Patent Application
20120149908
In a first aspect, the present invention relates to a method for the preparation of alkynylpiperidine and alkynylpiperidine derivatives. In particular, a method is provided for preparing alkynylpiperidine derivatives starting from epoxide compounds. Further, the alkynylpiperidine derivatives according to the present inventions are substituted trans-3,4-alkynylpiperidine derivatives. In another aspect, triazolylpiperidine compounds and methods for said preparation are provided. In particular, the triazolylpiperidine compounds according to the present invention are obtained by reacting an alkynylpiperidine derivative with an organic azide, preferably, in the presence of a Cu (I) or Ru catalyst. In a preferred embodiment, 1,4-disubstituted or 1,5-disubstituted 1,2,3-triazolylpiperidine compounds are provided.
Piperidine moieties are considered as one of the privileged structures in medicinal chemistry. These are small molecules capable of providing high affinity ligands for multiple receptors and enzymes (Mason, J. S. et. al., J Med Chem 1999, 42, (17), 3251-3264; Costantino, L. et. al., Curr Med Chem 2006, 13, (1), 65-85) and of these structures the piperidine ring is among the most common heterocycles occurring in pharmaceuticals. The vast number of substituted piperidine derivatives among biologically active compounds has motivated the development of a multitude of synthetic routes towards these structures, and these endeavours have yielded new routes to already known piperidines and also provided medicinal chemists with new building blocks e.g. Schramm, H. et. al., Synthesis 2009, (10), 1659-1662; Schramm, H. et. al., Eur J Org Chem 2010, 2010, (9), 1745-1753. In recent years, numerous reports on the facile and regioselective synthesis of disubstituted 1,2,3-triazoles from terminal alkynes and organic azides have appeared in the literature.
There is still an ongoing need for new piperidine derivatives, thus, providing useful scaffolds for pharmaceutically active compounds, e.g. having high affinity to receptors and enzymes as described for known piperidine compounds in the art.
Hence, one object of the present invention is to provide new methods and compounds based on a piperidine scaffold, in particular, providing alkynylpiperidine derivatives useful as intermediate compounds and starting material for the preparation of optionally substituted triazolylpiperidine derivatives. In another aspect, the object of the present invention is to provide new optionally substituted triazolylpiperidine compounds useful as scaffolds for new active pharmaceutical ingredients.
In a first aspect, the present invention relates to a compound of the general formula I
wherein R1 is hydrogen or a protecting group,
R2 and R3 are independently from each other hydrogen or a protection group, or an C1-C18 alkyl group, a C2-C18 alkenyl group, a C3-C18 aryl group, a C3-C18 heteroalkyl group, an aralkyl group, an arylalkyl group, an aryl group, an heteroarylalkyl group, an alkoxy group, an acyl group, like a carbonylalkyl group or a carbonylaryl group, all of said groups may be substituted with at least one substituent independently selected from the group of C1-C6 alkyl, C2-C6 alkenyl, halogen, CN, NO2, C1-C6 alkoxy, hydroxyl, carbamoyl, C1 to C8 alkylcarbamoyl, amido, C1-C6 alkoxycarbonyl, C1-C6 alkylcarbamoyloxy, C1-C6 alkoxycarbonylamino, amino, C1-C6 alkanoyloxy group, C1-C6 alkylthio and sulphur-containing analogs of oxygen containing substituents, preferably, R1 and R2 are not hydrogen at the same time, with the proviso that R1 and R2 are not hydrogen at the same time when the substituents at position 3 and position 4 of the piperidine ring are in cis-form.
In a preferred embodiment, the alkynylpiperidine derivative of general formula I is an ethynylpiperidine derivative wherein substituent R1 is hydrogen.
In another aspect, the present invention provides a method for the synthesis of a compound according to general formula I including the step of reacting an epoxide according to general formula II
In another aspect, an optionally substituted triazolylpiperidine compound of general formulas III or IV are provided. The compound of general formula III is a 1,4-disubstituted 1,2,3-triazolylpiperidine compound whereas general formula IV represents a substituted 1,5-disubstituted 1,2,3-triazolylpiperidine derivative.
In another aspect, the present invention provides a method for producing an optionally substituted triazolylpiperidine according to general formula III or IV according to the present invention. Said method comprising the step of reacting a compound of general formula I with an organic azide derivative to obtain a compound of general formula III or IV.
In
In
In
In a first aspect, the present invention relates to a compound of general formula I
wherein R1 is hydrogen or a protecting group,
R2 and R3 are independently from each other hydrogen or a protection group, or an C1-C18 alkyl group, a C2-C18 alkenyl group, a C3-C18 aryl group, a C3-C18 heteroalkyl group, an aralkyl group, an arylalkyl group, an aryl group, an heteroarylalkyl group, an alkoxy group, an acyl group, like a carbonylalkyl group or a carbonylaryl group, all of said groups may be substituted with at least one substituent independently selected from the group of C1-C6 alkyl, C2-C6 alkenyl, halogen, CN, NO2, C1-C6 alkenyl, hydroxyl, carbamoyl, C1 to C8 alkylcarbamoyl, amido, alkoxy, alkoxycarbonyl, alkylcarbamoyloxy, alkoxycarbonylamino, amino, alkanoyloxy group, alkylthio and sulphur-containing analogs of oxygen containing substituents, preferably, R1 and R2 are not hydrogen at the same time, with the proviso that R1 and R2 are not hydrogen at the same time when the substituents at position 3 and position 4 of the piperidine ring are in cis-form.
The term “C1 to 018” as used herein include compounds having C1, C2, C3, C4, C5, C6, C7, C8, C9, C10, C11, C12, C13, C14, C15, C16, C17, or C18 carbon atoms. The term “C1 to C6” include C1, C2, C3, C4, C5, C6 carbon atoms. The term “C2 to C6” include, C2, C3, C4, C5, C6 carbon atoms. The groups may be present in linear, branched or cyclic form.
“Alkyl” refers to a saturated aliphatic hydrocarbon including straight chain and branched chain groups. “Alkyl” may be exemplified by groups such as methyl, ethyl, n-propyl, isopropyl, n-butyl and the like. Alkyl groups may be substituted or unsubstituted. Substituents may also be themselves substituted. When substituted, the substituent group is preferably, but not limited to, C1-C4 alkyl, aryl, amino, cyano, halogen, alkoxy or hydroxyl.
“Alkenyl” refers to an unsaturated aliphatic hydrocarbon moiety including straight chain and branched chain groups. Alkenyl moieties contain at least one alkene. “Alkenyl” may be exemplified by groups such as ethenyl, n-propenyl, isopropenyl, n-butenyl and the like. Alkenyl groups may be substituted or unsubstituted. Substituents may also be themselves substituted. When substituted, the substituent group is preferably, but not limited to alkyl, halogen or alkoxy. Substituents may also be themselves substituted. Substituents may be located on the alkene itself and also on the adjacent member atoms of the alkenyl moiety.
“Alkynyl” refers to an unsaturated aliphatic hydrocarbon moiety including straight chain and branched chain groups. Alkynyl moieties contain at least one alkyne. “Alkynyl” may be exemplified by groups such as ethynyl, propynyl, n-butynyl and the like. Alkynyl groups may be substituted or unsubstituted. When substituted, the substituent group is preferably alkyl, amino, cyano, halogen, alkoxyl or hydroxyl. Substituents may also be themselves substituted. Substituents are not on the alkyne itself but on the adjacent member atoms of the alkynyl moiety.
“Acyl” or “carbonyl” refers to the group —C(O)R wherein R is H, alkyl, alkenyl, alkynyl, aryl, heteroaryl, carbocyclic, heterocarbocyclic, C1-C4 alkyl aryl or C1-C4 alkyl heteroaryl.
“Alkoxy” refers to the group —O—R wherein R is acyl, alkyl alkenyl, alkyl alkynyl, aryl, carbocyclic, heterocarbocyclic, heteroaryl, C1-C4 alkyl aryl or C1-C4 alkyl heteroaryl.
“Aralkyl” refers to a radical in which an aryl group is substituted for a hydrogen atom of an alkyl group; e.g., C6H5CH2—.
“Amino” refers to the group —NR′R″ wherein R′ and R″ are each, independently, hydrogen, alkyl, aryl, heteroaryl, C1-C4 alkyl aryl or C1-C4 alkyl heteroaryl. The R′ and R″ groups may themselves be linked to form a ring.
“Aryl” refers to an aromatic carbocyclic group. “Aryl” may be exemplified by phenyl. The aryl group may be substituted or unsubstituted. Substituents may also be themselves substituted. When substituted, the substituent group is preferably, but not limited to, alkyl, alkoxy, heteroaryl, acyl, carboxyl, carbonylamino, nitro, amino, cyano, halogen or hydroxyl. The substituents may be positioned at various locations on an aryl group. For example, substituents on a phenyl group may be located at an ortho-position, a meta-position, the para-position, or combinations thereof.
“Carboxyl” refers to the group —C(═O)OR, where R is a C1-C4 alkyl, aryl, The alkyl or aryl group may be substituted or unsubstituted. Substituents may also be themselves substituted. When substituted, the substituent group is preferably, but not limited to, alkyl, alkoxy, heteroaryl, acyl, carboxyl, carbonylamino, nitro, amino, cyano, halogen or hydroxyl. The substituents may be positioned at various locations on an aryl group.
“Carbonyl” refers to the group —C(O)R wherein each R is, independently, hydrogen, alkyl, aryl, cycloalkyl, heterocycloalkyl, heteroaryl, C1-C4 alkyl aryl or C1-C4 alkyl heteroaryl.
“Heteroaryl” or “heteroaromatic” refers to a monocyclic or bicyclic aromatic carbocyclic radical having one or more heteroatoms in the carbocyclic ring. Heteroaryl may be substituted or unsubstituted. When substituted, the substituents may themselves be substituted. Preferred, but non-limiting substituents, are aryl, C1-C4 alkyl aryl, amino, halogen, hydroxyl, cyano, nitro, carboxyl, carbonylamino or C1-C4 alkyl. Preferred heteroaromatic groups include tetrazoyl, thiazolyl, thienyl, thiophenyl, thiazolyl, purinyl, pyrimidyl, pyridyl, and furanyl. More preferred heteroaromatic groups include benzothiofuranyl, thiophenyl, thienyl, furanyl, tetrazoyl, triazolyl, and pyridyl.
“Heteroatom” means an atom other than carbon in the ring of a heterocyclic group or a heteroaromatic group or the chain of a heterogeneous group. Preferably, heteroatoms are selected from the group consisting of nitrogen, sulfur, phosphor and oxygen atoms. Groups containing more than one heteroatom may contain different heteroatoms.
“Heterocarbocyclic group” or “heterocycloalkyl” or “heterocyclic” means a monovalent saturated or unsaturated hydrocarbon ring containing at least one heteroatom. Heterocarbocyclic groups are monocyclic, or are fused, spiro, or bridged bicyclic ring systems. Monocyclic heterocarbocyclic groups contain 3 to 10 carbon atoms, preferably 4 to 7 carbon atoms, and more preferably 5 to 6 carbon atoms in the ring. Bicyclic heterocarbocyclic groups contain 8 to 12 carbon atoms, preferably 9 to 10 carbon atoms in the ring. Heterocarocyclic groups may be substituted or unsubstituted. Suitable substituents include, but are not limited to, lower alkyl, hydroxyl, nitrile, halogen and amino. Substituents may also be themselves substituted. Preferred heterocarbocyclic groups include epoxy, tetrahydrofuranyl, azacyclopentyl, azacyclohexyl, piperidyl, and homopiperidyl. More preferred heterocarbocyclic groups include piperidyl, and homopiperidyl. The most preferred heterocarbocyclic group is piperidyl. Heterocarbocyclic groups are not aromatic.
“Thioalkyl” refers to the group —S-alkyl.
That is, the present inventors were successful in obtaining compounds of the general formula I which represents useful as starting material and intermediates in the preparation of substituted piperidine derivatives, like triazolyl-substituted piperidine derivatives. In a preferred embodiment, the substituent R1 is hydrogen and R2 and R3 are different protection groups. For example, R1 is hydrogen and R2 is a silyl protecting group while R3 is a carbamate protecting group, preferably a tert-butoxycarbonyl group, or a sulfonamide group, or any other suitable amine protecting group described in the art.
The term “protecting group” refers to a group used to protect a certain functional group in a chemical synthesis as described in the art (P. J. Kocienski, Protecting groups, ISBN 9783131356031, Thieme publishing group), preferred protecting groups according to the present invention include tert-butoxycarbonyl, benzyloxycarbonyl, tosyl, nosyl, trimethylsilyl, dimethyl-tert-butylsilyl, carbobenzyloxy group, etc. When more than one protecting groups are present in the compounds, it is preferred that the protecting groups are different from each other.
The compounds of the general formula I are useful as intermediates in the production of triazolyl-substituted piperidine compounds.
The compound of the general formula I may be prepared as shown in
That is, as a starting material an epoxide derivative of a piperidine compound as shown in general formula II
is used as a starting material. Therein, R3 represents a protection group. The epoxide is reacted with a protected acetylide derivative, which is prepared by deprotonating a protected acetylene derivative using an alkyllithium compound, a Grignard Reagent, a lithium dialkylamide or hexamethyldisilazide, preferably n-BuLi, in the presence of a trialkylaluminium reagent, preferably AlMe3. Thereafter, the reaction mixture is cooled at a temperature below room temperature, preferably at −78° C.
With the term “protected acetylene derivative” is meant an acetylene derivative where one of the hydrogen atoms of acetylene is substituted with a protecting group like trimethylsilyl.
In a next step the epoxide is activated with a Lewis acid, preferably, BF3×OEt2, thus, allowing a ring opening in order to obtain a compound of general formula I wherein R2 is hydrogen.
That is, nucleophilic ring opening of an epoxide of general formula II can afford two different regioisomers, depending on the reagents and conditions used. Under neutral or basic conditions, formation of a 1:1 mixture of isomers is expected. However, if the reaction is carried out under acidic conditions, the formation of a cationic intermediate has been invoked to enhance the directing effect of the nitrogen atom of the piperidine ring. As a consequence the nucleophile will attack position 4 of the piperidine ring and afford only one regioisomer. By using a Lewis acid to coordinate the epoxide oxygen, thereby creating a cationic intermediate, the ethynyl nucleophile could be directed towards the 4-position of the piperidine. Thus, it is possible to synthesize specifically trans 3,4-disubstituted piperidine derivatives. In a preferred embodiment of the present invention, the reaction is carried out under conditions using a Lewis acid, thus, resulting in trans-3.4-disubstituted piperidine derivatives.
The ring opening of epoxide of general formula II (
In all cases where ring opening of the epoxide 2 occurred, only the product resulting from nucleophilic attack at the piperidine 4-position could be isolated. The regioselectivity was confirmed by X-ray single structure of 3, which also revealed that the piperidine substituents at C-3 and C-4 were situated trans to each other. Further details are given in the experimental section. Both the substituent at C-3 and C-4 are oriented in axial positions. The N-Boc protecting group is oriented in a pseudoequatorial position. In the X-ray structure, two enantiomers of the piperidine derivative are hydrogen bonded through the hydroxyl groups and the carbonyl oxygen atoms of the N-Boc protecting group (data not shown).
Hence, in a preferred embodiment, the compound of general formula I is a compound wherein the substituents at positions 3 and 4 of the piperidine ring, namely the residue OR2 and ethynyl-R1 are in trans position.
In a preferred embodiment, the method for preparing a compound according to general formula I according to any one of claims 1 to 3 comprising the step of
In a preferred embodiment, the reaction with the protected acetylene derivative is effected at a temperature of from 0° C. to room temperature and/or the reaction with the Lewis acid, in particular, BF3×OEt2, is conducted at a temperature below −50° C., preferably below −70° C., for example, at −78° C.
In another preferred embodiment, the method results in a compound of general formula I wherein the substituents at position 3 and 4 of the piperidine ring are in trans position.
In another aspect, the present invention relates to an optionally substituted triazolylpiperidine compound of general formula III or IV
In a preferred embodiment of the optionally substituted triazolylpiperidine compound according to the present invention, the substituent R2 is selected from the group of hydrogen, C1-C8 alkyl, a benzyl group, a naphthyl group, a carbonylbenzyl group, or a carbonylnaphthyl group. In another preferred embodiment, substituent R3 is hydrogen.
Furthermore, it is preferred that substituent R4 is selected from an aryl group optionally being substituted with an alkoxy group like a benzyl group. In particular preferred, the substituent R4 is an arylethyl group, in particular, a phenethyl group optionally substituted with a methoxy group. Alternatively, R4 is a phenyl group optionally substituted with a methoxy group.
In another preferred embodiment, the compound of general formula III or IV is a compound wherein the substituent R2 is a benzyl group or a naphthen-methyl group.
Moreover, another preferred embodiment of the compounds of general formula III or IV relates to compounds in the trans form at position 3 and 4 of the piperidine moiety.
Moreover, the present invention relates to a method for obtaining an optionally substituted triazolylpiperidine compound of general formula III or IV. Said method comprises the step of reacting a compound of general formula I wherein R1 and R2 are as defined herein or, alternatively, both R1 and R2 are hydrogen, with an organic azide, thus, obtaining a compound of general formula III or IV. It is preferred that the compound of general formula I is a compound wherein R1 is hydrogen while R2 is hydrogen or a protecting group, like TBDMS (tert-butyldimethylsilyloxy).
It is preferred that the reaction for obtaining the optionally substituted triazolylpiperidine according to the present invention is conducted in the presence of a catalyst, in particular of a Cu(I) catalyst or a Ru catalyst.
In particular, it is possible to obtain a 1,4-disubstituted 1,2,3-triazolylpiperidine of general formula III when reacting the compound of general formula I with an organic azide in the presence of a Cu(I) catalyst. Further, it is possible to obtain a 1,5-disubstituted 1,2,3-triazolylpiperidine when conducting the reaction in the presence of a Ru catalyst.
The reactions of acetylenes 1 and 4 with organic azides were conducted with the aim of getting triazoles. This reactions belong to the Huisgen 1,3-dipolar cycloadditions which generally give a mixture of the 1,4- and the 1,5-disubstituted 1,2,3-triazole (Huisgen, R., In 1,3-Dipolar cycloaddition chemistry, ed.; Padwa, A., Wiley: New York 1984, 1-176).
Based on recent advances in this field has lead to the discovery of metal-catalyzed reactions in which both 1,4- and 1,5-disubstituted 1,2,3-triazoles can be formed selectively. Cu(I) catalysis regiospecifically combines terminal acetylenes and organic azides to give only 1,4-disubstituted 1,2,3-triazoles (Tornøe, C. W. et. al., J Org Chem 2002, 67, (9), 3057-3064), whereas Ru catalysis preferably yields 1,5-disubstituted 1,2,3-triazoles (Zhang, L. et. al., J Am Chem Soc 2005, 127, (46), 15998-15999).
in the following, the invention will be described further in the examples. The examples are not intended to restrict the claimed matter but are used only to illustrate the invention further.
Firstly, the t-BuOH-water protocol developed by Sharpless and coworkers (Rostovtsev, V. V. et. al., Angew Chem Int Edit 2002, 41, (14), 2596-2599) was tried but this turned out to give 1,4-disubstituted 1,2,3-triazole 6 from the TBDMS protected 4 in 32% isolated yield only after 24 hrs reaction time (Table 1, entry 1); in addition 55% of the starting material was recovered. Changing the solvent to a CH2Cl2-water mixture dramatically increased the yield of 6 (Table 1, entry 2). When the same reaction was carried out with the unprotected alcohol 1, the 1,4-disubstituted 1,2,3-triazole 7 was isolated in high yield (Table 1, entry 3). Use of CHCl3-water as the solvent gave a comparable result (Table 1, entry 4). By using a Cu(I) salt, instead of in situ generating Cu(I) from Cu(II)SO4 and sodium ascorbate, and acetonitrile as the solvent at elevated temperature, triazole 7 could be isolated in 90% yield (Table 1, entry 5). Since acetonitrile was used as solvent, no base was added to stabilize the Cu(I) as has been described in the literature.
Because of their often small size, organic azides can be unstable and difficult to handle, thus in situ generation of organic azides from the corresponding halides by nucleophilic displacement with sodium azide can be advantageous (scheme 1). This principle can be applied for three-component syntheses of 1,2,3-triazoles.
Using acetonitrile-water as solvent for the in situ generation of the azide with CuI as the catalyst for the 1,3-dipolar cycloaddition (label 2, entry 7) gave as major product the diyne of compound 1 and triazole 7 as minor product (scheme 4). The diyene is presumably formed by terminal alkyne homocoupling (the Glaser alkyne homocoupling). Homocoupling was not observed when 7 was prepared from 1 and 2-phenylethyl azide using CuI in acetonitrile (Table 1, entry 5). This homocoupling is an oxidative dimerization, therefore high amount of oxygen are needed. When the azide is generated in situ, water is used as co-solvent which results in formation of the diyene 10.
First the azide was prepared from the bromide using NaN3 and Bu4NHSO4 as phase transfer catalyst. Next the piperidine moiety and the catalyst were added to the solution to obtain the 1,4-disubstituted 1,2,3-triazole compound (scheme 3). For the preparation of compound 6 (Table 2, entry 1 and 2) incomplete conversion was observed, even after 24 hrs, and starting material was recovered. Using the t-BuOH/H2O as solvent (Table 2, entry 3) did not give any reaction even at 60° C. and the starting material was recovered. For the preparation of triazole 8 (entry 4 and 5) increasing the temperature gave a significant increase in yield over the same reaction time (24 hrs). a similar result was obtained in the synthesis of triazole 9 using the same conditions (Table 2, entry 7).
It is preferred that the reaction for obtaining the disubstituted 1,2,3-triazolylpiperidine of either general formula III or general formula IV is effected in using CH2Cl2 or CHCl3 or MeCN as solvent. Of course, it is possible to use any other solvent, like tert-butanol/water, dimethylformamide, acetonitrile, etc.
Further, the 4-ethynyl piperidine derivatives could be converted into 1,5-disubstituted 1,2,3-triazoles. Several procedures to achieve this have been described in the literature, e.g. by Krasiński et al., Org Lett 2004, 6, (8), 1237-1240. In this protocol the addition of bromomagnesium acetylide to organic azides results in the formation of 1,5-disubstituted 1,2,3-triazoles after aqueous work-up. However, when submitting the alkyne 4 to these conditions, no reaction occurred and only starting material was recovered (Table 3, entry 1).
Using the method described by Zhang et al., J Am Chem Sac 2005, 127, (46), 15998-15999, where a ruthenium catalyst is used to facilitate [1+3] dipolar cycloaddition of acetylenes with organic azides the desired 1,5-disubstituted 1,2,3-triazoles were obtained (Table 3, entry 2 and 3). Under these conditions, both the silyl protected alcohol 4 and the unprotected alcohol 1 gave the desired products in high yield (Table 3, entry 2 and 3).
NMR spectra were recorded using a Bruker Spectrospin AC with CDCl3 as a solvent. The chemical shifts are reported in parts per million relative to TMS and the couplings constants are given in Hz. 13C peaks marked with * were identified from cross peaks in HSQC spectra.
Flash column chromatography was preformed using Silica gel for flash chromatography from J. T. Baker (“Baker Analyzed”, 0.063-0.200 mm). The eluents were composed of hexanes (mixture of isomers) and ethyl acetate.
TLC analysis of the reaction mixtures was done using Macherey-Nagel aluminium plates coated with silica gel 60 with fluorescent indicator UV254 with visualization using ultra violet light or a solution of 2% ninhydrine in ethanol containing 10 drops of conc. sulphuric acid pr. 100 mL solution.
Accurate mass determinations were performed using a Thermo Scientific LTQ Orbitrap MS.
TMS-acetylene (345 μL, 2.44 mmol) was dissolved in dry Et2O (15 mL) and was cooled at 0° C. under argon. Solutions of n-BuLi (1.6 M in hexane, 1.53 mL, 2.44 mmol) and Me3Al (1.12 mL, 2.0 M, 2.24 mmol) were added and the reaction mixture was allowed to warm up to rt. Epoxide 2 (0.405 g, 2.04 mmol) in dry Et2O (2 mL) was added and the reaction mixture was cooled at −78° C. before BF3.OEt2 (0.52 mL, 4.08 mmol) was added and the reaction was stirred for 2 h at −78° C. Dry CH3OH (3 mL) was added and after stirring for 15 min the reaction mixture was quenched with a saturated aqueous solution of NH4Cl (10 mL). The resulting mixture was allowed to warm up to rt over a period of 30 min. H2O was added and the mixture was extracted with Et2O (2×10 mL). The organic layers were combined, dried over Na2SO4 and the solvent was evaporated under reduced pressure. The crude product was purified by flash column chromatography using hexane/ethyl acetate (4:1) gave the title compound as a colorless solid (0.57 g, 80%), m.p. 67.4-69.0 Rf (hexanes/ethyl acetate 3:1): 0.22
1H NMR (400 MHz, CDCl3): δ 3.97 (m, 1H), 3.77 (m, 1H), 3.60 (m, 1H), 2.99 (m, 2H), 2.48 (m, 1H), 2.33 (m, 1H), 1.95 (m, 1H), 1.56 (m, 1H), 1.46 (s, 9H), 0.16 (s, 9H).
13C NMR (100 MHz, CDCl3): δ 155.3, 106.4, 88.3, 80.3, 69.7, 49*, 42*, 37*, 28.7, 0.4.
HR-MS (ESI): Calcd for C15H27NO3SiNa [M+Na]+: 320.1658, found 320.1649.
C15H27NO3Si, MW=297.47, triclinic, a=5.7413(15), b=11.872(3), c=14.437(5) Å, α=112.127(15), α=97.874(14), γ=98.495(10), V=881.4(4) Å3, and dcalc=1.121 g cm−3, T=123(2) K, space group P-1; Z=2. Data collected, 15714, Rint 0.0185. The structure was solved by direct methods, and least-squares refinement of the model based on 5471 independent data (4982 reflections with I>2.0σ(I)) converged to a final R1=0.0321 and wR2=0.0885, respectively. S=1.067. Selected geometric parameters (Å, °); N1-C1 1.4562(10), N1-C5 1.4646(10), N1-C11 1.3505(10), C1-C2 1.5242(11), C2-O2 1.4201(10), C2-C3 1.5432(11), C3-C4 1.5370(12), C3-C6 1.4706(12), C4-C5 1.5247(12), C6-C7 1.2068(13), C7-Si1 1.8339(11), C11-O2 1.2254(10), C11-O3 1.3441(10), O3-C12 1.4675(10), C11-N-1-C1 118.77(7), C11-N-1-C5 123.83(7), C1-N1-C5 114.35(6), N1-C1-C2 110.96(6), O1-C2-C1 111.74(6), O1-C2-C3-107.16(6), C1-C2-C3 111.00(6), C11-O3-C12 120.39(7), C6-C3-C4 112.00(7), C6-C3-C2 109.45(7), C4-C3-C2 109.88(6), C5-C4-C3 111.30(6), N1-C5-C4-109.66(6), C7-C6-C3 176.62(9), C6-C7-Si1 172.82(8), O2-C11-O3 123.90(7), O2-C11-N1 124.53(7), O3-C11-N1 111.54(7).
Compound 3 (0.58 g, 1.95 mmol) was dissolved in TBAF (1.0 M solution in THF, 5.85 mL, 5.85 mmol). After stirring for 15 min, ethyl acetate (50 mL) was added and the reaction mixture was extracted with a saturated aqueous solution of NaHCO3 (2×50 mL). The basic layers were combined and extracted with ethyl acetate (2×50 mL). Finally the organic layers were combined, washed with a saturated aqueous solution of NaCl, dried over MgSO4, filtered and evaporated to dryness. Purification by flash chromatography using hexane/ethyl acetate (3:1) gave the title compound as a colorless oil (0.42 g, 95%). Rf (hexane/ethyl acetate 3:1): 0.16.
1H NMR (400 MHz, CDCl3): δ 3.95 (dd, J=3.1, 1H), 3.73 (m, 1H), 3.62 (m, 1H), 2.99 (m, 2H), 2.89 (m, 1H), 2.47 (m, 1H), 2.19 (d, J=2.1, 1H), 1.97 (m, 1H), 1.57 (m, 1H), 1.45 (s, 9H).
13C NMR (100 MHz, CDCl3): δ 155.3, 84.5, 80.2, 71.5, 69.6, 48.5, 42.4, 35.7, 28.8, 28.7.
HR-MS (ESI): Calcd for C12H19NO3Na [M+Na]+: 248.1263, found 248.1250.
Alkyne 1 (0.42 g, 1.86 mmol) was dissolved in anhydrous DMF (8 mL) and to this solution imidazole (0.152 g, 2.23 mmol) and TBDMS-CI (0.336 g, 2.23 mmol) were added. The mixture was stirred overnight (20 hrs) at rt under argon. H2O (10 mL) was added and the reaction mixture was extracted with ethyl acetate (2×10 mL). The organic layers were combined, dried over Na2SO4, filtered and the solvent was removed under vacuum. The resulting crude product was purified by flash column chromatography using hexane/ethyl acetate (9:1) to give colorless oil (0.598 g, 95%). Rf (hexane/ethyl acetate 9:1): 0.44.
1H NMR (100 MHz, CDCl3): δ 3.81 (m, 1H), 3.67 (m, 1H), 3.58 (m, 1H), 3.12 (m, 1H), 2.98 (m, 1H), 2.43 (m, 1H), 2.11 (d, J=2.2, 1H), 1.98 (m, 1H), 1.55 (m, 1H), 1.45 (s, 9H), 0.90 (s, 9H), 0.12 (s, 6H).
13C NMR (100 MHz, CDCl3): δ 155.0, 85.4, 79.9, 71.0, 70.1, 49*, 42*, 36.0, 29*, 28.8, 26.1, 18.4, −4.4.
HR-MS (ESI): Calcd for C18H33NO3SiNa [M+Na]+: 362.2127; found 362.2148.
To a solution of alkyne 4 (93 mg, 0.27 mmol) and azide 5 (40 mg, 0.27 mmol) in a mixture of H2O and CH2Cl2 (1:1, 6 mL) were added CuSO4.5H2O (3.4 mg, 0.014 mmol) and sodium ascorbate (8.14 mg, 0.041 mmol). The reaction mixture was stirred at rt for 24 hrs. The mixture was filtered and the precipitate was washed with H2O. The filtrate was extracted with EtOAc (3×10 mL) and the organic layers were combined with the precipitate. These combined layers were washed with H2O (10 mL) and a saturated solution of NaCl in H2O (10 mL), dried over MgSO4, filtered, and the solvent was removed under reduced pressure. The crude product was purified by flash chromatography using hexane/ethyl acetate (1:1) to give the title compound as a colorless solid (0.113 g, 84%), m.p. 76.9-81.1 Rf (hexane/ethyl acetate 2:1): 0.32.
1H NMR (400 MHz, CDCl3): δ 7.26 (m, 3H), 7.15 (d, J=7.1, 2H), 7.11 (s, 1H), 4.54 (m, 2H), 4.16 (m, 1H), 4.06 (m, 1H), 3.70 (m, 1H), 3.19 (t, J=7.5, 2H), 2.74 (m, 1H), 2.69 (m, 2H), 1.96 (m, 1H), 1.86 (m, 1H), 1.47 (s, 9H), 0.76 (s, 9H), −0.04 (s, 3H), −0.31 (s, 3H).
13C NMR (100 MHz, CDCl3): δ 154.9, 148.9, 137.5, 129.2, 129.0, 127.5, 122.1, 80.0, 71.5, 51.6, 51*, 44*, 42.7, 37.2, 30.4, 28.8, 26.0, 18.2, −4.4, −4.9.
HR-MS (DART): Calcd for C26H43N4O3Si [M+H]+: 487.3104; found 487.3115.
Alkyne 1 (80 mg, 0.36 mmol) was dissolved in acetonitrile (2 mL) and the mixture was heated at 60° C. Azide 5 (58 mg, 0.39 mmol) and CuI (7 mg, 0.036 mmol) were added and the reaction mixture was stirred for 40 hrs at 60° C. The reaction mixture was cooled down and the solvent was evaporated. The crude product was purified by flash chromatography to yield a colorless solid (0.122 g, 90%).
Compound 6 (85 mg, 0.17 mmol) was dissolved in TBAF (1.0 M solution in THF, 520 μL, 0.52 mmol) and the reaction was stirred under argon at rt. After 1 hr EtOAc (20 mL) was added and the mixture was washed with an aqueous saturated solution of NaHCO3 (3×15 mL). The aqueous layers were combined and extracted with EtOAc (2×30 mL). The organic layers where combined, dried over MgSO4, filtered, and the solvent was removed. Purification by flash column chromatography using hexane/ethyl acetate (1:4) gave the title compound as a colorless solid (61 mg, 96%), m.p. 135.1-136.8. Rf (hexane/ethyl acetate 1:4): 0.22.
1H NMR (400 MHz, CDCl3): δ 7.28 (m, 3H), 7.08 (m, 2H), 7.04 (s, 1H), 4.58 (t, J=7.2, 2H), 4.35 (m, 1H), 4.18 (m, 1H), 3.60 (m, 1H), 3.20 (t, J=7.4, 2H), 2.71 (m, 3H), 1.91 (m, 1H), 1.58 (m, 1H), 1.46 (s, 9H).
13C NMR (100 MHz, CDCl3): δ 155.0, 150*, 137.3, 129.2, 129.2, 127.6, 121.3, 80.3, 70.8, 52.1, 49*, 42*, 41.3, 37.1, 28.8.
HR-MS (ESI): calcd for C20H30N4O3 [M+H]+: 373.2240; found 373.2261.
1-(Bromomethyl)-4-methoxybenzene (18 mg, 0.13 mmol) was dissolved in a mixture of CHCl3 (0.27 mL) and a saturated aqueous solution of NaHCO3 (0.55 mL). NaN3 (13 mg, 0.20 mmol), Bu4NHSO4 (43 mg, 0.13 mmol), alkyne 4 (44 mg, 0.13 mmol), CuSO4.5H2O (1.0 mg, 0.004 mmol), sodium ascorbate (3 mg, 0.013 mmol) and ethanol (0.12 mL) were added in this order and the mixture was heated to 60° C. in an oil bath. The reaction mixture was stirred for 21 hrs at this temperature and after completion cooled to rt. The reaction mixture was extracted with CHCl3 (2×5 mL). The organic layers were combined, washed with H2O (2×5 mL), dried (MgSO4) and the solvent was removed. Purification with flash chromatography gave the title compound as a colorless oil (47 mg, 70%). Rf (hexane/ethyl acetate 1:1): 0.28.
1H NMR (400 MHz, CDCl3): δ 7.13 (s, 1H), 7.08 (d, J=8.2, 2H), 6.84 (d, J=8.5, 2H), 4.50 (m, 2H), 4.13 (m, 1H), 4.11 (m, 2H), 3.79 (s, 1H), 3.71 (m, 1H), 3.12 (t, J=7.8, 2H), 2.70 (m, 3H), 1.99 (m, 1H), 1.85 (m, 1H), 1.47 (s, 9 H), 0.75 (s, 9H), −0.05 (s, 3H), −0.33 (s, 3H).
13C NMR (100 MHz, CDCl3): δ 159.0, 148.8, 130.0, 129.4, 122.2, 114.6, 80.0, 72*, 55.6, 51.9, 51*, 43*, 42.6, 36.4, 30.0, 28.8, 26.0, 18.2, 1.4, −5.0.
HR-MS (ESI): Calcd for C27H44N4O4SiNa [M+Na]+: 539.3030; found 539.3013.
The title compound was prepared from compound 8 as described for the preparation of compound 7 to give a colorless solid (quantitative).
The title compound was prepared from compound 1 as described for the preparation of compound 8. The crude product was purified by flash column chromatography using hexane/ethyl acetate (1:8) to give the title compound as colorless solid (0.192 g, 70%), m.p. 107.2-109.4 Rf (hexane/ethyl acetate 1:8): 0.17.
1H NMR (400 MHz, CDCl3): δ 7.10 (s, 1H), 6.99 (d, J=8.5, 2H), 6.82 (d, J=8.5, 2H), 4.53 (t, J=7.2, 2H), 4.35 (m, 1H), 4.16 (m, 1H), 3.78 (s, 3H), 3.61 (m, 1H), 3.14 (t, J=7.2, 2H), 2.70 (m, 3H), 1.93 (m, 1H), 1.59 (m, 1H), 1.46 (s, 9H).
13C NMR (100 MHz, CDCl3): δ 159.3, 155.1, 149.6, 130.0, 129.4, 121.1, 114.7, 80.2, 70.8, 55.7, 52.3, 49.8, 43*, 41.6, 36.3, 29.4, 28.8.
HR-MS (ESI): calcd for C21H30N4O4Na [M+Na]+: 425.2165; found 425.2179.
Alkyne 1 (75 mg, 0.22 mmol) was dissolved in dry THF (3 mL) and heated at 80° C. in an oil bath. To this mixture Cp*RuCl(PPh3)2 (1.8 mg, 0.002 mmol) and azide 5 (36 mg, 0.24 mmol) were added. The reaction mixture was stirred at 80° C. for 3 hours after which the solvent was removed using a rotary evaporator. The crude reaction mixture was purified by flash column chromatography using hexane/ethyl acetate (7:3) to give the title compound as a yellow oil (80 mg, 75%), Rf (hexane/ethyl acetate 7:3): 0.23.
1H NMR (400 MHz, CDCl3): δ 7.36 (s, 1H), 7.24 (m, 3H), 6.97 (m, 2H), 4.75 (m, 1H), 4.48 (m, 1H), 4.13 (m, 1H), 3.99 (m, 1H), 3.18 (m, 3H), 2.39 (m, 1H), 2.28 (m, 1H), 2.00 (m, 1H), 1.45 (m, 10H), 0.99 (m, 1H), 0.74 (s, 9 H), −0.12 (s, 3H), −0.42 (s, 3H).
13C NMR (100 MHz, CDCl3): δ 154.5, 139.9, 138.1, 130.6, 129.4, 129.1, 127.3, 80.4, 73.7, 51*, 49.8, 43*, 40.8, 37.6, 30.1, 28.7, 25.9, 18.0, −5.2.
HR-MS (ESI): calcd for C26H42N4O3SiNa [M+Na]: 509.2924; found 509.2907.
The deprotection of protected alcohol 11 to obtain the title compound was carried out as described for compound 7. The crude product was purified by flash column chromatography using hexane/ethyl acetate (1:9) giving the product as a colorless solid (192 mg, 75%).
Triazole 12 was prepared from compound 4 as described for 11. The crude product was purified by flash column chromatography using hexane/ethyl acetate (1:9) to give the title compound as a colourless solid (158 mg, 77%), m.p. 45.3-47.8. Rf (hexane/ethyl acetate 1:9): 0.26.
1H NMR (400 MHz, CDCl3): δ 7.24 (m, 3H), 7.16 (s, 1H), 7.01 (d, J=6.5, 2H), 4.60 (m, 2H), 4.25 (m, 1H), 4.00 (m, 1H), 3.40 (m, 1H), 3.18 (m, 2 H), 2.47 (m, 2H), 2.13 (m, 1H), 1.45 (m, 10H), 1.22 (m, 1H).
13C NMR (100 MHz, CDCl3): δ 154.8, 139.7, 138.2, 130.5, 129.3, 129.1, 127.3, 80.5, 71.6, 50.5, 49.8, 43.6, 40.6, 37.3, 30.3, 28.8.
HR-MS (ESI): calcd for C20H28N4O3Na [M+Na]+: 395.2059; found 395.2052.
In scheme 3 below, the reaction for formation of (±) Benzyl trans-4-ethynyl-3-hydroxypiperidine-1-carboxylate is shown.
Benzylchloroformate (0.939 mL, 6.58 mmol) was added dropwise to an ice cold solution of 1,2,3,6-tetrahydropiperidine (0.5 mL, 5.48 mmol) and NaHCO3 (0.554 g, 6.58 mmol) in H2O (13 mL). The resulting mixture was stirred at rt for 4 hrs after which CH2Cl2 (12 mL) and 5% aqueous Na2CO3 (5 mL) were added. The phases were separated and the aqueous phase was extracted with CH2Cl2 (20 mL). The combined organic layers were dried over Na2SO5 and after filtration the solvent was removed under reduced pressure. Purification by flash chromatography gave the title compound as a colourless oil (1.19 g, 83%); Rf=0.41 (hexane-EtAOc, 4:1); analytical data is in accordance with literature (Solares, L. F.; et al., Tetrahedron 2006, 62, (14), 3284-3291).
Cbz-protected pyridine obtained in the first step (0.369 g, 1.70 mmol) was dissolved in CH2Cl2 (2 mL) and cooled in at 0° C. A solution of mCPBA (0.411 g, 2.38 mmol) in CH2Cl2 (3 mL) was added drop wise to the reaction mixture over a period of 15 min. The reaction mixture was stirred at rt for 5 hrs after which TLC analysis indicated full conversion of the starting material. The completed reaction mixture was then washed three times with 5% aqueous K2CO2 (3×25 mL), and once with a saturated aqueous solution of NaCl (1×25 mL). The organic layer was dried over Na2SO4, filtered and the solvent was removed under reduced pressure. Purification by flash chromatography gave the title compound as a colourless oil (0.284 g, 72%); analytical data is in accordance with literature (Solares, L. F.; et al., Tetrahedron 2006, 62, (14), 3284-3291).
TMS-acetylene (82 μL, 0.58 mmol) was dissolved in dry Et2O (5 mL) and was cooled at 0° C. under argon. Solutions of n-BuLi (1.6 M in hexane, 0.363 mL, 0.58 mmol) and Me3Al (2.0 M, 0.264 mL, 0.53 mmol) were added and the reaction mixture was allowed to warm up to rt. The epoxide obtained in the second step (0.113 g, 0.48 mmol) in dry Et2O (1 mL) was added and the reaction mixture was cooled to −78° C. before BF3.Et2O (0.122 mL, 2 mmol) was added. The reaction mixture was stirred for 3 h at −78° C. Dry CH3OH (3 mL) was added and after stirring for 15 min the reaction mixture was quenched with a saturated aqueous solution of NH4Cl (5 mL). The resulting mixture was allowed to warm up to rt over a period of 30 min. H2O was added and the mixture was extracted with Et2O (2×10 mL). The organic layers were combined, dried over Na2SO4 and the solvent was evaporated under reduced pressure. Purification by flash chromatography gave the title compound as a colourless oil (86 mg, 55%); Rf=0.24 (hexanes-EtOAc, 1:2); 1H NMR (400 MHz, CDCl3) δ 7.47-7.28 (m, 5H), 5.13 (s, 2H), 4.13-3.93 (m, 1H), 3.91-3.74 (m, 1H), 3.74-3.55 (m, 1H), 3.22-2.95 (m, 1H), 2.59-2.45 (m, 1H), 2.21-2.10 (m, 1H), 1.69-1.53 (m, 1H), 1.44-1.14 (m, 1H), 0.15 (s, 9H); 13C NMR (101 MHz, CDCl3) δ 155.31, 137.01, 128.97, 128.40, 128.12, 83.98, 73.22, 69.89, 68.21, 48*, 42*, 36.01, 28.62, 0.40.
K2CO3 (38 mg, 0.28 mg) was to a solution of the alcohol obtained in the third step above (80 mg, 0.24 mmol) in MeOH/THF (1:5.6, 8.25 mL). The reaction mixture was stirred at rt for 3 hrs after which the solution was diluted with H2O (10 mL) and extracted with Et2O (2×10 mL). The organic layers were combined, dried over Na2SO3 and the solvent removed under reduced pressure to give the crude title compound as yellow oil. Purification by flash chromatography gave the title compound as a colourless oil; yield: 44 mg (71%); Rf=0.24 (hexanes-EtOAc, 2:1); 1H NMR (400 MHz, CDCl3) δ 7.33 (m, 5H), 5.13 (s, 2 H), 4.09-3.97 (m, 1H), 3.89-3.75 (m, 1H), 3.72-3.56 (m, 1H), 3.23-2.99 (m, 2H), 2.55-2.42 (m, 1H), 2.29-2.10 (m, 2H), 2.07-1.92 (m, 1H), 1.66-1.48 (m, 1H); 13C NMR (101 MHz, CDCl3) δ 155.67, 136.80, 128.85, 128.43, 128.24, 84.00, 71.86, 69.49, 67.71, 48.50, 42.57, 35.72, 28.58.
In
In addition, preliminary results demonstrate an enzyme inhibiting activity of the derivatives provided herein.
| Number | Date | Country | Kind |
|---|---|---|---|
| 10194913.9 | Dec 2010 | EM | regional |
