GB1409073A - 8-substituted dibenzobicyclo-3,2,1 octadienes - Google Patents
8-substituted dibenzobicyclo-3,2,1 octadienesInfo
- Publication number
- GB1409073A GB1409073A GB4974172A GB4974172A GB1409073A GB 1409073 A GB1409073 A GB 1409073A GB 4974172 A GB4974172 A GB 4974172A GB 4974172 A GB4974172 A GB 4974172A GB 1409073 A GB1409073 A GB 1409073A
- Authority
- GB
- United Kingdom
- Prior art keywords
- octadiene
- prepared
- dibenzobicyclo
- compound
- syn
- 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
- QTYUSOHYEPOHLV-UHFFFAOYSA-N octadiene group Chemical group C=CC=CCCCC QTYUSOHYEPOHLV-UHFFFAOYSA-N 0.000 title 1
- QTYUSOHYEPOHLV-FNORWQNLSA-N 1,3-Octadiene Chemical compound CCCC\C=C\C=C QTYUSOHYEPOHLV-FNORWQNLSA-N 0.000 abstract 10
- 150000001875 compounds Chemical class 0.000 abstract 7
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 abstract 6
- UORVGPXVDQYIDP-UHFFFAOYSA-N borane Chemical compound B UORVGPXVDQYIDP-UHFFFAOYSA-N 0.000 abstract 4
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 abstract 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 abstract 3
- -1 cyanomethyl Chemical group 0.000 abstract 3
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 abstract 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 abstract 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 abstract 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- 229910000085 borane Inorganic materials 0.000 abstract 2
- 230000000694 effects Effects 0.000 abstract 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 abstract 2
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 abstract 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 abstract 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 abstract 1
- 239000007818 Grignard reagent Substances 0.000 abstract 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 230000001430 anti-depressive effect Effects 0.000 abstract 1
- 239000000935 antidepressant agent Substances 0.000 abstract 1
- 229940005513 antidepressants Drugs 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 239000001569 carbon dioxide Substances 0.000 abstract 1
- 229910002092 carbon dioxide Inorganic materials 0.000 abstract 1
- 210000003169 central nervous system Anatomy 0.000 abstract 1
- 239000003937 drug carrier Substances 0.000 abstract 1
- 235000019253 formic acid Nutrition 0.000 abstract 1
- 150000002440 hydroxy compounds Chemical class 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 239000011777 magnesium Substances 0.000 abstract 1
- 229910052749 magnesium Inorganic materials 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- QARBMVPHQWIHKH-UHFFFAOYSA-N methanesulfonyl chloride Chemical compound CS(Cl)(=O)=O QARBMVPHQWIHKH-UHFFFAOYSA-N 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 238000007911 parenteral administration Methods 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- NNFCIKHAZHQZJG-UHFFFAOYSA-N potassium cyanide Chemical compound [K+].N#[C-] NNFCIKHAZHQZJG-UHFFFAOYSA-N 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract 1
- 150000003335 secondary amines Chemical group 0.000 abstract 1
- 239000007858 starting material Substances 0.000 abstract 1
- NYBWUHOMYZZKOR-UHFFFAOYSA-N tes-adt Chemical class C1=C2C(C#C[Si](CC)(CC)CC)=C(C=C3C(SC=C3)=C3)C3=C(C#C[Si](CC)(CC)CC)C2=CC2=C1SC=C2 NYBWUHOMYZZKOR-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C61/00—Compounds having carboxyl groups bound to carbon atoms of rings other than six-membered aromatic rings
- C07C61/16—Unsaturated compounds
- C07C61/39—Unsaturated compounds containing six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/12—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by halogen atoms or by nitro or nitroso groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US194056A US3860652A (en) | 1971-10-29 | 1971-10-29 | 8-Aminoalkyl substituted dibenzobicyclo {8 3.2.1{9 {0 octadienes |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1409073A true GB1409073A (en) | 1975-10-08 |
Family
ID=22716120
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB4974172A Expired GB1409073A (en) | 1971-10-29 | 1972-10-27 | 8-substituted dibenzobicyclo-3,2,1 octadienes |
| GB4095174A Expired GB1409075A (en) | 1971-10-29 | 1972-10-27 | 8-substituted dibenzobicyclo-3,2,1-octadienes |
| GB3443174A Expired GB1409074A (en) | 1971-10-29 | 1972-10-27 | 8-substituted dibenzobicyclo-3,2,1 octadienes |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB4095174A Expired GB1409075A (en) | 1971-10-29 | 1972-10-27 | 8-substituted dibenzobicyclo-3,2,1-octadienes |
| GB3443174A Expired GB1409074A (en) | 1971-10-29 | 1972-10-27 | 8-substituted dibenzobicyclo-3,2,1 octadienes |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US3860652A (enExample) |
| JP (1) | JPS5130066B2 (enExample) |
| AU (1) | AU451041B2 (enExample) |
| BE (1) | BE790673A (enExample) |
| CA (1) | CA1008853A (enExample) |
| CH (1) | CH579021A5 (enExample) |
| DE (1) | DE2252811A1 (enExample) |
| FR (1) | FR2158040B1 (enExample) |
| GB (3) | GB1409073A (enExample) |
| NL (1) | NL7214626A (enExample) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE794904A (fr) * | 1972-02-04 | 1973-08-02 | Roussel Uclaf | Nouveaux derives du dibenzocycloheptene et leur preparation |
| US3976774A (en) * | 1975-06-02 | 1976-08-24 | Riker Laboratories, Inc. | Antiemetic method |
| CA1087174A (en) * | 1976-12-08 | 1980-10-07 | Atsuyuki Kojima | Tetracyclic compounds and production thereof |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE665606A (enExample) * | 1964-06-19 | |||
| US3422104A (en) * | 1964-10-20 | 1969-01-14 | Geigy Chem Corp | 9,10-dihydro-11-amino-alkylene-9,10-ethanoanthracenes |
| US3452102A (en) * | 1966-08-17 | 1969-06-24 | Upjohn Co | 1,2-diphenyl-6-methoxy-1,2,3,4-tetrahydro-1,2-naphthalenediols |
-
0
- BE BE790673D patent/BE790673A/xx unknown
-
1971
- 1971-10-29 US US194056A patent/US3860652A/en not_active Expired - Lifetime
-
1972
- 1972-10-19 CA CA154,558A patent/CA1008853A/en not_active Expired
- 1972-10-27 NL NL7214626A patent/NL7214626A/xx not_active Application Discontinuation
- 1972-10-27 DE DE2252811A patent/DE2252811A1/de active Pending
- 1972-10-27 GB GB4974172A patent/GB1409073A/en not_active Expired
- 1972-10-27 GB GB4095174A patent/GB1409075A/en not_active Expired
- 1972-10-27 FR FR7238306A patent/FR2158040B1/fr not_active Expired
- 1972-10-27 AU AU48255/72A patent/AU451041B2/en not_active Expired
- 1972-10-27 GB GB3443174A patent/GB1409074A/en not_active Expired
- 1972-10-27 CH CH1575772A patent/CH579021A5/xx not_active IP Right Cessation
- 1972-10-28 JP JP47108399A patent/JPS5130066B2/ja not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| FR2158040B1 (enExample) | 1976-07-02 |
| NL7214626A (enExample) | 1973-05-02 |
| CA1008853A (en) | 1977-04-19 |
| GB1409074A (en) | 1975-10-08 |
| FR2158040A1 (enExample) | 1973-06-08 |
| BE790673A (fr) | 1973-04-27 |
| AU451041B2 (en) | 1974-07-25 |
| JPS5130066B2 (enExample) | 1976-08-30 |
| AU4825572A (en) | 1974-05-02 |
| GB1409075A (en) | 1975-10-08 |
| DE2252811A1 (de) | 1973-05-03 |
| CH579021A5 (enExample) | 1976-08-31 |
| US3860652A (en) | 1975-01-14 |
| JPS4852757A (enExample) | 1973-07-24 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| PCNP | Patent ceased through non-payment of renewal fee |