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(3S,4S)-1-benzyl-3-(N-tert-butoxycarbonyl)amino-4-methoxypyrrolidine | 174847-50-8

中文名称
——
中文别名
——
英文名称
(3S,4S)-1-benzyl-3-(N-tert-butoxycarbonyl)amino-4-methoxypyrrolidine
英文别名
(+)-trans-1-benzyl-3-(t-butoxycarbonylamino)-4-methoxypyrrolidine;tert.-Butyl N-(trans-1-benzyl-4-methoxypyrrolidin-3yl)carbamate;tert-butyl N-[(3S,4S)-1-benzyl-4-methoxypyrrolidin-3-yl]carbamate
(3S,4S)-1-benzyl-3-(N-tert-butoxycarbonyl)amino-4-methoxypyrrolidine化学式
CAS
174847-50-8
化学式
C17H26N2O3
mdl
——
分子量
306.405
InChiKey
RVUGUSZSDYIZMS-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):
    2.2
  • 重原子数:
    22
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.59
  • 拓扑面积:
    50.8
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    (3S,4S)-1-benzyl-3-(N-tert-butoxycarbonyl)amino-4-methoxypyrrolidine 在 palladium on activated charcoal lithium aluminium tetrahydride 、 氢气 作用下, 以 四氢呋喃乙醇 为溶剂, 反应 7.0h, 生成 (3S,4S)-3-(N-tert-butoxycarbonyl)methylamino-4-methoxypyrrolidine
    参考文献:
    名称:
    Practical synthesis of (3S,4S)-3-methoxy-4-methylaminopyrrolidine
    摘要:
    Three synthetic methods for the preparation of (3S,4S)-3-methoxy-4-methylaminopyrrolidine, an important intermediate in the synthesis of the novel quinolone antitumor agent, AG-7352, have been developed. By one route, an efficient and large-scale preparation of the chiral pyrrolidine could be achieved through resolution of (+/-)-1-Boc-3-benzylamino-4-hydroxypyrrolidine, which is prepared from either 3-pyrroline or 1,4-dichloro-2-butene. (C) 2002 Published by Elsevier Science Ltd.
    DOI:
    10.1016/s0957-4166(01)00530-4
  • 作为产物:
    参考文献:
    名称:
    Practical synthesis of (3S,4S)-3-methoxy-4-methylaminopyrrolidine
    摘要:
    Three synthetic methods for the preparation of (3S,4S)-3-methoxy-4-methylaminopyrrolidine, an important intermediate in the synthesis of the novel quinolone antitumor agent, AG-7352, have been developed. By one route, an efficient and large-scale preparation of the chiral pyrrolidine could be achieved through resolution of (+/-)-1-Boc-3-benzylamino-4-hydroxypyrrolidine, which is prepared from either 3-pyrroline or 1,4-dichloro-2-butene. (C) 2002 Published by Elsevier Science Ltd.
    DOI:
    10.1016/s0957-4166(01)00530-4
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文献信息

  • 7-(1-pyrrolidinyl)-3-quinolone- and -naphthyridonecarboxylic acid
    申请人:Bayer Aktiengesellschaft
    公开号:US04990517A1
    公开(公告)日:1991-02-05
    7-(1-Pyrrolidinyl)-3-quinolone- and -naphthyridonecarboxylic acid derivatives as antibacterial agents and feed additives, of the formula ##STR1## in which X.sup.1 is halogen, X.sup.2 is hydrogen, halogen, amino or other radical, R.sup.1 is alkyl, cycloalkyl, optionally substituted phenyl or other radical, R.sup.2 is hydrogen, alkyl or a dioxolylmethyl radical, R.sup.3 is ##STR2## A is N, CH, C-halogen, or the like, or forms a bridge with R.sup.1, and addition products thereof.
    7-(1-吡咯啉基)-3-喹啉基-和-啉基羧酸生物作为抗菌剂和饲料添加剂,其化学式为##STR1##其中X.sup.1为卤素,X.sup.2为氢、卤素、基或其他基团,R.sup.1为烷基、环烷基、可选择取代的苯基或其他基团,R.sup.2为氢、烷基或二氧杂环丙基基团,R.sup.3为##STR2##A为N、CH、C-卤素或类似物,或与R.sup.1形成桥梁的结合物。
  • Compounds, processes for the preparation thereof and anti-tumor agents
    申请人:Dainippon Pharmaceutical Co., Ltd.
    公开号:US05817669A1
    公开(公告)日:1998-10-06
    This invention relates to pyridone-carboxylic acid derivatives of the following formula or salts thereof: ##STR1## wherein R.sub.1 is a hydrogen atom, a halogen atom, etc., R.sub.2 is a carboxyl group etc., R.sub.3 is a hydrogen atom etc., A is a nitrogen atom or CH, m is 1 or 2, and Y is an eliminable group or a group having the following formula: ##STR2## wherein R.sub.4 is a hydrogen atom or a lower alkyl group, Z is a hydrogen atom, a lower alkyl group, etc., R.sub.5 is a hydrogen atom, a lower alkyl group, etc., n is 0 or 1, and p is 1, 2, 3 or 4 and to processes for the preparation of these compounds, and further to anti-tumor agents which contain the above compounds as effective ingredients.
    本发明涉及具有以下通式的吡啶酮羧酸生物或其盐:##STR1##其中R1为氢原子、卤素原子等,R2为羧基等,R3为氢原子等,A为氮原子或CH,m为1或2,Y为可消除基团或具有以下通式的基团:##STR2##其中R4为氢原子或低级烷基,Z为氢原子、低级烷基等,R5为氢原子、低级烷基等,n为0或1,p为1、2、3或4,以及制备这些化合物的方法,并且进一步涉及含有上述化合物作为有效成分的抗肿瘤药物。
  • NOVEL COMPOUND, PROCESS FOR PRODUCING THE SAME, AND ANTITUMOR AGENT
    申请人:DAINIPPON PHARMACEUTICAL CO., LTD.
    公开号:EP0787726B1
    公开(公告)日:2001-11-28
  • US4990517A
    申请人:——
    公开号:US4990517A
    公开(公告)日:1991-02-05
  • US5059597A
    申请人:——
    公开号:US5059597A
    公开(公告)日:1991-10-22
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同类化合物

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