4-(4-氨基苯氧基)-1-哌啶甲酸叔丁酯 | 138227-63-1

• 物质功能分类: 有机原料 - 杂环化合物
• 分子结构分类: 有机化合物 - 有机杂环化合物 - 哌啶类
• 中文名称: 4-(4-氨基苯氧基)-1-哌啶甲酸叔丁酯
• 中文别名: 1-BOC-4-(4-氨基苯氧基)哌啶；4-(4-氨基苯氧基)-1-哌啶羧酸-1,1-二甲基乙酯
• 英文名称: tert-butyl 4-(4-aminophenoxy)piperidine-1-carboxylate
• 英文别名: 4-(4-aminophenoxy)piperidine-1-carboxylic acid tert-butyl ester
• CAS: 138227-63-1
• 化学式: C₁₆H₂₄N₂O₃
• mdl: MFCD04115023
• 分子量: 292.378
• InChiKey: WEIBGUDKHYWNMW-UHFFFAOYSA-N

物化性质

• 沸点：
  430.3±35.0 °C(Predicted)
• 密度：
  1.140±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.7
• 重原子数：
  21
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.56
• 拓扑面积：
  64.8
• 氢给体数：
  1
• 氢受体数：
  4

安全信息

• 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：
  2-8°C

SDS

Material Safety Data Sheet

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Section 1. Identification of the substance
Product Name: 1-BOC-4-(4-aminophenoxy)piperidine
Synonyms: tert-Butyl 4-(4-aminophenoxy)piperidine-1-carboxylate

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

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Section 3. Composition/information on ingredients.
Ingredient name: 1-BOC-4-(4-aminophenoxy)piperidine
CAS number: 138227-63-1

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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.

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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.

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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.

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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:

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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.

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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: C16H24N2O3
Molecular weight: 292.4

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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.

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Section 11. Toxicological information
No data.

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Section 12. Ecological information
No data.

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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.

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

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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.

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SECTION 16 - ADDITIONAL INFORMATION
N/A

反应信息

• 作为反应物：
  描述：

  4-(4-氨基苯氧基)-1-哌啶甲酸叔丁酯 在 三乙酰氧基硼氢化钠 、 potassium carbonate 作用下， 以 二氯甲烷 、 溶剂黄146 、 N,N-二甲基甲酰胺 为溶剂， 反应 7.25h， 生成 ethyl N-{4-[(1-tert-butoxycarbonyl-4-piperidyl)oxy]phenyl}-N-[(7-cyano-2-naphthyl)methyl]carbamate
  参考文献：
  名称：

  The Discovery of YM-60828: A Potent, Selective and Orally-Bioavailable Factor Xa Inhibitor

  摘要：

  Since Factor Xa (FXa) is well known to play a central role in thrombosis and hemostasis, inhibition of FXa is an attractive target for antithrombotic strategies. As a part of our investigation of a non-peptide, orally available FXa inhibitor, we found that a series of N-[(7-amidino-2-naphthyl)methyl]aniline derivatives possessed potent and selective inhibitory activities. Structure-activity relationship (SAR) of the substituent (R-1) on the central aniline moiety suggested that increasing lipophilicity caused a detrimental effect on anticoagulant activity (prothrombin time assay) in plasma. Several compounds bearing a hydrophilic substituent in R-1 showed not only potent FXa inhibitory activities but also high anticoagulant activities. The best compound in this series was sulfamoylacetic acid derivative 8o (YM-60828) which was a potent, selective and orally bioavailable FXa inhibitor and was chosen for clinical development. (C) 2002 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0968-0896(01)00418-7
• 作为产物：
  描述：

  4-(4-硝基苯氧基)四氢-1(2H)-吡啶羧酸叔丁酯 在 palladium 10% on activated carbon 、 氢气 作用下， 以 甲醇 为溶剂， 20.0 ℃ 、103.42 kPa 条件下， 以88 %的产率得到4-(4-氨基苯氧基)-1-哌啶甲酸叔丁酯
  参考文献：
  名称：

  胶质母细胞瘤新型吲哚胺 2,3-双加氧酶 1 蛋白降解剂的鉴定和表征

  摘要：

  吲哚胺 2,3-双加氧酶 1 (IDO1) 是一种有效的免疫抑制酶，可通过色氨酸代谢和非酶功能抑制抗肿瘤免疫反应。迄今为止，大多数 IDO1 靶向方法都集中于抑制色氨酸代谢。然而，此类药物未能改善癌症患者的总体生存率。在这里，我们开发并表征了可降解 IDO1 蛋白的蛋白水解靶向嵌合体 (PROTAC)。测试了 IDO1-PROTAC 对 IDO1 酶和非酶活性的影响。在筛选 IDO1-PROTAC 衍生物文库后，鉴定出一种化合物可以通过 cereblon 介导的蛋白酶体降解有效降解 IDO1 蛋白。 IDO1-PROTAC：(i) 在培养的人胶质母细胞瘤 (GBM) 细胞中抑制 IDO1 酶活性和 IDO1 介导的 NF-κB 磷酸化，(ii) 在体内降解颅内脑肿瘤内的 IDO1 蛋白，以及 (iii) 介导存活对患有明确脑肿瘤的小鼠有益。这项研究鉴定并鉴定了一种新的 IDO1 蛋白降解剂

  DOI：

  10.1021/acs.jmedchem.2c00771

文献信息

• Phenoxypiperidines and analogs thereof useful as histamine H3 antagonists
  申请人：Mutahi W. Mwangi

  公开号：US20070167435A1

  公开（公告）日：2007-07-19

  Disclosed are compounds of the formula or a pharmaceutically acceptable salt or solvate thereof, wherein: M is CH or N; U and W are each CH, or one of U and W is CH and the other is N; X is a bond, alkylene, —C(O)—, —C(N—OR 5 )—, —C(N—OR 5 )—CH(R 6 )—, —CH(R 6 )—C(N—OR 5 )—, —O—, —OCH 2 —, —CH 2 O— or —S(O) 0-2 —; Y is —O—, —(CH 2 ) 2 —, —C(═O)—, —C(═NOR 7 )— or —SO 0-2 —; Z is a bond, optionally substituted alkylene or alkylene interrupted by a heteroatom or heterocyclic group; R 1 is optionally substituted alkyl, cycloalkyl, aryl, arylalkyl, heteroaryl, heterocycloalkyl, or benzimidazolyl or a derivative thereof; R 2 is optionally substituted alkyl, alkenyl, aryl, arylalkyl, heteroaryl, heteroarylalkyl, cycloalkyl or heterocycloalkyl; and the remaining variables are as defined in the specification; compositions and methods for treating an allergy-induced airway response, congestion, diabetes, obesity, an obesity-related disorder, metabolic syndrome and a cognition deficit disorder using said compounds, alone or in combination with other agents.

  揭示了以下化合物的结构式或其药学上可接受的盐或溶剂，其中：M为CH或N；U和W分别为CH，或者U和W中的一个为CH，另一个为N；X为键，烷基，—C(O)—，—C(N—OR5)—，—C(N—OR5)—CH(R6)—，—CH(R6)—C(N—OR5)—，—O—，—O —，—CH2O—或—S(O)0-2—；Y为—O—，—(CH2)2—，—C(═O)—，—C(═NOR7)—或—SO0-2—；Z为键，可选择地取代的烷基或被杂原子或杂环基中断的烷基；R1为可选择地取代的烷基，环烷基，芳基，芳基烷基，杂芳基，杂环烷基或苯并咪唑基或其衍生物；R2为可选择地取代的烷基，烯基，芳基，芳基烷基，杂芳基，杂芳基烷基，环烷基或杂环烷基；其余变量如规范中所定义；使用这些化合物，单独或与其他药剂联合使用，治疗由过敏引起的气道反应、充血、糖尿病、肥胖症、与肥胖有关的疾病、代谢综合征和认知缺陷障碍的组合物和方法。
• Discovery and Development of <i>N</i>-[4-(1-Cyclobutylpiperidin-4-yloxy)phenyl]-2-(morpholin-4-yl)acetamide Dihydrochloride (SUVN-G3031): A Novel, Potent, Selective, and Orally Active Histamine H₃ Receptor Inverse Agonist with Robust Wake-Promoting Activity
  作者：Ramakrishna Nirogi、Anil Shinde、Abdul Rasheed Mohammed、Rajesh Kumar Badange、Veena Reballi、Thrinath Reddy Bandyala、Sangram Keshari Saraf、Kumar Bojja、Sravanthi Manchineella、Pramod Kumar Achanta、Kiran Kumar Kandukuri、Ramkumar Subramanian、Vijay Benade、Raghava Choudary Palacharla、Pradeep Jayarajan、Santoshkumar Pandey、Venkat Jasti

  DOI：10.1021/acs.jmedchem.8b01280

  日期：2019.2.14

  histamine H3 receptor (H3R), physicochemical properties, and pharmacokinetics in rats resulted in identification of N-[4-(1-cyclobutyl-piperidin-4-yloxy)phenyl]-2-(morpholin-4-yl)acetamide dihydrochloride (17v, SUVN-G3031) as a clinical candidate. Compound 17v is a potent (hH3R Ki = 8.73 nM) inverse agonist at H3R with selectivity over other 70 targets, Compound 17v has adequate oral exposures and

  在大鼠中对组胺H3受体（H3R）的体外亲和力，理化性质和药代动力学指导下的一系列化学优化导致鉴定了N- [4-（1-环丁基-哌啶丁-4-基氧基）苯基] -2 -（吗啉-4-基）乙酰胺二盐酸盐（17v，SUVN-G3031）作为临床候选药物。化合物17v在H3R上是一种强效（hH3R Ki = 8.73 nM）反向激动剂，对其他70个靶标具有选择性。化合物17v在大鼠和狗中均具有足够的口服暴露量和良好的消除半衰期。它显示出高的受体占有率和明显的促醒作用，并减少了Orexin-B萨泊林损伤的大鼠的快速眼动睡眠，支持了其在治疗人类睡眠障碍中的潜在治疗作用。剂量比有效剂量高出几倍，对运动活性没有影响。它没有hERG和磷脂病的问题。已经成功完成了对动物的安全性，耐受性和药代动力学的第一阶段评估，以及对动物的长期安全性研究，而无需担心进一步的开发。
• UREIDO-PYRAZOLE DERIVATIVES AND THEIR USE AS KINASE INHIBITORS
  申请人：ELI LILLY AND COMPANY

  公开号：EP1609789A1

  公开（公告）日：2005-12-28

  The present invention provides kinase inhibitors of Formula I: wherein: R1 is hydrogen, methyl, or tolyl; W is piperidinyl, napthyl, or phenyl optionally substituted with halo; X is a bond, -CH2-, -O-(CH2)n-, -O-, or -C(O)-; n is 1 or 2; Y is phenyl, piperidinyl, or piperazinyl; Z is -C(O)-R2, -CH2-R3, or methylsulfonyl; R2 is C1-C4 alkyl, C1-C4 alkoxy, benzyloxy, C3-C5 cycloalkyl optionally substituted with phenyl, pyridyl optionally substituted with 1-2 C1-C4 alkoxy or 1-2 halo, thienyl optionally substituted with halo or C1-C4 alkyl, pyrrolyl, imidazolyl, pyrazolyl optionally substituted with C1-C4, alkyl, or phenyl optionally substituted from the group selected from trifluoromethyl, trifluoromethoxy, and 1-2 halo, and R3 is pyridyl; or a pharmaceutically acceptale salt thereof.

  本发明提供了化合物I的激酶抑制剂： 其中： R1为氢、甲基或甲苯基； W为哌啶基、萘基或苯基，可选择地取代为卤素； X为键、-CH2-、-O-( )n-、-O-或-C(O)-； n为1或2； Y为苯基、哌啶基或哌嗪基； Z为-C(O)-R2、- -R3或甲磺酰基； R2为C1-C4烷基、C1-C4烷氧基、苄氧基、C3-C5环烷基，可选择地取代为苯基，吡啶基，可选择地取代为1-2个C1-C4烷氧基或1-2个卤素，噻吩基，可选择地取代为卤素或C1-C4烷基，吡咯基，咪唑基，吡唑基，可选择地取代为C1-C4烷基，或苯基，可选择地取代为三氟甲基，三氟甲氧基和1-2个卤素中选择的一种，以及 R3为吡啶基； 或其药学上可接受的盐。
• [EN] PYRROLO[2,3-D]PYRIMIDINE DERIVATIVES AND THEIR USE IN THE TREATMENT OF CANCER<br/>[FR] DÉRIVÉS DE PYRROLO[2,3-D]PYRIMIDINE ET LEUR UTILISATION DANS LE TRAITEMENT DU CANCER
  申请人：SENTINEL ONCOLOGY LTD

  公开号：WO2021074251A1

  公开（公告）日：2021-04-22

  The invention provides compounds of the formula (1): or a salt or tautomer thereof wherein A, R1, R2, R3, R4, R5 and R6 are as defined herein. The compounds are inhibitors of Wee1 and/or PLK1 kinase and are envisaged to be useful in the treatment of cancers.

  这项发明提供了式（1）的化合物：或其盐或互变异构体，其中A、R1、R2、R3、R4、R5和R6如本文所定义。这些化合物是Wee1和/或PLK1激酶的抑制剂，预计在癌症治疗中有用。
• Bis-Heteroaryl Pyrazoles: Identification of Orally Bioavailable Inhibitors of Activin Receptor-Like Kinase-2 (R206H)
  作者：Katsuhiko Sekimata、Tomohiro Sato、Naoki Sakai、Hisami Watanabe、Chiemi Mishima-Tsumagari、Tomonori Taguri、Takehisa Matsumoto、Yoshifumi Fujii、Noriko Handa、Teruki Honma、Akiko Tanaka、Mikako Shirouzu、Shigeyuki Yokoyama、Kohei Miyazono、Yoshinobu Hashizume、Hiroo Koyama

  DOI：10.1248/cpb.c18-00598

  日期：2019.3.1

  Mutant activin receptor-like kinase-2 (ALK2) was reported to be closely associated with the pathogenesis of fibrodysplasia ossificans progressiva (FOP) and diffuse intrinsic pontine glioma (DIPG), and therefore presents an attractive target for therapeutic intervention. Through in silico virtual screenings and structure–activity relationship studies assisted by X-ray crystallographic analyses, a novel series of bis-heteroaryl pyrazole was identified as potent inhibitors of ALK2 (R206H). Derived from in silico hit compound RK-59638 (6a), compound 18p was identified as a potent inhibitor of ALK2 (R206H) with good aqueous solubility, liver microsomal stability, and oral bioavailability.

  突变的激活素受体样激酶-2（ALK2）被报道与进行性骨化性纤维发育不良（FOP）和弥漫性内在性脑桥胶质瘤（DIPG）的发病机制密切相关，因此成为一个有吸引力的治疗干预靶点。通过计算机虚拟筛选和结构-活性关系研究，借助X射线晶体学分析，发现了一系列新型双杂环吡唑类化合物，这些化合物是ALK2（R206H）的强效抑制剂。从计算机筛选的先导化合物RK-59638（6a）衍生而来，化合物18p被鉴定为具有良好水溶性、肝微粒体稳定性和口服生物利用度的ALK2（R206H）强效抑制剂。