BE837073A - Nouveau procede de preparation de composes bis-indoliques - Google Patents
Nouveau procede de preparation de composes bis-indoliquesInfo
- Publication number
- BE837073A BE837073A BE163109A BE163109A BE837073A BE 837073 A BE837073 A BE 837073A BE 163109 A BE163109 A BE 163109A BE 163109 A BE163109 A BE 163109A BE 837073 A BE837073 A BE 837073A
- Authority
- BE
- Belgium
- Prior art keywords
- bis
- preparation
- new process
- indolic compounds
- indolic
- Prior art date
Links
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
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Indole Compounds (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR7443221A FR2296418B1 (hu) | 1974-12-30 | 1974-12-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
BE837073A true BE837073A (fr) | 1976-06-24 |
Family
ID=9146736
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BE163109A BE837073A (fr) | 1974-12-30 | 1975-12-24 | Nouveau procede de preparation de composes bis-indoliques |
Country Status (10)
Country | Link |
---|---|
US (2) | US4769453A (hu) |
JP (1) | JPS6056719B2 (hu) |
BE (1) | BE837073A (hu) |
CA (1) | CA1132544A (hu) |
CH (1) | CH606023A5 (hu) |
DE (1) | DE2558124A1 (hu) |
FR (1) | FR2296418B1 (hu) |
GB (1) | GB1536407A (hu) |
HU (1) | HU177154B (hu) |
NL (1) | NL184418C (hu) |
Families Citing this family (40)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2296418B1 (hu) * | 1974-12-30 | 1978-07-21 | Anvar | |
GR68940B (hu) * | 1977-01-19 | 1982-03-29 | Lilly Co Eli | |
US4115388A (en) * | 1977-03-30 | 1978-09-19 | Eli Lilly And Company | 3'-Oxygenated derivatives of 4'-deoxy VLB "A" and "B" and related 1-formyl compounds |
HU180924B (en) | 1977-05-20 | 1983-05-30 | Richter Gedeon Vegyeszet | Process for producing leurosine-type alkaloides |
US4191688A (en) | 1977-08-08 | 1980-03-04 | Eli Lilly And Company | Amides of leurosine, leuroformine, desacetylleurosine and desacetylleuroformine |
HU181874B (en) * | 1977-08-08 | 1983-11-28 | Lilly Co Eli | Process for preparing amides of deacetyl-leurosine and deacetyl-leuroformine |
US4195022A (en) | 1978-03-27 | 1980-03-25 | Eli Lilly And Company | 4-Desacetoxy-4α-hydroxyvinblastine and related compounds |
FR2443470A1 (fr) * | 1978-12-08 | 1980-07-04 | Anvar | Nouveau procede de synthese de la vinblastine et de la leurosidine |
US4841045A (en) * | 1985-03-12 | 1989-06-20 | University Of Vermont & State Agricultural College | Synthesis of vinblastine and vincristine type compounds |
US4897477A (en) * | 1985-03-12 | 1990-01-30 | University Of Vermont & State Agricultural College | Synthesis of vinblastine and vincristine type compounds |
JPS62502684A (ja) * | 1985-03-12 | 1987-10-15 | ザ・ユニバ−シテイ・オブ・バ−モント・アンド・ステイト・アグリカルチユラル・カレツジ | ビンブラスチン及びビンクリスチン型化合物の合成 |
US4778885A (en) * | 1986-09-18 | 1988-10-18 | Allelix Inc. | Production of alkaloid dimers using ferric ion |
CA1341261C (en) * | 1987-01-22 | 2001-06-26 | James P. Kutney | Process for the synthesis of 3',4'-anhydrovinblastine, vinblastine and vincristine |
US5047528A (en) * | 1987-01-22 | 1991-09-10 | University Of Bristish Columbia | Process of synthesis of vinblastine and vincristine |
AU1066888A (en) * | 1987-01-22 | 1988-08-04 | University Of British Columbia, The | Process for the synthesis of vinblastine and vincristine |
USRE37449E1 (en) | 1987-02-06 | 2001-11-13 | University Of British Columbia | Process of synthesis of 3′,4′-anhydrovinblastine, vinblastine and vincristine |
US5037977A (en) * | 1988-08-11 | 1991-08-06 | Mitsui Petrochemical Industries Ltd. | Method for production of dimeric alkaloids |
FR2707988B1 (fr) * | 1993-07-21 | 1995-10-13 | Pf Medicament | Nouveaux dérivés antimitotiques des alcaloïdes binaires du catharantus rosesus, leur procédé de préparation et les compositions pharmaceutiques les comprenant. |
IL123220A0 (en) * | 1995-08-08 | 1998-09-24 | Albany Medical College | Ibogamine congeners |
FR2779146B1 (fr) | 1998-06-02 | 2002-01-18 | Roowin | Nouveaux derives de vinca-alcaloides et procedes de preparation |
CA2385528C (en) | 1999-10-01 | 2013-12-10 | Immunogen, Inc. | Compositions and methods for treating cancer using immunoconjugates and chemotherapeutic agents |
US7235564B2 (en) * | 2003-12-04 | 2007-06-26 | Amr Technology, Inc. | Vinorelbine derivatives |
EP1689395B1 (en) * | 2003-12-04 | 2016-02-17 | Albany Molecular Research, Inc. | Vinca derivatives |
US8039453B2 (en) * | 2006-09-12 | 2011-10-18 | Albany Molecular Research, Inc. | Vinca derivatives |
US20080125451A1 (en) * | 2006-09-12 | 2008-05-29 | Amr Technology, Inc. | Vinorelbine derivatives |
US9394294B2 (en) | 2010-05-11 | 2016-07-19 | Demerx, Inc. | Methods and compositions for preparing and purifying noribogaine |
US8765737B1 (en) | 2010-05-11 | 2014-07-01 | Demerx, Inc. | Methods and compositions for preparing and purifying noribogaine |
US8637648B1 (en) | 2010-06-22 | 2014-01-28 | Demerx, Inc. | Compositions comprising noribogaine and an excipient to facilitate transport across the blood brain barrier |
US8802832B2 (en) | 2010-06-22 | 2014-08-12 | Demerx, Inc. | Compositions comprising noribogaine and an excipient to facilitate transport across the blood brain barrier |
MX2013000733A (es) | 2010-07-23 | 2013-05-30 | Demerx Inc | Composiciones de noribogaina. |
EP2481740B1 (en) * | 2011-01-26 | 2015-11-04 | DemeRx, Inc. | Methods and compositions for preparing noribogaine from voacangine |
US8742096B2 (en) | 2011-03-28 | 2014-06-03 | Demerx, Inc. | Methods and compositions for preparing noribogaine from voacangine |
US9617274B1 (en) | 2011-08-26 | 2017-04-11 | Demerx, Inc. | Synthetic noribogaine |
WO2013085922A1 (en) | 2011-12-09 | 2013-06-13 | Demerx, Inc. | Phosphate esters of noribogaine |
US20130178618A1 (en) | 2012-01-10 | 2013-07-11 | William Allen Boulanger | Novel pharmaceutical intermediates and methods for preparing the same |
WO2013112673A1 (en) | 2012-01-25 | 2013-08-01 | Demerx, Inc. | Synthetic voacangine |
US9045481B2 (en) | 2012-12-20 | 2015-06-02 | Demerx, Inc. | Substituted noribogaine |
US8940728B2 (en) | 2012-12-20 | 2015-01-27 | Demerx, Inc. | Substituted noribogaine |
US9783535B2 (en) | 2012-12-20 | 2017-10-10 | Demerx, Inc. | Substituted noribogaine |
US12116372B1 (en) | 2023-12-14 | 2024-10-15 | William Allen Boulanger | Process for preparing methyl 3-bromo-2-(2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-yl)propanoate |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CH77A (de) * | 1889-01-09 | Christian Herren | Wurzelschneidmaschine | |
FR2210393B1 (hu) * | 1972-12-19 | 1976-07-02 | Richter Gedeon Vegyeszet | |
HU165986B (hu) * | 1973-02-16 | 1974-12-28 | ||
FR2296418B1 (hu) * | 1974-12-30 | 1978-07-21 | Anvar | |
US4279817A (en) * | 1975-05-30 | 1981-07-21 | The United States Of America As Represented By The Department Of Health & Human Services | Method for producing dimer alkaloids |
US4029663A (en) * | 1975-07-10 | 1977-06-14 | Eli Lilly And Company | Dimeric anhydro-vinca derivatives |
US4143041A (en) * | 1977-01-19 | 1979-03-06 | Eli Lilly And Company | 4'-Deoxyvincristine and related compounds |
HU180924B (en) * | 1977-05-20 | 1983-05-30 | Richter Gedeon Vegyeszet | Process for producing leurosine-type alkaloides |
HU178084B (en) * | 1977-05-31 | 1982-03-28 | Richter Gedeon Vegyeszet | New process for the extraction of native vindoline,catharantine,3',4'-anhydrovinblastine,leurosine and,if desired,of other diinodle alkaloids from vinca rosea l.drogue |
-
1974
- 1974-12-30 FR FR7443221A patent/FR2296418B1/fr not_active Expired
-
1975
- 1975-12-23 DE DE19752558124 patent/DE2558124A1/de active Granted
- 1975-12-23 GB GB52570/75A patent/GB1536407A/en not_active Expired
- 1975-12-24 CH CH1680175A patent/CH606023A5/xx not_active IP Right Cessation
- 1975-12-24 BE BE163109A patent/BE837073A/xx not_active IP Right Cessation
- 1975-12-30 JP JP50159649A patent/JPS6056719B2/ja not_active Expired
- 1975-12-30 HU HU75AA840A patent/HU177154B/hu unknown
- 1975-12-30 NL NLAANVRAGE7515193,A patent/NL184418C/xx not_active IP Right Cessation
- 1975-12-31 CA CA243,046A patent/CA1132544A/en not_active Expired
-
1981
- 1981-06-18 US US06/275,050 patent/US4769453A/en not_active Expired - Lifetime
-
1986
- 1986-04-29 US US06/857,075 patent/US4737586A/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
NL184418C (nl) | 1989-07-17 |
JPS6056719B2 (ja) | 1985-12-11 |
FR2296418A1 (hu) | 1976-07-30 |
US4769453A (en) | 1988-09-06 |
DE2558124A1 (de) | 1976-07-01 |
JPS5188999A (en) | 1976-08-04 |
FR2296418B1 (hu) | 1978-07-21 |
HU177154B (en) | 1981-08-28 |
NL7515193A (nl) | 1976-07-02 |
US4737586A (en) | 1988-04-12 |
CH606023A5 (hu) | 1978-10-13 |
NL184418B (nl) | 1989-02-16 |
GB1536407A (en) | 1978-12-20 |
DE2558124C2 (hu) | 1991-04-18 |
CA1132544A (en) | 1982-09-28 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
RE20 | Patent expired |
Owner name: CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE CNRS Effective date: 19951224 |