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

5-(4-fluorophenyl)-4-(4-methylthiophenyl)-1-(1-methyl-1-ethoxymethyl)-1H-imidazole | 177755-42-9

中文名称
——
中文别名
——
英文名称
5-(4-fluorophenyl)-4-(4-methylthiophenyl)-1-(1-methyl-1-ethoxymethyl)-1H-imidazole
英文别名
1-(1-ethoxyethyl)-5-(4-fluorophenyl)-4-(4-methylsulfanylphenyl)imidazole
5-(4-fluorophenyl)-4-(4-methylthiophenyl)-1-(1-methyl-1-ethoxymethyl)-1H-imidazole化学式
CAS
177755-42-9
化学式
C20H21FN2OS
mdl
——
分子量
356.464
InChiKey
AENKGAZZFWIBPM-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):
    4.6
  • 重原子数:
    25
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    52.4
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Benzenesulfonamide subtituted imidazolyl compounds for the treatment of
    摘要:
    描述了一类咪唑基化合物,用于治疗炎症和与炎症相关的疾病。特别感兴趣的化合物由式II定义,其中R.sup.1从较低的烷基、较低的卤代烷基、较低的羟基烷基、较低的芳基烯基、较低的芳氧基烷基、较低的芳硫基烷基和杂芳基中选择;其中R.sup.3从较低的烷基和氨基中选择;其中R.sup.4是从氢化物、卤素、较低的烷基和较低的烷氧基中选择的一个或多个基团;或者R.sup.4与苯基一起形成萘基或苯二氧杂基;在R.sup.3为甲基且R.sup.4为氢化物、甲基、甲氧基或氯时,提供R.sup.1不是较低烷基;或其药用盐。
    公开号:
    US05620999A1
  • 作为产物:
    参考文献:
    名称:
    Benzenesulfonamide subtituted imidazolyl compounds for the treatment of
    摘要:
    描述了一类咪唑基化合物,用于治疗炎症和与炎症相关的疾病。特别感兴趣的化合物由式II定义,其中R.sup.1从较低的烷基、较低的卤代烷基、较低的羟基烷基、较低的芳基烯基、较低的芳氧基烷基、较低的芳硫基烷基和杂芳基中选择;其中R.sup.3从较低的烷基和氨基中选择;其中R.sup.4是从氢化物、卤素、较低的烷基和较低的烷氧基中选择的一个或多个基团;或者R.sup.4与苯基一起形成萘基或苯二氧杂基;在R.sup.3为甲基且R.sup.4为氢化物、甲基、甲氧基或氯时,提供R.sup.1不是较低烷基;或其药用盐。
    公开号:
    US05620999A1
点击查看最新优质反应信息

文献信息

  • [EN] 4,5-SUBSTITUTED IMIDAZOLYL COMPOUNDS FOR THE TREATMENT OF INFLAMMATION<br/>[FR] COMPOSES D'IMIDAZOLYLE SUBSTITUES EN POSITIONS 4 ET 5, CONVENANT AU TRAITEMENT DE L'INFLAMMATION
    申请人:G.D. SEARLE & CO.
    公开号:WO1996003387A1
    公开(公告)日:1996-02-08
    (EN) A class of compounds is described for treating inflammation and inflammation-related disorders. Compounds of particular interest are defined by formula (I), wherein R1 is selected from lower alkyl, lower haloalkyl, lower hydroxyalkyl, lower alkoxyalkyl, lower alkenyloxyalkyl, mercapto, lower alkylcarbonyl, lower haloalkylcarbonyl, phenylcarbonyl, lower aralkylcarbonyl, lower aralkenyl, lower aryloxyalkyl, lower aralkyloxyalkyl, lower arylsulfonyl, lower aralkylsulfonyl, lower arylthioalkyl, lower heteroarylalkylthioalkyl, and heteroaryl selected from 2-thienyl, 2-furyl, 3-furyl, 2-pyridyl, 4-pyridyl and 2-benzofuryl; wherein R2 and R3 are independently selected from heteroaryl, cycloalkyl and aryl, wherein the heteroaryl, cycloalkyl and aryl radicals are substituted at a substitutable position with one or more radicals selected from hydrido, halo, lower alkylthio, lower alkylsulfinyl, lower alkylsulfonyl, aminosulfonyl, lower alkyl, cyano, carboxyl, lower alkoxycarbonyl, lower haloalkyl, hydroxyl, lower alkoxy, lower hydroxyalkyl, lower alkoxyalkyl, lower haloalkoxy, amino, lower alkylamino, phenylamino and nitro; and wherein R4 is selected from hydrido, lower alkyl and acyl; or a pharmaceutically acceptable salt thereof.(FR) La présente invention concerne une classe de composés convenant au traitement de l'inflammation et des troubles liés à l'inflammation. Les composés concernés en l'occurrence sont décrits par la formule générale (I). Dans cette formule générale (I), 'R1' est choisi parmi alkyle inférieur, haloalkyle inférieur, hydroxyalkyle inférieur, alcoxyalkyle inférieur, alcényloxyalkyle inférieur, mercapto, alkylcarbonyle inférieur, haloalkylcarbonyle inférieur, phénylcarbonyle, aralkylcarbonyle inférieur, aralcényle inférieur, aryloxyalkyle inférieur, aralkyloxyalkyle inférieur, arylsulfonyle inférieur, aralkylsulfonyle inférieur, arylthioalkyle inférieur, hétéroarylalkylthioalkyle inférieur, et hétéroaryle choisi parmi 2-thiényle, 2-furyle, 3-furyle, 2-pyridyle, 4-pyridyle et 2-benzofuryle. Dans la formule générale (I), 'R2' et 'R3' sont choisis séparément parmi hétéroaryle, cycloalkyle et aryle, les radicaux hétéroaryle, cycloalkyle et aryle étant substitués à des positions admettant la substitution par un ou plusieurs radicaux choisis parmi hydrido, halo, alkylthio inférieur, alkylsulfinyle inférieur, alkylsulfonyle inférieur, aminosulfonyle, alkyle inférieur, cyano, carboxyle, alcoxycarbonyle inférieur, haloalkyle inférieur, hydroxyle, alcoxy inférieur, hydroxyalkyle inférieur, alcoxyalkyle inférieur, haloalcoxy inférieur, amino, alkylamino inférieur, phénylamino et nitro. Dans la formule générale (I), 'R4' est choisi parmi hydrido, alkyle inférieur et acyle. L'invention concerne également des sels de ces composés de formule générale qui sont pharmaceutiquement acceptables.
    描述了一类用于治疗炎症和炎症相关疾病的化合物。特别感兴趣的化合物由式(I)定义,其中R1从较低的烷基,较低的卤代烷基,较低的羟基烷基,较低的氧烷基,较低的烯氧基烷基,巯基,较低的烷基羰基,较低的卤代烷基羰基,苯基羰基,较低的芳基烷基羰基,较低的芳基烯基,较低的芳氧基烷基,较低的芳基氧烷基,较低的芳基磺酰基,较低的芳基烷基磺酰基,较低的芳基硫代烷基,较低的杂环芳基烷基硫代烷基和杂环芳基,所述杂环芳基选择自2-噻吩基,2-呋喃基,3-呋喃基,2-吡啶基,4-吡啶基和2-苯并呋喃基;其中R2和R3分别选择自杂环芳基,环烷基和芳基,其中杂环芳基,环烷基和芳基基团在可取代位置上用一个或多个基团进行取代,所述基团选择自氢基,卤素基,较低的烷基硫基,较低的烷基亚砜基,较低的烷基磺酰基,氨基磺酰基,较低的烷基,氰基,羧基,较低的烷氧基羰基,较低的卤代烷基,羟基,较低的氧烷基,较低的羟基烷基,较低的氧烷基烷基,较低的卤代氧烷基,氨基,较低的烷基氨基,苯基氨基和硝基;其中R4选择自氢基,较低的烷基和酰基;或其药学上可接受的盐。
  • 4,5-subtstituted imdazolyl compounds for the treatment of inflammation
    申请人:G.D. Searle & Co.
    公开号:US20030050330A1
    公开(公告)日:2003-03-13
    A class of compounds is described for treating inflammation and inflammation-related disorders. Compounds of particular interest are defined by Formula I 1 wherein R 1 is selected from lower alkyl, lower haloalkyl, lower hydroxyalkyl, lower alkoxyalkyl, lower alkenyloxyalkyl, mercapto, lower alkylcarbonyl, lower haloalkylcarbonyl, phenylcarbonyl, lower aralkylcarbonyl, lower aralkenyl, lower aryloxyalkyl, lower aralkyloxyalkyl, lower arylsulfonyl, lower aralkylsulfonyl, lower arylthioalkyl, lower heteroarylalkylthioalkyl, and heteroaryl selected from 2 -thienyl, 2 -furyl, 3 -furyl, 2 -pyridyl, 4 -pyridyl and 2 -benzofuryl; wherein R 2 and R 3 are independently selected from heteroaryl, cycloalkyl and aryl, wherein the heteroaryl, cycloalkyl and aryl radicals are substituted at a substitutable position with one or more radicals selected from hydrido, halo, lower alkylthio, lower alkylsulfinyl, lower alkylsulfonyl, aminosulfonyl, lower alkyl, cyano, carboxyl, lower alkoxycarbonyl, lower haloalkyl, hydroxyl, lower alkoxy, lower hydroxyalkyl, lower alkoxyalkyl, lower haloalkoxy, amino, lower alkylamino, phenylamino and nitro; and wherein R 4 is selected from hydrido, lower alkyl and acyl; or a pharmaceutically-acceptable salt thereof.
    描述了一类化合物,用于治疗炎症和与炎症相关的疾病。特别感兴趣的化合物由公式I1定义,其中R1选自较低的烷基,较低的卤代烷基,较低的羟基烷基,较低的烷氧基烷基,较低的烯氧基烷基,巯基,较低的烷基羰基,较低的卤代烷基羰基,苯基羰基,较低的芳基烷基羰基,较低的芳基烯基,较低的芳氧基烷基,较低的芳基氧烷基,较低的芳基磺酰基,较低的芳基烷基磺酰基,较低的芳基硫代烷基,较低的杂芳基烷基硫代烷基,和杂芳基,所述杂芳基选自2-噻吩基,2-呋喃基,3-呋喃基,2-吡啶基,4-吡啶基和2-苯并呋喃基;其中R2和R3分别选自杂芳基,环烷基和芳基,所述杂芳基,环烷基和芳基基团在可取代的位置上用一个或多个基团选自氢,卤素,较低的烷基硫,较低的烷基亚砜,较低的烷基磺酰基,氨基磺酰基,较低的烷基,氰基,羧基,较低的烷氧基羰基,较低的卤代烷基,羟基,较低的烷氧基,较低的羟基烷基,较低的烷氧基烷基,较低的卤代芳基氧基,氨基,较低的烷基氨基,苯基氨基和硝基;其中R4选自氢,较低的烷基和酰基;或其药学上可接受的盐。
  • 4,5-substituted imidazolyl compounds for the treatment of inflammation
    申请人:G D Searle & Co.
    公开号:US06426360B1
    公开(公告)日:2002-07-30
    A class of compounds is described for treating inflammation and inflammation-related disorders. Compounds of particular interest are defined by Formula wherein R1 is selected from lower alkyl, lower haloalkyl, lower hydroxyalkyl, lower alkoxyalkyl, lower alkenyloxyalkyl, mercapto, lower alkylcarbonyl, lower haloalkylcarbonyl, phenylcarbonyl, lower aralkylcarbonyl, lower aralkenyl, lower aryloxyalkyl, lower aralkyloxyalkyl, lower arylsulfonyl, lower aralkylsulfonyl, lower arylthioalkyl, lower heteroarylalkylthioalkyl, and heteroaryl selected from 2-thienyl, 2-furyl, 3-furyl, 2-pyridyl, 4-pyridyl and 2-benzofuryl; wherein R2 and R3 are independently selected from heteroaryl, cycloalkyl and aryl, wherein the heteroaryl, cycloalkyl and aryl radicals are substituted at a substitutable position with one or more radicals selected from hydrido, halo, lower alkylthio, lower alkylsulfinyl, lower alkylsulfonyl, aminosulfonyl, lower alkyl, cyano, carboxyl, lower alkoxycarbonyl, lower haloalkyl, hydroxyl, lower alkoxy, lower hydroxyalkyl, lower alkoxyalkyl, lower haloalkoxy, amino, lower alkylamino, phenylamino and nitro; and wherein R4 is selected from hydrido, lower alkyl and acyl; or a pharmaceutically-acceptable salt thereof.
    描述了一类用于治疗炎症和炎症相关疾病的化合物。特别感兴趣的化合物由以下式子定义:其中R1选自较低的烷基、较低的卤代烷基、较低的羟基烷基、较低的烷氧基烷基、较低的烯氧基烷基、巯基、较低的烷基羰基、较低的卤代烷基羰基、苯基羰基、较低的芳基烷基羰基、较低的芳基烯基、较低的芳氧基烷基、较低的芳基氧基烷基、较低的芳基磺酰基、较低的芳基烷基磺酰基、较低的芳基硫代烷基、较低的杂芳基烷基硫代烷基和选自2-噻吩基、2-呋喃基、3-呋喃基、2-吡啶基、4-吡啶基和2-苯并呋喃基的杂芳基;其中R2和R3独立选自杂芳基、环烷基和芳基,其中杂芳基、环烷基和芳基基团在可取代位置上用一个或多个基团选自氢、卤、较低的烷基硫、较低的烷基亚砜、较低的烷基磺酰基、氨基磺酰基、较低的烷基、氰基、羧基、较低的烷氧羰基、较低的卤代烷基、羟基、较低的烷氧基、较低的羟基烷基、较低的卤代烷氧基、氨基、较低的烷基氨基、苯基氨基和硝基;其中R4选自氢、较低的烷基和酰基;或其药学上可接受的盐。
  • 4,5-substitued imidazolyl compounds for the treatment of inflammation
    申请人:G.D. Searle & Co.
    公开号:EP1211244A2
    公开(公告)日:2002-06-05
    A class of compounds is described for treating inflammation and inflammation-related disorders. Compounds of particular interest are defined by Formula I wherein R1 is selected from lower alkyl, lower haloalkyl, lower hydroxyalkyl, lower alkoxyalkyl, lower alkenyloxyalkyl, mercapto, lower alkylcarbonyl, lower haloalkylcarbonyl, phenylcarbonyl, lower aralkylcarbonyl, lower aralkenyl, lower aryloxyalkyl, lower aralkyloxyalkyl, lower arylsulfonyl, lower aralkylsulfonyl, lower arylthioalkyl, lower heteroarylalkylthioalkyl, and heteroaryl selected from 2-thienyl, 2-furyl, 3-furyl, 2-pyridyl, 4-pyridyl and 2-benzofuryl; wherein R2 and R3 are independently selected from heteroaryl, cycloalkyl and aryl, wherein the heteroaryl, cycloalkyl and aryl radicals are substituted at a substitutable position with one or more radicals selected from hydrido, halo, lower alkylthio, lower alkylsulfinyl, lower alkylsulfonyl, aminosulfonyl, lower alkyl, cyano, carboxyl, lower alkoxycarbonyl, lower haloalkyl, hydroxyl, lower alkoxy, lower hydroxyalkyl, lower alkoxyalkyl, lower haloalkoxy, amino, lower alkylamino, phenylamino and nitro; and wherein R4 is selected from lower alkyl and acyl; or a pharmaceutically-acceptable salt thereof.
    描述了一类用于治疗炎症和炎症相关疾病的化合物。特别感兴趣的化合物由式 I 定义 其中 R1 选自低级烷基、低级卤代烷基、低级羟基烷基、低级烷氧基烷基、低级烯氧基烷基、巯基、低级烷基羰基、低级卤代烷基羰基、苯基羰基、低级芳基羰基、低级芳烯基、低级芳氧基烷基、低级芳烷氧基烷基、低级芳烷氧基烷基、低级芳烷氧基烷基、低级芳烷氧基烷基、低级芳氧基烷基、低级芳氧基烷基、低级芳磺酰基、低级芳磺酰基、低级芳硫基烷基、低级杂芳基硫代烷基,以及选自 2-噻吩基、2-呋喃基、3-呋喃基、2-吡啶基、4-吡啶基和 2-苯并呋喃基的杂芳基;其中 R2 和 R3 独立选自杂芳基、环烷基和芳基,其中杂芳基、环烷基和芳基在可被取代的位置被一个或多个选自氢基、卤素基、低级烷硫基、低级烷亚硫基、低级烷亚基亚磺酰基、低级烷硫基和低级烷亚基亚磺酰基的基团取代、低级烷基亚磺酰基、低级烷基磺酰基、氨基磺酰基、低级烷基、氰基、羧基、低级烷氧基羰基、低级卤代烷基、羟基、低级烷氧基、低级羟基烷基、低级烷氧基烷基、低级卤代烷氧基、氨基、低级烷基氨基、苯基氨基和硝基;其中 R4 选自低级烷基和酰基;或其药学上可接受的盐。
  • 4,5-SUBSTITUTED IMIDAZOLYL COMPOUNDS FOR THE TREATMENT OF INFLAMMATION
    申请人:G.D. SEARLE & CO.
    公开号:EP0772601B1
    公开(公告)日:2002-09-18
查看更多

同类化合物

伊莫拉明 (5aS,6R,9S,9aR)-5a,6,7,8,9,9a-六氢-6,11,11-三甲基-2-(2,3,4,5,6-五氟苯基)-6,9-甲基-4H-[1,2,4]三唑[3,4-c][1,4]苯并恶嗪四氟硼酸酯 (5-氨基-1,3,4-噻二唑-2-基)甲醇 齐墩果-2,12-二烯[2,3-d]异恶唑-28-酸 黄曲霉毒素H1 高效液相卡套柱 非昔硝唑 非布索坦杂质Z19 非布索坦杂质T 非布索坦杂质K 非布索坦杂质E 非布索坦杂质67 非布索坦杂质65 非布索坦杂质64 非布索坦杂质61 非布索坦代谢物67M-4 非布索坦代谢物67M-2 非布索坦代谢物 67M-1 非布索坦-D9 非布索坦 非唑拉明 雷西纳德杂质H 雷西纳德 阿西司特 阿莫奈韦 阿米苯唑 阿米特罗13C2,15N2 阿瑞匹坦杂质 阿格列扎 阿扎司特 阿尔吡登 阿塔鲁伦中间体 阿培利司N-1 阿哌沙班杂质26 阿哌沙班杂质15 阿可替尼 阿作莫兰 阿佐塞米 镁(2+)(Z)-4'-羟基-3'-甲氧基肉桂酸酯 锌1,2-二甲基咪唑二氯化物 铵2-(4-氯苯基)苯并恶唑-5-丙酸盐 铬酸钠[-氯-3-[(5-二氢-3-甲基-5-氧代-1-苯基-1H-吡唑-4-基)偶氮]-2-羟基苯磺酸基][4-[(3,5-二氯-2-羟基苯 铁(2+)乙二酸酯-3-甲氧基苯胺(1:1:2) 钠5-苯基-4,5-二氢吡唑-1-羧酸酯 钠3-[2-(2-壬基-4,5-二氢-1H-咪唑-1-基)乙氧基]丙酸酯 钠3-(2H-苯并三唑-2-基)-5-仲-丁基-4-羟基苯磺酸酯 钠(2R,4aR,6R,7R,7aS)-6-(2-溴-9-氧代-6-苯基-4,9-二氢-3H-咪唑并[1,2-a]嘌呤-3-基)-7-羟基四氢-4H-呋喃并[3,2-D][1,3,2]二氧杂环己膦烷e-2-硫醇2-氧化物 野麦枯 野燕枯 醋甲唑胺