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(S)-2-amino-1-(azetidin-1-yl)-3,3-dimethylbutan-1-one | 1229007-82-2

中文名称
——
中文别名
——
英文名称
(S)-2-amino-1-(azetidin-1-yl)-3,3-dimethylbutan-1-one
英文别名
(2S)-2-amino-1-(azetidin-1-yl)-3,3-dimethylbutan-1-one
(S)-2-amino-1-(azetidin-1-yl)-3,3-dimethylbutan-1-one化学式
CAS
1229007-82-2
化学式
C9H18N2O
mdl
——
分子量
170.255
InChiKey
BTEWYVYQEYNZAY-SSDOTTSWSA-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):
    0.7
  • 重原子数:
    12
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.89
  • 拓扑面积:
    46.3
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    (S)-(-)-4-叔丁基氧氮杂环戊烷-2,5-二酮azetidine hydrochloride甲苯 作用下, 以 乙醇 为溶剂, 反应 0.17h, 以to provide the desired (S)-2-amino-1-(azetidin-1-yl)-3,3-dimethylbutan-1-one as a brown oil (1.7 g, 99%) that的产率得到(S)-2-amino-1-(azetidin-1-yl)-3,3-dimethylbutan-1-one
    参考文献:
    名称:
    Substituted imidazoheterocycle derivatives
    摘要:
    本发明提供了具有通式I结构的取代咪唑杂环化合物,其中Y从以下中选择:—O—、—OCRgRh—、—CRgRhO—、—CRgRh—、—(CRgRh)2—、—NRi—、—CRgRhNRi—和—NRiCRgRh—。还提供了通式I化合物的药学上可接受的盐、酸盐、水合物、溶剂化物和立体异构体。这些化合物可用作大麻素受体调节剂,并用于预防和治疗大麻素受体相关疾病和症状,如疼痛、炎症和瘙痒症。
    公开号:
    US08835422B2
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文献信息

  • 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。
  • SUBSTITUTED IMIDAZOHETEROCYCLE DERIVATIVES
    申请人:O'Connor Stephen J.
    公开号:US20120015930A1
    公开(公告)日:2012-01-19
    The present invention provides substituted imidazoheterocycles having the general structure of formula I: wherein Y is chosen from —O—, —OCR g R h —, —CR g R h O—, —CR g R h —, —(CR g R h ) 2 —, —NR i —, —CR g R h NR i — and —NR i CR g R h —. Also provided are pharmaceutically acceptable salts, acid salts, hydrates, solvates and stereoisomers of the compounds of formula I. The compounds are useful as modulators of cannabinoid receptors and for the prophylaxis and treatment of cannabinoid receptor-associated diseases and conditions, such as pain, inflammation and pruritis.
    本发明提供了具有公式I的一般结构的取代咪唑杂环化合物,其中Y从—O—,—OCRgRh—,—CRgRhO—,—CRgRh—,—(CRgRh)2—,—NRi—,—CRgRhNRi—和—NRiCRgRh—中选择。此外,还提供了公式I化合物的药学上可接受的盐、酸盐、水合物、溶剂物和立体异构体。这些化合物可用作大麻素受体调节剂,并用于预防和治疗与大麻素受体相关的疾病和病症,例如疼痛、炎症和瘙痒。
  • [EN] SUBSTITUTED IMIDAZOHETEROCYCLE DERIVATIVES<br/>[FR] DÉRIVÉS D'IMIDAZOHÉTÉROCYCLE SUBSTITUÉS
    申请人:CARA THERAPEUTICS INC
    公开号:WO2010068520A3
    公开(公告)日:2010-09-16
  • Compounds and Methods for Treatment of Visceral Pain
    申请人:Arena Pharmaceuticals, Inc.
    公开号:US20200078358A1
    公开(公告)日:2020-03-12
    The present invention relates to certain compounds of Formula Ia and pharmaceutical compositions thereof and their use in methods for the alleviation and/or treatment of visceral pain, for example abdominal pain; pelvic pain; male pelvic pain; pain from an internal organ; bladder pain; painful bladder syndrome; post-surgical abdominal pain (e.g., GI resection, hysterectomy, oophorectomy, C-section, and the like); or pain arising from or related to: pancreatitis (e.g., chronic pancreatitis), prostatitis (e.g., chronic prostatitis), inflammatory bowel disease (e.g., Crohn's disease), endometriosis, interstitial cystitis, prostatitis (e.g., chronic prostatitis), epididymitis (e.g., chronic epididymitis), or post-surgical abdominal lesions. In some embodiments, the visceral pain is consequent to inflammatory bowel disease, for example Crohn's disease.
  • US8778950B2
    申请人:——
    公开号:US8778950B2
    公开(公告)日:2014-07-15
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