首页> 外国专利> Imidazo 4,5-c quinolin-1 - 4 - amines and tetrahidroimidazo 4,5-c quinolin-1 - 4 - amines, Pharmaceutical compositions that include the use of such compounds in preparation of Medicines and Intermediates useful in the synthesis of such compounds

Imidazo 4,5-c quinolin-1 - 4 - amines and tetrahidroimidazo 4,5-c quinolin-1 - 4 - amines, Pharmaceutical compositions that include the use of such compounds in preparation of Medicines and Intermediates useful in the synthesis of such compounds

机译:咪唑并[4,5-c]喹啉1-4-胺和四氢咪唑并[4,5-c]喹啉1-4-胺,药物组合物,包括将这些化合物用于制备可用于药物治疗的药物和中间体这类化合物的合成

摘要

Imidazo [4,5-c] quinolin-1 - 4 - amines and tetrahidroimidazo [4,5-c] quinolin-1 - 4 - amines of formula (1), in which the links are represented by dotted lines are present or Absent, X is - chr5 chr5 alkyl -, -, - or - chr5 alquenilo; r1 is selected the Group consists of Cr3 - Z - R6 R4 - alkyl R4, R6 z Cr3 - - - - - - alquenilo Cr3, R4 Z - R6 R4 - aryl, heteroaryl Cr3 - Z - R6 R4, R6 z Cr3 - - - - heterociclilo,R4 - Cr3 - Z - H, - - - nr7 Cr3 R4 R6 alkyl R4, R6 nr7 Cr3 - - - - - - alquenilo R4, R6 nr7 Cr3 - aryl - - - - nr7 Cr3, R4 R6 R4 - heteroaryl, nr7 Cr3 - - - - - heterociclilo R4 R6, and nr7 - Cr3 - R8; each is independently NR5 - Z -, - O -, - S -; R2 is selected from the group consisting of hydrogen, alkyl, aryl, alquenilo, heteroari So, heterociclilo, alkyl and alkyl, alkyl and alkyl aryl - and alquenilo,,And alquenilo alkyl or substituted with one or more substituents selected from the group consisting of oh Halogen (R5), N, n 2, CO 2, CO (R5) C1 - 10 co alkyl, o-alkyl C1 - 10, N3, aryl, heteroaryl, aryl heterociclilo, co, and CO - heteroaryl; each is R3 = r4 = o or s; each is independently alkyl Or alquenilo,That can be interrupted by one or More groups or R5; each is independently H or alkyl of C1 - 10; R6 is a Link, alkyl, or alquenilo, which can be interrupted by one or More groups - or - C1; R7 is H, alkyl - 10Or arylalkyl or R4 and R7 can be United to form a Ring; R8 is H or alkyl of C1 - 10; and R7 and R8 may join together to form a ring, and each is independently - or or - S (o) 0 - 2 -; n is 0 to 4 and each R is present; independently selected from the group consisting of alkyl C1 - 10, Lac Oxy Hydroxy, halogen C1 - 10, and pharmaceutically acceptable Salts triflu00faormetilo; or the same.These compounds are useful as immune response modifiers. These compounds can induce the biosynthesis of several cytokines and are useful in the treatment of a variety of disorders including Viral Diseases and neoplastic diseases.Also disclosed are Pharmaceutical compositions that include the use of such compounds in preparation of Medicines and Intermediates useful in the synthesis of such compounds.
机译:式(1)的咪唑并[4,5-c]喹啉-1-胺和四氢咪唑并[4,5-c]喹啉1-4-胺,其中连接用虚线表示或不使用虚线表示X是-chr5 chr5烷基-,-,-或-chr5 Alquenilo;选择r1的基团为Cr3-Z-R6 R4-烷基R4,R6 z Cr3------Alquenilo Cr3,R4 Z-R6 R4-芳基,杂芳基Cr3-Z-R6 R4,R6 z Cr3-- --杂亚基,R4-Cr3-Z-H,---nr7 Cr3 R4 R6烷基R4,R6 nr7 Cr3-----Alquenilo R4,R6 nr7 Cr3-芳基----nr7 Cr3,R4 R6 R4-杂芳基,nr7 Cr3-----杂环基R4 R6和nr7-Cr3-R8;各自独立地为NR5-Z-,-O-,-S-; R 2选自氢,烷基,芳基,alquenilo,杂芳基。因此,杂环基,烷基和烷基,烷基和烷基芳基-和alquenilo,和alquenilo烷基或被一个或多个选自以下的取代基取代:卤素(R 5),N,n 2,CO 2,CO(R 5)C 1-10烷基,邻烷基C 1-10,N 3,芳基,杂芳基,芳基杂环,co和CO-杂芳基;每个是R3 = r4 = o或s;各自独立地为烷基或alquenilo,可以被一个或多个基团或R5打断;各自独立地为H或C 1-10的烷基; R6是一个Link,烷基或alquenilo,可以被一个或多个基团-或-C1打断; R7是H,烷基-10或芳烷基或R4和R7可以结合形成环; R8是H或C1-10的烷基; R7和R8可以连接在一起形成环,并且各自独立地为-或-或-S(o)0-2-; n为0至4,并且每个R存在;独立地选自烷基C 1-10,Lac Oxy Hydroxy,卤素C 1-10和药学上可接受的盐trifl u00metorilo。这些化合物可用作免疫反应调节剂。这些化合物可以诱导多种细胞因子的生物合成,并且可以用于治疗包括病毒性疾病和肿瘤性疾病在内的多种疾病。还公开了药物组合物,其包括将这些化合物用于制备可用于合成药物的药物和中间体。这样的化合物。

著录项

  • 公开/公告号AR035664A1

    专利类型

  • 公开/公告日2004-06-23

    原文格式PDF

  • 申请/专利权人 3M INNOVATIVE PROPERTIES COMPANY;

    申请/专利号AR2001P105726

  • 发明设计人

    申请日2001-12-10

  • 分类号C07D471/04;A61K31/421;A61K31/435;A61K31/437;A61P35/00;A61P31/12;C07D471/04;C07D235/00;C07D221/00;

  • 国家 AR

  • 入库时间 2022-08-21 23:12:26

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