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4-Boc-2-吗啉甲酸 | 189321-66-2

中文名称
4-Boc-2-吗啉甲酸
中文别名
N-BOC-2-吗啉甲酸;4-Boc-吗啉-2-羧酸;4-Boc-2-吗啡啉甲酸;4-BOC-2-吗啡啉甲酸;N-Boc-吗啉-2-羧酸
英文名称
4-(tert-butoxycarbonyl)morpholine-2-carboxylic acid
英文别名
morpholine-2,4-dicarboxylic acid 4-tert-butyl ester;4-[(2-methylpropan-2-yl)oxycarbonyl]morpholine-2-carboxylic acid
4-Boc-2-吗啉甲酸化学式
CAS
189321-66-2
化学式
C10H17NO5
mdl
MFCD01321006
分子量
231.249
InChiKey
LGWMTRPJZFEWCX-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:
    >139oC (dec.)
  • 沸点:
    369.5±42.0 °C(Predicted)
  • 密度:
    1.230±0.06 g/cm3(Predicted)
  • 溶解度:
    DMSO(轻微)、乙酸乙酯(轻微、加热)

计算性质

  • 辛醇/水分配系数(LogP):
    0.4
  • 重原子数:
    16
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.8
  • 拓扑面积:
    76.1
  • 氢给体数:
    1
  • 氢受体数:
    5

安全信息

  • 海关编码:
    2934999090
  • 危险性防范说明:
    P264,P273,P280,P305+P351+P338,P337+P313,P391,P501
  • 危险性描述:
    H319,H413
  • 储存条件:
    2-8°C

SDS

SDS:0cae028dd12ae7779e64f85ea76d1b02
查看
Material Safety Data Sheet

Section 1. Identification of the substance
4-Boc-2-morpholinecarboxylic acid
Product Name:
Synonyms:

Section 2. Hazards identification
Harmful by inhalation, in contact with skin, and if swallowed.
H319: Causes serious eye irritation
H411: Toxic to aquatic life with long lasting effects
P273: Avoid release to the environment
P305+P351+P338: IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present
and easy to do – continue rinsing

Section 3. Composition/information on ingredients.
Ingredient name: 4-Boc-2-morpholinecarboxylic acid
CAS number: 189321-66-2

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
This product should be handled only by, or under the close supervision of, those properly qualified
Handling:
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.
Storage: Store in closed vessels, refrigerated.

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
Melting point: No data
Flash point: No data
Density: No data
Molecular formula: C10H17NO5
Molecular weight: 231.2

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

制备方法与用途

用途

4-BOC-2-吗啡甲酸用于制备有效且选择性的3-磷酸肌苷依赖激酶1 (PDK 1) 抑制剂,特别适用于治疗多发性骨髓瘤。

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量
    • 1
    • 2

反应信息

  • 作为反应物:
    描述:
    4-Boc-2-吗啉甲酸硼烷四氢呋喃络合物 作用下, 以 四氢呋喃 为溶剂, 反应 2.5h, 以26%的产率得到4-Boc-2-羟甲基吗啡啉
    参考文献:
    名称:
    3,4-Di-substituted cyclobutene-1,2-diones as CXC-chemokine receptor ligands
    摘要:
    这里公开了用于治疗诸如急性和慢性炎症性疾病以及癌症的趋化因子介导疾病的公式1化合物或其药用可接受的盐或溶剂。
    公开号:
    US20040147559A1
  • 作为产物:
    描述:
    4-Boc-2-羟甲基吗啡啉2,2,6,6-四甲基哌啶氧化物三氯异氰尿酸碳酸氢钠 、 sodium bromide 作用下, 以 丙酮 为溶剂, 生成 4-Boc-2-吗啉甲酸
    参考文献:
    名称:
    SUBSTITUTED MORPHOLINES AS MODULATORS FOR THE CALCIUM SENSING RECEPTOR
    摘要:
    公式(I)的化合物以及用于制备这些化合物的方法,可用于治疗、管理和/或减轻与钙感受(CaSR)受体调节相关的疾病、紊乱、综合症或病况。治疗、管理和/或减轻与公式(I)的钙感受(CaSR)受体调节相关的疾病、紊乱、综合症或病况的方法。
    公开号:
    US20130345213A1
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文献信息

  • Pteridinone derivatives as PI3-kinases inhibitors
    申请人:Boehringer Ingelheim Pharma GmbH & Co. KG
    公开号:EP1953163A1
    公开(公告)日:2008-08-06
    New compounds of formula 1 are provided which by virtue of their pharmaceutical activity as PI3-kinase modulators may be used in the therapeutic field for the treatment of inflammatory or allergic diseases. Examples of these include inflammatory and allergic respiratory complaints, inflammatory diseases of the gastro-intestinal tract and motor apparatus, inflammatory and allergic skin diseases, inflammatory eye diseases, diseases of the nasal mucosa, inflammatory or allergic conditions involving autoimmune reactions or inflammations of the kidney.
    根据其作为PI3-激酶调节剂的药理活性,提供了公式1的新化合物,可用于治疗炎症或过敏性疾病的治疗领域。 这些例子包括炎症和过敏性呼吸道疾病,胃肠道和运动器官的炎症性疾病,炎症性和过敏性皮肤疾病,炎症性眼病,鼻黏膜疾病,涉及自身免疫反应或肾脏炎症的炎症性或过敏性疾病。
  • [EN] SPHINGOSINE-1-PHOSPHATE RECEPTOR AGONISTS<br/>[FR] AGONISTES DES RÉCEPTEURS SPHINGOSINE-1-PHOSPHATE
    申请人:BRISTOL MYERS SQUIBB CO
    公开号:WO2011017578A1
    公开(公告)日:2011-02-10
    Disclosed are compounds of Formula (I), or a stereoisomer or a pharmaceutically acceptable salt thereof, wherein: A is formula (II) Q is a substituted 5-membered monocyclic heteroaryl group; W is CH2, O, or NH; and R1, R2, R3, R4, R5, R6, m, n, t, and x are defined herein. Also disclosed are methods of using such compounds as selective agonists for G protein-coupled receptor S1P1, and pharmaceutical compositions comprising such compounds. These compounds are useful in treating, preventing, or slowing the progression of diseases or disorders in a variety of therapeutic areas, such as autoimmune diseases and vascular disease.
    揭示了Formula (I)的化合物,或其立体异构体或药用可接受的盐,其中:A为Formula (II),Q为取代的5-成员单环杂芳基团;W为CH2、O或NH;而R1、R2、R3、R4、R5、R6、m、n、t和x在此处有定义。还揭示了将这些化合物用作G蛋白偶联受体S1P1的选择性激动剂的方法,以及包含这些化合物的药物组合物。这些化合物在治疗、预防或减缓多种治疗领域的疾病或紊乱方面具有用处,如自身免疫疾病和血管疾病。
  • BICYCLIC HETEROARYL COMPOUNDS AND USES THEREOF
    申请人:Revolution Medicines, Inc.
    公开号:US20210139517A1
    公开(公告)日:2021-05-13
    The present disclosure is directed to modulators of SOS1 and their use in the treatment of disease. Also disclosed are pharmaceutical compositions comprising the same.
    本公开涉及SOS1的调节剂及其在治疗疾病中的应用。还公开了包含相同成分的药物组合物。
  • INHIBITORS OF INFLUENZA VIRUSES REPLICATION
    申请人:Charifson Paul S.
    公开号:US20120171245A1
    公开(公告)日:2012-07-05
    Methods of inhibiting the replication of influenza viruses in a biological sample or patient, of reducing the amount of influenza viruses in a biological sample or patient, and of treating influenza in a patient, comprises administering to said biological sample or patient an effective amount of a compound represented by Structural Formula (I): or a pharmaceutically acceptable salt thereof, wherein the values of Structural Formula (IA) are as described herein. A compound is represented by Structural Formula (IA) or a pharmaceutically acceptable salt thereof, wherein the values of Structural Formula (IA) are as described herein. A pharmaceutical composition comprises an effective amount of such a compound or pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier, adjuvant or vehicle.
    抑制生物样本或患者中流感病毒的复制、减少生物样本或患者中流感病毒量以及治疗患者流感的方法,包括向所述生物样本或患者施用有效量的由结构公式(I)表示的化合物: 或其药用可接受盐,其中结构公式(IA)的值如本文所述。由结构公式(IA)或其药用可接受盐表示的化合物,其中结构公式(IA)的值如本文所述。药物组合物包括有效量的上述化合物或其药用可接受盐,以及药用可接受载体、佐剂或车辆。
  • Inhibitors of influenza viruses replication
    申请人:Vertex Pharmaceuticals Incorporated
    公开号:US09345708B2
    公开(公告)日:2016-05-24
    Methods of inhibiting the replication of influenza viruses in a biological sample or patient, of reducing the amount of influenza viruses in a biological sample or patient, and of treating influenza in a patient, comprises administering to said biological sample or patient an effective amount of a compound represented by Structural Formula (I): or a pharmaceutically acceptable salt thereof, wherein the values of Structural Formula (IA) are as described herein. A compound is represented by Structural Formula (IA) or a pharmaceutically acceptable salt thereof, wherein the values of Structural Formula (IA) are as described herein. A pharmaceutical composition comprises an effective amount of such a compound or pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier, adjuvant or vehicle.
    抑制生物样本或患者中流感病毒的复制、减少生物样本或患者中流感病毒量以及治疗患者流感的方法,包括向所述生物样本或患者施用结构式(I)表示的化合物的有效量: 或其药用可接受盐,其中结构式(IA)的值如本文所述。一种化合物由结构式(IA)或其药用可接受盐表示,其中结构式(IA)的值如本文所述。一种药物组合物包括这样的化合物或其药用可接受盐的有效量,以及药用可接受载体、佐剂或赋形剂。
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