IE38387L - Phenylguanidine derivatives - Google Patents
Phenylguanidine derivativesInfo
- Publication number
- IE38387L IE38387L IE731854A IE185473A IE38387L IE 38387 L IE38387 L IE 38387L IE 731854 A IE731854 A IE 731854A IE 185473 A IE185473 A IE 185473A IE 38387 L IE38387 L IE 38387L
- Authority
- IE
- Ireland
- Prior art keywords
- carbon atoms
- radical
- radicals
- alkyl
- optionally carrying
- Prior art date
Links
- QRJZGVVKGFIGLI-UHFFFAOYSA-N 2-phenylguanidine Chemical class NC(=N)NC1=CC=CC=C1 QRJZGVVKGFIGLI-UHFFFAOYSA-N 0.000 title abstract 2
- -1 alkyl radical Chemical group 0.000 abstract 35
- 125000004432 carbon atom Chemical group C* 0.000 abstract 28
- 125000001424 substituent group Chemical group 0.000 abstract 9
- 125000005843 halogen group Chemical group 0.000 abstract 8
- 150000001875 compounds Chemical class 0.000 abstract 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 3
- 150000003254 radicals Chemical class 0.000 abstract 3
- 239000005864 Sulphur Chemical group 0.000 abstract 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 230000000507 anthelmentic effect Effects 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 150000005840 aryl radicals Chemical class 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 239000003085 diluting agent Substances 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 238000007911 parenteral administration Methods 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 238000011200 topical administration Methods 0.000 abstract 1
- 230000000699 topical effect Effects 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C281/00—Derivatives of carbonic acid containing functional groups covered by groups C07C269/00 - C07C279/00 in which at least one nitrogen atom of these functional groups is further bound to another nitrogen atom not being part of a nitro or nitroso group
- C07C281/16—Compounds containing any of the groups, e.g. aminoguanidine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C277/00—Preparation of guanidine or its derivatives, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C279/00—Derivatives of guanidine, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups
- C07C279/20—Derivatives of guanidine, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups containing any of the groups, X being a hetero atom, Y being any atom, e.g. acylguanidines
- C07C279/24—Y being a hetero atom
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Furan Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
1414244 Phenyl guanidine derivatives BAYER AG 17 Oct 1973 [18 Oct 1972] 48386/73 Heading C2C Novel compounds of Formula I wherein X is an alkyl radical with 1 to 6 carbon atoms; R<SP>1</SP> is an alkyl radical with 1 to 4 carbon atoms; R<SP>2</SP> is a hydrogen atom or an alkyl radical with 1 to 18 carbon atoms (optionally carrying one or more substituents selected from halogen and nitrile radicals, alkoxy radicals with 1 to 4 carbon atoms, alkoxycarbonyl radicals with 2 to 5 carbon atoms, phenoxy, halophenoxy; alkylphenoxy and alkoxyphenoxy radicals), or a cycloalkyl radical wih 5 to 8 carbon atoms, or an aralkyl radical (optionally carrying one or more substituents selected from halogen atoms, alkyl radicals with 1 to 4 carbon atoms and alkoxy radicals with 1 to 4 carbon atoms), or an aryl radical (optionally carrying one or more substituents selected from halogen atoms, alkyl radicals with 1 to 4 carbon atoms and alkoxy radicals with 1 to 4 carbon atoms), or a 1-furyl radical, or a radical of the general formula -NR<SP>11</SP>R<SP>111</SP> [in which R<SP>11</SP> is a hydrogen atom or an alkyl radical with 1 to 4 carbon atoms, and R<SP>111</SP> is a hydrogen atom or an alkyl radical with 1 to 18 carbon atoms (optionally carrying one or more substituents selected from halogen atoms, nitrile radicals, alkoxy radical with up to 4 carbon atoms and alkoxycarbonyl radicals with up to 5 carbon atoms), or a cycloalkyl radical with 5 to 8 carbon atoms, or an aralkyl radical (optionally carrying in the aryl part one or more substituents selected from halogen atoms, alkyl radicals with up to 6 carbon atoms and alkoxy radicals with up to 6 carbon atoms), a phenyl radical (optionally carrying at least one substituent selected from halogen atoms, alkyl radicals having up to 6 carbon atoms, and alkoxy radicals having up to 6 carbon atoms), or an acyl radical with up to 18 carbon atoms (optionally carrying at least one substituent selected from halogen atoms and alkoxy radicals having up to 6 carbon atoms), or an aroyl radical (optionally carrying as a substituent at least one radical selected from halogen atoms, alkyl radicals with up to 6 carbon atoms and alkoxy radicals with up to 6 carbon atoms), or an alkyl-sulphonyl radical with up to 18 carbon atoms, or an arylsulphonyl radical (optionally carrying at least one substituent selected from halogen atoms, amino radicals, alkyl radicals having up to 6 carbon atoms and alkoxy radical having up to 6 carbon atoms) or a dialkylamino radical with up to 4 carbon atoms; or R<SP>11</SP> and R<SP>111</SP>, together with the nitrogen atom between them, represent a heterocyclic ring with 4 to 7 carbon atoms optionally also containing at least one oxygen or sulphur atom]; with the proviso that X, R<SP>1</SP> and R<SP>2</SP> cannot in the same compound all represent methyl radicals are prepared by reacting compounds of formulae wherein R is C 1-4 alkyl. Pharmaceutical compositions in conventional forms for oral, rectal, topical and parenteral administration and having anthelmintic activity comprise and above novel compound and a carrier or diluent other than a solvent of molecular weight of less than 200.
[GB1414244A]
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE2250911A DE2250911A1 (en) | 1972-10-18 | 1972-10-18 | PHENYLGUANIDINE DERIVATIVES, A METHOD FOR THEIR PRODUCTION AND THEIR USE AS A MEDICINAL PRODUCT |
Publications (2)
Publication Number | Publication Date |
---|---|
IE38387L true IE38387L (en) | 1974-04-18 |
IE38387B1 IE38387B1 (en) | 1978-03-01 |
Family
ID=5859304
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
IE1854/73A IE38387B1 (en) | 1972-10-18 | 1973-10-17 | Phenylguanidine derivatives their production and their medicinal use |
Country Status (23)
Country | Link |
---|---|
JP (2) | JPS4971123A (en) |
AR (1) | AR199121A1 (en) |
AT (1) | AT338818B (en) |
AU (1) | AU475701B2 (en) |
BE (1) | BE806201A (en) |
CA (1) | CA992554A (en) |
CH (1) | CH586195A5 (en) |
CS (1) | CS168049B2 (en) |
DE (1) | DE2250911A1 (en) |
EG (1) | EG11195A (en) |
ES (1) | ES419721A1 (en) |
FR (1) | FR2203631B1 (en) |
GB (1) | GB1414244A (en) |
HU (1) | HU166358B (en) |
IE (1) | IE38387B1 (en) |
IL (1) | IL43431A (en) |
KE (1) | KE2628A (en) |
LU (1) | LU68627A1 (en) |
NL (1) | NL7314183A (en) |
PH (1) | PH10760A (en) |
SE (1) | SE386436B (en) |
SU (1) | SU489315A3 (en) |
ZA (1) | ZA738075B (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2651467A1 (en) * | 1976-11-11 | 1978-05-18 | Bayer Ag | SUBSTITUTED O-PHENYLENE DIAMINE DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE AS MEDICINAL PRODUCTS |
US6593466B1 (en) | 1999-07-07 | 2003-07-15 | Isis Pharmaceuticals, Inc. | Guanidinium functionalized nucleotides and precursors thereof |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2108835A1 (en) * | 1970-10-09 | 1972-05-26 | Rhone Poulenc Sa | Fungicidal guanidines from o phenylenediamine |
DE2109454A1 (en) * | 1971-02-27 | 1972-09-14 | Farbenfabriken Bayer Ag, 5090 Leverkusen | Fungicidal n-(2-acylaminophenyl)-n,n-bis(alkoxycarbonyl)-guanidines - from 2-acrylaminoanilines and s-alkyl n,n-bis(alkoxycarbonyl) isothiazole |
-
1972
- 1972-10-18 DE DE2250911A patent/DE2250911A1/en active Pending
-
1973
- 1973-10-12 SU SU1963844A patent/SU489315A3/en active
- 1973-10-15 NL NL7314183A patent/NL7314183A/xx not_active Application Discontinuation
- 1973-10-16 AR AR250542A patent/AR199121A1/en active
- 1973-10-16 EG EG403A patent/EG11195A/en active
- 1973-10-16 AT AT878973A patent/AT338818B/en not_active IP Right Cessation
- 1973-10-16 IL IL43431A patent/IL43431A/en unknown
- 1973-10-16 JP JP48115397A patent/JPS4971123A/ja active Pending
- 1973-10-16 CH CH1465073A patent/CH586195A5/xx not_active IP Right Cessation
- 1973-10-16 CS CS7129A patent/CS168049B2/cs unknown
- 1973-10-16 LU LU68627A patent/LU68627A1/xx unknown
- 1973-10-16 JP JP48115396A patent/JPS4986341A/ja active Pending
- 1973-10-17 SE SE7314109A patent/SE386436B/en unknown
- 1973-10-17 AU AU61505/73A patent/AU475701B2/en not_active Expired
- 1973-10-17 ES ES419721A patent/ES419721A1/en not_active Expired
- 1973-10-17 IE IE1854/73A patent/IE38387B1/en unknown
- 1973-10-17 CA CA183,615A patent/CA992554A/en not_active Expired
- 1973-10-17 BE BE136796A patent/BE806201A/en unknown
- 1973-10-17 ZA ZA738075*A patent/ZA738075B/en unknown
- 1973-10-17 GB GB4838673A patent/GB1414244A/en not_active Expired
- 1973-10-17 PH PH15116A patent/PH10760A/en unknown
- 1973-10-18 FR FR7337211A patent/FR2203631B1/fr not_active Expired
- 1973-10-18 HU HUBA2987A patent/HU166358B/hu unknown
-
1976
- 1976-05-18 KE KE2628*UA patent/KE2628A/en unknown
Also Published As
Publication number | Publication date |
---|---|
GB1414244A (en) | 1975-11-19 |
SE386436B (en) | 1976-08-09 |
IL43431A (en) | 1976-04-30 |
AU6150573A (en) | 1975-04-17 |
CA992554A (en) | 1976-07-06 |
PH10760A (en) | 1977-09-02 |
DE2250911A1 (en) | 1974-04-25 |
FR2203631B1 (en) | 1977-09-09 |
ATA878973A (en) | 1977-01-15 |
AU475701B2 (en) | 1976-09-02 |
AR199121A1 (en) | 1974-08-08 |
CH586195A5 (en) | 1977-03-31 |
CS168049B2 (en) | 1976-05-28 |
HU166358B (en) | 1975-03-28 |
AT338818B (en) | 1977-09-12 |
JPS4971123A (en) | 1974-07-10 |
JPS4986341A (en) | 1974-08-19 |
SU489315A3 (en) | 1975-10-25 |
ES419721A1 (en) | 1976-03-01 |
IL43431A0 (en) | 1974-01-14 |
KE2628A (en) | 1976-05-28 |
LU68627A1 (en) | 1973-12-27 |
FR2203631A1 (en) | 1974-05-17 |
EG11195A (en) | 1977-11-30 |
ZA738075B (en) | 1974-08-28 |
IE38387B1 (en) | 1978-03-01 |
BE806201A (en) | 1974-04-17 |
NL7314183A (en) | 1974-04-22 |
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