FI66360C - Analogifoerfarande foer framstaellning av saosom avstoetning motstaoende aemnen anvaendbara 2-fenyl-1h-perimidiner - Google Patents
Analogifoerfarande foer framstaellning av saosom avstoetning motstaoende aemnen anvaendbara 2-fenyl-1h-perimidiner Download PDFInfo
- Publication number
- FI66360C FI66360C FI783808A FI783808A FI66360C FI 66360 C FI66360 C FI 66360C FI 783808 A FI783808 A FI 783808A FI 783808 A FI783808 A FI 783808A FI 66360 C FI66360 C FI 66360C
- Authority
- FI
- Finland
- Prior art keywords
- perimidine
- preparation
- formula
- diaminonaphthalene
- reacted
- Prior art date
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- KXLJLJJNISGKPN-UHFFFAOYSA-N 2-phenyl-1h-perimidine Chemical compound C1=CC=CC=C1C(N1)=NC2=CC=CC3=CC=CC1=C23 KXLJLJJNISGKPN-UHFFFAOYSA-N 0.000 title claims description 9
- 238000010276 construction Methods 0.000 title 1
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- 238000000034 method Methods 0.000 claims description 13
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- YFOOEYJGMMJJLS-UHFFFAOYSA-N 1,8-diaminonaphthalene Chemical compound C1=CC(N)=C2C(N)=CC=CC2=C1 YFOOEYJGMMJJLS-UHFFFAOYSA-N 0.000 claims description 7
- 239000000460 chlorine Chemical group 0.000 claims description 5
- -1 p-trifluoromethylphenyl Chemical group 0.000 claims description 5
- AAQTWLBJPNLKHT-UHFFFAOYSA-N 1H-perimidine Chemical compound N1C=NC2=CC=CC3=CC=CC1=C32 AAQTWLBJPNLKHT-UHFFFAOYSA-N 0.000 claims description 3
- WKZXFTXRGGTUAF-UHFFFAOYSA-N 4-(1,1,2,2,2-pentafluoroethoxy)benzoyl chloride Chemical compound FC(F)(F)C(F)(F)OC1=CC=C(C(Cl)=O)C=C1 WKZXFTXRGGTUAF-UHFFFAOYSA-N 0.000 claims description 3
- UKJWAZZCGZQPTA-UHFFFAOYSA-N 4-(trifluoromethoxy)benzoyl fluoride Chemical compound FC(=O)C1=CC=C(OC(F)(F)F)C=C1 UKJWAZZCGZQPTA-UHFFFAOYSA-N 0.000 claims description 3
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- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 3
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- OXZYBOLWRXENKT-UHFFFAOYSA-N 4-(trifluoromethyl)benzoyl chloride Chemical compound FC(F)(F)C1=CC=C(C(Cl)=O)C=C1 OXZYBOLWRXENKT-UHFFFAOYSA-N 0.000 claims description 2
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- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 238000012754 cardiac puncture Methods 0.000 description 1
- 235000013351 cheese Nutrition 0.000 description 1
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- 230000005494 condensation Effects 0.000 description 1
- 210000002808 connective tissue Anatomy 0.000 description 1
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- 239000012895 dilution Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000003304 gavage Methods 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 208000024908 graft versus host disease Diseases 0.000 description 1
- 230000035931 haemagglutination Effects 0.000 description 1
- 208000006454 hepatitis Diseases 0.000 description 1
- 231100000283 hepatitis Toxicity 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 230000028993 immune response Effects 0.000 description 1
- 230000016784 immunoglobulin production Effects 0.000 description 1
- 229940073062 imuran Drugs 0.000 description 1
- 230000002779 inactivation Effects 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 210000003141 lower extremity Anatomy 0.000 description 1
- 206010025135 lupus erythematosus Diseases 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- MABCMWISTJAYLR-UHFFFAOYSA-N naphthalene-1,8-diamine 2-[3-(trifluoromethyl)phenyl]-1H-perimidine hydrochloride Chemical compound NC1=CC=CC2=CC=CC(=C12)N.Cl.FC(C=1C=C(C=CC1)C=1NC=2C=CC=C3C=CC=C(N1)C23)(F)F MABCMWISTJAYLR-UHFFFAOYSA-N 0.000 description 1
- IRGAPAYCZKPVFF-UHFFFAOYSA-N naphthalene-1,8-diamine;2-[4-(trifluoromethylsulfanyl)phenyl]-1h-perimidine;hydrochloride Chemical compound Cl.C1=CC(N)=C2C(N)=CC=CC2=C1.C1=CC(SC(F)(F)F)=CC=C1C(N1)=NC2=CC=CC3=CC=CC1=C23 IRGAPAYCZKPVFF-UHFFFAOYSA-N 0.000 description 1
- 239000012875 nonionic emulsifier Substances 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 239000008024 pharmaceutical diluent Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229940068918 polyethylene glycol 400 Drugs 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 206010039073 rheumatoid arthritis Diseases 0.000 description 1
- 201000005404 rubella Diseases 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 235000010356 sorbitol Nutrition 0.000 description 1
- 230000003393 splenic effect Effects 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000011421 subcutaneous treatment Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
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- 125000003944 tolyl group Chemical group 0.000 description 1
- 238000002054 transplantation Methods 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
-
- 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
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Immunology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Transplantation (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FI832540A FI66361C (fi) | 1977-12-19 | 1983-07-12 | Analogifoerfarande foer framstaellning av saosom avstoetning motstaoende aemnen anvaendbara 2,3-dihydro-2-fenyl-1h-perimidiner |
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US86173277A | 1977-12-19 | 1977-12-19 | |
| US86173277 | 1977-12-19 | ||
| US05/944,434 US4224326A (en) | 1978-09-21 | 1978-09-21 | Immunosuppressive agents |
| US94443478 | 1978-09-21 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| FI783808A7 FI783808A7 (fi) | 1979-06-20 |
| FI66360B FI66360B (fi) | 1984-06-29 |
| FI66360C true FI66360C (fi) | 1984-10-10 |
Family
ID=27127642
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI783808A FI66360C (fi) | 1977-12-19 | 1978-12-12 | Analogifoerfarande foer framstaellning av saosom avstoetning motstaoende aemnen anvaendbara 2-fenyl-1h-perimidiner |
Country Status (29)
| Country | Link |
|---|---|
| EP (1) | EP0002906B1 (cs) |
| JP (1) | JPS5488279A (cs) |
| AR (1) | AR218350A1 (cs) |
| AT (1) | AT367045B (cs) |
| AU (1) | AU522740B2 (cs) |
| CA (1) | CA1079281A (cs) |
| CH (1) | CH636863A5 (cs) |
| CS (1) | CS207699B2 (cs) |
| DD (1) | DD139849A5 (cs) |
| DE (1) | DE2861747D1 (cs) |
| DK (1) | DK144699C (cs) |
| ES (1) | ES476153A1 (cs) |
| FI (1) | FI66360C (cs) |
| FR (1) | FR2411834A1 (cs) |
| GB (1) | GB2010246B (cs) |
| GR (1) | GR70262B (cs) |
| HU (1) | HU178528B (cs) |
| IE (1) | IE47619B1 (cs) |
| IL (1) | IL56211A (cs) |
| IT (1) | IT1101673B (cs) |
| LU (1) | LU80662A1 (cs) |
| MX (1) | MX5563E (cs) |
| NZ (1) | NZ189150A (cs) |
| PL (1) | PL113258B1 (cs) |
| PT (1) | PT68903A (cs) |
| RO (1) | RO72250A (cs) |
| SU (1) | SU984409A3 (cs) |
| YU (1) | YU297678A (cs) |
| ZA (1) | ZA787054B (cs) |
-
1978
- 1978-12-12 AR AR274760A patent/AR218350A1/es active
- 1978-12-12 PT PT68903A patent/PT68903A/pt unknown
- 1978-12-12 FI FI783808A patent/FI66360C/fi not_active IP Right Cessation
- 1978-12-12 NZ NZ189150A patent/NZ189150A/xx unknown
- 1978-12-12 JP JP15407178A patent/JPS5488279A/ja active Pending
- 1978-12-12 AU AU42431/78A patent/AU522740B2/en not_active Expired
- 1978-12-13 FR FR7835084A patent/FR2411834A1/fr active Granted
- 1978-12-13 EP EP78300799A patent/EP0002906B1/en not_active Expired
- 1978-12-13 CA CA317,876A patent/CA1079281A/en not_active Expired
- 1978-12-13 GB GB7848213A patent/GB2010246B/en not_active Expired
- 1978-12-13 DE DE7878300799T patent/DE2861747D1/de not_active Expired
- 1978-12-14 IL IL56211A patent/IL56211A/xx unknown
- 1978-12-14 MX MX787596U patent/MX5563E/es unknown
- 1978-12-15 IT IT30926/78A patent/IT1101673B/it active
- 1978-12-15 LU LU80662A patent/LU80662A1/xx unknown
- 1978-12-18 DK DK567578A patent/DK144699C/da not_active IP Right Cessation
- 1978-12-18 SU SU782697059A patent/SU984409A3/ru active
- 1978-12-18 ZA ZA787054A patent/ZA787054B/xx unknown
- 1978-12-18 RO RO7895966A patent/RO72250A/ro unknown
- 1978-12-18 AT AT0904278A patent/AT367045B/de not_active IP Right Cessation
- 1978-12-18 YU YU02976/78A patent/YU297678A/xx unknown
- 1978-12-18 PL PL1978211890A patent/PL113258B1/pl unknown
- 1978-12-18 GR GR57920A patent/GR70262B/el unknown
- 1978-12-18 HU HU78EI827A patent/HU178528B/hu unknown
- 1978-12-18 IE IE2487/78A patent/IE47619B1/en unknown
- 1978-12-18 CH CH1284178A patent/CH636863A5/fr not_active IP Right Cessation
- 1978-12-19 CS CS788575A patent/CS207699B2/cs unknown
- 1978-12-19 DD DD78209925A patent/DD139849A5/de unknown
- 1978-12-19 ES ES476153A patent/ES476153A1/es not_active Expired
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| HF | Priority information amended | ||
| FD | Application lapsed | ||
| MM | Patent lapsed | ||
| MM | Patent lapsed |
Owner name: ELI LILLY AND COMPANY |