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2-甲基-2-丙基[(2R)-1-乙氧基-3-羟基-2-丙基]氨基甲酸酯 | 666718-81-6

中文名称
2-甲基-2-丙基[(2R)-1-乙氧基-3-羟基-2-丙基]氨基甲酸酯
中文别名
——
英文名称
(R)-tert-butyl 1-ethoxy-3-hydroxypropan-2-ylcarbamate
英文别名
tert-butyl N-[(2R)-1-ethoxy-3-hydroxypropan-2-yl]carbamate
2-甲基-2-丙基[(2R)-1-乙氧基-3-羟基-2-丙基]氨基甲酸酯化学式
CAS
666718-81-6
化学式
C10H21NO4
mdl
——
分子量
219.281
InChiKey
RAOQXIVLJZKEOR-MRVPVSSYSA-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):
    0.5
  • 重原子数:
    15
  • 可旋转键数:
    7
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.9
  • 拓扑面积:
    67.8
  • 氢给体数:
    2
  • 氢受体数:
    4

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
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • 6- (Heterocyclyl-substituted Benzyl) -4-Oxoquinoline Compound and Use Thereof as HIV Integrase Inhibitor
    申请人:SATOH Motohide
    公开号:US20080207618A1
    公开(公告)日:2008-08-28
    The present invention relates to a compound represented by the following formula [I] wherein each symbol is as defined in the specification, or a pharmaceutically acceptable salt thereof, or a solvate thereof, and a pharmaceutical composition, an anti-HIV agent and an HIV integrase inhibitor containing such compound. The compound of the present invention has an HIV integrase inhibitory activity, and is useful as an anti-HIV agent, or as an agent for the prophylaxis or treatment of AIDS. In addition, by the combined use with other anti-HIV agents such as a protease inhibitor, a reverse transcriptase inhibitor and the like, it can be a more effective anti-HIV agent. Because it shows integrase-specific high inhibitory activity, the compound can be a pharmaceutical agent safe on human body, which causes only a fewer side effects.
    本发明涉及以下式[I]所表示的化合物,其中每个符号如规范中所定义,或其药学上可接受的盐,或其溶剂合物,以及含有此类化合物的药物组合物,抗HIV药物和HIV整合酶抑制剂。本发明的化合物具有HIV整合酶抑制活性,并可用作抗HIV药物,或用作艾滋病的预防或治疗药物。此外,通过与其他抗HIV药物(如蛋白酶抑制剂、逆转录酶抑制剂等)的联合使用,可以使其成为更有效的抗HIV药物。由于它显示出整合酶特异性的高抑制活性,该化合物可以成为对人体安全的药物,仅引起较少的副作用。
  • FUSED HETEROAROMATIC PYRROLIDINONES AS SYK INHIBITORS
    申请人:Arikawa Yasuyoshi
    公开号:US20130116260A1
    公开(公告)日:2013-05-09
    Disclosed are compounds of Formula 1, and pharmaceutically acceptable salts thereof, wherein G, L 1 , L 2 , R 1 , R 2 , R 3 , and R 4 are defined in the specification. This disclosure also relates to materials and methods for preparing compounds of Formula 1, pharmaceutical compositions containing them, and their use for treating disorders, diseases, and conditions involving the immune system and inflammation, including rheumatoid arthritis, hematological malignancies, epithelial cancers (i.e., carcinomas), and other disorders, diseases, and conditions for which inhibition of SYK is indicated.
    本发明涉及式1的化合物及其药学上可接受的盐,其中G、L1、L2、R1、R2、R3和R4如规范中所定义。本公开还涉及制备式1化合物的材料和方法,包含它们的药物组合物,以及它们用于治疗涉及免疫系统和炎症的疾病、疾患和病况,包括类风湿性关节炎、血液恶性肿瘤、上皮癌(即癌症)和其他需要抑制SYK的疾病、疾患和病况。
  • Fused heteroaromatic pyrrolidinones
    申请人:Arikawa Yasuyoshi
    公开号:US08440689B2
    公开(公告)日:2013-05-14
    Disclosed are compounds of Formula 1, and pharmaceutically acceptable salts thereof, wherein G, L1, L2, R1, R2, R3, and R4 are defined in the specification. This disclosure also relates to materials and methods for preparing compounds of Formula 1, pharmaceutical compositions containing them, and their use for treating disorders, diseases, and conditions involving the immune system and inflammation, including rheumatoid arthritis, hematological malignancies, epithelial cancers (i.e., carcinomas), and other disorders, diseases, and conditions for which inhibition of SYK is indicated.
    本发明涉及一种公式1的化合物及其药学上可接受的盐,其中G、L1、L2、R1、R2、R3和R4在规范中定义。本公开还涉及制备公式1化合物的材料和方法、含有它们的制药组合物,以及它们用于治疗涉及免疫系统和炎症的疾病、疾病和病况,包括类风湿性关节炎、血液恶性肿瘤、上皮癌(即癌症)和其他需要抑制SYK的疾病、疾病和病况。
  • Fused heteroaromatic pyrrolidinones as SYK inhibitors
    申请人:Arikawa Yasuyoshi
    公开号:US09181255B2
    公开(公告)日:2015-11-10
    Disclosed are compounds of Formula 1, and pharmaceutically acceptable salts thereof, wherein G, L1, L2, R1, R2, R3, and R4 are defined in the specification. This disclosure also relates to materials and methods for preparing compounds of Formula 1, pharmaceutical compositions containing them, and their use for treating disorders, diseases, and conditions involving the immune system and inflammation, including rheumatoid arthritis, hematological malignancies, epithelial cancers (i.e., carcinomas), and other disorders, diseases, and conditions for which inhibition of SYK is indicated.
    本发明涉及公式1的化合物及其药学上可接受的盐,其中G、L1、L2、R1、R2、R3和R4在规范中定义。本公开还涉及制备公式1化合物的材料和方法、含有它们的药物组合物以及它们用于治疗涉及免疫系统和炎症的疾病、疾病和状况,包括类风湿性关节炎、血液恶性肿瘤、上皮癌(即癌瘤)和其他需要抑制SYK的疾病、疾病和状况。
  • PROCESS FOR THE PREPARATION OF FUSED HETEROAROMATIC PYRROLIDINONES
    申请人:Takeda Pharmaceutical Company Limited
    公开号:EP3489236A1
    公开(公告)日:2019-05-29
    Disclosed are compounds of Formula 1, and pharmaceutically acceptable salts thereof, wherein G, L1, L2, R1, R2, R3, and R4 are defined in the specification. This disclosure also relates to materials and methods for preparing compounds of Formula 1, pharmaceutical compositions containing them, and their use for treating disorders, diseases, and conditions involving the immune system and inflammation, including rheumatoid arthritis, hematological malignancies, epithelial cancers (i.e., carcinomas), and other disorders, diseases, and conditions for which inhibition of SYK is indicated.
    公开了式 1 的化合物、 及其药学上可接受的盐类,其中 G、L1、L2、R1、R2、R3 和 R4 的定义见说明书。本公开还涉及制备式 1 化合物的材料和方法、含有它们的药物组合物,以及它们在治疗涉及免疫系统和炎症的紊乱、疾病和病症方面的用途,包括类风湿性关节炎、血液恶性肿瘤、上皮癌(即癌),以及其它需要抑制 SYK 的紊乱、疾病和病症。
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