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2-环丙基嘧啶-5-胺 | 1152519-69-1

中文名称
2-环丙基嘧啶-5-胺
中文别名
2-环丙基-5氨基嘧啶
英文名称
2-cyclopropylpyrimidin-5-amine
英文别名
——
2-环丙基嘧啶-5-胺化学式
CAS
1152519-69-1
化学式
C7H9N3
mdl
MFCD11103237
分子量
135.169
InChiKey
OCOLSCGNKGPGKC-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):
    0.1
  • 重原子数:
    10
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.428
  • 拓扑面积:
    51.8
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    2-环丙基嘧啶-5-胺tris-(dibenzylideneacetone)dipalladium(0) 、 sodium hydride 、 caesium carbonate4,5-双二苯基膦-9,9-二甲基氧杂蒽 作用下, 以 1,4-二氧六环N,N-二甲基甲酰胺 、 mineral oil 为溶剂, 反应 40.08h, 生成 2-cyclopropyl-N-(pyrazin-2-yl)-N-({5-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]thiophen-2-yl}methyl)pyrimidin-5-amine
    参考文献:
    名称:
    [EN] OXADIAZOLYLTHIOPHENE DERIVATIVES USEFUL AS HISTONE DEACETYLASE INHIBITORS
    [FR] DÉRIVÉS D'OXADIAZOLYLTHIOPHÈNE À UTILISER EN TANT QU'INHIBITEURS DE L'HISTONE DÉSACÉTYLASE
    摘要:
    一种Formula I的化合物:(I)或其药学上可接受的盐,其中:每个R'是QR1;每个Q独立地选自键,-C1-C10烷基,-C2-C10烯基,-C(O)-,-C(O)O-,-C(O)N(R1)-,-C(O)N(R1)SO2-,-N(R1)C(O)-,-N(R1)-,-N(SO2(R1)),-N(R1)SO2-,-C(O)NR4R5-,-N(R4R5)C(O)-,-N(R4R5)-,-S-,-SO-,-SO2-,-S(O)O-,-SO2N(R1)-和-O-;每个R1独立地选自H,C1-C10烷基,C2-C10烯基,C2-C10炔基,C1-C10卤代烷基,C1-C10杂原子烷基,芳基,杂芳基,C3-C10环烷基,-(C1-C10烷基)-C3-C10环烷基,卤素,氰基,C1-C10烷基-芳基,C1-C10烷基-杂原子芳基,C1-C10杂环烷基和-(C1-C10烷基)-C1-C10杂环烷基。这些化合物是HDAC的抑制剂,因此在治疗包括癌症和炎症在内的多种疾病中具有潜在用途。
    公开号:
    WO2019166824A1
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文献信息

  • NOVEL COMPOUNDS
    申请人:Glaxo Group Limited
    公开号:US20150065507A1
    公开(公告)日:2015-03-05
    The present invention is directed to novel retinoid-related orphan receptor gamma (RORγ) modulators, processes for their preparation, pharmaceutical compositions containing these modulators, and their use in the treatment of inflammatory, metabolic and autoimmune diseases mediated by RORγ.
    本发明涉及新型视黄醛酸相关孤儿受体γ(RORγ)调节剂,其制备方法,含有这些调节剂的药物组合物,以及它们在治疗由RORγ介导的炎症性、代谢性和自身免疫疾病中的应用。
  • [EN] NOVEL COMPOUNDS<br/>[FR] NOUVEAUX COMPOSÉS
    申请人:GLAXO GROUP LTD
    公开号:WO2013160419A1
    公开(公告)日:2013-10-31
    The present invention is directed to novel retinoid-related orphan receptor gamma (RORγ) modulators, processes for their preparation, pharmaceutical compositions containing these modulators, and their use in the treatment of inflammatory, metabolic and autoimmune diseases mediated by RORγ.
    本发明涉及新型视黄醛相关孤儿受体γ(RORγ)调节剂,其制备方法,含有这些调节剂的药物组合物,以及它们在治疗由RORγ介导的炎症性、代谢性和自身免疫性疾病中的应用。
  • [EN] 6-AMINO-5,6,7,8-TETRAHYDRONAPHTHALEN-2-YL OR 3-AMINOCHROMAN-7-YL DERIVATIVES AS TAAR MODULATORS<br/>[FR] DÉRIVÉS 6-AMINO -5,6,7,8-TÉTRAHYDRONAPHTALÈNE -2-YLE OU 3-AMINOCHROMAN -7-YL COMME MODULATEURS DE TAAR
    申请人:HOFFMANN LA ROCHE
    公开号:WO2016016162A1
    公开(公告)日:2016-02-04
    The present invention relates to a compound of formula (I), wherein L is –C(O)NH-, -NHC(O)-, -S(O)2NH-, -NH- or -NHC(O)NH-; Ar is phenyl, benzyl, naphthyl or heteroaryl, selected from the group consisting of pyridinyl, pyrazolyl, pyrimidinyl, isoxazolyl or pyrazinyl, wherein Ar may be optionally substituted by one, two or three R1; R1 is hydrogen, lower alkyl, lower alkoxy, halogen, cyano, cycloalkyl, NHC(O)-lower alkyl, lower alkoxy substituted by halogen, lower alkyl substituted by halogen, or is phenyl optionally substituted by one or two halogen atoms, CF3O or lower alkyl, or is furanyl, thiazolyl or thiophenyl, optionally substituted by halogen or lower alkyl; X is CH or O; R is hydrogen or halogen; or a pharmaceutically suitable acid addition salt thereof, all racemic mixtures, all their corresponding enantiomers and/or optical isomers, which may be used for the treatment of depression, anxiety disorders, bipolar disorder, attention deficit hyperactivity disorder (ADHD), stress-related disorders, psychotic disorders, schizophrenia, neurological diseases, Parkinson's disease, neurodegenerative disorders, Alzheimer's disease, epilepsy, migraine, hypertension, substance abuse, metabolic disorders, eating disorders, diabetes, diabetic complications, obesity, dyslipidemia, disorders of energy consumption and assimilation, disorders and malfunction of body temperature homeostasis, disorders of sleep and circadian rhythm, and cardiovascular disorders.
    本发明涉及一种化合物,其化学式为(I),其中L为-C(O)NH-,-NHC(O)-,-S(O)2NH-,-NH-或-NHC(O)NH-;Ar为苯基,苄基,萘基或杂环基,所述杂环基选自吡啶基,吡唑基,嘧啶基,异噁唑基或吡嗪基,其中Ar可以选择性地由一个、两个或三个R1取代;R1为氢,低碳烷基,低烷氧基,卤素,氰基,环烷基,NHC(O)-低碳烷基,低烷氧基取代的卤素,低碳烷基取代的卤素,或为苯基,可选择性地由一个或两个卤素原子,CF3O或低碳烷基取代,或为呋喃基,噻唑基或噻吩基,可选择性地由卤素或低碳烷基取代;X为CH或O;R为氢或卤素;或其药学上适宜的酸加合物盐,所有的外消旋混合物,其对应的对映体和/或光学异构体,可用于治疗抑郁症,焦虑障碍,双相情感障碍,注意缺陷多动障碍(ADHD),与压力有关的障碍,精神病性障碍,精神分裂症,神经系统疾病,帕金森病,神经退行性疾病,阿尔茨海默病,癫痫,偏头痛,高血压,物质滥用,代谢障碍,进食障碍,糖尿病,糖尿病并发症,肥胖症,血脂异常,能量消耗和吸收障碍,体温稳态障碍,睡眠和昼夜节律障碍,以及心血管疾病。
  • Compounds
    申请人:Glaxo Group Limited
    公开号:US09242972B2
    公开(公告)日:2016-01-26
    The present invention is directed to novel retinoid-related orphan receptor gamma (RORγ) modulators, processes for their preparation, pharmaceutical compositions containing these modulators, and their use in the treatment of inflammatory, metabolic and autoimmune diseases mediated by RORγ.
    本发明涉及新型视黄醇相关孤儿受体γ(RORγ)调节剂,其制备过程,含有这些调节剂的制药组合物,以及它们在治疗由RORγ介导的炎症、代谢和自身免疫性疾病中的应用。
  • [EN] HETEROARYL COMPOUNDS USEFUL IN THE TREATMENT OF COGNITIVE DISORDERS<br/>[FR] COMPOSÉS HÉTÉROARYLE POUVANT ÊTRE UTILISÉS DANS LE TRAITEMENT DE TROUBLES COGNITIFS
    申请人:UNIV COLLEGE CARDIFF CONSULTANTS LTD
    公开号:WO2022234271A1
    公开(公告)日:2022-11-10
    The present invention provides compounds of formula (I), as well as pharmaceutically acceptable salts thereof: wherein X1, X2, X3, R3, Ring A and Ring B are as described herein. The compounds have affinity for α5-subunit-containing GABAAreceptors. The invention further provides the manufacture of the compounds of formula (I), pharmaceutical compositions comprising the compounds and their use as medicaments for the treatment of diseases and disorders associated with α5-GABAAreceptors, including depression and cognitive impairment, for example, congintive impairment associated with a psychotic disorder such as schizophrenia.
    本发明提供了式(I)的化合物,以及其药学上可接受的盐:其中X1,X2,X3,R3,环A和环B如本文所述。该化合物具有与α5亚单位含量的GABAA受体的亲和力。本发明进一步提供了制备式(I)化合物的方法,包括含有该化合物的药物组合物以及将其用作治疗与α5-GABAA受体相关的疾病和障碍的药物,包括抑郁症和认知障碍,例如与精神疾患如精神分裂症相关的认知障碍。
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