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(4S,8aS)-4-(2-naphthyl)-perhydropyrrolo[1,2-a]pyrazine-1,3-dione | 1397680-12-4

中文名称
——
中文别名
——
英文名称
(4S,8aS)-4-(2-naphthyl)-perhydropyrrolo[1,2-a]pyrazine-1,3-dione
英文别名
(4S,8aS)-4-naphthalen-2-yl-6,7,8,8a-tetrahydro-4H-pyrrolo[1,2-a]pyrazine-1,3-dione
(4S,8aS)-4-(2-naphthyl)-perhydropyrrolo[1,2-a]pyrazine-1,3-dione化学式
CAS
1397680-12-4
化学式
C17H16N2O2
mdl
——
分子量
280.326
InChiKey
NAEWBKVSOZGRQV-GJZGRUSLSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    2.7
  • 重原子数:
    21
  • 可旋转键数:
    1
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    49.4
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    (2S,αS)-1-(α-tert-butyl-carbamoyl-α-(2-naphthyl)methyl)-pyrrolidine-2-carboxylic acid methyl ester 在 boron trifluoride diacetate 、 sodium hydroxide 作用下, 以 乙醇 为溶剂, 生成 (4S,8aS)-4-(2-naphthyl)-perhydropyrrolo[1,2-a]pyrazine-1,3-dione 、 (4R,8aS)-4-(2-naphthyl)-perhydropyrrolo[1,2-a]pyrazine-1,3-dione
    参考文献:
    名称:
    Synthesis of bicyclic 2,6-diketopiperazines via a three-step sequence involving an Ugi five-center, four-component reaction
    摘要:
    A three-step sequence involving an Ugi five-center, four-component reaction (U-5C-4CR), amide N-detertbutylation and cyclocondensation has been developed for easy access to diverse bicyclic 2,6-diketopiperazine (2,6-DKP) derivatives. In the key step, aromatic aldehydes were successfully coupled with cyclic alpha-amino acids and isocyanides in the course of U-5C-4CR. Boron trifluoride-acetic acid complex was developed as a new N-detertbutylating agent effective at rt. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2012.07.064
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文献信息

  • Synthesis of bicyclic 2,6-diketopiperazines via a three-step sequence involving an Ugi five-center, four-component reaction
    作者:Maciej Dawidowski、Franciszek Herold、Marcin Wilczek、Jadwiga Turło、Andrzej Chodkowski、Anna Gomółka、Jerzy Kleps
    DOI:10.1016/j.tet.2012.07.064
    日期:2012.9
    A three-step sequence involving an Ugi five-center, four-component reaction (U-5C-4CR), amide N-detertbutylation and cyclocondensation has been developed for easy access to diverse bicyclic 2,6-diketopiperazine (2,6-DKP) derivatives. In the key step, aromatic aldehydes were successfully coupled with cyclic alpha-amino acids and isocyanides in the course of U-5C-4CR. Boron trifluoride-acetic acid complex was developed as a new N-detertbutylating agent effective at rt. (C) 2012 Elsevier Ltd. All rights reserved.
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