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2-脱氧-alpha-d-核糖1-磷酸二(环己基胺)

中文名称
2-脱氧-alpha-d-核糖1-磷酸二(环己基胺)
中文别名
——
英文名称
bis(cyclohexylamine) 2-deoxy-α-D-ribosyl-1-phosphate
英文别名
α-D-2′-deoxyribofuranose-1-O-phosphate bis(cyclohexylammonium) salt;O1-phosphono-α-D-erythro-2-deoxy-pentofuranose; compound with cyclohexylamine;O1-Phosphono-α-D-erythro-2-desoxy-pentofuranose; Verbindung mit Cyclohexylamin;2-deoxy-α-D-ribose 1-phosphate bis(cyclohexylamine) salt;2'-deoxyribose 1-phosphate di(monocyclohexylammonium) salt;cyclohexanamine;[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl] dihydrogen phosphate
2-脱氧-alpha-d-核糖1-磷酸二(环己基胺)化学式
CAS
——
化学式
C5H11O7P*2C6H13N
mdl
——
分子量
412.464
InChiKey
PJYWCLQUAQQXBV-KYWOWLQSSA-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):
    -0.16
  • 重原子数:
    20.0
  • 可旋转键数:
    3.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    142.47
  • 氢给体数:
    5.0
  • 氢受体数:
    6.0

反应信息

  • 作为反应物:
    描述:
    2-脱氧-alpha-d-核糖1-磷酸二(环己基胺) 在 Dowex-50 Na+ 作用下, 以 为溶剂, 反应 0.5h, 以96%的产率得到α-D-2′-deoxyribofuranose-1-O-phosphate disodium salt
    参考文献:
    名称:
    酶法合成2-脱氧核糖1-磷酸和核糖1磷酸及随后的核苷制备
    摘要:
    我们提供了一种从7-Me-Guo和7-Me-dGuo制备Rib-p和dRib-p的新型酶促方法。在存在PNP的情况下,7-Me-Guo和7-Me-dGuo的几乎不可逆的磷酸分解可确保起始核苷定量转化为异构纯α-Rib-p和α-dRib-p。分离和纯化后,Rib-p和dRib-p的收率为74–96%。
    DOI:
    10.1002/ejoc.201901454
  • 作为产物:
    描述:
    bis(cyclohexylamine) 3',5'-O-bis(4-chlorobenzoyl)-2-deoxy-α-D-ribosyl-1-phosphate 在 环己胺 作用下, 以 甲醇 为溶剂, 反应 72.0h, 以85%的产率得到2-脱氧-alpha-d-核糖1-磷酸二(环己基胺)
    参考文献:
    名称:
    First Stereoselective Synthesis of 2-Deoxy-α-d-ribosyl-1-phosphate:  Novel Application of Crystallization-Induced Asymmetric Transformation
    摘要:
    A first stereoselective synthesis of bis(cyclohexylamine) 2-deoxy-alpha-D-ribosyl-1-phosphate has been achieved. The synthesis features a key crystallization-induced asymmetric transformation (AT) to generate a desired alpha-anomer in 99% yield at a 98.8:1.2 ratio of alpha/beta.
    DOI:
    10.1021/jo025793h
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文献信息

  • Method for producing a pyrimidine nucleoside compound and a new pyrimidine nucleoside compound
    申请人:Araki Tadashi
    公开号:US20050074857A1
    公开(公告)日:2005-04-07
    A method for producing a pyrimidine nucleoside compound includes reacting a sugar phosphate and pyrimidine base derivative using an enzyme having cytosine nucleoside phosphorylase activity, the pyrimidine base derivative being represented by general formula (I): (wherein R1 represents an amino group that may be replaced with an acyl group having an alkyl group of 1 to 3 carbon atoms or an alkyl group of 1 to 3 carbon atoms, an alkyl group of 1 to 3 carbon atoms, or a thiol group; R2 represents an amino group, a thiol group, a hydroxyl group, or a hydrogen atom; R3 represents an alkyl group of 1 to 3 carbon atoms that may be replaced with a hydroxyl group, an amino group, or a hydrogen atom; R4 represents a hydroxyl group or a hydrogen atom; when R1 is an amino group, when R2 is a hydroxyl group, and when R4 is a hydrogen atom; R3 is neither an alkyl group of 1 to 3 carbon atoms nor a hydrogen atom).
    生产嘧啶核苷化合物的方法包括使用具有胞嘧啶核苷化酶活性的酶,通过反应糖磷酸嘧啶碱基衍生物来实现,其中嘧啶碱基衍生物由通用式(I)表示:(其中R1代表一个基,可以被具有1至3个碳原子的烷基或1至3个碳原子的烷基,1至3个碳原子的烷基或醇基替代;R2代表一个基,醇基,羟基或氢原子;R3代表1至3个碳原子的烷基,可以被羟基,基或氢原子替代;R4代表羟基或氢原子;当R1是基时,当R2是羟基时,当R4是氢原子时;R3既不是1至3个碳原子的烷基也不是氢原子)。
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