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3-氧杂-8-氮杂双环[3.2.1]辛烷盐酸盐 | 904316-92-3

中文名称
3-氧杂-8-氮杂双环[3.2.1]辛烷盐酸盐
中文别名
3-噁-8-氮杂双环[3.2.1]辛烷盐酸盐
英文名称
3-oxa-8-azabicyclo[3.2.1]octane hydrochloride
英文别名
3-oxa-8-azabicyclo[3.2.1]octane;hydrochloride
3-氧杂-8-氮杂双环[3.2.1]辛烷盐酸盐化学式
CAS
904316-92-3
化学式
C6H11NO*ClH
mdl
——
分子量
149.62
InChiKey
QCOHPFLNQAVPJE-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):
    0.56
  • 重原子数:
    9
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    21.3
  • 氢给体数:
    2
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2934999090
  • 危险性防范说明:
    P261,P280,P305+P351+P338
  • 危险性描述:
    H302,H315,H319,H332,H335

SDS

SDS:5d6662b6744ba281ae6dbe3f020e8efd
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Material Safety Data Sheet

Section 1. Identification of the substance
Product Name: 3-Oxa-8-azabicyclo[3.2.1]octane, HCl
Synonyms:

Section 2. Hazards identification
Harmful by inhalation, in contact with skin, and if swallowed.

Section 3. Composition/information on ingredients.
Ingredient name: 3-Oxa-8-azabicyclo[3.2.1]octane, HCl
CAS number: 904316-92-3

Section 4. First aid measures
Skin contact: Immediately wash skin with copious amounts of water for at least 15 minutes while removing
contaminated clothing and shoes. If irritation persists, seek medical attention.
Eye contact: Immediately wash skin with copious amounts of water for at least 15 minutes. Assure adequate
flushing of the eyes by separating the eyelids with fingers. If irritation persists, seek medical
attention.
Inhalation: Remove to fresh air. In severe cases or if symptoms persist, seek medical attention.
Ingestion: Wash out mouth with copious amounts of water for at least 15 minutes. Seek medical attention.

Section 5. Fire fighting measures
In the event of a fire involving this material, alone or in combination with other materials, use dry
powder or carbon dioxide extinguishers. Protective clothing and self-contained breathing apparatus
should be worn.

Section 6. Accidental release measures
Personal precautions: Wear suitable personal protective equipment which performs satisfactorily and meets local/state/national
standards.
Respiratory precaution: Wear approved mask/respirator
Hand precaution: Wear suitable gloves/gauntlets
Skin protection: Wear suitable protective clothing
Eye protection: Wear suitable eye protection
Methods for cleaning up: Mix with sand or similar inert absorbent material, sweep up and keep in a tightly closed container
for disposal. See section 12.
Environmental precautions: Do not allow material to enter drains or water courses.

Section 7. Handling and storage
Handling: This product should be handled only by, or under the close supervision of, those properly qualified
in the handling and use of potentially hazardous chemicals, who should take into account the fire,
health and chemical hazard data given on this sheet.
Store in closed vessels.
Storage:

Section 8. Exposure Controls / Personal protection
Engineering Controls: Use only in a chemical fume hood.
Personal protective equipment: Wear laboratory clothing, chemical-resistant gloves and safety goggles.
General hydiene measures: Wash thoroughly after handling. Wash contaminated clothing before reuse.

Section 9. Physical and chemical properties
Appearance: Not specified
Boiling point: No data
No data
Melting point:
Flash point: No data
Density: No data
Molecular formula: C6H11NO.ClH
Molecular weight: 149.6

Section 10. Stability and reactivity
Conditions to avoid: Heat, flames and sparks.
Materials to avoid: Oxidizing agents.
Possible hazardous combustion products: Carbon monoxide, nitrogen oxides, hydrogen chloride.

Section 11. Toxicological information
No data.

Section 12. Ecological information
No data.

Section 13. Disposal consideration
Arrange disposal as special waste, by licensed disposal company, in consultation with local waste
disposal authority, in accordance with national and regional regulations.

Section 14. Transportation information
Non-harzardous for air and ground transportation.

Section 15. Regulatory information
No chemicals in this material are subject to the reporting requirements of SARA Title III, Section
302, or have known CAS numbers that exceed the threshold reporting levels established by SARA
Title III, Section 313.


SECTION 16 - ADDITIONAL INFORMATION
N/A

制备方法与用途

用途

3-氧杂-8-氮杂双环[3.2.1]辛烷盐酸盐作为MDA受体亚单位NR2B拮抗剂,在治疗神经退行性疾病时效果更佳。其研究潜力较大。

合成方法

以廉价易得的己二酸(1)为初始原料,依次经酰化、代、苄胺环合、解、还原、脱环合、氢解脱苄和成盐等8步反应,合成3-氧杂-8-氮杂双环[3.2.1]辛烷盐酸盐。其合成路线图如下:

图1 3-氧杂-8-<a href=https://www.molaid.com/MS_300598 target="_blank">氮杂双环</a>[3.2.1]<a href=https://www.molaid.com/MS_38723 target="_blank">辛烷</a>盐酸盐的合成路线图

反应信息

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文献信息

  • [EN] PYRIMIDINE COMPOUNDS, COMPOSITIONS AND METHODS OF USE<br/>[FR] COMPOSÉS DE PYRIMIDINE, COMPOSITIONS ET PROCÉDÉS D'UTILISATION
    申请人:GENENTECH INC
    公开号:WO2010014939A1
    公开(公告)日:2010-02-04
    Disclosed are compounds of Formula I, including steroisomers, geometric isomers, tautomers, solvates, metabolites and pharmaceutically acceptable salts thereof, that are useful in modulating PIKK related kinase signaling, e.g., mTOR, and for the treatment of diseases (e.g., cancer) that are mediated at least in part by the dysregulation of the PIKK signaling pathway (e.g., mTOR).
    揭示了公式I的化合物,包括立体异构体、几何异构体、互变异构体、溶剂合物、代谢物和其药学上可接受的盐,这些化合物在调节PIKK相关激酶信号传导方面很有用,例如mTOR,并用于治疗至少部分由PIKK信号传导途径失调引起的疾病(例如癌症)。
  • [EN] TRICYCLIC DEGRADERS OF IKAROS AND AIOLOS<br/>[FR] AGENTS DE DÉGRADATION TRICYCLIQUES D'IKAROS ET D'AIOLOS
    申请人:C4 THERAPEUTICS INC
    公开号:WO2020210630A1
    公开(公告)日:2020-10-15
    Tricyclic cereblon binders for the degradation of Ikaros or Aiolos by the ubiquitin proteasome pathway for therapeutic applications are described.
    三环脑蛋白结合剂通过泛素蛋白酶体途径降解Ikaros或Aiolos以用于治疗应用的描述。
  • [EN] CHEMICAL COMPOUNDS<br/>[FR] COMPOSÉS CHIMIQUES
    申请人:GLAXOSMITHKLINE LLC
    公开号:WO2010120854A1
    公开(公告)日:2010-10-21
    The invention is directed to to substituted indazole derivatives. Specifically, the invention is directed to compounds according to Formula I: wherein R1 - R6 and X are defined herein. The compounds of the invention are inhibitors of PDK1 and can be useful in the treatment of disorders characterized by constitutively activated ACG kinases such as cancer and more specifically leukemia and cancers of the breast, colon, and lung. Accordingly, the invention is further directed to pharmaceutical compositions comprising a compound of the invention. The invention is still further directed to methods of inhibiting PDK1 activity and treatment of disorders associated therewith using a compound of the invention or a pharmaceutical composition comprising a compound of the invention.
    本发明涉及取代吲唑生物。具体而言,本发明涉及根据公式I的化合物:其中R1-R6和X在此定义。本发明的化合物是PDK1的抑制剂,可用于治疗由组成性激活的ACG激酶(如癌症,特别是白血病、乳腺癌、结肠癌和肺癌)引起的疾病。因此,本发明进一步涉及包含本发明化合物的药物组合物。本发明还进一步涉及使用本发明化合物或包含本发明化合物的药物组合物来抑制PDK1活性和治疗相关疾病的方法。
  • OXO-HETEROCYCLE FUSED PYRIMIDINE COMPOUNDS, COMPOSITIONS AND METHODS OF USE
    申请人:Bergeron Philippe
    公开号:US20100331305A1
    公开(公告)日:2010-12-30
    Disclosed are compounds of Formula I, including steroisomers, geometric isomers, tautomers, solvates, metabolites and pharmaceutically acceptable salts thereof, that are useful in modulating PIKK related kinase signaling, e.g., mTOR, and for the treatment of diseases (e.g., cancer) that are mediated at least in part by the dysregulation of the PIKK signaling pathway (e.g., mTOR).
    公开的是Formula I的化合物,包括立体异构体、几何异构体、互变异构体、溶剂合物、代谢物及其药学上可接受的盐,这些化合物在调节PIKK相关激酶信号传导方面很有用,例如mTOR,并用于治疗至少部分由PIKK信号传导途径失调引起的疾病(例如癌症)。
  • [EN] TETRAHYDROISOQUINOLINE DERIVED PRMT5-INHIBITORS<br/>[FR] INHIBITEURS DE PRMT5 DÉRIVÉS DE TÉTRAHYDROISOQUINOLÉINE
    申请人:CTXT PTY LTD
    公开号:WO2016034673A1
    公开(公告)日:2016-03-10
    A compound of formula I wherein: n is 1 or 2: p is 0 or 1; R1 is optionally one or more halo or methyl groups; R2a and R2b are independently selected from the group consisting of: (i) F; (ii) H; (iii) Me; and (iv) CH2OH; R2c and R2d are independently selected from the group consisting of: (i) F; (ii) H; (iii) Me; and (iv) CH2OH; R3a and R3b are independently selected from H and Me; R4 is either H or Me; R5 is either H or Me; R6a and R6b are independently selected from H and Me; A is either (i) optionally substituted phenyl; (ii) optionally substituted naphthyl; or (iii) optionally substituted C5-12 heteroaryl.
    式I的化合物,其中:n为1或2;p为0或1;R1可选地为一个或多个卤素或甲基基团;R2a和R2b分别选自以下组:(i) F;(ii) H;(iii) Me;和(iv) CH2OH;R2c和R2d分别选自以下组:(i) F;(ii) H;(iii) Me;和(iv) CH2OH;R3a和R3b分别选自H和Me;R4为H或Me;R5为H或Me;R6a和R6b分别选自H和Me;A为(i)可选地取代的苯基;(ii)可选地取代的基;或(iii)可选地取代的C5-12杂环基。
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