PL99366B1 - Sposob wytwarzania nowych dwu-n-tlenkow-/1,4/podstawionych 3-aminobenzo-1,2,4-triazyn - Google Patents
Sposob wytwarzania nowych dwu-n-tlenkow-/1,4/podstawionych 3-aminobenzo-1,2,4-triazyn Download PDFInfo
- Publication number
- PL99366B1 PL99366B1 PL1973183473A PL18347373A PL99366B1 PL 99366 B1 PL99366 B1 PL 99366B1 PL 1973183473 A PL1973183473 A PL 1973183473A PL 18347373 A PL18347373 A PL 18347373A PL 99366 B1 PL99366 B1 PL 99366B1
- Authority
- PL
- Poland
- Prior art keywords
- formula
- optionally substituted
- aminobenzo
- oxide
- triazine
- Prior art date
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- 239000003513 alkali Substances 0.000 description 1
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- 229910052791 calcium Inorganic materials 0.000 description 1
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- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 1
- 239000000292 calcium oxide Substances 0.000 description 1
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- 239000000378 calcium silicate Substances 0.000 description 1
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- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
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- 238000001816 cooling Methods 0.000 description 1
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- 239000002385 cottonseed oil Substances 0.000 description 1
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- 239000006071 cream Substances 0.000 description 1
- 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- KQWGXHWJMSMDJJ-UHFFFAOYSA-N cyclohexyl isocyanate Chemical compound O=C=NC1CCCCC1 KQWGXHWJMSMDJJ-UHFFFAOYSA-N 0.000 description 1
- WEPUZBYKXNKSDH-UHFFFAOYSA-N cyclopentanecarbonyl chloride Chemical compound ClC(=O)C1CCCC1 WEPUZBYKXNKSDH-UHFFFAOYSA-N 0.000 description 1
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- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 1
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- 239000008103 glucose Substances 0.000 description 1
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- MNQZXJOMYWMBOU-UHFFFAOYSA-N glyceraldehyde Chemical compound OCC(O)C=O MNQZXJOMYWMBOU-UHFFFAOYSA-N 0.000 description 1
- YQEMORVAKMFKLG-UHFFFAOYSA-N glycerine monostearate Natural products CCCCCCCCCCCCCCCCCC(=O)OC(CO)CO YQEMORVAKMFKLG-UHFFFAOYSA-N 0.000 description 1
- SVUQHVRAGMNPLW-UHFFFAOYSA-N glycerol monostearate Natural products CCCCCCCCCCCCCCCCC(=O)OCC(O)CO SVUQHVRAGMNPLW-UHFFFAOYSA-N 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
- 150000004820 halides Chemical class 0.000 description 1
- 150000002390 heteroarenes Chemical class 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- YWGHUJQYGPDNKT-UHFFFAOYSA-N hexanoyl chloride Chemical compound CCCCCC(Cl)=O YWGHUJQYGPDNKT-UHFFFAOYSA-N 0.000 description 1
- 235000001050 hortel pimenta Nutrition 0.000 description 1
- 239000003906 humectant Substances 0.000 description 1
- 238000001802 infusion Methods 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000007912 intraperitoneal administration Methods 0.000 description 1
- 125000003253 isopropoxy group Chemical group [H]C([H])([H])C([H])(O*)C([H])([H])[H] 0.000 description 1
- 239000000644 isotonic solution Substances 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 244000144972 livestock Species 0.000 description 1
- 239000000314 lubricant Substances 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
- 239000001525 mentha piperita l. herb oil Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 230000003641 microbiacidal effect Effects 0.000 description 1
- 239000003094 microcapsule Substances 0.000 description 1
- 235000019813 microcrystalline cellulose Nutrition 0.000 description 1
- 239000008108 microcrystalline cellulose Substances 0.000 description 1
- 229940016286 microcrystalline cellulose Drugs 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000012452 mother liquor Substances 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000003506 n-propoxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])O* 0.000 description 1
- LYGJENNIWJXYER-UHFFFAOYSA-N nitromethane Chemical compound C[N+]([O-])=O LYGJENNIWJXYER-UHFFFAOYSA-N 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- WTBAHSZERDXKKZ-UHFFFAOYSA-N octadecanoyl chloride Chemical compound CCCCCCCCCCCCCCCCCC(Cl)=O WTBAHSZERDXKKZ-UHFFFAOYSA-N 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000000312 peanut oil Substances 0.000 description 1
- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 description 1
- XGISHOFUAFNYQF-UHFFFAOYSA-N pentanoyl chloride Chemical compound CCCCC(Cl)=O XGISHOFUAFNYQF-UHFFFAOYSA-N 0.000 description 1
- 235000019319 peptone Nutrition 0.000 description 1
- 229940021222 peritoneal dialysis isotonic solution Drugs 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 244000144977 poultry Species 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- RIBFXMJCUYXJDZ-UHFFFAOYSA-N propanoyl bromide Chemical compound CCC(Br)=O RIBFXMJCUYXJDZ-UHFFFAOYSA-N 0.000 description 1
- RZWZRACFZGVKFM-UHFFFAOYSA-N propanoyl chloride Chemical compound CCC(Cl)=O RZWZRACFZGVKFM-UHFFFAOYSA-N 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- 229940007042 proteus vulgaris Drugs 0.000 description 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 229910001112 rose gold Inorganic materials 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
- 150000003839 salts Chemical class 0.000 description 1
- 239000013049 sediment Substances 0.000 description 1
- 239000008159 sesame oil Substances 0.000 description 1
- 235000011803 sesame oil Nutrition 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- UIIMBOGNXHQVGW-UHFFFAOYSA-M sodium bicarbonate Substances [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 1
- 229940001593 sodium carbonate Drugs 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000008174 sterile solution Substances 0.000 description 1
- 230000004936 stimulating effect Effects 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 150000003510 tertiary aliphatic amines Chemical class 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- BSYVTEYKTMYBMK-UHFFFAOYSA-N tetrahydrofurfuryl alcohol Chemical compound OCC1CCCO1 BSYVTEYKTMYBMK-UHFFFAOYSA-N 0.000 description 1
- 235000010487 tragacanth Nutrition 0.000 description 1
- 239000000196 tragacanth Substances 0.000 description 1
- 229940116362 tragacanth Drugs 0.000 description 1
- 229940035893 uracil Drugs 0.000 description 1
- 235000019871 vegetable fat Nutrition 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 229940075420 xanthine Drugs 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D253/00—Heterocyclic compounds containing six-membered rings having three nitrogen atoms as the only ring hetero atoms, not provided for by group C07D251/00
- C07D253/08—Heterocyclic compounds containing six-membered rings having three nitrogen atoms as the only ring hetero atoms, not provided for by group C07D251/00 condensed with carbocyclic rings or ring systems
- C07D253/10—Condensed 1,2,4-triazines; Hydrogenated condensed 1,2,4-triazines
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K20/00—Accessory food factors for animal feeding-stuffs
- A23K20/10—Organic substances
- A23K20/116—Heterocyclic compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Polymers & Plastics (AREA)
- Animal Husbandry (AREA)
- Zoology (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Cosmetics (AREA)
- Fodder In General (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2255947A DE2255947A1 (de) | 1972-11-15 | 1972-11-15 | Substituierte 3-amino-benzo-1,2,4triazin-di-n-oxide (1,4), verfahren zu ihrer herstellung sowie ihre verwendung als antimikrobielle mittel |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL99366B1 true PL99366B1 (pl) | 1978-07-31 |
Family
ID=5861794
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL1973183473A PL99366B1 (pl) | 1972-11-15 | 1973-11-13 | Sposob wytwarzania nowych dwu-n-tlenkow-/1,4/podstawionych 3-aminobenzo-1,2,4-triazyn |
| PL1973166510A PL87635B1 (en, 2012) | 1972-11-15 | 1973-11-13 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL1973166510A PL87635B1 (en, 2012) | 1972-11-15 | 1973-11-13 |
Country Status (19)
| Country | Link |
|---|---|
| JP (2) | JPS4980218A (en, 2012) |
| AR (3) | AR200888A1 (en, 2012) |
| AT (1) | AT331806B (en, 2012) |
| BE (1) | BE807309A (en, 2012) |
| BR (1) | BR7308877D0 (en, 2012) |
| CH (2) | CH592069A5 (en, 2012) |
| CS (1) | CS178138B2 (en, 2012) |
| DE (1) | DE2255947A1 (en, 2012) |
| DK (1) | DK593374A (en, 2012) |
| ES (3) | ES420536A1 (en, 2012) |
| FR (1) | FR2206104B1 (en, 2012) |
| GB (1) | GB1423585A (en, 2012) |
| HU (1) | HU168359B (en, 2012) |
| IL (1) | IL43614A (en, 2012) |
| LU (1) | LU68790A1 (en, 2012) |
| NL (1) | NL7315454A (en, 2012) |
| PL (2) | PL99366B1 (en, 2012) |
| SU (1) | SU519134A3 (en, 2012) |
| ZA (1) | ZA738726B (en, 2012) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL7801827A (nl) * | 1977-02-22 | 1978-08-24 | Ciba Geigy | Nieuwe heterocyclische verbindingen. |
| NZ194612A (en) * | 1979-08-31 | 1982-12-21 | Ici Australia Ltd | Benzotriazine derivatives intermediates and herbicidal compositions |
| US5672702A (en) * | 1995-12-04 | 1997-09-30 | Sanofi | Process for preparing 3 amino 1, 2, 4-benzotriazine dioxide |
| EP2543376A1 (en) | 2004-04-08 | 2013-01-09 | Targegen, Inc. | Benzotriazine inhibitors of kinases |
| NZ553492A (en) | 2004-08-25 | 2010-11-26 | Targegen Inc | Triazole derivatives and methods of use |
| CN115894385B (zh) * | 2023-01-09 | 2025-02-07 | 中国科学院长春应用化学研究所 | 替拉扎明衍生物及其制备方法和应用 |
-
1972
- 1972-11-15 DE DE2255947A patent/DE2255947A1/de active Pending
-
1973
- 1973-11-12 IL IL7343614A patent/IL43614A/en unknown
- 1973-11-12 NL NL7315454A patent/NL7315454A/xx not_active Application Discontinuation
- 1973-11-13 PL PL1973183473A patent/PL99366B1/pl unknown
- 1973-11-13 PL PL1973166510A patent/PL87635B1/pl unknown
- 1973-11-13 LU LU68790A patent/LU68790A1/xx unknown
- 1973-11-13 CH CH1594273A patent/CH592069A5/xx not_active IP Right Cessation
- 1973-11-13 SU SU1967994A patent/SU519134A3/ru active
- 1973-11-13 BR BR8877/73A patent/BR7308877D0/pt unknown
- 1973-11-13 JP JP48126879A patent/JPS4980218A/ja active Pending
- 1973-11-13 JP JP48126878A patent/JPS4980085A/ja active Pending
- 1973-11-13 CH CH200477A patent/CH592070A5/xx not_active IP Right Cessation
- 1973-11-14 HU HUBA2995A patent/HU168359B/hu unknown
- 1973-11-14 BE BE137737A patent/BE807309A/xx unknown
- 1973-11-14 ZA ZA738726A patent/ZA738726B/xx unknown
- 1973-11-14 CS CS7821A patent/CS178138B2/cs unknown
- 1973-11-14 ES ES420536A patent/ES420536A1/es not_active Expired
- 1973-11-15 AR AR251017A patent/AR200888A1/es active
- 1973-11-15 FR FR7340749A patent/FR2206104B1/fr not_active Expired
- 1973-11-15 GB GB5307073A patent/GB1423585A/en not_active Expired
- 1973-11-15 AT AT961273A patent/AT331806B/de not_active IP Right Cessation
-
1974
- 1974-11-14 DK DK593374A patent/DK593374A/da unknown
- 1974-11-15 AR AR256553A patent/AR203770A1/es active
- 1974-11-15 AR AR256554A patent/AR200983A1/es active
-
1976
- 1976-01-16 ES ES444360A patent/ES444360A1/es not_active Expired
- 1976-01-16 ES ES444359A patent/ES444359A1/es not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| AT331806B (de) | 1976-08-25 |
| JPS4980085A (en, 2012) | 1974-08-02 |
| BE807309A (fr) | 1974-05-14 |
| BR7308877D0 (pt) | 1974-09-24 |
| ES420536A1 (es) | 1976-07-01 |
| GB1423585A (en) | 1976-02-04 |
| FR2206104B1 (en, 2012) | 1977-09-02 |
| AR203770A1 (es) | 1975-10-15 |
| IL43614A0 (en) | 1974-03-14 |
| HU168359B (en, 2012) | 1976-04-28 |
| ATA961273A (de) | 1975-12-15 |
| ES444359A1 (es) | 1977-05-16 |
| ZA738726B (en) | 1974-09-25 |
| FR2206104A1 (en, 2012) | 1974-06-07 |
| CH592070A5 (en, 2012) | 1977-10-14 |
| AR200888A1 (es) | 1974-12-27 |
| ES444360A1 (es) | 1977-05-16 |
| PL87635B1 (en, 2012) | 1976-07-31 |
| AU6242873A (en) | 1975-05-15 |
| IL43614A (en) | 1977-06-30 |
| JPS4980218A (en, 2012) | 1974-08-02 |
| NL7315454A (en, 2012) | 1974-05-17 |
| CH592069A5 (en, 2012) | 1977-10-14 |
| CS178138B2 (en, 2012) | 1977-08-31 |
| AR200983A1 (es) | 1974-12-27 |
| LU68790A1 (en, 2012) | 1974-01-21 |
| SU519134A3 (ru) | 1976-06-25 |
| DK593374A (en, 2012) | 1975-05-20 |
| DE2255947A1 (de) | 1974-05-22 |
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