IE61911B1 - Indenofuran derivatives - Google Patents
Indenofuran derivativesInfo
- Publication number
- IE61911B1 IE61911B1 IE331488A IE331488A IE61911B1 IE 61911 B1 IE61911 B1 IE 61911B1 IE 331488 A IE331488 A IE 331488A IE 331488 A IE331488 A IE 331488A IE 61911 B1 IE61911 B1 IE 61911B1
- Authority
- IE
- Ireland
- Prior art keywords
- furan
- dione
- perhydroindeno
- indenofuran
- methoxybenzyl
- Prior art date
Links
- AYQFTEQCBBWCNZ-UHFFFAOYSA-N 2H-indeno[2,1-b]furan Chemical class C1=CC=C2C3=CCOC3=CC2=C1 AYQFTEQCBBWCNZ-UHFFFAOYSA-N 0.000 title claims abstract description 7
- 150000001875 compounds Chemical class 0.000 claims abstract description 14
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 3
- 238000002360 preparation method Methods 0.000 claims abstract description 3
- IAODRFIZLKITMK-UHFFFAOYSA-N furan-2,3-dione Chemical compound O=C1OC=CC1=O IAODRFIZLKITMK-UHFFFAOYSA-N 0.000 claims description 15
- 238000000034 method Methods 0.000 claims description 13
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 8
- 241001465754 Metazoa Species 0.000 claims description 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- 239000008194 pharmaceutical composition Substances 0.000 claims description 4
- 239000003085 diluting agent Substances 0.000 claims description 3
- 229910000104 sodium hydride Inorganic materials 0.000 claims description 3
- 238000002560 therapeutic procedure Methods 0.000 claims description 3
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 125000006487 butyl benzyl group Chemical group 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- 239000012312 sodium hydride Substances 0.000 claims description 2
- -1 2a-Benzyl-perhyd ro indeno [7,7a, 1-bc ] furan-2,3 -d Chemical compound 0.000 claims 1
- 241000575946 Ione Species 0.000 claims 1
- LTXREWYXXSTFRX-QGZVFWFLSA-N Linagliptin Chemical compound N=1C=2N(C)C(=O)N(CC=3N=C4C=CC=CC4=C(C)N=3)C(=O)C=2N(CC#CC)C=1N1CCC[C@@H](N)C1 LTXREWYXXSTFRX-QGZVFWFLSA-N 0.000 claims 1
- 239000000203 mixture Substances 0.000 abstract description 3
- 230000036783 anaphylactic response Effects 0.000 abstract description 2
- 208000003455 anaphylaxis Diseases 0.000 abstract description 2
- 230000001225 therapeutic effect Effects 0.000 abstract description 2
- 206010002198 Anaphylactic reaction Diseases 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
- 238000000921 elemental analysis Methods 0.000 description 7
- 238000010253 intravenous injection Methods 0.000 description 7
- 239000000843 powder Substances 0.000 description 7
- 206010006482 Bronchospasm Diseases 0.000 description 6
- NTYJJOPFIAHURM-UHFFFAOYSA-N Histamine Chemical compound NCCC1=CN=CN1 NTYJJOPFIAHURM-UHFFFAOYSA-N 0.000 description 6
- 238000002347 injection Methods 0.000 description 6
- 239000007924 injection Substances 0.000 description 6
- 238000002844 melting Methods 0.000 description 6
- 230000008018 melting Effects 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- 230000007885 bronchoconstriction Effects 0.000 description 5
- 241000700159 Rattus Species 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
- 208000024780 Urticaria Diseases 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 229960001340 histamine Drugs 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- HVAUUPRFYPCOCA-AREMUKBSSA-N 2-O-acetyl-1-O-hexadecyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCCOC[C@@H](OC(C)=O)COP([O-])(=O)OCC[N+](C)(C)C HVAUUPRFYPCOCA-AREMUKBSSA-N 0.000 description 2
- ORWQBKPSGDRPPA-UHFFFAOYSA-N 3-[2-[ethyl(methyl)amino]ethyl]-1h-indol-4-ol Chemical compound C1=CC(O)=C2C(CCN(C)CC)=CNC2=C1 ORWQBKPSGDRPPA-UHFFFAOYSA-N 0.000 description 2
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 2
- 241000699670 Mus sp. Species 0.000 description 2
- 108010003541 Platelet Activating Factor Proteins 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 239000005557 antagonist Substances 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000003480 eluent Substances 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 210000002966 serum Anatomy 0.000 description 2
- 239000000741 silica gel Substances 0.000 description 2
- 229910002027 silica gel Inorganic materials 0.000 description 2
- 230000001988 toxicity Effects 0.000 description 2
- 231100000419 toxicity Toxicity 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- WAUNFWSVXRPCDQ-UHFFFAOYSA-N 1-(bromomethyl)-2-methoxybenzene Chemical compound COC1=CC=CC=C1CBr WAUNFWSVXRPCDQ-UHFFFAOYSA-N 0.000 description 1
- HFWRFTPVXDWGAH-UHFFFAOYSA-N 2-oxatricyclo[5.3.1.04,11]undeca-1(10),4(11),6,8-tetraene-3,5-dione Chemical compound O1C=2C3=C(C1=O)C(C=C3C=CC=2)=O HFWRFTPVXDWGAH-UHFFFAOYSA-N 0.000 description 1
- OUURWLIJKXKYIV-UHFFFAOYSA-N 4-[(2-methoxyphenyl)methyl]-2-oxatricyclo[5.3.1.04,11]undecane-3,5-dione Chemical compound COC1=CC=CC=C1CC1(C(O2)=O)C(=O)CC3C1C2CCC3 OUURWLIJKXKYIV-UHFFFAOYSA-N 0.000 description 1
- OHSFLXQUIKJWOW-UHFFFAOYSA-N 4-cyclohex-2-en-1-yl-3-oxobutanoic acid Chemical compound OC(=O)CC(=O)CC1CCCC=C1 OHSFLXQUIKJWOW-UHFFFAOYSA-N 0.000 description 1
- 208000033399 Anaphylactic responses Diseases 0.000 description 1
- 206010002199 Anaphylactic shock Diseases 0.000 description 1
- 208000009079 Bronchial Spasm Diseases 0.000 description 1
- 208000014181 Bronchial disease Diseases 0.000 description 1
- COXVTLYNGOIATD-HVMBLDELSA-N CC1=C(C=CC(=C1)C1=CC(C)=C(C=C1)\N=N\C1=C(O)C2=C(N)C(=CC(=C2C=C1)S(O)(=O)=O)S(O)(=O)=O)\N=N\C1=CC=C2C(=CC(=C(N)C2=C1O)S(O)(=O)=O)S(O)(=O)=O Chemical compound CC1=C(C=CC(=C1)C1=CC(C)=C(C=C1)\N=N\C1=C(O)C2=C(N)C(=CC(=C2C=C1)S(O)(=O)=O)S(O)(=O)=O)\N=N\C1=CC=C2C(=CC(=C(N)C2=C1O)S(O)(=O)=O)S(O)(=O)=O COXVTLYNGOIATD-HVMBLDELSA-N 0.000 description 1
- 241000700198 Cavia Species 0.000 description 1
- 241000700199 Cavia porcellus Species 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 239000001828 Gelatine Substances 0.000 description 1
- 241000283973 Oryctolagus cuniculus Species 0.000 description 1
- 108010058846 Ovalbumin Proteins 0.000 description 1
- 230000006978 adaptation Effects 0.000 description 1
- 230000002052 anaphylactic effect Effects 0.000 description 1
- 230000003042 antagnostic effect Effects 0.000 description 1
- 230000002804 anti-anaphylactic effect Effects 0.000 description 1
- 239000000427 antigen Substances 0.000 description 1
- 230000007503 antigenic stimulation Effects 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229960003699 evans blue Drugs 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 229930184727 ginkgolide Natural products 0.000 description 1
- 238000011597 hartley guinea pig Methods 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 239000000644 isotonic solution Substances 0.000 description 1
- 210000004731 jugular vein Anatomy 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 229940092253 ovalbumin Drugs 0.000 description 1
- 210000003899 penis Anatomy 0.000 description 1
- 201000003144 pneumothorax Diseases 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 230000000241 respiratory effect Effects 0.000 description 1
- 230000029058 respiratory gaseous exchange Effects 0.000 description 1
- 230000001235 sensitizing effect Effects 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 230000002269 spontaneous effect Effects 0.000 description 1
- 238000013222 sprague-dawley male rat Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 210000003437 trachea Anatomy 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 230000003442 weekly effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/93—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems condensed with a ring other than six-membered
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/365—Lactones
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/08—Bronchodilators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pulmonology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Immunology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Furan Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Indole Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB878725872A GB8725872D0 (en) | 1987-11-04 | 1987-11-04 | Indenofuran derivative |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IE883314L IE883314L (en) | 1989-05-04 |
| IE61911B1 true IE61911B1 (en) | 1994-11-30 |
Family
ID=10626450
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IE331488A IE61911B1 (en) | 1987-11-04 | 1988-11-03 | Indenofuran derivatives |
Country Status (29)
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8418424D0 (en) * | 1984-07-19 | 1984-08-22 | Scras | Inhibition of platelets aggregation |
-
1987
- 1987-11-04 GB GB878725872A patent/GB8725872D0/en active Pending
-
1988
- 1988-10-20 ZA ZA887867A patent/ZA887867B/xx unknown
- 1988-10-24 GB GB8824858A patent/GB2211840B/en not_active Expired - Lifetime
- 1988-10-26 IN IN929DE1988 patent/IN173904B/en unknown
- 1988-10-26 GR GR880100727A patent/GR1000151B/el not_active IP Right Cessation
- 1988-10-27 NZ NZ226739A patent/NZ226739A/en unknown
- 1988-10-28 BE BE8801245A patent/BE1002161A3/fr not_active IP Right Cessation
- 1988-10-28 NL NL8802651A patent/NL8802651A/nl active Search and Examination
- 1988-10-31 SE SE8803932A patent/SE469382B/sv not_active IP Right Cessation
- 1988-11-01 MA MA21664A patent/MA21422A1/fr unknown
- 1988-11-02 AT AT0269788A patent/AT400300B/de not_active IP Right Cessation
- 1988-11-02 FI FI885047A patent/FI87779C/fi not_active IP Right Cessation
- 1988-11-02 ES ES8803333A patent/ES2009363A6/es not_active Expired
- 1988-11-03 KR KR1019880014440A patent/KR960016540B1/ko not_active Expired - Fee Related
- 1988-11-03 AU AU24645/88A patent/AU614242B2/en not_active Ceased
- 1988-11-03 CH CH4082/88A patent/CH675421A5/fr not_active IP Right Cessation
- 1988-11-03 PT PT88925A patent/PT88925B/pt not_active IP Right Cessation
- 1988-11-03 DK DK612888A patent/DK165743C/da not_active IP Right Cessation
- 1988-11-03 CA CA000582168A patent/CA1307279C/en not_active Expired - Lifetime
- 1988-11-03 TN TNTNSN88117A patent/TNSN88117A1/fr unknown
- 1988-11-03 NO NO884901A patent/NO171210C/no not_active IP Right Cessation
- 1988-11-03 IE IE331488A patent/IE61911B1/en not_active IP Right Cessation
- 1988-11-04 DE DE3837523A patent/DE3837523A1/de active Granted
- 1988-11-04 OA OA59463A patent/OA09021A/xx unknown
- 1988-11-04 IT IT8822494A patent/IT1227457B/it active
- 1988-11-04 FR FR888814395A patent/FR2622583B1/fr not_active Expired - Fee Related
- 1988-11-04 JP JP63277523A patent/JPH01151568A/ja active Granted
- 1988-11-04 FR FR8814394A patent/FR2622447B1/fr not_active Expired - Fee Related
- 1988-11-04 US US07/267,438 patent/US4904693A/en not_active Expired - Lifetime
-
1992
- 1992-04-29 SG SG48492A patent/SG48492G/en unknown
- 1992-11-05 HK HK855/92A patent/HK85592A/xx not_active IP Right Cessation
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4006237A (en) | Tetrahydrocarbostyril derivatives for the prophylaxis of asthma, hayfever and rhinitis | |
| EP0429685B1 (en) | Oxoindole derivative | |
| US4233303A (en) | Xanthine derivatives | |
| DE3833008A1 (de) | Pyrrolocarbozol-derivate, verfahren zu deren herstellung und deren verwendung als arzneimittel | |
| JPH0313235B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
| US6239278B1 (en) | Intermediates in the synthesis of (±)-camptothecin and related compounds and synthesis thereof | |
| EP0008802B1 (en) | Ergoline derivatives, their preparation and therapeutic composition containing them | |
| DE3304019A1 (de) | 3-acyloxy-1-phenyl-2-aminocarbonylindol-verbindungen sowie verfahren zu ihrer herstellung und diese verbindungen enthaltende arzneimittel | |
| US3933827A (en) | 9-Acyloxy-5,11-dimethyl-6H-pyrido[4,3-B]carbazoles | |
| EP0018857A1 (fr) | Pyrimido et imidazo-pyrido-indole-diones, leur préparation et leur application en thérapeutique | |
| EP0700914A1 (en) | Camptothecin derivatives, preparations thereof and antitumor agents | |
| IE61911B1 (en) | Indenofuran derivatives | |
| DE69028355T2 (de) | 4,5-Dihydro-6H-imidazo[4,5,1-ij]chinolin-6-on-6-oxim-O-sulfonsäurederivate | |
| EP0402232A1 (fr) | Dérivés de pyridobenzoindole, leur préparation et les compositions qui les contiennent | |
| US4022778A (en) | 10-Aryl-1,2,3,4-tetrahydropyrazino(1,2-α)indole and derivatives thereof | |
| NZ200218A (en) | Imidazo(1,2-a)quinoline derivatives | |
| EP0016255B1 (en) | Isoxazole derivative, preparation thereof and pharmaceutical compositions containing the same | |
| US3917833A (en) | Amino-substituted benzocycloheptenones for inducing sleep | |
| US4361579A (en) | Organogermanium compounds | |
| US4469694A (en) | 2-(1-Piperazinyl)-2,4,6-cycloheptatrien-1-one derivatives | |
| CA1110249A (en) | Indolopyrones having antiallergic activity | |
| US3979468A (en) | 4'-Chloro-4-ethynylbiphenyl and method of preparing same | |
| US4798832A (en) | Pyrido[1,2-a]pyrimidine compounds, corresponding intermediates and use as SRS-A antagonists | |
| US6201129B1 (en) | Tricyclic derivatives and their use as anti-cancer agents | |
| DE2521920A1 (de) | Neue derivate von 1h-triazolo(4,5-c) pyridin-7-carbonsaeuren und -saeureestern |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM4A | Patent lapsed |