FI70578C - Analogifoerfarande foer framstaellning av terapeutiskt anvaendbar 1-(4-klorfenyl)-1-(2,4-diklorfenyl)-2-(1,2,4,-triazol-1-yl)-etan-1-ol och dess salter - Google Patents
Analogifoerfarande foer framstaellning av terapeutiskt anvaendbar 1-(4-klorfenyl)-1-(2,4-diklorfenyl)-2-(1,2,4,-triazol-1-yl)-etan-1-ol och dess salter Download PDFInfo
- Publication number
- FI70578C FI70578C FI810743A FI810743A FI70578C FI 70578 C FI70578 C FI 70578C FI 810743 A FI810743 A FI 810743A FI 810743 A FI810743 A FI 810743A FI 70578 C FI70578 C FI 70578C
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- FI
- Finland
- Prior art keywords
- therapeutic
- acid
- triazol
- dichlorophenyl
- chlorophenyl
- Prior art date
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- 230000002538 fungal effect Effects 0.000 description 1
- 244000000004 fungal plant pathogen Species 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000007903 gelatin capsule Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 229940074076 glycerol formal Drugs 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 description 1
- 229960000890 hydrocortisone Drugs 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 150000002460 imidazoles Chemical class 0.000 description 1
- 150000002466 imines Chemical class 0.000 description 1
- 239000003701 inert diluent Substances 0.000 description 1
- 238000001802 infusion Methods 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000006210 lotion Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 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
- 239000000155 melt Substances 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 239000002516 radical scavenger Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 1
- 229940081974 saccharin Drugs 0.000 description 1
- 235000019204 saccharin Nutrition 0.000 description 1
- 239000000901 saccharin and its Na,K and Ca salt Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000008159 sesame oil Substances 0.000 description 1
- 235000011803 sesame oil Nutrition 0.000 description 1
- 239000004208 shellac Substances 0.000 description 1
- ZLGIYFNHBLSMPS-ATJNOEHPSA-N shellac Chemical compound OCCCCCC(O)C(O)CCCCCCCC(O)=O.C1C23[C@H](C(O)=O)CCC2[C@](C)(CO)[C@@H]1C(C(O)=O)=C[C@@H]3O ZLGIYFNHBLSMPS-ATJNOEHPSA-N 0.000 description 1
- 229940113147 shellac Drugs 0.000 description 1
- 235000013874 shellac Nutrition 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 150000003509 tertiary alcohols Chemical class 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- BSYVTEYKTMYBMK-UHFFFAOYSA-N tetrahydrofurfuryl alcohol Chemical compound OCC1CCCO1 BSYVTEYKTMYBMK-UHFFFAOYSA-N 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 235000010215 titanium dioxide Nutrition 0.000 description 1
- 239000000196 tragacanth Substances 0.000 description 1
- 235000010487 tragacanth Nutrition 0.000 description 1
- 229940116362 tragacanth Drugs 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
- MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 description 1
- FGQOOHJZONJGDT-UHFFFAOYSA-N vanillin Natural products COC1=CC(O)=CC(C=O)=C1 FGQOOHJZONJGDT-UHFFFAOYSA-N 0.000 description 1
- 235000012141 vanillin Nutrition 0.000 description 1
- 235000019871 vegetable fat Nutrition 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/10—Antimycotics
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (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)
- Public Health (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Dermatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Photoreceptors In Electrophotography (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE3010093 | 1980-03-15 | ||
DE19803010093 DE3010093A1 (de) | 1980-03-15 | 1980-03-15 | 1,1-diphenyl-2-(1.2.4-triazol-1-yl)-aethan-1-ole, verfahren zu ihrer herstellung und diese enthaltende therapeutische mittel |
Publications (3)
Publication Number | Publication Date |
---|---|
FI810743L FI810743L (fi) | 1981-09-16 |
FI70578B FI70578B (fi) | 1986-06-06 |
FI70578C true FI70578C (fi) | 1986-09-24 |
Family
ID=6097376
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FI810743A FI70578C (fi) | 1980-03-15 | 1981-03-10 | Analogifoerfarande foer framstaellning av terapeutiskt anvaendbar 1-(4-klorfenyl)-1-(2,4-diklorfenyl)-2-(1,2,4,-triazol-1-yl)-etan-1-ol och dess salter |
Country Status (20)
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4927839A (en) * | 1979-03-07 | 1990-05-22 | Imperial Chemical Industries Plc | Method of preventing fungal attack on wood, hides, leather or paint films using a triazole |
US4654332A (en) | 1979-03-07 | 1987-03-31 | Imperial Chemical Industries Plc | Heterocyclic compounds |
EP0123160B1 (en) * | 1980-08-18 | 1992-10-28 | Zeneca Limited | Triazole compounds, a process for preparing them, their use as plant fungicides and plant growth regulators and compositions containing them |
EP0048548B1 (en) * | 1980-08-28 | 1984-11-14 | Imperial Chemical Industries Plc | Pharmaceutical compositions of fungicidal triazole derivatives |
EP0122452A1 (en) * | 1983-03-18 | 1984-10-24 | Schering Corporation | Triazolyl- and imidazolyl-substituted fluoroalkane derivatives, process for their preparation and pharmaceutical compositions containing them |
US4482564A (en) * | 1983-06-03 | 1984-11-13 | Schering Corporation | Triazolyl-substituted propane derivatives |
GB8319984D0 (en) * | 1983-07-25 | 1983-08-24 | Ici Plc | Optically active fungicidal compound |
PH20855A (en) * | 1984-01-24 | 1987-05-19 | Pfizer | Antifungal agents |
DE3511409A1 (de) * | 1985-03-29 | 1986-10-02 | Basf Ag, 6700 Ludwigshafen | Herstellung von arzneimitteln gegen viruserkrankungen |
US4729986A (en) * | 1986-04-24 | 1988-03-08 | E. I. Du Pont De Nemours And Company | Fungicidal triazoles and imidazoles |
WO2010149758A1 (en) * | 2009-06-25 | 2010-12-29 | Basf Se | Antifungal 1, 2, 4-triazolyl derivatives |
CN107879991A (zh) * | 2017-11-24 | 2018-04-06 | 沈阳感光化工研究院有限公司 | 一种含氟三唑啉酮类化合物的合成方法 |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2324010C3 (de) * | 1973-05-12 | 1981-10-08 | Bayer Ag, 5090 Leverkusen | 1-Substituierte 2-Triazolyl-2-phenoxyäthanol-Verbindungen, Verfahren zu ihrer Herstellung und ihre Verwendung zur Bekämpfung von Pilzen |
DE2431407C2 (de) * | 1974-06-29 | 1982-12-02 | Bayer Ag, 5090 Leverkusen | 1,2,4-Triazol-1-yl-alkanone und -alkanole, Verfahren zu ihrer Herstellung sowie ihre Verwendung als Fungizide |
DE2547954A1 (de) * | 1975-10-27 | 1977-04-28 | Bayer Ag | 1-(2-halogen-2-phenyl-aethyl)-triazole, verfahren zu ihrer herstellung und ihre verwendung als fungizide |
IE44186B1 (en) * | 1975-12-03 | 1981-09-09 | Ici Ltd | 1,2,4-triazolyl alkanols and their use as pesticides |
IE45765B1 (en) * | 1976-08-19 | 1982-11-17 | Ici Ltd | Triazoles and imidazoles useful as plant fungicides and growth regulating agents |
-
1980
- 1980-03-15 DE DE19803010093 patent/DE3010093A1/de not_active Withdrawn
-
1981
- 1981-02-03 GR GR64042A patent/GR73187B/el unknown
- 1981-02-26 PT PT72574A patent/PT72574B/pt unknown
- 1981-03-07 EP EP81101668A patent/EP0036153B1/de not_active Expired
- 1981-03-07 AT AT81101668T patent/ATE5190T1/de not_active IP Right Cessation
- 1981-03-07 DE DE8181101668T patent/DE3161300D1/de not_active Expired
- 1981-03-09 IL IL62332A patent/IL62332A/xx unknown
- 1981-03-10 FI FI810743A patent/FI70578C/fi not_active IP Right Cessation
- 1981-03-11 CS CS811782A patent/CS221824B2/cs unknown
- 1981-03-11 IE IE533/81A patent/IE51146B1/en unknown
- 1981-03-11 DD DD81228201A patent/DD156808A5/de unknown
- 1981-03-13 ES ES500334A patent/ES500334A0/es active Granted
- 1981-03-13 NO NO810878A patent/NO155692C/no unknown
- 1981-03-13 HU HU8181646A patent/HU180630B/hu not_active IP Right Cessation
- 1981-03-13 SU SU813254444A patent/SU1355126A3/ru active
- 1981-03-13 DK DK114181A patent/DK114181A/da not_active Application Discontinuation
- 1981-03-13 AU AU68355/81A patent/AU544076B2/en not_active Ceased
- 1981-03-13 ZA ZA00811664A patent/ZA811664B/xx unknown
- 1981-03-13 YU YU00650/81A patent/YU65081A/xx unknown
- 1981-03-16 JP JP3670081A patent/JPS56142273A/ja active Pending
- 1981-03-23 IN IN313/CAL/81A patent/IN152638B/en unknown
Also Published As
Publication number | Publication date |
---|---|
CS221824B2 (en) | 1983-04-29 |
IE51146B1 (en) | 1986-10-15 |
IE810533L (en) | 1981-09-15 |
ATE5190T1 (de) | 1983-11-15 |
ES8201554A1 (es) | 1981-12-16 |
DE3161300D1 (en) | 1983-12-08 |
ES500334A0 (es) | 1981-12-16 |
NO810878L (no) | 1981-09-16 |
IN152638B (enrdf_load_stackoverflow) | 1984-02-25 |
ZA811664B (en) | 1982-11-24 |
SU1355126A3 (ru) | 1987-11-23 |
EP0036153A1 (de) | 1981-09-23 |
FI70578B (fi) | 1986-06-06 |
IL62332A (en) | 1984-08-31 |
GR73187B (enrdf_load_stackoverflow) | 1984-02-14 |
DE3010093A1 (de) | 1981-10-01 |
NO155692C (no) | 1987-05-13 |
DK114181A (da) | 1981-09-16 |
EP0036153B1 (de) | 1983-11-02 |
HU180630B (en) | 1983-03-28 |
FI810743L (fi) | 1981-09-16 |
JPS56142273A (en) | 1981-11-06 |
PT72574B (en) | 1982-02-12 |
YU65081A (en) | 1983-09-30 |
NO155692B (no) | 1987-02-02 |
AU6835581A (en) | 1981-09-24 |
IL62332A0 (en) | 1981-05-20 |
AU544076B2 (en) | 1985-05-16 |
DD156808A5 (de) | 1982-09-22 |
PT72574A (en) | 1981-03-01 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
MM | Patent lapsed |
Owner name: BASF AKTIENGESELLSCHAFT |