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(3-cyano-6-methyl-4-methoxymethyl-2-pyridylthio)acetic acid | 170885-42-4

中文名称
——
中文别名
——
英文名称
(3-cyano-6-methyl-4-methoxymethyl-2-pyridylthio)acetic acid
英文别名
Acetic acid, 2-[[3-cyano-4-(methoxymethyl)-6-methyl-2-pyridinyl]thio]-;2-[3-cyano-4-(methoxymethyl)-6-methylpyridin-2-yl]sulfanylacetic acid
(3-cyano-6-methyl-4-methoxymethyl-2-pyridylthio)acetic acid化学式
CAS
170885-42-4
化学式
C11H12N2O3S
mdl
MFCD00473875
分子量
252.294
InChiKey
MJLLTDZSIPEIAO-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):
    1.1
  • 重原子数:
    17
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.36
  • 拓扑面积:
    109
  • 氢给体数:
    1
  • 氢受体数:
    6

反应信息

  • 作为反应物:
    描述:
    (3-cyano-6-methyl-4-methoxymethyl-2-pyridylthio)acetic acidsodium ethanolate 作用下, 以 乙醇 为溶剂, 反应 2.0h, 以63%的产率得到3-Amino-4-methoxymethyl-6-methyl-thieno[2,3-b]pyridine-2-carboxylic acid
    参考文献:
    名称:
    Electrochemical synthesis and studies of substituted 2-thiopyridines
    摘要:
    A series of substituted 2-alkyl(aryl-, hetaryl-)thiopyridines was prepared by cathodic electrolysis of thiols in the presence of 2-chloro-3-cyano-4-methoxymethyl-6-methylpyridine or 4-chloro-6-methyl-3-oxo-1 H-furo[3,4-c]pyridine. The reaction of 3-cyano-4-methoxymethyl-6-methyl-2(1H)-thiopyridone with alkyl halides in the presence of KOH is regioselective and leads to S-alkyl derivatives. The advantages of electrosynthesis for the preparation of 2-alkylthiopyridines fused with 2(5H)-furanone and of 3-aminothieno[2,3-b]pyridines is demonstrated.
    DOI:
    10.1007/bf00700178
  • 作为产物:
    描述:
    2-chloro-3-cyano-4-methoxymethyl-6-methylpyridine 、 alkaline earth salt of/the/ methylsulfuric acid 在 氢氧化钾 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 以95%的产率得到(3-cyano-6-methyl-4-methoxymethyl-2-pyridylthio)acetic acid
    参考文献:
    名称:
    Electrochemical synthesis and studies of substituted 2-thiopyridines
    摘要:
    A series of substituted 2-alkyl(aryl-, hetaryl-)thiopyridines was prepared by cathodic electrolysis of thiols in the presence of 2-chloro-3-cyano-4-methoxymethyl-6-methylpyridine or 4-chloro-6-methyl-3-oxo-1 H-furo[3,4-c]pyridine. The reaction of 3-cyano-4-methoxymethyl-6-methyl-2(1H)-thiopyridone with alkyl halides in the presence of KOH is regioselective and leads to S-alkyl derivatives. The advantages of electrosynthesis for the preparation of 2-alkylthiopyridines fused with 2(5H)-furanone and of 3-aminothieno[2,3-b]pyridines is demonstrated.
    DOI:
    10.1007/bf00700178
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文献信息

  • Synthesis of substituted benzoxazinylthieno[2,3-b]pyridines by the reaction of (3-cyanopyridin-2-ylthio)acetic acids or their amides with o-aminophenyl(diphenyl)carbinol
    作者:E. A. Kaigorodova、L. D. Konyushkin、A. A. Osipova、E. A. Gavrilova、E. V. Gromachevskaya、G. D. Krapivin
    DOI:10.1007/s11172-005-0208-5
    日期:2004.12
    A general method for the synthesis of 3-amino-2-(4,4-diphenyl-4H-3,1-benzoxazin-2-yl)thieno[2,3-b]pyridines was proposed. The method involves reactions of (3-cyanopyridin-2-ylthio)acetic acids or their amides with o-aminophenyl(diphenyl)carbinol in nitromethane in the presence of perchloric acid followed by neutralization of the resulting salts.
    提出了一种合成 3-氨基-2-(4,4-二苯基-4H-3,1-苯并恶嗪-2-基)噻吩并[2,3-b]吡啶的通用方法。该方法包括(3-氰基吡啶-2-基硫基)乙酸或其酰胺与邻氨基苯基(二苯基)甲醇在高氯酸存在下在硝基甲烷中的反应,然后中和所得盐。
  • Electrochemical synthesis and studies of substituted 2-thiopyridines
    作者:E. A. Kaigorodova、L. D. Konyushkin、M. E. Niyazymbetov、S. N. Kvak、V. N. Zaplishny、V. P. Litvinov
    DOI:10.1007/bf00700178
    日期:1994.12
    A series of substituted 2-alkyl(aryl-, hetaryl-)thiopyridines was prepared by cathodic electrolysis of thiols in the presence of 2-chloro-3-cyano-4-methoxymethyl-6-methylpyridine or 4-chloro-6-methyl-3-oxo-1 H-furo[3,4-c]pyridine. The reaction of 3-cyano-4-methoxymethyl-6-methyl-2(1H)-thiopyridone with alkyl halides in the presence of KOH is regioselective and leads to S-alkyl derivatives. The advantages of electrosynthesis for the preparation of 2-alkylthiopyridines fused with 2(5H)-furanone and of 3-aminothieno[2,3-b]pyridines is demonstrated.
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