摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

[3-[5-(3-morpholin-4-ylphenoxy)pyridin-2-yl]amino]phenol | 1139717-74-0

中文名称
——
中文别名
——
英文名称
[3-[5-(3-morpholin-4-ylphenoxy)pyridin-2-yl]amino]phenol
英文别名
3-[[5-(3-Morpholin-4-ylphenoxy)pyridin-2-yl]amino]phenol
[3-[5-(3-morpholin-4-ylphenoxy)pyridin-2-yl]amino]phenol化学式
CAS
1139717-74-0
化学式
C21H21N3O3
mdl
——
分子量
363.416
InChiKey
SYYGNZMUCJGRGQ-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    3.7
  • 重原子数:
    27
  • 可旋转键数:
    5
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.19
  • 拓扑面积:
    66.8
  • 氢给体数:
    2
  • 氢受体数:
    6

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    (3-benzyloxyphenyl)-[5-(3-morpholin-4-ylphenoxy)pyridin-2-yl]-amine 在 20% palladium hydroxide on carbon 1,4-环己二烯 作用下, 以 乙酸乙酯 为溶剂, 反应 1.0h, 以29%的产率得到[3-[5-(3-morpholin-4-ylphenoxy)pyridin-2-yl]amino]phenol
    参考文献:
    名称:
    PYRIDINE DERIVATIVES FOR THE TREATMENT OF AMYLOID-RELATED DISEASES
    摘要:
    该化合物的结构式(I)或其药用可接受的盐或前药:其中X和Y分别独立为NR5或O;W和Z分别独立为键或(CH2)mCH(R7)(CH2)n;m=0-1,n=0-2;R为氢或卤素;R1和R2分别选自氢卤素,CF3,CN,OR8,NR9R10,NR9COR11,NR9SO2R11或C1-6烷基,可选择地被羟基,C1-6烷氧基或NR9R10取代;R3为氢,卤素,CF3,CN,OR8,SR8或SO2R11;R4为氢,卤素,CF3,OR9,NR9R10,NR9COR11,NR9SO2R11或C1-6烷基,可选择地被羟基,C1-6烷氧基或NR9R10取代;R5为氢或C1-6烷基,可选择地被羟基,C1-6烷氧基或NR9R10取代;R6为氢,氟,C1-6烷基或C1-6烷氧基;R7为氢,C1-6烷基,苯基或C1-3烷基苯基,其中所述苯基可选择地被一个或多个取代基取代,所述取代基选自卤素,C1-6烷基,CF3,OCF3或OR9;R8为氢或C1-6烷基,可选择地被氟,C1-6烷氧基或NR9R10取代;R9为氢,C1-6烷基或C1-3烷基苯基,其中所述苯基可选择地被一个或多个取代基取代,所述取代基选自卤素,C1-6烷基,CF3,OR8,NR9R10或OCF3;R10为氢,C1-6烷基,C1-6烯基,苯基或C1-3烷基苯基,其中所述苯基可选择地被一个或多个取代基取代,所述取代基选自卤素,C1-6烷基,CF3,OR8或OCF3;或当连接到氮原子时,R9和R10组合可形成一个可选择地含有来自NR9,S和O的进一步杂原子的5-或6-成员环;R11为C1-6烷基或一个苯基,可选择地被一个或多个取代基取代,所述取代基选自卤素,C1-6烷基,CF3,OCF3或OR8。这些化合物在治疗与淀粉样蛋白相关的疾病中很有用。
    公开号:
    US20100298325A1
点击查看最新优质反应信息

文献信息

  • [EN] PYRIDINE DERIVATIVES FOR THE TREATMENT OF AMYLOID-RELATED DISEASES<br/>[FR] DÉRIVÉS DE PYRIDINE POUR LE TRAITEMENT DE MALADIES SE RAPPORTANT AUX AMYLOÏDES
    申请人:SENEXIS LTD
    公开号:WO2009044160A1
    公开(公告)日:2009-04-09
    a compound of formula (I) or a pharmaceutically acceptable salt or prodrug thereof: wherein X and Y are independently NR5 or O; W and Z are independently a bond or (CH2)mCH(R7)(CH2)n; m = 0-1, n = 0-2; R is hydrogen or halogen; R1 and R2 are independently selected from hydrogen, halogen, CF3, CN, OR8, NR9R10, NR9COR11, NR9SO2R11 or C1-6 alkyl optionally substituted by hydroxyl, C1-6 alkoxy or NR9R10; R3 is hydrogen, halogen, CF3, CN, OR8, SR8 or SO2R 11.; R4 is hydrogen, halogen, CF3, OR9, NR9R10, NR9COR11, NR9SO2R11 or C1-6 alkyl optionally substituted by hydroxyl, C1-6 alkoxy or NR9R10; R5 is hydrogen or C1-6 alkyl optionally substituted by hydroxyl, C1-6 alkoxy or NR9R10;R6 is hydrogen, fluorine, C1-6 alkyl, or C1-6 alkoxy; R6 is hydrogen, fluorine, C1-6 alkyl, or C1-6 alkoxy; R7 is hydrogen, C1-6 alkyl, phenyl or C1-3 alkylphenyl wherein said phenyl groups are optionally substituted by one or more substituents selected from halogen, C1-6 alkyl, CF3, OCF3 or OR9; R8 is hydrogen or C1-6 alkyl optionally substituted by fluorine, C1-6 alkoxy or NR9R10; R9 is hydrogen, C1-6 alkyl or C1-3 alkylphenyl wherein said phenyl group is optionally substituted by one or more substituents selected from halogen, C1-6 alkyl, CF3, OR8, NR9R10Or OCF3; R10 is hydrogen, C1-6 alkyl, C1-6 alkenyl, phenyl or C1-3 alkylphenyl wherein said phenyl groups are optionally substituted by one or more substituents selected from halogen, C1-6 alkyl, CF3, OR8 or OCF3; or the groups R9 and R10 when they are attached to a nitrogen atom may together form a 5- or 6-membered ring which optionally contains one further heteroatom selected from NR9, S and O; and R11 is C1-6 alkyl or a phenyl group optionally substituted by one or more substituents selected from halogen, C1-6 alkyl, CF3, OCF3 or OR8 is provided. The compounds are useful in treating amyloid related diseases.
  • PYRIDINE DERIVATIVES FOR THE TREATMENT OF AMYLOID-RELATED DISEASES
    申请人:Scopes David Ian Carter
    公开号:US20100298325A1
    公开(公告)日:2010-11-25
    a compound of formula (I) or a pharmaceutically acceptable salt or prodrug thereof: wherein X and Y are independently NR 5 or O; W and Z are independently a bond or (CH2)mCH(R7)(CH2)n; m=0-1, n=0-2; R is hydrogen or halogen; R 1 and R 2 are independently selected from hydrogen halogen, CF 3 , CN, OR 8 , NR 9 R 10 , NR 9 COR 11 , NR 9 SO 2 R 11 or C 1-6 alkyl optionally substituted by hydroxyl, C 1-6 alkoxy or NR 9 R 10 ; R 3 is hydrogen, halogen, CF 3 , CN, OR 8 , SR 8 or SO 2 R 11 ; R 4 is hydrogen, halogen, CF 3 , OR 9 , NR 9 R 10 , NR 9 COR 11 , NR 9 SO 2 R 11 or C 1-6 alkyl optionally substituted by hydroxyl, C 1-6 alkoxy or NR 9 R 10 ; R 5 is hydrogen or C 1-6 alkyl optionally substituted by hydroxyl, C 1-6 alkoxy or NR 9 R 10 ; R6 is hydrogen, fluorine, C1-6 alkyl, or C1-6 alkoxy; R 6 is hydrogen, fluorine, C 1-6 alkyl, or C 1-6 alkoxy; R 7 is hydrogen, C 1-6 alkyl, phenyl or C 1-3 alkylphenyl wherein said phenyl groups are optionally substituted by one or more substituents selected from halogen, C 1-6 alkyl, CF 3 , OCF 3 or OR 9 ; R 8 is hydrogen or C 1-6 alkyl optionally substituted by fluorine, C 1-6 alkoxy or NR 9 R 10 , R 9 is hydrogen, C 1-6 alkyl or C 1-3 alkylphenyl wherein said phenyl group is optionally substituted by one or more substituents selected from halogen, C 1-6 alkyl, CF 3 , OR 8 , NR 9 R 10 Or OCF 3 ; R 10 is hydrogen, C 1-6 alkyl, C 1-6 alkenyl, phenyl or C 1-3 alkylphenyl wherein said phenyl groups are optionally substituted by one or more substituents selected from halogen, C 1-6 alkyl, CF 3 , OR 8 or OCF 3 ; or the groups R 9 and R 10 when they are attached to a nitrogen atom may together form a 5- or 6-membered ring which optionally contains one further heteroatom selected from NR 9 , S and O; and R 11 is C 1-6 alkyl or a phenyl group optionally substituted by one or more substituents selected from halogen, C 1-6 alkyl, CF 3 , OCF 3 or OR 8 is provided. The compounds are useful in treating amyloid related diseases.
    该化合物的结构式(I)或其药用可接受的盐或前药:其中X和Y分别独立为NR5或O;W和Z分别独立为键或(CH2)mCH(R7)(CH2)n;m=0-1,n=0-2;R为氢或卤素;R1和R2分别选自氢卤素,CF3,CN,OR8,NR9R10,NR9COR11,NR9SO2R11或C1-6烷基,可选择地被羟基,C1-6烷氧基或NR9R10取代;R3为氢,卤素,CF3,CN,OR8,SR8或SO2R11;R4为氢,卤素,CF3,OR9,NR9R10,NR9COR11,NR9SO2R11或C1-6烷基,可选择地被羟基,C1-6烷氧基或NR9R10取代;R5为氢或C1-6烷基,可选择地被羟基,C1-6烷氧基或NR9R10取代;R6为氢,氟,C1-6烷基或C1-6烷氧基;R7为氢,C1-6烷基,苯基或C1-3烷基苯基,其中所述苯基可选择地被一个或多个取代基取代,所述取代基选自卤素,C1-6烷基,CF3,OCF3或OR9;R8为氢或C1-6烷基,可选择地被氟,C1-6烷氧基或NR9R10取代;R9为氢,C1-6烷基或C1-3烷基苯基,其中所述苯基可选择地被一个或多个取代基取代,所述取代基选自卤素,C1-6烷基,CF3,OR8,NR9R10或OCF3;R10为氢,C1-6烷基,C1-6烯基,苯基或C1-3烷基苯基,其中所述苯基可选择地被一个或多个取代基取代,所述取代基选自卤素,C1-6烷基,CF3,OR8或OCF3;或当连接到氮原子时,R9和R10组合可形成一个可选择地含有来自NR9,S和O的进一步杂原子的5-或6-成员环;R11为C1-6烷基或一个苯基,可选择地被一个或多个取代基取代,所述取代基选自卤素,C1-6烷基,CF3,OCF3或OR8。这些化合物在治疗与淀粉样蛋白相关的疾病中很有用。
查看更多

同类化合物

(4-甲基环戊-1-烯-1-基)(吗啉-4-基)甲酮 (2-肟基-氰基乙酸乙酯)-N,N-二甲基-吗啉基脲六氟磷酸酯 鲸蜡基乙基吗啉氮鎓乙基硫酸盐 马啉乙磺酸钾 预分散OTOS-80 顺式4-(氮杂环丁烷-3-基)-2,2-二甲基吗啉 顺式-N-亚硝基-2,6-二甲基吗啉 顺式-3,5-二甲基吗啉 顺-2,6-二甲基-4-(4-硝基苯基)吗啉 非屈酯 雷奈佐利二聚体 阿瑞杂质9 阿瑞吡坦磷的二卞酯 阿瑞吡坦杂质 阿瑞吡坦杂质 阿瑞吡坦 阿瑞吡坦 阿瑞匹坦非对映异构体2R3R1R 阿瑞匹坦杂质A异构体 阿瑞匹坦杂质54 阿瑞匹坦-M3代谢物 钾[2 - (吗啉- 4 -基)乙氧基]甲基三氟硼酸 邻苯二甲酸单吗啉 调节安 试剂2-(4-Morpholino)ethyl2-bromoisobutyrate 茂硫磷 苯甲腈,2-(4-吗啉基)-5-[1,4,5,6-四氢-4-(羟甲基)-6-羰基-3-哒嗪基]- 苯甲曲秦 苯甲吗啉酮 苯基2-(2-苯基吗啉-4-基)乙基碳酸酯盐酸盐 苯二甲吗啉一氢酒石酸盐 苯二甲吗啉 苯乙酮 O-(吗啉基羰基甲基)肟 芬美曲秦 芬布酯盐酸盐 芬布酯 脾脏酪氨酸激酶(SYK)抑制剂 脱氯利伐沙班 脱氟雷奈佐利 羟基1-(3-氯苯基)-2-[(1,1-二甲基乙基)氨基]-1-丙酮盐酸盐 福沙匹坦苄酯 福沙匹坦杂质26 福曲他明 碘化N-甲基丙基吗啉 碘化N-甲基,乙基吗啉 硝酸吗啉 盐酸吗啡啉-D8 甲基吗啉-2-羧酸甲酯2,2,2-三氟乙酸盐 甲基N-[3-(乙酰基氨基)-4-[(2-氰基-4,6-二硝基苯基)偶氮]苯基]-N-乙基-&#x3B2-丙氨酸酸酯 甲基4-吗啉二硫代甲酸酯