CA1105936A - Method of preparation of 3-(3-carboxy-4- hydroxyphenyl)-4,5-dihydro-2-phenylbenz[e]indole and valuable intermediates ralated thereto - Google Patents
Method of preparation of 3-(3-carboxy-4- hydroxyphenyl)-4,5-dihydro-2-phenylbenz[e]indole and valuable intermediates ralated theretoInfo
- Publication number
- CA1105936A CA1105936A CA279,689A CA279689A CA1105936A CA 1105936 A CA1105936 A CA 1105936A CA 279689 A CA279689 A CA 279689A CA 1105936 A CA1105936 A CA 1105936A
- Authority
- CA
- Canada
- Prior art keywords
- dihydro
- compound
- phenacyl
- bromide
- phenylethyl
- 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
- 238000000034 method Methods 0.000 title claims abstract description 50
- HAWWPSYXSLJRBO-UHFFFAOYSA-N fendosal Chemical compound C1=C(O)C(C(=O)O)=CC(N2C(=CC=3C4=CC=CC=C4CCC=32)C=2C=CC=CC=2)=C1 HAWWPSYXSLJRBO-UHFFFAOYSA-N 0.000 title claims abstract description 12
- 238000002360 preparation method Methods 0.000 title claims abstract description 6
- 239000000543 intermediate Substances 0.000 title abstract description 7
- 150000001875 compounds Chemical class 0.000 claims abstract description 22
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 29
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 claims description 18
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical group OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 15
- 239000002904 solvent Substances 0.000 claims description 13
- 229960000583 acetic acid Drugs 0.000 claims description 11
- KBOPZPXVLCULAV-UHFFFAOYSA-N mesalamine Chemical compound NC1=CC=C(O)C(C(O)=O)=C1 KBOPZPXVLCULAV-UHFFFAOYSA-N 0.000 claims description 11
- 229960004963 mesalazine Drugs 0.000 claims description 11
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 6
- 238000006243 chemical reaction Methods 0.000 claims description 6
- 150000003839 salts Chemical class 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 238000009835 boiling Methods 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 239000012362 glacial acetic acid Substances 0.000 claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- SHLHKLFIKRKJRV-UHFFFAOYSA-M 1-phenyl-2-(2-pyrrolidin-1-ium-1-ylidene-3,4-dihydro-1h-naphthalen-1-yl)ethanone;bromide Chemical compound [Br-].C=1C=CC=CC=1C(=O)CC(C1=CC=CC=C1CC1)C1=[N+]1CCCC1 SHLHKLFIKRKJRV-UHFFFAOYSA-M 0.000 claims description 3
- WYJDRDMLKVLOFR-UHFFFAOYSA-N 2-[2-(dimethylamino)-3,4-dihydronaphthalen-1-yl]-1-phenylethanone;hydrobromide Chemical compound Br.C12=CC=CC=C2CCC(N(C)C)=C1CC(=O)C1=CC=CC=C1 WYJDRDMLKVLOFR-UHFFFAOYSA-N 0.000 claims description 3
- HMUQIUZPAYOZGT-UHFFFAOYSA-M dibutyl-(1-phenacyl-3,4-dihydro-1h-naphthalen-2-ylidene)azanium;bromide Chemical compound [Br-].CCCC[N+](CCCC)=C1CCC2=CC=CC=C2C1CC(=O)C1=CC=CC=C1 HMUQIUZPAYOZGT-UHFFFAOYSA-M 0.000 claims description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 3
- 125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims description 3
- 125000002112 pyrrolidino group Chemical group [*]N1C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims description 3
- 238000010992 reflux Methods 0.000 claims description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052794 bromium Inorganic materials 0.000 claims description 2
- 125000001246 bromo group Chemical group Br* 0.000 claims description 2
- 229910052801 chlorine Chemical group 0.000 claims description 2
- 239000000460 chlorine Chemical group 0.000 claims description 2
- GMDHZXTVMFIZNC-UHFFFAOYSA-M dimethyl-(1-phenacyl-3,4-dihydro-1h-naphthalen-2-ylidene)azanium;bromide Chemical compound [Br-].C[N+](C)=C1CCC2=CC=CC=C2C1CC(=O)C1=CC=CC=C1 GMDHZXTVMFIZNC-UHFFFAOYSA-M 0.000 claims description 2
- 150000001649 bromium compounds Chemical group 0.000 claims 2
- VXZZQJSYMFAJRL-UHFFFAOYSA-M 1-phenyl-2-(2-piperidin-1-ium-1-ylidene-3,4-dihydro-1h-naphthalen-1-yl)ethanone;bromide Chemical compound [Br-].C=1C=CC=CC=1C(=O)CC(C1=CC=CC=C1CC1)C1=[N+]1CCCCC1 VXZZQJSYMFAJRL-UHFFFAOYSA-M 0.000 claims 1
- UCGVRRXOEFAKFW-UHFFFAOYSA-N 2-[2-(dibutylamino)-3,4-dihydronaphthalen-1-yl]-1-phenylethanone;hydrobromide Chemical compound Br.C12=CC=CC=C2CCC(N(CCCC)CCCC)=C1CC(=O)C1=CC=CC=C1 UCGVRRXOEFAKFW-UHFFFAOYSA-N 0.000 claims 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical group [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims 1
- SXCMYIPMFYMQOU-UHFFFAOYSA-M dipentyl-(1-phenacyl-3,4-dihydro-1h-naphthalen-2-ylidene)azanium;bromide Chemical compound [Br-].CCCCC[N+](CCCCC)=C1CCC2=CC=CC=C2C1CC(=O)C1=CC=CC=C1 SXCMYIPMFYMQOU-UHFFFAOYSA-M 0.000 claims 1
- 230000000202 analgesic effect Effects 0.000 abstract description 2
- 230000003110 anti-inflammatory effect Effects 0.000 abstract description 2
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 18
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 13
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
- 239000011541 reaction mixture Substances 0.000 description 6
- 239000007787 solid Substances 0.000 description 5
- 239000000203 mixture Substances 0.000 description 4
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- LIGACIXOYTUXAW-UHFFFAOYSA-N phenacyl bromide Chemical compound BrCC(=O)C1=CC=CC=C1 LIGACIXOYTUXAW-UHFFFAOYSA-N 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- QUSLRVPVUZMBTO-UHFFFAOYSA-N n,n-dimethyl-3,4-dihydronaphthalen-2-amine Chemical compound C1=CC=C2CCC(N(C)C)=CC2=C1 QUSLRVPVUZMBTO-UHFFFAOYSA-N 0.000 description 2
- -1 naphtha-lene compound Chemical class 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 238000000967 suction filtration Methods 0.000 description 2
- KEIFWROAQVVDBN-UHFFFAOYSA-N 1,2-dihydronaphthalene Chemical compound C1=CC=C2C=CCCC2=C1 KEIFWROAQVVDBN-UHFFFAOYSA-N 0.000 description 1
- HFZZPWGYPHTLQU-UHFFFAOYSA-N 1-phenyl-3H-benzo[e]indole Chemical compound C=1NC2=CC=C3C=CC=CC3=C2C=1C1=CC=CC=C1 HFZZPWGYPHTLQU-UHFFFAOYSA-N 0.000 description 1
- JNUPLQLBLFNLMV-UHFFFAOYSA-N 2-phenyl-3h-benzo[e]indole Chemical compound N1C2=CC=C3C=CC=CC3=C2C=C1C1=CC=CC=C1 JNUPLQLBLFNLMV-UHFFFAOYSA-N 0.000 description 1
- NIVFNYHKXIXPMB-UHFFFAOYSA-N Br.C1=CCCC2=CC=CC=C12 Chemical compound Br.C1=CCCC2=CC=CC=C12 NIVFNYHKXIXPMB-UHFFFAOYSA-N 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 125000005610 enamide group Chemical group 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 description 1
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 239000002808 molecular sieve Substances 0.000 description 1
- ZUMAGUBZZXWNRS-UHFFFAOYSA-N n,n-dibutyl-3,4-dihydronaphthalen-2-amine Chemical compound C1=CC=C2CCC(N(CCCC)CCCC)=CC2=C1 ZUMAGUBZZXWNRS-UHFFFAOYSA-N 0.000 description 1
- ZFOQAJYJFVWBKU-UHFFFAOYSA-N n,n-dipentyl-3,4-dihydronaphthalen-2-amine Chemical compound C1=CC=C2CCC(N(CCCCC)CCCCC)=CC2=C1 ZFOQAJYJFVWBKU-UHFFFAOYSA-N 0.000 description 1
- 229940075566 naphthalene Drugs 0.000 description 1
- UFWIBTONFRDIAS-UHFFFAOYSA-N naphthalene-acid Natural products C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 1
- 230000000269 nucleophilic effect Effects 0.000 description 1
- ROFVJSWBDQUQGW-UHFFFAOYSA-N piperidin-1-ium;bromide Chemical compound Br.C1CCNCC1 ROFVJSWBDQUQGW-UHFFFAOYSA-N 0.000 description 1
- 150000003233 pyrroles Chemical class 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
- 239000012258 stirred mixture Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/10—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by doubly bound oxygen or sulphur atoms
- C07D295/112—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by doubly bound oxygen or sulphur atoms with the ring nitrogen atoms and the doubly bound oxygen or sulfur atoms separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/56—Ring systems containing three or more rings
- C07D209/58—[b]- or [c]-condensed
- C07D209/60—Naphtho [b] pyrroles; Hydrogenated naphtho [b] pyrroles
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (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)
- Pain & Pain Management (AREA)
- Public Health (AREA)
- Rheumatology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Indole Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Investigating Or Analysing Biological Materials (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA344,310A CA1092126A (en) | 1976-06-03 | 1980-01-24 | Method of preparation of 3-(3-carboxy-4- hydroxyphenyl)-4,5-dihydro-2-phenylbenz[e]indole and valuable intermediates related thereto |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/692,331 US4066659A (en) | 1976-06-03 | 1976-06-03 | Method of preparation of 3-(3-carboxy-4-hydroxyphenyl)-4,5-dihydro-2-phenylbenz (e) indole and valuable intermediates related thereto |
| US692,331 | 1991-04-26 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1105936A true CA1105936A (en) | 1981-07-28 |
Family
ID=24780138
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA279,689A Expired CA1105936A (en) | 1976-06-03 | 1977-06-02 | Method of preparation of 3-(3-carboxy-4- hydroxyphenyl)-4,5-dihydro-2-phenylbenz[e]indole and valuable intermediates ralated thereto |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US4066659A (en, 2012) |
| JP (1) | JPS5325556A (en, 2012) |
| AT (1) | AT353786B (en, 2012) |
| BE (1) | BE855406A (en, 2012) |
| CA (1) | CA1105936A (en, 2012) |
| CH (1) | CH629774A5 (en, 2012) |
| DE (1) | DE2724601A1 (en, 2012) |
| DK (1) | DK145296C (en, 2012) |
| ES (1) | ES459256A1 (en, 2012) |
| FI (1) | FI65059C (en, 2012) |
| HU (1) | HU176801B (en, 2012) |
| IT (1) | IT1076781B (en, 2012) |
| NL (1) | NL7705807A (en, 2012) |
| SE (1) | SE425391B (en, 2012) |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1356431A (en) * | 1971-06-03 | 1974-06-12 | Wyeth John & Brother Ltd | Substituted benz-g-indoles |
| US3931407A (en) * | 1973-03-01 | 1976-01-06 | American Hoechst Corporation | Method of treatment with and compositions containing condensed pyrroles bearing an N-phenyl substituent |
-
1976
- 1976-06-03 US US05/692,331 patent/US4066659A/en not_active Expired - Lifetime
-
1977
- 1977-05-26 NL NL7705807A patent/NL7705807A/xx not_active Application Discontinuation
- 1977-05-28 ES ES459256A patent/ES459256A1/es not_active Expired
- 1977-05-31 CH CH664677A patent/CH629774A5/de not_active IP Right Cessation
- 1977-06-01 IT IT24269/77A patent/IT1076781B/it active
- 1977-06-01 FI FI771747A patent/FI65059C/fi not_active IP Right Cessation
- 1977-06-01 DE DE19772724601 patent/DE2724601A1/de active Granted
- 1977-06-02 DK DK243677A patent/DK145296C/da active
- 1977-06-02 HU HU77HO1992A patent/HU176801B/hu not_active IP Right Cessation
- 1977-06-02 AT AT392877A patent/AT353786B/de not_active IP Right Cessation
- 1977-06-02 CA CA279,689A patent/CA1105936A/en not_active Expired
- 1977-06-03 SE SE7706526A patent/SE425391B/xx not_active IP Right Cessation
- 1977-06-03 BE BE178212A patent/BE855406A/xx not_active IP Right Cessation
- 1977-06-03 JP JP6568277A patent/JPS5325556A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| AT353786B (de) | 1979-12-10 |
| DE2724601C2 (en, 2012) | 1988-03-03 |
| DK243677A (da) | 1977-12-04 |
| HU176801B (en) | 1981-05-28 |
| FI771747A7 (en, 2012) | 1977-12-04 |
| DK145296B (da) | 1982-10-25 |
| BE855406A (fr) | 1977-12-05 |
| ATA392877A (de) | 1979-05-15 |
| FI65059B (fi) | 1983-11-30 |
| ES459256A1 (es) | 1978-03-01 |
| FI65059C (fi) | 1984-03-12 |
| CH629774A5 (de) | 1982-05-14 |
| DK145296C (da) | 1983-03-14 |
| DE2724601A1 (de) | 1977-12-22 |
| SE425391B (sv) | 1982-09-27 |
| US4066659A (en) | 1978-01-03 |
| NL7705807A (nl) | 1977-12-06 |
| SE7706526L (sv) | 1977-12-04 |
| IT1076781B (it) | 1985-04-27 |
| JPS5325556A (en) | 1978-03-09 |
| JPS6120546B2 (en, 2012) | 1986-05-22 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MKEX | Expiry |