CN1300289A - 新的三尖杉烷衍生物及其制备方法 - Google Patents
新的三尖杉烷衍生物及其制备方法 Download PDFInfo
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- CN1300289A CN1300289A CN99806044A CN99806044A CN1300289A CN 1300289 A CN1300289 A CN 1300289A CN 99806044 A CN99806044 A CN 99806044A CN 99806044 A CN99806044 A CN 99806044A CN 1300289 A CN1300289 A CN 1300289A
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- 238000000034 method Methods 0.000 title claims abstract description 177
- 230000008569 process Effects 0.000 title claims abstract 4
- 238000002360 preparation method Methods 0.000 title claims description 77
- DSRNKUZOWRFQFO-UHFFFAOYSA-N cephalotaxine Natural products COC1=CC23CCCN2CCc4cc5OCOc5cc4C3=C1O DSRNKUZOWRFQFO-UHFFFAOYSA-N 0.000 claims abstract description 124
- 150000001875 compounds Chemical class 0.000 claims abstract description 42
- 239000002243 precursor Substances 0.000 claims abstract description 24
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 227
- 239000000203 mixture Substances 0.000 claims description 194
- 239000002253 acid Substances 0.000 claims description 129
- HYFHYPWGAURHIV-UHFFFAOYSA-N homoharringtonine Natural products C1=C2CCN3CCCC43C=C(OC)C(OC(=O)C(O)(CCCC(C)(C)O)CC(=O)OC)C4C2=CC2=C1OCO2 HYFHYPWGAURHIV-UHFFFAOYSA-N 0.000 claims description 114
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 99
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 99
- WYURNTSHIVDZCO-UHFFFAOYSA-N tetrahydrofuran Substances C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 97
- 150000003839 salts Chemical class 0.000 claims description 88
- 239000002585 base Substances 0.000 claims description 83
- -1 heterocycle alkane Chemical class 0.000 claims description 80
- 229960002230 omacetaxine mepesuccinate Drugs 0.000 claims description 78
- HYFHYPWGAURHIV-JFIAXGOJSA-N omacetaxine mepesuccinate Chemical compound C1=C2CCN3CCC[C@]43C=C(OC)[C@@H](OC(=O)[C@@](O)(CCCC(C)(C)O)CC(=O)OC)[C@H]4C2=CC2=C1OCO2 HYFHYPWGAURHIV-JFIAXGOJSA-N 0.000 claims description 70
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- 238000006297 dehydration reaction Methods 0.000 claims description 53
- 229910052739 hydrogen Inorganic materials 0.000 claims description 41
- 239000001257 hydrogen Substances 0.000 claims description 41
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 38
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 38
- LRNKGNYRSLLFRU-KSZYUSJVSA-N 4'-demethyl homoharringtonine Chemical class C([C@@]12C=C([C@H]([C@H]2C2=C3)OC(=O)[C@@](O)(CCCC(C)(C)O)CC([O-])=O)OC)CC[NH+]1CCC2=CC1=C3OCO1 LRNKGNYRSLLFRU-KSZYUSJVSA-N 0.000 claims description 36
- 125000000217 alkyl group Chemical group 0.000 claims description 33
- LOUPRKONTZGTKE-WZBLMQSHSA-N Quinine Chemical compound C([C@H]([C@H](C1)C=C)C2)C[N@@]1[C@@H]2[C@H](O)C1=CC=NC2=CC=C(OC)C=C21 LOUPRKONTZGTKE-WZBLMQSHSA-N 0.000 claims description 31
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 28
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 27
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 25
- 239000000463 material Substances 0.000 claims description 25
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 claims description 25
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 25
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- LOUPRKONTZGTKE-UHFFFAOYSA-N cinchonine Natural products C1C(C(C2)C=C)CCN2C1C(O)C1=CC=NC2=CC=C(OC)C=C21 LOUPRKONTZGTKE-UHFFFAOYSA-N 0.000 claims description 20
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- 150000004703 alkoxides Chemical class 0.000 claims description 18
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 18
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- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 16
- 230000005526 G1 to G0 transition Effects 0.000 claims description 16
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims description 16
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 16
- 238000010168 coupling process Methods 0.000 claims description 16
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- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 claims description 11
- QOSSAOTZNIDXMA-UHFFFAOYSA-N Dicylcohexylcarbodiimide Chemical compound C1CCCCC1N=C=NC1CCCCC1 QOSSAOTZNIDXMA-UHFFFAOYSA-N 0.000 claims description 11
- 241000196324 Embryophyta Species 0.000 claims description 11
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- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 11
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- KWGRBVOPPLSCSI-UHFFFAOYSA-N d-ephedrine Natural products CNC(C)C(O)C1=CC=CC=C1 KWGRBVOPPLSCSI-UHFFFAOYSA-N 0.000 claims description 10
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- RZJRJXONCZWCBN-UHFFFAOYSA-N octadecane Chemical compound CCCCCCCCCCCCCCCCCC RZJRJXONCZWCBN-UHFFFAOYSA-N 0.000 claims description 10
- 238000007127 saponification reaction Methods 0.000 claims description 10
- KWGRBVOPPLSCSI-WPRPVWTQSA-N (-)-ephedrine Chemical compound CN[C@@H](C)[C@H](O)C1=CC=CC=C1 KWGRBVOPPLSCSI-WPRPVWTQSA-N 0.000 claims description 9
- 125000003342 alkenyl group Chemical group 0.000 claims description 9
- 125000000304 alkynyl group Chemical group 0.000 claims description 9
- 150000001718 carbodiimides Chemical class 0.000 claims description 9
- 239000003795 chemical substances by application Substances 0.000 claims description 9
- 125000000392 cycloalkenyl group Chemical group 0.000 claims description 9
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 9
- 229910052736 halogen Inorganic materials 0.000 claims description 9
- 125000004415 heterocyclylalkyl group Chemical group 0.000 claims description 9
- 238000007327 hydrogenolysis reaction Methods 0.000 claims description 9
- 238000000746 purification Methods 0.000 claims description 9
- KTGKQJVJRAXNGX-UHFFFAOYSA-N Anhydroharringtonine Natural products COC(=O)CC1(CCC(C)(C)O1)OC(=O)C2C3c4cc5OCOc5cc4CCN6CCCC36C=C2OC KTGKQJVJRAXNGX-UHFFFAOYSA-N 0.000 claims description 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 8
- 229910052799 carbon Inorganic materials 0.000 claims description 8
- 125000006239 protecting group Chemical group 0.000 claims description 8
- 125000001424 substituent group Chemical group 0.000 claims description 8
- RPOSUQSMDAYSCJ-UHFFFAOYSA-N Neoharringtonine Natural products C12C3=CC=4OCOC=4C=C3CCN3CCCC23C=C(OC)C1OC(=O)C(O)(CC(=O)OC)CC1=CC=CC=C1 RPOSUQSMDAYSCJ-UHFFFAOYSA-N 0.000 claims description 7
- 229910052728 basic metal Inorganic materials 0.000 claims description 7
- 150000003818 basic metals Chemical class 0.000 claims description 7
- 230000036961 partial effect Effects 0.000 claims description 7
- 238000000926 separation method Methods 0.000 claims description 7
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 6
- 238000005336 cracking Methods 0.000 claims description 6
- 125000004122 cyclic group Chemical group 0.000 claims description 6
- 150000002431 hydrogen Chemical class 0.000 claims description 6
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- 230000004913 activation Effects 0.000 claims description 5
- NWCHELUCVWSRRS-UHFFFAOYSA-N atrolactic acid Chemical compound OC(=O)C(O)(C)C1=CC=CC=C1 NWCHELUCVWSRRS-UHFFFAOYSA-N 0.000 claims description 5
- 238000001640 fractional crystallisation Methods 0.000 claims description 5
- 150000002500 ions Chemical class 0.000 claims description 5
- 229910052987 metal hydride Inorganic materials 0.000 claims description 5
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- 229940038384 octadecane Drugs 0.000 claims description 5
- 229960001404 quinidine Drugs 0.000 claims description 5
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 claims description 4
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 4
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 4
- 150000001263 acyl chlorides Chemical class 0.000 claims description 4
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- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical group CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims description 4
- 238000012544 monitoring process Methods 0.000 claims description 4
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical group OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
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- LMDZBCPBFSXMTL-UHFFFAOYSA-N 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide Chemical compound CCN=C=NCCCN(C)C LMDZBCPBFSXMTL-UHFFFAOYSA-N 0.000 claims description 3
- SNOFKGQEUYMNCE-UHFFFAOYSA-N 2,2,2-trifluoro-1-$l^{1}-oxidanylethanone Chemical compound [O]C(=O)C(F)(F)F SNOFKGQEUYMNCE-UHFFFAOYSA-N 0.000 claims description 3
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- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 14
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Images
Classifications
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- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
- C07D493/10—Spiro-condensed systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/12—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains three hetero rings
- C07D491/14—Ortho-condensed systems
- C07D491/147—Ortho-condensed systems the condensed system containing one ring with oxygen as ring hetero atom and two rings with nitrogen as ring hetero atom
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C57/00—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
- C07C57/02—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms with only carbon-to-carbon double bonds as unsaturation
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
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- C07C59/42—Unsaturated compounds containing hydroxy or O-metal groups
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
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- C07C59/42—Unsaturated compounds containing hydroxy or O-metal groups
- C07C59/48—Unsaturated compounds containing hydroxy or O-metal groups containing six-membered aromatic rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/66—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
- C07C69/73—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of unsaturated acids
- C07C69/732—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of unsaturated acids of unsaturated hydroxy carboxylic acids
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D203/00—Heterocyclic compounds containing three-membered rings with one nitrogen atom as the only ring hetero atom
- C07D203/04—Heterocyclic compounds containing three-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
- C07D203/06—Heterocyclic compounds containing three-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D203/08—Heterocyclic compounds containing three-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring nitrogen atom
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/08—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D263/16—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/48—Compounds containing oxirane rings with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms, e.g. ester or nitrile radicals
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- 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
- C07D305/02—Heterocyclic compounds containing four-membered rings having one oxygen atom as the only ring hetero atoms not condensed with other rings
- C07D305/04—Heterocyclic compounds containing four-membered rings having one oxygen atom as the only ring hetero atoms not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D305/08—Heterocyclic compounds containing four-membered rings having one oxygen atom as the only ring hetero atoms not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/04—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D307/10—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D307/16—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D309/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
- C07D309/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D309/08—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/10—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings
- C07D317/32—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D453/00—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids
- C07D453/02—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids containing not further condensed quinuclidine ring systems
- C07D453/04—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids containing not further condensed quinuclidine ring systems having a quinolyl-4, a substituted quinolyl-4 or a alkylenedioxy-quinolyl-4 radical linked through only one carbon atom, attached in position 2, e.g. quinine
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- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Tropical Medicine & Parasitology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Cephalosporin Compounds (AREA)
- Pyrane Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Epoxy Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
Description
Claims (87)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR98/03492 | 1998-03-20 | ||
FR9803492A FR2776292B1 (fr) | 1998-03-20 | 1998-03-20 | Cephalotaxanes porteurs de chaine laterale et leur procede de synthese |
Publications (2)
Publication Number | Publication Date |
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CN1300289A true CN1300289A (zh) | 2001-06-20 |
CN1220692C CN1220692C (zh) | 2005-09-28 |
Family
ID=9524328
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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CNB998060445A Expired - Lifetime CN1220692C (zh) | 1998-03-20 | 1999-03-17 | 三尖杉烷衍生物的制备方法 |
Country Status (19)
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US (5) | US6831180B1 (zh) |
EP (1) | EP1064285B1 (zh) |
JP (3) | JP4942871B2 (zh) |
KR (1) | KR20010042085A (zh) |
CN (1) | CN1220692C (zh) |
AT (1) | ATE289312T1 (zh) |
AU (1) | AU3270699A (zh) |
CA (1) | CA2324895A1 (zh) |
DE (1) | DE69923768T2 (zh) |
DK (1) | DK1064285T3 (zh) |
ES (1) | ES2237144T3 (zh) |
FR (1) | FR2776292B1 (zh) |
HU (1) | HUP0101375A3 (zh) |
IL (1) | IL138563A0 (zh) |
PL (1) | PL343032A1 (zh) |
PT (1) | PT1064285E (zh) |
TR (1) | TR200003613T2 (zh) |
WO (1) | WO1999048894A1 (zh) |
ZA (1) | ZA200005018B (zh) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN100396286C (zh) * | 2002-12-30 | 2008-06-25 | 北京大学第一医院 | 高三尖杉酯碱和三尖杉酯碱在制备抑制血管生成药物中的应用 |
CN102675327A (zh) * | 2012-03-01 | 2012-09-19 | 南开大学 | 三尖杉酯碱类生物碱及制备方法和应用 |
CN103635476A (zh) * | 2011-08-18 | 2014-03-12 | 杭州本生药业有限公司 | 高三尖杉酯碱的酰化衍生物、及其制备方法和应用 |
CN103687859A (zh) * | 2011-08-18 | 2014-03-26 | 杭州本生药业有限公司 | 高三尖杉酯碱的胺化衍生物、及其制备方法和应用 |
CN106866690A (zh) * | 2015-12-10 | 2017-06-20 | 南开大学 | 三尖杉酯类生物碱、其制备方法和用途 |
CN110577506A (zh) * | 2018-06-07 | 2019-12-17 | 中国科学院上海有机化学研究所 | (﹣)-三尖杉碱的酯类衍生物的合成方法及其中间体 |
Families Citing this family (20)
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FR2776292B1 (fr) * | 1998-03-20 | 2004-09-10 | Oncopharm | Cephalotaxanes porteurs de chaine laterale et leur procede de synthese |
AU7940500A (en) * | 2000-10-17 | 2002-04-29 | Oncopharm Corp | New cephalotaxanes, their method of preparation and their use in treatment of cancers, leukemias, parasites including thus resistant to usual chemotherapeutic agents and as reversal agents |
US7285546B2 (en) | 2000-10-17 | 2007-10-23 | Stragen Pharma S.A. | Cephalotaxanes, their method of preparation and their use in treatment of cancers, leukemias, parasites including those resistant to usual chemotherapeutic agents and as reversal agents |
EP1373275A2 (en) * | 2001-03-21 | 2004-01-02 | Oncopharm Corporation | Highly purified and crystalline form of harringtonine |
EP1534295A4 (en) * | 2002-07-17 | 2009-08-05 | Chemgenex Pharmaceuticals Inc | FORMULATIONS AND METHODS OF ADMINISTRATION OF CEPHALOTAXINS, INCLUDING HOMOHARRINGTONIN |
ITMI20051352A1 (it) * | 2005-07-15 | 2007-01-16 | Erregierre Spa | Processo di preparazi0ne di acido 2-metossicarbonilmetil-6,6-dimetil-2-tetraidropiran carbossilico |
EP2146690B1 (en) * | 2007-04-13 | 2018-03-21 | Teva Pharmaceuticals International GmbH | Oral cephalotaxine dosage forms |
US8466142B2 (en) * | 2008-03-03 | 2013-06-18 | Sloan-Kettering Institute For Cancer Research | Cephalotaxus esters, methods of synthesis, and uses thereof |
US20120022250A1 (en) * | 2009-03-11 | 2012-01-26 | Jean-Pierre Robin | Process for preparing cephalotaxine esters |
US20100240887A1 (en) * | 2009-03-23 | 2010-09-23 | Yaguang Liu | New methods of producing HHT |
US9428519B2 (en) | 2011-08-18 | 2016-08-30 | Hangzhou Bensheng Pharmaceutical Co., Ltd. | Acylated derivative of homoharringtonine, preparation method therefor, and application thereof |
EP2746286A4 (en) * | 2011-08-18 | 2015-01-07 | Hangzhou Bensheng Pharmaceutical Co Ltd | HOMOHARRINGTONIN AMINO DERIVATIVE, PREPARATION METHOD AND APPLICATION THEREOF |
CN102633806A (zh) * | 2012-04-05 | 2012-08-15 | 贵州博丰生物科技产业开发有限公司 | 一种三尖杉酯碱的提取分离方法 |
TN2016000269A1 (en) * | 2013-12-31 | 2017-10-06 | Thierry Bataille | Water soluble crystallin salts of certain harringtonines unambiguously protonated on their alkaloid nitrogen and their use as chemotherapeutic drugs. |
WO2015128463A1 (en) * | 2014-02-28 | 2015-09-03 | Jean-Pierre Robin | Water soluble salts of harringtonine and their pharmaceutical applications |
WO2015162217A2 (en) * | 2014-04-23 | 2015-10-29 | Jean-Pierre Robin | Crystalline salts of cephalotaxine and their use for its purification including enantiomers |
US10597401B2 (en) | 2015-05-08 | 2020-03-24 | Albany Molecular Research, Inc. | Methods and intermediates for the preparation of omacetaxine and cephalotaxine derivatives thereof |
EP3275875A1 (en) | 2016-07-28 | 2018-01-31 | INDENA S.p.A. | Dioxolanone intermediate useful in the synthesis of homoharringtonine |
EP3763715A1 (en) | 2019-07-11 | 2021-01-13 | Robin, Jean-Pierre | Harringtonines salts, in particular retinoates, their process of preparation and their uses in the treatment of leukemias, cancers, autoimmune, skin, alzheimer's and inflammatory bowel diseases and viral infections, combined with myelopoiesis stimulating agents |
CN114544849B (zh) * | 2022-02-22 | 2024-07-19 | 苏州正济医药研究有限公司 | 一种1h-1,2,4-三氮唑-1-甲脒单盐酸盐及杂质的检测方法 |
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-
1998
- 1998-03-20 FR FR9803492A patent/FR2776292B1/fr not_active Expired - Lifetime
-
1999
- 1999-03-16 US US09/270,006 patent/US6831180B1/en not_active Expired - Lifetime
- 1999-03-17 PT PT99942587T patent/PT1064285E/pt unknown
- 1999-03-17 WO PCT/IB1999/000491 patent/WO1999048894A1/en active IP Right Grant
- 1999-03-17 CA CA002324895A patent/CA2324895A1/en not_active Abandoned
- 1999-03-17 IL IL13856399A patent/IL138563A0/xx unknown
- 1999-03-17 TR TR2000/03613T patent/TR200003613T2/xx unknown
- 1999-03-17 ES ES99942587T patent/ES2237144T3/es not_active Expired - Lifetime
- 1999-03-17 DK DK99942587T patent/DK1064285T3/da active
- 1999-03-17 KR KR1020007010440A patent/KR20010042085A/ko not_active Application Discontinuation
- 1999-03-17 CN CNB998060445A patent/CN1220692C/zh not_active Expired - Lifetime
- 1999-03-17 AU AU32706/99A patent/AU3270699A/en not_active Abandoned
- 1999-03-17 EP EP99942587A patent/EP1064285B1/en not_active Expired - Lifetime
- 1999-03-17 HU HU0101375A patent/HUP0101375A3/hu unknown
- 1999-03-17 DE DE69923768T patent/DE69923768T2/de not_active Expired - Lifetime
- 1999-03-17 JP JP2000537877A patent/JP4942871B2/ja not_active Expired - Fee Related
- 1999-03-17 AT AT99942587T patent/ATE289312T1/de active
- 1999-03-17 PL PL99343032A patent/PL343032A1/xx unknown
-
2000
- 2000-09-20 ZA ZA200005018A patent/ZA200005018B/en unknown
-
2001
- 2001-03-27 US US09/817,176 patent/US6613900B2/en not_active Expired - Lifetime
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2004
- 2004-06-25 US US10/877,067 patent/US7169774B2/en not_active Expired - Lifetime
-
2006
- 2006-05-25 US US11/440,648 patent/US7842687B2/en not_active Ceased
-
2009
- 2009-03-16 JP JP2009063260A patent/JP5884005B2/ja not_active Expired - Fee Related
-
2012
- 2012-10-26 US US13/661,677 patent/USRE45128E1/en not_active Expired - Fee Related
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- 2015-03-19 JP JP2015056022A patent/JP6087381B2/ja not_active Expired - Lifetime
Cited By (11)
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CN100396286C (zh) * | 2002-12-30 | 2008-06-25 | 北京大学第一医院 | 高三尖杉酯碱和三尖杉酯碱在制备抑制血管生成药物中的应用 |
CN103635476A (zh) * | 2011-08-18 | 2014-03-12 | 杭州本生药业有限公司 | 高三尖杉酯碱的酰化衍生物、及其制备方法和应用 |
CN103687859A (zh) * | 2011-08-18 | 2014-03-26 | 杭州本生药业有限公司 | 高三尖杉酯碱的胺化衍生物、及其制备方法和应用 |
CN103635476B (zh) * | 2011-08-18 | 2016-03-09 | 杭州本生药业有限公司 | 高三尖杉酯碱的酰化衍生物、及其制备方法和应用 |
CN103687859B (zh) * | 2011-08-18 | 2016-08-17 | 杭州本生药业有限公司 | 高三尖杉酯碱的胺化衍生物、及其制备方法和应用 |
CN102675327A (zh) * | 2012-03-01 | 2012-09-19 | 南开大学 | 三尖杉酯碱类生物碱及制备方法和应用 |
CN102675327B (zh) * | 2012-03-01 | 2014-12-10 | 南开大学 | 三尖杉酯碱类似物及制备方法和应用 |
CN106866690A (zh) * | 2015-12-10 | 2017-06-20 | 南开大学 | 三尖杉酯类生物碱、其制备方法和用途 |
CN106866690B (zh) * | 2015-12-10 | 2019-10-11 | 南开大学 | 三尖杉酯类生物碱、其制备方法和用途 |
CN110577506A (zh) * | 2018-06-07 | 2019-12-17 | 中国科学院上海有机化学研究所 | (﹣)-三尖杉碱的酯类衍生物的合成方法及其中间体 |
CN110577506B (zh) * | 2018-06-07 | 2023-04-07 | 中国科学院上海有机化学研究所 | (﹣)-三尖杉碱的酯类衍生物的合成方法及其中间体 |
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Effective date of registration: 20100115 Address after: Vitoria Australia Patentee after: Chemical Gene Pharmaceutical Co.,Ltd. Address before: Geneva, Switzerland Patentee before: Stijen Pharmaceutical |
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Granted publication date: 20050928 |