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1-Boc-4-(Boc-氨基)哌啶-4-甲酸 | 189321-65-1

中文名称
1-Boc-4-(Boc-氨基)哌啶-4-甲酸
中文别名
N-BOC-氨基-(4-N-BOC-哌啶基)羧酸
英文名称
1-(tert-butoxycarbonyl)-4-((tert-butoxycarbonyl)amino)piperidine-4-carboxylic acid
英文别名
1-[(2-methylpropan-2-yl)oxycarbonyl]-4-[(2-methylpropan-2-yl)oxycarbonylamino]piperidine-4-carboxylic acid
1-Boc-4-(Boc-氨基)哌啶-4-甲酸化学式
CAS
189321-65-1
化学式
C16H28N2O6
mdl
——
分子量
344.408
InChiKey
AFEAWYLBSVKOAY-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

  • 沸点:
    479.5°C (rough estimate)
  • 密度:
    1.1158 (rough estimate)
  • 稳定性/保质期:

    遵照规定使用和储存,则不会发生分解。

计算性质

  • 辛醇/水分配系数(LogP):
    1.8
  • 重原子数:
    24
  • 可旋转键数:
    6
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.81
  • 拓扑面积:
    105
  • 氢给体数:
    2
  • 氢受体数:
    6

安全信息

  • 危险品标志:
    Xi
  • 安全说明:
    S26,S37/39
  • 危险类别码:
    R36/37/38
  • 海关编码:
    29225000
  • 危险性防范说明:
    P261,P305+P351+P338
  • 危险性描述:
    H315,H319,H335
  • 储存条件:
    存储在0至6°C的阴凉干燥处。

SDS

SDS:0bbf3fe5abd2525dc060038f83e3a114
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Name: N-BOC-Amino-(4-N-BOC-Piperidinyl)Carboxylic Acid 95% Material Safety Data Sheet
Synonym: None Known
CAS: 189321-65-1
Section 1 - Chemical Product MSDS Name:N-BOC-Amino-(4-N-BOC-Piperidinyl)Carboxylic Acid 95% Material Safety Data Sheet
Synonym:None Known

Section 2 - COMPOSITION, INFORMATION ON INGREDIENTS
CAS# Chemical Name content EINECS#
189321-65-1 N-BOC-Amino-(4-N-BOC-Piperidinyl)Carbo 95% unlisted
Hazard Symbols: XI
Risk Phrases: 36/37/38

Section 3 - HAZARDS IDENTIFICATION
EMERGENCY OVERVIEW
Irritating to eyes, respiratory system and skin.
Potential Health Effects
Eye:
Causes eye irritation. May cause chemical conjunctivitis.
Skin:
Causes skin irritation.
Ingestion:
May cause gastrointestinal irritation with nausea, vomiting and diarrhea.
Inhalation:
Causes respiratory tract irritation. Can produce delayed pulmonary edema.
Chronic:
Effects may be delayed.

Section 4 - FIRST AID MEASURES
Eyes: Immediately flush eyes with plenty of water for at least 15 minutes, occasionally lifting the upper and lower eyelids. Get medical aid.
Skin:
Get medical aid. Flush skin with plenty of water for at least 15 minutes while removing contaminated clothing and shoes. Wash clothing before reuse.
Ingestion:
Never give anything by mouth to an unconscious person. Get medical aid. Do NOT induce vomiting. If conscious and alert, rinse mouth and drink 2-4 cupfuls of milk or water. Wash mouth out with water.
Inhalation:
Remove from exposure and move to fresh air immediately. If not breathing, give artificial respiration. If breathing is difficult, give oxygen. Get medical aid. Do NOT use mouth-to-mouth resuscitation.
Notes to Physician:
Treat symptomatically and supportively.

Section 5 - FIRE FIGHTING MEASURES
General Information:
As in any fire, wear a self-contained breathing apparatus in pressure-demand, MSHA/NIOSH (approved or equivalent), and full protective gear. During a fire, irritating and highly toxic gases may be generated by thermal decomposition or combustion.
Extinguishing Media:
Use water spray, dry chemical, carbon dioxide, or chemical foam.

Section 6 - ACCIDENTAL RELEASE MEASURES
General Information: Use proper personal protective equipment as indicated in Section 8.
Spills/Leaks:
Vacuum or sweep up material and place into a suitable disposal container. Clean up spills immediately, observing precautions in the Protective Equipment section. Avoid generating dusty conditions.
Provide ventilation.

Section 7 - HANDLING and STORAGE
Handling:
Minimize dust generation and accumulation. Avoid breathing dust, vapor, mist, or gas. Avoid contact with eyes, skin, and clothing.
Keep container tightly closed. Avoid ingestion and inhalation. Use with adequate ventilation. Wash clothing before reuse.
Storage:
Store in a cool, dry place. Store in a tightly closed container.

Section 8 - EXPOSURE CONTROLS, PERSONAL PROTECTION
Engineering Controls:
Facilities storing or utilizing this material should be equipped with an eyewash facility and a safety shower. Use adequate ventilation to keep airborne concentrations low.
Exposure Limits CAS# 189321-65-1: Personal Protective Equipment Eyes: Wear appropriate protective eyeglasses or chemical safety goggles as described by OSHA's eye and face protection regulations in 29 CFR 1910.133 or European Standard EN166.
Skin:
Wear appropriate protective gloves to prevent skin exposure.
Clothing:
Wear appropriate protective clothing to prevent skin exposure.
Respirators:
Follow the OSHA respirator regulations found in 29 CFR 1910.134 or European Standard EN 149. Use a NIOSH/MSHA or European Standard EN 149 approved respirator if exposure limits are exceeded or if irritation or other symptoms are experienced.

Section 9 - PHYSICAL AND CHEMICAL PROPERTIES

Physical State: Powder
Color: white
Odor: Not available.
pH: Not available.
Vapor Pressure: Not available.
Viscosity: Not available.
Boiling Point: Not available.
Freezing/Melting Point: Not available.
Autoignition Temperature: Not available.
Flash Point: Not available.
Explosion Limits, lower: Not available.
Explosion Limits, upper: Not available.
Decomposition Temperature:
Solubility in water:
Specific Gravity/Density:
Molecular Formula: C16H28N2O6
Molecular Weight: 344.2058

Section 10 - STABILITY AND REACTIVITY
Chemical Stability:
Not currently available.
Conditions to Avoid:
Incompatible materials, dust generation, excess heat.
Incompatibilities with Other Materials:
Oxidizing agents.
Hazardous Decomposition Products:
Nitrogen oxides, carbon monoxide, carbon dioxide.
Hazardous Polymerization: Has not been reported

Section 11 - TOXICOLOGICAL INFORMATION
RTECS#:
CAS# 189321-65-1 unlisted.
LD50/LC50:
Not available.
Carcinogenicity:
N-BOC-Amino-(4-N-BOC-Piperidinyl)Carboxylic Acid - Not listed by ACGIH, IARC, or NTP.

Section 12 - ECOLOGICAL INFORMATION


Section 13 - DISPOSAL CONSIDERATIONS
Dispose of in a manner consistent with federal, state, and local regulations.

Section 14 - TRANSPORT INFORMATION

IATA
Not regulated as a hazardous material.
IMO
Not regulated as a hazardous material.
RID/ADR
Not regulated as a hazardous material.

Section 15 - REGULATORY INFORMATION

European/International Regulations
European Labeling in Accordance with EC Directives
Hazard Symbols: XI
Risk Phrases:
R 36/37/38 Irritating to eyes, respiratory system
and skin.
Safety Phrases:
S 26 In case of contact with eyes, rinse immediately
with plenty of water and seek medical advice.
S 37/39 Wear suitable gloves and eye/face
protection.
WGK (Water Danger/Protection)
CAS# 189321-65-1: No information available.
Canada
None of the chemicals in this product are listed on the DSL/NDSL list.
CAS# 189321-65-1 is not listed on Canada's Ingredient Disclosure List.
US FEDERAL
TSCA
CAS# 189321-65-1 is not listed on the TSCA inventory.
It is for research and development use only.


SECTION 16 - ADDITIONAL INFORMATION
N/A

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

反应信息

  • 作为反应物:
    描述:
    1-Boc-4-(Boc-氨基)哌啶-4-甲酸盐酸甲醇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 1,4-二氧六环醋酸异丙酯异丙醇 为溶剂, 反应 57.75h, 生成 3-[4-amino-1-(5-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)piperidine-4-carboxamido]phenyl N,N-dimethylcarbamate
    参考文献:
    名称:
    Discovery and Development of LX7101, a Dual LIM-Kinase and ROCK Inhibitor for the Treatment of Glaucoma
    摘要:
    The structure of LX7101, a dual LIM-kinase and ROCK inhibitor for the treatment of ocular hypertension and associated glaucoma, is disclosed. Previously reported LIM kinase inhibitors suffered from poor aqueous stability due to solvolysis of the central urea. Replacement of the urea with a hindered amide resulted in aqueous stable compounds, and addition of solubilizing groups resulted in a set of compounds with good properties for topical dosing in the eye and good efficacy in a mouse model of ocular hypertension. LX7101 was selected as a clinical candidate from this group based on superior efficacy in lowering intraocular pressure and a good safety profile. LX7101 completed IND enabling studies and was tested in a Phase 1 clinical trial in glaucoma patients, where it showed efficacy in lowering intraocular pressure.
    DOI:
    10.1021/ml500367g
  • 作为产物:
    描述:
    1-(tert-butyl) 4-methyl 4-((tert-butoxycarbonyl)amino)piperidine-1,4-dicarboxylate 以78的产率得到1-Boc-4-(Boc-氨基)哌啶-4-甲酸
    参考文献:
    名称:
    SUBSTITUTED PIPERIDINES HAVING PROTEIN KINASE INHIBITING ACTIVITY
    摘要:
    本发明提供了式(I)的PKA和PKB激酶抑制化合物,或其盐、溶剂化物、互变异构体或N-氧化物,其中E是一个五元杂环芳基环,包含1、2、3或4个从O、N和S中选择的杂原子,但不得多于1个杂原子不是N;q和r各自为0或1;前提是q+r为1或2;T为N或CR5基团;J1-J2为N═C(R6)、(R7)C═N、(R8)N—C(O)、(R8)2C—C(O)、N═N或(R7)C═C(R6);Q3为键或饱和的C1-3烃基连接基团,可选地被氟和羟基取代;G为NR2R3、CN或OH;m和n各自为0或1,前提是m+n为1或2,且当环E的相邻环成员为S或O时,m或n各自为0;R1a和R1b相同或不同,各自为氢或取代基R10;或R1a和R1b与它们所连接的碳原子或杂原子一起形成一个5或6元芳基或杂芳基环,其中芳基或杂芳基环可选地被一个或多个取代基R10取代;R2、R3、R4、R5、R7、R6、R8和R10如权利要求所定义。
    公开号:
    US20100093748A1
  • 作为试剂:
    描述:
    (S)-对氯-Β-苯丙氨醇1-Boc-4-(Boc-氨基)哌啶-4-甲酸1-Boc-4-(Boc-氨基)哌啶-4-甲酸 作用下, 以quant.的产率得到(S)-tert-butyl 4-(tert-butoxycarbonylamino)-4-(1-(4-chlorophenyl)-3-hydroxypropylcarbamoyl)piperidine-1-carboxylate
    参考文献:
    名称:
    Substituted pyrrolo[2,3-d]pyrimidine as a protein kinase B inhibitor
    摘要:
    本发明涉及一种新的化合物组,其化学式为(I)或其盐: 其中,Y,Z1,Z2,R1,R4,R5和n如说明书所述,可用于治疗或预防通过蛋白激酶B(PKB)介导的疾病或医疗条件,例如癌症。本发明还涉及包含化合物(I)的制药组合物,使用上述化合物治疗PKB介导的疾病的方法以及制备化合物(I)的方法。
    公开号:
    US08101623B2
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文献信息

  • LIMK2 INHIBITORS, COMPOSITIONS COMPRISING THEM, AND METHODS OF THEIR USE
    申请人:Burgoon Hugh Alfred
    公开号:US20090264450A1
    公开(公告)日:2009-10-22
    Inhibitors of LIM kinase 2 are disclosed, along with pharmaceutical compositions comprising them and methods of their use. Particular compounds are of the formula:
    LIM激酶2的抑制剂已被披露,以及包含它们的药物组合物和它们的使用方法。特定化合物的化学式如下:
  • [EN] PYRROLO [2, 3 -D] PYRIMIDIN DERIVATIVES AS PROTEIN KINASE B INHIBITORS<br/>[FR] DÉRIVÉS PYRROLO[2,3-D]PYRIMIDINE COMME INHIBITEURS DE LA PROTÉINE KINASE B
    申请人:ASTRAZENECA AB
    公开号:WO2009047563A1
    公开(公告)日:2009-04-16
    The invention relates to a novel group of compounds of Formula (I) or salts thereof: wherein Y, Z1, Z2, R1, R4, R5 and n are as described in the specification, which may be useful in the treatment or prevention of a disease or medical condition mediated through protein kinase B (PKB) such as cancer. The invention also relates to pharmaceutical compositions comprising said compounds, methods of treatment of diseases mediated by PKB using said compounds and methods for preparing compounds of Formula (I).
    该发明涉及一类新型化合物,其化学式为(I)或其盐:其中Y、Z1、Z2、R1、R4、R5和n如规范中所述,这些化合物可能在通过蛋白激酶B(PKB)介导的疾病或医疗状况的治疗或预防中有用,例如癌症。该发明还涉及包含所述化合物的药物组合物,使用所述化合物治疗通过PKB介导的疾病的方法,以及制备化合物(I)的方法。
  • [EN] AMINOPYRIMIDINE DERIVATIVES FOR USE AS MODULATORS OF KINASE ACTIVITY<br/>[FR] DÉRIVÉS AMINOPYRIMIDINES À UTILISER EN TANT QUE MODULATEURS D'ACTIVITÉ KINASE
    申请人:MERCK PATENT GMBH
    公开号:WO2013040044A1
    公开(公告)日:2013-03-21
    The invention provides novel heterocyclic amine compounds accord¬ ing to Formula (I) and their manufacture and use for the treatment of hyperproliferative diseases, such as cancer.
    这项发明提供了根据式(I)制备的新型杂环胺化合物,以及它们的制备和用于治疗高增殖性疾病,如癌症。
  • Sulfone derivatives, process for their production and use thereof
    申请人:——
    公开号:US20030187023A1
    公开(公告)日:2003-10-02
    A compound represented by the formula: 1 wherein R is a cyclic hydrocarbon group, or the like; W is a bond, or the like; X is a divalent hydrocarbon group, or the like; Y and Z are each independently —N(R 6 )— or the like; ring A is a nitrogen-containing heterocyclic ring, or the like; R5 and R6 are independently hydrogen atom, a hydrocarbon group, or the like; Z′ is imidoyl group, or the like; a is 0, 1 or 2; and b is 0 or 1, or a salt thereof.
    一个由以下式表示的化合物: 其中R是一个环烃基团,或类似物;W是一个键,或类似物;X是一个二价碳氢基团,或类似物;Y和Z分别独立地为—N(R6)—或类似物;环A是一个含氮杂环环,或类似物;R5和R6独立地为氢原子、一个碳氢基团,或类似物;Z′是亚胺基团,或类似物;a为0、1或2;b为0或1,或其盐。
  • NOVEL THIENOPYRROLE COMPOUNDS
    申请人:Wishart Neil
    公开号:US20110152243A1
    公开(公告)日:2011-06-23
    The invention provides a compound of Formula (I) pharmaceutically acceptable salts, pro-drugs, biologically active metabolites, stereoisomers and isomers thereof wherein the variable are defined herein. The compounds of the invention are useful for treating immunological and oncological conditions.
    该发明提供了公式(I)的化合物,包括药用盐、前药、生物活性代谢物、立体异构体和同分异构体,其中变量在此处定义。该发明的化合物可用于治疗免疫和肿瘤疾病。
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