EP0979233A1 - Verfahren zur synthese von oligonukleotiden in lösung - Google Patents
Verfahren zur synthese von oligonukleotiden in lösungInfo
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- EP0979233A1 EP0979233A1 EP98918629A EP98918629A EP0979233A1 EP 0979233 A1 EP0979233 A1 EP 0979233A1 EP 98918629 A EP98918629 A EP 98918629A EP 98918629 A EP98918629 A EP 98918629A EP 0979233 A1 EP0979233 A1 EP 0979233A1
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
Definitions
- This invention relates to the field of nucleic acid chemistry. Specifically, this invention describes a novel method for preparing oligonucleotides.
- the method utilized herein for preparing said oligonucleotides is called PASS, an acronym for Product Anchored Sequential Synthesis.
- oligonucleotides were not considered in any capacity other than strictly informational. Despite the fact that certain oligonucleotides were known to have interesting structural possibilities (e.g., t-RNAs) and other oligonucleotides were bound specifically by polypeptides in nature, very little attention had been focused on the non-informational capacities of oligonucleotides. For this reason, among others, little consideration had been given to using oligonucleotides as pharmaceutical compounds. There are currently at least three areas of exploration that have led to extensive studies regarding the use of oligonucleotides as pharmaceutical compounds.
- oligonucleotides are used to bind to certain coding regions in an organism to prevent the expression of proteins or to block various cell functions. Additionally, the discovery of RNA species with catalytic functions — ribozymes - has led to the study of RNA species that serve to perform intracellular reactions that will achieve desired effects. And lastly, the discovery of the SELEX process (Systematic Evolution of Ligands by Exponential Enrichment) (Tuerk and Gold (1990) Science 249:505) has shown that oligonucleotides can be identified that will bind to almost any biologically interesting target.
- SELEX is a method for identifying and producing nucleic acid ligands, termed "nucleic acid antibodies,” e.g., nucleic acids that interact with target molecules
- Such modifications are designed to increase cell penetration of the oligonucleotides, to stabilize them from nucleases and other enzymes that degrade or interfere with the structure or activity of the oligonucleotide analogs in the body, to enhance their binding to targeted RNA, to provide a mode of disruption (terminating event) once sequence-specifically bound to targeted RNA and to improve their pharmacokinetic properties.
- RNA secondary and tertiary structures can have important biological functions (Tinoco et al. (1987) Cold Spring Harb. Symp. Quant. Biol. 52:135; Larson et al. (1987) Mol. Cell. Biochem. 74:5; Tuerk et al. (1988) Proc. Natl. Acad. Sci. USA 85:1364; Resnekov et al. (1989) J. Biol. Chem. 264:9953).
- RNA Mimicry describes oligonucleotides or oligonucleotide analogs which mimic a portion of RNA able to interact with one or more proteins.
- the oligonucleotides contain modified internucleoside linkages rendering them nuclease- resistant, have enhanced ability to penetrate cells, and are capable of binding target oligonucleotide sequences.
- a nucleoside monomer is protected (P,) and the phosphoramidite is prepared (1).
- the phosphoramidite (referred to as the 5'-protected monomer unit) is then covalently attached to the growing oligonucleotide chain (2), via a phosphite triester linkage, through the 5'- hydroxy group of the ribose ring of the growing oligonucleotide chain to yield the oligonucleotide product (3), in which the majority of the growing oligonucleotide chain has been extended by one nucleotide, but a significant percent of chains are not extended.
- the product (3) is then oxidized to yield the phosphate triester (4).
- Each coupling reaction extends the oligonucleotide by one monomer via a phosphite triester linkage.
- the desired oligonucleotide (6 (n+1 sequence)) is deprotected and cleaved from the resin, together with all of the failure sequences (n, n-x).
- Automated oligonucleotide synthesis on solid supports is very efficient for the preparation of small amounts, 0.001 to 0.01 mmol, of a variety of sequences in a minimum amount of time with reasonable yield. It is, however, a highly inefficient process in terms of overall process yield based on input monomer. Typically a 16 fold excess of phosphoramidite is necessary per monomer addition. It has been recognized that the automated solid phase synthesis approach does not readily lend itself to be scaled to a level that allows efficient manufacture of oligonucleotide pharmaceuticals. (Zon and Geiser (1991) Anti-Cancer Drug Design 6:539-568).
- failure sequences As discussed above, must be blocked or capped in order to prevent the subsequent addition of monomers to incomplete oligonucleotides.
- the generation of failure sequences at every step of the synthesis produces a crude product contaminated with highly homologous byproducts, which must be carried through to the final crude product ⁇ see Scheme 1, structure 6 (n, n-x)).
- purification of crude synthetic oligonucleotides to a state acceptable for clinical studies is extremely cumbersome and inefficient.
- a large excess of monomer (approximately 16 fold) is used.
- Zon et al have suggested a block approach to the synthesis of oligonucleotides, in which a library of dimer or multimer oligonucleotide fragments are prepared in solution and then coupled to each other.
- the fragments are activated for coupling by differential 5'- deprotection and 3 '-phosphorylation.
- Phosphotriester coupling has been suggested for fragment preparation. (Bonora et al. (1993) Nucleic Acids Res. 21: 1213-1217). Due to the comparatively low yield of phosphotriester coupling this approach has not been widely accepted.
- the 5'-protecting group serves to prevent reaction of the 5'-hydroxyl group of one monomer with the phosphoramidite group of a second monomer during the coupling step.
- the 4,4'-dimethoxytrityl (DMT) group is commonly used as the 5'-protecting group (Schaller et al. (1963) J. Am. Chem. Soc.
- a fluorescent trityl analog has been used for the 5'-terminal protecting group during oligonucleotide synthesis to allow facile detection of full-length product in crude deprotected oligonucleotide (Fourrey et al. (1987) Tetrahedron Lett. 28:5157). Colored trityl groups were devised to allow monitoring of specific monomer additions during solid phase oligonucleotide synthesis (Fisher and Caruthers (1983) Nucleic Acids Res. U . : 1589).
- the Diels-Alder reaction is a cycloaddition reaction between a conjugated diene and an unsaturated molecule to form a cyclic compound with the ⁇ -electrons being used to form the new ⁇ bonds.
- the Diels-Alder reaction is an example of a [4 + 2] cycloaddition reaction, as it involves a system of 4- ⁇ electrons (the diene) and a system of 2- ⁇ electrons (the dienophile). The reaction can be made to occur very rapidly, under mild conditions, and for a wide variety of reactants.
- the Diels-Alder reaction is broad in scope and is well known to those knowledgeable in the art.
- samples of cholesterol containing ergosterol, a 1,3 diene which has been shown to react in a Diels-Alder fashion with RTAD derivatives (Barton et al. (1970) J. Chem. Soc. (D) 939), were treated with an excess of 3-aminopropyl-silica gel derivatized with various sulfonated 4-aryl-l,2,4 triazoline-3, 5 -diones (TDA-silica gel) at 25 °C. Following reaction nearly quantative yields of pure cholesterol were obtained.
- Other dienes which were trapped by this TAD-silica gel include 8,10-dodecadienol, 1-chloro-, 2-chloro- and 9-bromoanthracene.
- arylsulfonic acid derivatives of 4-aryl(2,6-diisoproply)- l,2,4-triazoline-3,5-diones were prepared and incorporated onto an amino silica gel.
- This TAD-silica gel also trapped ergosterol. After trapping of the ergosterol the silica gel was washed free of unreacted ergosterol and separated. Elution of the silica gel with an excess of triethyl amine in acetonitrile afforded the ergosterol-triazolinedione adduct. Treatment of this Diels-Alder adduct in refluxing THF containing excess LiAlH 4 liberated the ergosterol.
- the present invention is a method for the sequential solution phase synthesis of oligonucleotides that increases reaction yields and allows for predictable scale-up.
- the present invention is characterized by use of an anchor group attached to the 5 '-end of the growing oligonucleotide that allows successfully coupled product to be separated from unreacted starting materials.
- the anchor group also serves as the 5'-OH protecting group and the coupling reaction occurs in solution. The successfully reacted oligomer will contain the protecting group, while the unreacted oligomer will not, and the materials can be partitioned based on the presence of the anchor/protecting group.
- the anchor group reacts covalently with a derivatized solid support, such as a resin, membrane or polymer.
- a derivatized solid support such as a resin, membrane or polymer.
- the invention provides a method for the solution phase synthesis of a wide variety of oligonucleotides and modified oligonucleotides comprising reaction of a 5'-protected monomer unit with the 5'-end of a growing oligonucleotide chain in solution.
- the unreacted monomer may be oxidized to form a charged species that may be easily partitioned from the remainder of the reaction medium.
- the monomer units are phosphoramidites, which upon activation and oxidation are converted to phosphates. The charged phosphate species can be easily partitioned from the remainder of the reaction medium.
- the monomer unit consists of a 5'-protected phosphoramidite or H-phosphonate, wherein the protecting group is a substituted trityl group, levulinic acid group, or silyl ether group.
- the unreacted oligonucleotide starting material may be separated from the reacted oligonucleotide product based on the affinity of the protecting group for a chromatography resin.
- the unreacted oligonucleotide starting material may be separated from the reacted oligonucleotide product based on the specific reaction of the protecting group with a derivatized solid support, such as a resin, membrane or polymer.
- a derivatized solid support such as a resin, membrane or polymer.
- the partitioning method to remove unreacted oligonucleotide serves to allow for isolation and reuse of the unreacted oligonucleotide and also will allow the reacted oligonucleotide to be deprotected in preparation for the subsequent addition of the next 5 '-protected monomer unit.
- the method of this invention is not limited to phosphoramidite coupling chemistry, but is compatible with other coupling reactions such as H-phosphonate or phosphate triester coupling chemistry. This method also lends itself to automation and is ideally suited for the large scale manufacture of oligonucleotides with high efficiency.
- the methods of the present invention can be extended to all sequential polymerization reactions and thus to the sequential synthesis of any polymer.
- the present invention includes a method and apparatus to automatically separate the product from the unreacted 5'-protected monomer unit and the starting material.
- the apparatus is comprised of an extraction vessel and a chromatography resin filtration chamber, which contains a solid support. Upon completion of a monomer addition reaction, the reaction mixture is pumped into the extraction chamber, extracted and then eluted through the solid support, which retains only the 5'-protected monomer unit. The product is then separated from the starting material by eluting through a solid support that retains only the product.
- the chromatography resin filtration chamber contains a solid support which covalently reacts with both the 5 '-protected monomer unit and the product. The starting material is eluted from the solid support and the monomer and product are then released from the solid support with a dilute acid. The product is then separated from the 5'-protected monomer unit by passage through an ultrafiltration membrane.
- a material cost analysis reveals that the 5'-protected phosphoramidite is the most costly reaction component in oligonucleotide synthesis. The cost of the remaining materials are trivial in comparison. Therefore, it would be desirable to make the monomer the limiting reagent. Furthermore, a particular intermediate oligonucleotide sequence which failed to add to the incoming monomer could serve as an intermediate in a subsequent synthesis. Using the method of this invention, verification of the sequence and composition of oligonucleotide product becomes trivial. After every monomer addition cycle, a fully protected, neutral intermediate is obtained, which is easily analyzed by mass spectrometry without tedious sample preparation. Over the course of an oligonucleotide synthesis a library of analytical data for every sequential monomer addition can be obtained. Thus, product analysis becomes an integral part of the process.
- FIGURE 1 illustrates the reverse phase High Pressure Liquid Chromatography (HPLC) trace of the phosphoramidite coupling reaction mixture set forth in Example 1 prior to oxidation.
- FIGURE 2 illustrates the reverse phase HPLC trace of the phosphoramidite coupling reaction set forth in Example 1 after oxidation. The post oxidation trace has been superimposed on the preoxidation trace of Figure 1.
- HPLC High Pressure Liquid Chromatography
- FIGURE 3 illustrates the reverse phase HPLC traces of a mixture of oxidized phosphoramidite coupling reaction set forth in Example 1 , both prior to and after being passed through a DEAE Sephadex ® filter plug.
- FIGURE 4 illustrates the reverse phase HPLC traces of the oxidized phosphoramidite coupling reaction set forth in Example 1, after being eluted through a C18 resin with water/acetonitrile and after treatment with acetic acid and elution with water/acetonitrile.
- FIGURE 5 illustrates schematically an automated extraction and filtration system designed for use with the method of this invention.
- FIGURE 6 illustrates the anion exchange HPLC trace of the 15 base oligonucleotide prepared in Example 7 using 3'-PEG anchored solution phase synthesis.
- FIGURE 7 illustrates graphically the Diels-Alder capture data for the reaction of 5'-DHDTO-T-[3',3']-T-OSiPDBT-5' with polystyrene maleimide resins containing 1.0 eq, 2.5 eq, 5 eq and 10 eq of maleimide.
- FIGURE 8 illustrates schematically an automated extraction and filtration system designed for use with Diels-Alder product capture.
- FIGURE 9 illustrates graphically the precipitation and centrifugation of PEG- precipitated by ethyl ether, isopropyl ether and N-butyl ether.
- FIGURE 10 illustrates graphically the Diels-Alder reaction of diene subtituted trityl alcohol 5'-O-(4,4'-di-3,5-hexadienoxytrityl)thymidine (5'-DHDTO-dT) (31) with phenyltriazoline-dione (PTAD) (82) set forth in Example 17 (Scheme 22).
- PTAD phenyltriazoline-dione
- FIGURE 11 illustrates the use of a bis-TAD molecule in the PASS process.
- P is a solid support.
- FIGURE 12 illustrates schematically a PASS cycle for a preferred embodiment of the instant invention.
- FIGURES 13A-13E illustrate the HPLC traces of the reaction mixture for each step of PASS cycle described in Example 21.
- FIGURE 14 illustrates the reversed phase HPLC trace of the T-T dimer prepared in Example 30.
- FIGURE 15 illustrates the reversed phase HPLC trace of the T-T-T trimer prepared in Example 30.
- FIGURE 16A illustrates the reverse phase HPLC trace of the reaction of DHDT fC 3'-OH (153) with TBDPSi-Cl after 65 minutes (Example 31). Coupling from top to bottom: 5'-DHDT 2'-fC 3'-OH (153) (13.8 minutes), TBDPSi-Cl (11.3 minutes), and 5'- DHDT 2'-fC 3'-TBDPSi (154) (19.8 minutes).
- FIGURE 16B illustrates the reverse phase HPLC trace of the capture reaction of 5'-DHDT 2'-fC 3 * -TBDPS (154) on a PTAD-PS resin. From top to bottom: 5'-DHDT 2'- fC 3'-TBDPSi (154) (19.8 minutes) and capture solution (10.4 and 11.3 minutes).
- FIGURE 16C illustrates the reverse phase HPLC trace following the release and neutralization of compound 155. From top to bottom: aqueous solution 1 (1-2 minutes), aqueous solution 2 (no particular peaks) and 2'-fC 3'-TBDPS 5'-OH (155) (25.5 minutes).
- FIGURE 16D illustrates the NMR of compound (155) l'-cytidine (acetyl protected) 2'-flouro 3'-TBDPSi 5*-OH.
- the present invention includes a method for the solution phase synthesis of oligonucleotides, referred to herein as Product Anchored Sequential Synthesis (PASS).
- PASS Product Anchored Sequential Synthesis
- the present invention is characterized by utilization of an anchor group attached to the 5'-end of the growing oligonucleotide product that allows successfully coupled product to be separated from unreacted starting materials.
- the anchor group also serves as the 5'-OH protecting group.
- the successfully reacted oligonucleotide product will contain the protecting group, while the unreacted oligonucleotide starting material will not, and the product can be partitioned away from the starting material based on the presence of the blocking/protecting group. Unreacted starting material is recovered and can be reused in a subsequent synthesis batch of the same oligonucleotide.
- the improved method for oligonucleotide synthesis described herein does not employ a solid support for anchoring of the 3 '-end of the growing oligonucleotide chain.
- the invention provides a method for the solution phase synthesis of a wide variety of oligonucleotides and modified oligonucleotides comprising reaction of a 5'-protected monomer unit with the 5'-end of a growing oligonucleotide chain in solution. Performing these reactions in solution, rather than on solid supports, provides for better reaction kinetics.
- the unreacted 5'-protected monomer unit may be activated and oxidized to form a charged species that may be easily partitioned from the remainder of the reaction medium.
- the monomer units are phosphoramidites, that upon oxidation can be easily converted to phosphate diesters.
- the charged phosphate species can be easily partitioned from the remainder of the reaction medium.
- the oxidation may be performed in situ.
- H-phosphonate As the 5 '-protected monomer unit, which is a charged species (Example 2, Scheme 5), the oxidization of H-phosphonate is deferred until after the addition of the final monomer.
- the charged H-phosphonate monomers produce neutral H-phosphonate diester products after coupling, and the charged monomer species are readily removed by anion exchange filtration or extraction.
- the recovered H- phosphonate monomers are reusable.
- the 5'-protecting group that is utilized can be selected from any class of chemical functionalities that meets the basic requirements of the invention.
- the protecting group must be of a type that can be used to differentiate the product of the reaction from the remainder of the reaction mixture in order to effect a separation.
- the protecting group will have a strong affinity for or a reactivity with a particular phase or solid support and it must be easily cleaved or removed from the phase or solid support with high selectivity.
- the oligonucleotide product may be separated from unreacted oligonucleotide starting material using standard methods known to those skilled in the art including, but not limited to, centrifugation, separation on a resin, silica gel based separation, separation based on affinity for a metal, separation based on a magnetic force or electromagnetic force or separation based upon covalent attachment to a suitable solid support.
- the partitioning method to remove unreacted oligonucleotide starting material serves to both allow for the isolation for reuse of the unreacted oligonucleotide and also will result in a resin-bound oligonucleotide product which is easily deprotected in preparation for the subsequent addition of the next 5'- protected monomer unit.
- the protecting group will covalently react with a derivatized solid support, such as a resin, membrane or polymer, to give a covalently anchored protecting group which may easily be cleaved from the oligonucleotide with high selectivity.
- a derivatized solid support such as a resin, membrane or polymer
- the monomer unit consists of a 5 '-protected phosphoramidite or H-phosphonate, wherein the protecting group is a substituted trityl group, levulinic acid group or silyl ether group.
- the preferred substitution on the protecting group is a diene functionality, which can react, via a Diels- Alder reaction, with a solid support, such as a resin, membrane or polymer that has been derivatized with a dienophile, preferably a l,2,4-triazoline-3,5-dione (TAD).
- TAD l,2,4-triazoline-3,5-dione
- the unreacted oligonucleotide starting material is separated from the reacted nucleotide product based on the selective or specific covalent reaction of the 5'-protecting group with a derivatized resin.
- nucleoside means either a deoxyribonucleoside or a ribonucleoside or any chemical modifications thereof. Modifications of the nucleosides include, but are not limited to, 2'-position sugar modifications, 5-position pyrimidine modifications, 8-position purine modifications, modifications at cytosine exocyclic amines, substitution of 5-bromo- uracil, and the like.
- Oligonucleotide refers to either DNA or RNA or any chemical modifications thereof.
- the oligonucleotides synthesized by the method of this invention are depicted generally as follows:
- n 1 - 1,000
- a and A' are 2'-sugar substituents as defined below and B is a nucleobase as defined below.
- a "solid support” as used herein refers to a resin, membrane, phase, polymer, polymer precursor, or soluble polymer that can undergo phase transition.
- a solid support also refers to a resin, membrane, phase, polymer, polymer precursor, or soluble polymer that has been derivatized with a diene, dienophile, 1 ,3 dipole or a D group, as defined below.
- the term resin and solid support are used interchangeably and one of ordinary skill in the art will recognize what is intended by the term resin.
- solid supports include, but are not limited to, organic polymers, crosslinked organic polymers, maleimide derivatized polystyrene, polystyrene derivatized with D groups, as defined below, dienophile or diene derivatized polystyrene, TentagelTM derivatized with D groups, as defined below, dienophile or diene derivatized TentagelTM, l,2,4-triazoline-3,5-dione (TAD) derivatized resins, phenyltriazoline-dione (PTDA) derivatized resins, diene or dieonphile derivatized amino- functionalized resins, such as aminomethyl polystyrene, aminopropyl silica gel, aminopropyl CPG, NovaSynTM TG amino resin HL, and ArgoGelTM, amino-functionalized resins derivatized with D groups, as defined below, 4-(l,2,4-triazoline-3,5-di
- a "diene” is defined as a molecule bearing two adjacent double bonds, where the atoms forming these double bonds can be carbon or a heteroatom, which can undergo a [2+4] cycloaddition reaction with a dienophile.
- a "dienophile” is defined as a molecule bearing an alkene group, or a double between a carbon and a heteroatom, or a double bond between two heteroatoms, which can undergo a [2+4] cycloaddition reaction with a suitable diene.
- the dienophile can be any group, including but not limited to, a substituted or unsubstituted alkene, or a substituted or unsubstituted alkyne.
- dienophiles include, but are not limited to thiocarbonyl compounds, including thioaldehydes, thioesters, thioketones, thiocarbamates, thiocarbonates and thioamides and nitroso compounds.
- a "dienophile derivatized solid support” refers to a solid support that has been functionalized with a dienophile and a “diene derivatized solid support” refers to a solid support that has been functionalized with a diene.
- Preferred solid supports are inorganic oxides selected from the group consisting of silica, alumina, zeolites, controlled pore glass, that have hydroxyl groups that are capable of being functionalized, or organic supports such as polystyrene, as illustrated in Schemes 13 and 14.
- the dienophile is maleimide and the diene is 3,5-hexadiene.
- the dienophile is a l,2,4-triazoline-3,5-dione (TAD).
- a "[3+2] dipole” is defined as any moiety capable of undergoing a 3+2 cycloaddition reaction with a substituted or unsubstituted alkene, or a substituted or unsubstituted alkyne.
- Examples of [3+2] dipoles include, but are not limited to compounds of the formula:
- the "5'-protected monomer units" of this invention are generally depicted as follows including the conventional numbering for the ribose ring:
- B is a nucleobase;
- a and A' are 2'-sugar substituents;
- W is independently selected from the group consisting of a phosphoramidite, H- phosphonate, phosphotriester, phosphoramidate, protected oligonucleotide and methyl- phosphonate; and D-E is an alcohol protecting group(s) which serves as an anchor for partitioning the successfully reacted oligonucleotide product away from the unreacted oligonucleotide starting material.
- W is a phosphoramidite or H-phosphonate
- R 1 is selected from the group consisting of H and an alcohol protecting group
- R 3 is selected from the group consisting of R 2 , R 4 , CN, C(O)NH 2 , C(S)NH 2 , C(O)CF 3 , SO 2 R 4 , amino acid, peptide and mixtures thereof;
- R 4 is selected from the group consisting of an optionally substituted hydrocarbon (C,-C 20 alkyl, C 2 -C 20 alkenyl, C 2 -C 20 alkynyl), an optionally substituted heterocycle, t- butyldimethylsilyl ether, triisopropylsilyl ether, nucleoside, carbohydrate, fluorescent label and phosphate; most preferably A is selected from the group consisting of H, OH, NH 2 , Cl, F, NHOR 3 , OR 4 , OSiR 4 3 . (See United States Patent Application Serial No. 08/264,029, filed
- D-E can be any group that enables the partitioning of the "growing oligonucleotide chain" or
- oligonucleotide product away from unwanted side products and starting materials.
- the partitioning can be done by any suitable method, including but not limited to, silica gel based chromatography, centrifugation, or any other means known by those in the art for partitioning materials.
- the preferred method for partitioning is by binding to a resin.
- the most preferred method for partitioning is by covalent reaction between D and a derivatized solid support, such as a derivatized resin, polymer, or membrane.
- the protecting group D- E therefore, is preferably designed such that D has a strong affinity for a particular resin or phase, and E is designed such that the 5'-oxygen-E bond is easily cleaved with high selectivity.
- D may be omitted.
- the protecting group D-E is designed such that D can selectively or specifically form a covalent bond to a particular derivatized resin, polymer, or membrane. This covalent bond between D and a resin can be reversible.
- E includes, but is not limited to, the trityl group or the levulinic acid group or a silyl ether group, as depicted below.
- Y O, NH, S, P(H)(OR 4 ), P(OR 4 ) 2 , POH(O)(OR 4 ), NH(CO), (CO)NH, O(CO) (CO)O, NH(CO)NH, NH(CO)O, O(CO)NH, NH(CS)NH, NH(CS)O, O(CS)N omitted, SO, SO 2
- nucleobase will have the following definition.
- a nucleobase is a purine or a pyrimidine base.
- Nucleobase includes all purines and pyrimidines currently known to those skilled in the art or any chemical modifications thereof.
- the purines are attached to the ribose ring through the nitrogen in the 9 position of the purine ring and the pyrimidines are attached to the ribose ring through the nitrogen in the 1 position of the pyrimidine ring.
- the pyrimidine can be modified at the 5- or 6- position of the pyrimidine ring and the purine can be modified at positions 2-, 6- or 8- of the purine ring. Certain modifications are described in copending United States Patent Applications Serial Nos. 08/264,029, filed June 22, 1994, entitled "Novel Method of Preparation of
- a nucleobase includes, but is not limited to, uracil, cytosine, N4-protected cytosine, 4-thiouracil, isocytosine, 5-methyluracil (thymine), 5-substituted uracils, adenine, No-protected adenine, guanine, N2 -protected guanine 2,6-diaminopurine, halogenated purines as well as heterocycles meant to mimic the purine or pyrimidine ring, such as imidazole.
- Starting material refers to the compound that is reacted with the 5 '-protected monomer unit during each cycle of PASS to produce an oligomer that has been extended by one or more nucleotides.
- the starting material can be designed to produce a [5',3'] linkage between nucleotides or a [3', 3'] linkage between nucleotides, depending on the desired oligonucleotide product.
- the starting material is a 5'- deprotected otherwise protected oligonucleotide of length n
- the starting material is a 3 '-deprotected otherwise protected oligonucleotide of length n.
- the starting material is a 5'-deprotected otherwise protected oligonucleotide of length n, wherein n is an integer from 1-1000.
- the starting material is 2', 3'-protected by protecting groups, such as base labile groups, that are compatible with the reaction of the 5 '-protected monomer units with the starting material and with 5'-deprotection reactions.
- the PASS process consists of the controlled and sequential polymerization of an oligonucleotide, the starting material of one PASS cycle is typically the deprotected product from the previous PASS cycle. Because the PASS process does not require that the 3'- terminal nucleotide be anchored to a solid support, the starting material can include non- nucleoside modifications.
- Non-nucleoside modificiations can be introduced to the 3'- terminus which would not ordinarily be possible by solid phase synthesis.
- Non-nucleoside modifications to the 3 '-terminus of the starting material include, but are not limited to, the use of polyethylene glycol mono-methylether (molecular weight 5,000 to 100,000) (PEG) or other high molecular weight non-immunogenic units as the 3 '-terminal monomer for preparation of oligonucleotides with improved pharmacokinetic properties.
- PEG polyethylene glycol mono-methylether
- Product refers to an oligonucleotide that is produced by the covalent reaction of the 5'-protected monomer unit with the starting material during each PASS cycle.
- the starting material is a 5'-deprotected oligonucleotide of length n and the 5'-monomer unit is a single nucleotide
- the product of the reaction will be a 5'-protected oligonucleotide of length n+1. If the 5'-protected monomer unit is an oligonucleotide block of length m the product of the reaction will be a 5-protected oligonucleotide of length n+m.
- the product from a particular PASS cycle is then 5'- deprotected and becomes the starting material for the next cycle.
- a “failure sequence” refers to the starting material from a particular PASS cycle that fails to react with the 5'-protected monomer unit during that cycle.
- “Growing oligonucleotide chain” refers to either a 5'-deprotected oligonucleotide chain or a 5'-protected oligonucleotide chain that has been prepared by the sequential addition of nucleotides (N) beginning with the 3 '-terminal nucleotide of the desired nucleotide using the method of this invention. After each reaction cycle of the PASS process the growing oligonucleotide increases in length by at least one oligonucleotide, and becomes the starting material for the next reaction cycle.
- the term can refer to either starting material or product and one of ordinary skill in the art will recognize what is intended by the term in a particular context.
- Scheme 2 generally illustrates the method of this invention.
- a 5'-protected monomer unit such as phosphoramidite 7 is added to a starting material 8 in solution, in the presence of an activator, such as tetrazole or preferably 4,5-dicyanoimidazole (DCI) ⁇ see United States Patent Application Serial No. 08/730,556, filed October 15, 1996, entitled "Improved Coupling Activators for Oligonucleotide Synthesis"), to yield a product 9 to which one nucleotide has been added via a phosphite triester linkage.
- an activator such as tetrazole or preferably 4,5-dicyanoimidazole (DCI)
- the starting material 8 is a 5 '-deprotected otherwise protected oligonucleotide of length n, wherein n is an integer between 1 and 1000, and the product is a 5'-protected oligonucleotide of length n+1.
- the 5'-deprotected oligonucleotide starting material 8 is not anchored to a solid support, but rather, using standard methods, is simply 2', 3 '-protected by protecting groups, such as base labile groups, that are compatible with the reaction of the 5'- protected monomer units with the starting material and with 5'-deprotection reactions.
- the reaction mixture contains three species: unreacted 5 '-protected monomer unit 7, unreacted starting material 8, and the product of the reaction, compound 9, which is a 5 '-protected oligonucleotide of length n+1.
- the failure sequence any of the starting material 8 (a 5'-deprotected oligonucleotide of length n) which fails to react with the 5'-protected monomer unit 7 is referred to as the failure sequence, as this sequence was not extended.
- the product of the reaction, compound 9, is a 5 '-protected oligonucleotide chain extended by one nucleotide (length n+1), by the covalent reaction of the 5 '-hydroxy group of starting material 8, an oligonucleotide of length n with the 3 '-phosphoramidite group of the 5'-protected monomer unit 7.
- the product, compound 9, is the major component and the 5'- protected monomer unit 7 and the starting material 8 that did not react are present only in minor amounts.
- the unreacted 5'-protected monomer unit may optionally be removed from the reaction mixture, both to purify the materials and to recover the monomer starting material.
- non-reacted monomer is reacted to form an easily removable ionic species.
- Oxidation of the phosphite triester to phosphate triester may be carried out in the same reaction flask simply by addition of an oxidizing agent. In situ oxidation gives the desired oligonucleotide product 9, the phosphate salt 10 of monomer 7, as well as unreacted oligonucleotide starting material 8.
- the monomer phosphate salt 10 is the only free salt in the reaction mixture and thus is easily removed by techniques known to those in the art, including but not limited to, filtration through an anion exchange resin or membrane or extraction with an aqueous phase.
- the 3 '-terminal monomer is a polyethylene glycol mono-methylether of molecular weight 5,000 to 100,000, preferably 20,000.
- a simple molecular weight cut-off membrane can be used to remove monomer 10.
- the remaining filtrate may then be partitioned in any manner suitable to separate the "oligonucleotide product" from the "failure sequence.”
- the filtrate is applied to a material designed to interact selectively or specifically with the 5'-protecting group (D-E), such as a reverse phase resin.
- D-E the 5'-protecting group
- the product is captured or retained on the solid support by affinity of the 5 '-protecting group constituent D with the resin.
- the filtrate is applied to a material designed to covalently react with the 5'- protecting group (D-E), such as a dienophile derivatized resin where D contains a diene unit.
- the product is captured or retained on the solid support by covalent reaction of the 5'- protecting group constituent D with the resin.
- the unreacted oligonucleotide starting material 8 which does not carry the 5'-protecting group D, is washed away.
- the unreacted starting material may be isolated and stored to be used as an intermediate in a subsequent synthesis.
- the retained oligonucleotide product 9 is then released from the resin according to well known procedures.
- the oligonucleotide product is released by cleavage of the bond between the 5'-oxygen and the protecting group D-E.
- a reagent such as dilute dichloroacetic acid (DCA) may be used to cleave the trityl group, thereby releasing the oligonucleotide coupling product.
- DCA dilute dichloroacetic acid
- the liberated 5'-deprotected oligonucleotide coupling product 11 can then be used as the starting material in an additional coupling reaction.
- Utilization of the 5'-protecting group for anchoring of the oligonucleotide product allows for the possibility of using a wide variety of 3'-terminal modifications.
- These can be groups designed to facilitate separation of the product of the reaction from the 5'-protected monomer unit, such as a polymer of sufficient molecular weight to exploit molecular weight cut-off membranes for this separation, or a metal chelator to effect selective precipitation of the product.
- these groups contain a cleavable linker between the 3 '-terminus of the oligonucleotide and the modifying group, such as a succinate linker.
- non-nucleoside 3 '-terminal substituents may enhance pharmacokinetic properties of oligonucleotide products, such as a polyethylene glycol mono-methylether or a distearyl glycerol.
- oligonucleotide products such as a polyethylene glycol mono-methylether or a distearyl glycerol.
- the 3'-terminal monomer may also serve as a detector for diagnostic applications of oligonucleotides, such as a chelator designed to retain Tc99m for in vivo imaging.
- the oligonucleotide product is preferably separated from unreacted starting material each time a new coupling reaction is performed.
- the final oligonucleotide product is obtained in essentially pure form and the cumbersome removal of highly homologous failure sequences is eliminated.
- the reaction is performed in the solution phase, the yields of the reaction of the monomer with the oligonucleotide starting material are also significantly increased.
- a capping step becomes superfluous in this scheme, since only successful oligonucleotide coupling products enter the next step of the process. The elimination of the capping step amounts to another efficiency gain compared to the conventional process.
- oligonucleotide starting material that failed to undergo reaction with the 5 '-protected monomer unit is instead isolated and may be reused.
- failure sequence Each time a failure sequence is reisolated during a PASS iteration, it can be blended into the starting material at the same step or iteration in a subsequent synthesis of the same oligomer, or of an oligomer that shares the same 3'-terminal fragment. (See Scheme 3).
- Failure sequences therefore, become useful sequential building blocks for the subsequent manufacture of oligonucleotides. This not only increases the efficiency of the process, it also dramatically increases the purity of the final crude product. It further allows using the monomer as the limiting reagent and thus, dramatically increases process efficiency.
- the outlined synthetic scheme which exploits the 5 '-protecting group as the anchor for separation of product from starting materials and allows failure sequences to become intermediates for subsequent syntheses, is not limited to phosphoramidite coupling chemistry. It is compatible with other coupling reactions, such as, H-phosphonate or phosphate triester coupling chemistry. (See Gaffney and Jones (1988) Tetrahedron Lett. 29:2619-2622). This scheme also lends itself to automation of oligonucleotide synthesis and is ideally suited for the large scale manufacture of oligonucleotides with high efficiency.
- the covalent capture of desired or unwanted species in oligonucleotide synthesis can also be applied to a high resolution, single-step purification method in conventional solid phase or solution phase processes. If only the terminal monomer bears a diene modified trityl group at its 5'-terminus, then selective anchoring of the full length product on a dienophile derivatized resin or membrane removes all major failure sequences from the crude mixture. (See Scheme 1).
- a capping reagent which contains a moiety suitable for covalent capture (all D groups described above apply), such as a diene-modified acetic anhydride (or generally a D- modified acetic anhydride) or diene modified silyl chloride, such as 3,5-hexadienoxyacetic anhydride or tri-(3,5-hexadienoxy)silyl chloride, then all capped failure sequences can be removed from a crude oligonucleotide batch either after every monomer addition (in solution phase oligonucleotide synthesis processes) or after cleavage of the crude oligonucleotide from the solid support (in conventional solid phase oligonucleotide synthesis processes).
- the reaction of a diene modified trityl group with a dienophile modified resin allows facile preparation of cation exchange resins.
- a dimer of 2'-fTuoropyrimidine modified RNA oligonucleotides is assembled by the PASS process in Example 1 (Scheme 4).
- phosphoramidite coupling chemistry is employed to form a 3',3'-phosphodiester linkage. Oligonucleotides are often protected against 3'- to 5'-exonucleolytic degradation by incorporation of a 3',3'- phosphodiester linkage at the 3'-terminus.
- the reaction mixture is oxidized in situ to produce unreacted thymidine starting material 12, oxidized amidite monomer 15, and oxidized dimer product 14.
- the oxidized amidite monomer 15 is removed by filtering the reaction mixture through a bed of diethylaminoethylene (DEAE) Sephadex ® . HPLC analysis of the filtrate indicates that the oxidized amidite monomer 15 has been retained by the DEAE Sephadex ® as shown in Figure 3.
- the filtrate which contains the oxidized dimer product 14 and the unreacted thymidine starting material 12, is concentrated and redissolved in 60%) acetonitrile/water and loaded onto a C18 filter plug.
- the resin is washed with 70% water/acetonitrile followed by 50% water/acetonitrile to fully elute the unreacted thymidine starting material 12.
- Example 2 illustrates the method of this invention, wherein the 5'-protected monomer unit is an H-phosphonate, rather than a phosphoramidite.
- the 5'-protected monomer unit is an H-phosphonate, rather than a phosphoramidite.
- an H-phosphonate thymidine trimer bearing a 3',3'-internucleotidic linkage at the 3'-terminus (T-T-[3',3']-T trimer) 20 is prepared.
- the efficiency of the liquid phase coupling reaction was so high, that no unreacted 3'-terminal fragment 19 was detected.
- the reverse phase step is used only to cleave and separate the trityl group from the product.
- Example 3 describes the synthesis of a phosphoramidite monomer containing 5'-O-(4,4'-dioctadecyloxytrityl) (DOT) as the 5'-protecting group (D-E).
- DOT 5'-O-(4,4'-dioctadecyloxytrityl)
- Example 4 illustrates the ability to separate the coupling product from the unreacted oligonucleotide starting material (failure sequence) based upon the selective or specific interaction of the 5'-protecting group (D-E) with a particular resin or phase.
- D-E 5'-protecting group
- Example 4 illustrates the ability to separate the coupling product from the unreacted oligonucleotide starting material (failure sequence) based upon the selective or specific interaction of the 5'-protecting group (D-E) with a particular resin or phase.
- DOT 4,4'-dioctadecyltriphenylmethanol
- DMT dimethoxytritanol
- the coupled product can then be eluted from the chamber by cleavage of the trityl protecting group with a haloacetic acid in an organic solvent.
- the trityl group is retained on the resin.
- Example 5 describes the assembly of a hexamer oligonucleotide (5'-HO-T-T- A-C-T-[3',3']-T) in solution using an anion exchange medium to remove the excess monomer and C18 reverse phase resin to selectively capture the 5'-DMT protected product while not retaining the failure sequence.
- each monomer addition is accomplished in two steps.
- phosphoramidite coupling chemistry is employed to couple the 5'-protected monomer unit to the starting material. After coupling, the reaction mixture is oxidized in situ to produce unreacted starting material
- oxidized amidite monomer (failure sequence), oxidized amidite monomer, and oxidized product.
- the oxidized amidite monomer is removed by filtering the reaction mixture through an anion exchange medium, such as, DEAE Sephadex ® .
- the filtrate which contains the oxidized product and the unreacted starting material (failure sequence) is treated with a dilute acid to effect detritylation.
- dilute acids which can be used include, but are not limited to, dilute mineral acids, dilute trichloroacetic acid, dilute dichloroacetic acid (DCA), Lewis acids, such as, ZnBr 2 , nitromethane, tosic acid and perchloric acid.
- the mixture is then separated by chromatography.
- the mixture of product and unreacted starting material is first separated using a reverse phase resin followed by detritylation to release the detritylated product from the resin.
- the analytical data provided in Example 5 shows that the PASS process produces essentially pure oligonucleotide intermediates at every iteration with minimal consumption of cost-limiting monomer.
- Example 6 illustrates schematically an automated extraction/filtration system 110 designed for use with the method of this invention, to separate the unreacted 5'-protected monomer unit from the remainder of the reaction mixture.
- the automated extraction/filtration system 110 has two centers: an extraction vessel 112 and a chromatography resin filtration chamber 114.
- the extraction vessel is in fluid communication with the chromatography resin chamber by a tube 118.
- a first three way valve 120 controls the flow of the contents from the extraction vessel 112 into the chromatography chamber 114.
- a second valve 122 controls the addition of solvents into chamber 114.
- a third valve 124 controls the collection of effluent out of chamber 114. All three valves are electronically coupled to a controller 126, that provides signals that actuate all three valves 120, 122, and 124 between their various flow positions.
- Extraction vessel 112 is equipped with two inlet ports, 128 and 130, a stirrer 132, and an outlet port 134.
- the reaction mixture is pumped into the extraction vessel 112 through inlet port 128 and an extraction solvent, such as CH 2 C1 2 , and an aqueous buffer are pumped into the extraction vessel through inlet port 130.
- the mixture may be agitated with stirrer 132, after which time the layers are allowed to separate.
- the first three way valve 120 is then opened and the bottom organic layer flows through outlet port 134, into a conductivity monitor 136 and then through tube 118 into chamber 114.
- the conductivity monitor is electronically coupled to the controller 126.
- a rise in conductivity indicates that the organic layer has passed through the conductivity monitor and the aqueous layer has begun to enter.
- the rise in conductivity is recognized by the controller 126 which sends a signal to the first three-way valve 120 actuating the three-way valve to divert the aqueous layer away from chamber 114.
- Chamber 114 is equipped with three inlet ports 138, 140, and 142 and an outlet port 144.
- the organic layer enters chamber 114 through inlet port 138 and is pushed through the chamber 114 with a pressurized inert gas source, such as argon, which enters the chamber through inlet port 140.
- a pressurized inert gas source such as argon
- the chamber is then washed with solvent, i.e., CH 2 C1 2 , which enters the chamber through inlet port 142.
- solvent i.e., CH 2 C1 2
- the addition of solvent is controlled by the controller which selectively actuates the second valve 122.
- the organic effluent is collected through outlet port 144 by opening of the third valve 124 by the controller 126.
- the organic effluent contains the product of the reaction, which is the starting material extended by one nucleotide and unreacted oligonucleotide starting material (failure sequence).
- the unreacted 5'- protected monomer is retained in the chamber 114.
- the chamber 114 is washed with a buffered solution, added through inlet port 140, which elutes the unreacted 5'-protected monomer unit.
- Chamber 112 is then re-equilibrated with the organic solvent being used to elute the reaction mixture, i.e., CH 2 C1 2 .
- the organic effluent is next passed over a reverse phase resin, to separate the product from the unreacted oligonucleotide starting material (failure sequence). (See Example 6).
- Example 7 describes the solution phase synthesis of the 15 base oligonucleotide (5*-CTAAACGTAATGG-[3',3']-T-T-3') (SEQ ID NO:l) using polyethylene glycol of 20,000 molecular weight as a 3' residue modification.
- This example demonstrates the efficiency of solution phase synthesis and the potential for preparing 3 '-modified oligonucleotides in solution which can not be directly prepared using conventional solid phase synthesis.
- This example outlines the basic steps required for solution phase synthesis without the step wherein the oligonucleotide coupling product is captured on a resin as in a typical PASS cycle.
- this example also demonstrates the impact on efficiency and product purity that product capture provides as envisioned in PASS.
- Example 8 describes the synthesis of various diene modified trityl alcohols including a 5'-di-(3,5-hexadienoxy)tritylthymidine phosphoramidite monomer (32) and a 5'-di-(2,4-hexadienoxy)tritylthymidine phosphoramidite monomer.
- Example 9 (Scheme 9) demonstrates the use of dienes ⁇ 4,4'-di-3,5- hexadienoxytrityl alcohol (30) and 4,4'-di-2,4-hexadienoxytrityl alcohol (36)-- for efficient cycloaddition to maleimides (Reactions 1 and 2 respectively (Scheme 9)).
- Table 4 sets forth the reaction rates for these two reactions under various conditions. From the data set forth in Table 4, it is clear that modified trityl compound (30) reacts faster under the various reaction conditions. It is also clear that, as expected, both the increase in dienophile equivalents, as well as the addition of water to the reaction mixture increase the reaction rate.
- Example 10 describes the preparation of 3'-PEG derivatized oligonucleotides by PASS using the 4,4'-di-3,5-hexadienoxytrityl protecting group for capture of the oligonucleotide product on a substituted maleimide-polystyrene resin. This capture step removes the non-reacted starting oligonucleotide (failure sequence) from the reaction mixture.
- a 3'-PEG terminal modification is useful ter alia, for enhancing the pharmacokinetic behavior of therapeutic oligonucleotides in vivo.
- Example 11 describes a general reaction scheme for the preparation of non- PEG derivatized oligonucleotides by Diels-Alder product capture using a 5'-O-(4,4'-di-3,5- hexadienoxytrityl)-nucleoside (5'-O-DHDT-nucleoside) 46 as the diene and a maleimide substituted solid support 45 as the dienophile. (Scheme 11). As discussed above, the capture of full length oligonucleotides on a resin or membrane is integral to automating the PASS process.
- the general design of the capture involves a trityl group or trityl analog being irreversibly bound to a solid support, such as a resin, membrane, or polymer 47. Once bound, the oligonucleotide 49 is released by separating it from the irreversibly bound trityl group 48.
- a solid support such as a resin, membrane, or polymer 47.
- the oligonucleotide 49 is released by separating it from the irreversibly bound trityl group 48.
- Diels-Alder capture of the 5'-O-DHDT-nucleoside described above. Resin-bound active Diels-Alder dienophiles covalently react with diene trityls and conventional methods of detritylation release the nucleoside from the solid support and bound trityl group.
- This capture can be employed to prepare non-PEG derivatized oligonucleotides by PASS as described in Example 11 (Scheme
- solid supports are envisioned to be suitable for capture and release using the Diels-Alder reaction.
- Preferred solid supports are inorganic oxides selected from the group consisting of silica, alumina, zeolites, controlled pore glass, that have hydroxyl groups that are capable of being functionalized, as illustrated in Schemes 13 and 14.
- these inorganic oxides have been functionalized by silylating the hydroxyls with a silylating agent that has a more versatile or reactive functional group. (Scheme 13).
- the solid support is an organic support such as polystyrene, or amino-functionalized polystyrene.
- organic support such as polystyrene, or amino-functionalized polystyrene.
- These supports can be derivatized using standard methods known to those in the art.
- Examples 18-21 illustrate two methods of preparing triazoline dione derivatized amino-functionalized resins.
- Example 12 Scheme 15 describes the preparation of a dimer using product capture by Diels-Alder cycloaddition. The rate of capture of the 3',3'-linked 5'-DHDTO-T-T dimer is dependent on the excess of resin bound maleimide groups. Product capture proceeds quantitatively. The captured product is easily and quantitatively released from the resin with 3% dichloroacetic acid in dichloromethane. After neutralization and concentration, pure product is obtained.
- Example 13 describes a method for assembly of oligonucleotides from blocks by capturing one of the blocks on a resin using the cycloaddition of a 5'-O-(4,4'-di- 3,5-hexadienoxytrityl) protected oligonucleotide to a dienophile derivatized resin.
- Example 14 illustrates schematically an automated extraction/filtration system 200 and process designed for the automated preparation of an oligonucleotide bearing a 3'-terminal polyethylene glycol using covalent capture of the monomer addition product at every cycle, as described in Example 10.
- the PASS process which consists of a controlled, sequential polymerization of nucleoside phosphoramidites, is ideally suited for automation.
- Each monomer addition consists of a sequence of chemical processing steps. This sequence remains the same for each monomer addition (cycle). The only variable from cycle to cycle is the nature of the monomer that is added.
- a typical oligonucleotide consists of 2 to 12 different monomers, which are added typically more than once in a dedicated, programmable sequence.
- the automated extraction/filtration system 200 has three centers: a reaction vessel 212, a filtration chamber 214 ⁇ which contains the dienophile modified solid support 215 ⁇ and an ultrafiltration membrane system 218.
- Example 14 also lists various ultrafiltration membranes compatible with the conditions required for the separation of a product oligonucleotide and excess monomer after release from the capture resin. Membranes are evaluated based on reagent/product adsorption, retention, and reactivity. The membranes set forth in Example 14 were found to be suitable, based on flux rates as affected by solvent, loss of product due to adsorption, and finally by diffuse reflectance FTIR.
- Example 14 For purposes of illustration, the preparation of a 3'-terminal PEG oligonucleotide is described in Example 14, however, this automated method of synthesis can be done with or without a macromolecule attached to the oligonucleotide. In the latter case, the molecular weight cut-off membrane may be replaced by a liquid/liquid extraction step, as depicted in Figure 5.
- Example 15 describes the synthesis of maleimide derivatized trityl groups.
- an integral part of the PASS process is a method of removing n-1 sequences.
- One approach is oligonucleotide synthesis using monomers containing a maleimide-modified trityl group. These trityl groups are susceptible to reaction with diene- modified resins allowing separation of n-1 by simple washing of the resin followed by detritylation to release the full-length oligonucleotide.
- Example 16 describes the use of diene-modified capping reagents for the selective removal of failure sequences during solution phase synthesis and conventional solid phase synthesis.
- failure sequences are capped with acetic anhydride.
- the capping reaction with acetic anhydride proceeds rapidly and near quantitatively.
- diene modified analogs of acetic anhydride such as, 3,5-hexadienoic acid anhydride (74) and 3,5-hexadienoxyacetic anhydride (75) (Scheme 18) allows efficient capping of failure sequences and also enables removal of the capped failure sequence by cycloaddition to a dienophile derivatized resin or membrane at each cycle during solution phase synthesis as described in Example 7.
- the 5'-acetyl capping groups introduced during conventional solid phase synthesis are removed during the ammonia cleavage and deprotection step.
- the oligonucleotide In order to utilize reagents 74 or 75 as capping reagents in solid phase synthesis and as subsequent handles for selective removal of the failure sequences, the oligonucleotide must be bound to the support via a linker, such as described in Example 12, which is selectively cleavable under non-basic conditions.
- a capping reagent can be used which is not susceptible to removal under the typical basic deprotection conditions used at the end of conventional solid phase synthesis.
- the hexadienoxysilyl chlorides (76, 77 and 78), allow selective removal of the failure sequences once the crude oligonucleotide is cleaved from the support with ammonia.
- the silyl ether group is not removed under these conditions.
- the hexadienoxysilyl capped failures can be removed from the desired product by reaction with a dienophile derivatized resin or membrane.
- Scheme 19 illustrates generally a preferred method of this invention.
- integral to the PASS process is the chemoselective isolation of the product after every monomer addition, preferably by covalent anchoring on a resin, polymer or membrane.
- the method of covalent anchoring is via Diels-Alder reaction using a l,2,4-triazoline-3,5-dione (TAD) modified resin as the dienophile resin component.
- TAD l,2,4-triazoline-3,5-dione
- the use of triazoline diones not only dramatically accelerates the anchoring reaction, but also allows visual monitoring of this crucial step.
- a urazole is linked to a solid support.
- the immobilized urazole is oxidized to the triazoline dione with oxidizing agents such as NBS, N 2 O 4 , NCS or t-butyl hypochlorite.
- oxidizing agents such as NBS, N 2 O 4 , NCS or t-butyl hypochlorite.
- DHDT hexadiene labeled trityl groups
- reaction of TAD resin 80 with a diene-trityl modified oligonucleotide product, such as 46 produces the anchored product 81.
- the TAD group prior to anchoring by reaction with the diene-trityl modified product, displays a characteristic deep red/purple color.
- a urazole-derivatized resin is oxidized to the corresponding 1 ,2,4-triazoline-3,5-dione resin (TAD-resin) prior to use with an excess of oxidant.
- TAD-resin 1 ,2,4-triazoline-3,5-dione resin
- the oxidant is removed from the resin by washing the resin with the appropriate solvents.
- the solvent in which the Diels-Alder capture reaction is to take place in is added to the resin to allow the resin to swell.
- the di-hexadienoxytrityl (DHDT)-derivatized oligonucleotide is then added to an excess of at least 2 equivalents of the resin per equivalent of DHDT.
- the reaction is monitored for the disappearance of the oligonucleotide by either TLC or HPLC.
- the TAD-resin is added to the crude oligonucleotide product bearing a 5'- terminal DHDT group until the deep red color, characteristic of excess unreacted TAD- resin, persists.
- the resin is thoroughly washed with the appropriate solvents to remove any leachable material.
- the resin is then resuspended in the appropriate solvent and treated for 5 to 20 minutes with an acid sufficiently strong to effect detritylation and concomitant release of the 5 '-deprotected oligomer.
- a solution of 3% dichloroacetic acid in dichloromethane is used.
- the resin is removed from the solution via filtration and the combined organic layers are repeatedly washed with a basic aqueous solution, preferably a NaHCO 3 solution, followed by neutral aqueous solution, until the pH of the organic layer is between 6 and 7.
- the organic layer is then dried over Na ⁇ O,, and concentrated to yield the 5'-deprotected oligomer as a solid.
- Example 17 (Scheme 22, Figure 10) describes the Diels-Alder reaction of the diene subtituted trityl alcohol 5'-O-(4,4'-di-3,5-hexadienoxytrityl)thymidine (5'-DHDTO-dT) (31) with phenyltriazoline-dione (PTDA) (82).
- PTDA phenyltriazoline-dione
- Examples 18-21 illustrate two general methods for preparing triazoline dione derivatized resins.
- Examples 18 and 19 a urazole derivatized with benzoic acid is reacted with an amino-functionalized resin.
- Example 20 a urazole is formed directly on the resin.
- Example 21 describes a variety of methods for oxidizing urazole functionalized solid supports.
- Example 22 Scheme 27 describes the derivatization of a solid support with a urazole derivatized with caproic acid. Oxidation of this bound urazole with t-butyl hypochlorite produces the triazoline dione derivatized resin (99).
- Examples 19 and 22 illustrate the attachment of urazole to the solid support via an amide linkage. Urazole can also be attached to the solid support via an ester linkage.
- the solid support can be selected from a resin, membrane or polymer. Examples include, but are not limited to silica, cellulose, polypropylene, polyvinyl alcohols, methacrylates, polystyrene and polyethylene glycol.
- Example 23 illustrates the synthesis of a bis-TAD compound, the synthesis of a diene derivatized resin and the Diels-Alder reaction of the two compounds to generate a TAD resin without the need for on resin oxidation of the urazole to the TAD.
- thiocarbonyl compounds such as thioketones, thioaldehydes, thioesters, thiocarbamates, thiocarbonates and thioamides, ⁇ -nitroacrylic acid and nitroso compounds can also be attached to a solid support and used in the capture release step.
- Thiocarbonyl compounds are highly reactive dienophiles, much more so than their carbonyl counterparts. Diels-Alder reactions of thiocarbonyl compounds proceed in good yield with butadienes at room temperature. (Weinreb and Staib (1982) Tetrahedron 3_8.3087).
- Another reactive dienophile that can easily be covalently attached to a solid support is ⁇ -nitro acrylic acid. (Carruthers (1990) in Cycloaddition Reactions in Organic Synthesis. Pergamon Press, page 99). This dienophile also reacts with butadiene derivatives under mild conditions.
- Another potentially useful class of dienophiles are nitroso compounds. (Boger et al. (1985) J. Org. Chem. 50:19911). These compounds can be generated in situ from benzohydroxamic acids by treatment with tetraalkyl periodate solutions. Once formed, the nitroso group quickly undergoes a Diels- Alder cycloaddition with butadiene.
- Example 24 (Scheme 31) describes the use of a thiocarbonyl derivatized resin as the dienophile in the standard DHDT capture release cycle. This resin is easily prepared by standard synthetic organic methodologies and requires no oxidation step to produce the dienophile.
- Example 25 describes the use of a nitroacrylate derivatized resin as the dienophile in the standard DHDT capture release cycle. Like the thiocarbonyl resin, the nitroacrylate derivatized solid support requires no preactivation. This resin is used in the standard DHDT capture release cycle.
- Example 26 describes the use of a thioaldehyde resin generated in situ from a resin bound thiosulphinate. The thioaldehyde resin that is generated in the presence of the DHDT containing oligonucleotide is capable of undergoing a Diels-Alder reaction with the DHDT moiety thus capturing the desired product on the resin.
- Example 27 illustrates the use of a nitrosoformate resin as the dienophile in the standard DHDT capture release cycle.
- the nitrosoformate resin is generated in situ from a hydroxycarbamic ester derivatized resin by the excess tetra alkyl periodate present in the oligo mixture from the oxidation of the phosphite triester to the phosphate triester.
- the nitrosoformate group is a very reactive dienophile and will quickly capture the DHDT moiety on the resin via a Diels-Alder cycloaddition reaction.
- Figure 12 illustrates schematically one monomer addition cycle for Product Anchored Sequential Synthesis (PASS) of an oligonucloetide according to a preferred embodiment of this invention.
- the starting material a 3'-terminal oligonucleotide fragment
- an organic soluble oxidizing agent preferably tetrabutylammonium periodate
- oxidizing agents which are soluble in organic solvents, such as iodobenzene diacetate may also be used.
- the dienophile resin preferably a triazoline-dione derivatized resin
- the anchoring reaction is allowed to proceed until complete anchoring of the coupling product on the resin is achieved.
- the resin is washed and exposed to a reagent that removes the resin-anchored, 5'-terminal protecting group , preferably the DHDT group, from the 5 '-oxygen of the oligonucleotide fragment.
- This step which is preferably carried out with dilute dichloroacetic acid, releases the product from the resin.
- the acid reagent is removed by passing the reaction mixture over a DOWEX resin.
- the product is isolated by precipitation.
- the reaction solvent preferably a solvent mixture containing acetonitrile
- the anchoring step may be performed prior to oxidation.
- the resin-bound product is oxidized by exposure to an oxidizing agent that will convert a phosphite to a phospahte species, such as pyridine buffered aqueous iodine.
- an oxidizing agent that will convert a phosphite to a phospahte species, such as pyridine buffered aqueous iodine.
- DOWEX step for removal of excess dichloroacetic acid is not always necessary.
- the product can be precipitated, and acid removal is achieved either by washing the precipitate, by trituration or by recrystallization of the precipitate.
- Example 28 describes one monomer addition cycle of the PASS process wherein the product is covalently anchored to a l,2,4-triazoline-3,5-dione (TAD) modified resin via Diels-Alder reaction.
- TAD l,2,4-triazoline-3,5-dione
- Diels-Alder reaction is a preferred method for anchoring the product of the reaction to a solid support
- other methods are also contemplated as being within the scope of this invention.
- a 2+3 dipolar cycloaddition reaction may be applied to the anchoring step.
- an alkene group either part of the D group on the oligonucleotide product or on the resin, is reacted with a 1,3 -dipolar substituent to form the cylic five-membered addition product.
- a 2+2 cycloaddition reaction may also be applied to the anchoring step. (Scheme 20).
- a solid support derivatized with a ketene is prepared and treated with an olefin modified 5'-trityl oligonucleotide.
- ketene isocyanate or other reactive cummulene
- olefin modified 5'-trityl oligonucleotide is prepared and treated with an olefin modified 5'-trityl oligonucleotide.
- REP ring-opening methathesis polymerization
- a 7-oxanorbornene derivatized trityl is prepared and coupled to the 5' alcohol of a nucleoside.
- the phosphoramidite or H-phosphonate
- the ROMP polymerization is carried out and the resulting polymeric solution filtered and washed.
- the polymer is then treated with the CH 2 C1 2 /DCA mixture to liberate the full length oligonucleotide.
- Example 29 describes a general synthesis of diene-ols using hydroboration.
- Scheme 36 illustrates oligonucleotide synthesis using product anchoring by coupling to a resin bound monomer. This preferred embodiment retains the desired aspects of the PASS process without the need for producing diene trityl nucleoside phosphoramidites and without the need of preparing the triazoline dione resin.
- N-protected 5' and 3' hydroxyl nucleosides are known to react selectively at the 5' hydroxyl group with trityl chloride. (Beaucage and Radhakrishnan (1992) Tetrahedron 48:2223).
- trityl chloride resin available from Calbiochem-Novabiochem
- an N-protected nucleoside at the 5' hydroxyl group producing a 5' tritylated nucleoside directly attached to a solid support (137).
- This resin bound nucleoside can be phosphitilyated at the 3' end by treatment with excess phosphitilyating reagent. Since the nucleoside is attached to a solid support, the excess reagents can be easily removed by a wash step.
- the resulting phosphoramidite resin (139) can then be treated DCI and with a 5' hydroxyl N-protected, 3' protected nucleoside (or 5' hydroxyl oligonucleotide with all other sites protected) to produce a resin bound phosphotriester dimer (or in the case of the 5' hydroxyl oligonucleotide, the n+1 mer of the oligonucleotide). Any of the unreacted 5' hydroxyl (monomer or oligo) can be recovered by washing the resin.
- the resulting phosphite triester is oxidized to the phosphate triester by washing the resin with the appropriate oxidizing solution (either iodine or tetra alkyl periodate or for forming phosphorothioates the standard Beaucage reagent can be used).
- the desired product 141 can then be cleaved from the resin by running the standard deblock cycle.
- the trityl group stays bound to the resin (as in the Diels-Alder capture release example) and the product is washed off in the methylene chloride/dichloroacetic acid solution.
- This embodiment is not limited to the particular trityl resin shown or to the particular coupling chemistry described above. Rather, in a more generic sense, the present invention describes the preparation of a linear, sequential polymer by anchoring of the incoming monomer to a resin, soluble polymer, membrane, or immiscible liquid phase. The attachment of the incoming monomer is achieved through a removable protecting group, preferentially the 5'-protecting group in nucleoside monomers for oligonucleotide synthesis. In peptide synthesis, the monomer is preferentially anchored through the N- terminal protecting group.
- the growing polymer chain is attached to the anchored monomer by standard coupling chemistry, such as phosphoramidite, H-phosphonate or phosphate triester coupling in case of oligonucleotide synthesis.
- standard coupling chemistry such as phosphoramidite, H-phosphonate or phosphate triester coupling in case of oligonucleotide synthesis.
- all reagents and any remaining uncoupled polymer starting material are removed by simply washing the anchored product. This step is important, since it effects the purification of the growing polymer after every monomer addition without the need for complex purification techniques.
- the extended polymer chain is then released from the resin, soluble polymer, membrane or immiscible liquid phase by a reagent that cleaves the protecting group from the extended polymer chain.
- Example 30 (Schemes 37-39) illustrates the use of a trityl resin in the PASS process.
- the trityl chloride resin is derivatized with a thymidine nucleoside (through the 5'-hydroxyl), the resin bound nucleoside is phosphitilyated at the 3'- hydroxyl and then treated with a slight excess of 5'-diphenyl t-butyl silyl thymidine nucleoside (3' OH) in the presence of DCI activator. After the coupling and oxidation steps are complete the resin is washed to remove all unreacted material. The product (T-T dimer) is then removed from the resin by the usual detritylation method.
- Example 30 also illustrates the preparation of a trimer using this method.
- Example 31 illustrates the application of the PASS process to a high resolution, single-step method of purification.
- a 5'-DHDT derivatized nucleoside is protected at the 3 '-position with a tertbutyldiphenylsilyl group followed by purification using the PASS process.
- capture was 100% and the purity of the final product was 91%.
- This example demonstrates that column-based purifications can be replaced using the capture-release techniques employed in the PASS process.
- the following examples are provided for illustrative purposes only and are not intended to limit the scope of the invention.
- Example 1 Preparation of N-4-benzoyl-3'-(5'-tert-butyldimethylsilyl-3'-(2- cyanophosphoryl .thvmidyl.-2'-fluorocvtidine (16. (Scheme 4) 5'-tert-butyldimethylsilylthymidine 12 (5'-TBDMS-thymidine) (0.15 g, 0.42 mmol) was dissolved in dry acetonitrile (10 mL) under an argon atmosphere. Cytidine amidite 13 was added (0.43 g,O.50 mmol) followed by tetrazole (6.5 mL, 0.45 M in acetonitrile).
- Example 2 Preparation of a H-phosphonate thymidine trimer (T-T-[3',3']-T. (20. Assembly of a H-phosphonate thymidine trimer bearing a
- trimer 20 To a solution of dimer 19 (0.25 g, 0.39 mmol) in 1 :1 pyridine acetonitrile (23 mL) was added 17 (0.41 g, 0.58 mmol), followed by a solution of pivaloyl chloride (0.14 mL, 1.16 mmol) in 95:5 acetonitrile :pyridine (4.5 mL). The reaction was stirred under an argon atmosphere for 10 minutes, at which point HPLC analysis indicated complete conversion of dimer 19 to trimer 20.
- 5'-TBDPS-thymidine 12 (0.99 g, 2.07 mmol) was co-evaporated with dry methylene chloride and dissolved in 10 mL of dry methylene chloride.
- Thymidine amidite 2.0 g, 2.69 mmol was added followed by tetrazole 0.5 M in acetonitrile (21 mL, 10.5 mmol) and the reaction was stirred under argon. After 90 minutes, a solution of iodine/water/pyridine (0.2 M) was added until the dark brown color persisted, followed by 5% NaHSO 3 until the color returned to yellow.
- the concentrated reaction was partitioned (CH 2 Cl 2 /water) and the organic layer was dried with MgSO 4 and evaporated to dryness.
- the solid residue was dissolved in methanol/minimal methylene chloride and pipetted onto a 75 g bed of DEAE Sephadex ® equilibrated with water then methanol.
- the DEAE Sephadex ® was washed with 300 mL methanol and the combined methanol washes were concentrated to afford 2.42 g of a white foam.
- Detritylation The white foam was dissolved in 50 mL of 3% DCA and stirred at room temperature for 35 minutes, and then poured over 80 mL of silica gel equilibrated with methylene chloride.
- Detritylation The foam was stirred in 50 mL 3% DCA at room temperature, then pipetted onto a silica bed (approximately 120 mL) equilibrated with methylene chloride. The reaction mixture was eluted with 3% DCA then 100% methylene chloride through 10% methanol in methylene chloride. The appropriate fractions were combined and concentrated to give 1.41 g of the detritylated tetramer (S'-HO-A-C-T- ⁇ ' ⁇ 'l-T), 72% overall yield for the two step process.
- the yellow foam was dissolved in minimal methylene chloride and loaded onto a DEAE Sephadex ® bed equilibrated with water and then methanol.
- the Sephadex ® was washed with methanol, methylene chloride and then acetonitrile. The appropriate fractions were combined and concentrated to give 1.48 g of material.
- Detritylation The material was stirred in 40 mL 3% DCA at room temperature, and then pipetted onto a silica bed equilibrated with methylene chloride. It was eluted with 3% DCA, followed by solutions of 100% methylene chloride through 20% methanol in methylene chloride.
- the crude reaction mixture (1.48 g) was absorbed onto Cl 8 resin and loaded onto a bed of Cl 8 resin (approximately 125 g) which had been equilibrated with acetonitrile, followed by 70% water/acetonitrile.
- the resin was first washed with 1 :1 wate ⁇ acetonitrile to elute the monomer, followed by acetonitrile and methylene chloride to elute the hexamer.
- the appropriate fractions were combined and concentrated to give 0.83 g, (66% yield) of a solid.
- Detritylation The solid was stirred in 20 mL of 3% DCA at room temperature.
- Dowex Cl-form can be used to remove residual DCA from a solid sample.
- a T-A phosphoramidite dimer was found by NMR to contain approximately 1.2 equivalents of DCA following detritylation and hexane precipitation.
- a sample of this dimer (0.3 g) was dissolved in acetonitrile (5 mL) and loaded onto a column of Dowex Cl- form (15 g) which had been pre-equilibrated with acetonitrile. The liquid was eluted dropwise and the column was then washed with 35 mL of acetonitrile and concentrated to yield 0.26 g of a white foam.
- a sample checked by NMR shows approximately 95% reduction of acid.
- the reaction mixture is pumped into extraction vessel 112, through inlet port 128 ( Figure 5).
- Triethylammonium bicarbonate buffer (TBK) (0.05 M) and CH 2 C1 2 are added to the extraction vessel through inlet port 130, and the mixture is stirred.
- TK Triethylammonium bicarbonate buffer
- CH 2 C1 2 CH 2 C1 2 are added to the extraction vessel through inlet port 130, and the mixture is stirred.
- the layers are allowed to separate.
- valve 120 opens and the methylene chloride layer passes through conductivity meter 136, and onto a DEAE Sephadex ® plug 114.
- a rise in conductivity indicates that the CH 2 C1 2 has completely passed through the conductivity meter and the aqueous layer has now entered the meter.
- valve 120 automatically switches to divert the aqueous layer away from the DEAE Sephadex ® plug.
- the organic layer is pushed through the DEAE Sephadex ® plug with argon which enters the chamber through inlet port 140.
- the DEAE Sephadex ® plug is then washed with CH 2 C1 2 which is added through inlet port 142, controlled by valve 122.
- the CH 2 C1 2 effluent which contains the oligonucleotide product and unreacted oligonucleotide starting material (failure sequence), is collected through outlet port 144, controlled by valve 124.
- the unreacted phosphoramidite monomer which has been retained on the Sephadex ® plug, is eluted with the 1 M TBK.
- the Sephadex® plug is then re-equilibrated with CH 2 C1 2 .
- the CH 2 C1 2 eluent is then passed through a reverse phase resin to separate the coupled product from the failure sequence.
- the coupled product which has a DMT group attached to its 5 '-end, is retained on the resin, and the failure sequence is eluted from the chamber.
- the resin is then washed with, acidic dichloroacetic acid (3% in CH 2 C1 2 ), which cleaves the DMT protecting group and releases the coupled product from the chamber.
- the coupled product is eluted into a pH buffered solution to prevent decomposition due to excessive exposure to acid.
- the eluent is concentrated and the coupled product used as the starting material in the next reaction cycle.
- oligonucleotide of sequence 5'-CTAAACGTAATGG-[3',3']-T-T-3' was prepared by liquid phase synthesis, using polyethylene glycol (PEG) of molecular weight 20,000 as the 3 '-terminal modification.
- PEG polyethylene glycol
- Polyethylene glycol allows facile precipitation of the growing oligonucleotide chain during the individual steps.
- This example outlines the basic steps required for solution phase synthesis without the incorporation of the capture of the oligonucleotide coupling product onto a resin as in a typical PASS cycle. Thus, this example demonstrates the impact on efficiency and product purity, that product capture provides as envisioned in PASS.
- Detritylation 5'-DMT-nucleoside 3'-O-PEG (5.0 g) (20k, loading: 45 ⁇ mol/g) was dissolved in 50 mL of a mixture of dichloroacetic acid (DCA) and trihexylsilane (6.4 mL, 80 equivalents) in CH 2 C1 2 . After 9 minutes the detritylated 5'-HO-nucleoside 3'-O-PEG was precipitated with ether (2x), washed, filtered and dried under vacuum. Coupling reaction: The 5'-HO-nucleoside 3'-O-PEG was coevaporated 3 times with 20 mL of anhydrous acetonitrile and dried under high vacuum for 30 minutes.
- DCA dichloroacetic acid
- trihexylsilane 6.4 mL, 80 equivalents
- the flask was flushed with argon and closed to the outer atmosphere. Through the septa was injected: 50 mL of anhydrous acetonitrile to dissolve the 5'-HO-nucleoside 3'-O-PEG, 4.5 mL (0.1 M, 2.0 equivalents) of amidite in anhydrous acetonitrile and 1.4 mL (1.0 M, 6.0 equivalents) of DCI in acetonitrile. The solution was stirred under argon for 25 minutes, then precipitated with ether and dried by coevaporation with 20 mL of anhydrous acetonitrile.
- Oxidation The precipitate was dissolved in 50 mL of anhydrous acetonitrile, and 8 mL (0.1 M) of iodobenzene diacetate in acetonitrile was injected and the reaction mixture was stirred for 8 minutes.
- Capping reaction Acetic anhydride (6 mL), 2,6-lutidine (6 mL) and N-methylimidazole (6 mL) were simultaneously injected to the above solution and the reaction mixture was stirred for another 5 minutes.
- the capped oligonucleotide-PEG polymer was precipitated from ether as described above in the detritylation procedure.
- Example 8 (Schemes 7 and 8) describes the synthesis of various diene modified trityl alcohols including a 5'-O-(4,4'-di-3,5-hexadienoxytrityl) thymidine 3'- phosphoramidite monomer 32.
- Phenylmagnesium bromide (32 mL of a 1.0 M solution in THF, 32 mmol) was added to the solution and the mixture was stirred at room temperature under argon for 5 hours and evaporated to dryness under vacuum. The residue was redissolved in dichloromethane and washed with a saturated solution of ammonium chloride, followed by water. The organic phase was dried (MgSO 4 ), concentrated in vacuo, and purified by column chromatography (silica gel; hexane/CH 2 Cl 2 , 1/9) to yield 4.45 grams (62%) of compound 30 as a yellow oil.
- Thymidine (1.5 grams, 6.18 mmol), which had been coevaporated with pyridine and dissolved in anhydrous pyridine (42 mL), was then added to the solution containing the crude product. A catalytic amount of dimethylaminopyrimidine (DMAP) was added and the reaction mixture was stirred under argon overnight and the solvent was evaporated. The residue was redissolved in dichloromethane and washed with a 5% aqueous solution of sodium bicarbonate followed by water. The organic phase was dried (MgSO 4 ), evaporated and purified by column chromatography (silica gel; EtOAc/hexane, 1/1) to afford 3.53 grams (84%) of compound 31 as an off-white solid.
- DMAP dimethylaminopyrimidine
- Difluorobenzophenone (34) (4.8 grams, 22 mmol) was dissolved in anhydrous DMF (1 liter). NaH (95%; 5.6 grams, 220 mmol) was added and the solution was cooled to 0°C.
- 2,4-Hexadienol (5.8 mL, 51 mmol) was slowly added to the solution and the reaction mixture was allowed to warm to room temperature with stirring under argon overnight.
- the reaction mixture was concentrated in vacuo, dissolved in dichloromethane, and washed with water.
- the organic phase was dried (MgSO 4 ) and concentrated and purified by column chromatography (silica gel; hexane/ CH 2 C1 2 , 1/3) to afford 2.07 grams (25%) of compound 35 as a white solid.
- the 5'-di-(2,4-hexadienoxy)tritylthymidine phosphoramidite monomer can be prepared from compound 36 using the same procedure described above for the preparation of the 5'-O-(4,4'-di-3,5-hexadienoxytrityl)thymidine phosphoramidite (32).
- Example 9 describes the Diels-Alder reaction of diene substituted trityl alcohols ⁇ 4,4'-di-3,5-hexadienoxytrityl alcohol (30) and 4,4'-di-2,4- hexadienoxy trityl alcohol (36)-- with N-ethyl maleimide (Reactions 1 and 2 respectively). Table 4 sets forth the reaction rates for these two reactions under various reaction conditions. SCHEME 9
- Example 10 (Scheme 10) provide the general procedures to be followed for each monomer addition cycle, for the preparation of a 3'-PEG anchored oligonucleotide by solution phase synthesis using the Diels-Alder cycloaddition reaction for the covalent capture of the oligonucleotide product.
- Scheme 12 illustrates a general reaction scheme for the preparation of a non- PEG derivatized oligonucleotide by Diels-Alder product capture using a 5'-O-(4,4'-di-3,5- hexadienoxytrityl)nucleoside (5'-O-DHDT-nucleoside) as the diene and a maleimide substituted solid support as the dienophile.
- R oligonucleotide or 3'-blocking group
- the appropriate 3'-blocked oligonucleotide of length n (50) is coupled with 2.0 equivalents of the amidite monomer 51 by treatment with a 1.0 M solution of DCI in CH 3 CN.
- the 3'-blocking group can be a lipid or polysaccharide, or a more traditional solution-phase blocking group such as acetyl, pyranyl, or silyl group, such as tert-butyldiphenylsilyl ether.
- the coupling reaction takes less than 25 minutes and is monitored by TLC.
- the solution is treated directly with 8.0 equivalents of iodobenzene diacetate as a 0.1 M solution in CH 3 CN.
- the oxidation sequence is complete within 8 minutes and the crude reaction mixture is applied directly to the solid support bearing the dienophile.
- the Diels- Alder cycloaddition reaction is accelerated by utilizing a solvent of 1 : 1 CH 3 CN:H 2 O.
- the oligonucleotide, now covalently bound to the solid support 52, is easily separated from the unreacted starting oligonucleotide 50 (failure sequence) and reagents via simple filtration and washing of the resin beads.
- the amidite monomer 51 which also has a 5'-DHDT group is also bound to the resin (53).
- Detritylation/Release Sequence The washed and dried resin, bearing the covalently bound oligonucleotide (52), as well as, unreacted monomer phosphate (53), is washed with a solution of 3% DCA/CH 2 C1 2 , eluting into a neutralizing buffer to prevent acid-mediated decomposition of the oligonucleotide chain.
- the released oligomer (54) and monomer phosphate (55) are separated from one another via aqueous extraction.
- the product oligonucleotide in the organic phase is dried and exchanged into acetonitrile by ultrafiltration.
- 5'-DHDTO-T-r3'.3'l-T-OSiPDBT-5' (56).
- 5'-TBDPSiO-dT-3'-OH (12A) (0.21 g, 0.43 mmol) was dissolved in 10 mL acetonitrile.
- 5'-DHDTO-dT phosphoramidite (32) (0.5 g, 0.52 mmol) was added to this solution followed by 3.0 mL of 1.0 M DCI in acetonitrile (3.0 mmol). This solution was stirred under argon for 20 minutes, at which time 11 mL of a solution of 0.2 M I 2 in pyridine/water was added.
- Example 13 Preparation of an oligonucleotide from two blocks using fragment anchoring by Diels-Alder cvcloadditon
- the PASS oligonucleotide synthesis scheme allows facile and efficient preparation of oligonucleotide blocks, which can be coupled to each other in a modified PASS cycle as illustrated in Scheme 16. Briefly, the oligonucleotide block 59, prepared by PASS monomer addition cycles as outlined above, is reacted with a maleimide resin to give the resin anchored oligonucleotide block 61.
- the 3'-terminal PEG is removed from this block by reductive cleavage of linker L with titanium trichloride, yielding resin bound fragment 63, which has a free 3'-terminus. Phosphitylation of 63 with N,N-diisopropyl-2- cyanoethyl-chlorophosphine results in the 3'-terminal phosphoramidite 64. Compound 64 is then coupled to oligonucleotide block 62, obtained from detritylation of oligonucleotide block 60 after capture on a maleimide resin and subsequent detritylation.
- the coupling reaction is followed by oxidation of the phosphite triester linkage to the corresponding phosphate triester, followed by release of the product oligonucleotide from the resin with dichloroacetic acid, giving oligonucleotide fragment 60.
- reaction vessel 212 Figure 8
- reaction is allowed to proceed as described in Example 10.
- the reaction mixture is circulated through the diene or dienophile modified resin or membrane (hereafter referred to as the support), which is contained in vessel 214, to covalently capture the oligonucleotide.
- the time required for the capture step can be controlled by monitoring the disappearance of the coupling product from solution either by an HPLC or in line UV assay (not shown).
- the support is then rinsed to elute all failure sequences not containing the diene or dienophile.
- Oxidation can be accomplished either after the oligonucleotide is attached to the support or in solution prior to attachment to the dienophile support.
- the oxidation solution must be thoroughly removed from the resin prior to detritylation. This removal is conveniently controlled by in-line conductance monitoring (not shown).
- the support is then rinsed with DCA/CH 2 C1 2 to remove the growing oligomer and captured excess monomer from the resin, thus allowing the only species in the solution to be the 5'-deprotected oligonucleotide and monomer in a DCA/CH 2 C1 2 mixture.
- This mixture is then brought into contact with a membrane separator (218) to remove the DCA and the excess monomer, in addition to a solvent exchange to acetonitrile.
- the monomer may be separated by precipitation or extraction. The only species remaining in solution is the macromolecule attached oligomer in acetonitrile. This solution is now ready for the next coupling reaction.
- the dienophile support can contain a cleavable linker between the dienophile moiety and the resin or membrane, such as an amide bond. This cleavable linker allows facile regeneration of the dienophile support. Linkers such as these are well known to those skilled in the art. Membrane Evaluation Recovery of Pegylated Deoxythymidine after Exposure to a Polypropylene Ultrafiltration Membrane: Acetonitrile Solvent System.
- a solution of 2.74 mM 20k PEG-deoxythymidine (PEG-dT) was made by dissolving 1.49 grams of 46 ⁇ mol dT/gram PEG-dT in 25 ml of acetonitrile. Aliquots (2 mL) of the solution were then exposed to areas of 5.73 square centimeters of the working surface of a polypropylene ultrafiltration membrane (3M ® ) for periods of 0.25, 1 and 4 hours in 50 mL Falcon ® tubes. The starting solution was rinsed from the Falcon ® tubes and membranes with two 25 mL washes of acetonitrile.
- PEG-dT 20k PEG-deoxythymidine
- the wash solvent was assayed for PEG-dT spectrophotometrically by absorbance at 260 nm and balanced relative to the absorbance of the starting PEG-dT.
- a control to measure losses to the tube and glassware was performed by exposing a Falcon ® tube without a membrane to 2 mL of the starting solution for 4 hours and assaying for PEG-dT at 260 nm. Results are shown in Table 6. Recovery of Pegylated Deoxythymidine after Exposure to a Polypropylene Ultrafiltration Membrane: Methylene Chloride Solvent System.
- a solution of 2.72 mM 20k PEG- deoxythymidine (PEG-dT) was made by dissolving 1.48 grams of 46 ⁇ mol dT/gram PEG- dT in 25 mL of methylene chloride. Aliquots (2 mL) of the solution were then exposed to areas of 5.73 square centimeters of the working surface of a polypropylene ultrafiltration membrane (3M ® ) for periods of 0.25, 1 and 4 hours in 50 mL Falcon ® tubes. The starting solution was rinsed from the Falcon ® tubes and membranes with two 25 mL washes of methylene chloride.
- PEG-dT 20k PEG- deoxythymidine
- the wash solvent was assayed for PEG-dT spectrophotometrically by absorbance at 260 nm and balanced relative to the absorbance of the starting PEG-dT.
- a control to measure losses to the tube and glassware was performed by exposing a Falcon ® tube without a membrane to 2 mL of the starting solution for 4 hours and assaying for PEG- dT at 260 nm. Results are shown in Table 7.
- the starting solution was rinsed from the Falcon ® tubes and membranes with a 25 mL wash of acetonitrile.
- the membrane was soaked in 25 mL of acetonitrile for six days and then washed with an additional 25 mL of acetonitrile.
- the wash solvents were assayed for PEG- dT spectrophotometrically by absorbance at 260 nm and balanced relative to the absorbance of the starting PEG-dT.
- a control to measure losses to the tube and glassware was performed by exposing a Falcon ® tube without a membrane to 2 mL of the starting solution for 4 hours and assaying for PEG-dT at 260 nm. Results are shown in Table 8.
- the PEG-dT content of the supematants was determined spectrophotometrically and balanced relative to the starting- PEG-dT.
- a control to show losses to handling was performed by centrifuging and assaying 1.5 mL of the starting solution by the above method.
- the results are summarized in Figure 9. Compatibility by Flux and FTIR evaluations.
- PVDF Polyvinylidienedifluroride
- polypropylene membranes were evaluated by soaking them in the following solvent systems: acetonitrile, methylene chloride, the Coupling/Capping/Oxidation (c/c/0) solution in acetonitrile, and the mixture of 3% DCA in methylene chloride.
- Scheme 22 describes the Diels-Alder reaction of the diene subtituted trityl alcohol 5'-O-(4,4'-di-3,5-hexadienoxytrityl)thymidine (5'-DHDTO-dT) (31) with PTDA (82).
- SCHEME 22 describes the Diels-Alder reaction of the diene subtituted trityl alcohol 5'-O-(4,4'-di-3,5-hexadienoxytrityl)thymidine (5'-DHDTO-dT) (31) with PTDA (82).
- Scheme 24 illustrates a general procedure for the derivatization of amino- functionalized resins with 4-(4-urazole)benzoic acid (87). This general procedure has been successfully applied to a variety of amino-functionalized resins, including aminopropyl silica gel, aminopropyl CPG, ⁇ ovaSyn ® TG amino resin HL, and ArgoGelTM amino resin.
- urazol derivatized resin (88).
- a suspension of 10.1 g of aminomethyl polystyrene (loading 0.9 mmol/g), preswollen in 50 mL DMF, was added to a solution of 3.13 g (14 mmol) of urazole 87 and 2.3 g (16.9 mmol) HOBT in 100 mL DMF containing 5% pyridine.
- Example 20 Derivatization of amino-functionalized resins via direct formation of a urazole on resin
- Scheme 25 illustrates a general method for the derivatization of amino- functionalized resins via direct formation of the urazole on the resin.
- Example 21 Oxidation of a urazole functionalized solid support to the 1.2.4-triazoline- 3.5-dione (93)
- Example 20 describes a variety of methods for oxidizing a urazole functionalized solid support to the l,2,4-triazoline-3,5-dione (TAD) (Scheme 26). Oxidation of the PTAD is sensitive to the presence of nucleophiles. Oxidation of the urazole to TAD gives a bright red, orange or purple solution as described in the literature. (Keana et al. (1983) Org. Chem. 48:1982).
- Oxidation with dinitro en tetroxide One of the more widely used reagents for oxidizing urazoles to l,2,4-triazoline-3,5-diones is dinitrogen tetroxide (N 2 O 4 ). This oxidant proved effective in oxidizing the soluble urazole 87, as well as the TG amino resin which had been directly derivatized through the isocyanate to the urazole (see Example 20). This oxidant is not effective in oxidizing urazole bound to resins via an amide linker. Oxidation with N-bromosuccinimide.
- N-bromosuccinimide is a stable, relatively safely handled oxidant that forms TADs from the urazole precursors. It is freely soluble in DMF and relatively soluble in CH 2 C1 2 . This oxidant has proven effective in oxidizing the soluble urazole 87, as well as oxidizing urazole bound to a variety of resins via an amide linker (Example 19). This oxidant, however, is not effective in oxidizing the TG amino resin which had been directly derivatized through the isocyanate to the urazole (Example 20). Thus, this oxidant has complimentary reactivity to N 2 O 4 (see above).
- NBS or N 2 O 4 as oxidizing agents, is that both oxidants release acidic byproducts upon oxidation of the urazole substrate, which result in rapid detritylation of the DHDT moiety if not removed from the solid supports prior to introduction of the DHDT-protected oligonucleotide.
- TAD-caproamide resin (99).
- a suspension derivatized resin 98 (0.520 g, manufacturing loading 1.38 mmol per g, 0.718 mmol) in methylene chloride (10 mL) was allowed to gently shake for 10 minutes under argon.
- the suspension was cooled to 0°C and treated with t-butyl hypochlorite (0.173 g, 1.59 mmol).
- the suspension instantly turned bright pink and was gently shaken for 30 minutes while it reached room temperature.
- the solvent was drained off by filtration through a gas dispersion tube attached to a vacuum line.
- the resin was washed with methylene chloride (2x10 mL), DMF (2x10 mL) and methylene chloride (2x10 mL). The pH was monitored and at the end of the washes it was neutral. The resin was dried under high vacuum over P 2 O 5 for 15 hours to obtain 0.360 grams of a dark pink resin (99) (TAD-caproamide resin). IR (KBr) 1754, 1672 cm “1 . Analysis by titration using trans, trans- 1 ,4-diphenyl- 1,3 -butadiene showed loading of 0.46 mmol per gram. Oxidation and titration of a second batch of resin showed a loading of 0.78 mmol per gram.
- reaction mixture was poured into a 2 L separatory funnel and the aqueous phase removed and discarded. The mixture was washed with additional saturated NaHCO 3 (2x100 mL) and brine (1x100 mL). The organic phase was dried with Na 2 SO 4 , filtered and the solvent removed in vacuo.
- the resultant oil (101) was redissolved in toluene and transferred to a 1 L, 3 neck round bottom flask. Enough toluene was added to total 500 mL and the flask was purged with argon. Ethyl carbazate (25.5 g, 1.5 equiv.) was added all at once with vigorous stirring for 15 minutes.
- Derivatization of an aminomethylated polystyrene resin with hexadiene illustrates the derivatization of an aminomethylated polystyrene resin with hexadiene.
- Three different amino methylated resins 1% crosslinked polystyrene(l% DVB- PS-AM, 0.98 mmoles/gram); 2% crosslinked polystyrene (2% DVB-PS-AM, 1.38 mmoles/gram); and highly crosslinked polystyrene (HCL-PS-AM, loading 0.3 mmoles/gram) were functionalized with hexadiene.
- the mixture was allowed to stir for 10 minutes and transferred to the vessels containing the swelled resins, such that 1.5 equivalents of carboxylic hexadiene was transferred onto each resin (24.66 g onto the 2%DVB-PS-AM and 3.11 g onto the HCL-PS-AM).
- Diisopropylcarbodiimide (DIC) was then added to each of the resins (4.64 g onto the 2%DVB-PS-AM and 0.7 grams onto the HCL-PS-AM) and the resins were put on a shaker table for 17 hours with minimal agitation.
- the resins were then rinsed with 5x50 mL washes of DMF:CH 2 Cl 2 :pyridine (47.5:47.5:5) and 5x50 mL washes of CH 2 C1 2 , and dried under vacuum for 24 hours to yield the hexadiene derivatized resins (106).
- Bis-TAD (104) (3.12 g, 5.9 mmole) was brought up in 5 mL (6.42 g) of dichloromethane. 2.2 mL (2.8 grams, 1.96 mmole) of this solution was transferred directly onto three different dry resins: 1%DVB -PS -hexadiene (0.27 mmole), 2%DVB-PS-hexadiene (0.39 mmole) and HCL-PS-hexadiene (0.09 mmole) (106).
- the slurry of resin and bis-TAD was allowed to stir slowly for 16 hours, at which time the resins were all washed with methylene chloride (8x5 mL) and dried under a vacuum to the corresponding derivatized resins (107).
- the loading was evaluated by capture of diphenylbutadiene.
- Example 24 PASS using product capture by Diels-Alder cycloaddition with a thiocarbonyl derivatized resin.
- the coupling reaction mixture of a 5'-HO-oligonucleotide (DNA/RNA, any length) and a 5'-DHDT-nucleoside phosphoramidite with 4,5-dicyanoimidazole in acetonitrile (or propylenecarbonate or other suitable solvent or solvent mixture) is treated with a tetra-alkylamine periodate methylene chloride solution (or sulfurizing reagent for preparing phosphorothioates).
- This mixture which contains as the desired product the 5'- DHT-oligonucleotide phosphotriester which has had the DHT containing monomer incorporated onto it's 5' end (108), is then transferred into vessel containing an excess of the nitroacrylate derivatized resin (113).
- the resin (115) is washed to remove all non- DHDT containing species. Once the resin has been washed clean it is then treated with 3% DCA in methylene chloride to release the captured material. The resin is washed until all of the captured product is released. All of these washes are extracted with an aqueous phosphate buffer (pH approx. 7.0) to neutralize the acid and remove any unreacted hydrolyzed amidite. The dried methylene chloride layer is evaporated to give the desired product.
- Example 26. PASS using product capture by Diels-Alder cycloaddition with a thiocarbonyl derivatized resin generated in situ
- the coupling reaction mixture of a 5'-HO-oligonucleotide (DNA RNA, any length) and a 5'-DHDT-nucleoside phosphoramidite with 4,5-dicyanoimidazole in acetonitrile (or propylenecarbonate or other suitable solvent or solvent mixture) is treated with a tetra-alkylamine periodate methylene chloride solution (or sulfurizing reagent for preparing phosphorothioates).
- This mixture which contains as the desired product the 5'- DHDT-oligonucleotide phosphotriester, which has had the DHDT containing monomer incorporated onto it's 5' end (108), is then transferred into vessel containing an excess of the derivatized resin 117. This mixture is heated to cause the thiosulphinate (117) to decompose to the corresponding solid support tethered thioaldehyde (119).
- DHDT containing product has been removed from the solution by Diels-Alder reaction with the thioaldehyde dienophile (as determined by reversed phase HPLC analysis) the resin (121) is washed to remove all non-DHDT containing species. Once the resin has been washed clean it is then treated with 3% DCA in methylene chloride to release the captured material. The resin is washed until all of the captured product is released. All of these washes are extracted with an aqueous phosphate buffer (pH approx. 7.0) to neutralize the acid and remove any unreacted hydrolyzed amidite. The dried methylene chloride layer is evaporated to give the desired product.
- aqueous phosphate buffer pH approx. 7.0
- Example 27 PASS using product capture by Diels-Alder cycloaddition with a nitrsoformate derivatized resin generated in situ
- the coupling reaction mixture of a 5'-HO-oligonucleotide (DNA/RNA, any length) and a 5'-DHDT-nucleoside phosphoramidite with 4,5-dicyanoimidazole in acetonitrile (or propylenecarbonate or other suitable solvent or solvent mixture) is treated with an excess tetra-alkylamine periodate methylene chloride solution.
- This mixture which contains as the desired product the 5'-DHDT-oligonucleotide phosphotriester which has had the DHDT containing monomer incorporated onto it's 5' end (108), is then transferred into vessel containing an excess of the derivatized resin (123).
- Example 28 PASS Cycle using product capture by Diels-Alder cycloaddition with a triazole dione derivatized resin (Aqueous Free)
- Oxidation of PS-urazole Resin A suspension of 1.7 g of PS-urazole in 20 mL CH 2 C1 2 was treated with 2.7 g of NBS in 15 mL of DMF for 30 minutes. The reaction mixture was then filtered and the bright-red solids were washed with 3x10 mL of DMF and 5x20 mL of CH 2 C1 2 . The solids were dried under vacuum for 1 hour and resuspended in 15 mL of CH 2 C1 2 .
- Detritylation/Release Reaction The resin was then resuspended in 10 mL CH 2 C1 2 and treated with 20 mL of 3% DCA in CH 2 C1 2 to detritylate and release the captured material. A small amount of trityl (evident by the orange color) leached from the solids during the subsequent washes. The solids were washed with 5x30 mL CH 2 C1 2 , until TLC showed no more UV-active material leaching from them. The pale orange washes were then diluted to twice their volume with hexanes. The solvent was removed under vacuum to approximately 1/4 the total volume and the process was repeated with fresh hexanes to completely replace the CH 2 C1 2 with hexanes.
- the trimer-OH product precipitated from solution during the solvent exchange process.
- the solid precipitate was titurated 3x100 mL hexanes and redissolved in ACN.
- the ACN solution was washed through a pad of Dowex ® - 1 -chloride resin to remove residual DCA.
- the solvent was removed and 140 mg of peach-colored solids were isolated.
- An additional 12 mg was recovered from the hexane tituration washes for a total yield of 152 mg (89 % yield).
- the final HPLC and 31 P-NMR (d 3 -ACN) are depicted in Figures 13D and 13E.
- Scheme 27 illustrates a general synthesis of diene-ols via hydroboration.
- the alcohol may be synthesized using either 9-BBN (131) or (Sia) 2 BH (not shown).
- 9-BBN is preferred due to its stability, easy handling and the ease of purification of the product from the byproduct of the reaction --1,5-cyclooctanediol- by column chromatography.
- 3-Methyl-2-butanol (the major by-product produced from hydroboration with (Sia) 2 BH) boils at 112 °C and is removed by several coevaporations with pyridine leaving the desired alcohol which is then purified via silica gel column chromatography with SiO 2 . Distillation is known to lead to polymerization of the diene at temperatures above 70°C.
- the apparatus is charged with THF (10 mL) and 1,3,6-heptatriene, 129 (4.6 g, 48 mmol) via syringe.
- 9-BBN (131) (88 mL of a 0.5 M solution in THF, 44 mmol) is canulaed into the addition funnel.
- the flask is cooled to -10°C and the 9-BBN is added over 30 minutes.
- the reaction mixture is stirred for an additional 2.5 hours while the temperature is maintained between 0°C and -10°C.
- Aqueous NaH 2 PO 4 (13.3 mL of a 5 M solution) and NaOH (10.6 mL of a 6 M solution) is added to a 300 mL Erlenmeyer flask and cooled to 0°C.
- Aqueous H 2 O 2 (30 mL of a 30% solution) is added with stirring.
- the reaction mixture is then slowly added, with stirring, dropwise to the buffered oxidation mixture over 30 minutes.
- the mixture is kept at 0°C for an additional 1.5 hours followed by 2 hours at room temperature. If the solution is not cloudy this indicates that the mixture is not in two phases and additional water is added, with stirring, until it is cloudy.
- Solid K 2 CO 3 is added, with stirring, to aid in separating the aqueous phase.
- the mixture is then poured into a separatory funnel with 30 mL of brine and the mixture is shaken.
- the aqueous phase is extracted 2x with ether and the organic phases combined, dried with MgSO 4 filtered and the solvent removed.
- the alcohol (135) may be purified by vacuum distillation (decomposes at approximately 70 °C) or column chromatography (5% EtOAc in CH 2 C1 2 ).
- Example 30 PASS using a trityl derivatized solid support
- Example 129 (Schemes 37-39) illustrate the use of trityl derivatized solid supports in the PASS process.
- trityl thymidine resin (146).
- 4-Methoxytrityl chloride resin (143) (10 grams,l% cross linked polystyrene, obtained from Calbiochem-Novabiochem, trityl loading of 0.53 mmoles/gram) was treated with dry dimethylaminopyridine (DMAP) (130 mg) followed by thymidine (145) (1.99 grams, 1.5 equivalents based on trityl loading of the resin, dried by coevaporation from pyridine) and dry pyridine (60 mL). This slurry was mixed on an orbital shaker for 46 hours at room temperature.
- DMAP dry dimethylaminopyridine
- the slurry was placed on a sintered glass frit and washed with pyridine and methylene chloride until all unreacted thymidine had been removed.
- the washed resin was dried under vacuum for two hours giving 10.93 grams of a canary yellow solid (146).
- the dried resin (0.109 grams) was treated with 5 mL of 3% dichloroacetic acid in methylene chloride in a 10 mL volumetric flask, the solution was diluted to the mark with DMSO.
- the amount of thymidine released from the sample resin was determined by an HPLC assay (4.6 x 250 mm Phenomonex Jupiter C18 column, water/acetonitrile gradient, 2% to 40% acetonitrile over 20 minutes) and found to be 0.29 mmoles of thymidine per gram of resin (approx. 55% of theoretical).
- Preparation of trityl thymidine phosphoramidite resin (147).
- the trityl thymidine resin (146) (5.12 g, 1.48 mmole) was dried overnight under vacuum.
- the mixture was oxidized by the addition of tetrabutylammonium periodate (1.35 g, 3.1 mmoles) dissolved in 25 mL of methylene chloride. This solution was mixed on an orbital shaker for 8 minutes. The mixture filtered through a coarse glass frit and the polymer was washed with methylene chloride (20 x 50 mL) to remove all non-coupled reaction components. To the polymer (148) was added 750 mL of 3% dichloroacetic acid in methylene chloride in portions of 50 mL to detritylate the dimer product from the resin.
- the mixture was oxidized by the addition of tetrabutylammonium periodate (1.08 g, 2.5 mmoles) dissolved in 20 mL of methylene chloride. This solution was mixed on an orbital shaker and then filtered through a coarse glass frit and the polymer was washed with methylene chloride and acetonitrile to remove all non-coupled reaction components.
- trimer 152 was washed twice with 500 mL of phosphate buffer, dried over sodium sulfate, filtered, evaporated and placed under vacuum for 64 hours to give 1.04 g (87%) of trimer 152.
- 31 P NMR 121 MHz, DMSO
- ⁇ -1.50 and -1.54 s, diastereotopic
- - 2.49 and -2.55 s, diastereotopic
- the reversed phase HPLC of trimer 152 after cleavage from the resin is shown in Figure 15.
- DHDT 2'-fC 3'-TBDPS 1504. This experiment was carried out on the 2.70 mmol scale.
- DHDT 2'-fC 3'-TBDPS (154) was formed by combining imidazole (0.690 g, 9.86 mmol) in 3 mL DMF, TBDPSi-Cl (2.314 g, 8.43 mmol), and DHDT fC 3'-OH (153) (cytidine is acetyl protected) (1.97 g, 2.7 mmol) in 10 mL methylene chloride.
- the DHDT fC 3'-OH was added under argon to a 50 mL round-bottom flask, equipped with a stir bar.
- the capture solution was monitored using TLC. Capture was complete within 44 minutes as determined by reverse phase HPLC (C18 reversible column, 10%-90% acetonitile/NH 4 OAc over 30 minutes at 30 °C ( Figure 16B). The resin was subsequently washed with DCM until no UV active material was detectable by TLC (7x100 mL). Release: To release compound 154, the resin was washed with 3% DCA in DCM (5x70 mL). The resin was then washed with DCM (2x70 mL). Following each release-wash with DCA and DCM, the washes were immediately transferred into a separatory funnel containing 500 mL of a 0.2 M (7.5 pH) Na 2 HPO 4 buffer solution.
- FIG. 16C depicts the reverse phase HPLC chromatograms of both the organic and aqueous phase. As can be seen in Figure 16C the product (5'-HO 2'-fC 3'-TBDPS (155) is entirely in the organic phase. Table 10 sets forth the yield and purity of protected monomer 155. Capture was 100%. 'H NMR analysis (CDC1 3 ) of the product is shown in Figure 16D. MS expected weight of 525.64, found 525.4.
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US84382097A | 1997-04-21 | 1997-04-21 | |
US843820 | 1997-04-21 | ||
PCT/US1998/008192 WO1998047910A1 (en) | 1997-04-21 | 1998-04-20 | Method for solution phase synthesis of oligonucleotides |
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EP0979233A1 true EP0979233A1 (de) | 2000-02-16 |
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EP98918629A Withdrawn EP0979233A4 (de) | 1997-04-21 | 1998-04-20 | Verfahren zur synthese von oligonukleotiden in lösung |
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EP (1) | EP0979233A4 (de) |
JP (1) | JP2001520660A (de) |
AU (1) | AU7152098A (de) |
CA (1) | CA2286320A1 (de) |
IL (1) | IL132377A0 (de) |
WO (1) | WO1998047910A1 (de) |
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US7427678B2 (en) | 1998-01-08 | 2008-09-23 | Sigma-Aldrich Co. | Method for immobilizing oligonucleotides employing the cycloaddition bioconjugation method |
GB9825687D0 (en) * | 1998-11-25 | 1999-01-20 | Link Technologies Ltd | Oligonucleotide conjugation |
EP1287404A4 (de) * | 2000-05-01 | 2003-10-15 | Proligo Llc | Verfahren zur immobilisierung von oligonukleotiden, welches das cycloaddition-bikonjugierungs-verfahren anwendet |
DE10041221A1 (de) | 2000-08-22 | 2002-03-14 | Deutsches Krebsforsch | Verfahren zur Herstellung von wasserlöslichen Saccharidkonjugaten und Saccharidmimetika durch Diels-Alder-Reaktion und ihre Verwendung als Therapeutika oder Diagnostika |
US7172905B2 (en) | 2001-08-07 | 2007-02-06 | The University Of Chicago | Polypeptide immobilization |
US7098326B2 (en) | 2002-01-23 | 2006-08-29 | Sigma-Aldrich Co. | Methods for the integrated synthesis and purification of oligonucleotides |
GB0229423D0 (en) | 2002-12-18 | 2003-01-22 | Avecia Ltd | Process |
AU2002361255A1 (en) | 2002-12-31 | 2004-07-22 | Proligo Llc | Methods and compositions for the tandem synthesis of two or more oligonuleotides on the same solid support |
WO2005070859A1 (ja) * | 2004-01-27 | 2005-08-04 | Takeshi Wada | フルオラス担体およびそれを用いたオリゴヌクレオチド誘導体の製造方法 |
US9290617B2 (en) | 2005-07-06 | 2016-03-22 | Molly S. Shoichet | Method of biomolecule immobilization on polymers using click-type chemistry |
EP2147009A4 (de) | 2007-05-18 | 2014-01-08 | Dharmacon Inc | Neuartige chromophore silylschutzgruppen und ihre verwendung in der chemischen synthese von oligonukleotiden |
DE102010001987A1 (de) * | 2010-02-16 | 2011-08-18 | Evonik Röhm GmbH, 64293 | Funktionsmaterialien mit reversibler Vernetzung |
DE102010001992A1 (de) | 2010-02-16 | 2011-08-18 | Evonik Röhm GmbH, 64293 | Funktionsmaterialien mit steuerbarer Viskosität |
JP5705512B2 (ja) * | 2010-11-26 | 2015-04-22 | 農工大ティー・エル・オー株式会社 | 高分散性液相支持体を用いたオリゴヌクレオチド合成法 |
US9758546B2 (en) | 2013-10-21 | 2017-09-12 | Ionis Pharmaceuticals, Inc. | Method for solution phase detritylation of oligomeric compounds |
KR101889893B1 (ko) * | 2015-06-12 | 2018-08-22 | 애니젠 주식회사 | 선별적 용해도를 갖는 트리페닐메탄 유도체 및 그의 용도 |
AU2017284202B2 (en) * | 2016-06-14 | 2021-11-04 | Biogen Ma Inc. | Hydrophobic interaction chromatography for purification of oligonucleotides |
EP3473632B1 (de) * | 2016-06-20 | 2021-10-06 | Sekisui Medical Co., Ltd. | Neuartiges diphenylmethanschutzmittel |
JP6322350B1 (ja) * | 2016-11-11 | 2018-05-09 | 積水メディカル株式会社 | 新規トリチル保護剤 |
CN109963861B (zh) * | 2016-11-11 | 2021-09-28 | 积水医疗株式会社 | 新型三苯甲基保护剂 |
CN111491941B (zh) * | 2017-12-19 | 2023-08-08 | 积水医疗株式会社 | 新型烷基二苯甲烷保护剂 |
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WO1991011467A1 (en) * | 1990-01-26 | 1991-08-08 | Isp Investments Inc. | Alkenyl ethers and radiation curable compositions |
WO1994022802A1 (en) * | 1993-04-02 | 1994-10-13 | Laporte Plc | Protecting group for use in oligodeoxyribonucleotide synthesis |
EP0644196A1 (de) * | 1993-09-17 | 1995-03-22 | Ciba-Geigy Ag | TTTr als Schutzgruppe in der Nukleotidsynthese |
WO1997014706A1 (en) * | 1995-10-19 | 1997-04-24 | Nexstar Pharmaceuticals, Inc. | Method for solution phase synthesis of oligonucleotides |
WO1998030578A1 (en) * | 1997-01-08 | 1998-07-16 | Proligo Llc | Method for solution phase synthesis of oligonucleotides and peptides |
WO1998030575A1 (en) * | 1997-01-08 | 1998-07-16 | Proligo Llc | Bioconjugation of macromolecules |
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SU627134A1 (ru) * | 1977-06-16 | 1978-10-05 | Предприятие П/Я М-5885 | Способ получени тетрафурфурилоксисилана |
US5580731A (en) * | 1994-08-25 | 1996-12-03 | Chiron Corporation | N-4 modified pyrimidine deoxynucleotides and oligonucleotide probes synthesized therewith |
US5597909A (en) * | 1994-08-25 | 1997-01-28 | Chiron Corporation | Polynucleotide reagents containing modified deoxyribose moieties, and associated methods of synthesis and use |
-
1998
- 1998-04-20 EP EP98918629A patent/EP0979233A4/de not_active Withdrawn
- 1998-04-20 WO PCT/US1998/008192 patent/WO1998047910A1/en not_active Application Discontinuation
- 1998-04-20 IL IL13237798A patent/IL132377A0/xx unknown
- 1998-04-20 JP JP54450398A patent/JP2001520660A/ja active Pending
- 1998-04-20 AU AU71520/98A patent/AU7152098A/en not_active Abandoned
- 1998-04-20 CA CA002286320A patent/CA2286320A1/en not_active Abandoned
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WO1991011467A1 (en) * | 1990-01-26 | 1991-08-08 | Isp Investments Inc. | Alkenyl ethers and radiation curable compositions |
WO1994022802A1 (en) * | 1993-04-02 | 1994-10-13 | Laporte Plc | Protecting group for use in oligodeoxyribonucleotide synthesis |
EP0644196A1 (de) * | 1993-09-17 | 1995-03-22 | Ciba-Geigy Ag | TTTr als Schutzgruppe in der Nukleotidsynthese |
WO1997014706A1 (en) * | 1995-10-19 | 1997-04-24 | Nexstar Pharmaceuticals, Inc. | Method for solution phase synthesis of oligonucleotides |
WO1998030578A1 (en) * | 1997-01-08 | 1998-07-16 | Proligo Llc | Method for solution phase synthesis of oligonucleotides and peptides |
WO1998030575A1 (en) * | 1997-01-08 | 1998-07-16 | Proligo Llc | Bioconjugation of macromolecules |
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CHEMICAL ABSTRACTS, vol. 89, no. 25, 1978 Columbus, Ohio, US; abstract no. 215211, MUKHAMADALIEV, N. ET AL.: "Tetrafurfuryloxysilane" page 577; column l; XP002157922 & SU 627 134 A 5 October 1978 (1978-10-05) * |
H. SELIGER: "Scale-up of oligonucleotide synthesis in: Protocols for oligonucleotides and analogs (Editior: S. Agrawal)" METHODS IN MOLECULAR BIOLOGY, vol. 20, 1993, pages 391-403, XP002157921 * |
See also references of WO9847910A1 * |
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AU7152098A (en) | 1998-11-13 |
JP2001520660A (ja) | 2001-10-30 |
WO1998047910A1 (en) | 1998-10-29 |
IL132377A0 (en) | 2001-03-19 |
CA2286320A1 (en) | 1998-10-29 |
EP0979233A4 (de) | 2001-03-21 |
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