AR037231A1 - Procedimiento para la preparacion de derivados de 4-(imidazol-1-il) bencenosulfonamida e compuestos intermedios para la obtencion de los mismos - Google Patents

Procedimiento para la preparacion de derivados de 4-(imidazol-1-il) bencenosulfonamida e compuestos intermedios para la obtencion de los mismos

Info

Publication number
AR037231A1
AR037231A1 ARP020102972A ARP020102972A AR037231A1 AR 037231 A1 AR037231 A1 AR 037231A1 AR P020102972 A ARP020102972 A AR P020102972A AR P020102972 A ARP020102972 A AR P020102972A AR 037231 A1 AR037231 A1 AR 037231A1
Authority
AR
Argentina
Prior art keywords
alkyl
haloalkyl
aryl
derivatives
cyano
Prior art date
Application number
ARP020102972A
Other languages
English (en)
Inventor
Gonzalez Concepcion Gonzalez
Rosales Carmen Almansa
Original Assignee
Uriach & Cia Sa J
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 Uriach & Cia Sa J filed Critical Uriach & Cia Sa J
Publication of AR037231A1 publication Critical patent/AR037231A1/es

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

Abstract

Procedimiento para la preparación de derivados de 4-(imidazol-1-il) bencenosulfonamida de fórmula (1) con actividad intiinflamatoria, caracterizado porque comprende tratar un compuesto de fórmula (2) con un ácido. Se describe también los intermedios de fórmula (2), (3) y (4) utilizados en la obtención de dichos derivados. En los compuestos de fórmulas (1), (2), (3) y (4), R1 representa arilo o heteroarilo opcionalmente sustituido por uno o más grupos elegidos independientemente de entre halógeno, alquilo C1-8, haloalquilo C1-8, R2O alquilo C0-8, R2S alquilo C0-8, ciano, nitro, -NR2R4, -NR2SO2R3, -SOR3, -SO2R3, -SO2NR2R4 o -CONR2R4; R2 representa hidrógeno, alquilo C1-8 o aril alquilo C0-8 (donde el grupo arilo puede estar opcionalmente sustituido por uno o más grupo elegidos de entre alquilo C1-8, halógeno, haloalquilo C1-8, ciano, nitro, R5O alquilo C0-8, R5S alquilo C0-8, -NR5R6, -NR5COR3, -COR5 o -COOR5); R3 representa un grupo alquilo C1-8 o haloalquilo C1-8; R4 representa hidrógeno, alquilo C1-8, aril alquilo C1-8 (donde el grupo arilo puede estar opcionalmente sustituido por uno o más grupos elegidos de entre alquilo C1-8, halógeno, haloalquilo C1-8, ciano. Nitro, R5O alquilo C0-8, R5S alquilo C0-8, NR5R6, -NR5COR3, -COR5, COOR5), -COR6 o -COOR6; R5 representa hidrógeno, alquilo C1-8 o bencilo; R6 representa alquilo C1-8 o haloalquilo C1-8; arilo representa fenilo o naftilo; y heteroarilo representa piridina, pirazina, pirimidina o piridazina, que pueden estar opcionalmente fusionados a un anillo de benceno; en los compuestos de fórmulas (2), (3) y (4) But representa tert-butilo.
ARP020102972A 2001-08-07 2002-08-06 Procedimiento para la preparacion de derivados de 4-(imidazol-1-il) bencenosulfonamida e compuestos intermedios para la obtencion de los mismos AR037231A1 (es)

Applications Claiming Priority (1)

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.

Publications (1)

Publication Number Publication Date
AR037231A1 true AR037231A1 (es) 2004-11-03

Family

ID=8498662

Family Applications (2)

Application Number Title Priority Date Filing Date
ARP020102972A AR037231A1 (es) 2001-08-07 2002-08-06 Procedimiento para la preparacion de derivados de 4-(imidazol-1-il) bencenosulfonamida e compuestos intermedios para la obtencion de los mismos
ARP120101436A AR086065A2 (es) 2001-08-07 2012-04-25 Compuestos de imidazolsulfonamidas y un proceso para su produccion

Family Applications After (1)

Application Number Title Priority Date Filing Date
ARP120101436A AR086065A2 (es) 2001-08-07 2012-04-25 Compuestos de imidazolsulfonamidas y un proceso para su produccion

Country Status (17)

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

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IN2015DN00202A (es) 2012-07-12 2015-06-12 Chiesi Farma Spa
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.
DE69935913T2 (de) * 1998-07-02 2008-01-10 Cryptography Research Inc., San Francisco Leckresistente aktualisierung eines indexierten kryptographischen schlüssels
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
AR086065A2 (es) 2013-11-13
KR20040020079A (ko) 2004-03-06
ES2184633A1 (es) 2003-04-01
US8476456B2 (en) 2013-07-02
MXPA04001147A (es) 2004-07-08
ES2307817T3 (es) 2008-12-01
JP2005502659A (ja) 2005-01-27
CY1108861T1 (el) 2014-08-13
NO326162B1 (no) 2008-10-13
KR100888905B1 (ko) 2009-03-16
CA2456531A1 (en) 2003-02-27
BR0211749B1 (pt) 2013-09-10
DE60226879D1 (de) 2008-07-10
WO2003016285A8 (es) 2003-08-28
ATE396976T1 (de) 2008-06-15
EP1424329A1 (en) 2004-06-02
WO2003016285A1 (es) 2003-02-27
EP1424329B1 (en) 2008-05-28
US7351836B2 (en) 2008-04-01
BR0211749A (pt) 2004-10-13
US20090012307A1 (en) 2009-01-08
HK1066214A1 (en) 2005-03-18
NO20040981L (no) 2004-03-05
ES2184633B1 (es) 2004-08-01
BRPI0211749B8 (pt) 2021-05-25
DK1424329T3 (da) 2008-09-29
CA2456531C (en) 2010-12-14
JP4309262B2 (ja) 2009-08-05
PT1424329E (pt) 2008-08-06
US20040242872A1 (en) 2004-12-02

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