LU82079A1 - Nouveau procede de synthese de la vindesine - Google Patents
Nouveau procede de synthese de la vindesine Download PDFInfo
- Publication number
- LU82079A1 LU82079A1 LU82079A LU82079A LU82079A1 LU 82079 A1 LU82079 A1 LU 82079A1 LU 82079 A LU82079 A LU 82079A LU 82079 A LU82079 A LU 82079A LU 82079 A1 LU82079 A1 LU 82079A1
- Authority
- LU
- Luxembourg
- Prior art keywords
- vindesin
- deacetylvlb
- vindesine
- reaction
- acid
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 12
- 230000015572 biosynthetic process Effects 0.000 title description 4
- 238000003786 synthesis reaction Methods 0.000 title description 3
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical group C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 claims description 22
- NDMPLJNOPCLANR-UHFFFAOYSA-N 3,4-dihydroxy-15-(4-hydroxy-18-methoxycarbonyl-5,18-seco-ibogamin-18-yl)-16-methoxy-1-methyl-6,7-didehydro-aspidospermidine-3-carboxylic acid methyl ester Natural products C1C(CC)(O)CC(CC2(C(=O)OC)C=3C(=CC4=C(C56C(C(C(O)C7(CC)C=CCN(C67)CC5)(O)C(=O)OC)N4C)C=3)OC)CN1CCC1=C2NC2=CC=CC=C12 NDMPLJNOPCLANR-UHFFFAOYSA-N 0.000 claims description 13
- 229960004355 vindesine Drugs 0.000 claims description 13
- UGGWPQSBPIFKDZ-KOTLKJBCSA-N vindesine Chemical compound C([C@@H](C[C@]1(C(=O)OC)C=2C(=CC3=C([C@]45[C@H]([C@@]([C@H](O)[C@]6(CC)C=CCN([C@H]56)CC4)(O)C(N)=O)N3C)C=2)OC)C[C@@](C2)(O)CC)N2CCC2=C1N=C1[C]2C=CC=C1 UGGWPQSBPIFKDZ-KOTLKJBCSA-N 0.000 claims description 13
- 239000002253 acid Substances 0.000 claims description 9
- JXLYSJRDGCGARV-CFWMRBGOSA-N vinblastine Chemical class C([C@H](C[C@]1(C(=O)OC)C=2C(=CC3=C([C@]45[C@H]([C@@]([C@H](OC(C)=O)[C@]6(CC)C=CCN([C@H]56)CC4)(O)C(=O)OC)N3C)C=2)OC)C[C@@](C2)(O)CC)N2CCC2=C1NC1=CC=CC=C21 JXLYSJRDGCGARV-CFWMRBGOSA-N 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 125000003118 aryl group Chemical group 0.000 claims description 6
- 238000002360 preparation method Methods 0.000 claims description 5
- WLLGXSLBOPFWQV-UHFFFAOYSA-N MGK 264 Chemical compound C1=CC2CC1C1C2C(=O)N(CC(CC)CCCC)C1=O WLLGXSLBOPFWQV-UHFFFAOYSA-N 0.000 claims description 3
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 18
- 239000011541 reaction mixture Substances 0.000 description 15
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 14
- 239000000243 solution Substances 0.000 description 14
- 238000006243 chemical reaction Methods 0.000 description 13
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 6
- 150000001540 azides Chemical class 0.000 description 6
- IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 4
- 239000006227 byproduct Substances 0.000 description 4
- 239000000284 extract Substances 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 230000009466 transformation Effects 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- JQJPBYFTQAANLE-UHFFFAOYSA-N Butyl nitrite Chemical compound CCCCON=O JQJPBYFTQAANLE-UHFFFAOYSA-N 0.000 description 3
- 239000007868 Raney catalyst Substances 0.000 description 3
- NPXOKRUENSOPAO-UHFFFAOYSA-N Raney nickel Chemical compound [Al].[Ni] NPXOKRUENSOPAO-UHFFFAOYSA-N 0.000 description 3
- 229910000564 Raney nickel Inorganic materials 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 229910021529 ammonia Inorganic materials 0.000 description 3
- 150000003857 carboxamides Chemical class 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 230000008020 evaporation Effects 0.000 description 3
- 208000032839 leukemia Diseases 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
- IOVCWXUNBOPUCH-UHFFFAOYSA-N Nitrous acid Chemical compound ON=O IOVCWXUNBOPUCH-UHFFFAOYSA-N 0.000 description 2
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 150000003797 alkaloid derivatives Chemical class 0.000 description 2
- 238000004587 chromatography analysis Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000001953 recrystallisation Methods 0.000 description 2
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- 238000004809 thin layer chromatography Methods 0.000 description 2
- 101150020850 velB gene Proteins 0.000 description 2
- 229960004528 vincristine Drugs 0.000 description 2
- OGWKCGZFUXNPDA-XQKSVPLYSA-N vincristine Chemical compound C([N@]1C[C@@H](C[C@]2(C(=O)OC)C=3C(=CC4=C([C@]56[C@H]([C@@]([C@H](OC(C)=O)[C@]7(CC)C=CCN([C@H]67)CC5)(O)C(=O)OC)N4C=O)C=3)OC)C[C@@](C1)(O)CC)CC1=C2NC2=CC=CC=C12 OGWKCGZFUXNPDA-XQKSVPLYSA-N 0.000 description 2
- OGWKCGZFUXNPDA-UHFFFAOYSA-N vincristine Natural products C1C(CC)(O)CC(CC2(C(=O)OC)C=3C(=CC4=C(C56C(C(C(OC(C)=O)C7(CC)C=CCN(C67)CC5)(O)C(=O)OC)N4C=O)C=3)OC)CN1CCC1=C2NC2=CC=CC=C12 OGWKCGZFUXNPDA-UHFFFAOYSA-N 0.000 description 2
- NWZSZGALRFJKBT-KNIFDHDWSA-N (2s)-2,6-diaminohexanoic acid;(2s)-2-hydroxybutanedioic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O.NCCCC[C@H](N)C(O)=O NWZSZGALRFJKBT-KNIFDHDWSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 1
- 235000014066 European mistletoe Nutrition 0.000 description 1
- LPGWZGMPDKDHEP-HLTPFJCJSA-N Leurosine Chemical compound C([C@]1([C@@H]2O1)CC)N(CCC=1C3=CC=CC=C3NC=11)C[C@H]2C[C@]1(C(=O)OC)C1=CC([C@]23[C@H]([C@@]([C@H](OC(C)=O)[C@]4(CC)C=CCN([C@H]34)CC2)(O)C(=O)OC)N2C)=C2C=C1OC LPGWZGMPDKDHEP-HLTPFJCJSA-N 0.000 description 1
- 206010058467 Lung neoplasm malignant Diseases 0.000 description 1
- 206010028980 Neoplasm Diseases 0.000 description 1
- 235000012300 Rhipsalis cassutha Nutrition 0.000 description 1
- 241000863480 Vinca Species 0.000 description 1
- 241000221012 Viscum Species 0.000 description 1
- 229960000583 acetic acid Drugs 0.000 description 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
- 238000005903 acid hydrolysis reaction Methods 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 229930013930 alkaloid Natural products 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 239000011260 aqueous acid Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 239000003637 basic solution Substances 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 201000011510 cancer Diseases 0.000 description 1
- AIXAANGOTKPUOY-UHFFFAOYSA-N carbachol Chemical group [Cl-].C[N+](C)(C)CCOC(N)=O AIXAANGOTKPUOY-UHFFFAOYSA-N 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000001066 destructive effect Effects 0.000 description 1
- 235000019441 ethanol Nutrition 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000012458 free base Substances 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- IKDUDTNKRLTJSI-UHFFFAOYSA-N hydrazine monohydrate Substances O.NN IKDUDTNKRLTJSI-UHFFFAOYSA-N 0.000 description 1
- 238000007327 hydrogenolysis reaction Methods 0.000 description 1
- OWFXIOWLTKNBAP-UHFFFAOYSA-N isoamyl nitrite Chemical compound CC(C)CCON=O OWFXIOWLTKNBAP-UHFFFAOYSA-N 0.000 description 1
- 238000004811 liquid chromatography Methods 0.000 description 1
- 201000005296 lung carcinoma Diseases 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 238000011017 operating method Methods 0.000 description 1
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 235000010288 sodium nitrite Nutrition 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- KGKWFGPHYYEERW-UHFFFAOYSA-N velbanamine Chemical group C1CC2(C(C3)C(O)=O)N(C(=O)OC)C4=CC=CC=C4C22C4C31CCCN4CC2 KGKWFGPHYYEERW-UHFFFAOYSA-N 0.000 description 1
- 229960003048 vinblastine Drugs 0.000 description 1
- CXBGOBGJHGGWIE-IYJDUVQVSA-N vindoline Chemical group CN([C@H]1[C@](O)([C@@H]2OC(C)=O)C(=O)OC)C3=CC(OC)=CC=C3[C@]11CCN3CC=C[C@]2(CC)[C@@H]13 CXBGOBGJHGGWIE-IYJDUVQVSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
- C07D519/04—Dimeric indole alkaloids, e.g. vincaleucoblastine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6561—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Saccharide Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/003,442 US4210584A (en) | 1979-01-15 | 1979-01-15 | Vindesine synthesis |
| US344279 | 1979-01-15 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| LU82079A1 true LU82079A1 (fr) | 1980-04-23 |
Family
ID=21705894
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| LU82079A LU82079A1 (fr) | 1979-01-15 | 1980-01-14 | Nouveau procede de synthese de la vindesine |
Country Status (34)
| Country | Link |
|---|---|
| US (1) | US4210584A (ko) |
| EP (1) | EP0014053B1 (ko) |
| JP (1) | JPS5598195A (ko) |
| KR (1) | KR830002840B1 (ko) |
| AR (1) | AR223694A1 (ko) |
| AT (1) | AT371127B (ko) |
| AU (1) | AU5452280A (ko) |
| BE (1) | BE881078A (ko) |
| BG (1) | BG33295A3 (ko) |
| CA (1) | CA1148945A (ko) |
| CH (1) | CH645383A5 (ko) |
| CS (1) | CS214691B2 (ko) |
| DD (1) | DD148779A5 (ko) |
| DE (1) | DE3065852D1 (ko) |
| DK (1) | DK148961C (ko) |
| ES (2) | ES8101611A1 (ko) |
| FI (1) | FI800071A (ko) |
| FR (1) | FR2446290A1 (ko) |
| GB (1) | GB2040934B (ko) |
| GR (1) | GR72464B (ko) |
| HU (1) | HU182083B (ko) |
| IE (1) | IE49376B1 (ko) |
| IL (1) | IL59119A (ko) |
| IT (1) | IT1140506B (ko) |
| LU (1) | LU82079A1 (ko) |
| MY (1) | MY8500570A (ko) |
| NZ (1) | NZ192574A (ko) |
| PH (1) | PH15343A (ko) |
| PL (1) | PL124350B1 (ko) |
| PT (1) | PT70681A (ko) |
| RO (1) | RO77532A (ko) |
| SU (1) | SU906381A3 (ko) |
| YU (1) | YU5680A (ko) |
| ZA (1) | ZA80157B (ko) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60112895A (ja) * | 1983-11-24 | 1985-06-19 | Nippon Oil & Fats Co Ltd | 金属圧延用潤滑油 |
| FR2651348B1 (ko) * | 1989-08-04 | 1993-01-22 | Adir | |
| TW258739B (ko) * | 1992-04-04 | 1995-10-01 | Hoechst Ag | |
| CA2388844A1 (en) * | 1999-11-12 | 2001-05-25 | Angiotech Pharmaceuticals, Inc. | Compositions and methods for treating disease utilizing a combination of radioactive therapy and cell-cycle inhibitors |
| JP2006516548A (ja) | 2002-12-30 | 2006-07-06 | アンジオテック インターナショナル アクツィエン ゲゼルシャフト | 迅速ゲル化ポリマー組成物からの薬物送達法 |
| CN106831827B (zh) * | 2016-12-31 | 2019-03-29 | 广州白云山汉方现代药业有限公司 | 一种长春地辛的分离纯化方法 |
| CN106831826B (zh) * | 2016-12-31 | 2018-07-06 | 广州白云山汉方现代药业有限公司 | 一种从长春花中制备长春地辛的方法 |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2756235A (en) * | 1954-08-27 | 1956-07-24 | Lilly Co Eli | Method of producing lysergic acid amide |
-
1979
- 1979-01-15 US US06/003,442 patent/US4210584A/en not_active Expired - Lifetime
-
1980
- 1980-01-10 FR FR8000466A patent/FR2446290A1/fr active Granted
- 1980-01-10 CS CS80235A patent/CS214691B2/cs unknown
- 1980-01-10 NZ NZ192574A patent/NZ192574A/xx unknown
- 1980-01-10 GR GR60929A patent/GR72464B/el unknown
- 1980-01-10 GB GB8000870A patent/GB2040934B/en not_active Expired
- 1980-01-10 YU YU00056/80A patent/YU5680A/xx unknown
- 1980-01-10 BE BE1/9677A patent/BE881078A/fr not_active IP Right Cessation
- 1980-01-10 FI FI800071A patent/FI800071A/fi not_active Application Discontinuation
- 1980-01-10 CA CA000343455A patent/CA1148945A/en not_active Expired
- 1980-01-10 PT PT70681A patent/PT70681A/pt unknown
- 1980-01-10 AU AU54522/80A patent/AU5452280A/en not_active Abandoned
- 1980-01-10 EP EP80300095A patent/EP0014053B1/en not_active Expired
- 1980-01-10 ZA ZA00800157A patent/ZA80157B/xx unknown
- 1980-01-10 DE DE8080300095T patent/DE3065852D1/de not_active Expired
- 1980-01-11 JP JP250480A patent/JPS5598195A/ja active Granted
- 1980-01-11 AT AT0014080A patent/AT371127B/de not_active IP Right Cessation
- 1980-01-11 HU HU8052A patent/HU182083B/hu not_active IP Right Cessation
- 1980-01-13 IL IL59119A patent/IL59119A/xx unknown
- 1980-01-14 IT IT19210/80A patent/IT1140506B/it active
- 1980-01-14 PH PH23506A patent/PH15343A/en unknown
- 1980-01-14 ES ES487682A patent/ES8101611A1/es not_active Expired
- 1980-01-14 IE IE60/80A patent/IE49376B1/en unknown
- 1980-01-14 BG BG8046233A patent/BG33295A3/xx unknown
- 1980-01-14 SU SU802872553A patent/SU906381A3/ru active
- 1980-01-14 CH CH28780A patent/CH645383A5/fr not_active IP Right Cessation
- 1980-01-14 PL PL1980221359A patent/PL124350B1/pl unknown
- 1980-01-14 AR AR279615A patent/AR223694A1/es active
- 1980-01-14 DK DK14780A patent/DK148961C/da not_active IP Right Cessation
- 1980-01-14 LU LU82079A patent/LU82079A1/fr unknown
- 1980-01-15 ES ES487726A patent/ES487726A0/es active Granted
- 1980-01-15 KR KR1019800000134A patent/KR830002840B1/ko active
- 1980-01-15 RO RO8099874A patent/RO77532A/ro unknown
- 1980-01-15 DD DD80218466A patent/DD148779A5/de unknown
-
1985
- 1985-12-30 MY MY570/85A patent/MY8500570A/xx unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| FR1449628A (fr) | Procédé de préparation d'indoles polynucléaires désacylés, notamment d'esters de la série de la désacétyl-vincaleucoblastine et de la désacétyl-vincristine | |
| EP0340064A1 (fr) | Benzodiazépines, leur procédé et intermédiaires de préparation et leurs applications en thérapeutique | |
| LU82079A1 (fr) | Nouveau procede de synthese de la vindesine | |
| CA1325423C (fr) | Procede de synthese de l'azido-3'desozy-3'-thymidine et analogues | |
| EP0318392B1 (fr) | Nouveaux dérivés N-(vinblastinoyl-23) d'acide amino-1 méthylphosphonique, leurs procédés de préparation et les compositions pharmaceutiques qui les contiennent | |
| EP0635002B1 (fr) | Nouveaux derives de perhydroisoindole, et leur preparation | |
| EP0188947B1 (fr) | Peptides réduits, inhibiteurs de la sécrétion gastrique, procédé d'obtention et compositions pharmaceutiques les contenant | |
| EP0044238B1 (fr) | Dérivés de céphalosporines sulfoxydes, procédé de préparation et compositions pharmaceutiques en contenant | |
| CH655727A5 (fr) | Derives n-(vinblastinoyl-23) d'acides amines et composition pharmaceutique les contenant. | |
| US2944064A (en) | Process for preparing 5-hydroxy-tryptamine through new intermediates | |
| BE1001159A4 (fr) | Nouveaux derives d'ergolene, compositions pharmaceutiques les contenant et procede pour leur preparation. | |
| EP0115713A1 (fr) | (Pipérazinyl-1)-2 pyrimidines, leurs sels, procédé pour leur préparation et compositions pharmaceutiques en contenant | |
| CH637125A5 (fr) | Procede de preparation du 3-amino-5-(t-butyl)isoxazole. | |
| FR2667065A1 (fr) | Procede pour preparer la 1-[(2s)-3-mercapto-2-methyl-1-oxopropyl]-l-proline. | |
| FR2511677A1 (fr) | Procede de preparation d'esters des acides alcoxyvincaminiques et alcoxyapovincaminiques | |
| RU2192253C1 (ru) | Способ получения дигидроэргокристина | |
| KR0177901B1 (ko) | 멜라토닌의 신규한 제조방법 | |
| CH625519A5 (ko) | ||
| BE849244A (fr) | Nouveaux procedes de preparations de la 3',4'-didesoxykanamycine b. | |
| FR2577554A1 (fr) | Forme cristalline de la 7-(dimethylaminomethylene)-amino-9a-methoxymitosane | |
| FR2579206A1 (fr) | Nouvelles 5-h pyrido (3', 4' : 4,5) (pyrrolo 3,2-c) pyridones, leur procede de preparation et leur application en tant qu'intermediaires de synthese | |
| CH636595A5 (fr) | Procede de preparation de derives de l'acide n-(phosphonoacetyl)-l-aspartique et derives nouveaux ainsi obtenus. | |
| JPS58164573A (ja) | １−（４−クロロベンゾイル）−５−メトキシ−２−メチル−３−インド−ルアセトキシ酢酸類の製法 | |
| BE860309A (fr) | Derives de 5-fluorouracile leur procede de preparation et leur application therapeutique | |
| BE552107A (ko) |