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Espirocromanona substituted derivatives as inhibitors of ACC
专利权人:
BANYU PHARMACEUTICAL CO. LTD.
发明人:
TONOHARU IINO,HIDEKI JONA,JUN SHIBATA,TADASHI SHIMAMURA,TAKERU YAMAKAWA,LIHU YANG
申请号:
HN2009001276
公开号:
HN2009001276A
申请日:
2009.07.06
申请国别(地区):
HN
年份:
2012
代理人:
摘要:
THIS INVENTION REFERS TO ITS FORMULA (SEE APPLICATION). IN WHICH AR1 REPRESENTS A GROUP FORMED FROM AN AROMATIC RING SELECTED FROM THE GROUP CONSTITUTED BY INDOL, 1H-INDAZOL, 2H-INDAZOL, 1H-TIENO [2,3-C] PIRAZOL, 1H-PIRAZOLO [3,4-B ] PIRIDINA, VENZO [B] FURANO, BENZIMIDAZOL, BENZOXAZOL, 1,2-BENZISOXAZOL AND IMIDAZO [1,2-A] PIRIDINA; R1 AND R2 REPRESENT EACH ONE A HYDROGEN TOMATO, A HALOGEN TYPE, A CIANO GROUP, A C2-C6 ALQUENIL GROUP A C1-C6 ALCOXI GROUP, A C1-C6 HALOALCOXY GROUP, A C3-C3 GROUP , A C2-C7 ALCANOYLL GROUP, A C2-C7 HALOALCANOYL GROUP, A C2-C7 ALCOXICARBONYL GROUP, A C2-C7 HALOALCOXICARBONYL GROUP, A C3-C6 CYCLOALCOXICARBONYL GROUP,UN GRUPO ARALQUILOXICARBONILO UN GRUPO CARBAMOILALCOXI C1 -C6 UN GRUPO CARBOXIALQUENILO C2 -C6 O UN GRUPO DE -Q1-N (RA) -Q2-RB UN GRUPO ALQUILO C1 -C6 ARILO O HETEROARILO OPCIONALMENTE SUSTITUIDO O UN GRUPO ALQUILO C1 -C6 O ALQUENILO C3-C6 CYCALALKYL C3-C6-C6-C6-C6-C6-C6-C6-C6-C6-C6-C6-C6-C6-C6-C6-C6-C6-C6-C6-C6-C6-C6-C6-C6-C6-C6-C6-C6-C6-C6-C6-C6-C6-C6 OR A C1-C6 RENT GROUP, OPTIONALLY REPLACED; T AND U REPRESENT EACH ONE A NITRENE GENE OR A METINO GROUP; AND V REPRESENTS A OMTOMO DE OXIGENO OR A OMTOMO DE SULFRE. THE COMPOUND OF THE INVENTION IS USEFUL AS A THERAPEUTIC AGENT FOR DIFFERENT DISEASES RELATED TO ACC.ESTA INVENCION SE REFIERE A SU FORMULA (VER SOLICITUD) . EN LA QUE AR1 REPRESENTA UN GRUPO FORMADO DESDE UN ANILLO AROM�TICO SELECCIONADO DEL GRUPO CONSTITUIDO POR INDOL, 1H-INDAZOL, 2H-INDAZOL, 1H-TIENO [2,3-C]PIRAZOL, 1H-PIRAZOLO[3,4-B]PIRIDINA, VENZO[B]FURANO, BENZIMIDAZOL, BENZOXAZOL, 1,2-BENZISOXAZOL E IMIDAZO [1,2-A]PIRIDINA; R1 Y R2 REPRESENTAN CADA UNO UN �TOMO DE HIDROGENO, UN �TOMO DE HAL�GENO, UN GRUPO CIANO, UN GRUPO ALQUENILO C2 -C6 UN GRUPO ALCOXI C1 -C6, UN GRUPO HALOALCOXI C1 -C6,UN GRUPO CICLOALQUILOXI C3 -C6, UN GRUPO ALCANOILO C2-C7, UN GRUPO HALOALCANOILO C2-C7, UN ALCOXICARBONILO C2-C7, UN GRUPO HALOALCOXICARBONILO C2-C7, UN GRUPO CICLOALCOXICARBONILO C3 -C6, UN GRUPO ARALQUILOXICARBONILO, UN G
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