Boc-D-2-氨基已二酸 | 110544-97-3

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 中文名称: Boc-D-2-氨基已二酸
• 中文别名: Boc-D-2-氨基己二酸；BOC-D-2-氨基己二酸
• 英文名称: N^α-tert-butyloxycarbonyl-D-homoglutamic acid
• 英文别名: (R)-2-(tert-butoxycarbonylamino)hexanedioic acid；Boc-D-2-aminoadipic acid；(2R)-2-[(2-methylpropan-2-yl)oxycarbonylamino]hexanedioic acid
• CAS: 110544-97-3
• 化学式: C₁₁H₁₉NO₆
• 分子量: 261.275
• InChiKey: QDTDLMJRZPSKDM-SSDOTTSWSA-N

物化性质

• 熔点：
  122-123 °C
• 沸点：
  462.1±35.0 °C(Predicted)
• 密度：
  1.231±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  0.8
• 重原子数：
  18
• 可旋转键数：
  8
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.73
• 拓扑面积：
  113
• 氢给体数：
  3
• 氢受体数：
  6

安全信息

• 危险等级：
  IRRITANT

反应信息

• 作为反应物：
  描述：

  Boc-D-2-氨基已二酸 在 盐酸 、 4-(4,6-二甲氧基三嗪-2-基)-4-甲基吗啉盐酸盐 作用下， 以 四氢呋喃 、 乙醚 为溶剂， 反应 50.17h， 生成 (R)-1,6-bis(dodecylamino)-1,6-dioxohexan-2-aminium chloride
  参考文献：
  名称：

  Controlling the Position of Functional Groups at the Liquid/Solid Interface: Impact of Molecular Symmetry and Chirality

  摘要：

  With the aim of controlling the position of functional groups in a substrate-supported monolayer, a new family of functionalized linear alkyl chains was designed and synthesized, aided by molecular mechanics and dynamics simulations of its two-dimensional self-assembly on graphite. The self-assembly of these amino functionalized diamides at the liquid/solid interface was investigated with scanning tunneling microscopy. Intermolecular hydrogen-bonding interactions involving amides, combined with the effect of molecular symmetry and chirality, were found to guide the self-assembly. Control of the relative position and orientation of the amine groups was achieved, in the case of enantiopure compounds. Interestingly, racemates led to both racemic conglomerate and solid solution formation, with a concomitant loss of positional and orientational control of the amino groups as a result.

  DOI：

  10.1021/ja209018u
• 作为产物：
  描述：

  Nα,Nca-di-tert-butyloxycarbonyl-D-homoglutamine 在 sodium hydroxide 作用下， 以 甲醇 为溶剂， 反应 1.0h， 以92%的产率得到Boc-D-2-氨基已二酸
  参考文献：
  名称：

  Sakura, Naoki; Hirose, Kyoko; Hashimoto, Tadashi, Chemical and pharmaceutical bulletin, 1986, vol. 34, # 8, p. 3506 - 3509

  摘要：

  DOI：

文献信息

• [EN] ENZYME INHIBITORS<br/>[FR] INHIBITEURS D'ENZYMES
  申请人：KALVISTA PHARMACEUTICALS LTD

  公开号：WO2021032933A1

  公开（公告）日：2021-02-25

  The present invention provides compounds of formula (I): Formula (I) compositions comprising such compounds; the use of such compounds in therapy; and methods of treating patients with such compounds; wherein A, Y, n, R1, R2A, R2B, R3 and *1 are as defined herein.

  本发明提供了如下式(I)的化合物：化合物组合物；在治疗中使用这些化合物；以及使用这些化合物治疗患者的方法；其中A、Y、n、R1、R2A、R2B、R3和*1如本文所定义。
• PROCESS FOR PRODUCTION OF 4-(SUBSTITUTED PHENYL)HEXAHYDROPYRIDOÝ2,1-C¨Ý1,4¨OXAZIN-6-ONE
  申请人：Eisai R&D Management Co., Ltd.

  公开号：EP2226325A1

  公开（公告）日：2010-09-08

  4-(Substituted phenyl)hexahydropyrido[2,1-c][1,4]oxazin-6-one represented by formula (I) or a salt thereof is useful as an intermediate for the production of a bicyclic cinnamide compound which is an Aβ production inhibitor. 4-(Substituted phenyl)hexahydropyrido[2,1-c][1,4]oxazin-6-one or the salt thereof can be produced in an industrially advantageous manner by subjecting a compound represented by formula (II) or a salt thereof to an intramolecular condensation reaction.

  公式(I)表示的4-(取代苯基)六氢吡啶并[2,1-c][1,4]噁唑啉-6-酮或其盐可用作生产双环丁酰胺化合物的中间体，该化合物是Aβ产生抑制剂。通过将公式(II)表示的化合物或其盐经历分子内缩合反应，可以以工业上有利的方式生产4-(取代苯基)六氢吡啶并[2,1-c][1,4]噁唑啉-6-酮或其盐。
• PROCESS FOR PRODUCTION OF 4- (SUBSTITUTED PHENYL) HEXAHYDROPYRIDO [2,1-C] [1,4] OXAZIN-6-ONE
  申请人：Kayano Akio

  公开号：US20100280243A1

  公开（公告）日：2010-11-04

  4-(Substituted phenyl)hexahydropyrido[2,1-c][1,4]oxazin-6-one represented by formula (I) or a salt thereof is useful as an intermediate for the production of a bicyclic cinnamide compound which is an Aβ production inhibitor. 4-(Substituted phenyl)hexahydropyrido[2,1-c][1,4]oxazin-6-one or the salt thereof can be produced in an industrially advantageous manner by subjecting a compound represented by formula (II) or a salt thereof to an intramolecular condensation reaction.

  公式（I）表示的4-（取代苯基）六氢吡啶[2,1-c][1,4]噁唑-6-酮或其盐是生产双环丙烯酰胺化合物的中间体，该化合物是Aβ产生抑制剂。通过将公式（II）表示的化合物或其盐经历分子内缩合反应，可以以工业上优势的方式生产4-（取代苯基）六氢吡啶[2,1-c][1,4]噁唑-6-酮或其盐。
• BARTON, DEREK H. R.;HERVE, YOLANDE;POTIER, PIERRE;THIERRY, JOSIANE, TETRAHEDRON, 43,(1987) N 19, 4297-4308
  作者：BARTON, DEREK H. R.、HERVE, YOLANDE、POTIER, PIERRE、THIERRY, JOSIANE

  DOI：——

  日期：——
• ENZYME INHIBITORS
  申请人：Kalvista Pharmaceuticals Limited

  公开号：EP4017586A1

  公开（公告）日：2022-06-29