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4-amino-6-methyl-1-β-D-ribofuranosylpyrazolo<3,4-d>pyrimidine | 90414-42-9

中文名称
——
中文别名
——
英文名称
4-amino-6-methyl-1-β-D-ribofuranosylpyrazolo<3,4-d>pyrimidine
英文别名
4-amino-6-methyl-1-β-D-ribofuranosylpyrazolo[3,4-d]pyrimidine;4-Amino-6-methyl-1-beta-d-ribofuranosylpyrazolo[3,4-d]pyrimidine;(2R,3R,4S,5R)-2-(4-amino-6-methylpyrazolo[3,4-d]pyrimidin-1-yl)-5-(hydroxymethyl)oxolane-3,4-diol
4-amino-6-methyl-1-β-D-ribofuranosylpyrazolo<3,4-d>pyrimidine化学式
CAS
90414-42-9
化学式
C11H15N5O4
mdl
——
分子量
281.271
InChiKey
BCYCXVUXJLRUKT-KCGFPETGSA-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):
    -1.4
  • 重原子数:
    20
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.55
  • 拓扑面积:
    140
  • 氢给体数:
    4
  • 氢受体数:
    8

反应信息

  • 作为产物:
    参考文献:
    名称:
    某些吡唑并[3,4-d]嘧啶-4(5H)-硒代核苷及相关化合物的合成及抗病毒/抗肿瘤活性。
    摘要:
    几种吡唑并[3,4-d]嘧啶-4(5H)-硒代核糖核苷被制备为潜在的抗寄生虫剂。用硒基脲处理4-氯-1-(2,3,5-三-O-乙酰基-β-D-呋喃呋喃糖基)吡唑并[3,4-d]嘧啶(5a),然后脱乙酰化,得到1-β-D -核呋喃糖基吡唑并[3,4-d]嘧啶-4(5H)-硒酮(6a)。用硒脲对3-溴-4-氯-1-(2,3,5-三-O-苯甲酰基-β-D-呋喃呋喃糖基)吡唑并[3,4-d]嘧啶(5b)进行类似处理脱苯甲酰化,得到6a(6b)的3-溴衍生物。氨基甲酸酯化的4-氯-6-甲基-吡唑并[3,4-d]嘧啶(7)与四-O-乙酰基呋喃核糖的糖基化作用提供了关键的中间体4-氯-6-甲基-1-(2,3) ,5-(3-三-O-乙酰基-β-D-呋喃呋喃糖基)吡唑并[3,4-d]嘧啶(9)。进行9的氨解反应得到4-氨基-6-甲基-1-β-D-呋喃呋喃糖基吡唑并[3,4-d]嘧啶(10),而用氢氧化钠处理
    DOI:
    10.1021/jm00374a015
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文献信息

  • [EN] PYRROLOPYRIMIDINE NUCLEOSIDES AND ANALOGS THEREOF USEFUL AS ANTIVIRAL AGENTS<br/>[FR] NUCLÉOSIDES DE PYRROLOPYRIMIDINE ET ANALOGUES DE CEUX-CI UTILES EN TANT QU'AGENTS ANTIVIRAUX
    申请人:CHIMERIX INC
    公开号:WO2017024310A1
    公开(公告)日:2017-02-09
    The present disclosure provides pyrrolopyrimidine nucleoside analogs of the Formula I, Formula IA, Formula IB, or Formula II and phospholipid conjugates and pharmaceutical compositions thereof wherein Rc and A are defined herein. Also presented are methods of treating and/or preventing viral infection and/or viral infection-associated disease or disorder with one or more compounds of Formula I, Formula IA, Formula IB, or Formula II.
    本公开提供式I、式IA、式IB或式II的吡咯嘧啶嘧啶核苷类似物以及磷脂共轭物和制药组合物,其中Rc和A的定义如本文所述。还提供使用一种或多种式I、式IA、式IB或式II的化合物治疗和/或预防病毒感染和/或与病毒感染相关的疾病或障碍的方法。
  • Pyrrolopyrimidine nucleosides and analogs thereof
    申请人:Chimerix, Inc.
    公开号:US10407457B2
    公开(公告)日:2019-09-10
    The present disclosure provides pyrrolopyrimidine nucleoside analogs of the Formula I, Formula IA, Formula IB, or Formula II and phospholipid conjugates and pharmaceutical compositions thereof wherein Rc and A are defined herein. Also presented are methods of treating and/or preventing viral infection and/or viral infection-associated disease or disorder with one or more compounds of Formula I, Formula IA, Formula IB, or Formula II.
    本公开提供了式I、式IA、式IB或式II的吡咯嘧啶核苷类似物及其磷脂共轭物和药物组合物,其中Rc和A在本文中定义。还提出了用一种或多种式I、式IA、式IB或式II化合物治疗和/或预防病毒感染和/或病毒感染相关疾病或紊乱的方法。
  • PYRROLOPYRIMIDINE NUCLEOSIDES AND ANALOGS THEREOF
    申请人:Chimerix, Inc.
    公开号:US20170044202A1
    公开(公告)日:2017-02-16
    The present disclosure provides pyrrolopyrimidine nucleoside analogs of the Formula I, Formula IA, Formula IB, or Formula II and phospholipid conjugates and pharmaceutical compositions thereof wherein It c and A are defined herein. Also presented are methods of treating and/or preventing viral infection and/or viral infection-associated disease or disorder with one or more compounds of Formula I, Formula IA, Formula IB, or Formula II.
  • US9701706B2
    申请人:——
    公开号:US9701706B2
    公开(公告)日:2017-07-11
  • US9708359B2
    申请人:——
    公开号:US9708359B2
    公开(公告)日:2017-07-18
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同类化合物

硫代嘌呤醇核糖核苷 硝基苄基硫代间型霉素 别嘌呤醇核糖苷 [3,4-二乙酰氧基-5-(5-甲硫基-2,4,8,9-四氮杂双环[4.3.0]壬-2,4,7,10-四烯-9-基)四氢呋喃-2-基]甲基乙酸酯 6-氮杂卡德勾霉素 6-氨基别嘌呤醇核糖甙 4-氨基-3-苄基-1H-吡唑并[3,4-d]嘧啶-1-β-D-呋喃核糖 1 beta-呋喃核糖基-4-(甲硫基)吡唑并(3,4-d)嘧啶 1-β-D-ribofuranosylpyrazolo<3,4-d>pyrimidine-4-sulfenamide 4-amino-3-(3''-hydroxy-1''-propynyl)-1-(2',3',5'-tri-O-benzoyl-β-D-ribofuranosyl)-1H-pyrazolo[3,4-d]pyrimidine 1-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)pyrazolo<3,4-d>pyrimidine-4-carbonitrile 1-(2',3',5'-Tri-O-acetyl-β-D-ribofuranosyl)-3-cyano-4-methylmercaptopyrazolo<3,4-d>pyrimidine Acetic acid (2R,3R,4R,5R)-4-acetoxy-5-acetoxymethyl-2-(4-methanesulfonyl-pyrazolo[3,4-d]pyrimidin-1-yl)-tetrahydro-furan-3-yl ester 8-aza-7-deaza-7-[(5,7-di-tert-butylbenzoxazol-2-yl)ethynyl]adenosine (2R,3R,4S,5R)-2-{4-[(E)-3-(2,4-Dichloro-phenyl)-allylsulfanyl]-pyrazolo[3,4-d]pyrimidin-1-yl}-5-hydroxymethyl-tetrahydro-furan-3,4-diol 3-(methylthio)-1-β-D-ribofuranosylpyrazolo<3,4-d>pyrimidin-4(5H)-one 3-chloro-1-(β-D-ribofuranosyl)-1H-pyrazolo[3,4-d]pyrimidine-4,6-diamine 1-(2,3,4,6-Tetra-O-benzyl-β-D-glucopyranosyl)-1,5-dihydro-4H-pyrazolo-<3,4-d>pyrimidin-4-on (2R,3R,4S,5R)-2-{4-[(E)-3-(3,4-Dichloro-phenyl)-allylsulfanyl]-pyrazolo[3,4-d]pyrimidin-1-yl}-5-hydroxymethyl-tetrahydro-furan-3,4-diol 1-(2,3,4,6-Tetra-O-benzyl-β-D-glucopyranosyl)-1H-pyrazolo<3,4-d>pyrimidin-4-amin (2S,3R,4S,5R)-2-(4-amino-3-phenylpyrazolo[3,4-d]pyrimidin-1-yl)-5-hydroxymethyltetrahydrofuran-3,4-diol 1-(β-D-arabinofuranosyl)-1H-pyrazolo<3.4-d>pyrimidin-4-one 1-(2,3,5-tri-O-benzyl-β-D-arabinofuranosyl)-1H-pyrazolo<3.4-d>pyrimidin-4-one (2R,3R,4S,5R)-2-(4-Dihexylamino-pyrazolo[3,4-d]pyrimidin-1-yl)-5-hydroxymethyl-tetrahydro-furan-3,4-diol 4-(butylamino)-1-β-D-ribofuranosyl-1H-pyrazolo<3,4-d>pyrimidine 6-O-ethylinosine 1-(β-D-Ribofuranosyl)-3-carbamoyl-4,6-dimethylmercaptopyrazolo<3,4-d>pyrimidine 1-N-ethylinosine 6-amino-3-methyl-1-β-D-ribofuranosylpyrazolo<3,4-d>pyrimidin-4(5H)-one 1-(2',3',5'-tri-O-acetyl-β-D-ribofuranosyl)-3-thiocarbamoyl-4,6-dimethylmercaptopyrazolo<3,4-d>pyrimidine 1-(β-D-Ribofuranosyl)-4-amino-6-methylmercapto-3-carbamoylpyrazolo<3,4-d>pyrimidine 1-(β-D-Ribofuranosyl)-3-carbamoyl-4-amino-6-methylsulfonylpyrazolo<3,4-d>pyrimidine 6-Methylthio-4(5H)-oxo-1-β-D-ribofuranosylpyrazolo<3,4-d>pyrimidine 4,6-Dimethylthio-1-α-(2,3,5-tri-O-acetyl-D-xylofuranosyl)pyrazolo<3,4-d>pyrimidine 1-(β-D-Ribofuranosyl)-3-carbamoyl-4,6-diaminopyrazolo<3,4-d>pyrimidine 6-amino-4-methoxy-1-α-D-arabinofuranosylpyrazolo<3,4-d>pyrimidine 6-Methylthio-4(5H)-oxo-1-α-D-xylofuranosylpyrazolo<3,4-d>pyrimidine 6-Amino-4(5H)-oxo-1-α-D-xylofuranosylpyrazolo<3,4-d>pyrimidine N-<(6-amino-1-β-D-ribofuranosyl-4,5-dihydro-4-oxopyrazolo<3,4-d>pyrimidin-3-yl)carbonyl>glycine amide 4,6-Dimethylthio-1-α-D-xylofuranosylpyrazolo<3,4-d>pyrimidine 4,6-dimethylthio-1-α-D-arabinofuranosylpyrazolo<3,4-d>pyrimidine 4-methoxy-6-methylsulphonyl-1-α-(2,3,5-tri-O-acetyl-D-arabinofuranosyl)pyrazolo<3,4-d>pyrimidine 4-amino-6-methylthio-1-α-D-arabinofuranosylpyrazolo<3,4-d>pyrimidine 4-amino-6-methylsulphonyl-1-α-D-arabinofuranosylpyrazolo<3,4-d>pyrimidine 4-acetamido-6-methylsulphonyl-1-α-(2,3,5-tri-O-acetyl-D-arabinofuranosyl)pyrazolo<3,4-d>pyrimidine 4-amino-6-methoxy-1-α-D-arabinofuranosylpyrazolo<3,4-d>pyrimidine 4.6-Diamino-1-β-ribofuranosyl-1H-pyrazolo<3.4-d>pyrimidin 1-(N-Methyl-β-D-ribofuranuronamidosyl)-1H-pyrazolo<3,4-d>pyrimidin-4-amin 4-methoxy-6-methylthio-1-α-(2,3,5-tri-O-acetyl-D-arabinofuranosyl)pyrazolo<3,4-d>pyrimidine 1-β-D-ribofuranosyl-4(5H)-thioxopyrazolo<3,4-d>pyrimidine-3-carbonitrile