摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

3-((4aS,5aS)-3-carboxy-4,4a,5,5a-tetrahydro-1H-cyclopropa[4,5]cyclopenta[1,2-c]pyrazol-1-yl)pyrazine 1-oxide | 1268883-00-6

中文名称
——
中文别名
——
英文名称
3-((4aS,5aS)-3-carboxy-4,4a,5,5a-tetrahydro-1H-cyclopropa[4,5]cyclopenta[1,2-c]pyrazol-1-yl)pyrazine 1-oxide
英文别名
(2S,4S)-9-(4-oxidopyrazin-4-ium-2-yl)-8,9-diazatricyclo[4.3.0.0(2)]nona-1(6),7-diene-7-carboxylic acid;(2S,4S)-9-(4-oxidopyrazin-4-ium-2-yl)-8,9-diazatricyclo[4.3.0.02,4]nona-1(6),7-diene-7-carboxylic acid
3-((4aS,5aS)-3-carboxy-4,4a,5,5a-tetrahydro-1H-cyclopropa[4,5]cyclopenta[1,2-c]pyrazol-1-yl)pyrazine 1-oxide化学式
CAS
1268883-00-6
化学式
C12H10N4O3
mdl
——
分子量
258.236
InChiKey
JWVCWCNOPFCNFX-BQBZGAKWSA-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:
    629.0±55.0 °C(Predicted)
  • 密度:
    1.91±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -0.5
  • 重原子数:
    19
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    93.5
  • 氢给体数:
    1
  • 氢受体数:
    5

安全信息

  • 储存条件:
    存储条件:2-8°C,避光保存

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    3-((4aS,5aS)-3-carboxy-4,4a,5,5a-tetrahydro-1H-cyclopropa[4,5]cyclopenta[1,2-c]pyrazol-1-yl)pyrazine 1-oxide二乙胺基三氟化硫N,N-二异丙基乙胺 、 N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate 作用下, 以 二氯甲烷N,N-二甲基甲酰胺 为溶剂, 反应 0.75h, 生成 3-((4aS,5aS)-3-((3,3-difluoro-1-(hydroxymethyl)cyclobutyl)carbamoyl)-4,4a,5,5a-tetrahydro-1H-cyclopropa[4,5]cyclopenta[1,2-c]pyrazol-1-yl)pyrazine-1-oxide
    参考文献:
    名称:
    一种多环衍生物及其制备
    摘要:
    本发明公开一种式(I)、式(II)所示化合物及其立体异构体、药学上可接受的盐、溶剂化物、水合物、N‑氧化物、前药及其药物组合物、制备方法,以及在由大麻素CB2受体介导的疾病的预防和治疗中的用途。
    公开号:
    CN112480121A
  • 作为产物:
    描述:
    (1aS,5aS)-2-(pyrazin-2-yl)-1a,2,5,5a-tetrahydro-1H-2,3-diazacyclopropa[a]pentalene-4-carboxylic acid ethyl ester 在 甲酸双氧水 、 sodium hydroxide 作用下, 以 四氢呋喃甲醇 为溶剂, 反应 5.0h, 生成 3-((4aS,5aS)-3-carboxy-4,4a,5,5a-tetrahydro-1H-cyclopropa[4,5]cyclopenta[1,2-c]pyrazol-1-yl)pyrazine 1-oxide
    参考文献:
    名称:
    一种多环衍生物及其制备
    摘要:
    本发明公开一种式(I)、式(II)所示化合物及其立体异构体、药学上可接受的盐、溶剂化物、水合物、N‑氧化物、前药及其药物组合物、制备方法,以及在由大麻素CB2受体介导的疾病的预防和治疗中的用途。
    公开号:
    CN112480121A
点击查看最新优质反应信息

文献信息

  • [EN] PROCESSES FOR THE PREPARATION OF CANNABINOID RECEPTOR MODULATORS<br/>[FR] PROCÉDÉS DE PRÉPARATION DE MODULATEURS DES RÉCEPTEURS DE CANNABINOÏDES
    申请人:ARENA PHARM INC
    公开号:WO2016085941A1
    公开(公告)日:2016-06-02
    The present invention relates to processes, and process intermediates useful in the preparation of (1aS,5aS)-2-(4-oxy-pyrazin-2-yl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalene-4-carboxylic acid ((S)-1-hydroxymethyl-2,2-dimethyl-propyl)-amide (Compound 1) and crystalline forms thereof. The compound (1aS,5aS)-2-(4-oxy-pyrazin-2-yl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalene-4-carboxylic acid ((S)-1-hydroxymethyl-2,2-dimethyl-propyl)-amide has been identified as a modulator of the cannabinoid 2 (CB2) receptor and useful in the treatment of CB2 receptor-mediated disorders, for example, pain, disorders of the immune system (such as, autoimmune disorders, type 1 hypersensitivity and allergic response, conditions associated with CNS inflammation, conditions associated with vascular inflammation, and other disorders associated with aberrant or unwanted immune response), bone and joint diseases (such as, osteoporosis and arthritis), eye disease, cough, cancer, and regenerative medicine. The present invention further provides pharmaceutical compositions comprising Compound 1 and the use of the pharmaceutical compositions for the treatment of CB2 receptor-mediated disorders.
    本发明涉及用于制备(1aS,5aS)-2-(4-氧基吡嗪-2-基)-1a,2,5,5a-四氢-1H-2,3-二氮杂-环丙[a]戊二烯-4-羧酸((S)-1-羟甲基-2,2-二甲基-丙基)-酰胺(化合物1)及其结晶形式的过程和过程中间体。已确定该化合物(1aS,5aS)-2-(4-氧基吡嗪-2-基)-1a,2,5,5a-四氢-1H-2,3-二氮杂-环丙[a]戊二烯-4-羧酸((S)-1-羟甲基-2,2-二甲基-丙基)-酰胺为大麻素2(CB2)受体调节剂,并在治疗CB2受体介导的疾病中有用,例如疼痛、免疫系统疾病(如自身免疫疾病、1型超敏反应和过敏反应、与中枢神经系统炎症相关的疾病、与血管炎症相关的疾病以及其他与异常或不需要的免疫反应相关的疾病)、骨骼和关节疾病(如骨质疏松和关节炎)、眼疾、咳嗽、癌症和再生医学。本发明还提供包含化合物1的药物组合物以及用于治疗CB2受体介导的疾病的药物组合物的用途。
  • [EN] CRYSTALLINE FORMS AND PROCESSES FOR THE PREPARATION OF CONDENSED AZACYCLES ( CANNABINOID RECEPTOR MODULATORS)<br/>[FR] FORMES CRISTALLINES ET PROCÉDÉS DE PRÉPARATION D'AZACYCLES CONDENSÉS (MODULATEURS DES RÉCEPTEURS DES CANNABINOÏDES)
    申请人:ARENA PHARM INC
    公开号:WO2012116276A1
    公开(公告)日:2012-08-30
    The present invention relates to crystalline forms of (1aS,5aS)-2-(4-oxy-pyrazin-2-yl)- 1a,2,5.5a-tetrahydro- 1 H-2,3-diaza-cyclopropa[a]pentalene-4-carboxylic acid ((S)- 1 - hydroxymcthyl-2.2-dimcthyl-propyl)-amidc (Compound 1) and pharmaceutical compositions thereof that modulate the activity of the cannabinoid CB2 receptor and are therefore useful in t treatment of CB2 receptor-mediated disorders, for example, osteoarthritis; pain; hyperalgesia; allodynia; inflammatory hyperalgesia; neuropathic hyperalgesia; acute nociception; osteoporosis; multiple sclerosis-associated spasticity; autoimmune disorders; allergic reactions CNS inflammation for example; atherosclerosis; undesired immune cell activity, and inflammation associated with a disorder selected from: osteoarthritis, anaphylaxis, Behcet's disease, graft rejection, vasculitis, gout, spondylitis, viral disease, bacterial disease, lupus, inflammatory bowel disease, autoimmune hepatitis, and type 1 diabetes mellitus; age-related macular degeneration; cough; leukemia; lymphoma; CNS rumors; prostate cancer; Alzheimer's disease; stroke-induced damage; dementia; amyotrophic lateral sclerosis; and Parkinson's disease.
    本发明涉及(1aS,5aS)-2-(4-氧基吡嗪-2-基)-1a,2,5,5a-四氢-1H-2,3-二氮杂-环丙烯并[α]戊二烯-4-羧酸((S)-1-羟甲基-2,2-二甲基-丙基)-酰胺(化合物1)的晶型及其调节大麻素CB2受体活性的药物组合物,因此在治疗CB2受体介导的疾病方面具有用处,例如骨关节炎;疼痛;过敏性疼痛;触痛;炎症性过敏性疼痛;神经病性过敏性疼痛;急性疼痛感知;骨质疏松症;多发性硬化相关的痉挛;自身免疫性疾病;过敏反应中枢神经系统炎症,例如;动脉粥样硬化;不良的免疫细胞活性,以及与所选疾病相关的炎症:骨关节炎,过敏反应,贝赫切特氏病,移植排斥反应,血管炎,痛风,脊柱炎,病毒性疾病,细菌性疾病,红斑狼疮,炎症性肠病,自身免疫性肝炎和1型糖尿病;年龄相关性黄斑变性;咳嗽;白血病;淋巴瘤;中枢神经系统肿瘤;前列腺癌;阿尔茨海默病;中风引起的损伤;痴呆症;肌萎缩侧索硬化;和帕金森病。
  • CANNABINOID RECEPTOR MODULATORS
    申请人:Jones Robert M.
    公开号:US20120214766A1
    公开(公告)日:2012-08-23
    The present invention relates to certain compounds of Formula Ia and pharmaceutical compositions thereof that modulate the activity of the cannabinoid CB2 receptor. The present invention further relates to certain compounds of Formula Ia and pharmaceutical compositions thereof that modulate the activities of both the CB1 receptor and the CB2 receptor. Compounds of the present invention and pharmaceutical compositions thereof are directed to methods useful in the treatment of: pain, for example bone and joint pain, muscle pain, dental pain, migraine and other headache pain, inflammatory pain, neuropathic pain, pain that occurs as an adverse effect of therapeutics and pain associated with osteoarthritis; hyperalgesia; allodynia; inflammatory hyperalgesia; neuropathic hyperalgesia; acute nociception; osteoporosis; multiple sclerosis-associated spasticity; autoimmune disorders; allergic reactions; CNS inflammation; atherosclerosis; undesired immune cell activity and inflammation; age-related macular degeneration; cough; leukemia; lymphoma; CNS tumors; prostate cancer; Alzheimer's disease; stroke-induced damage; dementia; amyotrophic lateral sclerosis, and Parkinson's disease.
    本发明涉及公式Ia的某些化合物及其制药组合物,其调节大麻素CB2受体的活性。本发明还涉及公式Ia的某些化合物及其制药组合物,其调节CB1受体和CB2受体的活性。本发明的化合物和制药组合物适用于治疗以下疾病的方法:疼痛,例如骨骼和关节疼痛,肌肉疼痛,牙痛,偏头痛和其他头痛,炎性疼痛,神经痛,由治疗副作用引起的疼痛和与骨关节炎相关的疼痛;过敏症;炎性过敏症;神经病性过敏症;急性疼痛感受;骨质疏松症;多发性硬化症相关痉挛;自身免疫疾病;过敏反应;中枢神经系统炎症;动脉粥样硬化;不良的免疫细胞活动和炎症;年龄相关的黄斑变性;咳嗽;白血病;淋巴瘤;中枢神经系统肿瘤;前列腺癌;阿尔茨海默病;中风引起的损伤;痴呆症;肌萎缩性侧索硬化症和帕金森病。
  • CRYSTALLINE FORMS AND PROCESSES FOR THE PREPARATION OF CANNABINOID RECEPTOR MODULATORS
    申请人:Blackburn Anthony C.
    公开号:US20140135345A1
    公开(公告)日:2014-05-15
    The present invention relates to crystalline forms of (1aS,5aS)-2-(4-oxy-pyrazin-2-yl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalene-4-carboxylic acid ((S)-1-hydroxymethyl-2,2-dimethyl-propyl)-amide (Compound 1) and pharmaceutical compositions thereof that modulate the activity of the cannabinoid CB 2 receptor and are therefore useful in the treatment of CB 2 receptor-mediated disorders, for example, osteoarthritis; pain; hyperalgesia; allodynia; inflammatory hyperalgesia; neuropathic hyperalgesia; acute nociception; osteoporosis; multiple sclerosis-associated spasticity; autoimmune disorders; allergic reactions; CNS inflammation for example; atherosclerosis; undesired immune cell activity, and inflammation associated with a disorder selected from: osteoarthritis, anaphylaxis, Behcet's disease, graft rejection, vasculitis, gout, spondylitis, viral disease, bacterial disease, lupus, inflammatory bowel disease, autoimmune hepatitis, and type 1 diabetes mellitus; age-related macular degeneration; cough; leukemia; lymphoma; CNS tumors; prostate cancer; Alzheimer's disease; stroke-induced damage; dementia; amyotrophic lateral sclerosis; and Parkinson's disease.
    本发明涉及(1aS,5aS)-2-(4-氧基吡嗪-2-基)-1a,2,5,5a-四氢-1H-2,3-二氮杂环丙烷[a]五环-4-羧酸((S)-1-羟甲基-2,2-二甲基-丙基)-酰胺(化合物1)的晶体形式及其药物组成物,这些药物组成物调节大麻素CB2受体的活性,因此在治疗CB2受体介导的疾病方面非常有用,例如骨关节炎、疼痛、过敏症、炎症性疼痛、神经病性疼痛、急性疼痛、骨质疏松症、多发性硬化症相关痉挛、自身免疫性疾病、过敏反应、中枢神经系统炎症、动脉硬化、不良的免疫细胞活性以及与以下疾病相关的炎症:骨关节炎、过敏反应、Behcet氏病、移植排斥、血管炎、痛风、脊柱炎、病毒性疾病、细菌性疾病、狼疮、炎症性肠病、自身免疫性肝炎和1型糖尿病;年龄相关性黄斑变性;咳嗽;白血病;淋巴瘤;中枢神经系统肿瘤;前列腺癌;阿尔茨海默病;中风引起的损伤;痴呆;肌萎缩性侧索硬化症和帕金森病。
  • CRYSTALLINE FORMS AND PROCESSES FOR THE PREPARATION OF CONDENSED AZACYCLES (CANNABINOID RECEPTOR MODULATORS)
    申请人:Arena Pharmaceuticals, Inc.
    公开号:EP3395812A1
    公开(公告)日:2018-10-31
    The present invention relates to crystalline forms of (1aS,5aS)-2-(4-oxy-pyrazin-2-yl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalene-4-carboxylic acid ((S)-1-hydroxymethyl-2,2-dimethyl-propyl)-amide (Compound 1) and pharmaceutical compositions thereof that modulate the activity of the cannabinoid CB2 receptor and are therefore useful in the treatment of CB2 receptor-mediated disorders, for example, osteoarthritis; pain; hyperalgesia; allodynia; inflammatory hyperalgesia; neuropathic hyperalgesia; acute nociception; osteoporosis; multiple sclerosis-associated spasticity; autoimmune disorders; allergic reactions; CNS inflammation for example; atherosclerosis; undesired immune cell activity, and inflammation associated with a disorder selected from: osteoarthritis, anaphylaxis, Behcet's disease, graft rejection, vasculitis, gout, spondylitis, viral disease, bacterial disease, lupus, inflammatory bowel disease, autoimmune hepatitis, and type 1 diabetes mellitus; age-related macular degeneration; cough; leukemia; lymphoma; CNS tumors; prostate cancer; Alzheimer's disease; stroke-induced damage; dementia; amyotrophic lateral sclerosis; and Parkinson's disease.
    本发明涉及结晶形式的(1aS,5aS)-2-(4-氧基吡嗪-2-基)-1a,2,5,5a-四氢-1H-2,3-二氮杂环丙并[a]戊烯-4-羧酸((S)-1-羟甲基-2、(S)-1-羟甲基-2, 2-二甲基-丙基)-酰胺(化合物 1)及其药物组合物,可调节大麻素 CB2 受体的活性,因此可用于治疗 CB2 受体介导的疾病,例如骨关节炎;疼痛;痛觉减退;异动症;炎症性痛觉减退;神经病理性痛觉减退;急性痛觉;骨质疏松症;多发性硬化症相关痉挛;自身免疫性疾病;过敏反应;中枢神经系统炎症(例如);动脉粥样硬化;不希望出现的免疫细胞活性,以及与选自以下疾病的炎症相关的疾病:骨关节炎、过敏性休克、白塞氏病、移植物排斥、血管炎、痛风、脊柱炎、病毒性疾病、细菌性疾病、狼疮、炎症性肠病、自身免疫性肝炎和 1 型糖尿病;老年黄斑变性、咳嗽、白血病、淋巴瘤、中枢神经系统肿瘤、前列腺癌、阿尔茨海默病、中风引起的损伤、痴呆、肌萎缩性脊髓侧索硬化症和帕金森病。
查看更多

同类化合物

伊莫拉明 (5aS,6R,9S,9aR)-5a,6,7,8,9,9a-六氢-6,11,11-三甲基-2-(2,3,4,5,6-五氟苯基)-6,9-甲基-4H-[1,2,4]三唑[3,4-c][1,4]苯并恶嗪四氟硼酸酯 (5-氨基-1,3,4-噻二唑-2-基)甲醇 齐墩果-2,12-二烯[2,3-d]异恶唑-28-酸 黄曲霉毒素H1 高效液相卡套柱 非昔硝唑 非布索坦杂质Z19 非布索坦杂质T 非布索坦杂质K 非布索坦杂质E 非布索坦杂质67 非布索坦杂质65 非布索坦杂质64 非布索坦杂质61 非布索坦代谢物67M-4 非布索坦代谢物67M-2 非布索坦代谢物 67M-1 非布索坦-D9 非布索坦 非唑拉明 雷西纳德杂质H 雷西纳德 阿西司特 阿莫奈韦 阿米苯唑 阿米特罗13C2,15N2 阿瑞匹坦杂质 阿格列扎 阿扎司特 阿尔吡登 阿塔鲁伦中间体 阿培利司N-1 阿哌沙班杂质26 阿哌沙班杂质15 阿可替尼 阿作莫兰 阿佐塞米 镁(2+)(Z)-4'-羟基-3'-甲氧基肉桂酸酯 锌1,2-二甲基咪唑二氯化物 铵2-(4-氯苯基)苯并恶唑-5-丙酸盐 铬酸钠[-氯-3-[(5-二氢-3-甲基-5-氧代-1-苯基-1H-吡唑-4-基)偶氮]-2-羟基苯磺酸基][4-[(3,5-二氯-2-羟基苯 铁(2+)乙二酸酯-3-甲氧基苯胺(1:1:2) 钠5-苯基-4,5-二氢吡唑-1-羧酸酯 钠3-[2-(2-壬基-4,5-二氢-1H-咪唑-1-基)乙氧基]丙酸酯 钠3-(2H-苯并三唑-2-基)-5-仲-丁基-4-羟基苯磺酸酯 钠(2R,4aR,6R,7R,7aS)-6-(2-溴-9-氧代-6-苯基-4,9-二氢-3H-咪唑并[1,2-a]嘌呤-3-基)-7-羟基四氢-4H-呋喃并[3,2-D][1,3,2]二氧杂环己膦烷e-2-硫醇2-氧化物 野麦枯 野燕枯 醋甲唑胺