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PE20080769A1 - Derivados de biaril-sulfonamida - Google Patents

Derivados de biaril-sulfonamida

Info

Publication number
PE20080769A1
PE20080769A1 PE2007001190A PE2007001190A PE20080769A1 PE 20080769 A1 PE20080769 A1 PE 20080769A1 PE 2007001190 A PE2007001190 A PE 2007001190A PE 2007001190 A PE2007001190 A PE 2007001190A PE 20080769 A1 PE20080769 A1 PE 20080769A1
Authority
PE
Peru
Prior art keywords
amino
alkyl
benzen
sulfonyl
biphenyl
Prior art date
Application number
PE2007001190A
Other languages
English (en)
Inventor
Frederic Berst
Frederic Zecri
Philipp Grosche
Philipp Janser
Original Assignee
Novartis 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 Novartis Ag filed Critical Novartis Ag
Publication of PE20080769A1 publication Critical patent/PE20080769A1/es

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    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
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    • C07C311/15—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
    • C07C311/21—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
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    • A61K31/18—Sulfonamides
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    • C07C311/29—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
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    • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
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    • C07D333/52—Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes
    • C07D333/62—Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes 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 carbon atoms of the hetero ring

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Abstract

SE REFIERE A UN COMPUESTO DE FORMULA I DONDE X1, X2, X3, X4, X5, X6 Y X7 SON CADA UNO N, CR6; R6 ES H, HALOGENO, CIANO, OH, ENTRE OTROS; R1 Y R2 SON CADA UNO H, ALQUILO C1-C6, O TOMADOS JUNTOS SON O; R3 ES ALQUILO DE C1-C6, SUSTITUIDO EN CUALQUIER POSICION POR UNO O MAS R3'; R3' ES HIDROXILO, AMINO, ARILO, ARIL-ALQUILO, ENTRE OTROS; R4 ES H, ACILO, ALQUILO C1-C6, Y CUANDO SE ENLAZA CON R3 FORMAN UN ANILLO HETEROCICLICO DE 4 A 7 MIEMBROS; R5 ES ARILO O HETEROARILO SUSTUTUIDO O NO; R10 ES H O ALQUILO C1-C6, ALCOXILO C1-C6, ENTRE OTROS. SON COMPUESTOS PREFERIDOS: ACIDO (S)-3-METIL-2-{[3'-(2,4,5-TRICLORO-BENCEN-SULFONIL-AMINO)-BIFENIL-4-CARBONIL]-AMINO}-BUTIRICO; ACIDO {[3'-(4-CLORO-BENCEN-SULFONIL-AMINO)-BIFENIL-4-CARBONIL]-AMINO}-ACETICO; ACIDO 1-[3'-(4-CLORO-2,5-DIMETIL-BENCEN-SULFONIL-AMINO)-BIFENIL-4-IL-METIL]-AZETIDIN-3-CARBOXILO; ENTRE OTROS. TAMBIEN SE REFIERE A UN PROCEDIMIENTO DE PREPARACION Y COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON MODULADORES DE ESFINGOSINA-1-FOSFATO (S1P), UTILES EN EL TRATAMIENTO DE ENFERMEDADES AUTOINMUNES E HIPERPROLIFERATIVAS
PE2007001190A 2006-09-08 2007-09-06 Derivados de biaril-sulfonamida PE20080769A1 (es)

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