WO2003018002A2 - Cyclopropyl and cyclobutyl epothilone analogs - Google Patents
Cyclopropyl and cyclobutyl epothilone analogs Download PDFInfo
- Publication number
- WO2003018002A2 WO2003018002A2 PCT/EP2002/009407 EP0209407W WO03018002A2 WO 2003018002 A2 WO2003018002 A2 WO 2003018002A2 EP 0209407 W EP0209407 W EP 0209407W WO 03018002 A2 WO03018002 A2 WO 03018002A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- group
- compound
- independently selected
- formula
- radical
- Prior art date
Links
- 0 C[C@@](CCC[C@@](*1)[C@@]1CC(C(C)=CN)OC(C[C@@](C(C)(C)C([C@@]1C)=O)OC)=O)[C@@]1OC Chemical compound C[C@@](CCC[C@@](*1)[C@@]1CC(C(C)=CN)OC(C[C@@](C(C)(C)C([C@@]1C)=O)OC)=O)[C@@]1OC 0.000 description 5
- MNSKFUOZEJYSBS-OQVBTRJZSA-N C[C@@H](CCCC1=C[C@H]1C[C@@H](/C(/C)=C/c1ccc(C)cn1)OC(C[C@@H](C1(C)C)O)=O)[C@H](C)[C@@H](C)C1=O Chemical compound C[C@@H](CCCC1=C[C@H]1C[C@@H](/C(/C)=C/c1ccc(C)cn1)OC(C[C@@H](C1(C)C)O)=O)[C@H](C)[C@@H](C)C1=O MNSKFUOZEJYSBS-OQVBTRJZSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/08—Bridged systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D313/00—Heterocyclic compounds containing rings of more than six members having one oxygen atom as the only ring hetero atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/06—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
Definitions
- the invention is related to analogs of epothilone. More particularly, the invention is directed to analogs of cis- and frans-12,13-cyclopropyl and 12,13-cyclobutyl epothilones.
- One aspect of the invention is directed to compounds represented by any of the following structures:
- X is a diradical selected from the group consisting of -O-, -C(Y 1 )(Y 2 )-, and -C(Y 1 )(Y 2 )-C(Y 1 )(Y 2 )-.
- Y 1 and Y 2 are each radicals independently selected from the group consisting of -H, -F, -CI and -Br.
- Ar is a radical represented by the following structure:
- R 1 either forms a first fused ring structure with R 2 or is a radical selected from -H and a C1-C6 branched or straight chain alkyl represented by -(C(Z 1 )(Z 2 )(Z 3 )) n , where 1 ⁇ n>6.
- Z 1 , Z 2 , and Z 3 are each a radical independently selected from the group consisting of -H, -F, -CI, -Br, -OH, -NH 2 , and -(C(Z 1 )(Z 2 )(Z 3 )).
- Z 1 , Z 2 , or Z 3 is -OH or -NH 2
- each of the remaining Z 1 , Z 2 , and Z 3 is independently selected from the group consisting of -H and -(C(Z )(Z 2 )(Z 3 )).
- R 2 either forms the first fused ring structure with R 1 or forms a second fused ring structure with R 3 or is a radical selected from the group consisting of -H and a C1-C6 branched or straight chain alkyl represented by -(C(Z 1 )(Z 2 )(Z 3 )) n , where 1 ⁇ n>6.
- Z , Z 2 , and Z 3 are as defined above.
- R 3 either forms the second fused ring structure with R 2 or is a radical selected from the group consisting of -H and a C1-C6 branched or straight chain alkyl represented by -(C(Z 1 )(Z 2 )(Z 3 )) n , where 1 ⁇ n>6.
- Z 1 , Z 2 , and Z 3 are as defined above.
- the first or second fused ring structure is either an aromatic or heteroaromatic 5- or 6-membered fused ring with or without C1-C6 branched or straight chain alkyl substituents.
- Preferred species of this aspect of the invention include the following examples:
- Another aspect of the invention is directed to compounds represented by any of the following structures:
- X is a diradical selected from the group consisting of -C(Y 1 )(Y 2 )-, and -C(Y 1 )(Y 2 )-C(Y 1 )(Y 2 )-.
- Y 1 and Y 2 are each radicals independently selected from the group consisting of -H, -F, -CI and -Br.
- Preferred species of this aspect of the invention include the following examples:
- n is either 1 or 2.
- Another aspect of the invention is directed to an anticancer reagent comprising any of the compounds described above dissolved or suspended in a physiological solvent suitable for administration to a patient.
- the compound has a cnoncentration within the physiological solvent sufficient to be cytotoxic to a cancer cell.
- Another aspect of the invention is directed to a process for killing a cancer cell comprising the step of contacting the cancer cell with a solution containing a cytotoxic concentration of any compound described above.
- the present invention pertains to the use of a compound of formula I, l-S, II, II- S, III, lll-S, IV or IV-S or a pharmaceutically acceptable salt or a solvate or a hydrate of such a compound, in a method for the treatment of the human or animal body.
- the present invention pertains to the use of a compound of formula I, l-S, II, II- S, III, lll-S, IV or IV-S, or a pharmaceutically acceptable salt or a solvate or a hydrate of such a compound, for the preparation of a pharmaceutical product for the treatment of a neoplastic disease.
- neoplastic disease relates in particular to liquid tumor diseases, like leukemia, and solid tumor diseases.
- solid tumor disease especially means breast cancer, ovarian cancer, cancer of the colon and generally the Gl tract including gastric cancer, cervix cancer, lung cancer, e.g. small-cell lung cancer and non-small-cell lung cancer, pancreas cancer, renal cancer, glioma, melanoma, head and neck cancer, bladder cancer, thyroid cancer, hepatocellular cancer, prostate cancer and Kaposi's sarcoma.
- the present invention provides a method for the treatment of a neoplastic disease, which comprises administering a compound of formula I, l-S, II, ll-S, III, lll-S, IV or IV-S, or a pharmaceutically acceptable salt or a solvate or a hydrate of such a compound, in a quantity effective against said disease, to a warm-blooded animal requiring such treatment.
- the present invention relates to a pharmaceutical preparation, comprising a compound of formula I, l-S, II, ll-S, III, lll-S, IV or IV-S, or a pharmaceutically acceptable salt or a solvate or a hydrate of such a compound.and at least one pharmaceutically acceptable carrier that are suitable for topical, enteral, for example oral or rectal, or parenteral administration and that may be inorganic or organic, solid or liquid.
- diluents for example lactose, dextrose, mannitol, and/or glycerol, and/or lubricants and/or polyethylene glycol.
- Tablets may also comprise binders, for example magnesium aluminum silicate, starches, such as corn, wheat or rice starch, gelatin, methylcellulose, sodium carboxymethylcellulose and/or polyvinylpyrrolidone, and, if desired, disintegrators, for example starches, agar, alginic acid or a salt thereof, such as sodium alginate, and/or effervescent mixtures, or adsorbents, dyes, flavorings and sweeteners. It is also possible to use the pharmacologically active compounds of the present invention in the form of parenterally administrable compositions or in the form of infusion solutions.
- binders for example magnesium aluminum silicate, starches, such as corn, wheat or rice starch, gelatin, methylcellulose, sodium carboxymethylcellulose and/or polyvinylpyrrolidone
- disintegrators for example starches, agar, alginic acid or a salt thereof, such as sodium alginate, and/or effervescent mixtures, or
- the pharmaceutical compositions may be sterilized and/or may comprise excipients, for example preservatives, stabilisers, wetting agents and/or emulsifiers, solubilisers, salts for regulating the osmotic pressure and/or buffers.
- excipients for example preservatives, stabilisers, wetting agents and/or emulsifiers, solubilisers, salts for regulating the osmotic pressure and/or buffers.
- the present pharmaceutical compositions which may, if desired, comprise other pharmacologically active substances are prepared in a manner known per se, for example by means of conventional mixing, granulating, confectioning, dissolving or lyophilising processes, and comprise approximately from 1 % to 95%, especially from approximately 1 % to approximately 20%, active ingredient(s).
- the dosage of the active ingredient depends upon a variety of factors including type, species, age, weight, sex and medical condition of the patient; the severity of the condition to be treated; the route of administration; the renal and hepatic function of the patient; and the particular compound employed.
- a physician, clinician or veterinarian of ordinary skill can readily determine and prescribe the effective amount of the drug required to prevent, counter or arrest the progress of the condition.
- Optimal precision in achieving concentration of drug within the range that yields efficacy without toxicity requires a regimen based on the kinetics of the drug's availability to target sites. This involves a consideration of the distribution, equilibrium, and elimination of a drug.
- the compounds of the present invention can be administered alone or in combination with one or more other therapeutic agents, possible combination therapy taking the form of fixed combinations or the administration of a compound of the invention and one or more other therapeutic agents being staggered or given independently of one another, or the combined administration of fixed combinations and one or more other therapeutic agents.
- compounds of the present invention can be administered for example in the case of tumour therapy in combination with chemotherapy, radiotherapy, immunotherapy, surgical intervention, or a combination of these.
- Long-term therapy is equally possible as is adjuvant therapy in the context of other treatment strategies, as described above.
- Other possible treatments are therapy to maintain the patient's status after tumour regression, or even chemopreventive therapy, for example in patients at risk.
- Therapeutic agents for possible combination are especially one or more antiproliferative, cytostatic or cytotoxic compounds, for example a chemotherapeutic agent or several agents selected from the group which includes, but is not limited to, an inhibitor of polyamine biosynthesis, an inhibitor of a protein kinase, especially of a serine/threonine protein kinase, such as protein kinase C, or of a tyrosine protein kinase, such as the EGF receptor tyrosine kinase, e.g. PKI166, the VEGF receptor tyrosine kinase, e.g. PTK787, or the PDGF receptor tyrosine kinase, e.g.
- a chemotherapeutic agent for example a chemotherapeutic agent or several agents selected from the group which includes, but is not limited to, an inhibitor of polyamine biosynthesis, an inhibitor of a protein kinase, especially of a serine/thre
- STI571 a cytokine, a negative growth regulator, such as TGF- ⁇ or IFN- ⁇ , an aromatase inhibitor, e.g. letrozole or anastrozole, an inhibitor of the interaction of an SH2 domain with a phosphorylated protein, antiestrogens, topoisomerase I inhibitors, such as irinotecan, topoisomerase II inhibitors, microtubule active agents, e.g.
- paclitaxel paclitaxel, discodermolide or an epothilone, alkylating agents, antineoplastic antimetabolites, such as gemcitabine or capecitabine, platin compounds, such as carboplatin or cisplatin, anti- angiogenic compounds, gonadorelin agonists, anti-androgens, bisphosphonates, e.g. AREDIA® or ZOMETA®, and trastuzumab.
- the structure of the active agents identified by code nos., generic or trade names may be taken from the actual edition of the standard compendium 'The Merck Index" or from databases, e.g. Patents International (e.g. IMS World Publications). The corresponding content thereof is hereby incorporated by reference.
- Another aspect of the invention is a process for synthesizing any of the compounds described above or intermediates thereof, as described in the specification, in particular
- R 1 either forms a first fused ring structure with R 2 or is a radical selected from -H and a C1- C6 branched or straight chain alkyl represented by -(C(Z 1 )(Z 2 )(Z 3 )) n , where 1 ⁇ n>6 and Z 1 , Z 2 , and Z 3 are each a radical independently selected from the group consisting of -H, -F, -CI, -Br, -OH, -NH 2 , and -(C(Z 1 )(Z 2 )(Z 3 )), with a proviso that, if any one of Z 1 , Z 2 , or Z 3 is -OH or -NH 2 , then each of the remaining Z 1 , Z 2 , and Z 3 is independently selected from the group consisting of -H and -(C(Z 1 )(Z )(Z 3 ));
- R 2 either forms the first fused ring structure with R 1 or forms a second fused ring structure with R 3 or is a radical selected from the group consisting of -H and a C1-C6 branched or straight chain alkyl represented by -(C(Z 1 )(Z 2 )(Z 3 )) n , where 1 ⁇ n>6 and Z 1 , Z 2 , and Z 3 are each a radical independently selected from the group consisting of -H, -F, -CI, -Br, -OH, - NH 2 , and -(C(Z 1 )(Z 2 )(Z 3 )), with a proviso that, if any one of Z 1 , Z 2 , or Z 3 is -OH or -NH 2 , then each of the remaining Z Z 2 , and Z 3 is independently selected from the group consisting of - H and -(C(Z 1 )(Z 2 )(Z 3 ));
- R 3 either forms said second fused ring structure with R 2 or is a radical selected from the group consisting of -H and a C1-C6 branched or straight chain alkyl represented by - (C(Z 1 )(Z 2 )(Z 3 )) n , where 1 ⁇ n>6 and Z 1 , Z 2 , and Z 3 are each a radical independently selected from the group consisting of -H, -F, -CI, -Br, -OH, -NH 2 , and -(C(Z 1 )(Z 2 )(Z 3 )), with a proviso that, if any one of Z 1 , Z 2 , or Z 3 is -OH or -NH , then each of the remaining Z 1 , Z 2 , and Z 3 is independently selected from the group consisting of -H and -(C(Z 1 )(Z 2 )(Z 3 )); said first or second fused ring structure is either an aromatic or heteroaromatic 5- or
- X and Ar have the meaning as defined above for a compound fo formula I and PG is a protecting group for a hydroxy function, in a first step is condensed by a esterification reaction, optionally in the presence of a catalyst, and in a second step the protecting group is detached thus furnishing a lacton of formula I;
- X has the meaning as defined above for a compound fo formula III and PG is a protecting group for a hydroxy function, in a first step is condensed by a esterification reaction, optionally in the presence of a catalyst, and in a second step the protecting group is detached thus furnishing a lacton of formula III.
- Figure 1 illustrates the structure of the epothilones and preferred epothilone analogs.
- Figure 2 illustrates the retrosynthetic analysis used for the chemical synthesis of the designed 12,13-cycloalkane thiazole epothilone analogs 3-8.
- Figure 3 illustrates a scheme showing the preparation of building block 13.
- Figure 4 illustrates a scheme showing the synthesis of aldehyde 14.
- Figure 5 illustrates a scheme for the synthesis building block aldehydes 15 and 16.
- Figure 6 illustrates a scheme that illustrates the synthesis of thiazole vinyl iodide 17.
- Figures 7 and 8 illustrate a scheme showing the synthesis of epothilone analogs 3, 5 and 7.
- Figures 9 and 10 illustrate a scheme which shows the synthesis of cis-cyclobutyl epothilone analogs 4 and 6.
- Figures 11 and 12 illustrate a scheme showing the synthesis of the trans-cyclobutyl epothilone analog 8.
- Figure 13 illustrates the retrosynthetic analysis and key fragments for epothilone analogs 9- 12.
- Figure 14 illustrates a scheme for the synthesis of alcohols 85 and 86.
- Figure 15 illustrates the synthesis of pyridine iodide 87.
- Figures 16 and 17 illustrate a scheme for the synthesis of precursor aldehydes 107 and 113.
- Figures 18 and 19 illustrates the synthesis of cyclopropyl pyridine analogs of epothilone 9, 10, 11 and 12.
- Alcohol 25 was oxidized to the corresponding aldehyde (89% yield) with TPAP-NMO (for abbreviations of reagents and protecting groups, see legends in schemes), and then homologated to the desired aldehyde 13 via enol ether 26 by the two-step procedure described above for 20 (Wittig reaction followed by acidic hydrolysis), in 50% overall yield.
- TPAP-NMO for abbreviations of reagents and protecting groups, see legends in schemes
- c/s-aldehyde 34 was prepared by Dess-Martin periodinane oxidation (95% yield), while the corresponding fra ⁇ s-aldehyde 39 was conveniently available by base-catalyzed epimerization of 34 (88% from 33).
- 34 and 39 were homologated to 35 and 40, respectively, and the latter compounds were coupled with the chiral phosphorane derived from enantiomerically pure phosphonium salt 21 and NaHMDS-TMSCI to yield olefins 36 and 41 , respectively.
- the requisite vinyl iodide 17 was constructed from aldehyde 44 7 via a sequence involving (i) a modified Corey-Fuchs protocol (Grandjean, D.; et al. Tetrahedron Lett. 1994, 35, 3529- 3530) with in situ methylation of the intermediate acetylenide via intermediates 45 (88%) and 46 (97%); (ii) stereoselective hydrostannylation (Betzer, J.-F.; et al. Tetrahedron Lett. 1997, 38, 2279-2282) (84%); and (iii) iodine-tin exchange (99%), as shown in Scheme 5.
- This sequence represents a significant improvement, both regarding simplicity and yields, over the preliminary route previously disclosed (Nicolaou, K. C; et al. ChemBioChem 2001, 1, 69-75).
- the rans-cyclobutyl thiazole epothilone 8 was prepared by a similar sequence, as detailed in Scheme 8.
- the resulting alcohol was oxidized to the corresponding enone 75, which was then stereoselectively reduced with (-)-DIPCI (Brown, H. O; Ramachandran, P. V. Ace. Chem. Res. 1992, 25, 16-24; Brown, H. C; et al. J. Org. Chem. 1987, 52, 5406-5412) to afford only the (15S)-epimer 76.
- the remaining steps followed the same sequence described for the cis compounds (see Scheme 7), and proceeded smoothly and in similar yields, affording the targeted /rans-cyclobutyl epothilone 8.
- the required building blocks 85 and 86 were prepared as shown in Scheme 10.
- Hydrogenation of the double bond in 89 with concomitant cleavage of the benzyl ether gave primary alcohol 90 in 75% yield.
- This compound (90) was then converted into the corresponding iodide (91) in 93% yield by exposure to l 2 /PPh 3 .
- the starting materials used herein are commercially available or can be prepared in a manner known per se.
- R t and R 3 are H and R 2 is methyl.
- R 1 either forms a first fused ring structure with R 2 or is a radical selected from -H and a C1-C6 branched or straight chain alkyl represented by -(C(Z 1 )(Z 2 )(Z 3 )) n , where 1 ⁇ n>6 and Z 1 , Z 2 , and Z 3 are each a radical independently selected from the group consisting of -H, -F, -CI, -Br, -OH, -NH 2 , and -(C(Z 1 )(Z 2 )(Z 3 )), with a proviso that, if any one of Z 1 , Z 2 , or Z 3 is -OH or -NH 2 , then each of the remaining Z 1 , Z 2 , and Z 3 is independently selected from the group consisting of -H an -(C(Z 1 )(Z 2 )(Z 3 ));
- R 2 either forms the first fused ring structure with R 1 or forms a second fused ring structure with R 3 or is a radical selected from the group consisting of -H and a C1-C6 branched or straight chain alkyl represented by -(C(Z 1 )(Z 2 )(Z 3 )) n , where 1 ⁇ n>6 and Z 1 , Z 2 , and Z 3 are each a radical independently selected from the group consisting of -H, -F, -CI, -Br, -OH, - NH 2 , and -(C(Z 1 )(Z 2 )(Z 3 )), with a proviso that, if any one of Z 1 , Z 2 , or Z 3 is -OH or -NH 2 , then each of the remaining Z 1 , Z 2 , and Z 3 is independently selected from the group consisting of - H and -(C(Z 1 )(Z 2 )(Z 3 ));
- R 3 either forms said second fused ring structure with R 2 or is a radical selected from the group consisting of -H and a C1-C6 branched or straight chain alkyl represented by - (C(Z 1 )(Z )(Z 3 )) n , where 1 ⁇ n>6 and Z 1 , Z 2 , and Z 3 are each a radical independently selected from the group consisting of -H, -F, -CI, -Br, -OH, -NH 2 , and -(C(Z 1 )(Z 2 )(Z 3 )), with a proviso that, if any one of Z 1 , Z 2 , or Z 3 is -OH or -NH 2 , then each of the remaining Z 1 , Z 2 , and Z 3 is independently selected from the group consisting of -H and -(C(Z 1 )(Z 2 )(Z 3 )); said first or second fused ring structure is either an aromatic or heteroaromatic 5- or
- R 1 , R 2 and R 3 have the meanings as defined above, in a suitable solvent with HCCCH 3 in the presence of a Pd(ll)-catalyst and copper(l)iodide, furnishing a pyridine derivative of formula VIII,
- R 1 , R 2 and R 3 have the meanings as defined above, hydrostannylating the obtained product of formula VIII in a second step in order to obtain a pyridine derivative of formula IX,
- said iodide of formula X can, e.g., also be employed in the reaction sequence illustrated in Figure 9 instead of the iodide of number 17 thus furnishing compounds of formula I, wherein X is a diradical of formula -CH 2 -CH 2 - and Ar is a radical represented by the following structure: wherein R 1f R 2 and R 3 have the meanings as provided for a compound of formula X.
- protecting groups for a hydroxy group refers to acid labile protecting groups for a hydroxy group, which groups are known as such. It is a characteristic of protecting groups that they lend themselves readily, i.e. without undesired secondary reactions, to removal, typically by solvolysis, reduction, photolysis or also by enzyme activity, for example under conditions analogous to physiological conditions, and that they are not present in the end-products.
- the specialist knows, or can easily establish, which protecting groups are suitable with the reactions mentioned hereinabove and hereinafter.
- Preferred protecting groups are silyl ethers which are acid labile like fert-butyl-dimethyl-silyl (TBS) ether, triethylsilyl (TES) ether, triisopropylsilyl (TIPS) ether, diethylisopropylsilyl (DEIPS) ether, isopropyldimethylsilyl (IPDMS) ether or thexyldimethylsilyl (TDS) ether.
- TSS fert-butyl-dimethyl-silyl
- TES triethylsilyl
- TIPS triisopropylsilyl
- DEIPS diethylisopropylsilyl
- IPDMS isopropyldimethylsilyl
- TDS xyldimethylsilyl
- the cis analog 9 was also highly active, but was a factor of three to five less active than 11. Again, the 15f? isomeric analogs (10 and 12) were inactive.
- paclitaxel-selected clone PTX22 ( ⁇ 364) retains sensitivity to the epothilones, especially in the case of the most active analogs (9 and 11) where the relative resistance (RR) values are ⁇ 1.
- the cytotoxicity analysis was supplemented with data from two independent in vitro tubulin polymerization assays.
- one assay the fraction of tubulin polymerized into microtubules upon exposure to a given concentration of the respective compound was determined (see Table 2).
- tubulin polymerization kinetics upon exposure to the respective compounds was determined using purified rat brain tubulin through measurement of the absorbance at 350 nm (see Figure 3).
- paclitaxel, epothilone A (1) and epothilone B (2) were used as controls while compounds 9, 11 and 12 were selected for in vitro analysis.
- Compound 12 had no in vitro activity consistent with the lack of cytotoxic activity for this compound (Table 1 ).
- tubulin polymerization products of these compounds were examined by electron microscopy ( Figure 4) to rule out the potential increase in absorbance due to the formation of non-microtubule polymers. As seen in Figure 4, all compounds tested induced the formation of microtubule polymers with the exception of compound 12 where no microtubules were observed.
- Figure 1 shows the structures of a series of cyclopropyl and cyclobutyl epothilone analogs (3-12).
- Figure 2 illustrates the retrosynthetic analysis used for the chemical synthesis of the designed 12,13-cycloalkane thiazole epothilone analogs 3-8.
- Nozaki-Hiyama-Kishi coupling (Takai, K.; et al. Tetrahedron Lett. 1983, 24, 5281-5284; Jin, H.; et al. J. Am. Chem. Soc 1986, 108, 5644-5646), an aldol reaction and a Yamaguchi lactonization (Inanaga, J.; et al. Bull. Chem. Soc. Jpn. 1979, 52, 1989-1993; Mulzer, J.; et al. Synthesis 1992, 215-228; Nicolaou, K.
- Figure 3 is a scheme showing the preparation of building block 13. Reagents and Conditions: (a) (COCI) 2 (1.5 equiv), DMSO (2.0 equiv), Et 3 N (5.0 equiv), CH 2 CI 2 , -78 °C; (b) MeOCH 2 PPh 3 CI (1.5 equiv), NaHMDS (1.4 equiv), THF, -78 °C; (c) cat.
- Figure 4 is a scheme showing the synthesis of aldehyde 14. Reagents and Conditions: (a) DME (2.2 equiv), Et 2 Zn (2.2 equiv), CH 2 I 2 (4.4 equiv), 28 (1.2 equiv), CH 2 CI 2 , 98% yield, >90% ee; (b) Et 3 N (6.0 equiv), SO 3 » py (3.0 equiv), CH 2 CI 2 :DMSO 4:1, 0 °C, 2 h; (c) MeOCH 2 PPh 3 CI (1.5 equiv), NaHMDS (1.3 equiv), THF, -40 to 25 °C, 12 h, 81% over 2 steps; (d) TBAF (1.5 equiv), THF, 25 °C, 2 h; (e) NaH (1.5 equiv), BnBr (2.0 equiv), THF.-DMF 5:1, 0 to 25 °C, 10 h; (f
- Figure 5 is a scheme for the synthesis of building block aldehydes 15 and 16. Reagents and Conditions: (a) DMP (1.2 equiv), NaHCO 3 (5.0 equiv), CH 2 CI 2 , 25 °C, 3 h, 95%; (b) starting with alcohol 33: (COCI) 2 (1.1 equiv), DMSO (2.2 equiv), Et 3 N (5.0 equiv), CH 2 CI 2 , -78 °C; then Et 3 N, 25 °C, 5 days, 88% over 2 steps; c) MeOCH 2 PPh 3 CI (1.15 equiv), NaHMDS (1.10 equiv), THF, -78 to 25 °C, 89%; (d) 0.12 N HCI (aq):acetone (1:9), reflux, 1 h, 98% (35), 94% (40); (e) 21 (2.0 equiv), NaHMDS (3.8 equiv), THF, 0 °C
- DIBAL diisobutylaluminum hydride
- 4-DMAP 4-dimethylaminopyridine
- DMP Dess-Martin periodinane
- NaHMDS sodium hexamethyldisilazide
- py pyridine
- TMSCI chlorotrimethylsilane.
- FIG. 6 is a scheme that illustrates the synthesis of thiazole vinyl iodide 17.
- Reagents and Conditions (a) PPh 3 (4.0 equiv), CBr 4 (2.0 equiv), CH 2 CI 2 , 0 °C, 4 h, 88%; (b) NaHMDS (1.0 equiv), MeLi (2.0 equiv), Mel (5.0 equiv), -78 to 25 °C, 12 h, 97%; (c) ⁇ -BuLi (4.0 equiv), (n-Bu 3 Sn) 2 (4.0 equiv), CuCN (2.0 equiv), MeOH (110 equiv), THF, 87%; (d) l 2 (1.1 equiv), CH 2 CI 2 , 0 °C, 99%.
- NaHMDS sodium hexamethyldisilazide.
- Figures 7 and 8 are schemes showing the synthesis of epothilone analogs 3, 5, and 7.
- Reagents and Conditions (a) 17 (1.5-2.0 equiv), CrCI ⁇ (10-13 equiv), NiCI 2 (0.02-0.13 equiv), DMSO, 25 °C, 6-12 h, 56% (48), 91% from 32; (b) DMP (1.2 equiv), CH 2 CI 2 , 0 to 25 °C, 0.5 h, 83%; (c) (-)-DIPCI (3.0 equiv), Et 2 O, -15 to 25 °C, 18 h, 84%; (d) TBSOTf (1.1-2.0 equiv), 2,6-lutidine (2.5 equiv), CH 2 CI 2 , -78 °C, 0.5-1 h, 91-100%; (e) DIBAL (2.0-3.1 equiv), CH 2 CI 2 , -78 °C, 15 min-1 h,
- DIBAL diisobutylaluminum hydride
- DIPCI diisopinocampheyl chloroborane
- 4-DMAP 4-dimethyl- aminopyridine
- DMP Dess-Martin periodinane
- LDA lithium diisopropylamide
- NaHMDS sodium hexamethyldisilazide
- py pyridine
- TBAF tetrabutylammonium fluoride.
- Figures 9 and 10 are schemes which shows the synthesis of cis-cyclobutyl epothilone analogs 4 and 6.
- Reagents and Conditions (a) 17 (1.5 equiv), CrCI 2 (12.6 equiv), NiCI 2 (0.13 equiv), DMSO, 25 °C, 6 h, (89%, 2:3 mixture of C15 epimers); (b) TBSOTf (1.0 equiv), 2,6-lutidine (2.5 equiv), CH 2 CI 2 , -78 to 0 °C, 20 min; (c) DIBAL (2.0 equiv), CH 2 CI 2 , -78 °C, 5 min, 99% for 2 steps; (d) DMP (1.2 equiv), CH 2 CI 2 , 25 °C, 1.5 h; (e) LDA (3.1 equiv), 18 (3.0 equiv), THF, -78 °C, 4 min, 67% for 2 steps; (f) T
- 4-DMAP 4-dimethylamino-pyridine
- DMP Dess-Martin periodinane
- LDA lithium diisopropylamide
- py pyridine
- TBAF tetrabutylammonium fluoride.
- Figures 1 1 and 12 are schemes showing the synthesis of the trans-cyclobutyl epothilone analog 8.
- Reagents and Conditions (a) 17 (1.5 equiv), CrCI 2 (12.6 equiv), NiCI 2 (0.13 equiv), DMSO, 25 °C, 6 h, 91%; (b) DMP (1.2 equiv), NaHCO 3 (5.0 equiv), CH 2 CI 2 , 25 °C, 3 h; (c)
- Figure 14 is a scheme for the synthesis of alcohols 85 and 86.
- Reagents and Conditions (a) NaHMDS (2.1 equiv), TMSCI (1.1 equiv), THF, -78 to 25 °C, 6 h, 68%; (b) TBPDSCI (1.1 equiv), imidazole (2.0 equiv), DMF, 25 °C, 1 h, 89%; (c) 10% Pd/C, H 2 (1 atm), MeOH:THF 5:1, 50 °C, 10 h, 75%; (d) PPh 3 (1.4 equiv), 4-DMAP (0.01 equiv), l 2 (1.5 equiv), imidazole (2.0 equiv), MeCN/Et 2 O, 25 °C, 1 h, 93%; (e) n-BuU (3.3 equiv), 3-(tert-butyldimethylsilyloxy)propyne (3.5 equiv), THF/
- Figure 15 shows the synthesis of the pyridine vinyl alcohol 87.
- a Sonogashira coupling of 5-methyl-2-bromopyridine 99 with propyne (Arcadi, A.; et al. Tetrahedron 1994, 50, 437-452) yielded alkyne 100 in 98% yield.
- Figures 16 and 17 are schemes showing the synthesis of aldehydes 107 and 113.
- Reagents and Conditions (a) DMP (1.2 equiv), CH 2 CI 2 , 25 °C, 1.5 h; (b) LDA (2.5 equiv), 18 (2.4 equiv), THF, -78 °C, 4 min, 75% (102), 89% (108) over 2 steps, (c) TBDPSOTf (4.0 equiv), 2,6-lutidine (5.0 equiv), CH 2 CI 2 , -20 to 25 °C, 1 h, 93% (103), 100% (109); (d) HF-py, py, 25 °C, 2 h; (e) DMP (1.2 equiv), NaHCO 3 (1.5 equiv), CH 2 CI 2 , 25 °C, 6 h; (f) NaCIO 2 (5.0 equiv), 2-methyl-2-butene (7.5 equiv), NaH 2 PO
- Figures 18 and 19 show the synthesis of cyclopropyl pyridine analogs of epothilone, 9, 10, 11, and 12.
- Reagents and Conditions (a) NaBH 4 (1.1 equiv), CH 2 CI 2 /EtOH, -78 °C, 1 h, 72%; (b) LiOH, H 2 O/f-BuOH, 40 °C, 48 h, 98%; (c) EDC (2.0 equiv), 4-DMAP (0.5 equiv), TMSE-OH:CH 2 Cl 2 2:1 , 25 °C, 2 h, 83%; (d) DMP (2.5 equiv), py (10 equiv), CH 2 CI 2 , 0 °C, 2.5 h, 93%; (e) 87 (2.0 equiv), CrCI 2 (10 equiv), NiCI 2 (0.02 equiv), DMSO, 25 °C, 12 or 36 h, 43% (114), 71 % (121);
- 4-DMAP 4-dimethylaminopyridine
- DMP Dess-Martin periodinane
- EDC 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride
- py pyridine
- TBAF tetrabutylammonium fluoride
- TMSE 2-(trimethylsilyl)ethyl.
- Table 1 is a table that displays the cytotoxicity of epothilones 1 through 12 and paclitaxel against 1 A9 human ovarian carcinoma cells and ⁇ -tubulin mutant cell lines selected with paclitaxel or epothilone A.
- the antiproliferative effects of the tested compounds against the parental 1 A9 and the paclitaxel- and epothilone-selected drug resistant clones (PTX10, PTX22 and A8, respectively) were assessed in a 72 h growth inhibition assay using the SRB (sulforhodamine-B) assay (Skehan, P.; et al. J. Natl. Cancer Inst. 1990, 82, 1107-1112).
- IC 50 values for each compound are given in nM and represent the mean of 3-5 independent experiments ⁇ standard error of the mean.
- Relative resistance (RR) is calculated as an IC 50 value for each resistant subline divided by that for the parental cell line (1 A9).
- b Data from reference 3.
- CP cyclopropyl
- CB cyclobutyl
- na not applicable
- nd not determined
- py 5-methylpyridine side chain.
- Table 2 is a table of tubulin polymerization potency 3 and cytotoxicity ⁇ of epothilones 1 through 12 and paclitaxel against human epidermoid cancer cell lines.
- a %TP percent tubulin polymerized after incubation of tubulin with a known concentration of compound (typically 3 ⁇ M).
- KB-31 epidermoid Taxol ® -sensitive
- KB-8511 epidermoid Taxol ® -resistant (due to P-gp over expression).
- a %TP percent tubulin polymerized after incubation of tubulin with a known concentration of compound (typically 3 ⁇ M).
- KB-31 epidermoid Taxol®-sensitive
- KB-8511 epidermoid Taxol®-resistant (due to P- gp overexpression).
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Silicon Polymers (AREA)
Abstract
Description
Claims
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA002456280A CA2456280A1 (en) | 2001-08-23 | 2002-08-22 | Cyclopropyl and cyclobutyl epothilone analogs |
DE60229143T DE60229143D1 (en) | 2001-08-23 | 2002-08-22 | Cyclopropyl und cyclobutyl epothilon analoge |
AU2002331171A AU2002331171A1 (en) | 2001-08-23 | 2002-08-22 | Cyclopropyl and cyclobutyl epothilone analogs |
JP2003522522A JP4176015B2 (en) | 2001-08-23 | 2002-08-22 | Cyclopropyl and cyclobutyl epothilone analogs |
BR0212107-7A BR0212107A (en) | 2001-08-23 | 2002-08-22 | Cyclopropyl and cyclobutyl epothilone analogues |
EP02767418A EP1420780B1 (en) | 2001-08-23 | 2002-08-22 | Cyclopropyl and cyclobutyl epothilone analogs |
HK04109321.7A HK1066464A1 (en) | 2001-08-23 | 2004-11-25 | Cyclopropyl and cyclobutyl epothilone analogs |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US31469801P | 2001-08-23 | 2001-08-23 | |
US60/314,698 | 2001-08-23 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2003018002A2 true WO2003018002A2 (en) | 2003-03-06 |
WO2003018002A3 WO2003018002A3 (en) | 2003-09-04 |
Family
ID=23221047
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2002/009407 WO2003018002A2 (en) | 2001-08-23 | 2002-08-22 | Cyclopropyl and cyclobutyl epothilone analogs |
Country Status (13)
Country | Link |
---|---|
US (1) | US7358266B2 (en) |
EP (2) | EP2070534A3 (en) |
JP (2) | JP4176015B2 (en) |
CN (1) | CN100536841C (en) |
AT (1) | ATE409473T1 (en) |
AU (1) | AU2002331171A1 (en) |
BR (1) | BR0212107A (en) |
CA (1) | CA2456280A1 (en) |
DE (1) | DE60229143D1 (en) |
ES (1) | ES2315399T3 (en) |
HK (1) | HK1066464A1 (en) |
PT (1) | PT1420780E (en) |
WO (1) | WO2003018002A2 (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2004014919A1 (en) * | 2002-08-02 | 2004-02-19 | Novartis Ag | Epothilone derivatives |
JP2007525519A (en) * | 2004-02-27 | 2007-09-06 | スローン−ケッタリング インスティトュート フォア キャンサー リサーチ | Synthesis and use of epothilone, its intermediates and analogues |
US7825141B2 (en) | 2004-03-16 | 2010-11-02 | Novartis Ag | Epothilone derivatives |
US8871227B2 (en) | 2003-11-04 | 2014-10-28 | Bristol-Myers Squibb Company | Process and formulation containing epothilones and analogs thereof |
CN115850224A (en) * | 2022-07-22 | 2023-03-28 | 北京先通国际医药科技股份有限公司 | Synthetic method and application of modified long-chain fatty acid type PET reagent precursor |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6867305B2 (en) | 1996-12-03 | 2005-03-15 | Sloan-Kettering Institute For Cancer Research | Synthesis of epothilones, intermediates thereto and analogues thereof |
WO1999001124A1 (en) * | 1996-12-03 | 1999-01-14 | Sloan-Kettering Institute For Cancer Research | Synthesis of epothilones, intermediates thereto, analogues and uses thereof |
US20020058286A1 (en) * | 1999-02-24 | 2002-05-16 | Danishefsky Samuel J. | Synthesis of epothilones, intermediates thereto and analogues thereof |
DE60229143D1 (en) * | 2001-08-23 | 2008-11-13 | Novartis Ag | Cyclopropyl und cyclobutyl epothilon analoge |
ES2281692T3 (en) * | 2002-08-23 | 2007-10-01 | Sloan-Kettering Institute For Cancer Research | SYNTHESIS OF EPOTILONES, THEIR INTERMEDIARIES, THEIR ANALOGS AND THEIR USES. |
US7649006B2 (en) | 2002-08-23 | 2010-01-19 | Sloan-Kettering Institute For Cancer Research | Synthesis of epothilones, intermediates thereto and analogues thereof |
CN101535492A (en) | 2005-02-11 | 2009-09-16 | 南加州大学 | Method of expressing proteins with disulfide bridges |
AU2006318284A1 (en) * | 2005-11-22 | 2007-05-31 | The Scripps Research Institute | Chemical synthesis of a highly potent epothilone |
EP2029156A4 (en) * | 2006-05-01 | 2010-07-21 | Univ Southern California | Combination therapy for treatment of cancer |
JP5115729B2 (en) * | 2008-06-20 | 2013-01-09 | 信越化学工業株式会社 | Organosilicon compound containing acetoacetate group protected with trialkylsilyl group and process for producing the same |
WO2010056901A2 (en) | 2008-11-13 | 2010-05-20 | University Of Southern California | Method of expressing proteins with disulfide bridges with enhanced yields and activity |
WO2011146638A1 (en) | 2010-05-18 | 2011-11-24 | Cerulean Pharma Inc. | Compositions and methods for treatment of autoimmune and other diseases |
CN115141087B (en) * | 2022-09-06 | 2023-03-24 | 北京先通国际医药科技股份有限公司 | Synthesis method and application of isomers of PET precursor key intermediate |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998025929A1 (en) * | 1996-12-13 | 1998-06-18 | Novartis Ag | Epothilone analogs |
WO1999054318A1 (en) * | 1998-04-21 | 1999-10-28 | Bristol-Myers Squibb Company | 12,13-cyclopropane epothilone derivatives |
WO2000047584A2 (en) * | 1999-02-11 | 2000-08-17 | Schering Aktiengesellschaft | Epothilon derivatives, method for the production and the use thereof as pharmaceuticals |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5969145A (en) * | 1996-08-30 | 1999-10-19 | Novartis Ag | Process for the production of epothilones and intermediate products within the process |
US6380394B1 (en) * | 1996-12-13 | 2002-04-30 | The Scripps Research Institute | Epothilone analogs |
DE19848306A1 (en) * | 1998-10-14 | 2000-04-20 | Schering Ag | High yield preparation of cytotoxic or fungicidal compound epothilon B, from phenylsulfonyl-butanol derivative by multistage process via new thiazole derivative intermediates |
DE60229143D1 (en) * | 2001-08-23 | 2008-11-13 | Novartis Ag | Cyclopropyl und cyclobutyl epothilon analoge |
-
2002
- 2002-08-22 DE DE60229143T patent/DE60229143D1/en not_active Expired - Fee Related
- 2002-08-22 CN CNB028164415A patent/CN100536841C/en not_active Expired - Fee Related
- 2002-08-22 AT AT02767418T patent/ATE409473T1/en not_active IP Right Cessation
- 2002-08-22 AU AU2002331171A patent/AU2002331171A1/en not_active Abandoned
- 2002-08-22 BR BR0212107-7A patent/BR0212107A/en not_active IP Right Cessation
- 2002-08-22 ES ES02767418T patent/ES2315399T3/en not_active Expired - Lifetime
- 2002-08-22 PT PT02767418T patent/PT1420780E/en unknown
- 2002-08-22 CA CA002456280A patent/CA2456280A1/en not_active Abandoned
- 2002-08-22 EP EP08165542A patent/EP2070534A3/en not_active Withdrawn
- 2002-08-22 EP EP02767418A patent/EP1420780B1/en not_active Expired - Lifetime
- 2002-08-22 JP JP2003522522A patent/JP4176015B2/en not_active Expired - Fee Related
- 2002-08-22 WO PCT/EP2002/009407 patent/WO2003018002A2/en active IP Right Grant
- 2002-08-23 US US10/227,073 patent/US7358266B2/en not_active Expired - Fee Related
-
2004
- 2004-11-25 HK HK04109321.7A patent/HK1066464A1/en not_active IP Right Cessation
-
2008
- 2008-07-15 JP JP2008183765A patent/JP2009007367A/en active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998025929A1 (en) * | 1996-12-13 | 1998-06-18 | Novartis Ag | Epothilone analogs |
WO1999054318A1 (en) * | 1998-04-21 | 1999-10-28 | Bristol-Myers Squibb Company | 12,13-cyclopropane epothilone derivatives |
WO2000047584A2 (en) * | 1999-02-11 | 2000-08-17 | Schering Aktiengesellschaft | Epothilon derivatives, method for the production and the use thereof as pharmaceuticals |
Non-Patent Citations (8)
Title |
---|
ALTMANN K-H ET AL: "Synthesis and biological evaluation of highly potent analogues of epothilones B and D" BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, OXFORD, GB, vol. 10, no. 24, 18 December 2000 (2000-12-18), pages 2765-2768, XP004225345 ISSN: 0960-894X * |
JOHNSON J ET AL: "Synthesis, structure proof, and biological activity of epothilone cyclopropanes." ORGANIC LETTERS. UNITED STATES 1 JUN 2000, vol. 2, no. 11, 1 June 2000 (2000-06-01), pages 1537-1540, XP002235574 ISSN: 1523-7060 * |
NICOLAOU K C ET AL: "Chemical Biology of Epothilones" ANGEWANDTE CHEMIE. INTERNATIONAL EDITION, VERLAG CHEMIE. WEINHEIM, DE, vol. 37, no. 15, August 1998 (1998-08), pages 2014-2045, XP002131418 ISSN: 0570-0833 * |
NICOLAOU K C ET AL: "Chemical synthesis and biological evaluation of cis- and trans-12,13-cyclopropyl and 12,13-cyclobutyl epothilones and related pyridine side chain analogues." JOURNAL OF THE AMERICAN CHEMICAL SOCIETY. UNITED STATES 26 SEP 2001, vol. 123, no. 38, 26 September 2001 (2001-09-26), pages 9313-9323, XP002235576 ISSN: 0002-7863 * |
NICOLAOU K C ET AL: "DESIGNED EPOTHILONES: COMBINATORIAL SYNTHESIS, TUBULIN ASSEMBLY PROPERTIES, AND CYTOTOXIC ACTION AGAINST TAXOL.RESISTANT TUMOR CELLS" ANGEWANDTE CHEMIE. INTERNATIONAL EDITION, VERLAG CHEMIE. WEINHEIM, DE, vol. 36, no. 19, 1997, pages 2097-2103, XP002064441 ISSN: 0570-0833 * |
NICOLAOU K C ET AL: "Synthesis and biological evaluation of 12,13-cyclopropyl and 12,13-cyclobutyl epothilones." CHEMBIOCHEM: A EUROPEAN JOURNAL OF CHEMICAL BIOLOGY. GERMANY 8 JAN 2001, vol. 2, no. 1, 8 January 2001 (2001-01-08), pages 69-75, XP002235575 ISSN: 1439-4227 * |
NICOLAOU K C ET AL: "SYNTHESIS AND BIOLOGICAL PROPERTIES OF C12,13-CYCLOPROPYL-EPOTHILONE A AND RELATED EPOTHILONES" CHEMISTRY AND BIOLOGY, CURRENT BIOLOGY, LONDON, GB, vol. 5, no. 7, July 1998 (1998-07), pages 365-372, XP008010169 ISSN: 1074-5521 * |
NICOLAOU K C ET AL: "Total synthesis of 16-desmethylepothilone B, epothilone B10, epothilone F, and related side chain modified epothilone B analogues." CHEMISTRY (WEINHEIM AN DER BERGSTRASSE, GERMANY) GERMANY 4 AUG 2000, vol. 6, no. 15, 4 August 2000 (2000-08-04), pages 2783-2800, XP002223256 ISSN: 0947-6539 * |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2004014919A1 (en) * | 2002-08-02 | 2004-02-19 | Novartis Ag | Epothilone derivatives |
US8871227B2 (en) | 2003-11-04 | 2014-10-28 | Bristol-Myers Squibb Company | Process and formulation containing epothilones and analogs thereof |
JP2007525519A (en) * | 2004-02-27 | 2007-09-06 | スローン−ケッタリング インスティトュート フォア キャンサー リサーチ | Synthesis and use of epothilone, its intermediates and analogues |
US7825141B2 (en) | 2004-03-16 | 2010-11-02 | Novartis Ag | Epothilone derivatives |
CN115850224A (en) * | 2022-07-22 | 2023-03-28 | 北京先通国际医药科技股份有限公司 | Synthetic method and application of modified long-chain fatty acid type PET reagent precursor |
Also Published As
Publication number | Publication date |
---|---|
US20040039026A1 (en) | 2004-02-26 |
CA2456280A1 (en) | 2003-03-06 |
US7358266B2 (en) | 2008-04-15 |
WO2003018002A3 (en) | 2003-09-04 |
EP1420780B1 (en) | 2008-10-01 |
JP2009007367A (en) | 2009-01-15 |
DE60229143D1 (en) | 2008-11-13 |
JP4176015B2 (en) | 2008-11-05 |
PT1420780E (en) | 2008-12-29 |
AU2002331171A1 (en) | 2003-03-10 |
EP2070534A2 (en) | 2009-06-17 |
CN100536841C (en) | 2009-09-09 |
EP2070534A3 (en) | 2009-08-26 |
EP1420780A2 (en) | 2004-05-26 |
ES2315399T3 (en) | 2009-04-01 |
ATE409473T1 (en) | 2008-10-15 |
CN1545411A (en) | 2004-11-10 |
BR0212107A (en) | 2004-08-24 |
HK1066464A1 (en) | 2005-03-24 |
JP2005501107A (en) | 2005-01-13 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US7358266B2 (en) | Cyclopropyl and cyclobutyl epothilone analogs | |
US6958401B2 (en) | Method for synthesizing epothilones and epothilone analogs | |
US6531497B1 (en) | Epothilone derivatives and their synthesis and use | |
CN102015701B (en) | PIM kinase inhibitors and methods of their use | |
CA2496477C (en) | Synthesis of epothilones, intermediates thereto, analogues and uses thereof | |
US20060293527A1 (en) | Analogs of epothilone | |
JP2002512634A (en) | Epothilone derivative | |
JP2001507716A (en) | Synthesis of epothilone and its intermediates and analogues and their use | |
US8513429B2 (en) | Synthesis of epothilones, intermediates thereto and analogues thereof | |
US6350878B1 (en) | Intermediates for the synthesis of epothilones and methods for their preparation | |
US6906188B2 (en) | Method for synthesizing epothilones and epothilone analogs | |
CA2858164C (en) | Pyridone derivative and pharmaceutical containing same | |
US20040053995A1 (en) | Synthesis of epothilones, intermediates thereto and analogues thereof | |
US20040242928A1 (en) | Reverse hydroxamic acid derivatives | |
JP2005521694A (en) | Microtube stable compound | |
US20190218226A1 (en) | Prodrugs of anticancer agents indotecan and indimitecan | |
US20070203346A1 (en) | Method for synthesizing epothilones and epothilone analogs |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AK | Designated states |
Kind code of ref document: A2 Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE ES FI GB GD GE GH HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LT LU LV MA MD MK MN MX NO NZ OM PH PL PT RO RU SE SG SI SK TJ TM TN TR TT UA US UZ VC VN YU ZA ZW Kind code of ref document: A2 Designated state(s): AE AG AL AM AT AU AZ BA BB BG BY BZ CA CH CN CO CR CU CZ DE DM DZ EC EE ES FI GB GD GE GH HU ID IL IN IS JP KE KG KP KR KZ LK LT LU LV MA MD MK MN MX NO OM PH PL PT RO RU SE SG SI SK TJ TN TR TT UA US UZ VC VN YU ZA |
|
AL | Designated countries for regional patents |
Kind code of ref document: A2 Designated state(s): AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR IE IT LU MC NL PT SE SK TR Kind code of ref document: A2 Designated state(s): AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI GB GR IE IT LU MC NL PT SE SK TR |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
DFPE | Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101) | ||
WWE | Wipo information: entry into national phase |
Ref document number: 2002767418 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2456280 Country of ref document: CA |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2003522522 Country of ref document: JP Ref document number: 20028164415 Country of ref document: CN |
|
WWP | Wipo information: published in national office |
Ref document number: 2002767418 Country of ref document: EP |
|
WWG | Wipo information: grant in national office |
Ref document number: 2002767418 Country of ref document: EP |