(R)-1-甲氧基丙烷-2-胺盐酸盐 | 626220-76-6

• 分子结构分类: 有机化合物 - 有机氧化合物
• 中文名称: (R)-1-甲氧基丙烷-2-胺盐酸盐
• 中文别名: (R)-1-甲氧基-2-丙胺盐酸盐
• 英文名称: (R)-1-methoxypropan-2-amine hydrochloride
• 英文别名: (2R)-1-methoxypropan-2-amine hydrochloride；(2R)-1-methoxypropan-2-amine;hydrochloride
• CAS: 626220-76-6
• 化学式: C₄H₁₁NO*ClH
• mdl: MFCD12405301
• 分子量: 125.598
• InChiKey: RVDUOVVHQKMQLM-PGMHMLKASA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -0.26
• 重原子数：
  7
• 可旋转键数：
  2
• 环数：
  0.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  35.2
• 氢给体数：
  2
• 氢受体数：
  2

安全信息

• 海关编码：
  2922199090
• 危险性防范说明：
  P261,P280,P305+P351+P338
• 危险性描述：
  H302,H315,H319,H332,H335

SDS

Material Safety Data Sheet

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Section 1. Identification of the substance
Product Name: (R)-1-Methoxypropan-2-amine, HCl
Synonyms:

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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: (R)-1-Methoxypropan-2-amine, HCl
CAS number: 626220-76-6

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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: C4H11NO.ClH
Molecular weight: 125.6

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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, hydrogen chloride.

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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：

  氯乙基异氰酸酯 、 (R)-1-甲氧基丙烷-2-胺盐酸盐 在 吡啶 作用下， 以 四氢呋喃 为溶剂， 以50%的产率得到(S)-1-(2-chloroethyl)-3-(1-methoxypropan-2-yl)urea
  参考文献：
  名称：

  IMIDAZOLIDINONES AND ANALOGS EXHIBITING ANTI-CANCER AND ANTI-PROLIFERATIVE ACTIVITIES

  摘要：

  描述了一种化合物，其化学式为I，通过抑制c-FMS（CSF-1R）、c-KIT和/或PDGFR激酶，在治疗癌症、自身免疫疾病和代谢性骨疾病方面具有用途。这些化合物还在治疗其他由c-FMS、c-KIT或PDGFR激酶介导的哺乳动物疾病中发挥作用。

  公开号：

  US20140315917A1
• 作为产物：
  描述：

  2-((R)-2-methoxy-1-methyl-ethyl)isoindole-1,3-dione 在 肼 、 盐酸 作用下， 以 乙醇 、 乙醚 为溶剂， 反应 0.5h， 以100%的产率得到(R)-1-甲氧基丙烷-2-胺盐酸盐
  参考文献：
  名称：

  ISOINDOLYL COMPOUNDS

  摘要：

  式I的化合物：或其药用可接受盐，其中变量如本文所定义。还公开了制备这些化合物的方法，并将这些化合物用于治疗与P2X7嘌呤受体相关的疾病。

  公开号：

  US20120157494A1

文献信息

• [EN] BENZIMIDAZOLE DERIVATIVES AS BROMODOMAIN INHIBITORS<br/>[FR] DÉRIVÉS DE BENZIMIDAZOLE COMME INHIBITEURS DES BROMODOMAINES
  申请人：GLAXOSMITHKLINE IP DEV LTD

  公开号：WO2016146738A1

  公开（公告）日：2016-09-22

  Compounds of formula (I) and salts thereof: wherein R1, R2, R3, R4 are defined herein. Compounds of formula (I) and salts thereof have been found to inhibit the binding of the BET family of bromodomain proteins to, for example, acetylated lysine residues and thus may have use in therapy, for example in the treatment of autoimmune and inflammatory diseases, such as rheumatoid arthritis; and cancers.

  式（I）的化合物及其盐：其中R1、R2、R3、R4在此处定义。已发现式（I）的化合物及其盐能够抑制BET家族的溴结构域蛋白与例如乙酰化赖氨酸残基的结合，因此可能在治疗中发挥作用，例如在治疗自身免疫和炎症性疾病（如类风湿性关节炎）和癌症方面。
• [EN] MERTK DEGRADERS AND USES THEREOF<br/>[FR] AGENTS DE DÉGRADATION DE MERTK ET LEURS UTILISATIONS
  申请人：KYMERA THERAPEUTICS INC

  公开号：WO2020010210A1

  公开（公告）日：2020-01-09

  The present invention provides compounds, compositions thereof, and methods of using the same.

  本发明提供了化合物、其组合物以及使用相同的方法。
• [EN] METHODS AND COMPOUNDS FOR THE TREATMENT OF GENETIC DISEASE<br/>[FR] PROCÉDÉS ET COMPOSÉS POUR LE TRAITEMENT D'UNE MALADIE GÉNÉTIQUE
  申请人：DESIGN THERAPEUTICS INC

  公开号：WO2021158707A1

  公开（公告）日：2021-08-12

  The present disclosure relates to compounds and methods for modulating the expression of dmpk, and treating diseases and conditions in which dmpk plays an active role. The compound can be a transcription modulator molecule having a first terminus, a second terminus, and oligomeric backbone, wherein: a) the first terminus comprises a DNA-binding moiety capable of noncovalently binding to a nucleotide repeat sequence CAG or CTG; b) the second terminus comprises a protein-binding moiety binding to a regulatory molecule that modulates an expression of a gene comprising the nucleotide repeat sequence CAG or CTG; and c) the oligomeric backbone comprising a linker between the first terminus and the second terminus.

  本公开涉及化合物和方法，用于调节dmpk的表达，并治疗dmpk发挥积极作用的疾病和病况。该化合物可以是一种转录调节分子，具有第一末端、第二末端和寡聚骨架，其中：a）第一末端包括一种DNA结合基团，能够非共价结合到核苷酸重复序列CAG或CTG；b）第二末端包括结合到调节分子的蛋白结合基团，该调节分子调节包含核苷酸重复序列CAG或CTG的基因的表达；c）寡聚骨架包括连接第一末端和第二末端的连接物。
• [EN] 4-(8-METHOXY-1-((1-METHOXYPROPAN-2-YL)-2-(TETRAHYDRO-2H-PYRAN-4-YL)-1 H-IMIDAZO[4,5-C]QUINOLIN-7-YL)-3,5-DIMETHYLISOXAZOLE AND ITS USE AS BROMODOMAIN INHIBITOR<br/>[FR] 4-(8-MÉTHOXY-1-((1-MÉTHOXYPROPAN-2-YL)-2-(TÉTRAHYDRO-2H-PYRAN-4-YL)-1 H-IMIDAZO[4,5-C]QUINOLIN-7-YL)-3,5-DIMÉTHYLISOXAZOLE ET UTILISATION DE CE DERNIER EN TANT QU'INHIBITEUR DE BROMODOMAINES
  申请人：GLAXOSMITHKLINE LLC

  公开号：WO2013024104A1

  公开（公告）日：2013-02-21

  Novel quinoline compounds of formula (I), pharmaceutical compositions containing such compounds and their use in therapy, as bromodomain inhibitors.

  新型喹啉化合物的化学式（I），含有这种化合物的药物组合物以及它们在治疗中的应用，作为溴结构域抑制剂。
• In Vitro Intrinsic Clearance-Based Optimization of <i>N</i>³-Phenylpyrazinones as Corticotropin-Releasing Factor-1 (CRF₁) Receptor Antagonists
  作者：Richard A. Hartz、Vijay T. Ahuja、Maria Rafalski、William D. Schmitz、Allison B. Brenner、Derek J. Denhart、Jonathan L. Ditta、Jeffrey A. Deskus、Eddy W. Yue、Argyrios G. Arvanitis、Snjezana Lelas、Yu-Wen Li、Thaddeus F. Molski、Harvey Wong、James E. Grace、Kimberley A. Lentz、Jianqing Li、Nicholas J. Lodge、Robert Zaczek、Andrew P. Combs、Richard E. Olson、Ronald J. Mattson、Joanne J. Bronson、John E. Macor

  DOI：10.1021/jm900302q

  日期：2009.7.23

  identified as potent and orally active corticotropin-releasing factor-1 (CRF1) receptor antagonists. Selected compounds proved efficacious in an anxiety model in rats; however, pharmacokinetic properties were not optimal. In this article, we describe an in vitro intrinsic clearance-based approach to the optimization of pyrazinone-based CRF1 receptor antagonists wherein sites of metabolism were identified

  一系列基于吡嗪酮的杂环被鉴定为有效的和口服活性的促肾上腺皮质激素释放因子1（CRF 1）受体拮抗剂。所选择的化合物在大鼠焦虑模型中证明是有效的。但是，药代动力学特性不是最佳的。在本文中，我们描述了一种基于体外固有清除率的方法，用于优化基于吡嗪酮的CRF 1受体拮抗剂，其中通过与人肝微粒体孵育来确定代谢位点。发现通过在代谢的主要位点掺入适当的取代基可以降低代谢速率。这导致发现化合物12x，高效能（IC 50 = 1.0 nM）和选择性CRF1种受体拮抗剂，在大鼠中具有良好的口服生物利用度（F = 52％），并且在大鼠的防御性戒断焦虑测试中具有疗效。