2-Fluoromethyl-2-phthalimido-5-methane-sulfonyloxy-valeronitrile | 82212-58-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 异吲哚及其衍生物
• 英文名称: 2-Fluoromethyl-2-phthalimido-5-methane-sulfonyloxy-valeronitrile
• 英文别名: 2-(fluoromethyl)-5-(mesyloxy)-2-phthalimidopentanenitrile；2-fluoromethyl-2-phthalimido-5-methanesulfonyloxypentanenitrile；[4-cyano-4-(1,3-dioxoisoindol-2-yl)-5-fluoropentyl] methanesulfonate
• CAS: 82212-58-6
• 化学式: C₁₅H₁₅FN₂O₅S
• 分子量: 354.359
• InChiKey: BQZMQEFZGGYOAW-UHFFFAOYSA-N

物化性质

• 沸点：
  585.9±50.0 °C(Predicted)
• 密度：
  1.448±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1
• 重原子数：
  24
• 可旋转键数：
  7
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.4
• 拓扑面积：
  113
• 氢给体数：
  0
• 氢受体数：
  7

反应信息

• 作为反应物：
  描述：

  2-Fluoromethyl-2-phthalimido-5-methane-sulfonyloxy-valeronitrile 在 potassium tert-butylate 、 sodium iodide 作用下， 以 丙酮 为溶剂， 反应 63.5h， 生成 ethyl 2-(carbethoxy)-6-cyano-2,6-diphthalimido-7-fluoroheptanoate
  参考文献：
  名称：

  2-(4-Amino-4-carboxybutyl)aziridine-2-carboxylic acid. A potent irreversible inhibitor of diaminopimelic acid epimerase. Spontaneous formation from .alpha.-(halomethyl)diaminopimelic acids

  摘要：

  2-(4-Amino-4-carboxybutyl)aziridine-2-carboxylic acid (3) (aziridino-DAP) was identified as the product of spontaneous hydrolysis of alpha-(halomethyl)diaminopimelic acids (alpha-halomethyl-DAPs) 2a-c. Under physiological conditions, 3 is an extremely potent irreversible inhibitor of the bacterial enzyme diaminopimelic acid epimerase (DAP-epimerase; EC 5.1.1.7). This unusual mode of action of an alpha-halomethyl amino acid with a non-pyridoxal enzyme is investigated. Synthesis and characterization of 2a-c and 3, kinetics of spontaneous formation of 3 from alpha-halomethyl-DAPs, and kinetics of enzyme inhibition by both 3 and by alpha-halomethyl-DAPs are reported.

  DOI：

  10.1021/jm00170a018
• 作为产物：
  描述：

  2-fluoromethyl-2-amino-5-benzyloxy-pentanenitrile 在 吡啶 、 碘代三甲硅烷 、 三乙胺 作用下， 以 二氯甲烷 为溶剂， 反应 1.0h， 生成 2-Fluoromethyl-2-phthalimido-5-methane-sulfonyloxy-valeronitrile
  参考文献：
  名称：

  2-(4-Amino-4-carboxybutyl)aziridine-2-carboxylic acid. A potent irreversible inhibitor of diaminopimelic acid epimerase. Spontaneous formation from .alpha.-(halomethyl)diaminopimelic acids

  摘要：

  2-(4-Amino-4-carboxybutyl)aziridine-2-carboxylic acid (3) (aziridino-DAP) was identified as the product of spontaneous hydrolysis of alpha-(halomethyl)diaminopimelic acids (alpha-halomethyl-DAPs) 2a-c. Under physiological conditions, 3 is an extremely potent irreversible inhibitor of the bacterial enzyme diaminopimelic acid epimerase (DAP-epimerase; EC 5.1.1.7). This unusual mode of action of an alpha-halomethyl amino acid with a non-pyridoxal enzyme is investigated. Synthesis and characterization of 2a-c and 3, kinetics of spontaneous formation of 3 from alpha-halomethyl-DAPs, and kinetics of enzyme inhibition by both 3 and by alpha-halomethyl-DAPs are reported.

  DOI：

  10.1021/jm00170a018

文献信息

• Process for preparing fluorinated amino-nitriles
  申请人：Merrell Toraude et Compagnie

  公开号：US04405530A1

  公开（公告）日：1983-09-20

  Certain .alpha.-(fluoromethyl or difluoromethyl)-.alpha.-aminoacetonitriles are prepared by treating the appropriate .alpha.-(fluoromethyl or difluoromethyl) ketimine magnesium halide with hydrogen cyanide or with an alkali metal cyanide or ammonium cyanide and a proton source. The products are useful as intermediates for making .alpha.-(fluoromethyl or difluoromethyl)-.alpha.-amino acids having pharmacological activity.

  某些α-(氟甲基或二氟甲基)-α-氨基乙腈是通过将相应的α-(氟甲基或二氟甲基)酮亚胺镁卤化物与氢氰酸或与碱金属氰化物、氰化铵及质子源反应制备而成。这些产物作为中间体，可用于合成具有药理活性的α-(氟甲基或二氟甲基)-α-氨基酸。
• 2-halomethyl derivatives of 2-amino acids
  申请人：Merrell Dow France et Cie

  公开号：US04743691A1

  公开（公告）日：1988-05-10

  2-(Fluoromethyl or chloromethyl)-2,5-diaminopentanoic acid, 2-(fluoromethyl or chloromethyl)-2,6-diaminohexanoic acid, and 2-fluoromethyl-2-amino-5-guanidinopentanoic acid, and certain derivatives thereof, are inhibitors of ornithine decarboxylase. Methods of preparing the compounds and derivatives are also described.

  2-(氟甲基或氯甲基)-2,5-二氨基戊酸，2-(氟甲基或氯甲基)-2,6-二氨基己酸和2-氟甲基-2-氨基-5-胍基戊酸及其某些衍生物是鸟氨酸脱羧酶的抑制剂。本文还描述了制备这些化合物和衍生物的方法。
• 2-Halomethyl derivatives of 2-amino acids
  申请人：Merrell Dow France et Cie

  公开号：US04866206A1

  公开（公告）日：1989-09-12

  2-(Fluoromethyl or chloromethyl)-2,5-diaminopentanoic acid, 2-(fluoromethyl or chloromethyl)-2,6-diaminohexanoic acid, and 2-fluoromethyl-2-amino-5-guanidinopentanoic acid, and certain derivatives thereof, are inhibitors of ornithine decarboxylase. Methods of preparing the compounds and derivatives are also described.

  2-(氟甲基或氯甲基)-2,5-二氨基戊酸，2-(氟甲基或氯甲基)-2,6-二氨基己酸和2-氟甲基-2-氨基-5-胍基戊酸及其某些衍生物是鸟氨酸脱羧酶的抑制剂。本文还描述了制备这些化合物和衍生物的方法。
• Preparation of aminoacetonitrile derivatives
  申请人：MERRELL TORAUDE ET COMPAGNIE

  公开号：EP0046710A1

  公开（公告）日：1982-03-03

  2-Fluorinated methyl aminoacetonitriles are prepared by treating a corresponding fluorinated methyl ketimine magnesium halide with hydrogen cyanide or with an alkali metal cyanide or ammonium cyanide and a proton source.

  用氰化氢或碱金属氰化物或氰化铵和质子源处理相应的氟化甲基酮亚胺卤化镁，可制备 2-氟化甲基氨基乙腈。
• US4405530A
  申请人：——

  公开号：US4405530A

  公开（公告）日：1983-09-20