5-methyl-azabicyclo<3.3.0>octane-2-one | 137125-39-4

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡咯里西啶类
• 英文名称: 5-methyl-azabicyclo<3.3.0>octane-2-one
• 英文别名: 7a-methylhexahydro-3H-pyrrolizin-3-one；8-methyl-2,5,6,7-tetrahydro-1H-pyrrolizin-3-one
• CAS: 137125-39-4
• 化学式: C₈H₁₃NO
• 分子量: 139.197
• InChiKey: FSVVYIAVWCTTTL-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.5
• 重原子数：
  10
• 可旋转键数：
  0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.88
• 拓扑面积：
  20.3
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为产物：
  描述：

  5-氯-2-戊酮 在 sodium azide 、 potassium carbonate 作用下， 以 1,4-二氧六环 、 甲醇 、 N,N-二甲基甲酰胺 为溶剂， 反应 1.0h， 生成 5-methyl-azabicyclo<3.3.0>octane-2-one
  参考文献：
  名称：

  硼酸与γ-叠氮基-N-甲苯磺酰hydr的Csp3-Csp3 / Csp3-N过渡-无金属多米诺反应合成吡咯烷

  摘要：

  γ-叠氮基-N-甲苯磺酰hydr与硼酸之间的反应导致在多米诺骨牌过程中获得2,2-二取代的吡咯烷，包括1）重氮烷的形成，2）重氮化合物的分子间碳基化和3）分子内碳基化叠氮化物，并且包括在同一碳原子上形成Csp 3 -Csp 3和Csp 3 -N键。该反应在微波活化下无需任何过渡金属催化剂即可进行，并且在两个反应伙伴中均具有广泛的作用范围。它可以同等效率应用于烷基和芳基硼酸。与N衍生自2-（2-叠氮基乙基）-环戊酮和环己酮的-甲苯磺酰hydr反应的非对映选择性很高，导致顺式稠合双环系统成为独特的非对映异构体。超过60个示例说明了该过程的范围，包括天然生物碱中存在的支架，并且基于DFT的计算支持了该机制建议。

  DOI：

  10.1002/anie.202010528

文献信息

• Intramolecular Schmidt reactions of alkyl azides with ketals and enol ethers
  作者：Craig J. Mossman、Jeffrey Aubé

  DOI：10.1016/0040-4020(96)00037-3

  日期：1996.3

  The ketals or enol ethers of 1,5-azidoketones were converted into lactams using a two-stage process. Treatment of the ketals and enol ethers with acid (trifluoroacetic acid, triflic acid, or trimethylsilyl triflate) afforded an oxonium ion which reacted with the tethered azide to give a 1,1-azido-alkoxy intermediate. Bond reorganization led to an iminium ether that was reacted with sodium iodide in

  使用两步法将1，5-叠氮酮的缩酮或烯醇醚转化为内酰胺。用酸（三氟乙酸，三氟甲磺酸或三甲基三氟甲磺酸酯）处理缩酮和烯醇醚，得到氧鎓离子，其与束缚的叠氮化物反应，得到1，1-叠氮基-烷氧基中间体。键的重组产生了亚胺醚，该亚胺醚与碘化钠在丙酮中反应以暴露出酰胺产物。据报道，使用二甲基或二乙基缩酮，有七个分子内实例的收率在68％至≥95％之间。还描述了使用1，3-二氧戊环的尝试和一个分子间的实例。
• Intramolecular Schmidt Reactions of Alkyl Azides with Ketones: Scope and Stereochemical Studies
  作者：Gregory L. Milligan、Craig J. Mossman、Jeffrey Aube

  DOI：10.1021/ja00147a006

  日期：1995.10

  The intramolecular Schmidt reaction of alkyl azides and ketones has been demonstrated. The reaction is proposed to occur via initial attack of an azide on a ketone activated by a variety of protic or Lewis acids, including trifluoroacetic acid, titanium tetrachloride, and others. The resulting azidohydrin undergoes a direct rearrangement to afford the product amide and molecular nitrogen. When cyclic ketones are used, fused bicyclic lactams of types encountered in a wide variety of natural products are obtained. Although the distance allowed between the carbonyl group and the alkyl azide is quite restricted, the reaction is general with respect to the ketone component, including acyclic ketones and cyclic substrates ranging from standard to large ring sizes. The reaction also succeeds with aldehydes, although elimination or hydride migration products compete. In several cases examined, the reaction was found to proceed with retention of configuration at the migrating carbon. Competing reactions with beta-diketones and alpha,beta-unsaturated ketones were found to predominate over ring expansion.
• Intramolecular Schmidt reaction of alkyl azides
  作者：Jeffrey Aube、Gregory L. Milligan

  DOI：10.1021/ja00023a065

  日期：1991.11
• [EN] TEAD INHIBITORS<br/>[FR] INHIBITEURS DE TEAD
  申请人：[en]ORION CORPORATION

  公开号：WO2022219246A1

  公开（公告）日：2022-10-20

  The present invention relates to a compound of formula (I) wherein A, Z, L, R1, R2, R3, R4, R5and R33are as defined in claim 1, or a pharmaceutically acceptable salt thereof. The compounds of formula (I) possess utility as inhibitors of TEAD. The compounds are useful as medicaments in the treatment of diseases or conditions wherein inhibition of TEAD is desired, such as cancer and chronic pain.