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N-methylmorpholinium 5-cyano-4-(4-methoxyphenyl)-2-oxo-1,2,3,4-tetrahydropyridine-6-thiolate

中文名称
——
中文别名
——
英文名称
N-methylmorpholinium 5-cyano-4-(4-methoxyphenyl)-2-oxo-1,2,3,4-tetrahydropyridine-6-thiolate
英文别名
N-methylmorpholinium 5-cyano-4-(4-methoxyphenyl)-2-oxo-1,2,3,4-tetrahydro-6-pyridinethiolate;4-(4-methoxyphenyl)-2-oxo-6-sulfanyl-3,4-dihydro-1H-pyridine-5-carbonitrile;4-methylmorpholine
N-methylmorpholinium 5-cyano-4-(4-methoxyphenyl)-2-oxo-1,2,3,4-tetrahydropyridine-6-thiolate化学式
CAS
——
化学式
C5H11NO*C13H12N2O2S
mdl
——
分子量
361.465
InChiKey
ASNHXMMNMKNOCG-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

计算性质

  • 辛醇/水分配系数(LogP):
    1.91
  • 重原子数:
    25
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.44
  • 拓扑面积:
    75.6
  • 氢给体数:
    2
  • 氢受体数:
    6

反应信息

  • 作为反应物:
    描述:
    N-(4-氯苯基)-2-氯乙酰胺N-methylmorpholinium 5-cyano-4-(4-methoxyphenyl)-2-oxo-1,2,3,4-tetrahydropyridine-6-thiolate乙醇 为溶剂, 以79%的产率得到(4-chlorophenyl)carbamoylmethylthio-5-cyano-4-(4-methoxyphenyl)-1,2,3,4-tetrahydro-2-pyridinone
    参考文献:
    名称:
    摘要:
    DOI:
    10.1023/a:1002750402772
  • 作为产物:
    参考文献:
    名称:
    Design and Synthesis of Pyrido[2,1-b][1,3,5]thiadiazine Library via Uncatalyzed Mannich-Type Reaction
    摘要:
    This Research Article describes the synthesis of an over 700-member library of (8R/8S)-3-R-8-aryl-6-oxo-3,4,7,8-tetrahydro-2H,6H-pyrido[2,1-b][1,3,5]thiadiazin-9-carbonitriles by uncatalyzed Mannich-type reaction of N-methylmorpholinium (4R/4S)-4-aryl-3-cyano-6-oxo-1,4,5,6-tetrahydropyridin-2-thiolates with a set of primary amines and excessive HCHO. The scope and limitations of the reaction were studied. Starting thiolates were obtained in yields of 53-82% by multicomponent reaction of aromatic aldehydes, cyanothioacetamide, 2,2-dimethyl-1,3-dioxane-4,6-dione (Meldrum's acid), and N-methylmorpholine, followed by heterocyclization of the resulting Michael adducts.
    DOI:
    10.1021/co5000807
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文献信息

  • Synthesis of thiazolo[3,2-<i>a</i>]pyridines via an unusual Mannich-type cyclization
    作者:Victor V. Dotsenko、Ivan S. Bushmarinov、Alexander S. Goloveshkin、Elena A. Chigorina、Konstantin A. Frolov、Sergey G. Krivokolysko
    DOI:10.1080/10426507.2016.1224877
    日期:2017.1.2
    with 3-(1,3-benzodioxol-5-yl)-2-methylpropanal (ocean propanal) and p-toluidine afforded 7-aryl-2-(1,3-benzodioxol-5-ylmethyl)-2-methyl-3-[(4-methylphenyl)amino]-5-oxo-2,3,6,7-tetrahydro-5H-thiazolo[3,2-a]pyridine-8-carbonitriles in modest (25–46%) yields. The structure of the key compound was confirmed by X-ray crystal structure analysis. GRAPHICAL ABSTRACT
    摘要 N-甲基吗啉鎓 4-aryl-3-cyano-6-oxo-1,4,5,6-tetrahydropyridine-2-thiolates 与 3-(1,3-benzodioxol-5-yl)- 2-甲基丙醛(海洋丙醛)和对甲苯胺得到 7-芳基-2-(1,3-苯并二恶醇-5-基甲基)-2-甲基-3-[(4-甲基苯基)氨基]-5-氧代-2 ,3,6,7-四氢-5H-噻唑并[3,2-a]吡啶-8-腈的产率适中(25-46%)。通过X射线晶体结构分析确认了关键化合物的结构。图形概要
  • Mannich reaction in the synthesis of N,S-containing heterocycles. 14*. Unexpected formation of thiazolo[3,2-a]pyridines in the aminoalkylation of N-methylmorpholinium 4-aryl-3-cyano-6-oxo-1,4,5,6-tetrahydropyridine-2-thiolates by isobutyraldehyde and primary amines
    作者:V. V. Dotsenko、S. G. Krivokolysko
    DOI:10.1007/s10593-012-1042-y
    日期:2012.7
    Treatment of N-methylmorpholinium 4-aryl-3-cyano-6-oxo-1,4,5,6-tetrahydropyridine-2-thiolates with an excess of isobutyraldehyde and primary aromatic amines in refluxing ethanol gives the corresponding 7-aryl-3-arylamino-2,2-dimethyl-5-oxo-2,3,6,7-tetrahydro-5 H-thiazolo[3,2-a]pyridine-8-carbonitriles in 18-38 % yields.
  • A new method for the synthesis ofN-methylmorpholinium 4-aryl-5-cyano-2-oxo-1,2,3,4-tetrahydropyridine-6-thiolates and their properties
    作者:V. D. Dyachenko、S. G. Krivokolysko、V. P. Litvinov
    DOI:10.1007/bf02495131
    日期:1997.10
    N-Methylmorpholinium 4-aryl-5-cyano-2-oxo-1,2,3,4-tetrahydropyridine-6-thiolates were obtained by the condensation of aromatic aldehydes, cyanothioacetamide, and Meldrum's acid in the presence of N-methylmorpholine. They were then used in the syntheses of substituted 6-alkylthio-3,4-dihydropyridin-2(1H)-ones and 4,5-dihydrothieno[2,3-b]pyridin-6(7H)-ones.
  • ——
    作者:V. V. Dotsenko、S. G. Krivokolysko、A. N. Chernega、V. P. Litvinov
    DOI:10.1023/a:1024420930528
    日期:——
    The reactions of N-methylmorpholinium 4-aryl(hetaryl)-5-cyano-2-oxo-1,2,3,4-tetrahydropyridine-6-thiolates with malononitrile and acetone in ethanol afforded substituted tetrahydropyridothienopyridinones. In the absence of acetone, tetrahydropyridothiopyranopyridinones were isolated as the major reaction products. The latter were also synthesized independently by the reactions of the above-mentioned thiolates with 2-amino-1,1,3-tricyanopropene. The structure of 2,4-diamino-10-(2-chlorophenyl)-3-cyano-5-imino-8-oxo-7,8,9,10-tetrahydro-5H-pyrido[2',3':2,3]thiopyrano[4,5-b]pyridine was established by X-ray diffraction analysis.
  • Design and Synthesis of Pyrido[2,1-<i>b</i>][1,3,5]thiadiazine Library via Uncatalyzed Mannich-Type Reaction
    作者:Victor V. Dotsenko、Konstantin A. Frolov、Tatyana M. Pekhtereva、Olena S. Papaianina、Sergey Yu. Suykov、Sergey G. Krivokolysko
    DOI:10.1021/co5000807
    日期:2014.10.13
    This Research Article describes the synthesis of an over 700-member library of (8R/8S)-3-R-8-aryl-6-oxo-3,4,7,8-tetrahydro-2H,6H-pyrido[2,1-b][1,3,5]thiadiazin-9-carbonitriles by uncatalyzed Mannich-type reaction of N-methylmorpholinium (4R/4S)-4-aryl-3-cyano-6-oxo-1,4,5,6-tetrahydropyridin-2-thiolates with a set of primary amines and excessive HCHO. The scope and limitations of the reaction were studied. Starting thiolates were obtained in yields of 53-82% by multicomponent reaction of aromatic aldehydes, cyanothioacetamide, 2,2-dimethyl-1,3-dioxane-4,6-dione (Meldrum's acid), and N-methylmorpholine, followed by heterocyclization of the resulting Michael adducts.
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