CA2307548C - Process for converting 9-dihydro-13-acetylbaccatin iii into taxol and derivatives thereof - Google Patents
Process for converting 9-dihydro-13-acetylbaccatin iii into taxol and derivatives thereof Download PDFInfo
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- CA2307548C CA2307548C CA002307548A CA2307548A CA2307548C CA 2307548 C CA2307548 C CA 2307548C CA 002307548 A CA002307548 A CA 002307548A CA 2307548 A CA2307548 A CA 2307548A CA 2307548 C CA2307548 C CA 2307548C
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- substituted
- benzoyl
- iii
- taxol
- tosyl
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- RCINICONZNJXQF-MZXODVADSA-N taxol Chemical compound O([C@@H]1[C@@]2(C[C@@H](C(C)=C(C2(C)C)[C@H](C([C@]2(C)[C@@H](O)C[C@H]3OC[C@]3([C@H]21)OC(C)=O)=O)OC(=O)C)OC(=O)[C@H](O)[C@@H](NC(=O)C=1C=CC=CC=1)C=1C=CC=CC=1)O)C(=O)C1=CC=CC=C1 RCINICONZNJXQF-MZXODVADSA-N 0.000 title claims abstract description 43
- 229930012538 Paclitaxel Natural products 0.000 title claims abstract description 42
- 229960001592 paclitaxel Drugs 0.000 title claims abstract description 42
- WPPPFZJNKLMYBW-FAEUQDRCSA-N 13-acetyl-9-dihydrobaccatin iii Chemical compound O([C@@H]1[C@]2(O)C[C@@H](C(=C([C@@H](OC(C)=O)[C@H](O)[C@]3(C)[C@@H](O)C[C@H]4OC[C@]4([C@H]31)OC(C)=O)C2(C)C)C)OC(=O)C)C(=O)C1=CC=CC=C1 WPPPFZJNKLMYBW-FAEUQDRCSA-N 0.000 title claims abstract description 19
- 238000000034 method Methods 0.000 title claims abstract description 19
- FFCWRLFQIKDRNO-UHFFFAOYSA-N 9-dihydro-13-acetyl baccatin III Natural products CC(=O)OC1C2C(O)CC(OC(=O)C)C3(CO3)C2C(OC(=O)C)C4(O)CC(OC(=O)C)C(=C(C1OC(=O)C)C4(C)C)C FFCWRLFQIKDRNO-UHFFFAOYSA-N 0.000 title claims abstract description 17
- UYWQUFXKFGHYNT-UHFFFAOYSA-N Benzylformate Chemical class O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 claims abstract description 28
- 125000002088 tosyl group Chemical class [H]C1=C([H])C(=C([H])C([H])=C1C([H])([H])[H])S(*)(=O)=O 0.000 claims abstract description 20
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims abstract description 18
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims abstract description 16
- 150000001875 compounds Chemical class 0.000 claims abstract description 15
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 claims abstract description 10
- 230000001590 oxidative effect Effects 0.000 claims abstract description 10
- BUDQDWGNQVEFAC-UHFFFAOYSA-N Dihydropyran Chemical compound C1COC=CC1 BUDQDWGNQVEFAC-UHFFFAOYSA-N 0.000 claims abstract description 9
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 6
- OVMSOCFBDVBLFW-VHLOTGQHSA-N 5beta,20-epoxy-1,7beta,13alpha-trihydroxy-9-oxotax-11-ene-2alpha,4alpha,10beta-triyl 4,10-diacetate 2-benzoate Chemical compound O([C@@H]1[C@@]2(C[C@H](O)C(C)=C(C2(C)C)[C@H](C([C@]2(C)[C@@H](O)C[C@H]3OC[C@]3([C@H]21)OC(C)=O)=O)OC(=O)C)O)C(=O)C1=CC=CC=C1 OVMSOCFBDVBLFW-VHLOTGQHSA-N 0.000 claims description 17
- YWLXLRUDGLRYDR-ZHPRIASZSA-N 5beta,20-epoxy-1,7beta,10beta,13alpha-tetrahydroxy-9-oxotax-11-ene-2alpha,4alpha-diyl 4-acetate 2-benzoate Chemical compound O([C@H]1[C@H]2[C@@](C([C@H](O)C3=C(C)[C@@H](O)C[C@]1(O)C3(C)C)=O)(C)[C@@H](O)C[C@H]1OC[C@]12OC(=O)C)C(=O)C1=CC=CC=C1 YWLXLRUDGLRYDR-ZHPRIASZSA-N 0.000 claims description 15
- -1 benzoylmethyl Chemical group 0.000 claims description 11
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims description 8
- 229930014667 baccatin III Natural products 0.000 claims description 8
- 125000006239 protecting group Chemical group 0.000 claims description 6
- 239000003153 chemical reaction reagent Substances 0.000 claims description 5
- 238000010511 deprotection reaction Methods 0.000 claims description 5
- 230000000850 deacetylating effect Effects 0.000 claims description 4
- NPRDHMWYZHSAHR-UHFFFAOYSA-N pyridine;trioxochromium Chemical compound O=[Cr](=O)=O.C1=CC=NC=C1.C1=CC=NC=C1 NPRDHMWYZHSAHR-UHFFFAOYSA-N 0.000 claims description 4
- 229940123237 Taxane Drugs 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- DKPFODGZWDEEBT-QFIAKTPHSA-N taxane Chemical class C([C@]1(C)CCC[C@@H](C)[C@H]1C1)C[C@H]2[C@H](C)CC[C@@H]1C2(C)C DKPFODGZWDEEBT-QFIAKTPHSA-N 0.000 claims description 3
- XSYLUBKWRZCOQP-CXRLMVSZSA-N (3r,4s)-1-benzoyl-3-(1-ethoxyethoxy)-4-phenylazetidin-2-one Chemical compound N1([C@H]([C@H](C1=O)OC(C)OCC)C=1C=CC=CC=1)C(=O)C1=CC=CC=C1 XSYLUBKWRZCOQP-CXRLMVSZSA-N 0.000 claims description 2
- 239000007800 oxidant agent Substances 0.000 claims description 2
- 239000000543 intermediate Substances 0.000 abstract description 9
- 238000002360 preparation method Methods 0.000 abstract description 6
- 102000001324 CD59 Antigens Human genes 0.000 abstract 1
- 108010055167 CD59 Antigens Proteins 0.000 abstract 1
- MIYFJEKZLFWKLZ-UHFFFAOYSA-N Phenylmethyl benzeneacetate Chemical class C=1C=CC=CC=1COC(=O)CC1=CC=CC=C1 MIYFJEKZLFWKLZ-UHFFFAOYSA-N 0.000 abstract 1
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 90
- 239000000203 mixture Substances 0.000 description 36
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 27
- 238000006243 chemical reaction Methods 0.000 description 22
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 15
- 239000000047 product Substances 0.000 description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 12
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 11
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 10
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 10
- 229910000104 sodium hydride Inorganic materials 0.000 description 9
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 8
- 239000000741 silica gel Substances 0.000 description 8
- 229910002027 silica gel Inorganic materials 0.000 description 8
- HZNVUJQVZSTENZ-UHFFFAOYSA-N 2,3-dichloro-5,6-dicyano-1,4-benzoquinone Chemical compound ClC1=C(Cl)C(=O)C(C#N)=C(C#N)C1=O HZNVUJQVZSTENZ-UHFFFAOYSA-N 0.000 description 7
- 238000003818 flash chromatography Methods 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- LFTLOKWAGJYHHR-UHFFFAOYSA-N N-methylmorpholine N-oxide Chemical compound CN1(=O)CCOCC1 LFTLOKWAGJYHHR-UHFFFAOYSA-N 0.000 description 6
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 6
- 239000012044 organic layer Substances 0.000 description 6
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 5
- 150000004200 baccatin III derivatives Chemical class 0.000 description 5
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 5
- 239000012312 sodium hydride Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 238000004809 thin layer chromatography Methods 0.000 description 5
- 238000005160 1H NMR spectroscopy Methods 0.000 description 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 102000029749 Microtubule Human genes 0.000 description 4
- 108091022875 Microtubule Proteins 0.000 description 4
- 239000000872 buffer Substances 0.000 description 4
- 238000003381 deacetylation reaction Methods 0.000 description 4
- 239000000284 extract Substances 0.000 description 4
- YNESATAKKCNGOF-UHFFFAOYSA-N lithium bis(trimethylsilyl)amide Chemical compound [Li+].C[Si](C)(C)[N-][Si](C)(C)C YNESATAKKCNGOF-UHFFFAOYSA-N 0.000 description 4
- 210000004688 microtubule Anatomy 0.000 description 4
- 238000012746 preparative thin layer chromatography Methods 0.000 description 4
- 235000017557 sodium bicarbonate Nutrition 0.000 description 4
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 3
- 210000004027 cell Anatomy 0.000 description 3
- 229940125782 compound 2 Drugs 0.000 description 3
- 229940126214 compound 3 Drugs 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- 230000006196 deacetylation Effects 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000010410 layer Substances 0.000 description 3
- IHLVCKWPAMTVTG-UHFFFAOYSA-N lithium;carbanide Chemical compound [Li+].[CH3-] IHLVCKWPAMTVTG-UHFFFAOYSA-N 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- MZRVEZGGRBJDDB-UHFFFAOYSA-N n-Butyllithium Substances [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- 229910052938 sodium sulfate Inorganic materials 0.000 description 3
- 235000011152 sodium sulphate Nutrition 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- DPKBAXPHAYBPRL-UHFFFAOYSA-M tetrabutylazanium;iodide Chemical compound [I-].CCCC[N+](CCCC)(CCCC)CCCC DPKBAXPHAYBPRL-UHFFFAOYSA-M 0.000 description 3
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
- GHYOCDFICYLMRF-UTIIJYGPSA-N (2S,3R)-N-[(2S)-3-(cyclopenten-1-yl)-1-[(2R)-2-methyloxiran-2-yl]-1-oxopropan-2-yl]-3-hydroxy-3-(4-methoxyphenyl)-2-[[(2S)-2-[(2-morpholin-4-ylacetyl)amino]propanoyl]amino]propanamide Chemical compound C1(=CCCC1)C[C@@H](C(=O)[C@@]1(OC1)C)NC([C@H]([C@@H](C1=CC=C(C=C1)OC)O)NC([C@H](C)NC(CN1CCOCC1)=O)=O)=O GHYOCDFICYLMRF-UTIIJYGPSA-N 0.000 description 2
- YYROPELSRYBVMQ-UHFFFAOYSA-N 4-toluenesulfonyl chloride Chemical compound CC1=CC=C(S(Cl)(=O)=O)C=C1 YYROPELSRYBVMQ-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical class [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 2
- 238000005481 NMR spectroscopy Methods 0.000 description 2
- 206010028980 Neoplasm Diseases 0.000 description 2
- 230000000259 anti-tumor effect Effects 0.000 description 2
- 230000032823 cell division Effects 0.000 description 2
- 229940125773 compound 10 Drugs 0.000 description 2
- 229940125797 compound 12 Drugs 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- XYIBRDXRRQCHLP-UHFFFAOYSA-N ethyl acetoacetate Chemical compound CCOC(=O)CC(C)=O XYIBRDXRRQCHLP-UHFFFAOYSA-N 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 239000002808 molecular sieve Substances 0.000 description 2
- XSXHWVKGUXMUQE-UHFFFAOYSA-N osmium dioxide Inorganic materials O=[Os]=O XSXHWVKGUXMUQE-UHFFFAOYSA-N 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 2
- AOSZTAHDEDLTLQ-AZKQZHLXSA-N (1S,2S,4R,8S,9S,11S,12R,13S,19S)-6-[(3-chlorophenyl)methyl]-12,19-difluoro-11-hydroxy-8-(2-hydroxyacetyl)-9,13-dimethyl-6-azapentacyclo[10.8.0.02,9.04,8.013,18]icosa-14,17-dien-16-one Chemical compound C([C@@H]1C[C@H]2[C@H]3[C@]([C@]4(C=CC(=O)C=C4[C@@H](F)C3)C)(F)[C@@H](O)C[C@@]2([C@@]1(C1)C(=O)CO)C)N1CC1=CC=CC(Cl)=C1 AOSZTAHDEDLTLQ-AZKQZHLXSA-N 0.000 description 1
- GLGNXYJARSMNGJ-VKTIVEEGSA-N (1s,2s,3r,4r)-3-[[5-chloro-2-[(1-ethyl-6-methoxy-2-oxo-4,5-dihydro-3h-1-benzazepin-7-yl)amino]pyrimidin-4-yl]amino]bicyclo[2.2.1]hept-5-ene-2-carboxamide Chemical compound CCN1C(=O)CCCC2=C(OC)C(NC=3N=C(C(=CN=3)Cl)N[C@H]3[C@H]([C@@]4([H])C[C@@]3(C=C4)[H])C(N)=O)=CC=C21 GLGNXYJARSMNGJ-VKTIVEEGSA-N 0.000 description 1
- HYJVYOWKYPNSTK-UONOGXRCSA-N (2r,3s)-3-benzamido-2-hydroxy-3-phenylpropanoic acid Chemical compound N([C@H]([C@@H](O)C(O)=O)C=1C=CC=CC=1)C(=O)C1=CC=CC=C1 HYJVYOWKYPNSTK-UONOGXRCSA-N 0.000 description 1
- BDLSDHWCOJPHIE-YMVRPXFZSA-N (4r,4ar,7s,7ar,12bs)-9-methoxy-3-methyl-3-oxido-2,4,4a,7,7a,13-hexahydro-1h-4,12-methanobenzofuro[3,2-e]isoquinoline-3-ium-7-ol Chemical compound O[C@H]([C@@H]1O2)C=C[C@H]3[C@]4([H])[N+]([O-])(C)CC[C@]13C1=C2C(OC)=CC=C1C4 BDLSDHWCOJPHIE-YMVRPXFZSA-N 0.000 description 1
- MOHYOXXOKFQHDC-UHFFFAOYSA-N 1-(chloromethyl)-4-methoxybenzene Chemical compound COC1=CC=C(CCl)C=C1 MOHYOXXOKFQHDC-UHFFFAOYSA-N 0.000 description 1
- XVMSFILGAMDHEY-UHFFFAOYSA-N 6-(4-aminophenyl)sulfonylpyridin-3-amine Chemical compound C1=CC(N)=CC=C1S(=O)(=O)C1=CC=C(N)C=N1 XVMSFILGAMDHEY-UHFFFAOYSA-N 0.000 description 1
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical class [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 1
- 206010006187 Breast cancer Diseases 0.000 description 1
- 208000026310 Breast neoplasm Diseases 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- 206010008342 Cervix carcinoma Diseases 0.000 description 1
- 229940126657 Compound 17 Drugs 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 208000000461 Esophageal Neoplasms Diseases 0.000 description 1
- 206010033128 Ovarian cancer Diseases 0.000 description 1
- 206010061535 Ovarian neoplasm Diseases 0.000 description 1
- 208000000236 Prostatic Neoplasms Diseases 0.000 description 1
- 241001116500 Taxus Species 0.000 description 1
- 241000015728 Taxus canadensis Species 0.000 description 1
- 208000006105 Uterine Cervical Neoplasms Diseases 0.000 description 1
- NJZNINIVAJSDHL-UHFFFAOYSA-N [Na].Cl[O] Chemical compound [Na].Cl[O] NJZNINIVAJSDHL-UHFFFAOYSA-N 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 201000011510 cancer Diseases 0.000 description 1
- 230000005907 cancer growth Effects 0.000 description 1
- 230000003915 cell function Effects 0.000 description 1
- 201000010881 cervical cancer Diseases 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000002026 chloroform extract Substances 0.000 description 1
- 239000002036 chloroform fraction Substances 0.000 description 1
- 229940117975 chromium trioxide Drugs 0.000 description 1
- WGLPBDUCMAPZCE-UHFFFAOYSA-N chromium trioxide Inorganic materials O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
- GAMDZJFZMJECOS-UHFFFAOYSA-N chromium(6+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Cr+6] GAMDZJFZMJECOS-UHFFFAOYSA-N 0.000 description 1
- 210000001072 colon Anatomy 0.000 description 1
- 208000029742 colonic neoplasm Diseases 0.000 description 1
- 238000004440 column chromatography Methods 0.000 description 1
- 229940125904 compound 1 Drugs 0.000 description 1
- 229940125758 compound 15 Drugs 0.000 description 1
- 229940125898 compound 5 Drugs 0.000 description 1
- 239000002027 dichloromethane extract Substances 0.000 description 1
- 125000005448 ethoxyethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- ZLVXBBHTMQJRSX-VMGNSXQWSA-N jdtic Chemical compound C1([C@]2(C)CCN(C[C@@H]2C)C[C@H](C(C)C)NC(=O)[C@@H]2NCC3=CC(O)=CC=C3C2)=CC=CC(O)=C1 ZLVXBBHTMQJRSX-VMGNSXQWSA-N 0.000 description 1
- DLEDOFVPSDKWEF-UHFFFAOYSA-N lithium butane Chemical compound [Li+].CCC[CH2-] DLEDOFVPSDKWEF-UHFFFAOYSA-N 0.000 description 1
- 210000004185 liver Anatomy 0.000 description 1
- 208000014018 liver neoplasm Diseases 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
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- 230000002611 ovarian Effects 0.000 description 1
- 201000002628 peritoneum cancer Diseases 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 210000002307 prostate Anatomy 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 230000029305 taxis Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D305/00—Heterocyclic compounds containing four-membered rings having one oxygen atom as the only ring hetero atoms
- C07D305/14—Heterocyclic compounds containing four-membered rings having one oxygen atom as the only ring hetero atoms condensed with carbocyclic rings or ring systems
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Epoxy Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
A process for the preparation of taxol, analogs thereof and their intermediates is described. The process includes the steps of protecting the C- 7 hydroxy group of 9-dihydro-13-acetylbaccatin III with a suitable protectin g group; oxidizing the C-9 hydroxy group; and adding a suitable side chain to the C-13 position. The intermediates include a compound having formula (1) wherein R is selected from the group consisting of benzyl, substituted benzy l, benzylformate, substituted benzylformate, tosyl, substituted tosyl, dihydropyran, methoxymethyl, benzoyl and substituted benzoyl.
Description
TAXOL AND DERIVATIVES THEREOF
FIELD OF THE INVENTION
The present invention relates to a process for converting 9-dihydro-13-acetylbaccatin III into taxane, and is particularly concerned with a process for converting 9-dihydro-13-acetylbaccatin III into taxol, baccatin III, 10-deacetyIbaccatin III and their intermediates.
As used herein, taxol is a registered trademark.
BACKGROUND OF THE INVENTION
to Paclitaxel (taxol), represented by the following structural formula:
O
O O OH
\ /
,o s O NH O
. ~s \ '~:
OH O HO
/ \ O ~ CHI
O O
is a potent antitumor compound. Paclitaxel exhibits a unique mechanism for preventing the growth of cancer cells by affecting the microtubules, which play an important role in cell division and other cell functions. A.t the beginning of cell division. a large number of microtubules are produced, and as the division reaches an end, the microtubules are normally broken down. Taxol prevents microtubules from breaking down, which has the effect of clogging up cancer cells to an extent that the cells cease to grow and divide.
Taxol is clinically effective :for the treatment of refractory human ovarian and breast cancer, and has exhibit promising activity against a number of other types of cancers such as liver, peritoneal, cervical, prostate, colon, and esophageal cancers.
Taxol was primarily extracted from the bark of the Pacific yew Taxes brevi_ folia.
Unfortunately, the yew grows very slow, approximately eight inches per year, and therefore the tree is a limited source of taxol. This has lead researchers to seek alternative means for to producing taxol and analogs thereof which may display superior antitumor activity.
SUMMARY OF THE INVENTION
In one aspect of the present invention, there is provided a process for preparing a I5 taxane comprising the step of oxidizing the C-9 position of 9-dihydro-13-acetylbaccatin III
with a suitable oxidizing reagent such as tetra-n-propylammonium perruthenate, Collin's reagent or activated dimethylsulfoxide (DMSO).
In another aspect of the present invention, there is provided a process for preparing 2o taxol and a derivative thereof comprising the steps of (a) protecting the C-7 hydroxy group of 9-dihydro-I3-acetylbaccatin III with a suitable protecting group to obtain a protected product; and (b) oxidizing the C-9 hydroxy group of the protected product.
Preferably, the protecting group is selected from the group consisting of benzyl, substituted benzyl, benzylformate, substituted benzylformate, tosyl, substituted tosyl, dihydropyran, methoxymethyl, benzoyl and substituted benzoyl.
The process may fi.trther include the steps of deacetylating the C-13 position, and deprotection of the C-7 position to obtain baccatin III. Alternatively, following the C-13 deacetylation, the C-10 position can be deacetylated and the C-7 position can be deprotected to obtain 10-deacetylbaccatin III. Or alternatively, following the C-13 deacetylation, a suitable side chain can be added to the C-13 position and the resulting intermediate selectively deprotected to obtain a desired product such as taxol. To obtain taxol, the deprotection is 1u done at the C-7 and 2' positions. Suitable side chains are (2R, 2S)-N-benzoyl-O-(1-ethoxyethyl)-3-phenylisose;rine and (3R, 4S)-3-(1-ethoxyethoxy)-4-(phenyl)-N-benzoyl-2-azetidinone.
In accordance with another aspect of the present invention, there is provided a compound having the following chemical structure:
Ac:O OH
OR
0\ -o"
W m.. ~3 H3C H~iO
HC~ _ / \ ~O ~-CHa (I) wherein R is selected from the grotup consisting of benzyl, substituted benzyl, benzylformate, substituted benzylformate, tosyl, substituted tosyl, dihydropyran, methoxymethyl, benzoyl, 2o substituted benzoyl, benzoylmethyl and substituted benzoylmethyl.
SUSST1TUTE SHEET (RULE 26) In accordance with another aspect of the present invention, there is provided a compound of the formula:
Ac0 ~o s O
O
/ \ O ~CHa O O (II) wherein R is selected from the group consisting of benzyl, substituted benzyl, benzylformate, substituted benzylformate, tosyl, substituted tosyl, dihydropyran, methoxymethyl, benzoyl, substituted benzoyl, benzoylmethyl and substituted benzoylmethyl.
1o DETAILED DESCRIPTION OF THE INVENTION
Table 1 lists definitions and chemical structures of compounds as used herein, and those definitions and chemical structures are to be applied throughout the present specification.
SUBSTITUTE SHEET (RULE 26) Table 1: Definitions ,And Chemical Structures Name Definition/chemical structure Functional group an atom or group of atoms having a characteristic chemical reactivit Benzyl CHz Substituted benzyi a benzyl group as defined above substituted with one or more functional rou s Dihydropyran o Benzylformate o CHz C \
O-Substituted benzylformatea benzyiformate as defined above substituted with one or m r o e functional ~rou (s Methoxymethyl -cH2-o - cH3 Benzoylmethyl p -C -CH
z /
Substituted benzoylmethyla benzoylmethyl as defined above substituted with one or more functional rou s Tosyl -02S ~ / CHI
Substituted tosyl a tosyl as defined above substituted with one or more fianctional ~roup(s) SUBSTITUTE SHEET (RULE 26) The starting material, 9-dihydro-13-acetylbaccatin III, can be obtained by various means including by extraction of TczxuS species. Briefly, the isolation process entails collecting plant material such as stems and needles, and grounding and extracting the material with methanol. The extraction is carried through for about 24 hours, and the resulting mixture is filtered and the extract collected. The extract is concentrated to about 10°l0 of its original volume by evaporation, and further diluted with water. The aqueous solution is extracted several times with hexane to give an aqueous layer and a non-aqueous layer. The aqueous layer is extracted several times with chloroform or dichloromethane. The chloroform or dichloromethane extract is concentrated to dryness, and the residue is dissolved in a mixture of chloroform, methanol and acetone (10:1:0.5), and fractionated by dry column chromatography to obtain fractions of taxol and 9-dihydro-13-acetylbaccatin ID. The fractions are combined, extracted and the 9-dihydro-13-acetylbaccatin is crystallized out.
t>
Taxol and derivatives thereof may be synthesized from 9-dihydro-13-acetylbaccatin III
by a number of protection, oxidation, reaction and deprotection steps. For example, referring to the processes illustrated below in Schemes 1-3, 9-dihydro-13-acetylbaccatin III is first protected at the C-7 position by adding a protecting group such as a methoxybenzyl or tosyi 20~ group to form a protected intermediate such as compound 2 7 or 16. Other suitable protecting groups are substituted benzyl, dihydropyran, benzylformate (CBZ), substituted benzylformate, methoxymethyl (MOM), benzoylmethyl (BOM) and substituted benzoylmethyl.
The protected intermediate is oxidized at the C-9 position with a suitable oxidizing agent such as tetra-n-prop5~lammonium perruthenate (TPAP), Collin's reagent (chromium trioxide and pyridine in dichloromethane) or activated methyl sulfoxide (DMSO) to give an oxidized intermediate such as compound 3, 8 or 17. The oxidized intermediate may be deacetylated at the C-13 position by reaction with, for example butyliithium in hexane or methyllithium, to give a bac:catin LII analog such as compound 4 or 9 .
Depending of the desired product, the baccatin III analog can either be deprotected with, for example 2,3-dichloro-5,6-dicyanobenzoyuinone (DDQ) to yield baccatin III (15) or further reacted to eventually obtain 10-deacetylbaccatin III ( 13 ) or taxol ( 18) or other desirable products.
To obtain 10-deace~:ylbaccatin III , the baccatin III analog (4) is next deacetylated at the C-10 position by reaction with, for example triethylamine in sodium hydride, to compound 12 which is further deprotected. To obtain taxol, the C-13 taxol side chain is added to the baccatin III analog by reaction with, for example (2R, 2S)-N-benzoyl-O-( 1-t5 ethoxyethyl)-3-phenylisoserine and lithium hexamethyldisilazide, to give a taxol analog such as compound 5 or 10. The taxol analog is next deprotected at the 2' by reaction with, for example 1% hydrochloric a~~ed, and C-7 position by reaction with, for example triethylamine and UV light, to give taxol. Other suitable C-13 side chains such as (3R, 4S)-3-(1-ethoxyethoxy)-4-(phenyl)-Td-benzoyl-2-azetidinone may also be used to obtain taxol analogs.
It will be appreciate~~ by one skilled in the art that other reagents and reactants may be used to obtain the same results, and that protection, oxidation and deprotection steps may be carried out in varying order; or number of steps, as necessary, and that schemes 1-3 are intended to include such variations.
SUBSTITUTE SHEET (RULE 26) Ac0 OH SCHEME 1 AcO OH / \
OH OCHz~OMe s s _ CH~O / \ CH:CI
Ac01°' ~3 ACO nn", ~3 ,i, HO H = / O NaH, n-Bu4Nl HO H ~/ O
OAc \ ~ OAc 2 / \ O
TPAP
Ac0 O NMO
OCHz / \ OMe RT
s HO m, is ", CH3Li Ac0 O
OCH2 / ~ OMe H - / O - 44 degree s HO -4 OAc / \ O AcOm, ~3 "' _ H ~ WO
O HO
DDQ ~~ OAc / \
(18:1 ) ESN / \ NH 4 O
NaH
/ \ _ Ac0 O ~H LiHMDS
OH OEE
s Of E~O~, ,Ph HOin'. i3 ", \'Ph HO = ~ 0 0O
OAc / \ O
O
HO O OCHz / \ OMe HO O OH
s s HO ii" ~3 ", HO u"
DDQ =
HO ~ O CH2Ch-H20 HO H , O
OAc (20:1 ) OAc / \ O / \ O
O O
SUBSTITUTE SHEET (RULE 26) SCHEME 1 (cont'd) Ac0 OCH2 ~ ~ OMe NH O s / \ ~ ", O n~" ~3 OEE a -HO ~/
OAc / ~ O
1% HCI
O O
/ \ Ac0 OCHz ~ ~ OMe NH O
s / \
_ p m , ~3 ", OH H~ 'O
HO
OAc / ~ O
DDQ
CHzCh-H20 (20:1 ) O
Ac0 O
/ \ OH
NH O s / \
_ O m" ~ 3 "' OH
HO -OAc SUBSTITUTE SHEET (RULE 26) Ac0 OH
OH
Ac0 OH OSO2 ~ ~ CH3 CH3 ~ ~ S02C1 ,,, _ Ac0 "". ~s O NaH, n-Bu4Nl Ac0 i"" is , 7 HO
OAc H ~ ~p O HO
OAc O ~ ~ O
O
TPAP
NMO
RT
Ac0 O OS02 ~ ~ CH3 i Ac0 m. ~ 3 ,,, H~ ' i HO
OAc ~ O
O
n-BuLi -40 degree SUBSTITUTE SHEET (RULE 26) Ac0 O OSO~~~CH3 o SCHEME 2 (cont'd) HO ~~~~ is ~,, \ / NH O
H = ~O
HO = ' \ / off OAc -/ \ p OEE
LiHMDS
O
DDS
CH2Clz Hz0 - Ac0 O OS02 ~ ~ CH3 (18:1) \ / NH o s \ / ~O m, ~3 ~., Ac0 O OH OEE ~.~ _ ~O ~ 0 HO
s OAc / \ O
HO~~w ~g r.~
O
H~~ O 1°i° Hcl HO OAc / \ ~ o Ac0 O OSO2 ~ ~ CH3 O ~~~NH o s \ / Dln. 1g ~,, OH H - / O
HO -OAc / \ O
Et3N, by MeOH
P,cO
OH
\ / NH O s \ / O m. ~ 3 ~,, OH H = , O
Hc~ -OAc ~~O
~~-~,~~0 SUBSTITUTE SHEET (RULE 26) Ac0 OH OH
CHZBr Ac0 OH Q
AcOm",. t3 ", HO H =' 'O AcOm~,. ~3 ~"
OAc H ~ ~
/ \ HO -OAc O / \ O
TPAP
NaOCI
O
Q
AcO~ ~ ~".
HO H = '/
OAc / \
O
SUBSTITUTE SHEET (RULE 26) 1 9-dihydro-13-acetylbaccatin III
7-O-p-methoxybenzyl-9-dihydro-13-acetylbaccatin III
3 7-O-p-methoxybenzyl-13-acetylbaccatin III
4 7-O-p-methoxybenzylbaccati.n III
5 7-O-p-methoxybenzyl-(2'-ethoxyethyl) taxol 6 7-O-p-methoxybenzyl taxol 7 7-O-tosyl-9-dihydro-13-acet:ylbaccatin III
8 7-O-tosyl-13-acetylt>accatin III
9 7-O-tosylbaccatin III
l0 10 7-O-tosyl-( 2'-ethoxyethyl) taxol 11 7-O-tosyl taxol 12 10-deacetyl-7-O-p-methoxybenzylbaccatin III or 7-O-p-methoxybenryl-10-deacetylbaccatin III
13 10-deacetylbaccatin III
is I 5 Baccatin III
16 7-O-benzyl-9-dihydro-13-aceaylbaccatin III
17 7-O-benzyl-13-acetylbaccatin III
18 taxol or paclitaxel SUBSTITUTE SHEET (RULE 26) MATERIAL
All the reagents were obtained from Aldrich Chemicals, USA.
s Preparation of taaol Step 1(a): 7-O-p-methoxybenzyl-9-dihydro-13-acetylbaccatin III ( 2 ) 20 mg 9-dihydro-13-acetylbaccatin III ( 1 ) and 100 mg n-tetrabutylammonium iodide were dissolved in 3 mL of dichloromethane (CH2C12) in a 25 mL round bottom flask. 23 mg to of sodium hydride (NaH) was added and the mixture was stirred at room temperature for five minutes. 0. I mL of p-methoxybenzyl chloride was added dropwise over 5 minutes, and the temperature was raised to 45°C. 'The mixture was stirred for 24 hours, following which 30 mL of distilled water was added to stop the reaction. The product was extracted with dichloromethane, and purified by preparative thin layer chromatography (TLC) to yield 17 mg 15 7-O-p-methoxybenzyl-9-dihydro-I3-acetylbaccatin III, compound 2, as identified by NMR
spectroscopy.
'H-NMR (200 MHz, CDCI3), S: 8.10 (d,Ar-H-2,H-6), 7.60 (t, Ar-H-4), 7.50 (t, Ar-H-3, H-5), 7.21 (d, 2Ar-H), 6.90 (d, 2Ar-:(-i), 6.30 (d, H-10), 6.17 (t, H-13), 5.80 (d,H-2), 4.92 (d,H-2o S), 4.75 (dd, H-7), 4.50 (d, H-9), 4.31 (d,H-20a), 4.29 (d,H-20b), 4.15 (s, -OCHZ), 3.80 (s, OCH3), 3.01 (s, H-3), 2.59 (m,H-6), 2.26 (s, CH3C=O), 2.18 (s, CH3C=O), 2.10 (H-14a), 2.02 (s, CH3C=O), 1.97 (s, CH3), 1.85 (H-14b), i.77 (s, CH3), 1.75 (s, CH3), 1.26 (S, CH3) ppm.
Step 1(b): 7-O-methoxybenzyl-13-acetylbaccatin III ( 3 ) mg of the product of step 1 (a), compound 2, was added to 10.8 mg of 4-methylmorpholine N-oxide (NMO) in a 25 mL round bottom flask, and the mixture was dissolved in 3 mL of dichloromethane. 4d molecular sieve was added to the mixture which s was stirred for 5 minutes. 3.5 mg o~f tetra-n-propylammonium perruthenate (TPAP) was added, and the mixture wa;~ stirred for about 6 hours at room temperature, following which the temperature was raised to 40 °C'.. The mixture was maintained at that temperature overnight until the reaction was completed. Once the reaction was completed, the mixture was poured into a short silica gel column. The column was eluted with 50 mL of chloroform n> (CHCi3} to give a chloroform fraction which was concentrated to dryness.
The residue was purified by preparative TL(~ to yield 2 mg white needles which were identified as 7-O-methoxybenzyl-13-acetylbaccatin III, compound 3, by NMR spectroscopy.
'H-NMR (400 MHz, CDC'.13), b: 8.10 (d, Ar-H-2, H-6), 7.60 (t, Ar-H-4), 7.49 (t, Ar-H-3, H-S), 7.22 (s, 4Ar-H), 6.2f, (s, H-10), 6.18 (t, H-13), 5.65 (d, H-2), 5.60 (dd, H-7), 5.27 (s, OCH3), 4.95 (d, H-5), 4.33 (d, H-2l)a), 4.17 (d, H-20b), 3.95 (s, -OCHZ), 3.81 (d, H-3), 2.60 (m, H-6), 2.35 (s, CH;C=O), 2.22 (~dd, H-14a), 2.20 (s, CH3C=O), 2.15 (s, CHI), 2.05 (s, CH3C=O), 2.01 (H-14b), 1.96 (s, CH3), 1.24 (s, CH3), 1.18 (s, CH;) ppm.
2o Step 1(c): 7-O-p-methoxybenzylbaccatin III ( 4 ) SO mg of the produ~~t of step 1(b), compound 3, was dissolved in 5 mL of tetrahydrofuran at -44°C, <md 5 mole equivalent of methyllithium were added dropwise to remove the C-13 acetyl group. Upon completion of the deacetylation reaction, the mixture was partitioned between 50 mL of a mixture of saturated ammonium chloride buffer and SUBSTITUTE SHEET (RULE 26) dichloromethane ( 1:1 ). The organic layer was concentrated and purified by flash column chromatography on silica gel, eluting with a mixture of dichloromethane and methanol (97:3) to yield 22 mg of 7-O-p-methoxybenzylbaccatin III as white solid.
Step 1(d): 7-O-p-methoxybenzyl-(2'-ethoxyethyl) taxol ( S ) mg of the product of step 1 (c) (4) was combined with 6 mole equivalents of (2R, 2S)-N-benzoyl-O-(1-ethoxyethyl)-3-phenylisoserine or 5 mole equivalent of(3R, 4S)-3-(1-ethoxyethoxy)-4-(phenyl)-N-benzoyl-2-azetidinone and 3 mole equivalents of lithium hexamethyldisilazide (LiHNU7S) in 5 mL of tetrahydrofizran at -78 °C
for about 20 minutes in to a 25 mL round bottom flask. The reaction was warmed to 0 °C for about 6 hours, or until the reaction was completed as confirmed by TLC analysis. Once the reaction was completed, the mixture was quenched with 30 mL of a pH 7 buffer and the product was extracted with dichloromethane, dried and purified by flash column chromatography on silica gel, eluting with dichloromethane and methanol (97:3 ) to yield 16 mg of 7-O-p-methoxybenzyl-(2'-15 ethoxyethyl) taxol.
Step 1(e): 7-O-p-methoxybenzyl taxol ( 6 ) 10 mg of the product of step 1 (d) was dissolved in ethanol at room temperature in a ~
mL round bottom flask. An excess of 1% hydrochloric acid was added, and the reaction 2o continued for about 4 hours. The reaction product was poured into a 25 mL
separation funnel and 50 mL of a mixture of pH 7 buffer and dichloromethane ( 1:1 ) was added. The organic layer was evaporated to dryness to obtain a residue.
SUBSTITUTE SHEET (RULE 26) WO 98/50378 PCTlCA98/00401 Step 1(f): taxol or paciitax:el ( I 8) mL of dichloromethane was added to the residue obtained in step 1(e), and 0.25 mL
of water was mixed thereto. In this case, the ratio of water to dichloromethane was 1:20.
1.0-1.5 mole equivalent of :?,3-dichl~oro-5,6-dicyanobenzoquinone (DDQ) was added to the s mixture and the temperature was maintained at room temperature or 5°C. Upon completion, 10 mL of saturated aqueous sodium hydrogen carbonate (NaHC03) was added to the reaction, and the mixture was extracted with 10 mL of dichloromethane.
The extract was washed with S mL of saturated aqueous sodium hydrogen carbonate and dried over sodium sulfate (Na2S04). The solvent was evaporated and the residue was purified on a silica to gel column to give 3.5 mg of taxol.
Preparation of taxol Step 2(a): 7-O-tosyl-9-dihvydro-13-acetylbaccatin III ( 7 ) 1.0 g of 9-dihydro-13-acetylbaccatin III (1) was placed in a 50 mL round bottom flask with 454 mg of p-toluenesulfonyl chloride and 589 mg of tetrabutylammonium iodide. The mixture was dissolved in 1 S mL of dichloromethane and stirred at room temperature for S
2o minutes. 57 mg of sodium hydride was added slowly to the mixture, and the mixture was stirred at room temperature for 2 hours, following which 100 mL of water was added. The mixture was extracted with 70 mL of dichloromethane. The organic layer was concentrated to dryness, and the residue ,vas purified by flash column chromatography on silica gel, eluting SUBSTITUTE SHEET (RULE 26) with a mixture of dichloromethane and methanol (97:3) to yield 1.1 g of 7-O-tosyl-9-dihydro-13-acetylbaccatin III.
Step 2(b): 7-O-tosyl-13-acetylbaccatin III ( 8 ) 400 mg of the product of step 2(a), compound 7, was placed in a 50 mL round s bottom flask and 126 mg of 4-methylmorpholine N-oxide was added to thereto.
The mixture was dissolved in 5 mL of acetonitrile (CH3CN) and 126 mg of 4 6 molecular sieve was added The mixture was stirred at room temperature for about 10 minutes, following which 18 mg of TPAP was added. The mixture was stirred for 5 hours at room temperature and poured through a short silica gel column, eluting with dichloromethane. The fraction was further 1o purif ed by flash column chromatography on silica gel, eluting with a mixture of ethyl acetoacetate (EtOAc) and hexane (7:3) to yield about 350 mg of white crystals which were identified as 7-O-tosyl-13-acetylbaccatin III, purity 98%.
'H-NMR (400 MHz, CDCI3), 8: 8.05 (dd, 2H, Ar-H), 7.74 (d, 2H, tosyl), 7.60 (ddd, Ar-15 Hd), 7.47 (dd, 2H, Ar-H), 7.30 (d, 2H, tosyl), 6.69 (s, H,o), 6.16 (t, H,3), 5.66 (dd, H2), 5.30 (dd, H~), 4.85 (dd, H-5), 4.30 (d, H-20a), 4.10 (d, H-20b), 3.00 (s, 3H, tosyl), 3.92 (d, H-3), 2.60 (m, H-6a), 2.42 (s, -OCH3), 2.33 (s, -OCH3), 2.30 (dd, H-14a), 2.21 (s, -OCH;), 2.13 (s, CH3), 2.10 (dd, H-14b), 1.77 (s, CH3), 1.20 (s, CH3), 1.17 (s, CH3) ppm.
2o Step 2(c): 7-O-tosylbaccatin III ( 9 ) 100 mg of the product of step 2(b) (compound 8) was dissolved in 10 mL of tetrahydrofuran in a 25 mL round bottom flask. The flask was then placed into a container which was maintained at -43 °C. The solution was stirred and 0.4 mL of n-butyllithium in hexane was added dropwise for about 3 minutes. The mixture was stirred for about 30 SUBSTITUTE SHEET (RULE 26) minutes with the temperature raised to about 0 °C, and was further transferred into a 500 mL
separation funnel with 100 mL of water and extracted with 150 mL of dichloromethane. The product was purified by preparative TLC to yield about 62 mg of white crystals which were identified as 7-O-tosylbaccatin III.
Step 2(d): 7-O-tosyl-(2'-e;thoxyethyl) taxol ( 10 ) 100 mg of compound 8 was placed in a 25 mL round bottom flask , and 6 mole equivalents of (2R, 2S)-N-benzoyl-O-(1-ethoxyethyl)-3-phenylisoserine were dissolved in 5 mL of tetrahydrofuran at -'78 °C. 3 mole equivalents of LiHNIDS was added slowly. The to mixture was stirred at -78 "C for about 20 minutes, following which it was warmed to about 0 to 20 °C. The reaction progress was followed by TLC until completion.
Once completed, the reaction was quenched with pH 7 buffer and extracted with 40 mL of dichloromethane.
The organic layer was concentrated to dryness under vacuum, and the residue was purified by preparative TLC to yield about 85 rng of white crystals which were identified as 7-O-tosyl-(2'-ethaxyethyl) taxol.
Step 2(e): 7-O-tosyl taxol ( 11 ) 50 mg of the product of step 2(d), compound 10, was placed in a 25 mL round bottom flask and dissolved with 15 mL of ethanol at room temperature. An excess of 1 2o hydrochloric acid was added and the mixture was maintained at room temperature for about 5 hours. The reaction was then quenc;hed with 20 mL of water and 40 mL of dichloromethane.
The organic layer was evaporated to dryness under vacuum to yield 7-O-tosyl taxol.
Step 2(~: taxol or paclita~:el ( 18 ) SUBSTITUTE SHEET (RULE 26) The residue obtained in step 2(e) was dissolved in 10 mL of a 0.02 M solution of triethylamine in methanol and irradiated by UV light for about 6 hours or until the reaction is completed as shown by TLC. After irradiation, the triethylamine solvent was evaporated under vacuum. The residue was purified by flash column chromatography on silica gel, eluting with a mixture of clichloromethane and methanol (97:3) to yield about 25 mg of taxol which was characterized as natural taxol.
'H-NMR (400 MHz, CDI~l3), b: 8.12, 7.73, 7.6I, 7.51, 7.41, 7.38, 6.97, 6.27, 6.23, 5.78, 5.67, 4.94, 4.79, 4.40, 4.3 3, 4.19, 3.79, 3.54, 2.51, 2.46, 2.38, 2.36, 2.28, 2.24, 1.89, 1.89, l0 1.79, 1.68, 1.24, 1.14 pprr~.
Preparation of 10-deacetylbaccatin III
IS
Step 3(a): 7-O-p-methox~benzyl-10-deacetylbaccatin III ( 12 ) 70 mg of the prodG.ct of step 1 (c), compound 4, was placed in a 25 mL round bottom flask with 5 mL of dichloromethane. 1.5 mole equivalent of sodium hydride was added followed by 3 mL of trieth;ylamine, and the mixture was magnetically stirred for 2 to 3 hours.
2o The reaction progress was monitored by TLC. When the deacetylation was completed, the solution was poured into 25 mL of water and extracted with 30 mL
dichloromethane. The organic layer was concentrated to dryness under vacuum. The residue was purified by flash column chromatography to yield 42 mg of 7-O-p-methoxybenzyl-10-deacetylbaccatin III as white solid.
SUBSTITUTE SHEET (RULE 26) Step 3(b): 10-deacetylbaccatin IIIf ( 13 ) 30 mg of compound 12, i.e. 7-O-p-methoxybenzyl-10-deacetylbaccatin III, was placed into a 25 mL round bottom flask with 5 mL of dichloromethane which contained a small amount of water, thc: ratio of water to dichloromethane being 1:20. 1.0 mole equivalent of 2,3- dichloro-5,6-dicyanobenzoquinone (DDQ) was added and the mixture was stirred at room temperature for about 3 hours. Once the reaction was completed, 15 mL of staturated sodium hydrogen carbonate was added and the mixture was extracted with 20 mL
of dichloromethane. The extract was dried over sodium sulfate. The dichloromethane solution 1o was evaporated and the residue was purified with a silica gel column to yield 16 mg of 10-deacetylbaccatin III.
Preparation of baccatin III
25 mg of compound 4 (7-O-p-methoxybenzylbaccatin III) or 9 (7-O-tosylbaccatin III) containing a small amount of water was placed in a 25 mL round bottom flask and 5 mL of dichloromethane was added. In this case, the ratio of water to dichloromethane was 1:18. 1.0 to 1.5 mole equivalent of I)DQ was added to the mixture which was being stirred at about room temperature or S °C. Upon completion of the reaction, 20 mL of saturated aqueous 2o sodium hydrogen carbonate was added, and the mixture was extracted with 30 mL
dichloromethane, and dried over sodium sulfate. The solvent was evaporated and the residue was purified by flash column chromatography, eluting with a muxture of dichloromethane and methanol (96:4) to yield 1',~ mg of baccatin III, compound 15., as white solid.
SUBSTITUTE SHEET (RULE 26) EXAMPLE S
Preparation of 7-O-benzyl-13-acetylbaccatin IEI intermediate Step 4(a): 7-O-benzyl-9-dihydro-13-acetylbaccatin III ( 16 ) mg of 9-dihydro-13-acetylbaccatin III, compound 1, was dissolved in 3 mL of tetrahydrofi,rran (THF), and 20 mg of n-tetrabutylammonium iodide was added in a 5 mL
round bottom flask. The mixture was stirred for 5 minutes and 12 mg of sodium hydride was added. I 70 mg of ben2yl bromide was added dropwise and the mixture was stirred at 40°C.
The stirring continued overnight. 40 mL of distilled water was added to stop the reaction.
The product was extracted with chloroform. The chloroform solution was evaporated and the residue was purified by preparative TLC to yield 8 mg of 7-O-benzyl-9-dihydro-13-acetylbaccatin III.
Step 4(b): 7-O-benzyl-13-acetylbaccatin III ( 17 ) t.s In a similar manner as in step I(b), compound 17 can be made. In this case, the reagent methylmorphine N-oxide (NMO) is replaced by sodium chloroxide (NaOCI).
Taxol, 10-deacetylbaccatin III and baccatin III can be obtained from 7-O-benryl-13-acetylbaccatin III in similar manners as shown in the previous examples.
Although embodiments of the invention have been described above, it is not limited thereto and it will be apparent to those skilled in the art that numerous modifications form part of the present invention insofar as they do not depart from the spirit, nature and scope of the claimed and described invention.
FIELD OF THE INVENTION
The present invention relates to a process for converting 9-dihydro-13-acetylbaccatin III into taxane, and is particularly concerned with a process for converting 9-dihydro-13-acetylbaccatin III into taxol, baccatin III, 10-deacetyIbaccatin III and their intermediates.
As used herein, taxol is a registered trademark.
BACKGROUND OF THE INVENTION
to Paclitaxel (taxol), represented by the following structural formula:
O
O O OH
\ /
,o s O NH O
. ~s \ '~:
OH O HO
/ \ O ~ CHI
O O
is a potent antitumor compound. Paclitaxel exhibits a unique mechanism for preventing the growth of cancer cells by affecting the microtubules, which play an important role in cell division and other cell functions. A.t the beginning of cell division. a large number of microtubules are produced, and as the division reaches an end, the microtubules are normally broken down. Taxol prevents microtubules from breaking down, which has the effect of clogging up cancer cells to an extent that the cells cease to grow and divide.
Taxol is clinically effective :for the treatment of refractory human ovarian and breast cancer, and has exhibit promising activity against a number of other types of cancers such as liver, peritoneal, cervical, prostate, colon, and esophageal cancers.
Taxol was primarily extracted from the bark of the Pacific yew Taxes brevi_ folia.
Unfortunately, the yew grows very slow, approximately eight inches per year, and therefore the tree is a limited source of taxol. This has lead researchers to seek alternative means for to producing taxol and analogs thereof which may display superior antitumor activity.
SUMMARY OF THE INVENTION
In one aspect of the present invention, there is provided a process for preparing a I5 taxane comprising the step of oxidizing the C-9 position of 9-dihydro-13-acetylbaccatin III
with a suitable oxidizing reagent such as tetra-n-propylammonium perruthenate, Collin's reagent or activated dimethylsulfoxide (DMSO).
In another aspect of the present invention, there is provided a process for preparing 2o taxol and a derivative thereof comprising the steps of (a) protecting the C-7 hydroxy group of 9-dihydro-I3-acetylbaccatin III with a suitable protecting group to obtain a protected product; and (b) oxidizing the C-9 hydroxy group of the protected product.
Preferably, the protecting group is selected from the group consisting of benzyl, substituted benzyl, benzylformate, substituted benzylformate, tosyl, substituted tosyl, dihydropyran, methoxymethyl, benzoyl and substituted benzoyl.
The process may fi.trther include the steps of deacetylating the C-13 position, and deprotection of the C-7 position to obtain baccatin III. Alternatively, following the C-13 deacetylation, the C-10 position can be deacetylated and the C-7 position can be deprotected to obtain 10-deacetylbaccatin III. Or alternatively, following the C-13 deacetylation, a suitable side chain can be added to the C-13 position and the resulting intermediate selectively deprotected to obtain a desired product such as taxol. To obtain taxol, the deprotection is 1u done at the C-7 and 2' positions. Suitable side chains are (2R, 2S)-N-benzoyl-O-(1-ethoxyethyl)-3-phenylisose;rine and (3R, 4S)-3-(1-ethoxyethoxy)-4-(phenyl)-N-benzoyl-2-azetidinone.
In accordance with another aspect of the present invention, there is provided a compound having the following chemical structure:
Ac:O OH
OR
0\ -o"
W m.. ~3 H3C H~iO
HC~ _ / \ ~O ~-CHa (I) wherein R is selected from the grotup consisting of benzyl, substituted benzyl, benzylformate, substituted benzylformate, tosyl, substituted tosyl, dihydropyran, methoxymethyl, benzoyl, 2o substituted benzoyl, benzoylmethyl and substituted benzoylmethyl.
SUSST1TUTE SHEET (RULE 26) In accordance with another aspect of the present invention, there is provided a compound of the formula:
Ac0 ~o s O
O
/ \ O ~CHa O O (II) wherein R is selected from the group consisting of benzyl, substituted benzyl, benzylformate, substituted benzylformate, tosyl, substituted tosyl, dihydropyran, methoxymethyl, benzoyl, substituted benzoyl, benzoylmethyl and substituted benzoylmethyl.
1o DETAILED DESCRIPTION OF THE INVENTION
Table 1 lists definitions and chemical structures of compounds as used herein, and those definitions and chemical structures are to be applied throughout the present specification.
SUBSTITUTE SHEET (RULE 26) Table 1: Definitions ,And Chemical Structures Name Definition/chemical structure Functional group an atom or group of atoms having a characteristic chemical reactivit Benzyl CHz Substituted benzyi a benzyl group as defined above substituted with one or more functional rou s Dihydropyran o Benzylformate o CHz C \
O-Substituted benzylformatea benzyiformate as defined above substituted with one or m r o e functional ~rou (s Methoxymethyl -cH2-o - cH3 Benzoylmethyl p -C -CH
z /
Substituted benzoylmethyla benzoylmethyl as defined above substituted with one or more functional rou s Tosyl -02S ~ / CHI
Substituted tosyl a tosyl as defined above substituted with one or more fianctional ~roup(s) SUBSTITUTE SHEET (RULE 26) The starting material, 9-dihydro-13-acetylbaccatin III, can be obtained by various means including by extraction of TczxuS species. Briefly, the isolation process entails collecting plant material such as stems and needles, and grounding and extracting the material with methanol. The extraction is carried through for about 24 hours, and the resulting mixture is filtered and the extract collected. The extract is concentrated to about 10°l0 of its original volume by evaporation, and further diluted with water. The aqueous solution is extracted several times with hexane to give an aqueous layer and a non-aqueous layer. The aqueous layer is extracted several times with chloroform or dichloromethane. The chloroform or dichloromethane extract is concentrated to dryness, and the residue is dissolved in a mixture of chloroform, methanol and acetone (10:1:0.5), and fractionated by dry column chromatography to obtain fractions of taxol and 9-dihydro-13-acetylbaccatin ID. The fractions are combined, extracted and the 9-dihydro-13-acetylbaccatin is crystallized out.
t>
Taxol and derivatives thereof may be synthesized from 9-dihydro-13-acetylbaccatin III
by a number of protection, oxidation, reaction and deprotection steps. For example, referring to the processes illustrated below in Schemes 1-3, 9-dihydro-13-acetylbaccatin III is first protected at the C-7 position by adding a protecting group such as a methoxybenzyl or tosyi 20~ group to form a protected intermediate such as compound 2 7 or 16. Other suitable protecting groups are substituted benzyl, dihydropyran, benzylformate (CBZ), substituted benzylformate, methoxymethyl (MOM), benzoylmethyl (BOM) and substituted benzoylmethyl.
The protected intermediate is oxidized at the C-9 position with a suitable oxidizing agent such as tetra-n-prop5~lammonium perruthenate (TPAP), Collin's reagent (chromium trioxide and pyridine in dichloromethane) or activated methyl sulfoxide (DMSO) to give an oxidized intermediate such as compound 3, 8 or 17. The oxidized intermediate may be deacetylated at the C-13 position by reaction with, for example butyliithium in hexane or methyllithium, to give a bac:catin LII analog such as compound 4 or 9 .
Depending of the desired product, the baccatin III analog can either be deprotected with, for example 2,3-dichloro-5,6-dicyanobenzoyuinone (DDQ) to yield baccatin III (15) or further reacted to eventually obtain 10-deacetylbaccatin III ( 13 ) or taxol ( 18) or other desirable products.
To obtain 10-deace~:ylbaccatin III , the baccatin III analog (4) is next deacetylated at the C-10 position by reaction with, for example triethylamine in sodium hydride, to compound 12 which is further deprotected. To obtain taxol, the C-13 taxol side chain is added to the baccatin III analog by reaction with, for example (2R, 2S)-N-benzoyl-O-( 1-t5 ethoxyethyl)-3-phenylisoserine and lithium hexamethyldisilazide, to give a taxol analog such as compound 5 or 10. The taxol analog is next deprotected at the 2' by reaction with, for example 1% hydrochloric a~~ed, and C-7 position by reaction with, for example triethylamine and UV light, to give taxol. Other suitable C-13 side chains such as (3R, 4S)-3-(1-ethoxyethoxy)-4-(phenyl)-Td-benzoyl-2-azetidinone may also be used to obtain taxol analogs.
It will be appreciate~~ by one skilled in the art that other reagents and reactants may be used to obtain the same results, and that protection, oxidation and deprotection steps may be carried out in varying order; or number of steps, as necessary, and that schemes 1-3 are intended to include such variations.
SUBSTITUTE SHEET (RULE 26) Ac0 OH SCHEME 1 AcO OH / \
OH OCHz~OMe s s _ CH~O / \ CH:CI
Ac01°' ~3 ACO nn", ~3 ,i, HO H = / O NaH, n-Bu4Nl HO H ~/ O
OAc \ ~ OAc 2 / \ O
TPAP
Ac0 O NMO
OCHz / \ OMe RT
s HO m, is ", CH3Li Ac0 O
OCH2 / ~ OMe H - / O - 44 degree s HO -4 OAc / \ O AcOm, ~3 "' _ H ~ WO
O HO
DDQ ~~ OAc / \
(18:1 ) ESN / \ NH 4 O
NaH
/ \ _ Ac0 O ~H LiHMDS
OH OEE
s Of E~O~, ,Ph HOin'. i3 ", \'Ph HO = ~ 0 0O
OAc / \ O
O
HO O OCHz / \ OMe HO O OH
s s HO ii" ~3 ", HO u"
DDQ =
HO ~ O CH2Ch-H20 HO H , O
OAc (20:1 ) OAc / \ O / \ O
O O
SUBSTITUTE SHEET (RULE 26) SCHEME 1 (cont'd) Ac0 OCH2 ~ ~ OMe NH O s / \ ~ ", O n~" ~3 OEE a -HO ~/
OAc / ~ O
1% HCI
O O
/ \ Ac0 OCHz ~ ~ OMe NH O
s / \
_ p m , ~3 ", OH H~ 'O
HO
OAc / ~ O
DDQ
CHzCh-H20 (20:1 ) O
Ac0 O
/ \ OH
NH O s / \
_ O m" ~ 3 "' OH
HO -OAc SUBSTITUTE SHEET (RULE 26) Ac0 OH
OH
Ac0 OH OSO2 ~ ~ CH3 CH3 ~ ~ S02C1 ,,, _ Ac0 "". ~s O NaH, n-Bu4Nl Ac0 i"" is , 7 HO
OAc H ~ ~p O HO
OAc O ~ ~ O
O
TPAP
NMO
RT
Ac0 O OS02 ~ ~ CH3 i Ac0 m. ~ 3 ,,, H~ ' i HO
OAc ~ O
O
n-BuLi -40 degree SUBSTITUTE SHEET (RULE 26) Ac0 O OSO~~~CH3 o SCHEME 2 (cont'd) HO ~~~~ is ~,, \ / NH O
H = ~O
HO = ' \ / off OAc -/ \ p OEE
LiHMDS
O
DDS
CH2Clz Hz0 - Ac0 O OS02 ~ ~ CH3 (18:1) \ / NH o s \ / ~O m, ~3 ~., Ac0 O OH OEE ~.~ _ ~O ~ 0 HO
s OAc / \ O
HO~~w ~g r.~
O
H~~ O 1°i° Hcl HO OAc / \ ~ o Ac0 O OSO2 ~ ~ CH3 O ~~~NH o s \ / Dln. 1g ~,, OH H - / O
HO -OAc / \ O
Et3N, by MeOH
P,cO
OH
\ / NH O s \ / O m. ~ 3 ~,, OH H = , O
Hc~ -OAc ~~O
~~-~,~~0 SUBSTITUTE SHEET (RULE 26) Ac0 OH OH
CHZBr Ac0 OH Q
AcOm",. t3 ", HO H =' 'O AcOm~,. ~3 ~"
OAc H ~ ~
/ \ HO -OAc O / \ O
TPAP
NaOCI
O
Q
AcO~ ~ ~".
HO H = '/
OAc / \
O
SUBSTITUTE SHEET (RULE 26) 1 9-dihydro-13-acetylbaccatin III
7-O-p-methoxybenzyl-9-dihydro-13-acetylbaccatin III
3 7-O-p-methoxybenzyl-13-acetylbaccatin III
4 7-O-p-methoxybenzylbaccati.n III
5 7-O-p-methoxybenzyl-(2'-ethoxyethyl) taxol 6 7-O-p-methoxybenzyl taxol 7 7-O-tosyl-9-dihydro-13-acet:ylbaccatin III
8 7-O-tosyl-13-acetylt>accatin III
9 7-O-tosylbaccatin III
l0 10 7-O-tosyl-( 2'-ethoxyethyl) taxol 11 7-O-tosyl taxol 12 10-deacetyl-7-O-p-methoxybenzylbaccatin III or 7-O-p-methoxybenryl-10-deacetylbaccatin III
13 10-deacetylbaccatin III
is I 5 Baccatin III
16 7-O-benzyl-9-dihydro-13-aceaylbaccatin III
17 7-O-benzyl-13-acetylbaccatin III
18 taxol or paclitaxel SUBSTITUTE SHEET (RULE 26) MATERIAL
All the reagents were obtained from Aldrich Chemicals, USA.
s Preparation of taaol Step 1(a): 7-O-p-methoxybenzyl-9-dihydro-13-acetylbaccatin III ( 2 ) 20 mg 9-dihydro-13-acetylbaccatin III ( 1 ) and 100 mg n-tetrabutylammonium iodide were dissolved in 3 mL of dichloromethane (CH2C12) in a 25 mL round bottom flask. 23 mg to of sodium hydride (NaH) was added and the mixture was stirred at room temperature for five minutes. 0. I mL of p-methoxybenzyl chloride was added dropwise over 5 minutes, and the temperature was raised to 45°C. 'The mixture was stirred for 24 hours, following which 30 mL of distilled water was added to stop the reaction. The product was extracted with dichloromethane, and purified by preparative thin layer chromatography (TLC) to yield 17 mg 15 7-O-p-methoxybenzyl-9-dihydro-I3-acetylbaccatin III, compound 2, as identified by NMR
spectroscopy.
'H-NMR (200 MHz, CDCI3), S: 8.10 (d,Ar-H-2,H-6), 7.60 (t, Ar-H-4), 7.50 (t, Ar-H-3, H-5), 7.21 (d, 2Ar-H), 6.90 (d, 2Ar-:(-i), 6.30 (d, H-10), 6.17 (t, H-13), 5.80 (d,H-2), 4.92 (d,H-2o S), 4.75 (dd, H-7), 4.50 (d, H-9), 4.31 (d,H-20a), 4.29 (d,H-20b), 4.15 (s, -OCHZ), 3.80 (s, OCH3), 3.01 (s, H-3), 2.59 (m,H-6), 2.26 (s, CH3C=O), 2.18 (s, CH3C=O), 2.10 (H-14a), 2.02 (s, CH3C=O), 1.97 (s, CH3), 1.85 (H-14b), i.77 (s, CH3), 1.75 (s, CH3), 1.26 (S, CH3) ppm.
Step 1(b): 7-O-methoxybenzyl-13-acetylbaccatin III ( 3 ) mg of the product of step 1 (a), compound 2, was added to 10.8 mg of 4-methylmorpholine N-oxide (NMO) in a 25 mL round bottom flask, and the mixture was dissolved in 3 mL of dichloromethane. 4d molecular sieve was added to the mixture which s was stirred for 5 minutes. 3.5 mg o~f tetra-n-propylammonium perruthenate (TPAP) was added, and the mixture wa;~ stirred for about 6 hours at room temperature, following which the temperature was raised to 40 °C'.. The mixture was maintained at that temperature overnight until the reaction was completed. Once the reaction was completed, the mixture was poured into a short silica gel column. The column was eluted with 50 mL of chloroform n> (CHCi3} to give a chloroform fraction which was concentrated to dryness.
The residue was purified by preparative TL(~ to yield 2 mg white needles which were identified as 7-O-methoxybenzyl-13-acetylbaccatin III, compound 3, by NMR spectroscopy.
'H-NMR (400 MHz, CDC'.13), b: 8.10 (d, Ar-H-2, H-6), 7.60 (t, Ar-H-4), 7.49 (t, Ar-H-3, H-S), 7.22 (s, 4Ar-H), 6.2f, (s, H-10), 6.18 (t, H-13), 5.65 (d, H-2), 5.60 (dd, H-7), 5.27 (s, OCH3), 4.95 (d, H-5), 4.33 (d, H-2l)a), 4.17 (d, H-20b), 3.95 (s, -OCHZ), 3.81 (d, H-3), 2.60 (m, H-6), 2.35 (s, CH;C=O), 2.22 (~dd, H-14a), 2.20 (s, CH3C=O), 2.15 (s, CHI), 2.05 (s, CH3C=O), 2.01 (H-14b), 1.96 (s, CH3), 1.24 (s, CH3), 1.18 (s, CH;) ppm.
2o Step 1(c): 7-O-p-methoxybenzylbaccatin III ( 4 ) SO mg of the produ~~t of step 1(b), compound 3, was dissolved in 5 mL of tetrahydrofuran at -44°C, <md 5 mole equivalent of methyllithium were added dropwise to remove the C-13 acetyl group. Upon completion of the deacetylation reaction, the mixture was partitioned between 50 mL of a mixture of saturated ammonium chloride buffer and SUBSTITUTE SHEET (RULE 26) dichloromethane ( 1:1 ). The organic layer was concentrated and purified by flash column chromatography on silica gel, eluting with a mixture of dichloromethane and methanol (97:3) to yield 22 mg of 7-O-p-methoxybenzylbaccatin III as white solid.
Step 1(d): 7-O-p-methoxybenzyl-(2'-ethoxyethyl) taxol ( S ) mg of the product of step 1 (c) (4) was combined with 6 mole equivalents of (2R, 2S)-N-benzoyl-O-(1-ethoxyethyl)-3-phenylisoserine or 5 mole equivalent of(3R, 4S)-3-(1-ethoxyethoxy)-4-(phenyl)-N-benzoyl-2-azetidinone and 3 mole equivalents of lithium hexamethyldisilazide (LiHNU7S) in 5 mL of tetrahydrofizran at -78 °C
for about 20 minutes in to a 25 mL round bottom flask. The reaction was warmed to 0 °C for about 6 hours, or until the reaction was completed as confirmed by TLC analysis. Once the reaction was completed, the mixture was quenched with 30 mL of a pH 7 buffer and the product was extracted with dichloromethane, dried and purified by flash column chromatography on silica gel, eluting with dichloromethane and methanol (97:3 ) to yield 16 mg of 7-O-p-methoxybenzyl-(2'-15 ethoxyethyl) taxol.
Step 1(e): 7-O-p-methoxybenzyl taxol ( 6 ) 10 mg of the product of step 1 (d) was dissolved in ethanol at room temperature in a ~
mL round bottom flask. An excess of 1% hydrochloric acid was added, and the reaction 2o continued for about 4 hours. The reaction product was poured into a 25 mL
separation funnel and 50 mL of a mixture of pH 7 buffer and dichloromethane ( 1:1 ) was added. The organic layer was evaporated to dryness to obtain a residue.
SUBSTITUTE SHEET (RULE 26) WO 98/50378 PCTlCA98/00401 Step 1(f): taxol or paciitax:el ( I 8) mL of dichloromethane was added to the residue obtained in step 1(e), and 0.25 mL
of water was mixed thereto. In this case, the ratio of water to dichloromethane was 1:20.
1.0-1.5 mole equivalent of :?,3-dichl~oro-5,6-dicyanobenzoquinone (DDQ) was added to the s mixture and the temperature was maintained at room temperature or 5°C. Upon completion, 10 mL of saturated aqueous sodium hydrogen carbonate (NaHC03) was added to the reaction, and the mixture was extracted with 10 mL of dichloromethane.
The extract was washed with S mL of saturated aqueous sodium hydrogen carbonate and dried over sodium sulfate (Na2S04). The solvent was evaporated and the residue was purified on a silica to gel column to give 3.5 mg of taxol.
Preparation of taxol Step 2(a): 7-O-tosyl-9-dihvydro-13-acetylbaccatin III ( 7 ) 1.0 g of 9-dihydro-13-acetylbaccatin III (1) was placed in a 50 mL round bottom flask with 454 mg of p-toluenesulfonyl chloride and 589 mg of tetrabutylammonium iodide. The mixture was dissolved in 1 S mL of dichloromethane and stirred at room temperature for S
2o minutes. 57 mg of sodium hydride was added slowly to the mixture, and the mixture was stirred at room temperature for 2 hours, following which 100 mL of water was added. The mixture was extracted with 70 mL of dichloromethane. The organic layer was concentrated to dryness, and the residue ,vas purified by flash column chromatography on silica gel, eluting SUBSTITUTE SHEET (RULE 26) with a mixture of dichloromethane and methanol (97:3) to yield 1.1 g of 7-O-tosyl-9-dihydro-13-acetylbaccatin III.
Step 2(b): 7-O-tosyl-13-acetylbaccatin III ( 8 ) 400 mg of the product of step 2(a), compound 7, was placed in a 50 mL round s bottom flask and 126 mg of 4-methylmorpholine N-oxide was added to thereto.
The mixture was dissolved in 5 mL of acetonitrile (CH3CN) and 126 mg of 4 6 molecular sieve was added The mixture was stirred at room temperature for about 10 minutes, following which 18 mg of TPAP was added. The mixture was stirred for 5 hours at room temperature and poured through a short silica gel column, eluting with dichloromethane. The fraction was further 1o purif ed by flash column chromatography on silica gel, eluting with a mixture of ethyl acetoacetate (EtOAc) and hexane (7:3) to yield about 350 mg of white crystals which were identified as 7-O-tosyl-13-acetylbaccatin III, purity 98%.
'H-NMR (400 MHz, CDCI3), 8: 8.05 (dd, 2H, Ar-H), 7.74 (d, 2H, tosyl), 7.60 (ddd, Ar-15 Hd), 7.47 (dd, 2H, Ar-H), 7.30 (d, 2H, tosyl), 6.69 (s, H,o), 6.16 (t, H,3), 5.66 (dd, H2), 5.30 (dd, H~), 4.85 (dd, H-5), 4.30 (d, H-20a), 4.10 (d, H-20b), 3.00 (s, 3H, tosyl), 3.92 (d, H-3), 2.60 (m, H-6a), 2.42 (s, -OCH3), 2.33 (s, -OCH3), 2.30 (dd, H-14a), 2.21 (s, -OCH;), 2.13 (s, CH3), 2.10 (dd, H-14b), 1.77 (s, CH3), 1.20 (s, CH3), 1.17 (s, CH3) ppm.
2o Step 2(c): 7-O-tosylbaccatin III ( 9 ) 100 mg of the product of step 2(b) (compound 8) was dissolved in 10 mL of tetrahydrofuran in a 25 mL round bottom flask. The flask was then placed into a container which was maintained at -43 °C. The solution was stirred and 0.4 mL of n-butyllithium in hexane was added dropwise for about 3 minutes. The mixture was stirred for about 30 SUBSTITUTE SHEET (RULE 26) minutes with the temperature raised to about 0 °C, and was further transferred into a 500 mL
separation funnel with 100 mL of water and extracted with 150 mL of dichloromethane. The product was purified by preparative TLC to yield about 62 mg of white crystals which were identified as 7-O-tosylbaccatin III.
Step 2(d): 7-O-tosyl-(2'-e;thoxyethyl) taxol ( 10 ) 100 mg of compound 8 was placed in a 25 mL round bottom flask , and 6 mole equivalents of (2R, 2S)-N-benzoyl-O-(1-ethoxyethyl)-3-phenylisoserine were dissolved in 5 mL of tetrahydrofuran at -'78 °C. 3 mole equivalents of LiHNIDS was added slowly. The to mixture was stirred at -78 "C for about 20 minutes, following which it was warmed to about 0 to 20 °C. The reaction progress was followed by TLC until completion.
Once completed, the reaction was quenched with pH 7 buffer and extracted with 40 mL of dichloromethane.
The organic layer was concentrated to dryness under vacuum, and the residue was purified by preparative TLC to yield about 85 rng of white crystals which were identified as 7-O-tosyl-(2'-ethaxyethyl) taxol.
Step 2(e): 7-O-tosyl taxol ( 11 ) 50 mg of the product of step 2(d), compound 10, was placed in a 25 mL round bottom flask and dissolved with 15 mL of ethanol at room temperature. An excess of 1 2o hydrochloric acid was added and the mixture was maintained at room temperature for about 5 hours. The reaction was then quenc;hed with 20 mL of water and 40 mL of dichloromethane.
The organic layer was evaporated to dryness under vacuum to yield 7-O-tosyl taxol.
Step 2(~: taxol or paclita~:el ( 18 ) SUBSTITUTE SHEET (RULE 26) The residue obtained in step 2(e) was dissolved in 10 mL of a 0.02 M solution of triethylamine in methanol and irradiated by UV light for about 6 hours or until the reaction is completed as shown by TLC. After irradiation, the triethylamine solvent was evaporated under vacuum. The residue was purified by flash column chromatography on silica gel, eluting with a mixture of clichloromethane and methanol (97:3) to yield about 25 mg of taxol which was characterized as natural taxol.
'H-NMR (400 MHz, CDI~l3), b: 8.12, 7.73, 7.6I, 7.51, 7.41, 7.38, 6.97, 6.27, 6.23, 5.78, 5.67, 4.94, 4.79, 4.40, 4.3 3, 4.19, 3.79, 3.54, 2.51, 2.46, 2.38, 2.36, 2.28, 2.24, 1.89, 1.89, l0 1.79, 1.68, 1.24, 1.14 pprr~.
Preparation of 10-deacetylbaccatin III
IS
Step 3(a): 7-O-p-methox~benzyl-10-deacetylbaccatin III ( 12 ) 70 mg of the prodG.ct of step 1 (c), compound 4, was placed in a 25 mL round bottom flask with 5 mL of dichloromethane. 1.5 mole equivalent of sodium hydride was added followed by 3 mL of trieth;ylamine, and the mixture was magnetically stirred for 2 to 3 hours.
2o The reaction progress was monitored by TLC. When the deacetylation was completed, the solution was poured into 25 mL of water and extracted with 30 mL
dichloromethane. The organic layer was concentrated to dryness under vacuum. The residue was purified by flash column chromatography to yield 42 mg of 7-O-p-methoxybenzyl-10-deacetylbaccatin III as white solid.
SUBSTITUTE SHEET (RULE 26) Step 3(b): 10-deacetylbaccatin IIIf ( 13 ) 30 mg of compound 12, i.e. 7-O-p-methoxybenzyl-10-deacetylbaccatin III, was placed into a 25 mL round bottom flask with 5 mL of dichloromethane which contained a small amount of water, thc: ratio of water to dichloromethane being 1:20. 1.0 mole equivalent of 2,3- dichloro-5,6-dicyanobenzoquinone (DDQ) was added and the mixture was stirred at room temperature for about 3 hours. Once the reaction was completed, 15 mL of staturated sodium hydrogen carbonate was added and the mixture was extracted with 20 mL
of dichloromethane. The extract was dried over sodium sulfate. The dichloromethane solution 1o was evaporated and the residue was purified with a silica gel column to yield 16 mg of 10-deacetylbaccatin III.
Preparation of baccatin III
25 mg of compound 4 (7-O-p-methoxybenzylbaccatin III) or 9 (7-O-tosylbaccatin III) containing a small amount of water was placed in a 25 mL round bottom flask and 5 mL of dichloromethane was added. In this case, the ratio of water to dichloromethane was 1:18. 1.0 to 1.5 mole equivalent of I)DQ was added to the mixture which was being stirred at about room temperature or S °C. Upon completion of the reaction, 20 mL of saturated aqueous 2o sodium hydrogen carbonate was added, and the mixture was extracted with 30 mL
dichloromethane, and dried over sodium sulfate. The solvent was evaporated and the residue was purified by flash column chromatography, eluting with a muxture of dichloromethane and methanol (96:4) to yield 1',~ mg of baccatin III, compound 15., as white solid.
SUBSTITUTE SHEET (RULE 26) EXAMPLE S
Preparation of 7-O-benzyl-13-acetylbaccatin IEI intermediate Step 4(a): 7-O-benzyl-9-dihydro-13-acetylbaccatin III ( 16 ) mg of 9-dihydro-13-acetylbaccatin III, compound 1, was dissolved in 3 mL of tetrahydrofi,rran (THF), and 20 mg of n-tetrabutylammonium iodide was added in a 5 mL
round bottom flask. The mixture was stirred for 5 minutes and 12 mg of sodium hydride was added. I 70 mg of ben2yl bromide was added dropwise and the mixture was stirred at 40°C.
The stirring continued overnight. 40 mL of distilled water was added to stop the reaction.
The product was extracted with chloroform. The chloroform solution was evaporated and the residue was purified by preparative TLC to yield 8 mg of 7-O-benzyl-9-dihydro-13-acetylbaccatin III.
Step 4(b): 7-O-benzyl-13-acetylbaccatin III ( 17 ) t.s In a similar manner as in step I(b), compound 17 can be made. In this case, the reagent methylmorphine N-oxide (NMO) is replaced by sodium chloroxide (NaOCI).
Taxol, 10-deacetylbaccatin III and baccatin III can be obtained from 7-O-benryl-13-acetylbaccatin III in similar manners as shown in the previous examples.
Although embodiments of the invention have been described above, it is not limited thereto and it will be apparent to those skilled in the art that numerous modifications form part of the present invention insofar as they do not depart from the spirit, nature and scope of the claimed and described invention.
Claims (16)
EXCLUSIVE PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS
FOLLOWS:
1. A process for converting 9-dihydro-13-acetylbaccatin III into a taxane comprising the steps of:
protecting said 9-dihydro-13-acetylbaccatin III;
oxidizing said 9-dihydro-13-acetylbaccatin III to form an intermediate; and oxidizing the C-9 position of the 9-dihydro-13-acetylbaccatin III.
protecting said 9-dihydro-13-acetylbaccatin III;
oxidizing said 9-dihydro-13-acetylbaccatin III to form an intermediate; and oxidizing the C-9 position of the 9-dihydro-13-acetylbaccatin III.
2. The process as set forth in claim 1, wherein oxidizing is achieved by the addition of an oxidizing agent selected from the group consisting of tetra-n-propylammonium perruthenate, Collin's reagent and dimethylsulfoxide.
3. A process for preparing taxol and a derivative thereof comprising the steps of:
(a) protecting the C-7 hydroxy group of 9-dihydro-13-acetylbaccatin III with a protecting group to obtain a protected product;
(b) oxidizing the C-9 hydroxy group of the protected product; and (c) deacetylating said protected product to form a taxol and a derivative thereof.
(a) protecting the C-7 hydroxy group of 9-dihydro-13-acetylbaccatin III with a protecting group to obtain a protected product;
(b) oxidizing the C-9 hydroxy group of the protected product; and (c) deacetylating said protected product to form a taxol and a derivative thereof.
4. The process as set forth in claim 3, wherein said protecting group is selected from the group consisting of benzyl, substituted benzyl, benzylformate, substituted benzylformate, tosyl, substituted tosyl, dihydropyran, methoxymethyl, benzoyl and substituted benzoyl.
5. The process as set forth in claim 3, where oxidizing is achieved by the addition of an oxidizing reagent selected from the group consisting of tetra-n-propylammonium perruthenate, Collin's reagent and dimethylsulfoxide.
6. The process as set forth in claim 3, further comprising the step of deacetylating the C-13 position.
7. The process as set forth in claim 6, further comprising the step of deprotecting the C-7 position to obtain baccatin III.
8. The process as set forth in claim 6, further comprising the step of deacetylating the C-10 position.
9. The process as set forth in claim 8, further comprising the step of deprotecting the C-7 position to obtain 10-deacetylbaccatin III.
10. The process as set forth in claim 6, further comprising the steps of adding a side chain to the C-13 position and selectively deprotecting to obtain a desired product.
11. The process as set forth in claim 10, wherein the deprotection is done at the C-7 and 2' positions to obtain taxol.
12. The process as in claim 10, wherein said side chain is selected from the group consisting of (2R, 2S)-N-benzoyl-O-(1-ethoxyethyl)-3-phenylisoserine and (3R, 4S)-3-(1-ethoxyethoxy)-4-(phenyl)-N-benzoyl-2-azetidinone.
13. A compound having the formula ~
wherein R is selected from the group consisting of benzyl, substituted benzyl, tosyl, substituted tosyl, dihydropyran, methoxymethyl, benzoyl and substituted benzoyl.
wherein R is selected from the group consisting of benzyl, substituted benzyl, tosyl, substituted tosyl, dihydropyran, methoxymethyl, benzoyl and substituted benzoyl.
14. A compound as in claim 13, wherein the benzyl is benzylformate and the benzoyl is benzoylmethyl.
15. A compound having the formula:
wherein R is selected from the group consisting of benzyl, substituted benzyl, tosyl, substituted tosyl, dihydropyran, methoxymethyl, benzoyl and substituted benzoyl.
wherein R is selected from the group consisting of benzyl, substituted benzyl, tosyl, substituted tosyl, dihydropyran, methoxymethyl, benzoyl and substituted benzoyl.
16. A compound as in claim 15, wherein the benzyl is benzylformate and the benzoyl is benzoylmethyl.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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CA002307548A CA2307548C (en) | 1997-05-01 | 1998-05-01 | Process for converting 9-dihydro-13-acetylbaccatin iii into taxol and derivatives thereof |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA2,204,197 | 1997-05-01 | ||
CA002204197A CA2204197A1 (en) | 1997-05-01 | 1997-05-01 | Process for converting 9-dihydro-13-acetylbaccatin iii into taxol and derivatives thereof |
PCT/CA1998/000401 WO1998050378A1 (en) | 1997-05-01 | 1998-05-01 | Process for converting 9-dihydro-13-acetylbaccatin iii into taxol and derivatives thereof |
CA002307548A CA2307548C (en) | 1997-05-01 | 1998-05-01 | Process for converting 9-dihydro-13-acetylbaccatin iii into taxol and derivatives thereof |
Publications (2)
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CA2307548A1 CA2307548A1 (en) | 1998-11-12 |
CA2307548C true CA2307548C (en) | 2001-07-17 |
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CA002307548A Expired - Fee Related CA2307548C (en) | 1997-05-01 | 1998-05-01 | Process for converting 9-dihydro-13-acetylbaccatin iii into taxol and derivatives thereof |
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Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
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CA2538860A1 (en) * | 2006-03-08 | 2007-09-08 | Jian Liu | Conversion 9-dihydro-13-acetylbaccatin iii to 10-deacetylbaccatin iii |
WO2007143839A1 (en) * | 2006-06-12 | 2007-12-21 | 6570763 Canada Inc. | Semi-synthetic route for the preparation of paclitaxel, docetaxel and 10-deacetylbaccatin iii from 9-dihydro-13-acetylbaccatin iii |
US7847111B2 (en) | 2006-06-19 | 2010-12-07 | Canada Inc. | Semi-synthetic route for the preparation of paclitaxel, docetaxel, and 10-deacetylbaccatin III from 9-dihydro-13-acetylbaccatin III |
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1998
- 1998-05-01 CA CA002307548A patent/CA2307548C/en not_active Expired - Fee Related
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