GB1414244A - Phenylguanidine derivatives their production and their medicinal use - Google Patents

Phenylguanidine derivatives their production and their medicinal use

Info

Publication number
GB1414244A
GB1414244A GB4838673A GB4838673A GB1414244A GB 1414244 A GB1414244 A GB 1414244A GB 4838673 A GB4838673 A GB 4838673A GB 4838673 A GB4838673 A GB 4838673A GB 1414244 A GB1414244 A GB 1414244A
Authority
GB
United Kingdom
Prior art keywords
carbon atoms
radical
radicals
alkyl
optionally carrying
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
Application number
GB4838673A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Bayer AG
Original Assignee
Bayer AG
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Bayer AG filed Critical Bayer AG
Publication of GB1414244A publication Critical patent/GB1414244A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C281/00Derivatives 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
    • C07C281/16Compounds containing any of the groups, e.g. aminoguanidine
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C277/00Preparation of guanidine or its derivatives, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C279/00Derivatives of guanidine, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups
    • C07C279/20Derivatives 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
    • C07C279/24Y 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)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Furan 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.
GB4838673A 1972-10-18 1973-10-17 Phenylguanidine derivatives their production and their medicinal use Expired GB1414244A (en)

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 (1)

Publication Number Publication Date
GB1414244A true GB1414244A (en) 1975-11-19

Family

ID=5859304

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4838673A Expired GB1414244A (en) 1972-10-18 1973-10-17 Phenylguanidine derivatives their production and their medicinal use

Country Status (23)

Country Link
JP (2) JPS4986341A (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)

* Cited by examiner, † Cited by third party
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)

* Cited by examiner, † Cited by third party
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

Also Published As

Publication number Publication date
HU166358B (en) 1975-03-28
NL7314183A (en) 1974-04-22
JPS4971123A (en) 1974-07-10
SU489315A3 (en) 1975-10-25
IE38387B1 (en) 1978-03-01
CA992554A (en) 1976-07-06
IE38387L (en) 1974-04-18
SE386436B (en) 1976-08-09
AU6150573A (en) 1975-04-17
CH586195A5 (en) 1977-03-31
LU68627A1 (en) 1973-12-27
PH10760A (en) 1977-09-02
DE2250911A1 (en) 1974-04-25
AR199121A1 (en) 1974-08-08
FR2203631B1 (en) 1977-09-09
FR2203631A1 (en) 1974-05-17
JPS4986341A (en) 1974-08-19
IL43431A0 (en) 1974-01-14
EG11195A (en) 1977-11-30
ATA878973A (en) 1977-01-15
CS168049B2 (en) 1976-05-28
ES419721A1 (en) 1976-03-01
ZA738075B (en) 1974-08-28
BE806201A (en) 1974-04-17
AT338818B (en) 1977-09-12
KE2628A (en) 1976-05-28
IL43431A (en) 1976-04-30
AU475701B2 (en) 1976-09-02

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Legal Events

Date Code Title Description
PS Patent sealed [section 19, patents act 1949]
PCNP Patent ceased through non-payment of renewal fee