GB1198301A - Perfluoroalkylsulfonamides - Google Patents
PerfluoroalkylsulfonamidesInfo
- Publication number
- GB1198301A GB1198301A GB47927/67A GB4792767A GB1198301A GB 1198301 A GB1198301 A GB 1198301A GB 47927/67 A GB47927/67 A GB 47927/67A GB 4792767 A GB4792767 A GB 4792767A GB 1198301 A GB1198301 A GB 1198301A
- Authority
- GB
- United Kingdom
- Prior art keywords
- aqueous
- sulphonamides
- signifies
- oct
- heteroatom
- 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- 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
- C07D209/80—[b, c]- or [b, d]-condensed
- C07D209/82—Carbazoles; Hydrogenated carbazoles
- C07D209/88—Carbazoles; Hydrogenated carbazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the ring system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/36—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems
- C07D241/38—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems with only hydrogen or carbon atoms directly attached to the ring nitrogen atoms
- C07D241/40—Benzopyrazines
- C07D241/42—Benzopyrazines with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
-
- 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
- C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D249/14—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2603/00—Systems containing at least three condensed rings
- C07C2603/02—Ortho- or ortho- and peri-condensed systems
- C07C2603/04—Ortho- or ortho- and peri-condensed systems containing three rings
- C07C2603/06—Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members
- C07C2603/10—Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members containing five-membered rings
- C07C2603/12—Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members containing five-membered rings only one five-membered ring
- C07C2603/18—Fluorenes; Hydrogenated fluorenes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Abstract
1,198,301. Sulphonamide compositions. MINNESOTA MINING & MFG. CO. 20 Oct., 1967 [21 Oct., 1966], No. 47928/67. Headings A5B and A5E. [Also in Division C2] Anti-inflammatory, analgesic, antipyretic and antifibrinolytic, and antimicrobial, e.g. antiparasitic, antibacterial and antifugal, pesticidal, e.g. insecticidal and nematocidal and plant growth regulative penfluoralkylsulphonamides are of the general formula: R f SO 2 NR 2 R 3 ; wherein R f signifies a C 1-8 perfluoroalkyl group, R 2 signifies a hydrogen atom, a C 1-6 alkyl group or a cation (includes ammonium and substituted ammonium cations) and R 3 signifies a heteroatom containing organic group (the heteroatom can occur in a heterocyclic ring or in the form of an acylic grouping, e.g. in substituents of rings or in aliphatic groups) which is bonded to the nitrogen atom in the foregoing formula through an aromatic ring therein (includes aromatic heterocyclic). Pharmaceutical preparations in the form of aqueous solutions or as suspensions in an aqueous or non-aqueous suspending agent, e.g. gum acacia and containing the above sulphonamides can be administered orally or injected subcutaneously or intramuscularly. The sulphonamides may also 'be administered in the form of capsules, tablets, powders, sterile solutions of water or other solvents or other dosage forms in association with conventional diluents and adjuvants as well as other tableting aids and fillers. For application to plants the sulphonamides can be finely divided in an aqueous suspension and other agents may also be incorporated therein. Dry powders can also be utilized.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US58833866A | 1966-10-21 | 1966-10-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1198301A true GB1198301A (en) | 1970-07-08 |
Family
ID=24353436
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB47927/67A Expired GB1198301A (en) | 1966-10-21 | 1967-10-20 | Perfluoroalkylsulfonamides |
Country Status (5)
Country | Link |
---|---|
BR (1) | BR6794063D0 (en) |
CH (1) | CH513136A (en) |
DE (1) | DE1668420B2 (en) |
FR (1) | FR1579473A (en) |
GB (1) | GB1198301A (en) |
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6548547B1 (en) | 1998-07-08 | 2003-04-15 | Aventis Pharma Deutschland Gmbh | Sulfonylamino carboxylic acid N-arylamides as guanylate cyclase activators |
WO2006078283A3 (en) * | 2004-04-30 | 2006-10-12 | Genentech Inc | Quinoxaline inhibitors of hedgehog signalling |
US8722702B2 (en) | 2006-11-22 | 2014-05-13 | Plexxikon Inc. | Compounds modulating c-fms and/or c-kit activity and uses therefor |
US8741920B2 (en) | 2009-08-03 | 2014-06-03 | Hoffmann-La Roche, Inc. | Process for the manufacture of pharmaceutically active compounds |
US8865735B2 (en) | 2011-02-21 | 2014-10-21 | Hoffman-La Roche Inc. | Solid forms of a pharmaceutically active substance |
AU2012200933B2 (en) * | 2005-06-22 | 2015-04-30 | Plexxikon, Inc. | Pyrrolo [2, 3-B] pyridine derivatives as protein kinase inhibitors |
US9096593B2 (en) | 2009-11-06 | 2015-08-04 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
US9150570B2 (en) | 2012-05-31 | 2015-10-06 | Plexxikon Inc. | Synthesis of heterocyclic compounds |
EP2395004B1 (en) * | 2005-06-22 | 2016-01-20 | Plexxikon Inc. | Pyrrolo [2,3-b]pyridine derivatives as protein kinase inhibitors |
US9447089B2 (en) | 2009-04-03 | 2016-09-20 | Plexxikon Inc. | Compositions and uses thereof |
US9469640B2 (en) | 2007-07-17 | 2016-10-18 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
US9624213B2 (en) | 2011-02-07 | 2017-04-18 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
EP3760615A4 (en) * | 2018-02-27 | 2021-07-14 | Nippon Soda Co., Ltd. | Heteroaryl sulfonamide compound and pest control agent |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3661990A (en) * | 1970-04-13 | 1972-05-09 | Riker Laboratories Inc | N-alkylsulfonyl benzoylhaloalkylsulfonanilides |
US3647874A (en) * | 1970-04-13 | 1972-03-07 | Riker Laboratories Inc | N-cyanobenzoylhaloalkylsulfonanilides |
US3972926A (en) * | 1971-01-04 | 1976-08-03 | Riker Laboratories, Inc. | Substituted trifluoromethanesulfonanilides |
US3981914A (en) * | 1971-08-03 | 1976-09-21 | Minnesota Mining And Manufacturing Company | N-alkylsulfonylperfluoroalkanesulfonanilides |
US4005141A (en) | 1972-07-03 | 1977-01-25 | Minnesota Mining And Manufacturing Company | Perfluoroalkylsulfonamidoaryl compounds |
US3996277A (en) | 1974-11-14 | 1976-12-07 | Minnesota Mining And Manufacturing Company | 4-Methylthio-2-trifluoromethylmethanesulfonanilide and derivatives thereof |
EG16122A (en) * | 1981-08-10 | 1987-04-30 | Sumitomo Chemical Co | Trifluoromethanesulfonanilide derivatives,their production and herbicides containing them as active ingredients |
DE3834704A1 (en) * | 1988-10-07 | 1990-06-07 | Schering Ag | Fluorosubstituted benzene derivatives |
US20070238700A1 (en) * | 2006-04-10 | 2007-10-11 | Winzenberg Kevin N | N-phenyl-1,1,1-trifluoromethanesulfonamide hydrazone derivative compounds and their usage in controlling parasites |
-
1967
- 1967-10-20 GB GB47927/67A patent/GB1198301A/en not_active Expired
- 1967-10-20 BR BR194063/67A patent/BR6794063D0/en unknown
- 1967-10-20 FR FR1579473D patent/FR1579473A/fr not_active Expired
- 1967-10-20 DE DE1967M0075958 patent/DE1668420B2/en active Granted
- 1967-10-20 CH CH1466867A patent/CH513136A/en not_active IP Right Cessation
Cited By (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6809089B2 (en) | 1998-07-08 | 2004-10-26 | Aventis Pharma Deutschland Gmbh | Sulfonylaminocarboxylic acid N-arylamides as guanylate cyclase activators |
US7351703B2 (en) | 1998-07-08 | 2008-04-01 | Sanofi-Aventis Deutschland Gmbh | Sulfonylamino carboxylic acid N-arylamides as guanylate cyclase activators |
US6548547B1 (en) | 1998-07-08 | 2003-04-15 | Aventis Pharma Deutschland Gmbh | Sulfonylamino carboxylic acid N-arylamides as guanylate cyclase activators |
WO2006078283A3 (en) * | 2004-04-30 | 2006-10-12 | Genentech Inc | Quinoxaline inhibitors of hedgehog signalling |
JP2007535569A (en) * | 2004-04-30 | 2007-12-06 | ジェネンテック,インコーポレイティド | Quinoxaline inhibitors of hedgehog signaling |
AU2005325267B2 (en) * | 2004-04-30 | 2010-11-04 | Curis Inc. | Quinoxaline inhibitors of the hedgehog signalling pathway |
US8273743B2 (en) | 2004-04-30 | 2012-09-25 | Curis, Inc. | Quinoxaline inhibitors of the hedgehog signalling |
CN101018783B (en) * | 2004-04-30 | 2012-11-21 | 遗传技术研究公司 | Quinoxaline inhibitors of the HEDGEHOG signalling pathway |
AU2012200933B2 (en) * | 2005-06-22 | 2015-04-30 | Plexxikon, Inc. | Pyrrolo [2, 3-B] pyridine derivatives as protein kinase inhibitors |
EP2395004B1 (en) * | 2005-06-22 | 2016-01-20 | Plexxikon Inc. | Pyrrolo [2,3-b]pyridine derivatives as protein kinase inhibitors |
US9487515B2 (en) | 2006-11-22 | 2016-11-08 | Plexxikon Inc. | Compounds modulating c-fms and/or c-kit activity and uses therefor |
US9169250B2 (en) | 2006-11-22 | 2015-10-27 | Plexxikon Inc. | Compounds modulating c-fms and/or c-kit activity and uses therefor |
US8722702B2 (en) | 2006-11-22 | 2014-05-13 | Plexxikon Inc. | Compounds modulating c-fms and/or c-kit activity and uses therefor |
US9469640B2 (en) | 2007-07-17 | 2016-10-18 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
US9844539B2 (en) | 2007-07-17 | 2017-12-19 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
US10426760B2 (en) | 2007-07-17 | 2019-10-01 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
US9447089B2 (en) | 2009-04-03 | 2016-09-20 | Plexxikon Inc. | Compositions and uses thereof |
US9663517B2 (en) | 2009-04-03 | 2017-05-30 | Plexxikon Inc. | Compositions and uses thereof |
US8741920B2 (en) | 2009-08-03 | 2014-06-03 | Hoffmann-La Roche, Inc. | Process for the manufacture of pharmaceutically active compounds |
US9096593B2 (en) | 2009-11-06 | 2015-08-04 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
US9624213B2 (en) | 2011-02-07 | 2017-04-18 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
US11337976B2 (en) | 2011-02-07 | 2022-05-24 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
US8865735B2 (en) | 2011-02-21 | 2014-10-21 | Hoffman-La Roche Inc. | Solid forms of a pharmaceutically active substance |
US9150570B2 (en) | 2012-05-31 | 2015-10-06 | Plexxikon Inc. | Synthesis of heterocyclic compounds |
US9695169B2 (en) | 2012-05-31 | 2017-07-04 | Plexxikon Inc. | Synthesis of heterocyclic compounds |
EP3760615A4 (en) * | 2018-02-27 | 2021-07-14 | Nippon Soda Co., Ltd. | Heteroaryl sulfonamide compound and pest control agent |
Also Published As
Publication number | Publication date |
---|---|
BR6794063D0 (en) | 1973-09-18 |
DE1668420A1 (en) | 1970-06-25 |
FR1579473A (en) | 1969-08-29 |
DE1668420B2 (en) | 1976-11-25 |
CH513136A (en) | 1971-09-30 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
429A | Application made for amendment of specification (sect. 29/1949) | ||
429H | Application (made) for amendment of specification now open to opposition (sect. 29/1949) | ||
429D | Case decided by the comptroller ** specification amended (sect. 29/1949) | ||
PE20 | Patent expired after termination of 20 years |