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GB1030756A - Anti-inflammatory compositions comprising biphenylyl-alkane derivatives - Google Patents

Anti-inflammatory compositions comprising biphenylyl-alkane derivatives

Info

Publication number
GB1030756A
GB1030756A GB1284863A GB1284863A GB1030756A GB 1030756 A GB1030756 A GB 1030756A GB 1284863 A GB1284863 A GB 1284863A GB 1284863 A GB1284863 A GB 1284863A GB 1030756 A GB1030756 A GB 1030756A
Authority
GB
United Kingdom
Prior art keywords
biphenylyl
methyl
cooh
group
ch2oh
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
GB1284863A
Inventor
John Stuart Nicholson
Hugh Colin Richards
Stewart Sander Adams
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.)
Boots Pure Drug Co Ltd
Original Assignee
Boots Pure Drug Co Ltd
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 Boots Pure Drug Co Ltd filed Critical Boots Pure Drug Co Ltd
Priority to GB1284863A priority Critical patent/GB1030756A/en
Publication of GB1030756A publication Critical patent/GB1030756A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C59/00Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
    • C07C59/40Unsaturated compounds
    • C07C59/58Unsaturated compounds containing ether groups, groups, groups, or groups
    • C07C59/64Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/132Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group
    • C07C29/136Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH
    • C07C29/147Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of carboxylic acids or derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C33/00Unsaturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
    • C07C33/18Monohydroxylic alcohols containing only six-membered aromatic rings as cyclic part
    • C07C33/24Monohydroxylic alcohols containing only six-membered aromatic rings as cyclic part polycyclic without condensed ring systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C33/00Unsaturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
    • C07C33/26Polyhydroxylic alcohols containing only six-membered aromatic rings as cyclic part
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C57/00Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
    • C07C57/30Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms containing six-membered aromatic rings
    • C07C57/34Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms containing six-membered aromatic rings containing more than one carboxyl group
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C57/00Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
    • C07C57/30Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms containing six-membered aromatic rings
    • C07C57/38Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms containing six-membered aromatic rings polycyclic
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C57/00Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
    • C07C57/52Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms containing halogen
    • C07C57/58Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms containing halogen containing six-membered aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C57/00Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
    • C07C57/64Acyl halides

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)

Abstract

The invention comprises the compounds: 4-biphenylyl-a -chloracetic acid and its ethyl ester; 4-biphenylyl-a -methoxyacetic acid; 2-41-biphenylyl -propan - 1,3 - diol; 2 - 41 - biphenylyl -propanol; and 2 - 41 - biphenylyl - malonic acid and its 2-methyl derivative and its diethyl ester; and processes for preparing them. Biphenylyl intermediates obtained are: ethyl 4 - biphenylyl - a - methoxy - acetate; and 2 - (41 - biphenylyl) - 2 - methyl - malonic acid diethyl ester.ALSO:Analgesic, anti-inflammatory and anti-pyretic compositions comprise a carrier and a compound of the general formula <FORM:1030756/A5-A6/1> wherein R represents the group-CR1R2R2 wherein R1 is H or C1-4 alkyl and R2 represents -CH2OH, -COOR1, COOM or COOH.B wherein R1 is H or C1-4 alkyl optionally substituted with an amino or dialkylamino group, M is ammonium or a single equivalent of a non-toxic cation and B is a non-toxic organic base or R represents the group A-X wherein A represents -CH2-CH2-CH(CH3)- or -CHR\yM- wherein R3 is halogen, C1-4 alkoxy, methyl or C2-3 alkenyl and X represents COOR1, COOH.B, COOM, CH2OH or CONH2 provided that X is not COOH when R3 is methyl. They may be in conventional forms suitable for oral, parenteral and topical administration.
GB1284863A 1963-04-01 1963-04-01 Anti-inflammatory compositions comprising biphenylyl-alkane derivatives Expired GB1030756A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1284863A GB1030756A (en) 1963-04-01 1963-04-01 Anti-inflammatory compositions comprising biphenylyl-alkane derivatives

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1284863A GB1030756A (en) 1963-04-01 1963-04-01 Anti-inflammatory compositions comprising biphenylyl-alkane derivatives

Publications (1)

Publication Number Publication Date
GB1030756A true GB1030756A (en) 1966-05-25

Family

ID=10012252

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1284863A Expired GB1030756A (en) 1963-04-01 1963-04-01 Anti-inflammatory compositions comprising biphenylyl-alkane derivatives

Country Status (1)

Country Link
GB (1) GB1030756A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0020230A2 (en) * 1979-05-21 1980-12-10 Pierre Fabre S.A. p-Biphenyl-4-methyl-2-butenoic acids, process for their preparation, pharmaceutical compositions containing them and their use
WO2007020381A3 (en) * 2005-08-15 2007-05-03 Syngenta Participations Ag Process for the synthesis of mandipropamid and derivatives thereof

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0020230A2 (en) * 1979-05-21 1980-12-10 Pierre Fabre S.A. p-Biphenyl-4-methyl-2-butenoic acids, process for their preparation, pharmaceutical compositions containing them and their use
FR2457275A1 (en) * 1979-05-21 1980-12-19 Fabre Sa Pierre P-BIPHENYL-4 METHYL-2 BUTEN-3 OIC ACIDS USEFUL IN THE TREATMENT OF RHUMATISMS
EP0020230A3 (en) * 1979-05-21 1981-01-07 Pierre Fabre S.A. P-biphenyl-4-methyl-2-butenoic acids, process for their preparation, pharmaceutical compositions containing them and their use
WO2007020381A3 (en) * 2005-08-15 2007-05-03 Syngenta Participations Ag Process for the synthesis of mandipropamid and derivatives thereof
US8129560B2 (en) 2005-08-15 2012-03-06 Syngenta Crop Protection, Inc. Process for the synthesis of mandipropamid and derivatives thereof
TWI399363B (en) * 2005-08-15 2013-06-21 Syngenta Participations Ag Process
KR101305928B1 (en) * 2005-08-15 2013-09-12 신젠타 파티서페이션즈 아게 Process for the synthesis of mandipropamid and derivatives thereof

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