ES8105317A1 - Un procedimiento para la preparacion de 10, 11-dihidro-5-h- dibenzo (a,d) ciclohepten -5,10-iminas - Google Patents
Un procedimiento para la preparacion de 10, 11-dihidro-5-h- dibenzo (a,d) ciclohepten -5,10-iminasInfo
- Publication number
- ES8105317A1 ES8105317A1 ES492115A ES492115A ES8105317A1 ES 8105317 A1 ES8105317 A1 ES 8105317A1 ES 492115 A ES492115 A ES 492115A ES 492115 A ES492115 A ES 492115A ES 8105317 A1 ES8105317 A1 ES 8105317A1
- Authority
- ES
- Spain
- Prior art keywords
- hours
- temperature
- time
- treatment
- dihydro
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/08—Bridged systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D451/00—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D451/00—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof
- C07D451/02—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof
-
- 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)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Luminescent Compositions (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
PROCEDIMIENTO DE OBTENCION DE 10,11-DIHIDRO-5-H-DIBENZENO{A,D}CICLOEPTEN-5,10-IMINAS. CONSTA DE LAS SIGUIENTES ETAPAS: 1. TRATAMIENTO DE UNA CETONA CON AMONIACO GASEOSO EN PRESENCIA DE TETRACLORURO DE TITANIO; LA TEMPERATURA DE REACCION OSCILA DE -10 A 50GC, EMPLEANDOSE DE 2 A 10 HORAS. 2. ACILACION DE LA IMINA LIBRE POR TRATAMIENTO DE (I) CON UN HALURO DE ACILO; EL TIEMPO DE REACCION ES DE 1 A 6 HORAS A UNA TEMPERATURA DE 0 A 50GC. 3. ADICION DEL COMPUESTO R ELEVADO A 2 H SOBRE EL DOBLE ENLACE IMINICO; LA TEMPERATURA ES DE 0G A 50GC DURANTE UN TIEMPO DE 0,5 A 4 HORAS. 4. ADICION DEL GRUPO ACILAMINO SOBRE EL DOBLE ENLACE CONJUGADO; LA TEMPERATURA ES DE 150 A 170GC, EL TIEMPO, DE 24 A 48 HORAS. 5. DESACILACION DEL GRUPO IMINO POR HIDROLISIS ACIDA O BASICA A UNA TEMPERATURA DE 25 A 150GC DURANTE UN TIEMPO DE 2 A 48 HORAS. LOS COMPUESTOS QUE SE OBTIENEN TIENEN DE FORMULA GENERAL II. AGENTES ANSIOLITICOS: TRATAMIENTO DE TRASTORNOS EXTRAPIRAMIDALES (ENFERMEDAD DE PARKINSON). *FORMULA*
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US06/045,494 US4232158A (en) | 1979-06-04 | 1979-06-04 | 10,11-Dihydro-5H-dibenzo[a,d]cyclohepten-5,10-imines |
Publications (2)
Publication Number | Publication Date |
---|---|
ES8105317A1 true ES8105317A1 (es) | 1981-05-16 |
ES492115A0 ES492115A0 (es) | 1981-05-16 |
Family
ID=21938211
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES492115A Granted ES492115A0 (es) | 1979-06-04 | 1980-06-03 | Un procedimiento para la preparacion de 10, 11-dihidro-5-h- dibenzo (a,d) ciclohepten -5,10-iminas |
Country Status (16)
Country | Link |
---|---|
US (1) | US4232158A (es) |
EP (1) | EP0019866B1 (es) |
KR (1) | KR840000077B1 (es) |
AR (1) | AR230282A1 (es) |
AT (1) | ATE6651T1 (es) |
CA (1) | CA1142516A (es) |
DK (1) | DK238280A (es) |
ES (1) | ES492115A0 (es) |
FI (1) | FI64939C (es) |
GR (1) | GR68427B (es) |
HU (1) | HU181709B (es) |
NO (1) | NO152786C (es) |
PL (1) | PL124031B1 (es) |
PT (1) | PT71305B (es) |
SU (1) | SU1025328A3 (es) |
YU (1) | YU147180A (es) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4477668A (en) * | 1982-04-07 | 1984-10-16 | Merck & Co., Inc. | Process for 5-methyl-10,11-dihydro-5H-dibenzo[a,d]-cyclohepten-5,10-imine |
NZ221626A (en) * | 1986-09-08 | 1989-11-28 | Merck & Co Inc | Dibenzo(a,d cycloheptene derivatives and pharmaceutical compositions |
US6017910A (en) * | 1989-04-14 | 2000-01-25 | State Of Oregon, Acting By And Through The Oregon State Board Of Higher Education Acting For And On Behalf Of The Oregon Health Sciences University And The University Of Oregon | PCP receptor ligands and the use thereof |
US5011834A (en) * | 1989-04-14 | 1991-04-30 | State Of Oregon, Acting By And Through The Oregon State Board Of Higher Education, Acting For And On Behalf Of The Oregon Health Sciences University And The University Of Oregon | PCP receptor ligands and the use thereof |
US5196415A (en) * | 1989-05-09 | 1993-03-23 | The United States Of America As Represented By The Department Of Health And Human Services | 5-aminocarbonyl-5H-dibenzo[a.d]cyclohepten-5,10-imines for treatment of epilepsy and ***e addiction |
US5831095A (en) * | 1995-09-26 | 1998-11-03 | Research Triangle Institute | Synthesis of 5-aminocarbonyl-5H-dibenzo a,d!cyclohepten-5,10-imine |
WO2005030720A1 (ja) * | 2003-09-25 | 2005-04-07 | Shionogi & Co., Ltd. | Nmda受容体拮抗作用を有するピペリジン誘導体 |
MX2008002234A (es) * | 2005-08-19 | 2008-03-27 | Elan Pharm Inc | Inhibidores de sulfonamida n-biciclico puenteados de gamma secretasa. |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3542787A (en) * | 1968-06-25 | 1970-11-24 | American Home Prod | 10,11-dihydro-5,10-(iminomethano)-5h-dibenzo(a,d)cyclohepten-13-imine |
US3597433A (en) * | 1968-08-19 | 1971-08-03 | Ayerst Mckenna & Harrison | 10,11 - dihydro - 5,10 - (iminomethano)-5h-dibenzo(a,d)cycloheptene and derivatives thereof |
US3641038A (en) * | 1968-10-29 | 1972-02-08 | Ayerst Mckenna & Harrison | 10,11-dihydro - 10 5 - (iminomethano)-5h-dibenzo( ad)cyclohepten - 10 01acid addition salts the reofand process |
NL7007464A (es) * | 1969-05-30 | 1970-12-02 | ||
US3716541A (en) * | 1970-07-23 | 1973-02-13 | Ayerst Mckenna & Harrison | Substituted derivatives of 10,11-dihydro-5,10-(iminomethano)-5h-dibenzo, cycloheptenes and preparation thereof |
BE794904A (fr) * | 1972-02-04 | 1973-08-02 | Roussel Uclaf | Nouveaux derives du dibenzocycloheptene et leur preparation |
US4052508A (en) * | 1974-08-19 | 1977-10-04 | Merck & Co., Inc. | Heterocyclic dihydroanthracen imines |
US4064139A (en) * | 1975-04-07 | 1977-12-20 | Merck & Co., Inc. | Substituted 9,10-dihydroanthracen-9,10-imines |
US4123546A (en) * | 1977-07-01 | 1978-10-31 | E. I. Du Pont De Nemours And Company | Antidepressant compounds |
NL191488C (nl) * | 1977-09-19 | 1995-08-04 | Merck & Co Inc | Op de 5-plaats gesubstitueerde 10,11-dihydro-5H-dibenzo£a,d|cyclohepteen-5,10-iminen en farmaceutische preparaten die deze bevatten. |
-
1979
- 1979-06-04 US US06/045,494 patent/US4232158A/en not_active Expired - Lifetime
-
1980
- 1980-05-20 FI FI801622A patent/FI64939C/fi not_active IP Right Cessation
- 1980-05-21 AR AR281138A patent/AR230282A1/es active
- 1980-05-22 GR GR62025A patent/GR68427B/el unknown
- 1980-05-23 EP EP80102868A patent/EP0019866B1/en not_active Expired
- 1980-05-23 AT AT80102868T patent/ATE6651T1/de not_active IP Right Cessation
- 1980-05-23 SU SU802925102A patent/SU1025328A3/ru active
- 1980-05-25 PT PT71305A patent/PT71305B/pt unknown
- 1980-05-26 KR KR1019800002072A patent/KR840000077B1/ko active
- 1980-06-02 CA CA000353229A patent/CA1142516A/en not_active Expired
- 1980-06-02 PL PL1980224699A patent/PL124031B1/pl unknown
- 1980-06-03 NO NO801659A patent/NO152786C/no unknown
- 1980-06-03 DK DK238280A patent/DK238280A/da not_active Application Discontinuation
- 1980-06-03 YU YU01471/80A patent/YU147180A/xx unknown
- 1980-06-03 HU HU801391A patent/HU181709B/hu unknown
- 1980-06-03 ES ES492115A patent/ES492115A0/es active Granted
Also Published As
Publication number | Publication date |
---|---|
FI64939C (fi) | 1984-02-10 |
AR230282A1 (es) | 1984-03-01 |
NO152786B (no) | 1985-08-12 |
NO152786C (no) | 1985-11-20 |
EP0019866A1 (en) | 1980-12-10 |
FI64939B (fi) | 1983-10-31 |
PT71305B (en) | 1981-09-21 |
DK238280A (da) | 1980-12-05 |
CA1142516A (en) | 1983-03-08 |
SU1025328A3 (ru) | 1983-06-23 |
YU147180A (en) | 1983-04-30 |
FI801622A (fi) | 1980-12-05 |
PT71305A (en) | 1980-06-01 |
ATE6651T1 (de) | 1984-03-15 |
ES492115A0 (es) | 1981-05-16 |
KR840000077B1 (ko) | 1984-02-08 |
HU181709B (en) | 1983-11-28 |
KR830002764A (ko) | 1983-05-30 |
PL224699A1 (es) | 1981-05-08 |
GR68427B (es) | 1981-12-30 |
EP0019866B1 (en) | 1984-03-14 |
NO801659L (no) | 1980-12-05 |
US4232158A (en) | 1980-11-04 |
PL124031B1 (en) | 1982-12-31 |
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