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9-氮杂吲哚-5-硼酸 | 913835-63-9

中文名称
9-氮杂吲哚-5-硼酸
中文别名
咪唑并[1,2-A]吡啶-6-硼酸
英文名称
imidazo[1,2-a]pyridin-6-ylboronic acid
英文别名
Imidazo[1,2-a]pyridine-6-boronic acid
9-氮杂吲哚-5-硼酸化学式
CAS
913835-63-9
化学式
C7H7BN2O2
mdl
MFCD06739225
分子量
161.956
InChiKey
IPJIKGJKMCILGV-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

  • 熔点:
    115-117
  • 密度:
    1.31±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.63
  • 重原子数:
    12
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    57.8
  • 氢给体数:
    2
  • 氢受体数:
    3

安全信息

  • 危险品标志:
    Xi
  • 危险性防范说明:
    P261,P280,P305+P351+P338
  • 危险性描述:
    H302,H315,H319,H332,H335
  • 储存条件:
    -20°C,保存于惰性气体中

SDS

SDS:b47c301dc43ccdcd4b0b96b8471518fc
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Material Safety Data Sheet

Section 1. Identification of the substance
Product Name: Imidazo[1,2-a]pyridine-6-boronic acid
Synonyms: 3a-Azaindole-5-boronic acid

Section 2. Hazards identification
Harmful by inhalation, in contact with skin, and if swallowed.
H317: May cause an allergic skin reaction
P280: Wear protective gloves/protective clothing/eye protection/face protection

Section 3. Composition/information on ingredients.
Ingredient name: Imidazo[1,2-a]pyridine-6-boronic acid
CAS number: 913835-63-9

Section 4. First aid measures
Immediately wash skin with copious amounts of water for at least 15 minutes while removing
Skin contact:
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, under −20◦C.
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
Not specified
Appearance:
Boiling point: No data
Melting point: No data
Flash point: No data
Density: No data
Molecular formula: C7H7BN2O2
Molecular weight: 162.0

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.

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

反应信息

  • 作为反应物:
    参考文献:
    名称:
    镍(II)催化的芳基和杂芳基硼酸和二氧化硫替代物DABSO的亚磺酸盐合成
    摘要:
    我们报告易于获得的芳基和杂芳基硼酸的氧化还原中性Ni(II)催化的硫化。使用市售的,空气稳定的NiBr 2 ·(甘醇二甲醚),市售的菲咯啉配体和DABSO的组合,硼酸可以有效地转化为相应的亚磺酸盐,可以进一步精加工成有价值的含磺酰基基团,包括砜,磺酰胺,磺酰氟和磺酸酯。催化剂的加入量可以以克为单位降低至2.5摩尔%。这种实际上简单的方案可耐受前所未有的药学上相关的和电子贫(杂)芳基硼酸,可直接合成活性药物成分。
    DOI:
    10.1021/acscatal.9b04363
  • 作为产物:
    描述:
    6-溴-咪唑并[1,2-a]吡啶联硼酸频那醇酯tris-(dibenzylideneacetone)dipalladium(0)sodium acetate三环己基膦 作用下, 以 1,4-二氧六环 为溶剂, 反应 24.0h, 以72%的产率得到9-氮杂吲哚-5-硼酸
    参考文献:
    名称:
    奥普力农及9-氮杂吲哚-5-硼酸的制备方法
    摘要:
    本发明涉及奥普力农及9‑氮杂吲哚‑5‑硼酸的制备方法。本发明尤其涉及经过Suzuki偶联获得奥普力农的方法。本发明奥普力农及9‑氮杂吲哚‑5‑硼酸的制备方法,开创性设计出汇聚式的合成路线,相对于现有的三种串联式的合成工艺,原子利用率高,整体的反应收率优于现有的合成路线;本发明的合成反应条件温和,操作简便,有利于实现工业化生成。获得的奥普力农可进一步经成盐得到盐酸奥普力农,制得的盐酸奥普力具有杂质低、纯度高、收率高、反应条件温和等优点。
    公开号:
    CN106349246B
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文献信息

  • [EN] SUBSTITUTED PYRAZOLE AND PYRROLE COMPOUNDS AND METHODS FOR USING THEM FOR INHIBITION OF INITIATION OF TRANSLATION AND TREATMENT OF DISEASES AND DISORDERS RELATING THERETO<br/>[FR] COMPOSÉS PYRAZOLE ET PYRROLE SUBSTITUÉS ET PROCÉDÉS D'UTILISATION DE CES DERNIERS POUR L'INHIBITION DE L'INITIATION DE LA TRADUCTION ET LE TRAITEMENT DE MALADIES ET DE TROUBLES ASSOCIÉS À CETTE DERNIÈRE
    申请人:BANTAM PHARMACEUTICAL LLC
    公开号:WO2016196644A1
    公开(公告)日:2016-12-08
    Disclosed are pyrazole compounds, as well as pharmaceutical compositions and methods of use thereof. One embodiment is a compound having the structure (I) and pharmaceutically acceptable salts and /V-oxides thereof, wherein X1, X2, Z1, Z2, the ring system denoted by "a", R1, A1A, L1B, A1B, L1A, L2, Q, L3, R3, A4A, L4B, A4B, L4A, R4, L5, and R5 are as described herein. In certain embodiments, compounds disclosed herein disrupt the elF4E/eiF4G interaction, and can be used to treat hyperproliferative disorder, a neurological disease or disorder, or autism.
    揭示了吡唑化合物,以及其药物组合物和使用方法。其中一种实施例是具有结构(I)及其药用可接受的盐和/或氧化物,其中X1、X2、Z1、Z2、由“a”表示的环系统、R1、A1A、L1B、A1B、L1A、L2、Q、L3、R3、A4A、L4B、A4B、L4A、R4、L5和R5如本文所述。在某些实施例中,本文所披露的化合物破坏elF4E/eiF4G相互作用,并可用于治疗过度增殖性疾病、神经系统疾病或障碍,或自闭症。
  • [EN] IMIDAZO[1,2-A]PYRAZINE MODULATORS OF THE ADENOSINE A2A RECEPTOR<br/>[FR] MODULATEURS DE 5,6-BICYCLO-IMIDAZO[1,2-A]PYRAZINE DU RÉCEPTEUR A2A DE L'ADÉNOSINE
    申请人:SELVITA S A
    公开号:WO2019002606A1
    公开(公告)日:2019-01-03
    The present invention relates to the compound of formula (I) and salts, stereoisomers, tautomers, isotopologues,or N-oxides thereof. The present invention is further concerned with the use of such a compound or salt, stereoisomer, tautomer, isotopologues,or N-oxide thereof as medicament and a pharmaceutical composition comprising said compound.
    本发明涉及式(I)的化合物及其盐、立体异构体、互变异构体、同位素同分异构体或N-氧化物。本发明进一步涉及将该化合物或盐、立体异构体、互变异构体、同位素同分异构体或N-氧化物用作药物的用途,以及包含该化合物的药物组合物。
  • [EN] APOPTOSIS SIGNAL-REGULATING KINASE INHIBITORS AND USES THEREOF<br/>[FR] INHIBITEURS DE KINASE DE RÉGULATION DU SIGNAL DE L'APOPTOSE ET LEURS UTILISATIONS
    申请人:FRONTHERA U S PHARMACEUTICALS LLC
    公开号:WO2019051265A1
    公开(公告)日:2019-03-14
    Described herein are ASK1 inhibitors and pharmaceutical compositions comprising said compounds. The subject compounds and compositions are useful for the treatment of blood disease, autoimmune disorders, pulmonary disorders, hypertension, inflammatory diseases, fibrotic diseases, diabetes, diabetic nephropathy, renal diseases, respiratory diseases, cardiovascular diseases, acute lung injuries, acute or chronic liver diseases, and neurodegenerative diseases.
    本文描述了ASK1抑制剂和包含该化合物的药物组合物。所述化合物和组合物对于治疗血液疾病、自身免疫性疾病、肺部疾病、高血压、炎症性疾病、纤维化疾病、糖尿病、糖尿病肾病、肾脏疾病、呼吸系统疾病、心血管疾病、急性肺损伤、急性或慢性肝病以及神经退行性疾病具有用处。
  • [EN] SUBSTITUTED INDOLE COMPOUNDS<br/>[FR] COMPOSÉS D'INDOLE SUBSTITUÉS
    申请人:BRISTOL MYERS SQUIBB CO
    公开号:WO2019099336A1
    公开(公告)日:2019-05-23
    Disclosed are compounds of Formula (I) or salts thereof, wherein Ring Het, R1, R2, R3, R4, R5, m, n, and p are defined herein. Also disclosed are methods of using such compounds as inhibitors of signaling through Toll-like receptor 7, or 8, or 9, and pharmaceutical compositions comprising such compounds. These compounds are useful in treating inflammatory and autoimmune diseases.
    公开了公式(I)的化合物或其盐,其中环杂环、R1、R2、R3、R4、R5、m、n和p在本发明中定义。还公开了将此类化合物用作通过Toll样受体7、8或9的信号传递的抑制剂的方法,以及包含此类化合物的药物组合物。这些化合物在治疗炎症和自身免疫疾病方面是有用的。
  • [EN] HETEROCYCLIC COMPOUNDS AS BIOGENIC AMINE TRANSPORT MODULATORS<br/>[FR] COMPOSÉS HÉTÉROCYCLIQUES EN TANT QUE MODULATEURS DU TRANSPORT D'AMINES BIOGÈNES
    申请人:ANANTHAN SUBRAMANIAM
    公开号:WO2016090296A1
    公开(公告)日:2016-06-09
    The present disclosure relates to certain amine derivatives of fused bicyclic heterocycles that inhibit the amine reuptake function of the biogenic amine transporters, dopamine transporter (DAT), serotonin transporter (SERT) and norepinephrine transporter (NET). Compounds of the present disclosure are potent inhibitors of the reuptake of dopamine (DA), serotonin (5-hydroxytryptamine, 5-HT) and norepinephrine (NE) with full or partial maximal efficacy. The compounds with partial maximal efficacy in inhibiting reuptake of all three biogenic amines are herein referred to as partial triple uptake inhibitors (PTRIs). Compounds of the present disclosure are useful for treating depression, pain and substance abuse and relapse to substance abuse and addiction to substances such as cocaine, methamphetamine, nicotine and alcohol. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.
    本公开涉及抑制生物胺转运体多巴胺转运体(DAT)、5-羟色胺转运体(SERT)和去甲肾上腺素转运体(NET)的某些融合双环杂环生物胺衍生物的化合物。本公开的化合物是多巴胺(DA)、5-羟色胺(5-HT)和去甲肾上腺素(NE)的重摄取的有效抑制剂,具有完全或部分最大效力。在抑制所有三种生物胺的重摄取中具有部分最大效力的化合物在此被称为部分三重摄取抑制剂(PTRIs)。本公开的化合物可用于治疗抑郁症、疼痛、物质滥用、物质滥用复发以及对可卡因、甲基苯丙胺、尼古丁和酒精等物质的成瘾。本摘要旨在作为在特定领域进行搜索的扫描工具,并不意在限制本发明。
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