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Similar deamidas heteroarilicas as antagonists of P2X7

机译:类似的杂食性拟螺螺作为P2X7的拮抗剂

摘要

Or a pharmaceutically acceptable Salt thereof, wherein: T, u and V are selected independently between Cr3, CRA and N, such that (i) exactly one T, u and V is CRA; and (ii) IF x is CH2 and phenyl, and u and V are both carbons replaced then t is n; W - C (= o) - NR4.- nr4c (= o) - or NR4 NR4 - C (= o) - X is absent or is alquileno C1 - C6 is replaced with 0 to 4 substituents chosen independently between: (i) c1-c4 alkyl,(cycloalkyl alkyl C0 - C1 - C2 and C8) fenilalquilo C0 C2; (ii) substituents are taken together to form a ring heterocicloalquilo cycloalkyl or 3 to 7 members; and (iii) substituents are taken together to form a heterocicloalquilo R4 4 - to 7 - is cicloalqu members; and ILO - C16 heterocicloalquilo C3, 4 - 16 - member6 - to 16 - aryl or heteroaryl - member of 5 to 16 members, each of whom is replaced with 0 to 6 chosen independently between hydroxy substituents, halogen, Nitro, cyano, amino, Oxo, aminocarbonilo, aminosulfonilo alquiloc1, COOH, - C2 - C6, alquenilo alquinilo C2 - C6 c6a, haloalqu ILO - C6 C1 - C6, hidroxialquiloc1, aminoalquilo C1 - C6, alcoxic1 - haloalcoxic1 - C6 C6C2 - C6 alkyl ether, alcanoilo C1 - C6, alquilsulfoniloc1 - (C3 - C7 C6, cycloalkyl) alkyl C0 C4 -, mono - or di - (alquilc1 - C6) alcanoilamino C1 - C6 amino, mono - or di - (alquilc1 - C6) aminocarbonilo, mono or di (alquilc1 - C6) aminosulfonilo and (alquilc1 - C6) sulfonylamino; Z1 and Z3 N or CR2 are independently; Z2 is n, CR2 or CRA; each R2 and R3 are each independently selected from Hydrogen, halogen, a cyano,Aminocarbonilo, amino, Nitro, aminosulfonilo, COOH, c1-c6 alkyl, alquenilo C2 - C6, alquinilo C2 - C6, haloalquilo C1 - C6, hidroxialquilo c1-c6 alkoxy, aminoalquilo C1 - C6 C1 - C6, haloalcoxi C1 - C6, alcanoilo C1 - C2 - C6 C6 alkyl ether, (cicloalquilc3 - C7) C0 C4 alkyl -, mono - or di - (alquilc1 - C6 amino alkyd) Ilsulfonilo C1 - C6, alcanoilamino C1 - C6, mono - or di - (alquilc1 - C6) aminocarbonilo,Mono - or di - (alquilc1 - aminosulfonilo (C6) and alquilc1 sulfonylamino - C6) each independently; R4 is Hydrogen, alkyl (C1 - C6, C8 alkyl - cicloalquilc3) C0 C2...
机译:或其药学上可接受的盐,其中:T,u和V独立地选自Cr 3,CRA和N,使得(i)恰好一个T,u和V为CRA; (ii)如果x是CH 2和苯基,并且u和V都被碳取代,则t是n;和W-C(= o)-NR4.- nr4c(= o)-或NR4 NR4-C(= o)-X不存在或被Alquileno C1-C6替换为0至4个在以下之间独立选择的取代基:(i) C 1 -C 4烷基,(环烷基烷基C 0 -C 1 -C 2和C 8)苯丙醇基C 0 C 2; (ii)取代基一起形成环杂环烷基或3至7个成员; (iii)取代基一起形成异环基的R4 4至7-是环基的成员;和ILO-C16杂环氯基C3,4-16-成员6--16-芳基或杂芳基-成员5-16,其中每个被0-6取代,其独立地选自羟基取代基,卤素,硝基,氰基,氨基,羰基,氨基羰基,氨基磺基alquiloc1,COOH--C2-C6,alquenilo alquinilo C2-C6 c6a,卤代allo ILO-C6 C1-C6,hidroxialquiloc1,氨基代alquilo C1-C6,醇解1-卤代烷氧基1-C6 C6C2- C6,链烷磺酰基1-(C3-C7 C6,环烷基)烷基C0-C4-,单-或二-(alquilc1-C6)链烷醇氨基C1-C6氨基,单-或双-(alquilc1-C6)氨基羰基,单或二(alquilc1 -C6)氨基磺酰基和(alquilc1-C6)磺酰基氨基; Z 1和Z 3 N或CR 2独立地; Z2为n,CR2或CRA;每个R 2和R 3各自独立地选自氢,卤素,氰基,氨基羰基,氨基,硝基,氨基磺酰基,COOH,c1-c6烷基,alquenilo C2-C6,alquinilo C2-C6,卤代alquilo C1-C6,hidroxialquilo c1-c6烷氧基,氨基芳基C1-C6 C1-C6,卤代醇C1-C6,阿尔卡诺基C1-C2-C6 C6烷基醚,(cicloalquilc3-C7)C0 C4烷基-,单-或二-(alquilc1-C6氨基醇酸)异磺酰基C1- C6,链烷醇氨基C1-C6,单-或二-(alquilc1-C6)氨基羰基,单-或二-(alquilc1-氨基磺酰基(C6)和alquilc1-磺酰基氨基-C6)各自; R4为氢,烷基(C1-C6,C8烷基-环氯基3)C0 C2 ...

著录项

  • 公开/公告号CO6241110A2

    专利类型

  • 公开/公告日2011-01-20

    原文格式PDF

  • 申请/专利权人 H.LUNDBECK A/S;

    申请/专利号CO20090127786

  • 申请日2009-11-10

  • 分类号A61K31/437;A61P25;A61P29;C07D471/04;

  • 国家 CO

  • 入库时间 2022-08-21 18:06:57

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