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1H-Pyrazole-3-carboxylic acid, 4-fluoro-5-propyl- | 681034-64-0

中文名称
——
中文别名
——
英文名称
1H-Pyrazole-3-carboxylic acid, 4-fluoro-5-propyl-
英文别名
4-fluoro-5-propyl-1H-pyrazole-3-carboxylic acid
1H-Pyrazole-3-carboxylic acid, 4-fluoro-5-propyl-化学式
CAS
681034-64-0
化学式
C7H9FN2O2
mdl
——
分子量
172.16
InChiKey
PLFOBBQEOBUECU-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

物化性质

  • 沸点:
    371.3±42.0 °C(Predicted)
  • 密度:
    1.355±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.4
  • 重原子数:
    12
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.43
  • 拓扑面积:
    66
  • 氢给体数:
    2
  • 氢受体数:
    4

文献信息

  • [EN] MORPHOLIN-PYRIDINE DERIVATIVES<br/>[FR] DÉRIVÉS MORPHOLINE-PYRIDINE
    申请人:HOFFMANN LA ROCHE
    公开号:WO2015165835A1
    公开(公告)日:2015-11-05
    The present invention relates to compounds of formula (I) wherein X is CR or N; R is hydrogen, halogen or lower alkyl; L is a bond, -C(O)- or -C(O)NH-; Ar is phenyl or a five or six membered heteroaryl group, containing one or two N atoms; R1 is halogen, lower alkyl, lower alkyl substituted by halogen, lower alkoxy, lower alkoxy substituted by halogen or cycloalkyl; n is 0, 1, 2 or 3; or to a pharmaceutically suitable acid addition salt thereof, to 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.
    本发明涉及以下式(I)的化合物,其中X为CR或N;R为氢、卤素或较低的烷基;L为键,-C(O)-或-C(O)NH-;Ar为苯基或含有一个或两个N原子的五元或六元杂环芳基;R1为卤素、较低的烷基、被卤素取代的较低烷基、较低的烷氧基、被卤素取代的较低烷氧基或环烷基;n为0、1、2或3;或其药学适宜的酸加合物,所有外消旋混合物,所有对应的对映体和/或光学异构体,可用于治疗抑郁症、焦虑症、双相情感障碍、注意缺陷多动障碍(ADHD)、与压力有关的障碍、精神障碍、精神分裂症、神经疾病、帕森病、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、体温稳态障碍和功能障碍、睡眠和昼夜节律障碍,以及心血管疾病。
  • [EN] 2-OXA-5-AZABICYCLO[2.2.1]HEPTAN-3-YL DERIVATIVES<br/>[FR] DÉRIVÉS DU 2-OXA -5-AZABICYCLO [2.2.1] HEPTAN -3-YL
    申请人:HOFFMANN LA ROCHE
    公开号:WO2016016292A1
    公开(公告)日:2016-02-04
    The present invention relates to compounds of formula (I), wherein L is a bond, -C(O)NH-, -NHC(O)-, -CH2NHC(O)-, CH2C(O)NH-, -CH2NH-, -NH- or -NHC(O)NH-; R1 is hydrogen, lower alkyl, halogen, lower alkoxy-alkyl, lower alkoxy substituted by halogen, lower alkyl substituted by halogen or is phenyl or heteroaryl selected from the group consisting of pyridinyl, pyrimidinyl, pyrazinyl or pyrazolyl, and wherein phenyl and heteroaryl are optionally substituted by one, two or three substituents selected from the group consisting of halogen, lower alkyl, lower alkoxy, lower alkyl substituted by halogen, lower alkoxy substituted by halogen, cycloalkyl or O-CH2-cycloalkyl; or to a pharmaceutically suitable acid addition salt thereof, to 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.
    本发明涉及以下化合物的公式(I),其中L是键,-C(O)NH-,-NHC(O)-,- NHC(O)-, C(O)NH-,- NH-,-NH-或-NHC(O)NH-;R1是氢,较低的烷基,卤素,较低的烷氧基烷基,受卤素取代的较低的烷氧基,受卤素取代的较低的烷基或为苯基或杂环芳基,所述苯基和杂环芳基从吡啶基、嘧啶基、吡啉基或吡唑基中选择,其中苯基和杂环芳基可以选择地被来自卤素、较低的烷基、较低的烷氧基、受卤素取代的较低的烷基、受卤素取代的较低的烷氧基、环烷基或O-CH2-环烷基的一个、两个或三个取代基取代;或其药用合适的酸盐,所有的消旋混合物,它们所有对应的对映体和/或光学异构体,可用于治疗抑郁症、焦虑症、躁郁症、注意力缺陷多动障碍(ADHD)、与压力有关的障碍、精神病性障碍、精神分裂症、神经疾病、帕森病、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、心血管障碍。
  • [EN] 5-SUBSTITUTED 2H-PYRAZONE-3-CARBOXYLIC ACID DERIVATIVES AS ANTILIPOLYTIC AGENTS FOR THE TREATMENT OF METABOLIC-RELATED DISORDERS SUCH AS DYSLIPIDEMIA<br/>[FR] DERIVES D'ACIDE 2H-PYRAZOLE-3-CARBOXYLIQUE SUBSTITUE EN 5 UTILISES EN TANT QU'AGENTS ANTILIPOTYQUES POUR LE TRAITEMENT DE TROUBLES METABOLIQUES, TELS QUE LA DYSLIPIDEMIE
    申请人:ARENA PHARM INC
    公开号:WO2004032928A1
    公开(公告)日:2004-04-22
    The present invention relates to certain pyrazole carboxylic acid derivatives of Formula (Ia), and pharmaceutically acceptable salts thereof, as antilipolytic agents and against for the receptor RUP25, wherein: R2 is H, halogen, C1-12 alkyl or C1-12 haloalkyl; and R3 is C3-6 cycloalkyl, C1-12 alkyl, C1-12 haloalkyl, C3-6 cycloalkyl-C1-4-alkylene, aryl-C1-4-alkylene or heteroaryl-C1-4-alkylene, wherein said aryl-C1-4-alkylene and heteroaryl-C1-4-alkylene can be optionally substituted 1 to 5 substituents selected from the substituents listed in the claims. Also provided by the present invention are pharmaceutical compositions containing compounds of the invention, and methods of using the compounds and compositions of the invention in the treatment of metabolic-related disorders, including dyslipidemia, atherosclerosis, coronary heart disease, insulin resistance, type 2 diabetes, Syndrome-X and the like. In addition, the present invention also provides for pharmaceutical compositions in combination with other active agents, for example, those agents belonging to the class of α-glucosidase inhibitors, aldose reductase inhibitors, biguanides, HMG-CoA reductase inhibitors, squalene synthesis inhibitors, fibrates, LDL catabolism enhancers, angiotensin converting enzyme (ACE) inhibitors, insulin secretion enhancers, thiazolidinedione and the like.
    本发明涉及具有化学式(Ia)的某些吡唑羧酸生物及其药学上可接受的盐,作为抗脂解作用剂和针对受体RUP25的药物,在该化合物中:R2为H、卤素、C1-12烷基或C1-12卤代烷基;R3为C3-6环烷基、C1-12烷基、C1-12卤代烷基、C3-6环烷基-C1-4-烷基、芳基-C1-4-烷基或杂环芳基-C1-4-烷基,其中所述的芳基-C1-4-烷基和杂环芳基-C1-4-烷基可以选择性地取代1至5个选自权利要求中所列取代基的取代基。本发明还提供了含有该化合物的药物组合物,以及在治疗代谢相关疾病,包括脂质代谢紊乱、动脉粥样硬化、冠心病、胰岛素抵抗、2型糖尿病、综合征X等方面使用该化合物和组合物的方法。此外,本发明还提供了与其他活性剂结合的药物组合物,例如,属于α-葡萄糖苷酶抑制剂、醛糖还原酶抑制剂、双胍类、HMG-CoA还原酶抑制剂角鲨烯合成抑制剂、贝特类药物、LDL降解增强剂、血管紧张素转化酶(ACE)抑制剂胰岛素分泌增强剂、噻唑烷二酮类药物等类别的药物。
  • 5-substituted 2h-pyrazone-3-carbixylic acid derivatives as antilipolytic agents for the treatment of metabolic-related disorders such as dyslipidemia
    申请人:Semple Graeme
    公开号:US20060167270A1
    公开(公告)日:2006-07-27
    The present invention relates to certain pyrazole carboxylic acid derivatives of Formula (Ia), and pharmaceutically acceptable salts thereof, as antilipolytic agents and against for the receptor RUP25, wherein: R 2 is H, halogen, C 1-12 alkyl or C 1-12 haloalkyl; and R 3 is C 3-6 cycloalkyl, C 1-12 alkyl, C 1-12 haloalkyl, C 3-6 cycloalkyl-C 1-4 -alkylene, aryl-C 1-4 -alkylene or heteroaryl-C 1-4 -alkylene, wherein said aryl-C 1-4 -alkylene and heteroaryl-C 1-4 -alkylene can be optionally substituted 1 to 5 substituents selected from the substituents listed in the claims. Also provided by the present invention are pharmaceutical compositions containing compounds of the invention, and methods of using the compounds and compositions of the invention in the treatment of metabolic-related disorders, including dyslipidemia, atherosclerosis, coronary heart disease, insulin resistance, type 2 diabetes, Syndrome-X and the like. In addition, the present invention also provides for pharmaceutical compositions in combination with other active agents, for example, those agents belonging to the class of α-glucosidase inhibitors, aldose reductase inhibitors, biguanides, HMG-CoA reductase inhibitors, squalene synthesis inhibitors, fibrates, LDL catabolism enhancers, angiotensin converting enzyme (ACE) inhibitors, insulin secretion enhancers, thiazolidinedione and the like.
    本发明涉及公式(Ia)的某些吡唑羧酸生物及其药学上可接受的盐,作为抗脂解作用剂和对RUP25受体的作用剂,其中:R2为H、卤素、C1-12烷基或C1-12卤代烷基;R3为C3-6环烷基、C1-12烷基、C1-12卤代烷基、C3-6环烷基-C1-4-烷基、芳基-C1-4-烷基或杂环芳基-C1-4-烷基,其中所述的芳基-C1-4-烷基和杂环芳基-C1-4-烷基可以选择性地被1至5个在权利要求书中列出的取代基所取代。本发明还提供了含有该化合物的药物组合物,并且提供了使用该化合物和该组合物治疗代谢相关疾病的方法,包括血脂异常、动脉粥样硬化、冠心病、胰岛素抵抗、2型糖尿病、X综合症等。此外,本发明还提供了与其他活性剂组合的药物组合物,例如属于α-葡萄糖苷酶抑制剂、醛还原酶抑制剂、双胍类、HMG-CoA还原酶抑制剂角鲨烷合成抑制剂、纤维酸类、LDL降解增强剂、血管紧张素转换酶(ACE)抑制剂胰岛素分泌增强剂、噻唑烷二酮等类别的活性剂。
  • 5-SUBSTITUTED 2H-PYRAZONE-3-CARBOXYLIC ACID DERIVATIVES AS ANTILIPOLYTIC AGENTS FOR THE TREATMENT OF METABOLIC-RELATED DISORDERS SUCH AS DYSLIPIDEMIA
    申请人:Arena Pharmaceuticals, Inc.
    公开号:EP1551403A1
    公开(公告)日:2005-07-13
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