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methyl 3,3,3-trifluoro-2-(3-methyl-5-oxo-1-phenyl-4,5-dihydro-1Н-pyrazol-4-ylidene)propanoate | 312517-66-1

中文名称
——
中文别名
——
英文名称
methyl 3,3,3-trifluoro-2-(3-methyl-5-oxo-1-phenyl-4,5-dihydro-1Н-pyrazol-4-ylidene)propanoate
英文别名
methyl 3,3,3-trifluoro-2-(3-methyl-5-oxo-1-phenyl-1,5-dihydro-4H-pyrazol-4-ylidene)propanoate;methyl 3,3,3-trifluoro-2-(3-methyl-5-oxo-1-phenyl-1,5-dihydro-4H-pyrazol-4-ylidene)propionate;(Z)-4-(1-methoxycarbonyl-2,2,2-trifluoroethylidene)-1-phenyl-3-methylpyrazol-5-one;2-(1,5-dihydro-3-methyl-5-oxo-1-phenyl-4H-pyrazol-4-ylidene)-3,3,3-trifluoro-propanoic acid methyl ester;Methyl 3,3,3-trifluoro-2-(3-methyl-5-oxo-1-phenyl-1h-pyrazol-4(5h)ylidene)propionate;methyl 3,3,3-trifluoro-2-(3-methyl-5-oxo-1-phenylpyrazol-4-ylidene)propanoate
methyl 3,3,3-trifluoro-2-(3-methyl-5-oxo-1-phenyl-4,5-dihydro-1Н-pyrazol-4-ylidene)propanoate化学式
CAS
312517-66-1
化学式
C14H11F3N2O3
mdl
MFCD01571388
分子量
312.248
InChiKey
UOFNXKCTHAQBME-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:
    374.6±52.0 °C(Predicted)
  • 密度:
    1.35±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.3
  • 重原子数:
    22
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.21
  • 拓扑面积:
    59
  • 氢给体数:
    0
  • 氢受体数:
    7

反应信息

点击查看最新优质反应信息

文献信息

  • Modification of biologically active amides and amines with fluorine-containing heterocycles 6. Methyl 3,3,3-trifluoro-2-(3-methyl-5-oxo-1-phenyl-1,5-dihydro-4H-pyrazol-4-ylidene)propionate in cyclocondensation with 1,3-binucleophiles
    作者:V. B. Sokolov、A. Yu. Aksinenko
    DOI:10.1007/s11172-012-0272-6
    日期:2012.10
    A reaction of methyl 3,3,3-trifluoro-2-(3-methyl-5-oxo-1-phenyl-1,5-dihydro-4H-pyrazol-4-ylidene)propionate with 1,3-binucleophiles (N-benzylurea, N-substituted 3-aminocrotonates, N-substituted 3-aminocyclohexenones, and 6-aminouracyls), leading to the formation of fluorine-containing heterocyclic 3-methyl-1-phenylpyrazol-5-one derivatives, was studied.
    3,3,3-三氟-2-(3-甲基-5-氧代-1-苯基-1,5-二氢-4H-吡唑-4-亚基)丙酸甲酯与1,3-双亲核试剂(N -苄基脲、N-取代的3-氨基巴豆酸酯、N-取代的3-氨基环己烯酮和6-氨基尿酰基),导致形成含氟研究了杂环3-甲基-1-苯基吡唑-5-酮衍生物。
  • Indoledione derivative
    申请人:MSD K.K.
    公开号:US08106086B2
    公开(公告)日:2012-01-31
    A compound represented by the general formula (I-a): [wherein R1a and R2a each means hydrogen, lower cycloalkyl, lower alkyl, etc.; R3a means hydrogen, lower cycloalkyl, lower alkyl, etc.; R4a and R5a each means lower alkyl, lower cycloalkyl, etc. or R4a and R5a are bonded to each other to form lower cycloalkylidene; and R6a means lower alkyl, lower haloalkyl, etc.]. This compound functions as an LCE inhibitor and is useful as a therapeutic agent for various circulatory diseases, nervous diseases, metabolic diseases, reproductive diseases, digestive tract diseases, neoplasm, infectious diseases, etc.
    化合物的一般式为(I-a):[其中R1a和R2a各表示氢,较低的环烷基,较低的烷基等;R3a表示氢,较低的环烷基,较低的烷基等;R4a和R5a各表示较低的烷基,较低的环烷基等,或R4a和R5a相互连接形成较低的环烷基亚基;R6a表示较低的烷基,较低的卤代烷基等]。该化合物作为LCE抑制剂,可用作各种循环系统疾病、神经系统疾病、代谢性疾病、生殖系统疾病、消化道疾病、肿瘤、感染性疾病等的治疗剂。
  • Fluoro-containing 4-ethylidene-2,4-dihydropyrazol-3-ones in the Diels-Alder reaction with cyclopentadiene and cyanamines
    作者:V. B. Sokolov、A. Yu. Aksinenko、T. A. Epishina、T. V. Goreva
    DOI:10.1134/s1070363212100155
    日期:2012.10
    The fluorinated 4-ethylidene-2,4-dihydropyrazol-3-ones act as heterodienes and dienophiles in the Diels-Alder reaction with amines and cyclopentadiene to give 1,4-dihydropyrazolo[4,3-e]-1,3-oxazines and spirobicyclo[2.2.1]hept-5-ene-2,4'-pyrazolones, respectively.
  • INDOLEDIONE DERIVATIVE
    申请人:MSD K.K.
    公开号:EP2145884B1
    公开(公告)日:2014-08-06
  • Reactions of highly electrophilic polyfluoro unsaturated compounds with pyrazole derivatives
    作者:A. S. Golubev、V. Yu. Tyutin、N. D. Chkanikov、A. F. Kolomiets、A. V. Fokin
    DOI:10.1007/bf00863375
    日期:1992.11
    Pyrazole derivatives were hydroxyalkylated at the C4 atom by hexafluoroacetate and methyl trifluoropyruvate. The products of the hydroxyalkylation were dehydrated to the corresponding alkylidene derivatives which were reacted with nucleophiles. Dicyanoethylenes, obtained from polyfluorocarbonyl compounds, alkylated pyrazol-5-ones with the formation of pyrazolopyran derivatives.
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