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18F-labelled 5-fluorouracil | 823-63-2

中文名称
——
中文别名
——
英文名称
18F-labelled 5-fluorouracil
英文别名
5-(fluoro-18F)pyrimidine-2,4(1H,3H)-dione;5-(18F)fluoranyl-1H-pyrimidine-2,4-dione
<sup>18</sup>F-labelled 5-fluorouracil化学式
CAS
823-63-2
化学式
C4H3FN2O2
mdl
——
分子量
129.08
InChiKey
GHASVSINZRGABV-SFIIULIVSA-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

  • 熔点:
    281-283 °C

计算性质

  • 辛醇/水分配系数(LogP):
    -0.9
  • 重原子数:
    9
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    58.2
  • 氢给体数:
    2
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    盐酸 作用下, 以 为溶剂, 反应 0.03h, 生成 18F-labelled 5-fluorouracil
    参考文献:
    名称:
    通过金属转移反应,可以从[18F]氟化物合成用于人类PET成像的[18F] 5-氟尿嘧啶。
    摘要:
    Translation of new F-18-fluorination reactions to produce radiotracers for human positron emission tomography (PET) imaging is rare because the chemistry must have useful scope and the process for F-18-labeled tracer production must be robust and simple to execute. The application of transition metal mediators has enabled impactful F-18-fluorination methods, but to date none of these reactions have been applied to produce a human-injectable PET tracer. In this article we present chemistry and process innovations that culminate in the first production from [F-18]fluoride of human doses of [F-18]5-fluorouracil, a PET tracer for cancer imaging in humans. The first preparation of nickel 6-aryl complexes by transmetalation from arylboronic acids or esters was developed and enabled the synthesis of the [F-18]5-fluorouracil precursor. Routine production of >10 mCi doses of [F-18]5-fluorouracil was accomplished with a new instrument for azeotrope-free [F-18]fluoride concentration in a process that leverages the tolerance of water in nickel-mediated F-18-fluorination.
    DOI:
    10.1021/acs.organomet.6b00059
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文献信息

  • [EN] SOLID-PHASE FLUORINATION OF URACIL AND CYTOSINE<br/>[FR] FLUORATION EN PHASE SOLIDE D'URACILE ET DE CYTOSINE
    申请人:HAMMERSMITH IMANET LTD
    公开号:WO2004056400A1
    公开(公告)日:2004-07-08
    The invention relates to a process for the production of an 18F-labelled tracer which comprises treatment of a solid support-bound precursor of formula (I): SOLID SUPPORT-LINKER-I+ -TRACER (I) Y- wherein the TRACER is of formula (A): or an amine protected derivative thereof, wherein Y- is an anion, preferably trifluoromethylsulphonate (triflate) anion; and R1 is either (i) a group CH-NP1AP2A in which P1A and P2A are each independently hydrogen or a protecting group, or (ii) a carbonyl group; with 18F- to produce the labelled tracer of formula (II) or an amine protected derivative thereof, wherein R1 is as defined for the compound of formula (I).
    本发明涉及一种制备18F标记示踪剂的方法,其中包括对式(I)的固体支持前体进行处理:SOLID SUPPORT-LINKER-I+ -TRACER (I) Y-,其中TRACER的式(A)为:或其氨基保护衍生物,其中Y-是阴离子,优选为三氟甲磺酸盐(三氟甲磺酸盐)阴离子;R1要么是(i)CH-NP1AP2A基团,其中P1A和P2A各自独立地是氢或保护基,要么是(ii)羰基基团;用18F-处理,以产生式(II)的标记示踪剂或其氨基保护衍生物,其中R1如式(I)化合物中所定义。
  • New syntheses of fluoro-compounds by fluorination in water
    作者:Mirko Diksic、Pasquale Di Raddo
    DOI:10.1016/s0040-4039(01)91250-x
    日期:1984.1
  • Brown; Brady; Roberts, Journal of labelled compounds and radiopharmaceuticals, 1999, vol. 42, # SUPPL. 1, p. S533-S535
    作者:Brown、Brady、Roberts、Osman、Luthra、Price
    DOI:——
    日期:——
  • VINE E. N.; YOUNG D.; VINE W. H.; WOLF W., INT. J. APPL. RADIAT. AND ISOTOP., 1979, 30, NO 7, 401-405
    作者:VINE E. N.、 YOUNG D.、 VINE W. H.、 WOLF W.
    DOI:——
    日期:——
  • OBERDORFER, FRANZ;HOFMANN, EVELYN;MAIER-BORST, WOLFGANG, J. LABELL. COMPOUNDS AND RADIOPHARM., 27,(1989) N, C. 137-145
    作者:OBERDORFER, FRANZ、HOFMANN, EVELYN、MAIER-BORST, WOLFGANG
    DOI:——
    日期:——
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