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4-amino-3,3-dimethyl-piperidine-1-carboxylic acid ethyl ester | 544443-46-1

中文名称
——
中文别名
——
英文名称
4-amino-3,3-dimethyl-piperidine-1-carboxylic acid ethyl ester
英文别名
4-Amino-1-carbethoxy-3,3-dimethylpiperidine;ethyl 4-amino-3,3-dimethylpiperidine-1-carboxylate
4-amino-3,3-dimethyl-piperidine-1-carboxylic acid ethyl ester化学式
CAS
544443-46-1
化学式
C10H20N2O2
mdl
——
分子量
200.281
InChiKey
LMBHFRKOOBDTIT-UHFFFAOYSA-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

物化性质

  • 沸点:
    271.1±33.0 °C(Predicted)
  • 密度:
    1.013±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.9
  • 重原子数:
    14
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.9
  • 拓扑面积:
    55.6
  • 氢给体数:
    1
  • 氢受体数:
    3

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    trifluoromethanesulfonic acid 6-chloro-2-oxo-2H-chromen-4-yl ester4-amino-3,3-dimethyl-piperidine-1-carboxylic acid ethyl ester 在 sodium hydride 作用下, 以 DMF (N,N-dimethyl-formamide) 为溶剂, 反应 72.17h, 以56%的产率得到4-(6-chloro-2-oxo-2H-chromen-4-ylamino)-3,3-dimethyl-piperidine-1-carboxylic acid ethyl ester
    参考文献:
    名称:
    [EN] ANTAGONISTS OF MELANIN CONCENTRATING HORMONE RECEPTOR
    [FR] ANTAGONISTES DU RECEPTEUR DE L'HORMONE DE MELANO-CONCENTRATION
    摘要:
    公开号:
    WO2003106452A3
  • 作为产物:
    描述:
    3,3-dimethyl-4-oxo-piperidine-1-carboxylic acid ethyl ester 在 ammonium acetate 、 sodium tetrahydroborate 作用下, 以 甲醇 为溶剂, 反应 144.0h, 以73%的产率得到4-amino-3,3-dimethyl-piperidine-1-carboxylic acid ethyl ester
    参考文献:
    名称:
    [EN] ANTAGONISTS OF MELANIN CONCENTRATING HORMONE RECEPTOR
    [FR] ANTAGONISTES DU RECEPTEUR DE L'HORMONE DE MELANO-CONCENTRATION
    摘要:
    公开号:
    WO2003106452A3
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文献信息

  • Generation triple-targeting, chiral, broad-spectrum antimicrobial 7-substituted piperidino-quinolone carboxylic acid derivatives, their preparation,compositions and use as medicaments
    申请人:WOCKHARDT LIMITED
    公开号:US20030216568A1
    公开(公告)日:2003-11-20
    This invention relates to new generation triple-targeting, chiral, broad-spectrum antimicrobial 7-substituted piperidino-quinolone carboxylic acid derivatives, to their optical isomers, diastereomers or enantiomers, as well as pharmaceutically acceptable salts, hydrates, prodrugs, polymorphs and pseudopolymorphs thereof, to their preparation, to their compositions and to their use.
    本发明涉及新一代三重靶向手性广谱抗菌7-取代哌啶酮羧酸衍生物,以及它们的光学异构体、对映异构体或对映体,以及其药学上可接受的盐、水合物、前药、多晶形和假多晶形,以及它们的制备、组成和用途。
  • Antagonists of melanin concentrating hormone receptor
    申请人:Millennium Pharmaceuticals, Inc.
    公开号:US20040106645A1
    公开(公告)日:2004-06-03
    This invention provides compounds that are antagonists of melanin concentrating hormone receptor-1 (MCH-R1). The compounds are represented by formula I: 1 where m is zero or one, n is zero to two, Y is oxygen or —N(R 9 )—, R 1 , R 2 , R 3 , R 4 , R 5 , R 9 and Ring A are defined in the specification. Coumarin and quinolone compounds where R 1 and R 2 together form a fused benzo ring are preferred. The invention also provides compounds of formula VI where the coumarin moiety is replaced by a quinazolinone ring. The compounds are useful for treating MCH-R1-related disorders, particularly overweight conditions including obesity.
    这项发明提供了一些与黑色素浓集激素受体-1 (MCH-R1) 相对抗的化合物。这些化合物由公式 I 表示:其中 m 为零或一,n 为零至二,Y 为氧或 —N(R9)—,R1、R2、R3、R4、R5、R9 和环 A 在说明书中有定义。偏好使用 R1 和 R2 结合形成融合苯环的香豆素和喹啉类化合物。该发明还提供了公式 VI 的化合物,其中香豆素基团被喹嗪酮环替换。这些化合物可用于治疗与 MCH-R1 相关的疾病,特别是超重症,包括肥胖症。
  • Generation triple-targeting, chiral, broad-spectrum antimicrobial 7-substituted piperidino-quinolone carboxylic acid derivatives, their preparation, compositions and use as medicaments
    申请人:De Souza John Noel
    公开号:US20050065164A1
    公开(公告)日:2005-03-24
    This invention relates to new generation triple-targeting, chiral, broad-spectrum antimicrobial 7-substituted piperidino-quinolone carboxylic acid derivatives, to their optical isomers, diastereomers or enantiomers, as well as pharmaceutically acceptable salts, hydrates, prodrugs, polymorphs and pseudopolymorphs thereof, to their preparation, to their compositions and to their use.
    本发明涉及新一代三重靶向、手性、广谱抗微生物的7-取代哌啶酮羧酸衍生物,以及它们的光学异构体、对映异构体或对映体、药学上可接受的盐、水合物、前药、多晶型和假多晶型,以及它们的制备、组合物和用途。
  • New generation triple-targeting, chiral, broad-spectrum antimicrobial 7-substituted piperidino-quinolone carboxylic acid derivatives, their preparation, compositions and use as medicaments
    申请人:De Souza Noel John
    公开号:US20080214608A1
    公开(公告)日:2008-09-04
    This invention relates to new generation triple-targeting, chiral, broad-spectrum antimicrobial 7-substituted piperidino-quinolone carboxylic acid derivatives, to their optical isomers, diastereomers or enantiomers, as well as pharmaceutically acceptable salts, hydrates, prodrugs, polymorphs and pseudopolymorphs thereof, to their preparation, to their compositions and to their use.
    本发明涉及新一代三重靶向手性广谱抗微生物7-取代哌啶酮羧酸衍生物,以及它们的光学异构体、对映异构体或对映体,以及药学上可接受的盐、水合物、前药、多晶形和伪多晶形,以及它们的制备、组成和使用。
  • NEW GENERATION TRIPLE-TARGETING, CHIRAL, BROAD-SPECTRUM ANTIMICROBIAL 7-SUBSTITUTED PIPERIDINO-QUINOLONE CARBOXYLIC ACID DERIVATIVES, THEIR PREPARATION, COMPOSITIONS AND USE AS MEDICAMENTS
    申请人:Wockhardt Limited
    公开号:EP1453824A1
    公开(公告)日:2004-09-08
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