2-(1-羟乙基)吡咯烷-1-羧酸叔丁酯 | 916145-68-1

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡咯烷类
• 中文名称: 2-(1-羟乙基)吡咯烷-1-羧酸叔丁酯
• 英文名称: tert-butyl 2-(1-hydroxyethyl)pyrrolidine-1-carboxylate
• CAS: 916145-68-1
• 化学式: C₁₁H₂₁NO₃
• mdl: MFCD20232789
• 分子量: 215.293
• InChiKey: JNNOAQQODYAQBD-UHFFFAOYSA-N

物化性质

• 沸点：
  299.8±13.0 °C(Predicted)
• 密度：
  1.076±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.4
• 重原子数：
  15
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.909
• 拓扑面积：
  49.8
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  2-(1-羟乙基)吡咯烷-1-羧酸叔丁酯 在 三乙胺 作用下， 以 乙腈 为溶剂， 反应 74.0h， 生成 1-tert-butyl-6-fluoro-7-[(S)-2-((S)-1-hydroxyethyl)pyrrolidin-1-yl]-4-oxo-1,4-dihydro[1,8]naphthyridine-3-carboxylic acid ethyl ester
  参考文献：
  名称：

  Novel Antibacterial Class:  A Series of Tetracyclic Derivatives

  摘要：

  We describe the synthesis and antibacterial activity of a series of tetracyclic naphthyridones. The members of this series act primarily via inhibition of bacterial translation and belong to the class of novel ribosome inhibitors (NRIs). In this paper we explore the structure-activity relationships (SAR) of these compounds to measure their ability both to inhibit bacterial translation and also to inhibit the growth of bacterial cells in culture. The most active of these compounds inhibit Streptococcus pneumoniae translation at concentrations of < 5 mu M and have minimum inhibitory concentrations (MICs) of < 8 mu g/mL against clinically relevant strains of bacteria.

  DOI：

  10.1021/jm060010w
• 作为产物：
  描述：

  2-羟基-3-(2-苯基-2-氧代)乙基-1,4-萘醌 、 乙基溴化镁 在 水 、 氯化铵 作用下， 以 四氢呋喃 为溶剂， 反应 3.0h， 生成 2-(1-羟乙基)吡咯烷-1-羧酸叔丁酯
  参考文献：
  名称：

  WO2006/125641

  摘要：

  公开号：

文献信息

• Substituted Imidazopyridines as HDM2 Inhibitors
  申请人：Merck Sharp & Dohme Corp.

  公开号：US20140179680A1

  公开（公告）日：2014-06-26

  The present invention provides substituted imidazopyridines as described herein or a pharmaceutically acceptable salt or solvate thereof. The representative compounds are useful as inhibitors of the HDM2 protein. Also disclosed are pharmaceutical compositions comprising the above compounds and potential methods of treating cancer using the same.

  本发明提供了如本文所述的取代咪唑吡啶或其药用可接受的盐或溶剂。代表性化合物可用作HDM2蛋白的抑制剂。还公开了包括上述化合物的药物组合物以及使用它们治疗癌症的潜在方法。
• [EN] KRAS G12D INHIBITORS<br/>[FR] INHIBITEURS DE KRAS G12D
  申请人：MIRATI THERAPEUTICS INC

  公开号：WO2021041671A1

  公开（公告）日：2021-03-04

  The present invention relates to compounds that inhibit KRas G12D. In particular, the present invention relates to compounds that inhibit the activity of KRas G12D, pharmaceutical compositions comprising the compounds and methods of use therefor.

  本发明涉及抑制KRas G12D的化合物。具体地，本发明涉及抑制KRas G12D活性的化合物，包括这些化合物的药物组合物以及使用方法。
• Substituted isoquinoline-1,3(2H,4H)-diones, 1-thioxo-1,4-dihydro-2H-isoquinoline-3-ones and 1,4-dihydro-3 (2H)-isoquinolones and methods of use thereof
  申请人：Tsou Hwei-Ru

  公开号：US20080085890A1

  公开（公告）日：2008-04-10

  This invention provides compounds of Formula (I), having the structure where G 1 , G 2 , G 3 , G 4 , A 1 , A 2 , Y 1 , Y 2 , L 1 , Z, e and f are defined herein, or a pharmaceutically acceptable salt thereof, which are useful for treating or preventing cancer.

  这项发明提供了具有结构的化合物（I），其中G1、G2、G3、G4、A1、A2、Y1、Y2、L1、Z、e和f在此处定义，或其药用可接受盐，用于治疗或预防癌症。
• Substituted heterocyclic compounds and methods of use
  申请人：Cao Guo-Qiang

  公开号：US20050182072A1

  公开（公告）日：2005-08-18

  The present invention relates to therapeutic diazobicyclo pyridines and their use in the treatment of arthritis, rheumatoid arthritis, psoriatic arthritis or osteoarthritis, organ transplant, acute transplant or heterograft and homograft rejection, ischemic and reperfusion injury, transplantation tolerance induction, multiple sclerosis, inflammatory bowel disease, ulcerative colitis, Crohn's disease, lupus, graft vs. host diseases, T -cell mediated hypersensitivity diseases, contact hypersensitivity, delayed-type hypersensitivity, gluten-sensitive enteropathy, Type 1 diabetes, psoriasis, contact dermatitis, Hashimoto's thyroiditis, Sjogren's syndrome, autoimmune hyperthyroidism, Graves' Disease, Addison's disease, autoimmune polyglandular disease, autoimmune alopecia, pernicious anemia, vitiligo, autoimmune hypopituatarism, Guillain-Barre syndrome, autoimmune diseases, glomerulonephritis, serum sickness, uticaria, respiratory allergies, asthma, hayfever, allergic rhinitis, skin allergies, scleracielma, mycosis flugoides, acute inflammatory responses, acute respiratory distress syndrome, dermatomyositis, alopecia areata, chronic actinic dermatitis, eczema, Behcet's disease, Pustulosis palmoplanteris, Pyoderma gangrenum, Sezary's syndrome, atopic dermatitis, systemic schlerosis, morphea, Type II diabetes and cancers where PKC theta or other PKC-family kinases are activated, overexpressed or facilitate tumor growth or survival of tumor cells, T cell leukemia, thymoma, T and B cell lymphoma, colon carcinoma, breast carcinoma and lung carcinoma or provides resistance to chemotherapeutic drugs.

  本发明涉及治疗用的二氮杂双环吡啶及其在治疗关节炎、类风湿性关节炎、银屑病性关节炎或骨关节炎、器官移植、急性移植或异种移植和同种移植排斥、缺血再灌注损伤、移植耐受诱导、多发性硬化症、炎症性肠病、溃疡性结肠炎、克罗恩病、红斑狼疮、移植物抗宿主病、T细胞介导的超敏反应性疾病、接触性超敏反应、迟发型超敏反应、麦糊疹性肠病、1型糖尿病、银屑病、接触性皮炎、桥本甲状腺炎、干燥综合症、自身免疫性甲状腺功能亢进症、格雷夫斯病、亚当逊病、自身免疫性多发性内分泌腺疾病、自身免疫性脱发症、恶性贫血、白癜风、自身免疫性下丘脑功能减退症、格林-巴利综合症、自身免疫性疾病、肾小球肾炎、血清病、荨麻疹、呼吸道过敏、哮喘、花粉热、过敏性鼻炎、皮肤过敏、硬皮病、浆液性腺瘤、急性炎症反应、急性呼吸窘迫综合症、皮肌炎、斑秃、慢性光化性皮炎、湿疹、Behcet病、掌跖角化症、脓疱性荨麻疹、Sezary综合症、特应性皮炎、系统性硬化病、硬皮症、2型糖尿病和PKC theta或其他PKC家族激酶被激活、过度表达或促进肿瘤生长或肿瘤细胞存活、T细胞白血病、胸腺瘤、T和B细胞淋巴瘤、结肠癌、乳腺癌和肺癌或提供对化疗药物的抗性。
• Pyridine Compounds For Combating Arthropod Pests and Nematodes
  申请人：Puhl Michael

  公开号：US20080176826A1

  公开（公告）日：2008-07-24

  The present invention relates to new pyridine compounds which are useful for combating animal pests, in particular insects, arachnids and nematodes. The invention also relates to a method for combating insects, nematodes and arachnids. The pyridine compounds have the formula I as defined below. Likewise, compounds of the formula II are suitable for combating pests. In formulae I and II n is 1 or 2, and R 1 , R 2 , R 3 , R 4 and R 5 are as defined in the claims and in the specification.

  本发明涉及一种新的吡啶化合物，可用于对抗动物害虫，尤其是昆虫、蜘蛛和线虫。本发明还涉及一种用于对抗昆虫、线虫和蜘蛛的方法。吡啶化合物的化学式I如下所定义。同样，化学式II的化合物也适用于对抗害虫。在式I和II中，n为1或2，R1、R2、R3、R4和R5如权利要求和说明书中所定义。