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

2-tert-butyl-5-ethenylpyridine | 910487-14-8

中文名称
——
中文别名
——
英文名称
2-tert-butyl-5-ethenylpyridine
英文别名
——
2-tert-butyl-5-ethenylpyridine化学式
CAS
910487-14-8
化学式
C11H15N
mdl
——
分子量
161.247
InChiKey
NOJVJWVMLPWLSQ-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):
    3.3
  • 重原子数:
    12
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.36
  • 拓扑面积:
    12.9
  • 氢给体数:
    0
  • 氢受体数:
    1

文献信息

  • Substituted sulfonylaminoarylmethyl cyclopropanecarboxamide as VR1 receptor antagonists
    申请人:Hanazawa Takeshi
    公开号:US20060211741A1
    公开(公告)日:2006-09-21
    This invention provides a compound of the formula (I): wherein A and B are independently CR 12 or N; D and E are each independently CR 9 or N; R 1 represents (C 1 -C 6 )alkyl; R 2 represents hydrogen, halogen, hydroxy, (C 1 -C 6 )alkyl, halo(C 1 -C 6 )alkyl, hydroxy(C 1 -C 6 )alkyl, (C 1 -C 6 )alkoxy or (C 1 -C 6 )alkoxy-(C 1 -C 6 )alkyl; R 3 , R 4 , R 5 , R 6 , R 10 and R 11 each independently represent hydrogen, halogen, (C 1 -C 6 )alkyl, halo(C 1 -C 6 )alkyl, (C 1 -C 6 )alkoxy, hydroxy(C 1 -C 6 )alkyl or (C 1 -C 6 )alkoxy-(C 1 -C 6 )alkyl; or R 3 and R 4 are taken together with the carbon atom to which they are attached to form a 3- to 7-membered carbocyclic ring or heterocyclic ring in which one or two non-adjacent carbon atoms are optionally replaced by an oxygen atom, a sulfur atom or NH; R 7 and R 9 each independently represent hydrogen, halogen, (C 1 -C 6 )alkyl, halo(C 1 -C 6 )alkyl, hydroxy(C 1 -C 6 )alkyl, (C 1 -C 6 )alkoxy, hydroxy(C 1 -C 6 )alkoxy, (C 1 -C 6 )alkoxy-(C 1 -C 6 )alkyl, (C 1 -C 6 )alkoxy-(C 1 -C 6 )alkoxy, (C 1 -C 6 )alkylthio, (C 1 -C 6 )alkylsulfinyl, (C 1 -C 6 )alkylsulfonyl, NH 2 , [(C 1 -C 6 )alkyl]NH—, [(C 1 -C 6 )alkyl] 2 N—, H 2 N—(C 1 -C 6 )alkoxy, (C 1 -C 6 )alkyl-NH—(C 1 -C 6 )alkoxy, [(C 1 -C 6 )alkyl] 2 N(C 1 -C 6 )alkoxy; H 2 N—(C 1 -C 6 )alkoxy-(C 1 -C 6 )alkyl, (C 1 C 6 )alkyl-NH—(C 1 -C 6 )alkoxy-(C 1 -C 6 )alkyl, [(C 1 -C 6 )alkyl] 2 N(C 1 -C 6 )alkoxy-(C 1 -C 6 )alkyl or 5- or 6-membered heterocyclic ring containing at least one nitrogen atom; R 8 represents halogen, (C 1 -C 6 )alkyl, halo(C 1 -C 6 )alkyl, hydroxy(C 1 -C 6 )alkyl, (C 1 -C 6 )alkoxy, hydroxy(C 1 -C 6 )alkoxy, (C 1 -C 6 )alkoxy-(C 1 -C 6 )alkyl, (C 1 -C 6 )alkoxy-(C 1 -C 6 )alkoxy, halo(C 1 -C 6 )alkylsulfonyl, halo(C 1 -C 6 )alkylsulfinyl, halo(C 1 -C 6 )alkoxy, halo(C 1 -C 6 )alkylthio, [(C 1 -C 6 )alkyl]NH— or [(C 1 -C 6 )alkyl] 2 N—; or R 7 and R 8 , when E is CR 9 , are taken together with the carbon atoms to which they are attached form a 5-8 membered carbocyclic or heterocyclic ring, in which one or two non-adjacent carbon atoms are optionally replaced by oxygen, sulfur, N or NH groups, wherein the carbocyclic ring or the heterocyclic ring is unsubstituted or substituted with one or more substituents each independently selected from the group consisting of hydroxy, (C 1 -C 6 )alkyl, (C 1 -C 6 )alkoxy and hydroxy(C 1 -C 6 )alkyl; and R 12 represents hydrogen, halogen, (C 1 -C 6 )alkyl or hydroxy(C 1 -C 6 )alkyl; or a pharmaceutically acceptable salt or solvate thereof. These compounds are useful for the treatment of disease conditions caused by overactivation of VR1 receptor such of pain, or the like in mammalian. This invention also provides a pharmaceutical composition comprising the above compound.
    这项发明提供了一个化合物的结构式(I):其中A和B分别独立地为CR12或N;D和E分别独立地为CR9或N;R1代表(C1-C6)烷基;R2代表氢、卤素、羟基、(C1-C6)烷基、卤代(C1-C6)烷基、羟基(C1-C6)烷基、(C1-C6)氧烷基或(C1-C6)氧烷基-(C1-C6)烷基;R3、R4、R5、R6、R10和R11分别独立地代表氢、卤素、(C1-C6)烷基、卤代(C1-C6)烷基、(C1-C6)氧烷基、羟基(C1-C6)烷基或(C1-C6)氧烷基-(C1-C6)烷基;或者R3和R4一起与它们连接的碳原子形成一个3-至7-成员的碳环或杂环,其中一个或两个非相邻的碳原子可以选择性地被氧原子、硫原子或NH取代;R7和R9分别独立地代表氢、卤素、(C1-C6)烷基、卤代(C1-C6)烷基、羟基(C1-C6)烷基、(C1-C6)氧烷基、羟基(C1-C6)氧烷基、(C1-C6)氧烷基-(C1-C6)烷基、(C1-C6)氧烷基-(C1-C6)氧烷基、(C1-C6)烷基硫、(C1-C6)烷基亚硫基、(C1-C6)烷基磺基、NH2、[(C1-C6)烷基]NH—、[(C1-C6)烷基]2N—、H2N—(C1-C6)氧烷基、(C1-C6)烷基-NH—(C1-C6)氧烷基、[(C1-C6)烷基]2N(C1-C6)氧烷基;H2N—(C1-C6)氧烷基-(C1-C6)烷基、(C1C6)烷基-NH—(C1-C6)氧烷基-(C1-C6)烷基、[(C1-C6)烷基]2N(C1-C6)氧烷基-(C1-C6)烷基或含有至少一个氮原子的5-或6-成员杂环,R8代表卤素、(C1-C6)烷基、卤代(C1-C6)烷基、羟基(C1-C6)烷基、(C1-C6)氧烷基、羟基(C1-C6)氧烷基、(C1-C6)氧烷基-(C1-C6)烷基、(C1-C6)氧烷基-(C1-C6)氧烷基、卤代(C1-C6)烷基磺基、卤代(C1-C6)烷基亚硫基、卤代(C1-C6)烷基氧基、卤代(C1-C6)烷基硫基、[(C1-C6)烷基]NH—或[(C1-C6)烷基]2N—;或者当E为CR9时,R7和R8一起与它们连接的碳原子形成一个5-8成员的碳环或杂环,其中一个或两个非相邻的碳原子可以选择性地被氧、硫、N或NH基团取代,其中碳环或杂环未取代或取代有一个或多个取代基,每个取代基独立地选自羟基、(C1-C6)烷基、(C1-C6)氧烷基和羟基(C1-C6)烷基;R12代表氢、卤素、(C1-C6)烷基或羟基(C1-C6)烷基;或其药学上可接受的盐或溶剂。这些化合物对于治疗由VR1受体过度激活引起的疾病状况,如哺乳动物中的疼痛等,是有用的。这项发明还提供了包含上述化合物的药物组合物。
  • SUBSTITUTED SULFONYLAMINOARYLMETHYL CYCLOPROPANECARBOXAMIDE AS VR1 RECEPTOR ANTAGONISTS
    申请人:HANAZAWA TAKESHI
    公开号:US20100035880A1
    公开(公告)日:2010-02-11
    This invention provides a compound of the formula (I): wherein A and B are independently CR 12 or N; D and E are each independently CR 9 or N; R 1 represents (C 1 -C 6 )alkyl; R 2 represents hydrogen, halogen, hydroxy, (C 1 -C 6 ) alkyl, halo(C 1 -C 6 ) alkyl, hydroxy(C 1 -C 6 )alkyl, (C 1 -C 6 )alkoxy or (C 1 -C 6 )alkoxy-(C 1 -C 6 )alkyl; R 3 , R 4 , R 5 , R 6 , R 10 and R 11 each independently represent hydrogen, halogen, (C 1 -C 6 )alkyl, halo(C 1 -C 6 )alkyl, (C 1 -C 6 )alkoxy, hydroxy(C 1 -C 6 )alkyl or (C 1 -C 6 )alkoxy-(C 1 -C 6 )alkyl; or R 3 and R 4 are taken together with the carbon atom to which they are attached to form a 3- to 7-membered carbocyclic ring or heterocyclic ring in which one or two non-adjacent carbon atoms are optionally replaced by an oxygen atom, a sulfur atom or NH; R 7 and R 9 each independently represent hydrogen, halogen, (C 1 -C 6 )alkyl, halo(C 1 -C 6 )alkyl, hydroxy(C 1 -C 6 )alkyl, (C 1 -C 6 )alkoxy, hydroxy(C 1 -C 6 )alkoxy, (C 1 -C 6 )alkoxy-(C 1 -C 6 )alkyl, (C 1 -C 6 )alkoxy-(C 1 -C 6 )alkoxy, (C 1 -C 6 )alkylthio, (C 1 -C 6 )alkylsulfinyl, (C 1 -C 6 )alkylsulfonyl, NH 2 , [(C 1 -C 6 )alkyl]NH—, [(C 1 -C 6 )alkyl] 2 N—, H 2 N—(C 1 -C 6 )alkoxy, (C 1 -C 6 )alkyl-NH—(C 1 -C 6 )alkoxy, [(C 1 -C 6 )alkyl] 2 N(C 1 -C 6 )alkoxy; H 2 N—(C 1 -C 6 )alkoxy-(C 1 -C 6 )alkyl, (C 1 -C 6 )alkyl-NH—(C 1 -C 6 )alkoxy-(C 1 -C 6 )alkyl, [(C 1 -C 6 )alkyl] 2 N(C 1 -C 6 )alkoxy-(C 1 -C 6 )alkyl or 5- or 6-membered heterocyclic ring containing at least one nitrogen atom; R 8 represents halogen, (C 1 -C 6 )alkyl, halo(C 1 -C 6 )alkyl, hydroxy(C 1 -C 6 )alkyl, (C 1 -C 6 )alkoxy, hydroxy(C 1 -C 6 )alkoxy, (C 1 -C 8 )alkoxy-(C 1 -C 6 )alkyl, (C 1 -C 6 )alkoxy-(C 1 -C 6 )alkoxy, halo(C 1 -C 6 )alkylsulfonyl, halo(C 1 -C 6 )alkylsulfinyl, halo(C 1 -C 6 )alkoxy, halo(C 1 -C 6 )alkylthio, [(C 1 -C 6 )alkyl]NH— or [(C 1 -C 6 )alkyl] 2 N—; or R 7 and R 8 , when E is CR 9 , are taken together with the carbon atoms to which they are attached form a 5-8 membered carbocyclic or heterocyclic ring, in which one or two non-adjacent carbon atoms are optionally replaced by oxygen, sulfur, N or NH groups, wherein the carbocyclic ring or the heterocyclic ring is unsubstituted or substituted with one or more substituents each independently selected from the group consisting of hydroxy, (C 1 -C 6 )alkyl, (C 1 -C 6 )alkoxy and hydroxy(C 1 -C 6 )alkyl; and R 12 represents hydrogen, halogen, (C 1 -C 6 )alkyl or hydroxy(C 1 -C 6 )alkyl; or a pharmaceutically acceptable salt or solvate thereof. These compounds are useful for the treatment of disease conditions caused by overactivation of VR1 receptor such of pain, or the like in mammalian. This invention also provides a pharmaceutical composition comprising the above compound.
    本发明提供了一种公式(I)的化合物:其中A和B分别独立表示CR12或N; D和E分别独立表示CR9或N; R1表示(C1-C6)烷基; R2表示氢,卤素,羟基,(C1-C6)烷基,卤代(C1-C6)烷基,羟基(C1-C6)烷基,(C1-C6)氧烷基或(C1-C6)氧烷基-(C1-C6)烷基; R3、R4、R5、R6、R10和R11分别独立表示氢,卤素,(C1-C6)烷基,卤代(C1-C6)烷基,(C1-C6)氧烷基,羟基(C1-C6)烷基或(C1-C6)氧烷基-(C1-C6)烷基; 或R3和R4与它们所附着的碳原子一起形成3-至7-成员的碳环或杂环,其中一个或两个非相邻的碳原子可以选择地被氧原子,硫原子或NH代替; R7和R9分别独立表示氢,卤素,(C1-C6)烷基,卤代(C1-C6)烷基,羟基(C1-C6)烷基,(C1-C6)氧烷基,羟基(C1-C6)氧烷基,(C1-C6)氧烷基-(C1-C6)烷基,(C1-C6)氧烷基-(C1-C6)氧烷基,(C1-C6)烷基硫,(C1-C6)烷基亚磺酰基,(C1-C6)烷基磺酰基,NH2,[(C1-C6)烷基] NH-,[(C1-C6)烷基] 2N-,H2N-(C1-C6)氧烷基,(C1-C6)烷基-NH-(C1-C6)氧烷基,[(C1-C6)烷基] 2N(C1-C6)氧烷基; H2N-(C1-C6)氧烷基-(C1-C6)烷基,(C1-C6)烷基-NH-(C1-C6)氧烷基-(C1-C6)烷基,[(C1-C6)烷基] 2N(C1-C6)氧烷基-(C1-C6)烷基或含有至少一个氮原子的5-或6-成员杂环,R8表示卤素,(C1-C6)烷基,卤代(C1-C6)烷基,羟基(C1-C6)烷基,(C1-C6)氧烷基,羟基(C1-C6)氧烷基,(C1-C8)氧烷基-(C1-C6)烷基,(C1-C6)氧烷基-(C1-C6)氧烷基,卤代(C1-C6)烷基磺酰基,卤代(C1-C6)烷基亚磺酰基,卤代(C1-C6)氧烷基,卤代(C1-C6)烷基硫,[(C1-C6)烷基] NH-或[(C1-C6)烷基] 2N-; 或者当E为CR9时,R7和R8与它们所附着的碳原子一起形成5-8成员的碳环或杂环,其中一个或两个非相邻的碳原子可以选择地被氧,硫,N或NH基团代替,其中碳环或杂环未被取代或被一个或多个取代基取代,每个取代基独立地选择自羟基,(C1-C6)烷基,(C1-C6)氧烷基和羟基(C1-C6)烷基; R12表示氢,卤素,(C1-C6)烷基或羟基(C1-C6)烷基; 或其药学上可接受的盐或溶剂。这些化合物对于治疗由VR1受体过度激活引起的疾病状况,如哺乳动物中的疼痛等非常有用。本发明还提供了包含上述化合物的药物组成物。
  • COSMETIC POLYMER COMPOSITION AND COSMETIC
    申请人:HIWATASHI Tomoaki
    公开号:US20070166250A1
    公开(公告)日:2007-07-19
    The present invention discloses a cosmetic polymer composition containing a straight-chain block copolymer, where the copolymer having a unit derived from a compound having an ethylenic unsaturated bond, having a number-average molecular weight of 1.0×10 3 to 1.0×10 6 , and having at least two or more glass transition points or melting points; a hair cosmetic polymer composition containing a copolymer a copolymer capable of forming a film having a Young's modulus of 50 MPa or larger and a fracture-point elongation of 100% or larger, and dispersible into water and/or alcohol; and a cosmetic material containing these compositions.
    本发明揭示了一种化妆品聚合物组合物,其中包含一种直链嵌段共聚物,该共聚物具有从具有乙烯不饱和键的化合物导出的单元,具有1.0×103至1.0×106的数均分子量,并且具有至少两个或更多的玻璃转变点或熔点;一种头发化妆品聚合物组合物,其中包含一种共聚物,该共聚物能够形成具有50 MPa或更大的杨氏模量和100%或更大的断裂点延伸的膜,并且能够分散到水和/或酒精中;以及包含这些组合物的化妆品材料。
  • Graft copolymer and process for production thereof
    申请人:MITSUBISHI CHEMICAL CORPORATION
    公开号:EP0939090A1
    公开(公告)日:1999-09-01
    The present invention discloses a graft copolymer comprising an olefin polymer or a block copolymer, and an ionic group-containing polymer grafted to the olefin polymer or the block copolymer by a bridging group whose bridging chain has 4 or more atoms. The invention also discloses a process for producing the graft copolymer, which comprises reacting a radical polymerizable unsaturated compound (b) with a modified olefin polymer (a1) or a modified block copolymer (a2) to form a radical polymerizable olefin polymer (c1) or a radical polymerizable block copolymer (c2), the modified olefin polymer (a1) or the radical polymerizable block copolymer (c2) having a functional group selected from the group consisting of a hydroxyl group, a carboxyl group, an anhydrous carboxyl group, an epoxy group, and an isocyanate group, and the radical polymerizable unsaturated compound (b) having a functional group reactive with the above functional group; and then radical copolymerizing a radical polymerizable unsaturated compound (d) having an ionic group with the radical polymerizable olefin polymer (c1) or the radical polymerizable block copolymer (c2). When applied to a surface of a molded product of a thermoplastic resin or the like, the graft copolymer of the invention can impart coating properties, printing properties and antistatic properties to the molded product while maintaining sufficient adhesion to the molded product.
    本发明公开了一种接枝共聚物,包括烯烃聚合物或嵌段共聚物,以及通过桥接基(其桥接链具有 4 个或更多原子)接枝到烯烃聚合物或嵌段共聚物上的含离子基团聚合物。本发明还公开了一种生产接枝共聚物的工艺,包括将可自由基聚合的不饱和化合物(b)与改性烯烃聚合物(a1)或改性嵌段共聚物(a2)反应,形成可自由基聚合的烯烃聚合物(c1)或可自由基聚合的嵌段共聚物(c2)、改性烯烃聚合物(a1)或可自由基聚合的嵌段共聚物(c2)具有选自羟基、羧基、无水羧基、环氧基和异氰酸酯基的官能团,以及可自由基聚合的不饱和化合物(b)具有与上述官能团反应的官能团;然后将具有离子基团的可自由基聚合的不饱和化合物 (d) 与可自由基聚合的烯烃聚合物 (c1) 或可自由基聚合的嵌段共聚物 (c2) 进行自由基共聚。将本发明的接枝共聚物涂抹到热塑性树脂或类似材料的模制产品表面时,可赋予模制产品涂层性能、印刷性能和抗静电性能,同时与模制产品保持足够的粘附性。
  • Cosmetic polymer composition and cosmetic
    申请人:MITSUBISHI CHEMICAL CORPORATION
    公开号:US20040223933A1
    公开(公告)日:2004-11-11
    The present invention discloses a cosmetic polymer composition containing a straight-chain block copolymer, where the copolymer having a unit derived from a compound having an ethylenic unsaturated bond, having a number-average molecular weight of 1.0×10 3 to 1.0×10 6 , and having at least two or more glass transition points or melting points; a hair cosmetic polymer composition containing a copolymer a copolymer capable of forming a film having a Young's modulus of 50 MPa or larger and a fracture-point elongation of 100% or larger, and dispersible into water and/or alcohol; and a cosmetic material containing these compositions.
    本发明公开了一种含有直链嵌段共聚物的化妆品聚合物组合物,该共聚物的单元来源于具有乙烯不饱和键的化合物,其数均分子量为 1.0×10 3 至 1.0×10 6 一种头发化妆品聚合物组合物,其中含有一种共聚物,该共聚物能形成一层膜,膜的杨氏模量大于或等于 50 兆帕,断裂点伸长率大于或等于 100%,并可分散于水和/或酒精中;以及一种含有这些组合物的化妆品材料。
查看更多

同类化合物

(S)-氨氯地平-d4 (R,S)-可替宁N-氧化物-甲基-d3 (R)-N'-亚硝基尼古丁 (5E)-5-[(2,5-二甲基-1-吡啶-3-基-吡咯-3-基)亚甲基]-2-亚磺酰基-1,3-噻唑烷-4-酮 (5-溴-3-吡啶基)[4-(1-吡咯烷基)-1-哌啶基]甲酮 (5-氨基-6-氰基-7-甲基[1,2]噻唑并[4,5-b]吡啶-3-甲酰胺) (2S)-2-[[[9-丙-2-基-6-[(4-吡啶-2-基苯基)甲基氨基]嘌呤-2-基]氨基]丁-1-醇 (2R,2''R)-(+)-[N,N''-双(2-吡啶基甲基)]-2,2''-联吡咯烷四盐酸盐 黄色素-37 麦斯明-D4 麦司明 麝香吡啶 鲁非罗尼 鲁卡他胺 高氯酸N-甲基甲基吡啶正离子 高氯酸,吡啶 高奎宁酸 马来酸溴苯那敏 马来酸左氨氯地平 顺式-双(异硫氰基)(2,2'-联吡啶基-4,4'-二羧基)(4,4'-二-壬基-2'-联吡啶基)钌(II) 顺式-二氯二(4-氯吡啶)铂 顺式-二(2,2'-联吡啶)二氯铬氯化物 顺式-1-(4-甲氧基苄基)-3-羟基-5-(3-吡啶)-2-吡咯烷酮 顺-双(2,2-二吡啶)二氯化钌(II) 水合物 顺-双(2,2'-二吡啶基)二氯化钌(II)二水合物 顺-二氯二(吡啶)铂(II) 顺-二(2,2'-联吡啶)二氯化钌(II)二水合物 非那吡啶 非洛地平杂质C 非洛地平 非戈替尼 非尼拉朵 非尼拉敏 阿雷地平 阿瑞洛莫 阿培利司N-6 阿伐曲波帕杂质40 间硝苯地平 间-硝苯地平 锇二(2,2'-联吡啶)氯化物 链黑霉素 链黑菌素 银杏酮盐酸盐 铬二烟酸盐 铝三烟酸盐 铜-缩氨基硫脲络合物 铜(2+)乙酸酯吡啶(1:2:1) 铁5-甲氧基-6-甲基-1-氧代-2-吡啶酮 钾4-氨基-3,6-二氯-2-吡啶羧酸酯 钯,二氯双(3-氯吡啶-κN)-,(SP-4-1)-