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2-(hydroxymethyl)-4-methylpiperidine | 38299-77-3

中文名称
——
中文别名
——
英文名称
2-(hydroxymethyl)-4-methylpiperidine
英文别名
(4-methyl-piperidin-2-yl)-methanol;(4-Methylpiperidin-2-yl)methanol
2-(hydroxymethyl)-4-methylpiperidine化学式
CAS
38299-77-3
化学式
C7H15NO
mdl
——
分子量
129.202
InChiKey
QAGSWXPHVBZSKN-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:
    9
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    32.3
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    2-(hydroxymethyl)-4-methylpiperidine盐酸氯化亚砜 、 sodium azide 、 potassium carbonate红铝 作用下, 以 二氯甲烷N,N-二甲基甲酰胺乙腈丁酮 为溶剂, 反应 15.0h, 生成 1-Benzyl-5-methyl-azepan-3-ylamine
    参考文献:
    名称:
    Development of Potent Serotonin-3 (5-HT3) Receptor Antagonists. I. Structure-Activity Relationships of 2-Alkoxy-4-amino-5-chlorobenzamide Derivatives.
    摘要:
    合成了一系列新的2-烷氧基-4-氨基-5-氯苯甲酰胺衍生物,这些衍生物在氨基部分包含五到七元的杂环非芳香环,并通过测试其对大鼠冯·贝佐尔德-雅里希反射的拮抗能力来评估其对血清素-3(5-HT3)受体的拮抗活性。五到七元的杂环包括吡咯烷、吗啉、1,4-噻嗪、哌啶、哌嗪、1,4-噁唑烯、1,4-噻唑烯、七元环及1,4-二唑烯环。其中,某些具有1,4-二唑烯环的苯甲酰胺衍生物表现出了强效的5-HT3受体拮抗活性。特别是4-氨基-5-氯-N-(1,4-二甲基六氢-1H-1,4-二唑啉-6-基)-2-乙氧基苯甲酰胺(96)和1-苄基-4-甲基六氢-1H-1,4-二唑啉类似物103展现了强效的5-HT3受体拮抗活性,而未表现出对5-HT4受体的结合亲和力。
    DOI:
    10.1248/cpb.43.1364
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文献信息

  • SUBSTITUTED THIAZOLIDINEDIONE INDAZOLES, INDOLES AND BENZOTRIAZOLES AS ESTROGEN-RELATED RECEPTOR-a MODULATORS
    申请人:Bignan Gilles
    公开号:US20110294780A1
    公开(公告)日:2011-12-01
    The present invention relates to compounds of Formula (I), methods for preparing these compounds, compositions, intermediates and derivatives thereof and for treating a condition including but not limited to ankylosing spondylitis, artherosclerosis, arthritis (such as rheumatoid arthritis, infectious arthritis, childhood arthritis, psoriatic arthritis, reactive arthritis), bone-related diseases (including those related to bone formation), breast cancer (including those unresponsive to anti-estrogen therapy), cardiovascular disorders, cartilage-related disease (such as cartilage injury/loss, cartilage degeneration, and those related to cartilage formation), chondrodysplasia, chondrosarcoma, chronic back injury, chronic bronchitis, chronic inflammatory airway disease, chronic obstructive pulmonary disease, diabetes, disorders of energy homeostasis, gout, pseudogout, lipid disorders, metabolic syndrome, multiple myeloma, obesity, osteoarthritis, osteogenesis imperfecta, osteolytic bone metastasis, osteomalacia, osteoporosis, Paget's disease, periodontal disease, polymyalgia rheumatica, Reiter's syndrome, repetitive stress injury, hyperglycemia, elevated blood glucose level, and insulin resistance.
    本发明涉及式(I)的化合物,制备这些化合物的方法,组合物,中间体及其衍生物,并用于治疗包括但不限于强直性脊柱炎,动脉粥样硬化,关节炎(如类风湿关节炎,感染性关节炎,儿童关节炎,银屑病性关节炎,反应性关节炎),与骨相关的疾病(包括与骨形成有关的疾病),乳腺癌(包括对抗雌激素治疗无效的癌症),心血管疾病,软骨相关疾病(如软骨损伤/丧失,软骨退化以及与软骨形成有关的疾病),软骨发育不良,软骨肉瘤,慢性腰部损伤,慢性支气管炎,慢性炎症性气道疾病,慢性阻塞性肺疾病,糖尿病,能量稳态紊乱,痛风,假性痛风,脂质紊乱,代谢综合征,多发性骨髓瘤,肥胖,骨关节炎,遗传性骨发育不全,骨溶解性骨转移,软骨软化症,骨质疏松症,帕金森病,牙周病,多肌痛风,Reiter综合征,重复性应激损伤,高血糖,血糖水平升高和胰岛素抵抗等病症的方法。
  • [EN] TETRASUBSTITUTED PYRIMIDINE DERIVATIVES FOR CONTROLLING PHYTOPATHOGENIC FUNGI<br/>[FR] DÉRIVÉS DE PYRIMIDINE TÉTRASUBSTITUÉS PERMETTANT DE CONTRÔLER DES CHAMPIGNONS PHYTOPATHOGÈNES
    申请人:BASF SE
    公开号:WO2009019099A1
    公开(公告)日:2009-02-12
    The present invention relates to pyrimidine compounds of the formula (I) in which the substituents are as defined in the claims and the specification and to the use of said compounds for the control of phytopathogenic fungi.
    本发明涉及式(I)的嘧啶化合物,其中取代基如索引和说明书中所定义的,并且涉及利用这些化合物控制植物病原真菌。
  • Fungicidal Azolopyrimidines, Process for Their Preparation and Their Use For Controlling Harmful Fungi, and Also Compositions Comprising Them
    申请人:Dietz Jochen
    公开号:US20100160311A1
    公开(公告)日:2010-06-24
    The present invention relates to azolopyrimidines of the formula I in which the substituents are defined according to the description, to processes and intermediates for preparing these compounds, to compositions comprising them and to their use for controlling phytopathogenic harmful fungi.
    本发明涉及公式I的咪唑嘧啶类化合物,其中取代基根据描述进行定义,涉及制备这些化合物的方法和中间体,包括这些化合物的组合物以及它们用于控制植物病原真菌的用途。
  • Pyrimidine compounds for combating pathogenic fungi and cancer
    申请人:Dietz Jochen
    公开号:US20090264447A1
    公开(公告)日:2009-10-22
    The present invention relates to the use of pyrimidine compounds of formula I wherein the variables have the meanings stated in the claims and in the description, for combating pathogenic fungi, new pyrimidine compounds of formula (I), and fungicidal and pharmaceutical agents containing the same.
    本发明涉及使用式I中变量具有所述声明和说明中的含义的嘧啶化合物来对抗病原真菌,以及公式(I)的新嘧啶化合物和含有其的杀真菌和药物制剂。
  • Cahill,R.; Crabb,T.A., Journal of Heterocyclic Chemistry, 1972, vol. 9, p. 875 - 878
    作者:Cahill,R.、Crabb,T.A.
    DOI:——
    日期:——
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