摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

methyl 4-(2-bromo-4-fluorophenyl)-6-methyl-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate | 1092952-99-2

中文名称
——
中文别名
——
英文名称
methyl 4-(2-bromo-4-fluorophenyl)-6-methyl-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate
英文别名
Methyl 4-(2-Bromo-4-fluorophenyl)-6-methyl-2-(2-thiazolyl)-1,4-dihydropyrimidine-5-carboxylate;methyl 4-(2-bromo-4-fluorophenyl)-6-methyl-2-(1,3-thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate
methyl 4-(2-bromo-4-fluorophenyl)-6-methyl-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate化学式
CAS
1092952-99-2
化学式
C16H13BrFN3O2S
mdl
——
分子量
410.267
InChiKey
LLYBOQJNOCWNPF-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:
    483.3±55.0 °C(Predicted)
  • 密度:
    1.63±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.1
  • 重原子数:
    24
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.19
  • 拓扑面积:
    91.8
  • 氢给体数:
    1
  • 氢受体数:
    6

反应信息

  • 作为反应物:
    描述:
    methyl 4-(2-bromo-4-fluorophenyl)-6-methyl-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate 在 Chiralpak IG 5 μm 20 mm * 250 mm 作用下, 以 甲醇二氧化碳 为溶剂, 生成 (R)-methyl 4-(2-bromo-4-fluorophenyl)-6-methyl-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate 、 (S)-methyl 4-(2-bromo-4-fluorophenyl)-6-methyl-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate
    参考文献:
    名称:
    [EN] HETEROARYLDIHYDROPYRIMIDINE DERIVATIVES AND METHODS OF TREATING HEPATITIS B INFECTIONS
    [FR] DÉRIVÉS D'HÉTÉROARYLDIHYDROPYRIMIDINE ET PROCÉDÉS DE TRAITEMENT D'INFECTIONS PAR LE VIRUS DE L'HÉPATITE B
    摘要:
    本文提供了用于治疗需要HBV感染的患者的化合物,其制药组合物以及抑制、抑制或预防患者HBV感染的方法。
    公开号:
    WO2020125729A1
  • 作为产物:
    参考文献:
    名称:
    [EN] HETEROARYLDIHYDROPYRIMIDINE DERIVATIVES AND METHODS OF TREATING HEPATITIS B INFECTIONS
    [FR] DÉRIVÉS D'HÉTÉROARYLDIHYDROPYRIMIDINE ET PROCÉDÉS DE TRAITEMENT D'INFECTIONS PAR LE VIRUS DE L'HÉPATITE B
    摘要:
    本文提供了用于治疗需要HBV感染的患者的化合物,其制药组合物以及抑制、抑制或预防患者HBV感染的方法。
    公开号:
    WO2020125729A1
点击查看最新优质反应信息

文献信息

  • [EN] COMBINATION OF HEPATITIS B VIRUS (HBV) VACCINES AND DIHYDROPYRIMIDINE DERIVATIVES AS CAPSID ASSEMBLY MODULATORS<br/>[FR] COMBINAISON DE VACCINS CONTRE LE VIRUS DE L'HÉPATITE B (VHB) ET DE DÉRIVÉS DE DIHYDROPYRIMIDINE EN TANT QUE MODULATEURS DE L'ASSEMBLAGE DES CAPSIDES
    申请人:JANSSEN SCIENCES IRELAND UNLIMITED CO
    公开号:WO2020255016A1
    公开(公告)日:2020-12-24
    Therapeutic combinations of hepatitis B virus (HBV) vaccines and capsid assembly modulators (CAMs), such as dihydropyrimidine derivatives are described. Methods of inducing an immune response against HBV or treating an HBV-induced disease, particularly in individuals having chronic HBV infection, using the disclosed therapeutic combinations are also described.
    描述了乙型肝炎病毒(HBV)疫苗与壳蛋白组装调节剂(CAMs)的治疗组合,例如二氢嘧啶生物。还描述了利用所述治疗组合诱导免疫应答抗击HBV或治疗HBV引起的疾病的方法,尤其是在患有慢性HBV感染的个体中。
  • DIHYDROPYRIMIDINE COMPOUNDS AND THEIR APPLICATION IN PHARMACEUTICALS
    申请人:SUNSHINE LAKE PHARMA CO., LTD.
    公开号:US20160206616A1
    公开(公告)日:2016-07-21
    Provided herein are dihydropyrimidine compounds and their pharmaceutical applications, especially for use in treating and preventing HBV diseases. Specifically, provided herein are compounds having Formula (I) or (Ia), or an enantiomer, a diastereoisomer, a tautomer, a hydrate, a solvate, or a pharmaceutically acceptable salt thereof, wherein the variables of the formulas are as defined in the specification. Also provided herein is the use of the compounds having Formula (I) or (Ia), or an enantiomer, a diastereoisomer, a tautomer, a hydrate, a solvate, or a pharmaceutically acceptable salt thereof for treating and preventing HBV diseases.
    本文提供二氢嘧啶化合物及其医药应用,特别是用于治疗和预防乙型肝炎疾病。具体而言,提供的化合物具有公式(I)或(Ia),或其对映异构体、顺反异构体、互变异构体、合物、溶剂化物或其药学上可接受的盐,其中公式中的变量如规范中所定义。此外,还提供了使用具有公式(I)或(Ia)或其对映异构体、顺反异构体、互变异构体、合物、溶剂化物或其药学上可接受的盐来治疗和预防乙型肝炎疾病的方法。
  • Discovery and Pre-Clinical Characterization of Third-Generation 4-H Heteroaryldihydropyrimidine (HAP) Analogues as Hepatitis B Virus (HBV) Capsid Inhibitors
    作者:Zongxing Qiu、Xianfeng Lin、Weixing Zhang、Mingwei Zhou、Lei Guo、Buelent Kocer、Guolong Wu、Zhisen Zhang、Haixia Liu、Houguang Shi、Buyu Kou、Taishan Hu、Yimin Hu、Mengwei Huang、S. Frank Yan、Zhiheng Xu、Zheng Zhou、Ning Qin、Yue Fen Wang、Shuang Ren、Hongxia Qiu、Yuxia Zhang、Yi Zhang、Xiaoyue Wu、Kai Sun、Sheng Zhong、Jianxun Xie、Giorgio Ottaviani、Yuan Zhou、Lina Zhu、Xiaojun Tian、Liping Shi、Fang Shen、Yi Mao、Xue Zhou、Lu Gao、John A. T. Young、Jim Zhen Wu、Guang Yang、Alexander V. Mayweg、Hong C. Shen、Guozhi Tang、Wei Zhu
    DOI:10.1021/acs.jmedchem.7b00083
    日期:2017.4.27
    Described herein are the discovery and structure activity relationship (SAR) studies of the third-generation 4-H heteroaryldihydropyrimidines (4-H HAPs) featuring the introduction of a C6 carboxyl group as novel HBV capsid inhibitors. This new series of 4-H HAPs showed improved anti-HBV activity and better drug-like properties compared to the first- and second-generation 4-H HAPs. X-ray crystallographic study of.analogue 12 (HAP_iR01) with Cp149 Y132A mutant hexamer clearly elucidated the role of C6 carboxyl group played for the increased binding affinity, which formed strong hydrogen' onding interactions with capsid protein and coordinated waters. The representative analogue 10 (HAP_R10) was extensively characterized in vitro (ADMET) and in vivo (mouse PK and PD) and subsequently selected for further devehipffientas oral anti-HBV infection agent.
  • HETEROARYLDIHYDROPYRIMIDINE DERIVATIVES AND METHODS OF TREATING HEPATITIS B INFECTIONS
    申请人:Janssen Phrmaceutica NV
    公开号:US20220048919A1
    公开(公告)日:2022-02-17
    Provided herein are compounds useful for the treatment of HBV infection in a subject in need thereof, pharmaceutical compositions thereof, and methods of inhibiting, suppressing, or preventing HBV infection in the subject.
  • US9498479B2
    申请人:——
    公开号:US9498479B2
    公开(公告)日:2016-11-22
查看更多