washed four times with water until neutral, dried on sodium sulphate and evaporated to dryness in vacuo. The crude product thus obtained is purified by column chromatography through silica gel (eluant: petroleum ether/ethyl acetate 4:1).
C18H29NO6S (387.49)
[M+H]+=388
TLC: silica gel, petroleum ether/ethyl acetate 7:3, Rf value=0.59
53c)
A mixture of 6.80 g (17.55 mmol) of product from 53b, 8 ml TFA and 100 ml dichloromethane is stirred for 2.5 hours at ambient temperature. The reaction mixture is then evaporated to dryness in vacuo. The residue is combined with 1 M sodium hydroxide solution and extracted twice with ethyl acetate (organic extracts are discarded). The aqueous phase is acidified with 2 M HCl, then extracted again with ethyl acetate. The organic extracts are washed with water, dried on sodium sulphate and evaporated to dryness in vacuo.
C14H21NO6S (331.29)
[M+H]+=332
HPLC (Method 4): retention time=3.4 min
53d)
53d is prepared analogously to 28c from 1.00 g (6.10 mmol) of 4-chloro-2-methylpyridine hydrochloride (Alfa Aesar) and 2.08 g (12.20 mmol) of N-methyl-N-piperidin-4-ylmethyl-acetamide (DE 1100635, Rhône-Poulenc, 1961).
C15H23N3O (261.36)
[M+H]+=262
HPLC (Method 4): retention time=1.9 min
53e)
A mixture of 1.37 g (5.24 mmol) of product from 53d and 15 ml semiconcentrated HCl is refluxed for four days. The reaction mixture is made alkaline with 20% sodium hydroxide solution and extracted with dichloromethane. The organic extracts are dried on sodium sulphate and evaporated to dryness in vacuo.
C13H21N3 (219.33)
[M+H]+=220
TLC: silica gel, dichloromethane/methanol/ammonia 8:2:0.2, Rf value=0.48
53f)
Example 53 is prepared analogously to 1f from 0.099 g (0.30 mmol) of product from 53c, 0.066 g (0.30 mmol) of product from 53e, 0.10 ml (0.75 mmol) of triethylamine and 0.12 g (0.36 mmol) of TBTU in 8 ml THF and 1 ml DMF.
C27H40N4O5S×HCl (569.16)
[M+H]+=533
HPLC (Method 4): retention time=3.1 min
54a)
54a is prepared analogously to 1f from 2.00 g (8.27 mmol) of product from 38d, 8.28 ml (16.55 mmol) of methylamine 2 M in THF (Aldrich), 3.46 ml (24.82 mmol) of triethylamine and 3.19 g (9.93 mmol) of TBTU in 30 ml THF.
C13H18N2O (218.29)
[M+H]+=219
TLC: silica gel, dichloromethane/methanol 8:2, Rf value=0.14
54b)
54b is prepared analogously to 38f from 1.00 g (4.58 mmol) of product from 54a and 9.00 ml (9.00 mmol) of lithium aluminium hydride 1 M in THF (Aldrich) in 30 ml THF.
C13H20N2 (204.31)
[M+H]+=205
TLC: silica gel, dichloromethane/methanol 8:2, Rf value=0.07
54c)
Example 54 is prepared analogously to 1f from 0.099 g (0.30 mmol) of product from 53c, 0.088 g (0.30 mmol) of product from 54b, 0.10 ml (0.75 mmol) of triethylamine and 0.12 g (0.36 mmol) of TBTU in 7 ml THF and 1 ml DMF.
C27H39N3O5S×HCl (554.14)
[M+H]+=518
HPLC (Method 4): retention time=3.1 min
55a)
A mixture of 3.20 g (34.00 mmol) of 2-aminopyridine (Aldrich), 2.75 g (11.31 mmol) of 4-bromoacetylbenzoic acid (Fluorochem) and 100 ml of ethanol is refluxed for six hours at reflux temperature and stirred overnight at ambient temperature. The precipitate formed is filtered off and dried.
C14H10N2O2 (238.24)
[M+H]+=239
55b)
55b is prepared analogously to 27c from 1.7 g (7.14 mmol) of product from 55a and 30 ml of thionyl chloride.
C14H9ClN2O×HCl (293.15)
55c)
2.10 g (7.14 mmol) of product from 55b in 100 ml dichloromethane are combined with 25 ml (50.00 mmol) of methylamine 2 M in THF (Aldrich) while cooling with an ice bath. The reaction mixture is then stirred for two hours at ambient temperature and then evaporated to dryness in vacuo. The residue is triturated with water, filtered off and dried. The crude product thus obtained is purified by column chromatography through silica gel (eluant: dichloromethane/methanol 97:3).
C15H13N3O (251.28)
[M+H]+=252
55d)
A mixture of 0.70 g (2.79 mmol) of product from 55c, 0.15 g palladium on charcoal (20%), 100 ml of methanol and 30 ml dichloromethane is hydrogenated at ambient temperature in the autoclave. The catalyst is filtered off, the filtrate is evaporated to dryness in vacuo.
C15H17N3O (255.32)
[M+H]+=256
55e)
55e is prepared analogously to 38f from 0.80 g (3.13 mmol) of product from 55d and 20.00 ml (20.00 mmol) of lithium aluminium hydride 1 M in THF (Aldrich) in 50 ml of pyridine.
C15H19N3 (241.33)
[M+H]+=242
55f)
Example 55 is prepared analogously to 1f from 0.14 g (0.42 mmol) of product from 53c, 0.10 g (0.41 mmol) of product from 55e, 0.14 ml (0.99 mmol) of triethylamine and 0.15 g (0.46 mmol) of TBTU in 30 ml THF and 5 ml DMF.
C29H38N4O5S×HCl (591.16)
[M+H]+=555
TLC: silica gel, dichloromethane/methanol 9:1, Rf value=0.26
56a)
56a is prepared analogously to 27c from 1.35 g (5.59 mmol) of 1-benzyl-pyrrolidine-3-carboxylic acid (J. Org. Chem. 33, 1968, 3637-3639) and 10 ml of thionyl chloride.
C12H14ClNO×HCl (260.16)
56b)
56b is prepared analogously to 55c from 1.45 g (5.57 mmol) of product from 56a, 10 ml (50.00 mmol) of methylamine 2 M in THF (Aldrich) in 50 ml THF.
C13H18N2O (218.29)
[M+H]+=219
56c)
A mixture of 1.10 g (5.04 mmol) of product from 56b, 0.20 g palladium hydroxide and 40 ml of methanol is hydrogenated at 50° C. in the autoclave. The catalyst is filtered off, the filtrate is evaporated to dryness in vacuo.
C6H12N2O (128.17)
[M+H]+=129
56d)
56d is prepared analogously to 28c from 0.76 g (5.08 mmol) of 4-chloropyridine hydrochloride (Aldrich), 0.65 g (5.07 mmol) of product from 56c and 1.52 ml (10.88 mmol) of triethylamine in 10 ml of ethanol.
C11H15N3O (205.26)
[M+H]+=206
56e)
56e is prepared analogously to 38f from 0.45 g (2.19 mmol) of product from 56d and 7.00 ml (7.00 mmol) of lithium aluminium hydride 1 M in THF (Aldrich) in 30 ml THF.
C11H17N3 (191.27)
[M+H]+=192
56f)
Example 56 is prepared analogously to 1f from 0.14 g (0.42 mmol) of product from 53c, 0.10 g (0.42 mmol) of product from 56e, 0.18 ml (1.29 mmol) of triethylamine and 0.18 g (0.56 mmol) of TBTU in 30 ml THF and 5 ml DMF.
C25H36N4O5S×HCl (541.10)
[M+H]+=505
HPLC (Method 5): retention time=1.51 min
Example 57 is prepared analogously to 1f from 0.10 g (0.30 mmol) of product from 53c, 0.066 g (0.30 mmol) of product from 8b, 0.13 ml (0.91 mmol) of triethylamine and 0.097 g (0.30 mmol) of TBTU in 5 ml DMF.
C27H40N4O5S×C2HF3O2 (646.72)
[M+H]+=533
HPLC (Method 5): retention time=1.51 min
Example 58 is prepared analogously to 1f from 0.10 g (0.30 mmol) of product from 53c, 0.07 g (0.30 mmol) of product from 33a, 0.13 ml (0.91 mmol) of triethylamine and 0.097 g (0.30 mmol) of TBTU in 5 ml DMF.
C28H42N4O5S×C2HF3O2 (660.75)
[M+H]+=547
HPLC (Method 5): retention time=1.48 min
59a)
59a is prepared analogously to 1f from 2.00 g (11.16 mmol) of terephthalic acid monomethylamide (EMKA), 1.90 ml (22.32 mmol) of isopropylamine (Aldrich), 3.11 ml (22.32 mmol) of triethylamine and 4.30 g (13.40 mmol) of TBTU in 60 ml THF.
C12H16N2O2 (220.27)
[M+H]+=221
HPLC (Method 4): retention time=2.3 min
59b)
59b is prepared analogously to 38f from 1.34 g (6.08 mmol) of product from 59a and 25.00 ml (25.00 mmol) of lithium aluminium hydride 1 M in THF (Aldrich) in 150 ml THF.
C12H20N2 (192.30)
[M+H]+=193
TLC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.17
59c)
Example 59 is prepared analogously to 1f from 0.099 g (0.30 mmol) of product from 53c, 0.058 g (0.30 mmol) of product from 59b, 0.10 ml (0.75 mmol) of triethylamine and 0.12 g (0.36 mmol) of TBTU in 8 ml THF.
C26H39N3O5S×HCl (542.13)
[M+H]+=506
HPLC (Method 4): retention time=3.1 min
60a)
A mixture of 3.00 g (13.91 mmol) of methyl 4-aminoethylbenzoate (EMKA), 1.94 ml (13.91 mmol) of triethylamine and 50 ml THF is stirred for 10 min at ambient temperature and then combined with 1.13 ml (15.30 mmol) of acetone. The reaction mixture is stirred for another 30 min at ambient temperature, then 3.24 g (15.30 mmol) of sodium triacetoxyborohydride and 1.19 ml (20.86 mmol) of acetic acid are added. The mixture is stirred for 16 hours at ambient temperature. The reaction mixture is evaporated to dryness in vacuo, the residue is taken up in 1 M HCl and extracted with ethyl acetate (organic phase is discarded). The aqueous phase is made alkaline with saturated potassium carbonate solution and extracted with ethyl acetate. The organic extracts are dried on sodium sulphate and evaporated to dryness in vacuo.
C13H19NO2 (221.30)
[M+H]+=222
HPLC (Method 4): retention time=2.2 min
60b)
A mixture of 2.52 g (11.39 mmol) of product from 60a, 11.40 ml (22.80 mmol) of methylamine 2 M in THF (Aldrich), 0.54 g (5.70 mmol) of magnesium chloride (Aldrich) and 100 ml THF is stirred for 17 hours at 120° C. in the autoclave. The reaction mixture is filtered, the filtrate is evaporated to dryness in vacuo. The crude product thus obtained is purified by column chromatography through silica gel (eluant: dichloromethane/methanol/ammonia 9:1:0.1).
C13H20N2O (220.31)
[M+H]+=221
TLC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.21
60c)
60c is prepared analogously to 38f from 1.49 g (6.76 mmol) of product from 60b and 10.00 ml (10.00 mmol) of lithium aluminium hydride 1 M in THF (Aldrich) in 60 ml THF.
C13H22N2 (206.33)
[M+H]+=207
TLC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.10
60d)
Example 60 is prepared analogously to 1f from 0.099 g (0.30 mmol) of product from 53c, 0.062 g (0.30 mmol) of product from 60c, 0.083 ml (0.60 mmol) of triethylamine and 0.12 g (0.36 mmol) of TBTU in 8 ml THF.
C27H41N3O5S (519.70)
[M+H]+=520
HPLC (Method 4): retention time=3.2 min
61a)
61a is prepared analogously to 28c from 1.00 g (6.67 mmol) of 4-chloropyridine hydrochloride (Aldrich) and 2.55 g (15.00 mmol) of N-methyl-N-piperidin-4-ylmethyl-acetamide (DE 110635, Rhône-Poulenc, 1961) in 1 ml of water.
C14H21N3O (247.34)
[M+H]+=248
61b)
A mixture of 1.00 g (4.04 mmol) of product from 61a and 10 ml semiconcentrated HCl is refluxed for three days. The reaction mixture is then diluted with water, made alkaline with 20% sodium hydroxide solution and extracted with ethyl acetate. The organic extracts are dried on sodium sulphate and evaporated to dryness in vacuo.
C12H19N3 (205.30)
TLC: silica gel, dichloromethane/ethanol 9:1, Rf value=0.2
61c)
Example 61 is prepared analogously to 1f from 0.099 g (0.30 mmol) of product from 53c, 0.062 g (0.30 mmol) of product from 61b, 0.083 ml (0.60 mmol) of triethylamine and 0.12 g (0.36 mmol) of TBTU in 8 ml THF and 1 ml DMF.
C26H38N4O5S (518.67)
[M+H]+=519
HPLC (Method 4): retention time=3.2 min
62a)
A mixture of 1.69 g (10.00 mmol) of 4-(1H-imidazol-4-yl)-benzonitrile (J. Am. Chem. Soc. 93, 1971, 4256-4263), 1.12 g (10.00 mmol) of potassium-tert-butoxide and 25 ml DMSO is first stirred for 30 min at ambient temperature, then slowly combined with 0.62 ml (10.00 mmol) of methyl iodide and stirred for another 2.5 hours at ambient temperature. The reaction mixture is then added to water, the precipitate formed is filtered off and dried in vacuo. The crude product thus obtained is purified by column chromatography through silica gel (eluant: dichloromethane/ethanol 19:1).
C11H9N3 (183.21)
[M+H]+=184
HPLC (Method 4): retention time=1.9 min
62b)
62b is prepared analogously to 34b from 1.02 g (5.57 mmol) of product from 62a, 0.20 g Raney nickel and 30 ml of methanolic ammonia solution.
C11H13N3 (187.24)
TLC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.27
62c)
Example 62 is prepared analogously to 1f from 0.099 g (0.30 mmol) of product from 53c, 0.056 g (0.30 mmol) of product from 62b, 0.083 ml (0.60 mmol) of triethylamine and 0.12 g (0.36 mmol) of TBTU in 7 ml THF and 1 ml DMF.
C25H32N4O5S×HCl (537.07)
[M+H]+=501
HPLC (Method 4): retention time=3.2 min
63a)
5.00 g (22.32 mmol) of 2-bromo-4′-cyano-acetophenone (Aldrich) and 10.00 g (169.29 mmol) of acetamide (Merck) are heated together with stirring for two hours to 210° C. After cooling, the reaction mixture is stirred into water and acidified with 2 M HCl. The precipitate is filtered off and discarded. The filtrate is made alkaline with concentrated ammonia solution, the precipitate is filtered off and dried in vacuo. The crude product thus obtained is purified by column chromatography through silica gel (eluant: dichloromethane/ethanol 9:1).
C11H9N3 (183.21)
[M−H]-=182
HPLC (Method 4): retention time=1.9 min
63b)
63b is prepared analogously to 62a from 2.39 g (13.05 mmol) of product from 63a, 1.46 g (13.05 mmol) of potassium-tert-butoxide and 0.81 ml (13.05 mmol) of methyl iodide in 50 ml DMSO.
C12H11N3 (197.24)
[M+H]+=198
HPLC (Method 4): retention time=1.9 min
63c)
63c is prepared analogously to 34b from 2.04 g (10.34 mmol) of product from 63b, 0.40 g Raney nickel and 50 ml of methanolic ammonia solution.
C12H15N3 (201.27)
TLC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.19
63d)
Example 63 is prepared analogously to 1f from 0.099 g (0.30 mmol) of product from 53c, 0.060 g (0.30 mmol) of product from 63c, 0.083 ml (0.60 mmol) of triethylamine and 0.12 g (0.36 mmol) of TBTU in 7 ml THF and 1 ml DMF.
C26H34N4O5S×HCl (551.10)
[M+H]+=515
HPLC (Method 4): retention time=3.2 min
64a)
64a is prepared analogously to 1f from 4.00 g (19.21 mmol) of ethyl 4-carboxymethyl-benzoate (J. Med. Chem. 41, 1998, 5219-5246), 19.21 ml (38.42 mmol) of dimethylamine 2 M in THF (Aldrich), 5.36 ml (38.42 mmol) of triethylamine and 7.39 g (23.00 mmol) of TBTU in 100 ml THF.
C13H17NO3 (235.28)
[M+H]+=236
HPLC (Method 4): retention time=3.3 min
64b)
A mixture of 3.07 g (13.05 mmol) of product from 64a, 9.75 ml (39.00 mmol) of 4 M sodium hydroxide solution, 9.75 ml of water and 50 ml of ethanol is stirred overnight at ambient temperature. Then the ethanol is eliminated in vacuo. The aqueous residue is acidified with 4 M HCl and extracted with ethyl acetate. The organic extracts are dried on sodium sulphate and evaporated to dryness in vacuo. The product thus obtained is triturated with diethyl ether and dried.
C11H13NO3 (207.23)
[M+H]+=208
HPLC (Method 4): retention time=2.3 min
64c)
64c is prepared analogously to 1f from 2.30 g (11.10 mmol) of product from 64b, 11.10 ml (22.20 mmol) of dimethylamine 2 M in THF (Aldrich), 3.09 ml (22.20 mmol) of triethylamine and 4.28 g (13.32 mmol) of TBTU in 70 ml THF.
C12H16N2O2 (220.27)
[M+H]+=221
TLC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.44
64d)
64d is prepared analogously to 38f from 1.92 g (8.72 mmol) of product from 64c and 40.00 ml (40.00 mmol) of lithium aluminium hydride 1 M in THF (Aldrich) in 150 ml THF.
C12H20N2 (192.30)
[M+H]+=193
TLC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.10
64e)
Example 64 is prepared analogously to 1f from 0.099 g (0.30 mmol) of product from 53c, 0.058 g (0.30 mmol) of product from 64d, 0.083 ml (0.60 mmol) of triethylamine and 0.12 g (0.36 mmol) of TBTU in 7 ml THF and 1 ml DMF.
C26H39N3O5S (505.67)
[M+H]+=508
HPLC (Method 4): retention time=3.0 min
65a)
65a is prepared analogously to 34b from 0.40 g (1.82 mmol) of 4-imidazo[1,2-a]pyridin-2-yl-benzonitrile (J. Med. Chem. 41, 1998, 4317-4328), 0.10 g Raney nickel and 40 ml of methanolic ammonia solution.
C14H13N3 (223.27)
[M+H]+=224
TLC: silica gel, dichloromethane/methanol 9:1, Rf value=0.06
65b)
A mixture of 0.40 g (1.79 mmol) of product from 65a, 0.05 g platinum oxide and 40 ml of methanol is hydrogenated at 50° C. in the autoclave. The catalyst is filtered off, the filtrate is evaporated to dryness in vacuo.
C14H17N3 (227.30)
[M+H]+=228
65c)
Example 65 is prepared analogously to 1f from 0.15 g (0.44 mmol) of product from 53c, 0.10 g (0.44 mmol) of product from 65b, 0.15 ml (1.09 mmol) of triethylamine and 0.16 g (0.48 mmol) of TBTU in 30 ml THF and 10 ml DMF.
C28H36N4O5S×HCl (577.14)
[M+H]+=541
HPLC (Method 5): retention time=1.57 min
66a)
A mixture of 0.50 g (2.06 mmol) of 4-bromoacetylbenzoic acid (Fluorochem) and 5 ml formamide is stirred for one hour at 150° C. in the microwave. After cooling the precipitated product is filtered off, washed with diethyl ether and dried.
C10H8N2O2 (188.18)
[M+H]+=189
66b)
A mixture of 1.60 g (8.50 mmol) of product from 66a, 5.40 g (38.04 mmol) of methyl iodide, 7.00 g (25.33 mmol) of potassium carbonate and 30 ml DMF is stirred overnight at ambient temperature. The reaction mixture is filtered, the filtrate is evaporated to dryness in vacuo. The crude product thus obtained is purified by column chromatography through silica gel (eluant: dichloromethane/methanol 100:1 to 75:1).
C12H12N2O2 (216.24)
[M+H]+=217
66c)
A mixture of 0.75 g (3.47 mmol) of product from 66b and 20 ml methylamine 33% in ethanol (Fluka) is heated to 160° C. overnight in the autoclave. The reaction mixture is evaporated to dryness in vacuo. The crude product thus obtained is purified by column chromatography through silica gel (eluant: dichloromethane/methanol 50:1 to 25:1).
C12H13N3O (215.25)
[M+H]+=216
66d)
66d is prepared analogously to 38f from 0.41 g (1.91 mmol) of product from 66c and 3.00 ml (3.00 mmol) of lithium aluminium hydride 1 M in THF (Aldrich) in 70 ml THF.
C12H15N3 (201.27)
[M+H]+=202
TLC: silica gel, dichloromethane/methanol/ammonia 8:2:0.01, Rf value=0.16
66e)
Example 66 is prepared analogously to 1f from 0.15 g (0.45 mmol) of product from 53c, 0.09 g (0.45 mmol) of product from 66d, 0.11 ml (1.09 mmol) of triethylamine and 0.16 g (0.50 mmol) of TBTU in 30 ml THF and 5 ml DMF.
C26H34N4O5S×HCl (551.10)
[M+H]+=515
TLC: silica gel, dichloromethane/methanol 9:1, Rf value=0.52
67a)
A mixture of 1.21 g (6.14 mmol) of product from 63b, 20 ml 20% sodium hydroxide solution and 40 ml of ethanol is refluxed overnight with stirring. The ethanol is eliminated in vacuo. The residue is diluted with water and acidified with 4 M HCl. The precipitated product is filtered off and dried at 50° C. in the circulating air dryer.
C12H12N2O2 (252.70)
[M+H]+=217
HPLC (Method 4): retention time=1.7 min
67b)
67b is prepared analogously to 1f from 1.55 g (6.13 mmol) of product from 67a, 4.60 ml (9.20 mmol) of methylamine 2 M in THF (Aldrich), 1.71 ml (12.30 mmol) of triethylamine and 2.38 g (7.40 mmol) of TBTU in 50 ml THF.
C13H15N3O (229.28)
[M+H]+=230
TLC: silica gel, dichloromethane/methanol 9:1, Rf value=0.47
67c)
67c is prepared analogously to 38f from 1.33 g (5.80 mmol) of product from 67b and 15.00 ml (15.00 mmol) of lithium aluminium hydride 1 M in THF (Aldrich) in 80 ml THF.
C13H17N3 (215.29)
[M+H]+=216
TLC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.29
67d)
Example 67 is prepared analogously to 1f from 0.099 g (0.30 mmol) of product from 53c, 0.065 g (0.30 mmol) of product from 67c, 0.083 ml (0.60 mmol) of triethylamine and 0.12 g (0.36 mmol) of TBTU in 7 ml THF and 1 ml DMF.
C27H36N4O5S×HCl (565.13)
[M+H]+=529
HPLC (Method 4): retention time=3.1 min
68a)
68a is prepared analogously to 1f from 5.39 g (20.16 mmol) of 1-benzhydryl-azetidine-3-carboxylic acid (Acros), 15 ml (30.00 mmol) of methylamine 2 M in THF (Aldrich), 5.58 ml (40.00 mmol) of triethylamine and 7.71 g (24.00 mmol) of TBTU in 150 ml THF.
C18H20N2O (280.36)
HPLC (Method 4): retention time=2.5 min
68b)
A mixture of 5.32 g (18.98 mmol) of product from 68a, 0.50 g palladium on charcoal (10%) and 100 ml of methanol is hydrogenated for 24 hours at ambient temperature in the autoclave. The catalyst is filtered off, the filtrate is evaporated to dryness in vacuo. The crude product thus obtained is purified by column chromatography through silica gel (eluant: dichloromethane/methanol/ammonia 70:30:3).
C5H10N2O (114.15)
TLC: silica gel, dichloromethane/methanol/ammonia 7:3:0.3, Rf value=0.17
68c)
68c is prepared analogously to 28c from 1.31 g (8.76 mmol) of 4-chloropyridine hydrochloride (Aldrich), 1.00 g (8.76 mmol) of product from 68b and 2.40 ml (17.22 mmol) of triethylamine in 5 ml of ethanol.
C10H13N3O (191.23)
[M+H]+=192
TLC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.25
68d)
68d is prepared analogously to 38f from 0.46 g (2.41 mmol) of product from 68c and 5.00 ml (5.00 mmol) of lithium aluminium hydride 1 M in THF (Aldrich) in 20 ml THF.
C10H15N3 (177.25)
[M+H]+=178
TLC: silica gel, dichloromethane/methanol/ammonia 8:2:0.2, Rf value=0.40
68e)
Example 68 is prepared analogously to 1f from 0.083 g (0.25 mmol) of product from 53c, 0.044 g (0.25 mmol) of product from 68d, 0.070 ml (0.50 mmol) of triethylamine and 0.096 g (0.30 mmol) of TBTU in 7 ml THF and 1 ml DMF.
C24H34N4O5S (490.62)
[M+H]+=491
HPLC (Method 4): retention time=2.9 min
Example 69 is prepared analogously to 1f from 0.083 g (0.25 mmol) of product from 53c, 0.041 g (0.25 mmol) of 4-(2-dimethylamino-ethyl)-phenylamine (JW Pharmlab), 0.070 ml (0.50 mmol) of triethylamine and 0.096 g (0.30 mmol) of TBTU in 7 ml THF and 1 ml DMF.
C24H35N3O5S×HCl (514.08)
[M+H]+=478
HPLC (Method 4): retention time=3.1 min
Example 70 is prepared analogously to 1f from 0.083 g (0.25 mmol) of product from 53c, 0.048 g (0.25 mmol) of 3-(2-diethylamino-ethyl)-phenylamine (analogously to J. Med. Chem. 28, 1985, 1533-1536), 0.070 ml (0.50 mmol) of triethylamine and 0.096 g (0.30 mmol) of TBTU in 7 ml THF and 1 ml DMF.
C26H39N3O5S (505.67)
[M+H]+=506
HPLC (Method 4): retention time=3.4 min
Example 71 is prepared analogously to 1f from 0.083 g (0.25 mmol) of product from 53c, 0.038 g (0.25 mmol) of 4-dimethylaminomethyl-phenylamine (J. Chem. Soc. 1935, 871), 0.070 ml (0.50 mmol) of triethylamine and 0.096 g (0.30 mmol) of TBTU in 7 ml THF and 1 ml DMF.
C23H33N3O5S (463.59)
[M+H]+=464
HPLC (Method 4): retention time=3.1 min
72a)
72a is prepared analogously to 60a from 0.82 g (5.00 mmol) of 4-formyl-benzoic acid methylamide (EMKA), 0.50 ml (5.00 mmol) of cyclopentylamine (Aldrich), 0.37 ml (6.50 mmol) of acetic acid and 1.59 g (7.50 mmol) of sodium triacetoxyborohydride in 30 ml THF.
C14H20N2O (232.32)
TLC: silica gel, dichloromethane/ethanol 9:1, Rf value=0.15
72b)
72b is prepared analogously to 38f from 1.00 g (4.30 mmol) of product from 72a and 9.00 ml (9.00 mmol) of lithium aluminium hydride 1 M in THF (Aldrich) in 40 ml THF.
C14H22N2 (218.34)
[M+H]+=219
TLC: silica gel, dichloromethane/ethanol 9:1, Rf value=0.2
72c)
Example 72 is prepared analogously to 1f from 0.20 g (0.60 mmol) of product from 53c, 0.13 g (0.60 mmol) of product from 72b, 0.21 ml (1.50 mmol) of triethylamine and 0.23 g (0.72 mmol) of TBTU in 10 ml THF.
C28H41N3O5S×HCl (568.17)
[M+H]+=532
HPLC (Method 5): retention time=1.60 min
73a)
A mixture of 2.60 g (11.65 mmol) of product from 65a, 2.55 g (11.68 mmol) of Boc-anhydride and 100 ml DMF is stirred for two hours at ambient temperature. Then 100 ml of water are slowly added thereto. The precipitated product is filtered off, washed with water and petroleum ether and dried.
C19H21N3O2 (323.39)
[M+H]+=324
TLC: silica gel, dichloromethane/methanol 9:1, Rf value=0.78
73b)
73b is prepared analogously to 62a from 1.00 g (3.09 mmol) of product from 73a, 0.70 g (6.24 mmol) of potassium-tert-butoxide and 0.98 ml (6.90 mmol) of methyl iodide in 30 ml DMSO.
C17H17N3O2 (295.34)
[M+H]+=296
73c)
A mixture of 0.59 g (1.75 mmol) of product from 73b, 2 ml TFA and 30 ml dichloromethane is stirred for three hours at ambient temperature. The reaction mixture is then washed with water, dried on sodium sulphate and evaporated to dryness in vacuo.
C15H15N3 (237.30)
[M+H]+=238
73d)
Example 73 is prepared analogously to 1f from 0.14 g (0.42 mmol) of product from 53c, 0.10 g (0.42 mmol) of product from 73c, 0.10 ml (0.99 mmol) of triethylamine and 0.15 g (0.46 mmol) of TBTU in 30 ml THF and 5 ml DMF.
C29H34N4O5S×HCl (587.13)
[M+H]+=551
HPLC (Method 5): retention time=1.58 min
74a)
74a is prepared analogously to 53b from 4.08 g (14.93 mmol) of product from 53a, 4.68 g (22.39 mmol) of tert-butyl 2-bromopropionate (TCI), 1.38 g (4.98 mmol) of tetrabutylammonium chloride (Fluka) and 70 ml of 35% sodium hydroxide solution in 70 ml of toluene.
C19H31NO6S (401.52)
[M+H]+=402
TLC: silica gel, petroleum ether/ethyl acetate 7:3, Rf value=0.69
74b)
74b is prepared analogously to 53c from 5.12 g (12.75 mmol) of product from 74a and 5.89 ml TFA in 80 ml dichloromethane.
C15H23NO6S (345.41)
[M+H]+=346
TLC: silica gel, dichloromethane/ethanol 19:1, Rf value=0.25
74c)
Example 74 is prepared analogously to 1f from 0.10 g (0.30 mmol) of product from 74b, 0.058 g (0.30 mmol) of product from 64d, 0.084 ml (0.60 mmol) of triethylamine and 0.12 g (0.36 mmol) of TBTU in 7 ml THF and 1 ml DMF.
C27H41N3O5S (519.70)
[M+H]+=520
HPLC (Method 4): retention time=3.1 min
75a)
75a is prepared analogously to 60a from 0.82 g (5.00 mmol) of 4-formyl-benzoic acid methylamide (EMKA), 0.67 ml (5.00 mmol) of 4-methylcyclohexylamine cis/trans mixture (Acros), 0.37 ml (6.50 mmol) of acetic acid and 1.59 g (7.50 mmol) of sodium triacetoxyborohydride in 30 ml THF.
C16H24N2O (260.37)
TLC: silica gel, dichloromethane/ethanol 9:1, Rf value=0.25
75b)
75b is prepared analogously to 38f from 1.30 g (4.99 mmol) of product from 75a and 10.00 ml (10.00 mmol) of lithium aluminium hydride 1 M in THF (Aldrich) in 50 ml THF.
C16H26N2 (246.39)
TLC: silica gel, dichloromethane/ethanol 9:1, Rf value=0.2
75c)
Example 75 is prepared analogously to 1f from 0.20 g (0.60 mmol) of product from 53c, 0.15 g (0.60 mmol) of product from 75b, 0.21 ml (1.50 mmol) of triethylamine and 0.23 g (0.72 mmol) of TBTU in 10 ml THF.
C30H45N3O5S×HCl (596.22)
[M+H]+=560
HPLC (Method 5): retention time=1.65 min
Example 76 is prepared analogously to 1f from 0.10 g (0.30 mmol) of product from 74b, 0.060 g (0.30 mmol) of product from 63c, 0.084 ml (0.60 mmol) of triethylamine and 0.12 g (0.36 mmol) of TBTU in 7 ml THF and 1 ml DMF.
C27H36N4O5S (528.66)
[M+H]+=529
HPLC (Method 4): retention time=3.2 min
77a)
77a is prepared analogously to 60a from 0.82 g (5.00 mmol) of 4-formyl-benzoic acid methylamide (EMKA), 0.58 ml (5.00 mmol) of 3-pentylamine (Aldrich), 0.37 ml (6.50 mmol) of acetic acid and 1.59 g (7.50 mmol) of sodium triacetoxyborohydride in 30 ml THF.
C14H22N2O (234.34)
[M+H]+=235
TLC: silica gel, dichloromethane/ethanol 9:1, Rf value=0.4
77b)
77b is prepared analogously to 38f from 1.10 g (4.69 mmol) of product from 77a and 9.40 ml (9.40 mmol) of lithium aluminium hydride 1 M in THF (Aldrich) in 40 ml THF.
C14H24N2 (220.35)
TLC: silica gel, dichloromethane/ethanol 9:1, Rf value=0.1
77c)
Example 77 is prepared analogously to 1f from 0.20 g (0.60 mmol) of product from 53c, 0.13 g (0.60 mmol) of product from 77b, 0.21 ml (1.50 mmol) of triethylamine and 0.23 g (0.72 mmol) of TBTU in 10 ml THF.
C28H43N3O5S×HCl (570.18)
[M+H]+=534
TLC: silica gel, dichloromethane/ethanol 9:1, Rf value=0.45
78a)
78a is prepared analogously to 60a from 0.82 g (5.00 mmol) of 4-formyl-benzoic acid methylamide (EMKA), 0.53 ml (5.00 mmol) of tert-butylamine (Fluka), 0.37 ml (6.50 mmol) of acetic acid and 1.59 g (7.50 mmol) of sodium triacetoxyborohydride in 30 ml THF.
C13H20N2O (220.31)
[M+H]+=221
TLC: silica gel, dichloromethane/ethanol 9:1, Rf value=0.15
78b)
78b is prepared analogously to 38f from 1.00 g (4.54 mmol) of product from 78a and 9.10 ml (9.10 mmol) of lithium aluminium hydride 1 M in THF (Aldrich) in 40 ml THF.
C13H22N2 (206.33)
78c)
Example 78 is prepared analogously to 1f from 0.20 g (0.60 mmol) of product from 53c, 0.12 g (0.60 mmol) of product from 78b, 0.21 ml (1.50 mmol) of triethylamine and 0.23 g (0.72 mmol) of TBTU in 10 ml THF.
C27H41N3O5S (519.70)
[M+H]+=520
HPLC (Method 5): retention time=1.58 min
79a)
A mixture of 0.50 ml (4.70 mmol) of 1-fluoro-3-nitrobenzene (Fluka), 1.34 g (9.39 mmol) of 4-(N,N-dimethylaminomethyl)-piperidine (Eur. J. Med. Chem. Chim. Ther. 37, 2002, 487-502), 0.65 g (4.70 mmol) of potassium carbonate and 6.6 ml DMSO is stirred for five days at 110° C. The reaction mixture is then poured onto ice, the precipitate formed is filtered off. The product thus obtained is dried overnight in the vacuum desiccator.
C14H21N3O2 (263.34)
[M+H]+=264
TLC: silica gel, dichloromethane/methanol 9:1, Rf value=0.20
79b)
A mixture of 0.95 ml (3.60 mmol) of product from 79a, 0.095 g palladium on charcoal (5%) and 72 ml of ethanol is hydrogenated at ambient temperature in the autoclave. The catalyst is filtered off, the filtrate is evaporated to dryness in vacuo.
C14H23N3 (233.35)
[M+H]+=234
79c)
Example 79 is prepared analogously to 1f from 0.15 g (0.46 mmol) of product from 53c, 0.11 g (0.46 mmol) of product from 79b, 0.084 ml (0.60 mmol) of triethylamine and 0.18 g (0.56 mmol) of TBTU in 3 ml DMF.
C28H42N4O5S (546.72)
[M+H]+=547
HPLC (Method 5): retention time=1.49 min
80a)
80a is prepared analogously to 33a from 0.70 g (3.01 mmol) of 4-(4-dimethylamino-piperidin-1-yl)-benzaldehyde (Tetrahedron 57, 2001, 4781-4785), 3.00 ml (31.88 mmol) of methylamine 33% in ethanol (Aldrich), 0.20 g Raney nickel in 25 ml of ethanol.
C15H25N3 (247.38)
[M+H]+=248
TLC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.16
80b)
Example 80 is prepared analogously to 1f from 0.15 g (0.45 mmol) of product from 53c, 0.11 g (0.45 mmol) of product from 80a, 0.13 ml (0.90 mmol) of triethylamine and 0.17 g (0.54 mmol) of TBTU in 5 ml DMF.
C29H44N4O5S×HCl (597.21)
[M+H]+=561
HPLC (Method 1): retention time=2.33 min
81a)
81a is prepared analogously to 33a from 1.00 g (4.90 mmol) of 4-(4-methyl-piperazin-1-yl)-benzaldehyde (Chem. Pharm Bull. 45, 1997, 1458-1469), 4.00 ml (42.50 mmol) of methylamine 33% in ethanol (Aldrich), 0.20 g Raney nickel in 30 ml of ethanol.
C13H21N3 (219.33)
[M+H]+=220
TLC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.15
81b)
Example 81 is prepared analogously to 1f from 0.15 g (0.45 mmol) of product from 53c, 0.099 g (0.45 mmol) of product from 81a, 0.13 ml (0.90 mmol) of triethylamine and 0.17 g (0.54 mmol) of TBTU in 5 ml DMF.
C27H40N4O5S×HCl (569.16)
[M+H]+=533
HPLC (Method 1): retention time=2.28 min
Example 82 is prepared analogously to 1f from 0.15 g (0.45 mmol) of product from 53c, 0.092 g (0.45 mmol) of product from 19b, 0.13 ml (0.90 mmol) of triethylamine and 0.17 g (0.54 mmol) of TBTU in 5 ml DMF.
C26H38N4O5S×HCl (555.13)
[M+H]+=519
HPLC (Method 1): retention time=2.29 min
83a)
83a is prepared analogously to 51a from 1.35 g (5.16 mmol) of product from 41b, 1.24 g (5.68 mmol) of Boc-anhydride and 0.80 ml (5.68 mmol) of triethylamine in 50 ml dichloromethane.
C21H35N3O2 (361.52)
[M+H]+=362
TLC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.42
83b)
83b is prepared analogously to 51b from 1.80 g (4.98 mmol) of product from 83a and 0.57 g (15.00 mmol) of lithium aluminium hydride (Aldrich) in 25 ml THF.
C17H29N3 (275.43)
[M+H]+=276
HPLC (Method 1): retention time=1.77 min
83c)
Example 83 is prepared analogously to 1f from 0.14 g (0.50 mmol) of product from 22c, 0.15 g (0.50 mmol) of product from 83b, 0.14 ml (1.00 mmol) of triethylamine and 0.18 g (0.55 mmol) of TBTU in 6 ml DMF.
C30H46N4O4S×HCl (595.24)
[M+H]+=559
HPLC (Method 1): retention time=2.46 min
Example 84 is prepared analogously to 1f from 0.15 g (0.50 mmol) of product from 22c, 0.10 g (0.50 mmol) of 4-(1-methylpiperidin-4-yloxy)-phenylamine (ART-CHEM), 0.14 ml (1.00 mmol) of triethylamine and 0.18 g (0.55 mmol) of TBTU in 6 ml DMF.
C25H35N3O5S×HCl (526.09)
[M+H]+=490
HPLC (Method 1): retention time=2.40 min
Example 85 is prepared analogously to 1f from 0.15 g (0.50 mmol) of product from 22c, 0.09 g (0.50 mmol) of 4-(2-dimethylamino-ethoxy)-phenylamine (Collect. Czech. Chem. Commun. 55, 1990, 282-295), 0.14 ml (1.00 mmol) of triethylamine and 0.18 g (0.55 mmol) of TBTU in 6 ml DMF.
C23H33N3O5S×HCl (500.05)
[M+H]+=464
HPLC (Method 1): retention time=2.35 min
Example 86 is prepared analogously to 1f from 0.14 g (0.45 mmol) of product from 22c, 0.099 g (0.45 mmol) of product from 81a, 0.13 ml (0.90 mmol) of triethylamine and 0.17 g (0.54 mmol) of TBTU in 5 ml DMF.
C26H38N4O5S×HCl (539.13)
[M+H]+=503
HPLC (Method 1): retention time=2.43 min
87a)
A mixture of 0.11 g (0.33 mmol) of product from 27c, 0.043 g (0.33 mmol) of 3-amino-6-chloropyridazine (Acros), 0.12 ml (0.66 mmol) of DIPEA and 10 ml dichloromethane is refluxed for three days with stirring. The precipitate is then filtered off. The filtrate is evaporated to dryness in vacuo and the crude product is purified by preparative HPLC.
C17H21ClN4O4S (412.89)
[M+H]+=413/415
87b)
A mixture of 0.03 g (0.073 mmol) of product from 87a and 0.013 g (0.073 mmol) of diethyl-piperidin-4-ylmethyl-amine (Chem. Pharm. Bull. 42, 1994, 74-84) is melted at 173° C. The product is then recovered from the reaction mixture by preparative HPLC.
C27H42N6O4S (546.73)
[M+H]+=547
HPLC (Method 6): retention time=2.12 min
88a)
88a is prepared analogously to 51a from 0.70 g (3.18 mmol) of product from 27b, 0.80 g (3.65 mmol) of Boc-anhydride and 5.50 ml (11.00 mmol) of 2 M sodium hydroxide solution in 40 ml dioxane and 20 ml of water.
C17H28N4O2 (320.43)
[M+H]+=321
TLC: silica gel, dichloromethane/methanol/ammonia 4:1:0.2, Rf value=0.83
88b)
88b is prepared analogously to 51b from 0.60 g (1.87 mmol) of product from 88a and 0.21 g (5.60 mmol) of lithium aluminium hydride (Aldrich) in 20 ml THF.
C13H22N4 (234.34)
[M+H]+=235
TLC: silica gel, dichloromethane/methanol/ammonia 4:1:0.2, Rf value=0.62
88c)
Example 88 is prepared analogously to 27d from 0.16 g (0.50 mmol) of product from 27c, 0.12 g (0.50 mmol) of product from 88b and 0.17 ml (1.00 mmol) of DIPEA in 5 ml THF.
C26H39N5O4S×HCl (554.15)
[M+H]+=518
TLC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.61
89a)
89a is prepared analogously to 8a from 0.70 g (4.18 mmol) of 4-piperidinopiperidine (Aldrich), 0.44 ml (4.18 mmol) of 1-fluoro-4-nitrobenzene (Acros) and 1.33 ml (9.61 mmol) of triethylamine in 12 ml DMF.
C16H23N3O2 (289.37)
[M+H]+=290
TLC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.3
89b)
89b is prepared analogously to 8b from 0.96 g (3.32 mmol) of product from 89a and 0.093 g palladium on charcoal (5%) in 45 ml of ethanol.
C16H25N3 (259.39)
[M+H]+=260
TLC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.2
89c)
Example 89 is prepared analogously to 1f from 0.10 g (0.33 mmol) of product from 22c, 0.086 g (0.33 mmol) of product from 89b, 0.14 ml (1.00 mmol) of triethylamine and 0.11 g (0.33 mmol) of TBTU in 2 ml THF.
C29H42N4O4S×C2HF3O2 (656.76)
[M+H]+=543
HPLC (Method 5): retention time=1.47 min
90a)
90a is prepared analogously to 8a from 0.84 g (4.18 mmol) of 4-N-Boc-aminopiperidine (Acros), 0.44 ml (4.18 mmol) of 1-fluoro-4-nitrobenzene (Acros) and 1.33 ml (9.61 mmol) of triethylamine in 12 ml DMF.
C16H23N3O4 (321.37)
[M+H]+=322
90b)
90b is prepared analogously to 8b from 1.01 g (3.43 mmol) of product from 90a and 0.11 g palladium on charcoal (5%) in 45 ml of ethanol.
C16H25N3O2 (291.39)
[M+H]+=292
90c)
90c is prepared analogously to 1f from 0.10 g (0.33 mmol) of product from 22c, 0.097 g (0.33 mmol) of product from 90b, 0.14 ml (1.00 mmol) of triethylamine and 0.11 g (0.33 mmol) of TBTU in 2 ml THF.
C29H42N4O6S (574.73)
[M+H]+=575
HPLC (Method 5): retention time=1.62 min
90d)
Example 90 is prepared analogously to 18b from 0.19 g (0.33 mmol) of product from 90c and 0.33 ml TFA in 0.5 ml dichloromethane.
C24H34N4O4S×C2HF3O2 (588.64)
[M+H]+=475
HPLC (Method 5): retention time=1.41 min
91a)
91a is prepared analogously to 8a from 0.90 g (4.18 mmol) of tert-butyl methyl-piperidin-4-yl-carbamate (Fluorochem), 0.44 ml (4.18 mmol) of 1-fluoro-4-nitrobenzene (Acros) and 1.33 ml (9.61 mmol) of triethylamine in 12 ml DMF.
C17H25N3O4 (335.40)
[M+H]+=336
TLC: silica gel, dichloromethane/methanol 30:1, Rf value=0.6
91b)
91b is prepared analogously to 8b from 1.08 g (3.22 mmol) of product from 91a and 0.11 g palladium on charcoal (5%) in 45 ml of ethanol.
C17H27N3O2 (305.42)
[M+H]+=306
TLC: silica gel, dichloromethane/methanol 30:1, Rf value=0.4
91c)
91c is prepared analogously to 1f from 0.10 g (0.33 mmol) of product from 22c, 0.10 g (0.33 mmol) of product from 91b, 0.14 ml (1.00 mmol) of triethylamine and 0.11 g (0.33 mmol) of TBTU in 2 ml THF.
C30H44N4O6S (588.76)
[M+H]+=589
HPLC (Method 5): retention time=1.69 min
91d)
Example 91 is prepared analogously to 18b from 0.21 g (0.36 mmol) of product from 91c and 0.36 ml TFA in 0.6 ml dichloromethane.
C25H36N4O4S×C2HF3O2 (602.67)
[M+H]+=489
HPLC (Method 5): retention time=1.42 min
92a)
A mixture of 0.66 g (5.16 mmol) of 4-dimethylamino-piperidine (Alfa Aesar), 1.00 g (4.69 mmol) of tert-butyl (4-oxocyclohexyl)-carbamate (Fluorochem), 1.19 g (5.16 mmol) of sodium triacetoxyborohydride and 20 ml dichloromethane is stirred under nitrogen for four hours at ambient temperature. The reaction mixture is then diluted with dichloromethane, washed with saturated sodium hydrogen carbonate solution, dried on sodium sulphate and evaporated to dryness in vacuo.
C18H35N3O2 (325.49)
92b)
A mixture of 0.80 g (2.46 mmol) of product from 92a, 4 ml 6 M HCl, 3 ml 37% HCl and 3 ml of methanol is stirred for two hours at 50° C. The reaction mixture is then evaporated to dryness in vacuo.
C13H27N3×3HCl (334.76)
92c)
Example 92 is prepared analogously to 1f from 0.10 g (0.33 mmol) of product from 22c, 0.13 g (0.40 mmol) of product from 92b, 0.23 ml (1.66 mmol) of triethylamine and 0.13 g (0.40 mmol) of TBTU in 8 ml DMF.
C26H44N4O4S×2HCl (581.64)
[M+H]+=509
HPLC (Method 5): retention time=1.36 min
93a)
93a is carried out analogously to 92a from 0.63 g (3.70 mmol) of diethyl-piperidin-4-ylmethyl-amine (Chem. Pharm. Bull. 42, 1994, 74-84), 0.72 g (3.37 mmol) of tert-butyl (4-oxocyclohexyl)-carbamate (Fluorochem) and 0.86 g (4.04 mmol) of sodium triacetoxyborohydride in 20 ml dichloromethane.
C21H41N3O2 (367.57)
93b)
93b is prepared analogously to 92b from 0.90 g (2.45 mmol) of product from 93a, 4 ml 6 M HCl and 3 ml 37% HCl in 3 ml of methanol.
C16H33N3×3HCl (376.84)
93c)
Example 93 is prepared analogously to 1f from 0.10 g (0.33 mmol) of product from 22c, 0.14 g (0.37 mmol) of product from 93b, 0.23 ml (1.66 mmol) of triethylamine and 0.13 g (0.40 mmol) of TBTU in 8 ml DMF.
C29H50N4O4S×2HCl (623.72)
[M+H]+=551
HPLC (Method 5): retention time=1.39 min
94a)
A mixture of 0.88 g (6.88 mmol) of 4-dimethylamino-piperidine (Alfa Aesar), 1.00 g (4.93 mmol) of 3-bromo-6-nitropyridine (Aldrich), 0.18 g (0.49 mmol) of tetrabutyl-ammonium iodide, 0.74 g (5.33 mmol) of potassium carbonate and 5 ml DMSO is stirred for two hours at 80° C. Then the reaction mixture is poured onto water and extracted with dichloromethane. The organic extracts are washed with saturated sodium hydrogen carbonate solution and saturated sodium chloride solution, dried on sodium sulphate and evaporated to dryness in vacuo. The crude product thus obtained is purified by preparative HPLC.
C12H18N4O2×CH2O2 (296.32)
HPLC (Method 1): retention time=1.49 min
94b)
94b is prepared analogously to 8b from 0.50 g (2.00 mmol) of product from 94a and 0.08 g palladium on charcoal (10%) in 40 ml of methanol.
C12H20N4 (220.31)
94c)
A mixture of 0.63 g (2.10 mmol) of product from 22c, 0.91 g (9.00 mmol) of N-methylmorpholine, 0.45 g (2.04 mmol) of product from 94b and 50 ml THF is stirred for 10 minutes at ambient temperature and then combined with 5.22 ml (9.00 mmol) of propylphosphonic anhydride 50% in ethyl acetate (Fluka). The reaction mixture is stirred overnight at ambient temperature and then evaporated to dryness in vacuo. The residue is combined with 2 N potassium carbonate solution and extracted with dichloromethane. The organic extracts are washed with water and saturated sodium chloride solution, dried on sodium sulphate and evaporated to dryness in vacuo. The crude product thus obtained is purified by preparative HPLC.
C25H37N5O4S×C2HF3O2 (617.68)
[M+H]+=504
HPLC (Method 5): retention time=1.38 min
Example 95 is prepared analogously to 1f from 0.08 g (0.27 mmol) of product from 22c, 0.066 g (0.27 mmol) of product from 80a, 0.11 ml (0.80 mmol) of triethylamine and 0.085 g (0.27 mmol) of TBTU in 2 ml THF.
C28H42N4O4S×C2HF3O2 (644.75)
[M+H]+=531
HPLC (Method 5): retention time=1.50 min
Example 96 is prepared analogously to 1f from 0.08 g (0.27 mmol) of product from 22c, 0.054 g (0.27 mmol) of product from 19b, 0.11 ml (0.80 mmol) of triethylamine and 0.085 g (0.27 mmol) of TBTU in 2 ml THF.
C25H36N4O4S×C2HF3O2 (602.67)
[M+H]+=489
HPLC (Method 5): retention time=1.49 min
97a)
97a is prepared analogously to 8a from 1.00 g (5.87 mmol) of diethyl-piperidin-4-ylmethyl-amine (Chem. Pharm. Bull. 42, 1994, 74-84), 0.91 g (5.87 mmol) of 1-fluoro-2-methyl-4-nitrobenzene (ABCR) and 1.14 ml (8.20 mmol) of triethylamine in 12 ml DMF.
C17H27N3O2 (305.42)
[M+H]+=306
97b)
97b is prepared analogously to 8b from 0.91 g (2.98 mmol) of product from 97a and 0.20 g palladium on charcoal (10%) in 50 ml of methanol.
C17H29N3 (275.43)
97c)
Example 97 is prepared analogously to 1f from 0.15 g (0.50 mmol) of product from 22c, 0.14 g (0.50 mmol) of product from 97b, 0.21 ml (1.50 mmol) of triethylamine and 0.16 g (0.50 mmol) of TBTU in 7 ml THF and 1 ml DMF.
C30H46N4O4S×HCl (595.24)
[M+H]+=559
HPLC (Method 5): retention time=1.44 min
98a)
98a is prepared analogously to 8a from 0.75 g (5.87 mmol) of 4-dimethylamino-piperidine (Alfar Aesar), 0.91 g (5.87 mmol) of 1-fluoro-2-methyl-4-nitrobenzene (ABCR) and 1.14 ml (8.20 mmol) of triethylamine in 12 ml DMF.
C14H21N3O2 (263.34)
98b)
98b is prepared analogously to 8b from 0.30 g (1.14 mmol) of product from 98a and 0.10 g palladium on charcoal (10%) in 25 ml of methanol.
C14H23N3 (233.35)
98r)
Example 98 is prepared analogously to 1f from 0.32 g (1.07 mmol) of product from 22c, 0.25 g (1.07 mmol) of product from 98b, 0.42 ml (3.00 mmol) of triethylamine and 0.34 g (1.07 mmol) of TBTU in 7 ml THF and 1 ml DMF.
C27H40N4O4S×HCl (553.16)
[M+H]+=517
HPLC (Method 5): retention time=1.52 min
99a)
99a is prepared analogously to 8a from 0.92 g (5.87 mmol) of dimethyl-(2-piperidin-4-yl-ethyl)-amine (J. Med. Chem. 36, 1993, 162-165), 0.91 g (5.87 mmol) of 1-fluoro-2-methyl-4-nitrobenzene (ABCR) and 2.49 g (18.00 mmol) of potassium carbonate in 12 ml DMF.
C16H25N3O2 (291.39)
[M+H]+=292
99b)
99b is prepared analogously to 8b from 0.60 g (1.14 mmol) of product from 99a and 0.20 g palladium on charcoal (10%) in 50 ml of methanol.
C16H27N3 (261.41)
99c)
Example 99 is prepared analogously to 1f from 0.15 g (0.50 mmol) of product from 22c, 0.13 g (0.50 mmol) of product from 99b, 0.21 ml (1.50 mmol) of triethylamine and 0.16 g (0.50 mmol) of TBTU in 7 ml THF and 1 ml DMF.
C29H44N4O4S×HCl (581.21)
[M+H]+=545
HPLC (Method 5): retention time=1.42 min
100a)
100a is prepared analogously to 8a from 1.00 g (4.47 mmol) of 4-(3-methyl-3H-imidazol-4-yl)-piperidine (J. Med. Chem. 46, 2003, 5445-5457), 0.63 g (4.47 mmol) of 4-fluoro-nitrobenzene (ABCR) and 2.10 g (15.20 mmol) of potassium carbonate in 50 ml DMF.
C14H16N4O2 (272.30)
[M+H]+=273
100b)
10b-1 and 100b-2 are prepared analogously to 62a from 1.10 g (4.04 mmol) of product from 100a, 0.60 g (4.23 mmol) of methyl iodide and 0.46 g (4.10 mmol) of potassium-tert-butoxide in 50 ml DMSO. The resulting mixture of isomers is separated by column chromatography through silica gel (eluant: dichloromethane/methanol 100:1 to 30:1).
100b-1: C15H18N4O2 (286.33)
[M+H]+=287
TLC: silica gel, dichloromethane/methanol 9:1, Rf value=0.50
100b-2: C15H18N4O2 (286.33)
[M+H]+=287
TLC: silica gel, dichloromethane/methanol 9:1, Rf value=0.38
100c)
100c is prepared analogously to 8b from 0.10 g (0.35 mmol) of 100b-2 and 0.20 g palladium on charcoal (10%) in 30 ml of methanol.
C15H20N4 (256.35)
TLC: silica gel, dichloromethane/methanol 9:1, Rf value=0.10
Example 100 is prepared analogously to 1f from 0.085 g (0.28 mmol) of product from 22c, 0.070 g (0.27 mmol) of product from 100c, 0.048 ml (0.35 mmol) of triethylamine and 0.095 g (0.30 mmol) of TBTU in 20 ml THF and 3 ml DMF.
C28H37N5O4S×HCl (576.15)
[M+H]+=540
HPLC (Method 5): retention time=1.41 min
101a)
101a is prepared analogously to 8b from 0.35 g (1.22 mmol) of 100b-1 and 0.50 g palladium on charcoal (10%) in 50 ml of methanol.
C15H20N4 (256.35)
TLC: silica gel, dichloromethane/methanol 9:1, Rf value=0.14
101b)
Example 101 is prepared analogously to 1f from 0.12 g (0.40 mmol) of product from 22c, 0.10 g (0.39 mmol) of product from 101a, 0.05 ml (0.50 mmol) of triethylamine and 0.14 g (0.42 mmol) of TBTU in 30 ml THF and 5 ml DMF.
C28H37N5O4S (539.69)
[M+H]+=540
TLC: silica gel, dichloromethane/methanol 9:1, Rf value=0.47
102a)
102a is prepared analogously to 60a from 0.50 g (5.00 mmol) of N-methylcyclohexylamine (CHESS), 0.82 g (5.00 mmol) of 4-formyl-benzoic acid methylamide (EMKA), 1.59 g (7.50 mmol) of sodium triacetoxyborohydride and 0.37 ml (6.50 mmol) of acetic acid in 30 ml THF.
C15H22N2 (246.35)
102b)
102b is prepared analogously to 38f from 1.06 g (4.30 mmol) of product from 102a and 8.60 ml (8.60 mmol) of lithium aluminium hydride 1 M in THF (Aldrich) in 40 ml THF.
C15H24N2 (232.36)
102c)
Example 102 is prepared analogously to 1f from 0.20 g (0.60 mmol) of product from 53c, 0.14 g (0.60 mmol) of product from 102b, 0.21 ml (1.50 mmol) of triethylamine and 0.23 g (0.72 mmol) of TBTU in 10 ml THF.
C29H43N3O5S×HCl (582.20)
[M+H]+=546
HPLC (Method 5): retention time=1.58 min
103a)
A mixture of 0.04 g (0.079 mmol) of 70, 4.8 mg (0.12 mmol) of sodium hydride 60%, 1 ml THF and 0.5 ml DMF is stirred for 30 minutes at ambient temperature. Then 4.9 μl (0.079 mmol) of methyl iodide are added and the mixture is stirred for a further two hours at ambient temperature. The reaction mixture is then evaporated to dryness in vacuo, the residue is mixed with water and extracted with ethyl acetate. The organic extracts are dried on sodium sulphate and evaporated to dryness in vacuo. The crude product thus obtained is purified by column chromatography (eluant: dichloromethane/methanol/ammonia 95:5:0.5).
C13H22N2 (206.33)
[M+H]+=207
103b)
Example 103 is prepared analogously to 1f from 0.08 g (0.24 mmol) of product from 53c, 0.05 g (0.24 mmol) of product from 103a, 0.067 ml (0.48 mmol) of triethylamine and 0.093 g (0.29 mmol) of TBTU in 7 ml THF and 1 ml DMF.
C27H41N3O5S (519.70)
[M+H]+=520
HPLC (Method 4): retention time=3.2 min
104a)
104a is prepared analogously to 60a from 0.35 g (1.72 mmol) of 4-(2-methyl-1.3-thiazol-4-yl)-benzaldehyde (Maybridge), 1.50 ml (3.00 mmol) of methylamine 2 M in THF (Acros), 0.70 g (3.30 mmol) of sodium triacetoxyborohydride and 0.23 ml (4.00 mmol) of acetic acid in 20 ml THF.
C12H14N2S (218.32)
[M+H]+=219
104b)
Example 104 is prepared analogously to 1f from 0.16 g (0.47 mmol) of product from 53c, 0.10 g (0.46 mmol) of product from 104a, 0.11 ml (1.09 mmol) of triethylamine and 0.16 g (0.48 mmol) of TBTU in 30 ml THF and 5 ml DMF.
C26H33N3O5S2 (531.69)
[M+H]+=532
TLC: silica gel, dichloromethane/methanol 9:1, Rf value=0.66
Example 105 is prepared analogously to 1f from 0.14 g (0.41 mmol) of product from 53c, 0.10 g (0.40 mmol) of methyl-[3-(2-morpholin-4-yl-ethoxy)-benzyl]-amine (Maybridge), 0.14 ml (0.99 mmol) of triethylamine and 0.14 g (0.44 mmol) of TBTU in 30 ml THF and 5 ml DMF.
C28H41N3O7S×HCl (600.17)
[M+H]+=564
TLC: silica gel, dichloromethane/methanol 9:1, Rf value=0.59
Example 106 is prepared analogously to 1f from 0.17 g (0.51 mmol) of product from 53c, 0.10 g (0.50 mmol) of methyl-(3-pyrimidin-5-yl-benzyl)-amine (Maybridge), 0.17 ml (1.19 mmol) of triethylamine and 0.17 g (0.53 mmol) of TBTU in 30 ml THF and 5 ml DMF.
C26H32N4O5S×HCl (549.08)
[M+H]+=513
HPLC (Method 5): retention time=1.78 min
Example 107 is prepared analogously to 1f from 0.18 g (0.54 mmol) of product from 53c, 0.10 g (0.53 mmol) of (4-furan-2-yl-benzyl)-methyl-amine (Maybridge), 0.18 ml (1.29 mmol) of triethylamine and 0.18 g (0.56 mmol) of TBTU in 30 ml THF and 5 ml DMF.
C26H32N2O6S (500.61)
[M+H]+=501
HPLC (Method 5): retention time=2.09 min
108a)
107a is prepared analogously to 79a from 2.41 g (18.78 mmol) of 4-dimethylamino-piperidine (Alfa Aesar), 1.00 ml (9.39 mmol) of 1-fluoro-3-nitrobenzene (Fluka) and 1.30 g (9.39 mmol) of potassium carbonate in 15 ml DMSO.
C13H19N3O2 (249.31)
[M+H]+=250
108b)
A mixture of 1.74 g (6.98 mmol) of product from 108a, 12.00 g (68.92 mmol) of sodium dithionite, 10.00 g (72.35 mmol) of potassium carbonate, 60 ml THF and 30 ml of water six hours is heated to 80° C. After cooling the organic phase is separated off, washed with saturated sodium chloride solution, dried on sodium sulphate and evaporated to dryness in vacuo.
C13H21N3 (219.33)
108c)
Example 108 is prepared analogously to 1f from 0.13 g (0.40 mmol) of product from 53c, 0.10 g (0.47 mmol) of product from 108b, 0.067 ml (0.48 mmol) of triethylamine and 0.15 g (0.48 mmol) of TBTU in 5 ml DMF.
C27H40N4O5S (532.70)
[M+H]+=533
HPLC (Method 5): retention time=1.56 min
109a)
A mixture of 0.59 g (3.12 mmol) of 4-pyrrolidin-1-ylmethyl-benzylamine (Enamine-BB), 0.29 ml (3.75 mmol) of methyl chloroformate (Fluka), 0.52 ml (3.75 mmol) of triethylamine and 10 ml dichloromethane is stirred for two hours at ambient temperature. The reaction mixture is diluted with 10 ml dichloromethane, washed twice with water, dried on sodium sulphate and evaporated to dryness in vacuo.
C14H20N2O2 (248.32)
109b)
109b is prepared analogously to 51b from 0.61 g (2.44 mmol) of product from 109a and 5.00 ml (5.00 mmol) of lithium aluminium hydride 1 M in THF (Aldrich) in 5 ml THF.
C13H20N2 (204.31)
109c)
Example 109 is prepared analogously to 1f from 0.18 g (0.54 mmol) of product from 53c, 0.17 g (0.81 mmol) of product from 109b, 0.15 ml (1.07 mmol) of triethylamine and 0.21 g (0.65 mmol) of TBTU in 4 ml DMF.
C27H39N3O5S×CH2O2 (631.71)
[M+H]+=518
HPLC (Method 5): retention time=1.56 min
Example 110 is prepared analogously to 1f from 0.12 g (0.36 mmol) of product from 53c, 0.096 g (0.51 mmol) of 4-pyrrolidin-1-ylmethyl-benzylamine (Enamine-BB), 0.10 ml (0.72 mmol) of triethylamine and 0.14 g (0.44 mmol) of TBTU in 4 ml DMF.
C26H37N3O5S×CH2O2 (617.68)
[M+H]+=504
HPLC (Method 5): retention time=1.56 min
111a)
A mixture of 1.00 g (4.25 mmol) of tert-butyl (4-formylbenzyl)-carbamate (Acros) and 10 ml dichloromethane is combined successively with 1.15 ml (8.50 mmol) of cis-2,6-dimethylpiperidine (Aldrich) and 1.80 g (8.50 mmol) of sodium triacetoxyborohydride while cooling with an ice bath. The reaction mixture is stirred for three days at ambient temperature, then slowly quenched with saturated sodium hydrogen carbonate solution and extracted with dichloromethane. The organic extracts are washed with water and saturated sodium chloride solution, dried on sodium sulphate and evaporated to dryness in vacuo. The crude product thus obtained is purified by column chromatography (eluant: dichloromethane/methanol 93:7).
C20H32N2O2 (332.48)
[M+H]+=333
HPLC (Method 5): retention time=1.47 min
111b)
111b is prepared analogously to 51b from 0.92 g (2.76 mmol) of product from 111a and 8.27 ml (8.27 mmol) of lithium aluminium hydride 1 M in THF (Aldrich) in 30 ml THF.
C16H26N2 (246.39)
[M+H]+=247
HPLC (Method 5): retention time=1.03 min
111c)
Example 111 is prepared analogously to 1f from 0.08 g (0.24 mmol) of product from 53c, 0.059 g (0.24 mmol) of product from 111b, 0.10 ml (0.72 mmol) of triethylamine and 0.078 g (0.24 mmol) of TBTU in 2 ml THF.
C30H45N3O5S×C2HF3O2 (673.78)
[M+H]+=560
HPLC (Method 5): retention time=1.59 min
112a)
250.00 ml (500.00 mmol) of methylamine 2 M in methanol (Fluka) are slowly combined with 54.00 g (250.00 mmol) of 4-nitrobenzylbromide (Fluka) while cooling with an ice bath. The reaction mixture is stirred for one hour while cooling with an ice bath and for 30 minutes at ambient temperature and then evaporated to dryness in vacuo. The residue is stirred with diethyl ether and filtered off. The filtrate is evaporated to dryness in vacuo, combined with sodium carbonate solution and extracted with diethyl ether. The organic extracts are dried on sodium sulphate and evaporated to dryness in vacuo. The crude product thus obtained is purified by column chromatography (eluant: dichloromethane/methanol 5:0 to 5:1).
C8H10N2O2 (166.18)
[M+H]+=167
112b)
A mixture of 13.40 g (80.64 mmol) of product from 112a and 25 ml ethyl acetate is slowly combined with 17.68 g (81.00 mmol) of Boc-anhydride while cooling with an ice bath. The reaction mixture is stirred for three hours at ambient temperature, then washed with water, dried on sodium sulphate and evaporated to dryness in vacuo.
C13H18N2O4 (266.29)
112c)
A mixture of 23.00 g (86.37 mmol) of product from 112b, 2.30 g Raney nickel, 230 ml of ethanol and 230 ml ethyl acetate is hydrogenated in the autoclave at ambient temperature. The catalyst is filtered off, the filtrate is evaporated to dryness in vacuo. The crude product thus obtained is purified by column chromatography (eluant: petroleum ether/ethyl acetate 1:1).
C13H20N2O2 (236.31)
[M+H]+=237
TLC: silica gel, petroleum ether/ethyl acetate 1:1, Rf value=0.55
112d)
A mixture of 0.50 g (2.12 mmol) of product from 112c, 0.48 g (3.56 mmol) of trimethylsilyl isocyanate (Fluka) and 15 ml THF is refluxed over the weekend with stirring. Then the reaction mixture is evaporated to dryness in vacuo.
C14H21N3O3 (279.33)
[2M+H]+=559
112e)
A mixture of 0.64 g (2.29 mmol) of product from 112d and 10 ml of methanolic HCl is stirred for three hours at ambient temperature and for two hours at 50° C. Then the reaction mixture is evaporated to dryness in vacuo. The residue is dried overnight in vacuo.
C9H13N3×HCl (215.68)
[M+H]+=180
112f)
Example 112 is prepared analogously to 1f from 0.20 g (0.60 mmol) of product from 53c, 0.13 g (0.60 mmol) of product from 112e, 0.42 ml (3.02 mmol) of triethylamine and 0.22 g (0.66 mmol) of TBTU in 4 ml DMF.
C23H32N4O6S (492.59)
[M+H]+=493
HPLC (Method 6): retention time=2.93 min
113a)
A mixture of 2.00 g (9.92 mmol) of 4-methylaminomethyl-benzoic acid hydrochloride (J. Med. Chem. 26, 1983, 309-312) and 25 ml of ethanolic HCl is stirred for 1.5 hours at reflux temperature. Then the reaction mixture is evaporated to dryness in vacuo.
C11H15NO2×HCl (229.70)
[M+H]+=194
HPLC (Method 6): retention time=1.39 min
113b)
113b is prepared analogously to 1f from 0.70 g (2.11 mmol) of product from 53c, 0.49 g (2.11 mmol) of product from 113a, 0.88 ml (6.34 mmol) of triethylamine and 0.78 g (2.32 mmol) of TBTU in 12 ml DMF.
C25H34N2O7S (506.61)
[M+H]+=507
HPLC (Method 6): retention time=3.95 min
113c)
A mixture of 1.06 g (2.09 mmol) of product from 133b, 7.00 ml (7.00 mmol) of 1 M sodium hydroxide solution, 15 ml THF and 1.5 ml of ethanol is stirred for four hours at 50° C. The reaction mixture is then combined with 7 ml 1 M HCl and evaporated to dryness in vacuo. The residue is taken up in acetone, dried on magnesium sulphate and evaporated to dryness in vacuo.
C23H30N2O7S (478.56)
[M+H]+=479
HPLC (Method 6): retention time=3.21 min
113d)
Example 113 is prepared analogously to 1f from 0.50 g (1.05 mmol) of product from 113c, 4.00 ml (2.00 mmol) of ammonia 0.5 M in dioxane, 0.44 ml (3.14 mmol) of triethylamine and 0.38 g (1.15 mmol) of TBTU in 4 ml DMF.
C23H31N3O6S (477.57)
[M+H]+=478
HPLC (Method 6): retention time=2.92 min
A mixture of 0.075 g (0.15 mmol) of 61, 0.1 g (0.71 mmol) of methyl iodide and 5 ml dichloromethane is stirred overnight at ambient temperature. The reaction mixture is then evaporated to dryness in vacuo.
C27H41N4O5S×I (660.61)
[M+H]+=533
HPLC (Method 5): retention time=1.55 min
Example 115 is prepared analogously to 114 from 0.03 g (0.059 mmol) of 64 and 0.05 g (0.35 mmol) of methyl iodide in 5 ml dichloromethane.
C27H42N3O5S×I (647.61)
[M+H]+=520
HPLC (Method 5): retention time=1.55 min
116a)
116a is prepared analogously to 1f from 0.50 g (1.05 mmol) of product from 113c, 0.14 g (1.05 mmol) of tert-butyl hydrazine carboxylate (Aldrich), 0.58 ml (4.18 mmol) of triethylamine and 0.38 g (1.15 mmol) of TBTU in 6 ml DMF.
C28H40N4O8S (592.71)
[M+H]+=593
HPLC (Method 6): retention time=3.46 min
116b)
Example 116 is prepared analogously to 112e from 0.68 g (1.15 mmol) of product from 116a and 10 ml of methanolic HCl.
C23H32N4O6S×C2HF3O2 (606.61)
[M+H]+=493
HPLC (Method 6): retention time=3.46 min
117a)
A mixture of 3.20 g (17.47 mmol) of product from 63a, 50 ml 20% sodium hydroxide solution and 50 ml of ethanol is refluxed overnight with stirring. Then the ethanol is eliminated in vacuo and the aqueous residue is neutralised with concentrated HCl. The precipitate formed is filtered off and dried.
C11H10N2O2 (202.21)
[M+H]+=203
117b)
A mixture of 2.70 g (13.35 mmol) of product from 117a, 8.00 g (57.89 mmol) of potassium carbonate and 100 ml DMF is stirred for one hour at 60° C. After cooling the reaction mixture is combined with 3.50 g (27.65 mmol) of benzyl chloride (Aldrich) at ambient temperature and then stirred over the weekend at 60° C. The reaction mixture is poured onto water and stirred for one hour at ambient temperature. The precipitate formed is filtered off and dried.
C25H22N2O2 (382.45)
[M+H]+=383
TLC: silica gel, dichloromethane/methanol 9:1, Rf value=0.64
117c)
A mixture of 1.80 g (4.71 mmol) of product from 117b and 100 ml methylamine 33% in ethanol (Aldrich) is stirred for six hours at 180° C. and overnight at 160° C. in the autoclave. The reaction mixture is then evaporated to dryness in vacuo. The crude product thus obtained is purified by column chromatography (eluant: dichloromethane/methanol 19:1).
C19H19N3O (305.37)
[M+H]+=306
117d)
A mixture of 1.20 g (3.93 mmol) of product from 117c, 0.20 g palladium on charcoal (20%) and 50 ml of methanol is hydrogenated at 50° C. in the autoclave. The catalyst is filtered off, the filtrate is evaporated to dryness in vacuo.
C12H13N3O (215.25)
[M+H]+=216
117e)
117e is prepared analogously to 38f from 0.70 g (3.25 mmol) of product from 117d and 10.00 ml (10.00 mmol) of lithium aluminium hydride 1 M in THF (Aldrich) in 200 ml THF.
C12H15N3 (201.27)
[M+H]+=202
117f)
Example 117 is prepared analogously to 1f from 0.17 g (0.51 mmol) of product from 53c, 0.10 g (0.50 mmol) of product from 117e, 0.17 ml (1.19 mmol) of triethylamine and 0.17 g (0.53 mmol) of TBTU in 30 ml THF and 5 ml DMF.
C26H34N4O5S (514.64)
[M+H]+=515
TLC: silica gel, dichloromethane/methanol 9:1, Rf value=0.28
118a)
118a is prepared analogously to 13a from 0.75 g (4.05 mmol) of 5-bromo-m-xylene (Aldrich), 0.55 ml (8.30 mmol) of chlorosulphonic acid (Aldrich) and 10 ml dichloromethane.
C8H8BrClO2S (283.57)
HPLC (Method 6): retention time=4.76 min
118b)
118b is prepared analogously to 3a from 0.65 g (2.29 mmol) of product from 118a and 0.28 ml (3.44 mmol) of N-methylaminoethanol (BASF) in 5 ml THF.
C11H16BrNO3S (322.22)
HPLC (Method 6): retention time=3.38 min
118c)
118c is first prepared analogously to 53b from 0.74 g (2.29 mmol) of product from 118b, 0.75 g (5.06 mmol) of tert-butyl 2-bromopropionate (Fluka), 0.42 g (1.14 mmol) of tetrabutylammonium iodide (Aldrich) and 8.67 g (75.90 mmol) of 35% sodium hydroxide solution in 40 ml of toluene. The tert-butyl ester is then stirred overnight together with 2 ml HCl 4 M in dioxane (Aldrich) in 4 ml dioxane at ambient temperature. The product is then obtained by evaporating the reaction mixture in vacuo.
C13H18BrNO5S (380.26)
HPLC (Method 6): retention time=3.48 min
118d)
Example 118 is prepared analogously to 1f from 0.10 g (0.26 mmol) of product from 118c, 0.054 g (0.26 mmol) of product from 61b, 0.11 ml (0.79 mmol) of triethylamine and 0.084 g (0.26 mmol) of TBTU in 10 ml THF and 3 ml DMF.
C25H35BrN4O4S (567.54)
[M+H]+=568/569/571
HPLC (Method 6): retention time=2.77 min
A mixture of 0.03 g (0.053 mmol) of 118 and 0.03 g palladium on charcoal in 5 ml of methanol is hydrogenated in the autoclave at ambient temperature. The catalyst is filtered off, the filtrate is evaporated to dryness in vacuo. The crude product thus obtained is purified by preparative HPLC.
C25H36N4O4S (488.64)
[M+H]+=489
HPLC (Method 6): retention time=2.45 min
120a)
120a is prepared analogously to 3a from 0.50 g (2.29 mmol) of 2,4,6-trimethylbenzene-sulphonic acid chloride (Fluka) and 0.19 g (2.52 mmol) of N-methylaminoethanol (BASF) in 5 ml THF.
C12H19NO3S (257.35)
[M+H]+=258
120b)
120b is prepared analogously to 118c from 0.56 g (2.18 mmol) of product from 120a, 0.48 ml (3.26 mmol) of tert-butyl 2-bromopropionate (Fluka), 0.18 g (0.65 mmol) of tetrabutylammonium chloride (Fluka) and 7.46 g (65.28 mmol) of 35% sodium hydroxide solution in 20 ml of toluene and subsequent stirring in 2 ml HCl 4 M in dioxane.
C14H21NO5S (315.39)
120c)
Example 120 is prepared analogously to 1f from 0.10 g (0.32 mmol) of product from 120b, 0.065 g (0.32 mmol) of product from 61b, 0.13 ml (0.95 mmol) of triethylamine and 0.20 g (0.63 mmol) of TBTU in 10 ml THF.
C26H38N4O4S (502.67)
[M+H]+=503
HPLC (Method 5): retention time=1.57 min
121a)
A mixture of 0.98 g (7.05 mmol) of sarcosine methylester hydrochloride (Fluka), 1.65 g (7.05 mmol) of product from 13a and 50 ml of pyridine is stirred for one hour at ambient temperature. The reaction mixture is then evaporated to dryness in vacuo. The residue is then taken up in 1 M HCl and extracted with ethyl acetate. The organic extracts are dried on sodium sulphate and evaporated to dryness in vacuo.
C13H19NO5S (301.36)
[M+H]+=302
121b)
A mixture of 1.90 g (6.29 mmol) of product from 121a, 6.45 ml (12.90 mmol) of 2 M sodium hydroxide solution and 9 ml of methanol is stirred for three days at ambient temperature. The methanol is eliminated in vacuo, the aqueous residue is poured onto 1 M HCl. The precipitate formed is filtered off and dried overnight in the vacuum desiccator.
C12H17NO5S (287.33)
[M+H]+=288
121c)
121c is prepared analogously to 1f from 0.20 g (0.70 mmol) of product from 121b, 0.087 g (0.70 mmol) of glycine methylester hydrochloride (Aldrich), 0.29 ml (2.09 mmol) of triethylamine and 0.22 g (0.70 mmol) of TBTU in 5 ml THF.
C15H22N2O6S (358.41)
[M+H]+=359
HPLC (Method 5): retention time=1.72 min
121d)
121d is prepared analogously to 121b from 0.23 g (0.63 mmol) of product from 121c and 0.64 ml (1.29 mmol) of 2 M sodium hydroxide solution in 1 ml of methanol.
C14H20N2O6S (344.38)
[M+H]+=345
121e)
121e is prepared analogously to 28c from 3.00 g (14.00 mmol) of tert-butyl piperidine-4-ylmethyl-carbamate (EMKA), 2.10 g (14.00 mmol) of 4-chloropyridine hydrochloride (Aldrich) and 7.80 ml (56.32 mmol) of triethylamine in 15 ml isopropanol.
C16H25N3O2 (291.39)
[M+H]+=292
HPLC (Method 5): retention time=1.40 min
121f)
121f is prepared analogously to 18b from 1.44 g (4.95 mmol) of product from 121e and 4.95 ml TFA in 8 ml dichloromethane.
C11H17N3×2C2HF3O2 (419.32)
[M+H]+=192
HPLC (Method 5): retention time=0.36 min
121g)
Example 121 is prepared analogously to 1f from 0.09 g (0.26 mmol) of product from 121d, 0.11 g (0.26 mmol) of product from 121f, 0.15 ml (1.05 mmol) of triethylamine and 0.084 g (0.26 mmol) of TBTU in 1.9 ml THF.
C25H35N5O5S×C2HF3O2 (631.67)
[M+H]+=518
HPLC (Method 5): retention time=1.46 min
Example 122 is prepared analogously to 1f from 0.09 g (0.26 mmol) of product from 121d, 0.054 g (0.26 mmol) of product from 61b, 0.11 ml (0.78 mmol) of triethylamine and 0.084 g (0.26 mmol) of TBTU in 1.9 ml THF.
C26H37N5O5S×C2HF3O2 (645.69)
[M+H]+=532
HPLC (Method 5): retention time=1.50 min
123a)
123a is prepared analogously to 1f from 0.20 g (0.70 mmol) of product from 121b, 0.097 g (0.70 mmol) of sarcosine methylester hydrochloride (Fluka), 0.29 ml (2.09 mmol) of triethylamine and 0.22 g (0.70 mmol) of TBTU in 5 ml THF.
C16H24N2O6S (372.44)
[M+H]+=373
HPLC (Method 5): retention time=1.78 min
123b)
123b is prepared analogously to 121b from 0.23 g (0.60 mmol) of product from 123a and 0.62 ml (1.24 mmol) of 2 M sodium hydroxide solution in 1 ml of methanol.
C15H22N2O6S (258.41)
[M+H]+=359
123c)
Example 123 is prepared analogously to 1f from 0.094 g (0.26 mmol) of product from 123b, 0.11 g (0.26 mmol) of product from 121f, 0.15 ml (1.05 mmol) of triethylamine and 0.084 g (0.26 mmol) of TBTU in 1.9 ml THF.
C26H37N5O5S×C2HF3O2 (645.69)
[M+H]+=532
HPLC (Method 5): retention time=1.47 min
Example 124 is prepared analogously to 1f from 0.094 g (0.26 mmol) of product from 123b, 0.054 g (0.26 mmol) of product from 61b, 0.11 ml (0.78 mmol) of triethylamine and 0.084 g (0.26 mmol) of TBTU in 1.9 ml THF.
C27H39N5O5S×C2HF3O2 (659.72)
[M+H]+=548
HPLC (Method 5): retention time=1.49 min
Example 125 is prepared analogously to 1f from 0.09 g (0.26 mmol) of product from 121d, 0.076 g (0.26 mmol) of product from 54b, 0.11 ml (0.78 mmol) of triethylamine and 0.084 g (0.26 mmol) of TBTU in 1.9 ml THF.
C27H38N4O5S (530.68)
[M+H]+=531
HPLC (Method 1): retention time=2.43 min
Example 126 is prepared analogously to 1f from 0.09 g (0.26 mmol) of product from 121d, 0.05 g (0.26 mmol) of product from 59b, 0.11 ml (0.78 mmol) of triethylamine and 0.084 g (0.26 mmol) of TBTU in 1.9 ml THF.
C26H38N4O5S×HCl (555.13)
[M+H]+=519
HPLC (Method 1): retention time=2.42 min
Example 127 is prepared analogously to 1f from 0.09 g (0.26 mmol) of product from 121d, 0.065 g (0.26 mmol) of product from 80a, 0.11 ml (0.78 mmol) of triethylamine and 0.084 g (0.26 mmol) of TBTU in 1.9 ml THF.
C29H43N5O5S×HCl (610.21)
[M+H]+=574
HPLC (Method 1): retention time=2.38 min
Example 128 is prepared analogously to 1f from 0.09 g (0.26 mmol) of product from 121d, 0.057 g (0.26 mmol) of product from 81a, 0.11 ml (0.78 mmol) of triethylamine and 0.084 g (0.26 mmol) of TBTU in 1.9 ml THF.
C27H39N5O5S×C2HF3O2 (610.21)
[M+H]+=546
HPLC (Method 5): retention time=1.51 min
Example 129 is prepared analogously to 1f from 0.09 g (0.26 mmol) of product from 121d, 0.056 g (0.26 mmol) of product from 67c, 0.11 ml (0.78 mmol) of triethylamine and 0.084 g (0.26 mmol) of TBTU in 1.9 ml THF.
C27H35N5O5S×C2HF3O2 (655.69)
[M+H]+=542
HPLC (Method 5): retention time=1.52 min
130a)
130a is prepared analogously to 10d from 0.50 g (2.13 mmol) of product from 13a, 0.42 g (2.13 mmol) of ethyl 5-methylaminovalerate (J. Am. Chem. Soc. 55, 1933, 1233-1241) and 1.18 ml (8.52 mmol) of triethylamine in 15 ml THF.
C17H27NO5S (357.47)
[M+H]+=358
HPLC (Method 6): retention time=4.10 min
130b)
130b is prepared analogously to 121b from 0.62 g (1.73 mmol) of product from 130a and 7.00 ml (7.00 mmol) of 1 M sodium hydroxide solution in 1.5 ml of methanol and 15 ml THF.
C15H23NO5S (329.41)
[M+H]+=330
HPLC (Method 6): retention time=3.24 min
130c)
Example 130 is prepared analogously to 1f from 0.18 g (0.54 mmol) of product from 130b, 0.10 g (0.49 mmol) of product from 61b, 0.14 ml (0.97 mmol) of triethylamine and 0.18 g (0.54 mmol) of TBTU in 3 ml DMF.
C27H40N4O4S (516.70)
[M+H]+=517
HPLC (Method 6): retention time=2.65 min
Example 131 is prepared analogously to 1f from 0.069 g (0.21 mmol) of product from 130b, 0.088 g (0.21 mmol) of product from 121f, 0.087 ml (0.63 mmol) of triethylamine and 0.077 g (0.23 mmol) of TBTU in 1 ml DMF.
C26H38N4O4S×CH2O2 (548.71)
[M+H]+=503
HPLC (Method 6): retention time=2.52 min
132a)
A mixture of 2.50 g (9.15 mmol) of product from 53a, 1.39 ml (10.00 mmol) of triethylamine and 50 ml THF is combined at ambient temperature with 0.77 ml (10.00 mmol) of methanesulphonic acid chloride (Aldrich). The reaction mixture is then stirred overnight at ambient temperature. The precipitate formed is filtered off. The filtrate is evaporated to dryness in vacuo. The residue is taken up in ethyl acetate and washed with water and saturated sodium chloride solution, dried on sodium sulphate and evaporated to dryness in vacuo.
C13H21NO6S2 (351.44)
[M+H]+=352
TLC: silica gel, dichloromethane/methanol 9.5:0.5, Rf value=0.95
132b)
A mixture of 0.50 g (1.42 mmol) of product from 132a, 0.20 g (1.42 mmol) of sarcosine methylester hydrochloride (Aldrich), 0.52 ml (3.00 mmol) of DIPEA and 5 ml DMF is stirred for 24 hours at 80° C. The reaction mixture is evaporated down in vacuo. The residue is taken up in dichloromethane and washed with water and saturated sodium hydrogen carbonate solution, dried on sodium sulphate and evaporated to dryness in vacuo. The crude product thus obtained is purified by column chromatography (eluant: dichloromethane/0-3% methanol).
C16H26N2O5S (358.45)
[M+H]+=359
132c)
132c is prepared analogously to 1c from 0.29 g (0.81 mmol) of product from 132b and 0.17 g (4.00 mmol) of lithium hydroxide monohydrate (Aldrich) in 5 ml THF and 4 ml of water.
C15H24N2O5S (344.43)
HPLC (Method 1): retention time=2.32 min
132d)
Example 132 is prepared analogously to 1f from 0.10 g (0.29 mmol) of product from 132c, 0.06 g (0.29 mmol) of product from 61b, 0.084 ml (0.60 mmol) of triethylamine and 0.096 g (0.30 mmol) of TBTU in 10 ml DMF.
C27H41N5O4S×2HCl (604.63)
[M+H]+=532
HPLC (Method 5): retention time=1.39 min
Example 133 is prepared analogously to 1f from 0.10 g (0.29 mmol) of product from 132c, 0.12 g (0.29 mmol) of product from 121f, 0.17 ml (1.20 mmol) of triethylamine and 0.096 g (0.30 mmol) of TBTU in 60 ml DMF.
C26H39N5O4S×2HCl (590.61)
[M+H]+=518
HPLC (Method 5): retention time=1.37 min
134a)
A mixture of 1.60 g (4.55 mmol) of product from 132a, 2.10 g (14.00 mmol) of sodium iodide and 30 ml acetone is stirred for eight hours at reflux temperature. The reaction mixture is then filtered through silica gel. The filtrate is evaporated to dryness in vacuo. The residue is taken up in ethyl acetate, washed with water, dried on sodium sulphate and evaporated to dryness in vacuo.
C12H18INO3S (383.25)
[M+H]+=384
HPLC (Method 1): retention time=3.75 min
134b)
134b is prepared analogously to 132b from 1.30 g (3.39 mmol) of product from 134a, 1.28 g (10.20 mmol) of glycine methylester hydrochloride (Aldrich) and 3.48 ml (20.00 mmol) of DIPEA in 15 ml acetonitrile.
C15H24N2O5S (344.43)
[M+H]+=345
TLC: silica gel, dichloromethane/methanol 9.5:0.5, Rf value=0.38
134c)
A mixture of 0.46 g (1.34 mmol) of product from 134b, 0.33 g (1.50 mmol) of Boc-anhydride, 0.21 ml (1.50 mmol) of triethylamine and 30 ml dichloromethane is stirred overnight at ambient temperature. The reaction mixture is then diluted with dichloromethane and washed with saturated sodium hydrogen carbonate solution and saturated sodium chloride solution, dried on sodium sulphate and evaporated to dryness in vacuo.
C20H32N2O7S (444.54)
[M+H]+=445
TLC: silica gel, dichloromethane/methanol 9.5:0.5, Rf value=0.45
134d)
134d is prepared analogously to 1c from 0.59 g (1.33 mmol) of product from 134c and 0.28 g (6.60 mmol) of lithium hydroxide monohydrate (Aldrich) in 7 ml THF and 6.6 ml of water.
C19H30N2O7S (430.52)
[M+H]+=431
134e)
134e is prepared analogously to 1f from 0.15 g (0.35 mmol) of product from 134d, 0.072 g (0.35 mmol) of product from 61b, 0.098 ml (0.70 mmol) of triethylamine and 0.11 g (0.35 mmol) of TBTU in 7 ml DMF.
C31H47N5O6S (617.80)
[M+H]+=618
HPLC (Method 1): retention time=2.62 min
134f)
Example 134 is prepared analogously to 18b from 0.16 g (0.26 mmol) of product from 134e and 3 ml TFA in 3 ml dichloromethane.
C26H39N5O4S×2HCl (590.61)
[M+H]+=518
HPLC (Method 5): retention time=1.40 min
135a)
135a is prepared analogously to 1f from 0.15 g (0.35 mmol) of product from 134d, 0.15 g (0.35 mmol) of product from 121f, 0.20 ml (1.40 mmol) of triethylamine and 0.11 g (0.35 mmol) of TBTU in 7 ml DMF.
C30H45N5O6S (603.77)
[M+H]+=604
TLC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.48
135b)
Example 135 is prepared analogously to 18b from 0.16 g (0.27 mmol) of product from 135a and 5 ml TFA in 5 ml dichloromethane.
C25H37N5O4S×2HCl (576.58)
[M+H]+=504
HPLC (Method 1): retention time=2.17 min
136a)
A mixture of 0.21 g (0.60 mmol) of product from 132a, 0.065 ml (0.60 mmol) of ethyl mercaptoacetate (Aldrich), 0.17 g (1.20 mmol) of potassium carbonate and 10 ml acetonitrile is stirred for 24 hours at ambient temperature. The precipitate is filtered off, the filtrate is evaporated down in vacuo. The crude product thus obtained is purified by preparative HPLC.
C16H25NO5S2 (375.51)
[M+H]+=376
136b)
136b is prepared analogously to 121b from 0.070 g (0.19 mmol) of product from 136a and 2.00 ml (2.00 mmol) of 1 M sodium hydroxide solution in 5 ml THF.
C14H21NO5S2 (347.45)
[M+H]+=348
136c)
Example 136 is prepared analogously to 1f from 0.064 g (0.18 mmol) of product from 136b, 0.038 g (0.18 mmol) of product from 61b, 0.079 ml (0.46 mmol) of DIPEA and 0.059 g (0.18 mmol) of TBTU in 5 ml DMF.
C26H38N4O4S2 (534.74)
[M+H]+=535
HPLC (Method 6): retention time=2.68 min
Example 137 is prepared analogously to 1f from 0.073 g (0.21 mmol) of product from 136b, 0.088 g (0.21 mmol) of product from 121f, 0.11 ml (0.63 mmol) of DIPEA and 0.087 g (0.27 mmol) of TBTU in 5 ml DMF.
C25H36N4O4S2×C2HF3O2 (634.73)
[M+H]+=521
HPLC (Method 6): retention time=2.57 min
138a)
138a is prepared analogously to 3a from 2.0 g (8.52 mmol) of product of 13a, 1.37 μg (8.55 mmol) of N-Boc-ethylenediamine (Fluka) and 1.0 g (9.89 mmol) of triethylamine in 50 ml THF.
C16H26N2O5S (358.45)
[M−H]-=357
HPLC (Method 6): retention time=3.63 min
138b)
138b is prepared analogously to 3b from 3.38 g (9.43 mmol) of the product of 138a, 0.53 ml (8.55 mmol) of methyl iodide, 1.77 g (12.83 mmol) of potassium carbonate under anhydrous conditions in 30 ml DMSO.
C17H28N2O5S (372.48)
[M+H]+=373
HPLC (Method 6): retention time=3.89 min
138c)
138b is prepared analogously to 28d from 3.61 g (9.69 mmol) of the product of 138b and 10 ml TFA in 50 ml dichloromethane.
C127H20N2O3S (272.36)
[M+H]+=273
HPLC (Method 6): retention time=1.95 min
138d)
A mixture of 0.50 g (1.84 mmol) of the product of 138c, 0.56 ml (5.51 mmol) of triethylamine and 25 ml dichloromethane is combined with 0.38 ml (2.75 mmol) of monoethyl oxalate chloride (Fluka) in 5 ml dichloromethane while cooling with an ice bath and the mixture is stirred for two hours at ambient temperature. The reaction mixture is then diluted with dichloromethane, washed with 10% aqueous citric acid solution, saturated sodium sulphate solution and with water, dried on sodium sulphate and evaporated to dryness in vacuo.
C16H24N2O6S (372.44)
[M+H]+=373
138e)
A mixture of 0.60 g (1.60 mmol) of the product of 138d, 5.6 ml 1 M sodium hydroxide solution and 6 ml of ethanol is stirred for four hours at ambient temperature and then evaporated to dryness in vacuo. The residue is combined with 8 ml 1 M hydrochloric acid and extracted with ethyl acetate. The combined organic extracts are washed with water and saturated sodium chloride solution, dried on sodium sulphate and evaporated to dryness in vacuo.
C14H20N2O6S (344.38)
[M+H]+=345
138f)
Example 138 is prepared analogously to 1f from 40.0 mg (0.12 mmol) of the product of 138e, 48.2 mg (0.12 mmol) of N,N-dimethyl-N′-(4-methylaminomethyl-phenyl)-ethan-1,2-diamine (analogously to J. Chem. Soc 1960, 3163-3165), 0.038 ml (0.29 mmol) of DIPEA and 38.9 mg (0.12 mmol) of TBTU in 1.5 ml DMF.
C26H39N5O5S (533.68)
[M+H]+=534
HPLC (Method 6): retention time=1.61 min
Example 139 is prepared analogously to 1f from 40.0 mg (0.12 mmol) of the product of 138e, 22.5 mg (0.12 mmol) of N-(4-aminomethyl-phenyl)-N′,N′-dimethylethan-1,2-diamine (analogously to J. Chem. Soc 1960, 3163-3165), 0.038 ml (0.29 mmol) of DIPEA and 38.9 mg (0.12 mmol) of TBTU in 1.5 ml DMF.
C25H37N5O5S (519.66)
[M+H]+=520
HPLC (Method 6): retention time=1.53 min
The following compounds were prepared analogously to Example 22:
C27H33N5O4S×C2HF3O2 (637.67)
[M+H]+=524
HPLC (Method 6): retention time=2.43 min
C29H29N3O4S×C2HF3O2 (629.65)
[M+H]+=516
HPLC (Method 6): retention time=3.39 min
C28H35N5O4S (537.67)
[M+H]+=538
HPLC (Method 6): retention time=2.45 min
C31H44N6O4S×C2HF3O2 (710.81)
[M+H]+=597
HPLC (Method 6): retention time=2.30 min
C23H27N5O5S×C2HF3O2 (599.58)
[M+H]+=486
HPLC (Method 6): retention time=2.46 min
C26H39N3O4S (489.67)
[M+H]+=490
HPLC (Method 6): retention time=2.66 min
C34H39N5O4S (613.77)
[M+H]+=614
HPLC (Method 6): retention time=3.07 min
C26H39N3O4S×C2HF3O2 (603.70)
[M+H]+=490
HPLC (Method 6): retention time=2.60 min
C24H34N4O5S×CH2O2 (536.64)
[M+H]+=491
HPLC (Method 6): retention time=2.29 min
C25H36N4O5S×CH2O2 (550.67)
[M+H]+=505
HPLC (Method 6): retention time=2.32 min
C25H36N4O5S (504.64)
[M+H]+=505
HPLC (Method 6): retention time=2.31 min
C26H38N4O5S×CH2O2 (564.70)
[M+H]+=519
HPLC (Method 6): retention time=2.34 min
C27H41N5O4S×2C2HF3O2 (759.76)
[M+H]+=532
HPLC (Method 5): retention time=1.40 min
C30H46N4O5S×HCl (611.24)
[M+H]+=575
HPLC (Method 1): retention time=2.12 min
C29H44N4O5S×HCl (597.21)
[M+H]+=561
HPLC (Method 8): retention time=3.12 min
C27H40N4O5S×HCl (569.16)
[M+H]+=533
HPLC (Method 11): retention time=1.67 min
C25H35N3O4S×HCl (510.09)
[M+H]+=474
HPLC (Method 7): retention time=1.90 min
C24H33N3O4S×C2HF3O2 (573.63)
[M+H]+=460
HPLC (Method 5): retention time=1.52 min
C26H35N3O4S×C2HF3O2 (599.66)
[M+H]+=486
HPLC (Method 5): retention time=1.55 min
C26H37N3O4S×C2HF3O2 (601.68)
[M+H]+=488
HPLC (Method 5): retention time=1.54 min
C25H35N3O5S×C2HF3O2 (603.65)
[M+H]+=490
HPLC (Method 5): retention time=1.54 min
C26H40N4O4S×HCl (541.15)
[M+H]+=505
HPLC (Method 5): retention time=1.59 min
C25H38N4O4S×HCl (527.12)
[M+H]+=491
HPLC (Method 5): retention time=1.55 min
C25H37N3O4S×HCl (512.11)
[M+H]+=476
HPLC (Method 5): retention time=1.56 min
C26H37N3O4S×HCl (524.12)
[M+H]+=488
HPLC (Method 5): retention time=1.54 min
C24H36N4O4S×HCl (513.09)
[M+H]+=477
HPLC (Method 7): retention time=1.88 min
C25H38N4O4S×HCl (527.12)
[M+H]+=491
HPLC (Method 7): retention time=1.92 min
C23H34N4O4S×HCl (499.07)
[M+H]+=463
HPLC (Method 7): retention time=1.79 min
C24H36N4O4S×HCl (513.09)
[M+H]+=477
HPLC (Method 7): retention time=1.86 min
C24H34N4O4S×C2HF3O2 (588.64)
[M+H]+=475
HPLC (Method 5): retention time=1.39 min
C29H45N5O4S×2HCl (632.69)
[M+H]+=560
DC: silica gel, dichloromethane/ethanol 9:1, Rf value=0.22
C26H39N5O4S×2HCl (590.61)
[M+H]+=518
DC: silica gel, dichloromethane/ethanol 4:1, Rf value=0.68
C28H43N5O4S×2HCl (618.66)
[M+H]+=546
HPLC (Method 5): retention time=1.26 min
C29H42N4O4S (542.73)
[M+H]+=543
HPLC (Method 4): retention time=2.8 min
C27H41N5O4S×2HCl (604.63)
[M+H]+=532
HPLC (Method 5): retention time=1.39 min
C26H37FN4O4S×HCl (557.12)
[M+H]+=521
DC: silica gel, dichloromethane/ethanol 9:1, Rf value=0.25
C29H43FN4O4S×HCl (599.20)
[M+H]+=563
DC: silica gel, dichloromethane/ethanol 9:1, Rf value=0.40
C28H41FN4O4S×HCl (585.17)
[M+H]+=549
DC: silica gel, dichloromethane/ethanol 9:1, Rf value=0.35
C27H40N4O4S (516.70)
[M+H]+=517
DC: silica gel, dichloromethane/ethanol/ammonia 8:2:0.01, Rf value=0.41
C29H42N4O4S×HCl (579.19)
[M+H]+=543
DC: silica gel, dichloromethane/ethanol/ammonia 8:2:0.01, Rf value=0.47
C26H37ClN4O4S×HCl (573.58)
[M+H]+=537/539
DC: silica gel, dichloromethane/ethanol 9:1, Rf value=0.26
C29H43ClN4O4S×HCl (615.66)
[M+H]+=579/581
DC: silica gel, dichloromethane/ethanol 9:1, Rf value=0.45
C28H41ClN4O4S×HCl (601.63)
[M+H]+=565/567
DC: silica gel, dichloromethane/ethanol 9:1, Rf value=0.30
C27H39FN4O4S×HCl (571.15)
[M+H]+=535
DC: silica gel, dichloromethane/ethanol/ammonia 8:2:0.01, Rf value=0.26
C27H39BrN4O4S×HCl (632.05)
[M+H]+=595/597
DC: silica gel, dichloromethane/ethanol/ammonia 8:2:0.01, Rf value=0.51
C30H44N4O4S×HCl (593.22)
[M+H]+=557
DC: silica gel, dichloromethane/ethanol/ammonia 8:2:0.01, Rf value=0.63
C27H39ClN4O4S×HCl (587.60)
[M+H]+=551
DC: silica gel, dichloromethane/ethanol/ammonia 8:2:0.01, Rf value=0.58
C30H37N5O4S×HCl (600.17)
[M+H]+=564
HPLC (Method 4): retention time=3.0 min
C29H41ClN4O4S×HCl (613.64)
[M+H]+=577/579
DC: silica gel, dichloromethane/methanol 9:1, Rf value=0.24
C26H33N5O4S2 (543.70)
[M+H]+=544
HPLC (Method 6): retention time=3.11 min
C26H38N4O5S (518.67)
[M+H]+=519
HPLC (Method 6): retention time=2.44 min
C19H25N3O4S×C2HF3O2 (505.51)
[M+H]+=392
HPLC (Method 6): retention time=2.04 min
C27H35N5O5S (541.66)
[M+H]+=542
HPLC (Method 6): retention time=2.51 min
C25H36N4O5S (504.64)
[M+H]+=505
HPLC (Method 6): retention time=2.43 min
C29H36N4O4S (536.69)
[M+H]+=537
HPLC (Method 6): retention time=2.19 min
C28H38N6O4S (554.71)
[M+H]+=555
HPLC (Method 6): retention time=2.37 min
C26H38N4O4S (502.67)
[M+H]+=503
HPLC (Method 6): retention time=2.35 min
C26H38N4O4S (502.67)
[M+H]+=503
HPLC (Method 6): retention time=2.00 min
C27H38N4O5S×C2HF3O2 (644.70)
[M+H]+=531
HPLC (Method 6): retention time=2.45 min
C27H38N4O5S (530.68)
[M+H]+=531
HPLC (Method 6): retention time=2.53 min
C25H35N5O4S (501.64)
[M+H]+=502
HPLC (Method 6): retention time=2.05 min
C24H31N5O4S (485.60)
[M+H]+=486
HPLC (Method 6): retention time=2.41 min
C24H35FN4O4S×CH2O2 (540.65)
[M+H]+=495
HPLC (Method 6): retention time=2.50 min
C27H38N4O5S (530.68)
[M+H]+=531
HPLC (Method 6): retention time=2.36 min
C28H42N4O4S (530.72)
[M+H]+=531
HPLC (Method 6): retention time=2.60 min
C28H40N4O5S (544.71)
[M+H]+=545
HPLC (Method 6): retention time=2.21 min
C27H39ClN4O4S (551.14)
[M+H]+=551/553
HPLC (Method 6): retention time=2.65 min
C27H40N4O4S×C2HF3O2 (630.72)
[M+H]+=517
HPLC (Method 6): retention time=2.51 min
C27H38N4O5S×CH2O2 (576.71)
[M+H]+=531
HPLC (Method 6): retention time=2.33 min
C28H44N6O4S×C2HF3O2 (674.78)
[M+H]+=561
HPLC (Method 6): retention time=2.14 min
C28H44N6O4S×C2HF3O2 (674.78)
[M+H]+=561
HPLC (Method 6): retention time=2.43 min
C25H38N6O4S×C2HF3O2 (632.70)
[M+H]+=519
HPLC (Method 6): retention time=2.11 min
C30H43N3O4S×C2HF3O2 (655.77)
[M+H]+=542
HPLC (Method 6): retention time=2.75 min
C25H38N6O4S×C2HF3O2 (632.70)
[M+H]+=519
HPLC (Method 6): retention time=2.30 min
C27H42N6O4S×C2HF3O2 (660.75)
[M+H]+=547
HPLC (Method 6): retention time=2.08 min
C27H42N6O4S×C2HF3O2 (660.75)
[M+H]+=547
HPLC (Method 6): retention time=2.34 min
C28H40ClN5O4S×CH2O2 (624.19)
[M+H]+=578/580
HPLC (Method 6): retention time=2.64 min
C28H41N5O4S×CH2O2 (589.75)
[M+H]+=544
HPLC (Method 6): retention time=2.09 min
C27H38N6O4S×CH2O2 (588.72)
[M+H]+=543
HPLC (Method 9): retention time=1.67 min
C28H40N6O4S (556.72)
[M+H]+=557
HPLC (Method 9): retention time=1.71 min
C26H36N6O4S×CH2O2 (574.69)
[M+H]+=529
HPLC (Method 9): retention time=1.61 min
C26H44N4O4S (508.72)
[M+H]+=509
HPLC (Method 9): retention time=1.23 min
C27H46N4O4S×2C2HF3O2 (750.79)
[M+H]+=523
HPLC (Method 9): retention time=1.30 min
C28H48N4O4S×2C2HF3O2 (764.82)
[M+H]+=537
HPLC (Method 9): retention time=1.31 min
C26H43N3O4S (493.70)
[M+H]+=494
HPLC (Method 9): retention time=1.72 min
C24H41N3O4S×C2HF3O2 (581.69)
[M+H]+=468
HPLC (Method 9): retention time=1.69 min
C25H36N4O4S×C2HF3O2 (602.67)
[M+H]+=489
HPLC (Method 5): retention time=1.39 min
C29H38N5O4S×I (679.61)
[M+H]+=552
HPLC (Method 5): retention time=1.55 min
C29H50N4O4S (550.80)
[M+H]+=551
HPLC (Method 5): retention time=1.38 min
C29H50N4O4S (550.80)
[M+H]+=551
HPLC (Method 5): retention time=1.40 min
C28H40N4O4S×2HCl (601.63)
[M+H]+=529
HPLC (Method 5): retention time=1.41 min
C29H43N5O4S (557.75)
[M+H]+=558
HPLC (Method 1): retention time=1.90 min
C29H49N5O4S (563.80)
[M+H]+=564
HPLC (Method 5): retention time=1.33 min
C27H47N5O4S×2HCl (610.68)
[M+H]+=538
HPLC (Method 7): retention time=1.74 min
C27H38N4O4S (610.68)
[M+H]+=515
HPLC (Method 5): retention time=1.41 min
C29H43N5O4S (557.75)
[M+H]+=558
HPLC (Method 5): retention time=1.43 min
C28H40N4O4S×2C2HF3O2 (756.75)
[M+H]+=529
HPLC (Method 5): retention time=1.42 min
C28H48N4O4S×2HCl (609.69)
[M+H]+=537
HPLC (Method 7): retention time=1.70 min
C26H38N4O4S×2C2HF3O2 (730.72)
[M+H]+=503
HPLC (Method 5): retention time=1.40 min
C26H44N4O4S×2HCl (581.64)
[M+H]+=509
HPLC (Method 5): retention time=1.38 min
C26H44N4O4S×2HCl (581.64)
[M+H]+=509
HPLC (Method 5): retention time=1.40 min
C27H46N4O4S×2HCl (595.67)
[M+H]+=523
DC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.13
C27H46N4O4S×2HCl (595.67)
[M+H]+=523
DC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.13
C28H46N4O4S×2HCl (607.68)
[M+H]+=535
HPLC (Method 5): retention time=1.10 min
C27H46N4O4S×2HCl (595.67)
[M+H]+=523
DC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.25
C27H46N4O4S×2HCl (595.67)
[M+H]+=523
DC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.25
C27H46N4O4S×2C2HF3O2 (750.79)
[M+H]+=523
HPLC (Method 5): retention time=1.38 min
C29H48N4O4S×2C2HF3O2 (776.83)
[M+H]+=549
HPLC (Method 5): retention time=1.39 min
C29H48N4O4S×2C2HF3O2 (776.83)
[M+H]+=549
HPLC (Method 5): retention time=1.39 min
C28H48N4O4S×2HCl (609.69)
[M+H]+=537
HPLC (Method 5): retention time=1.38 min
C28H48N4O4S×2HCl (609.69)
[M+H]+=537
HPLC (Method 11): retention time=1.60 min
C28H48N4O4S×2HCl (609.69)
[M+H]+=537
HPLC (Method 7): retention time=1.71 min
C30H43N5O4S×HCl (606.22)
[M+H]+=570
DC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.29
C28H39ClN4O4S×HCl (599.61)
[M+H]+=563/565
HPLC (Method 5): retention time=1.59 min
C28H41ClN4O4S×HCl (601.63)
[M+H]+=565/567
DC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.46
C30H45ClN4O4S×HCl (629.68)
[M+H]+=593/595
DC: silica gel, dichloromethane/methanol 9:1, Rf value=0.42
C29H43ClN4O4S×HCl (615.66)
[M+H]+=579/581
DC: silica gel, dichloromethane/methanol 9:1, Rf value=0.23
C30H37N5O4S×HCl (600.17)
[M+H]+=564
DC: silica gel, dichloromethane/methanol/ammonia 8:2:0.1, Rf value=0.67
C30H43N5O4S (569.76)
[M+H]+=570
DC: silica gel, dichloromethane/methanol/ammonia 8:2:0.2, Rf value=0.65
C30H43ClN4O4S×HCl (627.67)
[M+H]+=591/593
DC: silica gel, dichloromethane/methanol 9:1, Rf value=0.20
C29H43ClN4O4S×HCl (615.66)
[M+H]+=579/581
DC: silica gel, dichloromethane/methanol 9:1, Rf value=0.17
C28H46N4O4S×2HCl (607.68)
[M+H]+=535
DC: silica gel, dichloromethane/methanol/ammonia 8:2:0.2, Rf value=0.23
C31H52N4O4S×2HCl (649.76)
[M+H]+=577
DC: silica gel, dichloromethane/methanol/ammonia 8:2:0.2, Rf value=0.69
C28H46N4O4S (534.76)
[M+H]+=535
DC: silica gel, dichloromethane/methanol/ammonia 8:2:0.2, Rf value=0.58
C31H52N4O4S (576.84)
[M+H]+=577
DC: silica gel, dichloromethane/methanol/ammonia 8:2:0.2, Rf value=0.56
C28H46N4O4S×2HCl (607.68)
[M+H]+=535
DC: silica gel, dichloromethane/methanol/ammonia 8:2:0.2, Rf value=0.58
C27H46N4O4S (522.74)
[M+H]+=523
HPLC (Method 9): retention time=1.30 min
C27H46N4O4S (522.74)
[M+H]+=523
HPLC (Method 9): retention time=1.28 min
C29H48N4O4S×CH2O2 (594.81)
[M+H]+=549
HPLC (Method 6): retention time=1.96 min
C309H44N4O4S (556.76)
[M+H]+=557
HPLC (Method 9): retention time=1.71 min
C24H42N4O4S×C2HF3O2 (596.70)
[M+H]+=483
HPLC (Method 9): retention time=1.23 min
C27H46N4O4S (522.74)
[M+H]+=523
HPLC (Method 9): retention time=1.23 min
C25H44N4O4S (496.71)
[M+H]+=497
HPLC (Method 9): retention time=1.25 min
C28H49N5O4S×2HCl (624.71)
[M+H]+=552
HPLC (Method 10): retention time=1.06 min
C29H50N4O4S×CH2O2 (596.82)
[M+H]+=551
HPLC (Method 9): retention time=1.31 min
C27H45N5O5S×CH2O2 (597.77)
[M+H]+=552
HPLC (Method 9): retention time=1.20 min
C28H48N4O4S (536.77)
[M+H]+=537
HPLC (Method 6): retention time=1.32 min
C27H45N5O5S×C2HF3O2 (665.77)
[M+H]+=552
HPLC (Method 9): retention time=1.18 min
C27H46N4O4S×2 C2HF3O2 (750.79)
[M+H]+=523
HPLC (Method 9): retention time=1.29 min
C24H34ClN5O4S (524.08)
[M+H]+=524/526
HPLC (Method 9): retention time=1.60 min
C23H38N4O4S×2C2HF3O2 (694.69)
[M+H]+=467
HPLC (Method 9): retention time=1.16 min
C26H38ClN5O4S×C2HF3O2 (666.15)
[M+H]+=552/554
HPLC (Method 9): retention time=1.68 min
C26H44N4O4S×2HCl (581.64)
[M+H]+=509
HPLC (Method 5): retention time=1.36 min
C29H48N4O4S×2HCl (621.70)
[M+H]+=549
HPLC (Method 5): retention time=1.38 min
C29H48N4O4S (548.78)
[M+H]+=549
HPLC (Method 5): retention time=1.38 min
C29H48N4O4S (548.78)
[M+H]+=549
HPLC (Method 5): retention time=1.36 min
C29H46F2N4O4S (584.76)
[M+H]+=585
HPLC (Method 5): retention time=1.38 min
C29H47FN4O4S (566.77)
[M+H]+=567
HPLC (Method 5): retention time=1.38 min
C29H47FN4O4S (566.77)
[M+H]+=567
HPLC (Method 5): retention time=1.36 min
C29H48N4O5S (564.78)
[M+H]+=565
HPLC (Method 5): retention time=1.37 min
C30H50N4O4S (562.81)
[M+H]+=563
HPLC (Method 5): retention time=1.39 min
C29H50N4O4S (550.80)
[M+H]+=551
HPLC (Method 5): retention time=1.36 min
C30H50N4O4S (562.81)
[M+H]+=563
HPLC (Method 5): retention time=1.28 min
C27H47N5O4S×3C2HF3O2 (879.83)
[M+H]+=538
HPLC (Method 5): retention time=1.33 min
C30H50N4O4S×2HCl (635.73)
[M+H]+=563
HPLC (Method 5): retention time=1.37 min
C29H46F2N4O4S×2C2HF3O2 (584.76)
[M+H]+=585
HPLC (Method 5): retention time=1.38 min
C29H47FN4O4S×2C2HF3O2 (794.82)
[M+H]+=567
HPLC (Method 5): retention time=1.35 min
C29H47FN4O4S×2C2HF3O2 (794.82)
[M+H]+=567
HPLC (Method 5): retention time=1.36 min
C29H48N4O5S (564.78)
[M+H]+=565
HPLC (Method 5): retention time=1.36 min
C30H50N4O4S (562.81)
[M+H]+=563
HPLC (Method 5): retention time=1.37 min
C29H50N4O4S (550.80)
[M+H]+=551
HPLC (Method 5): retention time=1.37 min
C30H50N4O4S (562.81)
[M+H]+=563
HPLC (Method 5): retention time=1.37 min
C30H50N4O4S×3C2HF3O2 (877.81)
[M+H]+=536
HPLC (Method 5): retention time=1.34 min
C30H50N4O4S (562.81)
[M+H]+=563
HPLC (Method 5): retention time=1.37 min
C29H49N5O4S×3C2HF3O2 (905.87)
[M+H]+=564
HPLC (Method 5): retention time=1.08 min
C28H46N4O4S×2HCl (607.68)
[M+H]+=535
DC: silica gel, dichloromethane/methanol/ammonia 8:2:0.2, Rf value=0.19
C27H40N4O4S×C2HF3O4 (630.72)
[M+H]+=517
HPLC (Method 9): retention time=1.40 min
C29H48N4O4S (548.78)
[M+H]+=549
HPLC (Method 6): retention time=1.24 min
C27H46N4O4S (522.74)
[M+H]+=523
HPLC (Method 9): retention time=1.29 min
C26H44N4O4S (508.72)
[M+H]+=509
HPLC (Method 9): retention time=1.30 min
C26H44N4O4S (508.72)
[M+H]+=509
HPLC (Method 9): retention time=1.23 min
C26H44N4O4S (508.72)
[M+H]+=509
HPLC (Method 6): retention time=1.20 min
C25H35N3O5S×HCl (526.09)
[M+H]+=490
HPLC (Method 10): retention time=1.16 min
C26H37N3O5S×HCl (540.12)
[M+H]+=504
HPLC (Method 10): retention time=1.22 min
C24H38N4O5S×C2HF3O2 (608.67)
[M+H]+=495
HPLC (Method 9): retention time=1.47 min
C24H40N4O4S (480.66)
[M+H]+=481
HPLC (Method 9): retention time=1.21 min
C24H40N4O4S×C2HF3O2 (594.69)
[M+H]+=481
HPLC (Method 9): retention time=1.19 min
C27H39N3O5S×HCl (554.14)
[M+H]+=518
HPLC (Method 5): retention time=1.36 min
C26H38N4O4S×HCl (539.13)
[M+H]+=503
HPLC (Method 5): retention time=1.29 min
C27H40N4O4S×HCl (553.16)
[M+H]+=517
HPLC (Method 5): retention time=1.35 min
C25H36N4O4S×HCl (525.10)
[M+H]+=489
HPLC (Method 5): retention time=1.31 min
C26H38N4O4S×HCl (539.13)
[M+H]+=503
HPLC (Method 5): retention time=1.35 min
C26H37N3O5S×HCl (540.12)
[M+H]+=504
HPLC (Method 10): retention time=1.18 min
C29H48N4O4S×C2HF3O2 (662.81)
[M+H]+=549
HPLC (Method 9): retention time=1.27 min
C27H45N5O4S×3HCl (645.13)
[M+H]+=536
HPLC (Method 5): retention time=1.14 min
C29H48N4O4S×2HCl (621.70)
[M+H]+=549
HPLC (Method 5): retention time=1.16 min
C29H48N4O4S (548.78)
[M+H]+=549
HPLC (Method 5): retention time=1.16 min
C30H50N4O4S×C2HF3O2 (676.83)
[M+H]+=563
HPLC (Method 9): retention time=1.14 min
C29H48N4O4S×C2HF3O2 (662.81)
[M+H]+=549
HPLC (Method 9): retention time=1.30 min
C30H50N4O4S×2HCl (635.73)
[M+H]+=563
HPLC (Method 11): retention time=1.70 min
C28H48N4O4S×2HCl (609.69)
[M+H]+=537
HPLC (Method 11): retention time=1.67 min
C27H44N4O4S×2HCl (593.65)
[M+H]+=521
HPLC (Method 11): retention time=1.61 min
C29H48N4O4S×2HCl (621.70)
[M+H]+=549
HPLC (Method 4): retention time=2.39 min
C29H48N4O4S×2HCl (621.70)
[M+H]+=549
HPLC (Method 4): retention time=2.34 min
The following compounds were prepared analogously to Example 53:
C23H30N2O7S (478.56)
[M+H]+=479
HPLC (Method 6): retention time=3.21 min
C26H33N5O6S (543.64)
[M+H]+=544
HPLC (Method 6): retention time=2.51 min
C26H38N4O6S (534.67)
[M+H]+=535
HPLC (Method 6): retention time=2.48 min
C26H398N3O6S (521.67)
[M+H]+=522
HPLC (Method 6): retention time=2.60 min
C27H41N3O5S (519.70)
[M+H]+=520
HPLC (Method 6): retention time=2.61 min
C27H42N4O5S×HCl (571.17)
[M+H]+=535
HPLC (Method 5): retention time=1.57 min
C29H34N4O5S×C2HF3O2 (664.69)
[M+H]+=551
HPLC (Method 5): retention time=1.60 min
C26H40N4O5S×HCl (557.15)
[M+H]+=521
HPLC (Method 5): retention time=1.53 min
C28H41N3O5S×C2HF3O2 (645.73)
[M+H]+=532
HPLC (Method 5): retention time=1.54 min
C25H37N3O5S×HCl (528.11)
[M+H]+=492
HPLC (Method 5): retention time=1.53 min
C26H39N3O6S×C2HF3O2 (635.69)
[M+H]+=522
HPLC (Method 5): retention time=1.53 min
C26H37N3O5S×HCl (540.12)
[M+H]+=504
HPLC (Method 7): retention time=1.93 min
C26H39N3O5S×HCl (542.13)
[M+H]+=506
HPLC (Method 5): retention time=1.54 min
C28H41N3O5S×HCl (568.17)
[M+H]+=532
DC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.30
C26H37N3O5S×HCl (540.12)
[M+H]+=504
HPLC (Method 5): retention time=1.51 min
C28H42N4O5S×HCl (583.18)
[M+H]+=547
HPLC (Method 5): retention time=1.54 min
C28H42N4O5S×HCl (583.18)
[M+H]+=547
HPLC (Method 10): retention time=1.24 min
C29H44N4O5S×HCl (597.21)
[M+H]+=561
HPLC (Method 5): retention time=1.55 min
C27H45N3O5S×HCl (560.19)
[M+H]+=524
DC: silica gel, dichloromethane/methanol/ammonia 8:2:0.01, Rf value=0.39
C27H39N3O5S×HCl (554.14)
[M+H]+=518
HPLC (Method 4): retention time=3.4 min
C28H41N3O5S×HCl (568.17)
[M+H]+=532
DC: silica gel, dichloromethane/methanol 9:1, Rf value=0.14
C24H30N4O5S×C2HF3O2 (600.61)
[M+H]+=487
HPLC (Method 6): retention time=2.58 min
C25H35N3O5S×C2HF3O2 (603.65)
[M+H]+=490
HPLC (Method 6): retention time=2.61 min
C23H29N5O5S×C2HF3O2 (601.60)
[M+H]+=488
HPLC (Method 6): retention time=3.28 min
C27H39FN4O6S (566.69)
[M+H]+=567
HPLC (Method 6): retention time=2.59 min
C25H37FN4O5S (524.65)
[M+H]+=525
HPLC (Method 6): retention time=2.59 min
C27H38N4O5S (530.68)
[M+H]+=531
HPLC (Method 6): retention time=2.65 min
C26H33N5O6S (543.64)
[M+H]+=544
HPLC (Method 6): retention time=2.39 min
C26H35N5O5S (529.65)
[M+H]+=530
HPLC (Method 6): retention time=2.43 min
C28H40N4O5S (544.71)
[M+H]+=545
HPLC (Method 6): retention time=2.65 min
C27H39N5O5S (545.70)
[M+H]+=546
HPLC (Method 6): retention time=2.19 min
C26H39ClN4O5S (555.13)
[M+H]+=555/557
HPLC (Method 6): retention time=2.63 min
C25H44N4O5S (512.71)
[M+H]+=513
HPLC (Method 6): retention time=1.94 min
C27H41N3O6S (535.70)
[M+H]+=536
HPLC (Method 6): retention time=2.56 min
C26H38ClN3O6S×CH2O2 (602.14)
[M+H]+=556/558
HPLC (Method 6): retention time=2.65 min
C30H44N4O5S (572.76)
[M+H]+=573
HPLC (Method 6): retention time=2.69 min
C27H42N4O5S (534.71)
[M+H]+=535
HPLC (Method 6): retention time=2.54 min
C24H42N4O5S (498.68)
[M+H]+=499
HPLC (Method 6): retention time=1.95 min
C28H41ClN4O5S (581.17)
[M+H]+=581/583
HPLC (Method 6): retention time=2.77 min
C27H36N4O6S (544.66)
[M+H]+=545
HPLC (Method 6): retention time=2.59 min
C28H41N3O6S (547.71)
[M+H]+=548
HPLC (Method 6): retention time=2.59 min
C25H44N4O5S (512.71)
[M+H]+=513
HPLC (Method 6): retention time=1.94 min
C25H32N4O5S (500.61)
[M+H]+=501
HPLC (Method 6): retention time=2.41 min
C23H31N5O5S (489.59)
[M+H]+=490
HPLC (Method 6): retention time=2.46 min
C27H39N3O5S×C2HF3O2 (631.71)
[M+H]+=518
HPLC (Method 6): retention time=2.54 min
C26H41N5O5S×CH2O2 (581.73)
[M+H]+=536
HPLC (Method 6): retention time=2.58 min
C25H39N5O5S×CH2O2 (567.70)
[M+H]+=522
HPLC (Method 6): retention time=2.31 min
C27H36N4O5S×C2HF3O2 (642.69)
[M+H]+=529
HPLC (Method 6): retention time=2.56 min
C21H30N4O5S (450.55)
[M+H]+=451
HPLC (Method 6): retention time=2.31 min
C26H34N4O5S (514.64)
[M+H]+=515
HPLC (Method 6): retention time=2.51 min
C29H41N5O5S×C2HF3O2 (685.76)
[M+H]+=572
HPLC (Method 6): retention time=2.14 min
C24H33N5O5S×C2HF3O2 (617.64)
[M+H]+=504
HPLC (Method 9): retention time=1.61 min
C24H33N5O5S×C2HF3O2 (617.64)
[M+H]+=504
HPLC (Method 9): retention time=1.59 min
C27H45N3O5S×C2HF3O2 (637.75)
[M+H]+=524
HPLC (Method 9): retention time=1.70 min
C26H46N4O5S (526.73)
[M+H]+=527
HPLC (Method 5): retention time=1.43 min
C28H41N3O5S×C2HF3O2 (645.73)
[M+H]+=532
HPLC (Method 5): retention time=1.56 min
C28H43N5O5S×C2HF3O2 (675.76)
[M+H]+=562
HPLC (Method 5): retention time=1.41 min
C26H39N5O5S×C2HF3O2 (647.71)
[M+H]+=534
HPLC (Method 5): retention time=1.42 min
C28H41N3O6S (547.71)
[M+H]+=548
HPLC (Method 5): retention time=1.53 min
C26H41N5O5S (535.70)
[M+H]+=536
HPLC (Method 5): retention time=1.42 min
C29H44N4O5S×HCl (597.21)
[M+H]+=561
HPLC (Method 7): retention time=1.91 min
C29H43N3O5S×C2HF3O2 (659.76)
[M+H]+=546
HPLC (Method 5): retention time=1.59 min
C28H43N5O5S×2C2HF3O2 (789.78)
[M+H]+=562
HPLC (Method 5): retention time=1.40 min
C30H46N4O5S×C2HF3O2 (688.80)
[M+H]+=575
HPLC (Method 5): retention time=1.56 min
C25H39N5O5S×2HCl (594.60)
[M+H]+=522
HPLC (Method 5): retention time=1.40 min
C26H46N4O5S×2HCl (599.65)
[M+H]+=527
HPLC (Method 5): retention time=1.41 min
C27H46N4O5S×HCl (575.20)
[M+H]+=539
DC: silica gel, dichloromethane/methanol/ammonia 8:2:0.01, Rf value=0.35
C28H42N4O5S×HCl (583.18)
[M+H]+=547
DC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.32
C28H41N3O5S×HCl (568.17)
[M+H]+=532
DC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.35
C26H44N4O5S×HCl (561.18)
[M+H]+=525
DC: silica gel, dichloromethane/methanol/ammonia 8:2:0.01, Rf value=0.12
C29H44N4O5S×HCl (597.21)
[M+H]+=561
DC: silica gel, dichloromethane/methanol 9:1, Rf value=0.30
C28H44N4O5S×HCl (585.20)
[M+H]+=549
DC: silica gel, dichloromethane/methanol 9:1, Rf value=0.15
C28H47N3O5S×HCl (574.22)
[M+H]+=538
DC: silica gel, dichloromethane/methanol 9:1, Rf value=0.05
C26H45N3O5S×HCl (548.18)
[M+H]+=512
HPLC (Method 5): retention time=1.56 min
C26H43N3O5S×HCl (546.16)
[M+H]+=510
DC: silica gel, dichloromethane/methanol 9:1, Rf value=0.05
C25H42N4O5S×2HCl (583.61)
[M+H]+=511
DC: silica gel, dichloromethane/ethanol/ammonia 9:1:0.1, Rf value=0.22
C25H42N4O5S×2HCl (583.61)
[M+H]+=511
HPLC (Method 5): retention time=1.37 min
C25H43N3O5S×HCl (534.15)
[M+H]+=498
DC: silica gel, dichloromethane/methanol/ammonia 8:2:0.01, Rf value=0.58
C25H43N3O5S×HCl (534.15)
[M+H]+=498
DC: silica gel, dichloromethane/methanol/ammonia 8:2:0.01, Rf value=0.57
C26H44N4O5S×2HCl (597.64)
[M+H]+=525
DC: silica gel, dichloromethane/methanol/ammonia 8:2:0.2, Rf value=0.52
C27H46N4O5S×2HCl (611.67)
[M+H]+=539
HPLC (Method 12): retention time=2.45 min
C27H46N4O5S×2HCl (611.67)
[M+H]+=539
HPLC (Method 12): retention time=2.35 min
C26H44N4O5S×2HCl (597.64)
[M+H]+=525
HPLC (Method 12): retention time=2.3 min
C26H44N4O5S×2HCl (597.64)
[M+H]+=525
HPLC (Method 12): retention time=2.3 min
C28H41N3O6S (547.71)
[M+H]+=548
HPLC (Method 9): retention time=1.7 min
C27H36N4O6S (544.66)
[M+H]+=545
HPLC (Method 9): retention time=1.69 min
C26H37N5O5S (531.67)
[M+H]+=532
HPLC (Method 6): retention time=1.56 min
C26H39FN4O5S (538.68)
[M+H]+=539
HPLC (Method 6): retention time=2.60 min
C26H46N4O5S×2HCl (599.65)
[M+H]+=527
HPLC (Method 7): retention time=1.78 min
C26H46N4O5S×2HCl (599.65)
[M+H]+=527
HPLC (Method 7): retention time=1.77 min
C26H36N4O5S (516.65)
[M+H]+=517
HPLC (Method 9): retention time=1.65 min
C25H42N4O6S×C2HF3O2 (640.71)
[M+H]+=527
HPLC (Method 9): retention time=1.55 min
C27H44N4O6S×C2HF3O2 (666.75)
[M+H]+=553
HPLC (Method 9): retention time=1.57 min
C26H44N4O6S×C2HF3O2 (654.74)
[M+H]+=541
HPLC (Method 9): retention time=1.57 min
C27H45N3O5S×C2HF3O2 (637.75)
[M+H]+=524
HPLC (Method 6): retention time=1.71 min
C23H30N4O5S (474.57)
[M+H]+=475
HPLC (Method 9): retention time=1.53 min
C21H35N3O5S (441.59)
[M+H]+=442
HPLC (Method 9): retention time=1.48 min
C28H46N4O6S×C2HF3O2 (680.78)
[M+H]+=567
HPLC (Method 9): retention time=1.60 min
C27H44N4O6S×C2HF3O2 (666.75)
[M+H]+=553
HPLC (Method 9): retention time=1.57 min
C24H40N4O6S×C2HF3O2 (626.69)
[M+H]+=513
HPLC (Method 9): retention time=1.53 min
C30H43N3O6S×CH2O2 (619.77)
[M+H]+=574
HPLC (Method 9): retention time=1.73 min
C31H52N4O5S×C2HF3O2 (706.86)
[M+H]+=593
HPLC (Method 9): retention time=1.34 min
C27H46N4O5S (538.74)
[M+H]+=539
HPLC (Method 9): retention time=1.43 min
C26H44N4O5S×C2HF3O2 (638.74)
[M+H]+=525
HPLC (Method 6): retention time=1.53 min
C26H44N4O5S×C2HF3O2 (638.74)
[M+H]+=525
HPLC (Method 6): retention time=1.41 min
C29H49N3O5S×C2HF3O2 (665.81)
[M+H]+=552
HPLC (Method 9): retention time=1.74 min
C29H41N3O5S (543.72)
[M+H]+=544
HPLC (Method 6): retention time=1.73 min
C26H43N3O5S×C2HF3O2 (623.73)
[M+H]+=510
HPLC (Method 9): retention time=1.63 min
C22H37N3O5S (455.61)
[M+H]+=456
HPLC (Method 6): retention time=1.55 min
C26H44N4O6S (540.72)
[M+H]+=541
HPLC (Method 6): retention time=1.59 min
C27H48N4O5S×2HCl (613.68)
[M+H]+=541
HPLC (Method 7): retention time=1.65 min
C27H48N4O5S×2HCl (613.68)
[M+H]+=541
HPLC (Method 11): retention time=1.64 min
C26H46N4O5S×2C2HF3O2 (754.78)
[M+H]+=527
HPLC (Method 5): retention time=1.16 min
C26H46N4O5S×2HCl (599.65)
[M+H]+=527
HPLC (Method 7): retention time=1.82 min
C26H46N4O5S×2HCl (599.65)
[M+H]+=527
HPLC (Method 7): retention time=1.82 min
C26H44N4O5S×2HCl (597.64)
[M+H]+=525
HPLC (Method 12): retention time=2.3 min
C27H46N4O5S×2HCl (611.67)
[M+H]+=539
DC: silica gel, dichloromethane/methanol/ammonia 8:2:0.2, Rf value=0.65
C27H45N3O5S (523.73)
[M+H]+=524
HPLC (Method 6): retention time=1.29 min
C24H40N4O5S×CH2O2 (542.69)
[M+H]+=497
HPLC (Method 9): retention time=1.25 min
C26H44N4O5S×CH2O2 (570.74)
[M+H]+=525
HPLC (Method 9): retention time=1.31 min
C25H42N4O5S×CH2O2 (556.72)
[M+H]+=511
HPLC (Method 9): retention time=1.31 min
C27H45N3O5S (523.73)
[M+H]+=524
HPLC (Method 6): retention time=1.67 min
C25H44N4O5S×C2HF3O2 (626.73)
[M+H]+=513
HPLC (Method 9): retention time=1.29 min
C28H48N4O5S×2HCl (625.69)
[M+H]+=553
HPLC (Method 9): retention time=1.35 min
C28H48N4O5S×2HCl (625.69)
[M+H]+=553
HPLC (Method 9): retention time=1.32 min
C28H48N4O5S (552.77)
[M+H]+=553
HPLC (Method 9): retention time=1.37 min
C28H48N4O5S×CH2O2 (598.80)
[M+H]+=553
HPLC (Method 9): retention time=1.35 min
C30H43ClN4O5S (607.21)
[M+H]+=608
HPLC (Method 6): retention time=1.80 min
C26H44N4O5S×2HCl (597.64)
[M+H]+=525
HPLC (Method 12): retention time=2.4 min
C26H44N4O5S×2HCl (597.64)
[M+H]+=525
HPLC (Method 12): retention time=2.4 min
C29H48N4O5S×2HCl (637.70)
[M+H]+=565
HPLC (Method 12): retention time=2.3 min
C29H48N4O5S×2HCl (637.70)
[M+H]+=565
HPLC (Method 12): retention time=2.92 min
C26H44N4O5S×2HCl (597.64)
[M+H]+=525
DC: silica gel, dichloromethane/methanol/ammonia 8:2:0.2, Rf value=0.60
C27H46N4O5S×2HCl (611.67)
[M+H]+=539
DC: silica gel, dichloromethane/methanol/ammonia 8:2:0.2, Rf value=0.62
C27H45N3O5S×HCl (560.19)
[M+H]+=524
HPLC (Method 12): retention time=3.01 min
C28H48N4O5S×2HCl (625.69)
[M+H]+=553
HPLC (Method 12): retention time=2.45 min
C25H42N4O5S×2HCl (583.61)
[M+H]+=511
HPLC (Method 12): retention time=2.33 min
C24H42N4O5S×C2HF3O2 (612.70)
[M+H]+=499
HPLC (Method 9): retention time=1.32 min
C25H42N4O5S×2C2HF3O2 (738.74)
[M+H]+=511
HPLC (Method 9): retention time=1.24 min
C25H42N4O5S×2C2HF3O2 (738.74)
[M+H]+=511
HPLC (Method 9): retention time=1.27 min
C28H46N4O5S×CH2O2 (596.78)
[M+H]+=551
HPLC (Method 6): retention time=1.31 min
C26H43N3O5S×C2HF3O2 (623.73)
[M+H]+=510
HPLC (Method 9): retention time=1.62 min
C25H40N4O6S×C2HF3O2 (638.70)
[M+H]+=525
HPLC (Method 9): retention time=1.49 min
C26H42N4O6S×C2HF3O2 (652.72)
[M+H]+=539
HPLC (Method 9): retention time=1.51 min
C26H42N4O6S×C2HF3O2 (652.72)
[M+H]+=539
HPLC (Method 9): retention time=1.52 min
C28H47N3O5S (537.76)
[M+H]+=538
HPLC (Method 9): retention time=1.71 min
C28H48N4O5S (552.77)
[M+H]+=553
HPLC (Method 9): retention time=1.39 min
C28H46N4O5S×CH2O2 (596.78)
[M+H]+=551
HPLC (Method 6): retention time=1.32 min
C26H46N4O5S (526.73)
[M+H]+=527
HPLC (Method 9): retention time=1.27 min
C24H41N3O5S (483.67)
[M+H]+=484
HPLC (Method 6): retention time=1.60 min
C30H50N4O5S×CH2O2 (624.83)
[M+H]+=579
HPLC (Method 6): retention time=1.31 min
C23H36Cl2N4O5S (551.53)
[M+H]+=551/553/555
HPLC (Method 9): retention time=1.30 min
C26H43N3O5S (509.70)
[M+H]+=510
HPLC (Method 6): retention time=1.67 min
C30H50N4O5S×C2HF3O2 (692.83)
[M+H]+=579
HPLC (Method 9): retention time=1.39 min
C30H50N4O5S×C2HF3O2 (692.83)
[M+H]+=579
HPLC (Method 9): retention time=1.39 min
C29H50N4O5S×C2HF3O2 (680.82)
[M+H]+=567
HPLC (Method 9): retention time=1.40 min
C29H49N3O5S (551.78)
[M+H]+=552
HPLC (Method 9): retention time=1.72 min
C28H46N4O6S×C2HF3O2 (680.78)
[M+H]+=567
HPLC (Method 9): retention time=1.60 min
C29H50N4O5S×C2HF3O2 (680.82)
[M+H]+=567
HPLC (Method 9): retention time=1.41 min
C27H45N3O5S×C2HF3O2 (637.75)
[M+H]+=524
HPLC (Method 9): retention time=1.69 min
C29H48N4O5S×2HCl (637.70)
[M+H]+=565
HPLC (Method 12): retention time=2.4 min
C27H44N4O6S×C2HF3O2 (666.75)
[M+H]+=553
HPLC (Method 9): retention time=1.61 min
C26H42N4O6S×C2HF3O2 (652.72)
[M+H]+=539
HPLC (Method 9): retention time=1.60 min
C26H42N4O6S (538.70)
[M+H]+=539
HPLC (Method 9): retention time=1.47 min
C25H40N4O6S (524.67)
[M+H]+=525
HPLC (Method 9): retention time=1.48 min
C26H44N4O5S (524.72)
[M+H]+=525
HPLC (Method 9): retention time=1.30 min
C27H46N4O5S (538.74)
[M+H]+=539
HPLC (Method 9): retention time=1.34 min
C28H46N4O5S×2HCl (623.68)
[M+H]+=551
DC: silica gel, dichloromethane/methanol/ammonia 8:2:0.2, Rf value=0.71
C27H44N4O6S×C2HF3O2 (666.75)
[M+H]+=553
HPLC (Method 9): retention time=1.62 min
C26H44N4O5S×2C2HF3O2 (752.76)
[M+H]+=525
HPLC (Method 9): retention time=1.33 min
C26H42N4O6S×C2HF3O2 (652.72)
[M+H]+=539
HPLC (Method 9): retention time=1.50 min
C25H44N4O5S (512.71)
[M+H]+=513
HPLC (Method 9): retention time=1.27 min
C28H47N3O5S×C2HF3O2 (651.78)
[M+H]+=538
HPLC (Method 9): retention time=1.71 min
C27H46N4O5S (538.74)
[M+H]+=539
HPLC (Method 9): retention time=1.37 min
C27H46N4O5S (538.74)
[M+H]+=539
HPLC (Method 9): retention time=1.44 min
C25H43N3O6S×HCl (550.15)
[M+H]+=514
HPLC (Method 5): retention time=1.34 min
C29H50N4O5S×2HCl (639.72)
[M+H]+=567
HPLC (Method 5): retention time=1.21 min
C29H50N4O5S×2HCl (639.72)
[M+H]+=567
HPLC (Method 5): retention time=1.20 min
C32H54N4O5S×C2HF3O2 (720.88)
[M+H]+=607
HPLC (Method 9): retention time=1.37 min
C26H44N4O5S×2C2HF3O2 (752.76)
[M+H]+=525
HPLC (Method 9): retention time=1.41 min
C25H44N4O5S (512.71)
[M+H]+=513
HPLC (Method 9): retention time=1.35 min
C28H48N4O5S×2C2HF3O2 (780.82)
[M+H]+=553
HPLC (Method 9): retention time=1.40 min
C26H43N3O5S (509.70)
[M+H]+=510
HPLC (Method 9): retention time=1.70 min
C27H45N3O6S×HCl (576.19)
[M+H]+=540
HPLC (Method 5): retention time=1.37 min
C25H43N3O6S×HCl (550.15)
[M+H]+=514
HPLC (Method 5): retention time=1.36 min
C27H45N3O6S×HCl (576.19)
[M+H]+=540
HPLC (Method 5): retention time=1.38 min
C27H47N3O5S×HCl (562.21)
[M+H]+=526
HPLC (Method 4): retention time=3.0 min
C28H47N3O5S×HCl (574.22)
[M+H]+=538
HPLC (Method 4): retention time=3.1 min
C26H44N4O5S (524.72)
[M+H]+=525
HPLC (Method 9): retention time=1.32 min
C27H46N4O5S (538.74)
[M+H]+=539
HPLC (Method 9): retention time=1.57 min
C27H45N3O6S (539.73)
[M+H]+=540
HPLC (Method 9): retention time=1.65 min
C25H43N3O5S (497.69)
[M+H]+=498
HPLC (Method 9): retention time=1.65 min
C28H47N3O5S×HCl (574.22)
[M+H]+=538
HPLC (Method 9): retention time=1.68 min
C25H41N3O5S×C2HF3O2 (609.70)
[M+H]+=496
HPLC (Method 9): retention time=1.62 min
C27H44N4O6S×C2HF3O2 (666.76)
[M+H]+=553
HPLC (Method 9): retention time=1.57 min
C26H44N4O6S×C2HF3O2 (654.75)
[M+H]+=541
HPLC (Method 9): retention time=1.56 min
C26H43N5O6S×C2HF3O2 (667.74)
[M+H]+=554
HPLC (Method 9): retention time=1.00 min
C27H45N5O6S×C2HF3O2 (681.77)
[M+H]+=568
HPLC (Method 9): retention time=1.03 min
C24H40N4O6S×C2HF3O2 (626.69)
[M+H]+=513
HPLC (Method 9): retention time=1.50 min
C26H42N4O6S×C2HF3O2 (654.72)
[M+H]+=539
HPLC (Method 9): retention time=1.55 min
C25H42N4O6S×C2HF3O2 (640.71)
[M+H]+=527
HPLC (Method 9): retention time=1.63 min
C27H44N4O6S (552.73)
[M+H]+=553
HPLC (Method 9): retention time=1.65 min
C28H47N3O6S×HCl (590.22)
[M+H]+=554
HPLC (Method 5): retention time=1.44 min
C27H44N4O6S×C2HF3O2 (666.75)
[M+H]+=553
HPLC (Method 9): retention time=1.59 min
C27H44N4O6S×C2HF3O2 (666.75)
[M+H]+=553
HPLC (Method 9): retention time=1.61 min
C26H44N4O6S×C2HF3O2 (590.22)
[M+H]+=541
HPLC (Method 9): retention time=1.56 min
C27H44N4O6S×C2HF3O2 (666.75)
[M+H]+=553
HPLC (Method 9): retention time=1.55 min
C26H42N4O6S×C2HF3O2 (652.72)
[M+H]+=539
HPLC (Method 9): retention time=1.55 min
C25H38F3N3O4S (533.66)
[M+H]+=534
C25H38F3N3O4S (533.66)
[M+H]+=534
C24H37Cl2N3O4S (534.55)
[M+H]+=535
C25H37ClF3N3O4S (568.10)
[M+H]+=569
The following compounds wurden analogously to Example 121 prepared:
C25H34N4O5S×C2HF3O2 (616.65)
[M+H]+=503
HPLC (Method 6): retention time=2.30 min
C25H36N4O5S×HCl (541.10)
[M+H]+=505
HPLC (Method 5): retention time=1.49 min
C28H39FN4O5S×C2HF3O2 (676.72)
[M+H]+=563
HPLC (Method 5): retention time=1.55 min
C26H36N4O5S×HCl (553.11)
[M+H]+=517
HPLC (Method 11): retention time=1.73 min
C25H34N4O5S×C2HF3O2 (616.65)
[M+H]+=503
HPLC (Method 5): retention time=1.49 min
C27H36N4O5S×C2HF3O2 (642.69)
[M+H]+=529
HPLC (Method 5): retention time=1.50 min
C27H38N4O5S×C2HF3O2 (644.70)
[M+H]+=531
HPLC (Method 5): retention time=1.54 min
C26H36N4O6S×C2HF3O2 (646.68)
[M+H]+=533
HPLC (Method 5): retention time=1.51 min
C27H41N5O5S×HCl (584.17)
[M+H]+=548
HPLC (Method 5): retention time=1.53 min
C26H39N5O5S×HCl (570.15)
[M+H]+=534
HPLC (Method 5): retention time=1.52 min
C26H38N4O5S×HCl (555.13)
[M+H]+=519
HPLC (Method 5): retention time=1.51 min
C26H33N5O5S (527.64)
[M+H]+=528
HPLC (Method 4): retention time=3.0 min
C28H40N4O5S×HCl (581.17)
[M+H]+=545
HPLC (Method 4): retention time=3.1 min
C26H36N4O5S×HCl (553.11)
[M+H]+=517
HPLC (Method 5): retention time=1.48 min
C28H41N5O5S×HCl (596.18)
[M+H]+=560
HPLC (Method 5): retention time=1.52 min
C28H41N5O5S×HCl (596.18)
[M+H]+=560
HPLC (Method 5): retention time=1.52 min
C29H43N5O5S×HCl (610.21)
[M+H]+=574
HPLC (Method 5): retention time=1.57 min
C27H44N4O5S×HCl (573.19)
[M+H]+=537
DC: silica gel, dichloromethane/methanol/ammonia 8:2:0.01, Rf value=0.66
C27H38N4O5S×HCl (567.14)
[M+H]+=531
HPLC (Method 4): retention time=3.0 min
C28H40N4O5S×HCl (581.17)
[M+H]+=545
DC: silica gel, dichloromethane/methanol 9:1, Rf value=0.18
C28H41N5O5S×HCl (596.18)
[M+H]+=560
DC: silica gel, ethyl acetate/methanol/ammonia 9:1:0.1, Rf value=0.42
C27H38N6O5S (558.69)
[M+H]+=559
HPLC (Method 6): retention time=2.23 min
C28H39N5O5S (557.71)
[M+H]+=558
HPLC (Method 6): retention time=2.35 min
C26H38ClN5O5S×CH2O2 (614.16)
[M+H]+=568/570
HPLC (Method 6): retention time=2.55 min
C27H40N4O6S (548.70)
[M+H]+=549
HPLC (Method 6): retention time=2.49 min
C25H43N5O5S (525.71)
[M+H]+=526
HPLC (Method 6): retention time=1.85 min
C30H43N5O5S (585.76)
[M+H]+=586
HPLC (Method 6): retention time=2.66 min
C27H38N4O5S (530.68)
[M+H]+=531
HPLC (Method 6): retention time=2.52 min
C27H41N5O5S (547.71)
[M+H]+=548
HPLC (Method 6): retention time=2.44 min
C26H37ClN4O6S (569.11)
[M+H]+=570
HPLC (Method 6): retention time=2.56 min
C24H41N5O5S (511.68)
[M+H]+=512
HPLC (Method 6): retention time=1.80 min
C28H40ClN5O5S (594.17)
[M+H]+=594/596
HPLC (Method 6): retention time=2.68 min
C27H35N5O6S (557.66)
[M+H]+=558
HPLC (Method 6): retention time=2.51 min
C28H40N4O6S (560.71)
[M+H]+=561
HPLC (Method 6): retention time=2.51 min
C25H31N5O5S (513.61)
[M+H]+=514
HPLC (Method 6): retention time=2.35 min
C27H39N5O5S×C2HF3O2 (659.72)
[M+H]+=546
HPLC (Method 6): retention time=2.44 min
C23H30N6O5S (502.59)
[M+H]+=503
HPLC (Method 6): retention time=2.37 min
C27H39N5O5S×C2HF3O2 (659.72)
[M+H]+=546
HPLC (Method 6): retention time=2.52 min
C28H41N5O5S×C2HF3O2 (673.75)
[M+H]+=560
HPLC (Method 6): retention time=2.58 min
C28H39N5O5S×C2HF3O2 (671.73)
[M+H]+=558
HPLC (Method 6): retention time=2.57 min
C27H38N4O5S×C2HF3O2 (644.70)
[M+H]+=531
HPLC (Method 6): retention time=2.45 min
C26H40N6O5S (548.70)
[M+H]+=549
HPLC (Method 6): retention time=2.52 min
C29H43N5O5S×C2HF3O2 (687.77)
[M+H]+=574
HPLC (Method 6): retention time=2.72 min
C30H43N5O5S (585.76)
[M+H]+=586
HPLC (Method 6): retention time=2.70 min
C25H38N6O5S×CH2O2 (580.70)
[M+H]+=535
HPLC (Method 6): retention time=2.16 min
C27H35N5O5S×C2HF3O2 (655.69)
[M+H]+=542
HPLC (Method 6): retention time=2.48 min
C28H41N5O5S×C2HF3O2 (673.75)
[M+H]+=560
HPLC (Method 6): retention time=2.61 min
C21H29N5O5S (463.55)
[M+H]+=464
HPLC (Method 9): retention time=1.47 min
C26H33N5O5S (527.64)
[M+H]+=528
HPLC (Method 9): retention time=1.60 min
C29H40N6O5S (584.73)
[M+H]+=585
HPLC (Method 9): retention time=1.37 min
C24H32N6O5S×C2HF3O2 (630.64)
[M+H]+=517
HPLC (Method 9): retention time=1.58 min
C24H32N6O5S×C2HF3O2 (630.64)
[M+H]+=517
HPLC (Method 9): retention time=1.57 min
C27H44N4O5S×C2HF3O2 (650.75)
[M+H]+=537
HPLC (Method 9): retention time=1.68 min
C26H45N5O5S×2HCl (612.65)
[M+H]+=540
HPLC (Method 5): retention time=1.39 min
C28H40N4O5S×C2HF3O2 (658.73)
[M+H]+=545
HPLC (Method 5): retention time=1.53 min
C26H38N4O6S×C2HF3O2 (648.69)
[M+H]+=535
HPLC (Method 5): retention time=1.43 min
C28H40N4O6S (560.71)
[M+H]+=561
HPLC (Method 5): retention time=1.50 min
C26H40N6O5S (548.70)
[M+H]+=549
HPLC (Method 5): retention time=1.39 min
C29H43N5O5S×HCl (610.21)
[M+H]+=574
HPLC (Method 7): retention time=1.88 min
C29H42N4O5S×C2HF3O2 (672.76)
[M+H]+=559
HPLC (Method 5): retention time=1.55 min
C25H38N6O5S×2HCl (607.59)
[M+H]+=535
HPLC (Method 5): retention time=1.39 min
C30H45N5O5S×C2HF3O2 (701.80)
[M+H]+=588
HPLC (Method 5): retention time=1.55 min
C28H40N4O5S×HCl (581.17)
[M+H]+=545
HPLC (Method 4): retention time=3.3 min
C27H45N5O5S×2HCl (624.66)
[M+H]+=552
DC: silica gel, dichloromethane/methanol/ammonia 8:2:0.01, Rf value=0.25
C26H43N5O5S×HCl (574.18)
[M+H]+=538
DC: silica gel, dichloromethane/methanol/ammonia 8:2:0.01, Rf value=0.10
C29H43N5O5S×HCl (610.21)
[M+H]+=574
DC: silica gel, dichloromethane/methanol 9:1, Rf value=0.25
C31H44N4O5S×HCl (621.23)
[M+H]+=585
HPLC (Method 12): retention time=3.0 min
C28H43N5O5S×HCl (598.20)
[M+H]+=562
DC: silica gel, dichloromethane/methanol 9:1, Rf value=0.14
C29H42N4O5S×HCl (595.19)
[M+H]+=559
DC: silica gel, dichloromethane/methanol/ammonia 9:1:0.1, Rf value=0.32
C28H40N4O6S (560.71)
[M+H]+=561
HPLC (Method 9): retention time=1.66 min
C27H35N5O6S (557.66)
[M+H]+=558
HPLC (Method 9): retention time=1.64 min
C26H38FN5O5S (551.68)
[M+H]+=552
HPLC (Method 6): retention time=2.30 min
C26H36N6O5S (544.67)
[M+H]+=545
HPLC (Method 6): retention time=1.48 min
C26H35N5O5S (529.65)
[M+H]+=530
HPLC (Method 9): retention time=1.61 min
C23H29N5O5S (487.57)
[M+H]+=488
HPLC (Method 9): retention time=1.53 min
C27H47N5O5S×2HCl (626.68)
[M+H]+=554
HPLC (Method 7): retention time=1.61 min
C27H47N5O5S×2HCl (626.68)
[M+H]+=554
HPLC (Method 7): retention time=1.61 min
C28H47N5O5S×CH2O2 (611.80)
[M+H]+=566
HPLC (Method 9): retention time=1.33 min
C25H41N5O5S×2HCl (596.61)
[M+H]+=524
HPLC (Method 12): retention time=2.3 min
C26H43N5O5S×2HCl (610.64)
[M+H]+=538
DC: silica gel, dichloromethane/methanol/ammonia 8:2:0.2, Rf value=0.53
C29H42N4O5S×HCl (595.19)
[M+H]+=559
HPLC (Method 12): retention time=2.8 min
C26H38N4O5S×C2HF3O2 (632.69)
[M+H]+=519
HPLC (Method 9): retention time=1.61 min
C29H40N4O5S (556.72)
[M+H]+=557
HPLC (Method 9): retention time=1.69 min
C30H42N4O6S (586.74)
[M+H]+=587
HPLC (Method 9): retention time=1.74 min
C29H49N5O5S×2HCl (652.72)
[M+H]+=580
HPLC (Method 10): retention time=1.11 min
C30H51N5O5S×2HCl (666.74)
[M+H]+=594
HPLC (Method 10): retention time=1.11 min
C29H42N4O5S×HCl (595.19)
[M+H]+=559
HPLC (Method 12): retention time=3.1 min
C29H42N4O5S×HCl (595.19)
[M+H]+=559
DC: silica gel, dichloromethane/methanol/ammonia 8:2:0.01, Rf value=0.68
C27H44N4O6S×HCl (589.19)
[M+H]+=553
HPLC (Method 5): retention time=1.35 min
C25H42N4O6S×HCl (563.15)
[M+H]+=527
HPLC (Method 5): retention time=1.38 min
C27H44N4O6S×HCl (589.19)
[M+H]+=553
HPLC (Method 5): retention time=1.35 min
C25H42N4O6S×HCl (563.15)
[M+H]+=527
HPLC (Method 5): retention time=1.32 min
The following compounds were prepared analogously to Example 130:
C26H44N4O4S×2C2HF3O2 (736.76)
[M+H]+=509
HPLC (Method 6): retention time=1.36 min
C28H41N3O4S×C2HF3O2 (629.73)
[M+H]+=516
HPLC (Method 6): retention time=1.77 min
The following compounds were prepared analogously to Example 136:
C25H42N4O4S2×C2HF3O2 (640.78)
[M+H]+=527
HPLC (Method 6): retention time=1.35 min
C27H39N3O4S2 (533.75)
[M+H]+=534
HPLC (Method 6): retention time=1.74 min
The following compound was prepared analogously to Example 138:
C26H38N4O5S×CH2O2 (564.70)
[M+H]+=519
HPLC (Method 6): retention time=2.33 min
572a)
A mixture of 88.0 mg (0.167 mmol) of 569, 0.15 g (0.61 mmol) of 70% m-chloroper-benzoic acid (Fluka) and 3 ml dichloromethane is stirred for 30 minutes at ambient temperature and then evaporated to dryness in vacuo. The residue is dissolved in methanol and membrane-filtered. The product is then obtained by preparative HPLC from the filtrate.
C25H42N4O8S2 (590.76)
[M+H]+=591
572b)
A mixture of 90.0 mg (0.15 mmol) of the product of 572a, 20.0 mg Raney nickel and 10 ml THF is stirred for one hour in the autoclave at ambient temperature. Then the catalyst is filtered off and the filtrate is evaporated to dryness in vacuo. The crude product thus obtained is purified by preparative HPLC.
C25H42N4O6S2×CH2O2 (604.78)
[M+H]+=559
HPLC (Method 6): retention time=1.33 min
573a)
573a is prepared analogously to 1f from 2.16 g (7.50 mmol) of the product of 121b, 1.20 g (7.50 mmol) of N-Boc-ethylenediamine (Fluka), 3.14 ml (22.50 mmol) of triethylamine and 2.41 g (7.50 mmol) of TBTU in 28 ml THF and 4 ml DMF.
C19H31N3O6S (429.53)
DC: silica gel, dichloromethane/ethanol 19:1, Rf value=0.35
573b)
573b is prepared analogously to 28d from 2.70 g (6.29 mmol) of the product of 573a and 7 ml TFA in 50 ml dichloromethane.
C14H23N3O4S (329.42)
DC: silica gel, dichloromethane/ethanol 9:1, Rf value=0.15
573c)
Example 573 is prepared analogously to 1f from 0.119 g (0.50 mmol) of 4-(2-diethylaminoethoxy)-benzoic acid (J. Med. Chem. 14, 1971, 836-842), 0.165 g (0.50 mmol) of the product of 573b, 0.21 ml (1.50 mmol) of triethylamine and 0.16 g (0.50 mmol) of TBTU in 7 ml THF and 1 ml DMF.
C27H40N4O6S×HCl (585.16)
HPLC (Method 5): retention time=1.44 min
The following compounds were prepared analogously to Example 573:
C26H36N4O5S×HCl (553.11)
[M+H]+=517
HPLC (Method 5): retention time=1.40 min
C28H40N4O5S×HCl (581.17)
[M+H]+=545
HPLC (Method 12): retention time=3.51 min
635a)
A mixture of 0.78 g (4.98 mmol) of monomethylmalonate potassium salt (Fluka), 0.52 g (5.47 mmol) of magnesium chloride and 30 ml THF is stirred for four hours at 50° C. A second mixture of 1.00 g (3.32 mmol) of the product of 22c, 0.65 g (3.98 mmol) of CDI and 20 ml THF is stirred first for one hour at RT and then added to the first mixture. The mixture is stirred overnight at RT and then the precipitate formed is filtered off. The filtrate is evaporated to dryness in vacuo. The crude product thus obtained is triturated with water, filtered off and dried at 45° C. in the vacuum dryer.
C16H23NO6S (357.42)
[M+H]+=358
HPLC (Method 9): retention time=2.19 min
635b)
635b is prepared analogously to 60a from 0.47 ml (4.07 mmol) of 1-methyl-4-piperidone (Fluka), 0.76 g .(4.07 mmol) of (R)-3-(Boc-amino)-pyrrolidine (Fluka), 1.72 g (8.13 mmol) of sodium triacetoxyborohydride and 0.23 ml (4.07 mmol) of acetic acid in 10 ml dichloromethane.
C15H29N3O2 (283.41)
[M+H]+=284
635c)
635c is prepared analogously to 38f from 0.90 g (3.18 mmol) of the product of 635b and 5.0 ml (10.00 mmol) of lithium aluminium hydride (2M in THF) in 15 ml THF.
C11H23N3 (197.32)
[M+H]+=198
635d)
A mixture of 0.56 g (1.58 mmol) of the product of 635a, 0.54 g (2.73 mmol) of the product of 635c and 5 ml of toluene is heated to 120° C. for 24 hours. Then the reaction mixture is evaporated to dryness in vacuo. The crude product thus obtained is purified by preparative HPLC.
C26H42N4O5S (522.70)
[M+H]+=523
HPLC (Method 9): retention time=1.33 min
The following Examples describe pharmaceutical formulations which contain as active substance any desired compound of general formula I:
Active compound and mannitol are dissolved in water. The charged ampoules are freeze dried. Water for injection is used to dissolve to give the solution ready for use.
(1), (2) and (3) are mixed and granulated with an aqueous solution of (4). (5) is admixed to the dry granules. Tablets are compressed from this mixture, biplanar with a bevel on both sides and dividing groove on one side.
Diameter of the tablets: 9 mm.
(1), (2) and (3) are mixed and granulated with an aqueous solution of (4). (5) is admixed to the dry granules. Tablets are compressed from this mixture, biplanar with a bevel on both sides and dividing groove on one side.
Diameter of the tablets: 12 mm.
(1) is triturated with (3). This trituration is added to the mixture of (2) and (4) with vigorous mixing.
This powder mixture is packed into hard gelatine two-piece capsules of size 3 in a capsule-filling machine.
(1) is triturated with (3). This trituration is added to the mixture of (2) and (4) with vigorous stirring.
This powder mixture is packed into hard gelatine two-piece capsules of size 0 in a capsule-filling machine.
| Number | Date | Country | Kind |
|---|---|---|---|
| 102006039003 | Aug 2006 | DE | national |
