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2-(1-异丙基-1H-吡唑-3-基)乙醇 | 177940-21-5

中文名称
2-(1-异丙基-1H-吡唑-3-基)乙醇
中文别名
乙基4-(4-氯苯基)-4-羟基哌啶-1-羧酸酯
英文名称
2-(1-isopropyl-1H-pyrazol-3-yl)-1-ethanol
英文别名
2-(1-Isopropyl-1H-pyrazol-3-yl)ethanol;2-(1-propan-2-ylpyrazol-3-yl)ethanol
2-(1-异丙基-1H-吡唑-3-基)乙醇化学式
CAS
177940-21-5
化学式
C8H14N2O
mdl
——
分子量
154.212
InChiKey
SENLEHBGLMHBRX-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):
    0.5
  • 重原子数:
    11
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.62
  • 拓扑面积:
    38
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    2-(1H-吡唑-3-基)-乙醇disodium;carbonate2-碘代丙烷二氯甲烷Sodium sulfate-III 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 18.0h, 以to give 0.36 gm (26.0%) of the title compound as a brown oil的产率得到2-(1-异丙基-1H-吡唑-3-基)乙醇
    参考文献:
    名称:
    Methods of treating or ameliorating the symptoms of common cold or allergic rhinitis with serotonin 5-HT1F agonists
    摘要:
    本发明提供了一种治疗或缓解普通感冒或过敏性鼻炎症状的方法,包括向需要该治疗的哺乳动物施用一种5-羟色胺5-HT1F激动剂。
    公开号:
    US06380201B1
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文献信息

  • [EN] SUBSTITUTED 2-CARBONYLAMINO-6-PIPERIDINAMINOPYRIDINES AND SUBSTITUTED 1-CARBONYLAMINO-3-PIPERIDINAMINOBENZENES AS 5-HT1F AGONISTS<br/>[FR] 2-CARBONYLAMINO-6-PIPERIDINAMINOPYRIDINES SUBSTITUES ET 1-CARBONYLAMINO-3-PIPERIDINAMINOBENZENES SUBSTITUES UTILISES EN TANT QU'AGONISTES DE 5-HT1F
    申请人:LILLY CO ELI
    公开号:WO2005035499A1
    公开(公告)日:2005-04-21
    ABSTRACT The present invention relates to compounds of formula I: (I) or a pharmaceutically acceptable acid addition salt thereof, where; X is C(R3c= or N=; R1 is C2-C6 alkyl, substituted C2-C6 alkyl, C3-C7 cycloalkyl, substituted C3-C7 cycloalkyl, phenyl, substituted phenyl, heterocycle, or substituted heterocycle; R2 is hydrogen, C1-C3 n-alkyl, C3-C6 cycloalkyl-C1-C3 alkyl, or a group of formula II (II) provided that when R1 is C2-C6 alkyl or substituted C2-C6 alkyl, R2 is hydrogen or methyl; R3a, R3b, and, when X is C(R3c)=, R3c, are each independently hydrogen, fluoro, or methyl, provided that no more than one of R3a, R3b, and R3c may be other than hydrogen; R4 is hydrogen or C1-C3 alkyl; R5 is hydrogen, C1-C3 alkyl, or C3-C6 cycloalkylcarbonyl, provided that when R3a is other than hydrogen, R5 is hydrogen; R6 is hydrogen or C1-C6 alkyl; and n is an integer from 1 to 6 inclusively. The compounds of the present invention are useful for activating 5-HT1F receptors, inhibiting neuronal protein extravasation, and for the treatment or prevention of migraine in a mammal.
    本发明涉及以下化合物的公式I:(I)或其药学上可接受的酸加盐,其中;X为C(R3c=或N=;R1为C2-C6烷基,取代的C2-C6烷基,C3-C7环烷基,取代的C3-C7环烷基,苯基,取代的苯基,杂环烷基,或取代的杂环烷基;R2为氢,C1-C3正烷基,C3-C6环烷基-C1-C3烷基,或公式II的基团(II),但当R1为C2-C6烷基或取代的C2-C6烷基时,R2为氢或甲基;R3a,R3b,和当X为C(R3c)=时,R3c,各自独立地为氢,,或甲基,但R3a,R3b,和R3c中的最多一个可能不是氢;R4为氢或C1-C3烷基;R5为氢,C1-C3烷基,或C3-C6环烷基甲酰,但当R3a不是氢时,R5为氢;R6为氢或C1-C6烷基;n为1到6的整数(包括1和6)。本发明的化合物可用于激活5-HT1F受体,抑制神经蛋白外渗,以及用于治疗或预防哺乳动物的偏头痛。
  • 1H-indole and benzo(b)thiophene derivatives with 4-(1,2,3,6-tetra:hydro:pyridinyl)- and 4-piperidinyl-groups bound to the heterocyclic ring as inhibitors of serotonin reuptake
    申请人:ELI LILLY AND COMPANY
    公开号:EP0812826A1
    公开(公告)日:1997-12-17
    The pharmaceutical use of novel compounds of formula I: where Z is a structure of formula A-B is -C=CH- or -C(R5)-CH2-; X is S or NR4; R1 is H, halo, formyl, C1-C4 alkyl, C1-C4 alkoxy, thienylmethyloxy, 4,5-dihydrothiazol-2-yl, cyano, nitro, carboxamido, trifluoromethyl or hydroxy; R2 is H or halo; R3 is H, C1-C4 alkyl, (C1-C4 alkylene)-aryl, or -CH2-Y-NR7R8; R4 is H, C1-C4 alkyl, C1-C5 acyl, or phenylsulfonyl; R5 is H or OH; R6 is H or methyl; Y is -CH2- or -C(O)-; R7 is pyridinyl; and R8 is H or -C(O)-(C3-C6 cycloalkyl); and pharmaceutically acceptable salts thereof.
    化合物的药用途:其中Z是formulaA-B结构,-C=CH-或-C(R5)-CH2-;X是S或NR4;R1是H、卤素、甲酰基、C1-C4烷基、C1-C4烷氧基、噻吩甲氧基、4,5-二氢噻唑-2-基、基、硝基、羧酰胺基、三甲基或羟基;R2是H或卤素;R3是H、C1-C4烷基、(C1-C4烷基)-芳基,或- -Y-NR7R8;R4是H、C1-C4烷基、C1-C5酰基,或苯基磺酰基;R5是H或OH;R6是H或甲基;Y是- -或-C(O)-;R7是吡啶基;R8是H或-C(O)-(C3-C6环烷基);以及其药用上可接受的盐。
  • [EN] A METHOD FOR THE PREVENTION OF MIGRAINE<br/>[FR] METHODE DE PREVENTION DE MIGRAINE
    申请人:ELI LILLY AND COMPANY
    公开号:WO1998011895A1
    公开(公告)日:1998-03-26
    (EN) This invention provides methods for the prevention of migraine which comprises administering to a mammal in need thereof a serotonin 5-HT1F agonist.(FR) L'invention concerne une méthode de prévention de migraine, qui consiste à administrer à un patient mammifère un agoniste 5-HT1F de la sérotonine.
    这项发明提供了预防偏头痛的方法,包括向需要的哺乳动物施用5-HT1F血清素激动剂。
  • [EN] TREATMENT OF THE COMMON COLD OR ALLERGIC RHINITIS<br/>[FR] TRAITEMENT DU RHUME DE CERVEAU ET DES RHINITES ALLERGIQUES
    申请人:ELI LILLY AND COMPANY
    公开号:WO1998006402A1
    公开(公告)日:1998-02-19
    (EN) This invention provides methods for the treatment or amelioration of the symptoms of the common cold or allergic rhinitis which comprises administering to a mammal in need thereof a serotonin 5-HT1F agonist.(FR) La présente invention concerne une thérapie permettant de traiter le rhume de cerveau ou les rhinites allergiques, ou d'en atténuer les signes cliniques. Cette thérapie consiste en l'administration, à un mammifère le justifiant, d'un agoniste de la sérotonine 5-HTF1.
    这项发明提供了治疗或缓解普通感冒或过敏性鼻炎症状的方法,包括向需要治疗的哺乳动物施用5-羟色胺5-HT1F激动剂。
  • 5-HT.sub.1F agonists for the treatment of migraine
    申请人:Eli Lilly and Company
    公开号:US05521196A1
    公开(公告)日:1996-05-28
    This invention provides novel 5-HT.sub.1F agonists which are useful for the treatment of migraine and associated disorders.
    这项发明提供了新型的5-HT.sub.1F激动剂,可用于治疗偏头痛及相关疾病。
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