DK1424329T3 - Fremgangsmåde til fremstillingen af 4-(imidazol-1-yl)benzensulfonamid - Google Patents

Fremgangsmåde til fremstillingen af 4-(imidazol-1-yl)benzensulfonamid

Info

Publication number
DK1424329T3
DK1424329T3 DK02794802T DK02794802T DK1424329T3 DK 1424329 T3 DK1424329 T3 DK 1424329T3 DK 02794802 T DK02794802 T DK 02794802T DK 02794802 T DK02794802 T DK 02794802T DK 1424329 T3 DK1424329 T3 DK 1424329T3
Authority
DK
Denmark
Prior art keywords
imidazol
formula
preparation
benzenesulfonamide
chem
Prior art date
Application number
DK02794802T
Other languages
English (en)
Inventor
Gonzalez Concepcion Gonzalez
Rosales Carmen Almansa
Original Assignee
Palau Pharma Sa
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 Palau Pharma Sa filed Critical Palau Pharma Sa
Application granted granted Critical
Publication of DK1424329T3 publication Critical patent/DK1424329T3/da

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic 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
    • C07D233/64Heterocyclic 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 substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C303/00Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
    • C07C303/36Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids
    • C07C303/40Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids by reactions not involving the formation of sulfonamide groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/30Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/37Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
    • C07C311/38Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring having sulfur atoms of sulfonamide groups and amino groups bound to carbon atoms of six-membered rings of the same carbon skeleton
    • C07C311/39Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring having sulfur atoms of sulfonamide groups and amino groups bound to carbon atoms of six-membered rings of the same carbon skeleton having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom
    • C07C311/40Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring having sulfur atoms of sulfonamide groups and amino groups bound to carbon atoms of six-membered rings of the same carbon skeleton having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom to an acyclic carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic 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
    • C07D233/66Heterocyclic 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
    • C07D233/68Halogen atoms
DK02794802T 2001-08-07 2002-08-01 Fremgangsmåde til fremstillingen af 4-(imidazol-1-yl)benzensulfonamid DK1424329T3 (da)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
ES200101853A ES2184633B1 (es) 2001-08-07 2001-08-07 Procedimiento para la preparacion de derivados de 4-(imidazol-1-il) bencenosulfonamida.
PCT/ES2002/000385 WO2003016285A1 (es) 2001-08-07 2002-08-01 Procedimiento para la preparacion de derivados de 4-(imidazol-1-il)bencenosulfonamida

Publications (1)

Publication Number Publication Date
DK1424329T3 true DK1424329T3 (da) 2008-09-29

Family

ID=8498662

Family Applications (1)

Application Number Title Priority Date Filing Date
DK02794802T DK1424329T3 (da) 2001-08-07 2002-08-01 Fremgangsmåde til fremstillingen af 4-(imidazol-1-yl)benzensulfonamid

Country Status (17)

Country Link
US (2) US7351836B2 (da)
EP (1) EP1424329B1 (da)
JP (1) JP4309262B2 (da)
KR (1) KR100888905B1 (da)
AR (2) AR037231A1 (da)
AT (1) ATE396976T1 (da)
BR (1) BRPI0211749B8 (da)
CA (1) CA2456531C (da)
CY (1) CY1108861T1 (da)
DE (1) DE60226879D1 (da)
DK (1) DK1424329T3 (da)
ES (2) ES2184633B1 (da)
HK (1) HK1066214A1 (da)
MX (1) MXPA04001147A (da)
NO (1) NO326162B1 (da)
PT (1) PT1424329E (da)
WO (1) WO2003016285A1 (da)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2872509B1 (en) 2012-07-12 2016-09-14 Chiesi Farmaceutici S.p.A. Inhibition of enzymes
WO2022269384A1 (en) * 2021-06-24 2022-12-29 Ami Organics Ltd. A process for the direct synthesis of fedratinib intermediate

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TNSN99111A1 (fr) * 1998-06-11 2005-11-10 Pfizer Derives de sulfonylbenzene nouveaux, procede pour leur preparation et compositions pharmaceutiques les contenant.
US6539092B1 (en) * 1998-07-02 2003-03-25 Cryptography Research, Inc. Leak-resistant cryptographic indexed key update
AR024222A1 (es) * 1998-10-16 2002-09-25 Palau Pharma Sa Imidazoles con actividad antiinflamatoria un procedimiento para su preparacion y composiciones farmaceuticas que lo contienen
ES2159489B1 (es) * 2000-03-23 2002-04-16 Uriach & Cia Sa J Nuevos derivados de imidazol con actividad antiinflamatoria.

Also Published As

Publication number Publication date
CA2456531A1 (en) 2003-02-27
ES2307817T3 (es) 2008-12-01
WO2003016285A8 (es) 2003-08-28
HK1066214A1 (en) 2005-03-18
US7351836B2 (en) 2008-04-01
AR086065A2 (es) 2013-11-13
ES2184633A1 (es) 2003-04-01
EP1424329B1 (en) 2008-05-28
ATE396976T1 (de) 2008-06-15
DE60226879D1 (de) 2008-07-10
WO2003016285A1 (es) 2003-02-27
NO20040981L (no) 2004-03-05
US8476456B2 (en) 2013-07-02
CY1108861T1 (el) 2014-08-13
BR0211749B1 (pt) 2013-09-10
BR0211749A (pt) 2004-10-13
KR20040020079A (ko) 2004-03-06
JP4309262B2 (ja) 2009-08-05
MXPA04001147A (es) 2004-07-08
JP2005502659A (ja) 2005-01-27
US20090012307A1 (en) 2009-01-08
EP1424329A1 (en) 2004-06-02
NO326162B1 (no) 2008-10-13
ES2184633B1 (es) 2004-08-01
CA2456531C (en) 2010-12-14
BRPI0211749B8 (pt) 2021-05-25
AR037231A1 (es) 2004-11-03
PT1424329E (pt) 2008-08-06
US20040242872A1 (en) 2004-12-02
KR100888905B1 (ko) 2009-03-16

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