DE2100242C2 - 1-Methyl-2-(3a,4,5,6,7,7a-hexahydro-1,2-benzisoxazol-3-yl)-5-nitroimidazol, Verfahren zu dessen Herstellung und dieses enthaltende Veterinärarzneimittel - Google Patents

1-Methyl-2-(3a,4,5,6,7,7a-hexahydro-1,2-benzisoxazol-3-yl)-5-nitroimidazol, Verfahren zu dessen Herstellung und dieses enthaltende Veterinärarzneimittel

Info

Publication number
DE2100242C2
DE2100242C2 DE2100242A DE2100242A DE2100242C2 DE 2100242 C2 DE2100242 C2 DE 2100242C2 DE 2100242 A DE2100242 A DE 2100242A DE 2100242 A DE2100242 A DE 2100242A DE 2100242 C2 DE2100242 C2 DE 2100242C2
Authority
DE
Germany
Prior art keywords
methyl
nitroimidazole
hexahydro
preparation
benzisoxazol
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
DE2100242A
Other languages
German (de)
English (en)
Other versions
DE2100242A1 (de
Inventor
Peter Scotch Plains N.J. Kulsa
Clarence Stanley Beaconsfield Quebec Rooney
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.)
Merck and Co Inc
Original Assignee
Merck and Co Inc
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 Merck and Co Inc filed Critical Merck and Co Inc
Publication of DE2100242A1 publication Critical patent/DE2100242A1/de
Application granted granted Critical
Publication of DE2100242C2 publication Critical patent/DE2100242C2/de
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
    • C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
    • C07D493/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members 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
    • C07D233/91—Nitro radicals
    • C07D233/92—Nitro radicals attached in position 4 or 5
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members 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
    • C07D233/91—Nitro radicals
    • C07D233/92—Nitro radicals attached in position 4 or 5
    • C07D233/94—Nitro radicals attached in position 4 or 5 with hydrocarbon radicals, substituted by oxygen or sulfur atoms, attached to other ring members
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members 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
    • C07D233/91—Nitro radicals
    • C07D233/92—Nitro radicals attached in position 4 or 5
    • C07D233/95—Nitro radicals attached in position 4 or 5 with hydrocarbon radicals, substituted by nitrogen atoms, attached to other ring members
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D495/04—Ortho-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (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)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
DE2100242A 1970-01-07 1971-01-05 1-Methyl-2-(3a,4,5,6,7,7a-hexahydro-1,2-benzisoxazol-3-yl)-5-nitroimidazol, Verfahren zu dessen Herstellung und dieses enthaltende Veterinärarzneimittel Expired DE2100242C2 (de)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US130770A 1970-01-07 1970-01-07

Publications (2)

Publication Number Publication Date
DE2100242A1 DE2100242A1 (de) 1971-07-15
DE2100242C2 true DE2100242C2 (de) 1984-07-19

Family

ID=21695371

Family Applications (1)

Application Number Title Priority Date Filing Date
DE2100242A Expired DE2100242C2 (de) 1970-01-07 1971-01-05 1-Methyl-2-(3a,4,5,6,7,7a-hexahydro-1,2-benzisoxazol-3-yl)-5-nitroimidazol, Verfahren zu dessen Herstellung und dieses enthaltende Veterinärarzneimittel

Country Status (11)

Country Link
US (1) US3711495A (enExample)
JP (1) JPS511717B1 (enExample)
CA (1) CA988089A (enExample)
CH (1) CH555852A (enExample)
DE (1) DE2100242C2 (enExample)
FR (1) FR2081416B1 (enExample)
GB (1) GB1316221A (enExample)
NL (1) NL7018072A (enExample)
OA (1) OA03554A (enExample)
ZA (1) ZA707997B (enExample)
ZM (1) ZM14570A1 (enExample)

Families Citing this family (38)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3915978A (en) * 1970-01-07 1975-10-28 Merck & Co Inc Nitroimidazoles
DE2229248C3 (de) * 1971-07-30 1980-03-27 Gruppo Lepetit S.P.A., Mailand (Italien) 5-Iminomethyl-2-nitroimidazoI-Derivate und Verfahren zu deren Herstellung
US4010176A (en) * 1972-10-27 1977-03-01 Merck & Co., Inc. Isoxazole substituted nitroimidazoles
US4080340A (en) * 1975-07-30 1978-03-21 Merck & Co., Inc. Nitroimidazoles
DE2613167A1 (de) * 1976-03-27 1977-10-06 Bayer Ag Oximcarbamate, verfahren zu ihrer herstellung und ihre verwendung als insektizide, akarizide und nematozide
US4268674A (en) * 1977-11-14 1981-05-19 The Dow Chemical Company Preparation of substituted oxatriazoles
US4144345A (en) * 1977-11-30 1979-03-13 Merck & Co., Inc. Dihydroxybenzisoxazolin-3-yl-substituted-5-nitroimidazoles as antibacterials and antiprotozoals
IT7852095A0 (it) * 1977-11-30 1978-11-28 Merck & Co Inc Diidrossiisossazolin-3-il-sostitui to-5-nitroimidazoli e relativo procedimento di produzione
US4269830A (en) * 1979-05-17 1981-05-26 Merck & Co., Inc. Compositions and methods for the treatment of chronic trypanosomiasis infections
GB2101886B (en) * 1981-05-22 1985-07-31 Merck & Co Inc Compositions for the treatment of chronic trypanosomiasis infections
IE59813B1 (en) * 1986-05-09 1994-04-06 Warner Lambert Co Styryl pyrazoles, isoxazoles and analogs thereof having activity as 5-lipoxy-genase inhibitors and pharmaceutical compositions containing them
US4767868A (en) * 1987-04-10 1988-08-30 Pennwalt Corporation 3-Phenyl-3-(1H-imidazol-1-ylmethyl)-2-methyl-5-[(phenylamino)methyl]isoxazolidines
US4723021A (en) * 1986-08-27 1988-02-02 Pennwalt Corporation Substituted 5-(phenoxyalkyl)-3-phenyl-3-(1H-imidazol-1-ylmethyl)-2-methylisoxazolidines
US4767867A (en) * 1987-04-10 1988-08-30 Pennwalt Corporation 5-(alkoxyalkyl)-3-phenyl-3-(1H-imidazol-1-ylmethyl)-2-methylisoxazolidines
US4831154A (en) * 1987-04-10 1989-05-16 Pennwalt Corporation 5-alkyl(or alkenyl)-3-phenyl-3-(1H-imidazol-1-ylmethyl)-2-methylisoxazolidines
US4727156A (en) * 1986-08-27 1988-02-23 Pennwalt Corporation 3-(Substituted phenyl)-3-(1H-imidazol-1-ylmethyl)-2-methyl-5-{[(substituted phenyl)thio]me}isoxazolidine derivatives
US4727157A (en) * 1986-08-27 1988-02-23 Pennwalt Corporation 3-(Substituted phenyl)-3-(1H-1,2,4-triazol-1-yl)methyl-2-methyl-5-[(substituted phenoxy)methyl]isoxazolidine derivatives
US4719306A (en) * 1986-08-27 1988-01-12 Pennwalt Corporation Substituted 3,5-diphenyl-3-(1H-imidazol-1-ylmethyl)-2-methylisoxazolidines
US4767866A (en) * 1987-04-10 1988-08-30 Pennwalt Corporation 3-Phenyl-3-(1H-1,2,4-triazol-1-ylmethyl)-2-methyl-5-alkylisoxazolidines
US4769471A (en) * 1987-04-10 1988-09-06 Pennwalt Corporation Substituted 3,5-diphenyl-3-(1H-1,2,4-triazol-1-yl-methyl)-2-methylisoxazolidines
US4769468A (en) * 1987-04-10 1988-09-06 Penwalt Corporation 5-(acyloxyalkyl)-3-phenyl-3-(1H-imidazol-1-ylmethyl)-2-methylisoxazolidines
US4769469A (en) * 1987-04-10 1988-09-06 Pennwalt Corporation 5-(phenyl or phenoxyalkyl)-3-(2-furanyl)-3-(1H-imidazol-1-ylmethyl)-2-methylisoxazolidines
US4769470A (en) * 1987-10-02 1988-09-06 Pennwalt Corporation 5-(phenyl or phenoxyalkyl)-3-(2-thienyl)-3-(1H-imidazol-1-ylmethyl)-2-methylisoxazolidines
US4777262A (en) * 1987-10-02 1988-10-11 Pennwalt Corporation 5-(substituted thiomethyl)-3-phenyl-3-(1H-imidazol-1-ylmethyl)-2-methylisoxazolidine derivatives
US4749793A (en) * 1987-10-02 1988-06-07 Pennwalt Corporation 5-substituted-3-phenyl-3-[1H-imidazol-1-ylmethyl) or (1H-1,2,4-triazol-1-ylmethyl]-2-benzylisoxazolidines (ir 3011)
US4777264A (en) * 1987-10-02 1988-10-11 Pennwalt Corporation 5-carbonyl derivatives of 3-phenyl-3-(1H-imadazol-1-ylmethyl)-2-methylisoxazolidines and related compounds thereof
US4785117A (en) * 1987-10-02 1988-11-15 Pennwalt Corporation 5,5-disubstituted-3-phenyl-3-phenyl-3-[(1H-imidazol-1-ylmethyl) or (1H-1,2,4-triazol-1-ylmethyl)]-2-methylisoxazolidine derivatives (IR 3012)
US4754042A (en) * 1987-10-02 1988-06-28 Pennwalt Corporation 5-{[naphthyl(or 2-oxo-1,3-benzoxathiol-6-yl)oxy]methyl}-3-phenyl-3-(1H-imidazol-1-ylmethyl)-2-methylisoxazolidines
US4777263A (en) * 1987-10-02 1988-10-11 Pennwalt Corporation 5-substituted-3-(2-naphthalenyl)-3-((1H-imidazol-1-ylmethyl) or (1H-1,2,4-triazol-1-ylmethyl))-2-methylisoxazolidines
US4835283A (en) * 1988-03-07 1989-05-30 Pennwalt Corporation 3,5-diphenyl-3-[(1H-imidazol-1-ylmethyl) or (1H-1,2,4-triazol-1-ylmethyl)]-2
US6072057A (en) * 1996-06-06 2000-06-06 Gliatech Inc. 1H-4(5)-cyclo-substituted imidazole derivatives as histamine H3 receptor agents
US6329342B1 (en) 1997-08-19 2001-12-11 Eli Lilly And Company Treatment of congestive heart failure with growth hormone secretagogues
AU3180999A (en) * 1998-02-25 1999-09-15 Pharmacia & Upjohn Company Substituted aminomethyl isoxazoline derivatives useful as antimicrobials
US6639076B1 (en) * 1998-08-18 2003-10-28 Eli Lilly And Company Growth hormone secretagogues
US6828331B1 (en) * 1999-02-19 2004-12-07 Eli Lilly And Company Growth hormone secretagogues
US7125840B2 (en) * 2001-10-09 2006-10-24 Eli Lilly And Company Substituted dipeptides as growth hormone secretagogues
US20060167268A1 (en) * 2002-04-09 2006-07-27 Eli Lilly And Company, Patent Division, Growth hormone secretagogues
EP1497316B1 (en) * 2002-04-09 2006-07-05 Eli Lilly And Company Growth hormone secretagogues

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1162257A (en) * 1965-09-22 1969-08-20 Danippon Pharmaceutical Co Ltd 3-(5-Nitro-2-Furyl) Isoxazole Derivatives and methods of preparation thereof
FR1510315A (fr) * 1966-02-03 1968-01-19 Ciba Geigy Procédé pour la préparation de 4-diaza-cyclo-alcano-pyrazoles substitués en position 1 par des restes hétérocycliques bicycliques
US3452035A (en) * 1966-12-23 1969-06-24 American Cyanamid Co 2 - amino - 5 - (5 - nitro - 1 - substituted-2 - imidazolyl) - 1,3,4 - thiadiazoles and oxadiazoles

Also Published As

Publication number Publication date
NL7018072A (enExample) 1971-07-09
CH555852A (de) 1974-11-15
US3711495A (en) 1973-01-16
FR2081416B1 (enExample) 1974-09-27
ZA707997B (en) 1972-07-26
DE2100242A1 (de) 1971-07-15
GB1316221A (en) 1973-05-09
CA988089A (en) 1976-04-27
JPS511717B1 (enExample) 1976-01-20
FR2081416A1 (enExample) 1971-12-03
OA03554A (fr) 1971-03-30
ZM14570A1 (en) 1972-08-21

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OD Request for examination
D2 Grant after examination
8364 No opposition during term of opposition
8339 Ceased/non-payment of the annual fee