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5-p-t-butylphenoxy-1-pentanol | 92584-43-5

中文名称
——
中文别名
——
英文名称
5-p-t-butylphenoxy-1-pentanol
英文别名
5-(4-tert-butylphenoxy)pentan-1-ol
5-p-t-butylphenoxy-1-pentanol化学式
CAS
92584-43-5
化学式
C15H24O2
mdl
MFCD17455281
分子量
236.354
InChiKey
PAGUWKONJTUNNT-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
  • 重原子数:
    17
  • 可旋转键数:
    7
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    29.5
  • 氢给体数:
    1
  • 氢受体数:
    2

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:
    参考文献:
    名称:
    BERGER, F. M.;DEGRAW, J. I. ,, JR.;JOHNSON, H. L.
    摘要:
    DOI:
  • 作为试剂:
    描述:
    4-(tert-butyl)-1-(pent-4-en-1-yloxy)benzene 、 9-Borabicyclononane 、 sodium hydroxide双氧水乙醚magnesium sulfate 、 silica gel 、 5-p-t-butylphenoxy-1-pentanol 作用下, 以 四氢呋喃 为溶剂, 反应 1.0h, 生成 5-p-t-butylphenoxy-1-pentanol
    参考文献:
    名称:
    Treatment of allergic conditions using indanyloxy-alkanol derivatives
    摘要:
    提供具有以下结构的p-烯丙基或环烷基苯氧基脂肪醇和酯类化合物:##STR1## 其中:R.sub.1是具有1到6个碳原子的烷基,优选是三级的,更优选是叔丁基;或者是与苯基相邻环碳原子紧密结合的二价环烷基,例如茚烷;R.sub.2是具有1到3个碳原子的低级烷基或氢;R.sub.3是羟基或由未取代和羟基取代的一元羧酸和由未取代和羟基取代的二元羧酸衍生的COOR.sub.4和OOCR.sub.4的酯基,其中酸被选择自脂肪酸(包括具有1到约12个碳原子的碳酸酸),环烷基酸(具有3到约12个碳原子),碳环芳香酸(具有6到约20个碳原子)和氮杂环芳香酸(具有5到约12个碳原子),其中R.sub.4是一价的烷基,环烷基,芳香族或氮杂环芳香族,R.sub.5是二价的烷基,环烷基,芳香族或氮杂环芳香族,其中酸被醇类酯化,所述醇具有1到6个碳原子;和碳酸单烷酯,所述烷基具有1到3个碳原子;n.sub.1,n.sub.2和n.sub.3分别表示CH.sub.2,C(R.sub.2).sub.2和CH.sub.2基团的数量,是在0到10范围内的数字;且n.sub.1,n.sub.2和n.sub.3中至少有一个不为零。这些化合物通过抑制释放导致过敏疾病症状的化学介质,包括过敏性鼻炎,哮喘,皮肤和胃肠道的过敏反应以及刺激物和引起炎症的物质产生的刺激和炎症症状,防止移植细胞和器官的排斥,特别是骨髓和胰岛素产生的Langerhans细胞的排斥。
    公开号:
    US04816491A1
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文献信息

  • T-Butyl-phenoxy-alkylene esters of benzoic and nicotinic acids,
    申请人:Berger; Frank M.
    公开号:US04451474A1
    公开(公告)日:1984-05-29
    p-Alkyl or cycloalkyl phenoxy alkanols and esters are provided having the structure: ##STR1## in which: R.sub.1 is an alkyl group having from one to six carbon atoms, preferably tertiary, and still more preferably tertiary-butyl; or a bivalent cycloalkylene group condensed with the phenyl group at adjacent ring carbons thereof, such as in indane; R.sub.2 is lower alkyl having from one to three carbon atoms or hydrogen; R.sub.3 is hydroxyl or an ester group selected from the group consisting of COOR.sub.4 and OOCR.sub.4 derived from unsubstituted and hydroxy-substituted monocarboxylic acids and COOR.sub.5 OOC and OOCR.sub.5 COO derived from unsubstituted and hydroxy-substituted dicarboxylic acids, the acids being selected from the group consisting of aliphatic acids, including carbamic acid, having from one to about twelve carbon atoms; cycloaliphatic acids having from three to about twelve carbon atoms; carbocyclic aromatic acids having from six to about twenty carbon atoms; and nitrogen heterocyclic aromatic acids having from five to about twelve carbon atoms, R.sub.4 being monovalent aliphatic, cycloaliphatic, aromatic, or nitrogen heterocyclic aromatic, and R.sub.5 being divalent aliphatic, cycloaliphatic, aromatic, or nitrogen heterocyclic aromatic, the acids being esterified with aliphatic alcohols having from one to six carbon atoms; and carbonic acid monoalkyl esters, the alkyl having from one to three carbon atoms; and n.sub.1, n.sub.2 and n.sub.3 represent the number of CH.sub.2, C(R.sub.2).sub.2 and CH.sub.2 groups, respectively, and are numbers within the range from 0 to 10; and at least one of n.sub.1, n.sub.2 and n.sub.3 is other than zero. These compounds inhibit abnormal tissue reactivity due to specific allergic hypersensitivity or due to specific irritants by inhibiting the release of chemical mediators that are responsible for the symptoms of allergic diseases, including allergic rhinitis, asthma, hypersensitivity of the skin and of the gastrointestinal canal, and the many symptoms of irritation and inflammation produced by irritants and inflammation-causing substances.
    提供具有结构的p-烷基或环烷基苯氧基烷醇和酯物:其中:R.sub.1是具有从一个到六个碳原子的烷基基团,最好是三级,更好是三级丁基;或者是与苯基在相邻环碳上紧密结合的二价环烷基烯基团,例如在茚中;R.sub.2是具有从一个到三个碳原子或氢的较低烷基;R.sub.3是羟基或从未取代和羟基取代的单羧酸和从未取代和羟基取代的二羧酸衍生的COOR.sub.4和OOCR.sub.4组成的酯基,所述酸被选择自具有从一个到大约十二个碳原子的脂肪酸,具有从三到大约十二个碳原子的环脂肪酸,具有从六到大约二十个碳原子的环芳香族酸以及具有从五到大约十二个碳原子的氮杂环芳香族酸,其中R.sub.4是一价的脂肪、环脂肪、芳香族或氮杂环芳族,R.sub.5是二价的脂肪、环脂肪、芳香族或氮杂环芳族,所述酸与具有从一个到六个碳原子的脂肪醇酯化;和碳酸单烷酯,该烷基具有从一个到三个碳原子;n.sub.1、n.sub.2和n.sub.3分别代表CH.sub.2、C(R.sub.2).sub.2和CH.sub.2基的数量,它们是从0到10范围内的数字;并且n.sub.1、n.sub.2和n.sub.3中至少有一个不为零。这些化合物通过抑制释放导致过敏性疾病症状的化学介质来抑制由于特定过敏性过敏或特定刺激物引起的异常组织反应,包括过敏性鼻炎、哮喘、皮肤和胃肠道过敏以及由刺激物和引起炎症的物质产生的刺激和炎症症状。
  • Phenoxy alkanol esters for treatment of allergic conditions
    申请人:Berger; Frank M.
    公开号:US05242936A1
    公开(公告)日:1993-09-07
    Compounds of the formula: ##STR1## wherein R.sub.1 is at position 4 and either is an alkyl group of 1-6 C or is an --(CH.sub.2).sub.3 -- which is additionally linked to the phenyl at position 3 thereof; R.sub.2 is a lower alkyl of 1-3 C or is hydrogen; n.sub.1, n.sub.2 and n.sub.3 represent the number of CH.sub.2, C(R.sub.2).sub.2 and CH.sub.2 groups, respectively, wherein n.sub.1 is 2, 3, 4, 5, 6, 8, or 11, n.sub.2 is 0 or 1 and n.sub.3 is 0 and R.sub.4 is an alkyl residue of 1-12 C or is selected from phenyl and pyridyl; and their pharmaceutical compositions are useful in inhibiting the release of chemical mediators which cause allergic symptoms. Compounds, compositions, and methods for treatment of allergic conditions are disclosed.
    化学式为:##STR1##的化合物,其中R.sub.1位于位置4,可以是1-6个碳的烷基或是与其位置3的苯基额外连接的--(CH.sub.2).sub.3 -;R.sub.2是1-3个碳的低烷基或氢;n.sub.1,n.sub.2和n.sub.3分别表示CH.sub.2,C(R.sub.2).sub.2和CH.sub.2的数目,其中n.sub.1为2、3、4、5、6、8或11,n.sub.2为0或1,n.sub.3为0,R.sub.4为1-12个碳的烷基残基或选择自苯基和吡啶基;它们的药物组成物在抑制导致过敏症状的化学介质释放方面有用。公开了用于治疗过敏症状的化合物、组成物和方法。
  • P-alkyl phenoxy alkanols for the treatment of allergic conditions
    申请人:Berger; Frank M.
    公开号:US05021460A1
    公开(公告)日:1991-06-04
    p-Alkyl or cycloalkyl phenoxy alkanols and esters are provided having the structure: ##STR1## in which: R.sub.1 is an alkyl group having from one to six carbon atoms, preferably tertiary, and still more preferably tertiary-butul; or a bivalent cycloalkylene group condensed with the phenyl group at adjacent ring carbons thereof, such as in indane; R.sub.2 is lower alkyl having from one to three carbon atoms or hydrogen; R.sub.3 is hydroxyl or an ester group selected from the group consisting of COOR.sub.4 and OOCR.sub.4 derived from unsubstituted and hydroxy-substituted monocarboxylic acids and COOR.sub.5 OOC and OOCR.sub.5 COO derived from unsubstituted and hydroxy-substituted dicarboxylic acids, the acids being selected from the group consisting of aliphatic acids, including carbamic acid, having from one to about twelve carbon atoms; cycloaliphatic acids having from three to about twelve carbon atoms; carbocyclic aromatic acids having from six to about twenty carbon atoms; and nitrogen heterocyclic aromatic acids having from five to about twelve carbon atoms, R.sub.4 being monovalent aliphatic, cycloaliphatic, aromatic, or nitrogen heterocyclic aromatic, and R.sub.5 being divalent aliphatic, cycloaliphatic, aromatic, or nitrogen heterocyclic aromatic, the acids being esterified with aliphatic alcohols having from one to six carbon atoms; and carbonic acid monoalkyl esters, the alkyl having from one to three carbon atoms; and n.sub.1, n.sub.2 and n.sub.3 represent the number of CH.sub.2, C(R.sub.2),.sub.2 and CH.sub.2 groups, respectively, and are numbers within the range from 0 to 10; and at least one of n.sub.1, n.sub.2 and n.sub.3 is other than zero. These compounds inhibit abnormal tissue reactivity due to specific allergic hypersensitivity or due to specific irritants by inhibiting the release of chemical mediators that are responsible for the symptoms of allergic diseases, including allergic rhinitis, asthma, hypersensitivity of the skin and of the gastrointestinal canal, and the many symptoms of irritation and inflammation produced by irritants and inflammation-causing substances, and prevent rejection of transplanted cells and organs and particularly of bone marrow and insulin-producing Langerhans cells.
    提供了具有以下结构的p-烷基或环烷基苯氧基烷醇和酯类化合物:##STR1## 其中:R.sub.1是具有1至6个碳原子的烷基,优选是三级的,更优选是三级丁基;或者是与苯基相邻环碳原子上紧密连接的二价环烷基,例如在茚中;R.sub.2是具有1至3个碳原子的低级烷基或氢;R.sub.3是羟基或酯基,所述酯基选自由未取代和羟基取代的一元羧酸和二元羧酸,所述酸选自具有1至约12个碳原子的脂肪族酸,包括碳酸酯酸;具有3至约12个碳原子的环脂肪族酸;具有6至约20个碳原子的碳环芳香族酸;以及具有5至约12个碳原子的氮杂环芳香族酸,其中R.sub.4是一价的脂肪族、环脂肪族、芳香族或氮杂环芳香族,而R.sub.5是二价的脂肪族、环脂肪族、芳香族或氮杂环芳香族,所述酸被烷基醇酯化,所述烷基具有1至6个碳原子;以及碳酸单烷酯,所述烷基具有1至3个碳原子;n.sub.1、n.sub.2和n.sub.3分别代表CH.sub.2、C(R.sub.2),.sub.2和CH.sub.2基团的数量,且它们是在0至10范围内的数字;并且至少一个n.sub.1、n.sub.2和n.sub.3不为零。这些化合物通过抑制释放导致过敏性疾病症状的化学介质,包括过敏性鼻炎、哮喘、皮肤和胃肠道的过敏性,以及刺激物和引起炎症的物质产生的许多刺激和炎症症状,抑制异常组织反应,防止移植细胞和器官的排异反应,特别是骨髓和胰岛素产生的朗格汉斯细胞的排异反应。
  • P-Alkyl or cycloalkyl phenoxy alkanols and alkanol esters and process
    申请人:Berger; Frank M.
    公开号:US04543362A1
    公开(公告)日:1985-09-24
    p-Alkyl or cycloalkyl phenoxy alkanols and esters are provided having the structure: ##STR1## in which: R.sub.1 is an alkyl group having from one to six carbon atoms, preferably tertiary, and still more preferably tertiary-butyl; or a bivalent cycloalkylene group condensed with the phenyl group at adjacent ring carbons thereof, such as in indane; R.sub.2 is lower alkyl having from one to three carbon atoms or hydrogen; R.sub.3 is hydroxyl or an ester group selected from the group consisting of COOR.sub.4 and OOCR.sub.4 derived from unsubstituted and hydroxy-substituted monocarboxylic acids and COOR.sub.5 OOC and OOCR.sub.5 COO derived from unsubstituted and hydroxy-substituted dicarboxylic acids, the acids being selected from the group consisting of aliphatic acids, including carbamic acid, having from one to about twelve carbon atoms; cycloaliphatic acids having from three to about twelve carbon atoms; carbocyclic aromatic acids having from six to about twenty carbon atoms; and nitrogen heterocyclic aromatic acids having from five to about twelve carbon atoms, R.sub.4 being monovalent aliphatic, cycloaliphatic, aromatic, or nitrogen heterocyclic aromatic, and R.sub.5 being divalent aliphatic, cycloaliphatic, aromatic, or nitrogen heterocyclic aromatic, the acids being esterified with aliphatic alcohols having from one to six carbon atoms; and carbonic acid monoalkyl esters, the alkyl having from one to three carbon atoms; and n.sub.1, n.sub.2 and n.sub.3 represent the number of CH.sub.2, C(R.sub.2).sub.2 and CH.sub.2 groups, respectively, and are numbers within the range from 0 to 10; and at least one of n.sub.1, n.sub.2 and n.sub.3 is other than zero. These compounds inhibit abnormal tissue reactivity due to specific allergic hypersensitivity or due to specific irritants by inhibiting the release of chemical mediators.
    提供p-烷基或环烷基苯氧基脂肪醇和酯,其结构为:##STR1## 其中:R.sub.1是具有1至6个碳原子的烷基,优选是三级的,更优选是叔丁基;或是与苯基相邻环碳原子上凝结的二价环烷基,例如在茚中;R.sub.2是具有1至3个碳原子的低级烷基或氢;R.sub.3是羟基或酯基,所述酯基选自由未取代和羟基取代的单羧酸和由未取代和羟基取代的二羧酸衍生的COOR.sub.4和OOCR.sub.5 COO,所述酸选自包括具有1至约12个碳原子的脂肪酸,包括碳酸酯,具有从3到约12个碳原子的环脂肪酸,具有从6到约20个碳原子的碳环芳香酸和具有从5到约12个碳原子的氮杂环芳香酸,其中R.sub.4是一价的脂肪烷基,环脂肪烷基,芳香族或氮杂环芳香族,R.sub.5是二价的脂肪烷基,环脂肪烷基,芳香族或氮杂环芳香族,所述酸被醇类醇酯化,其碳原子数为1至6;和碳酸单烷基酯,该烷基具有从1至3个碳原子;n.sub.1,n.sub.2和n.sub.3分别代表CH.sub.2,C(R.sub.2).sub.2和CH.sub.2基团的数量,分别是从0到10的数字;并且n.sub.1,n.sub.2和n.sub.3中至少有一个不为零。这些化合物通过抑制化学介质的释放来抑制由特定过敏过敏或特定刺激物引起的异常组织反应。
  • P-alkyl or cycloalkyl phenoxy alkanols and alkanol esters and use for the treatment of allergic conditions
    申请人:PHARMACO DEVELOPMENT PARTNERS
    公开号:EP0162975A1
    公开(公告)日:1985-12-04
    Compounds of the formula and the pharmaceutically acceptable esters thereof wherein R is alkyl (1-6C) or cycloalkyl (1-6C) optionally fused to the benzene of th ecompound of formula I at positions 3 and 4; and Z is a straight chain alkylene (1-15C) optionally substituted by one or two lower alkyl 11-3C); with the proviso that if the compound of formula I is unesterified, Z cannot be unsubstituted prpylene are disclosed. These compounds, as well as unesterified forms wherein Z is unsubstituted propylene are useful in preventing allergic reactions in humans.
    本发明公开了式 I 的化合物及其药学上可接受的酯类,其中 R 是烷基(1-6C)或环烷基(1-6C),可选择在位置 3 和 4 与式 I 化合物的苯融合;Z 是直链亚烷基(1-15C),可选择被一个或两个低级烷基 11-3C 取代;但如果式 I 化合物是未酯化的,则 Z 不能是未取代的丙烯。 这些化合物以及 Z 是未取代的丙烯的未酯化形式可用于预防人类的过敏反应。
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(βS)-β-氨基-4-(4-羟基苯氧基)-3,5-二碘苯甲丙醇 (S)-(-)-7'-〔4(S)-(苄基)恶唑-2-基]-7-二(3,5-二-叔丁基苯基)膦基-2,2',3,3'-四氢-1,1-螺二氢茚 (S)-盐酸沙丁胺醇 (S)-3-(叔丁基)-4-(2,6-二甲氧基苯基)-2,3-二氢苯并[d][1,3]氧磷杂环戊二烯 (S)-2,2'-双[双(3,5-三氟甲基苯基)膦基]-4,4',6,6'-四甲氧基联苯 (S)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (R)富马酸托特罗定 (R)-(-)-盐酸尼古地平 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[((6-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-3-(叔丁基)-4-(2,6-二苯氧基苯基)-2,3-二氢苯并[d][1,3]氧杂磷杂环戊烯 (R)-2-[((二苯基膦基)甲基]吡咯烷 (N-(4-甲氧基苯基)-N-甲基-3-(1-哌啶基)丙-2-烯酰胺) (5-溴-2-羟基苯基)-4-氯苯甲酮 (5-溴-2-氯苯基)(4-羟基苯基)甲酮 (5-氧代-3-苯基-2,5-二氢-1,2,3,4-oxatriazol-3-鎓) (4S,5R)-4-甲基-5-苯基-1,2,3-氧代噻唑烷-2,2-二氧化物-3-羧酸叔丁酯 (4-溴苯基)-[2-氟-4-[6-[甲基(丙-2-烯基)氨基]己氧基]苯基]甲酮 (4-丁氧基苯甲基)三苯基溴化磷 (3aR,8aR)-(-)-4,4,8,8-四(3,5-二甲基苯基)四氢-2,2-二甲基-6-苯基-1,3-二氧戊环[4,5-e]二恶唑磷 (2Z)-3-[[(4-氯苯基)氨基]-2-氰基丙烯酸乙酯 (2S,3S,5S)-5-(叔丁氧基甲酰氨基)-2-(N-5-噻唑基-甲氧羰基)氨基-1,6-二苯基-3-羟基己烷 (2S,2''S,3S,3''S)-3,3''-二叔丁基-4,4''-双(2,6-二甲氧基苯基)-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2S)-(-)-2-{[[[[3,5-双(氟代甲基)苯基]氨基]硫代甲基]氨基}-N-(二苯基甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[[((1R,2R)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2-硝基苯基)磷酸三酰胺 (2,6-二氯苯基)乙酰氯 (2,3-二甲氧基-5-甲基苯基)硼酸 (1S,2S,3S,5S)-5-叠氮基-3-(苯基甲氧基)-2-[(苯基甲氧基)甲基]环戊醇 (1-(4-氟苯基)环丙基)甲胺盐酸盐 (1-(3-溴苯基)环丁基)甲胺盐酸盐 (1-(2-氯苯基)环丁基)甲胺盐酸盐 (1-(2-氟苯基)环丙基)甲胺盐酸盐 (-)-去甲基西布曲明 龙胆酸钠 龙胆酸叔丁酯 龙胆酸 龙胆紫 龙胆紫 齐达帕胺 齐诺康唑 齐洛呋胺 齐墩果-12-烯[2,3-c][1,2,5]恶二唑-28-酸苯甲酯 齐培丙醇 齐咪苯 齐仑太尔 黑染料 黄酮,5-氨基-6-羟基-(5CI) 黄酮,6-氨基-3-羟基-(6CI) 黄蜡,合成物 黄草灵钾盐