3,4-dichloro-N-isopropylbenzamide | 28394-52-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 3,4-dichloro-N-isopropylbenzamide
• 英文别名: N-Isopropyl-3,4-dichlorbenzamid；3,4-Dichlor-benzoesaeure-isopropylamid；3,4-dichloro-N-propan-2-ylbenzamide
• CAS: 28394-52-7
• 化学式: C₁₀H₁₁Cl₂NO
• mdl: MFCD00460933
• 分子量: 232.109
• InChiKey: HRQFVHHYFOMACR-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4
• 重原子数：
  14
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  29.1
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  3,4-dichloro-N-isopropylbenzamide 在 五氯化磷 作用下， 以 苯 为溶剂， 生成 N-Isopropyl-3,4-dichlorbenzimidylchlorid
  参考文献：
  名称：

  Aromatic substituted amidines

  摘要：

  公开号：

  US03850909A1
• 作为产物：
  描述：

  异丙胺 、 3,4-二氯苯甲酰氯 在 三乙胺 作用下， 以 二氯甲烷 为溶剂， 反应 6.0h， 以95%的产率得到3,4-dichloro-N-isopropylbenzamide
  参考文献：
  名称：

  仲酰胺的还原宝石-氰化-膦酰基化反应化学合成α-氨基-α-氰基膦酸酯

  摘要：

  已经开发出一种新的方法来制备α-氨基-α-氰基膦酸酯。该方法的特征在于Tf 2 O介导的仲酰胺还原性双氰胺氰基化/膦酰基化。温和的反应条件，高的键形成效率，廉价的易得原料以及具有宽泛的官能团相容性的良好至优异的收率构成了该方法的主要优点。该协议可以以克为单位运行。

  DOI：

  10.1021/acs.orglett.9b01257

文献信息

• Ketone Synthesis by Direct, Orthogonal Chemoselective Hydroacylation of Alkenes with Amides: Use of Alkenes as Surrogates of Alkyl Carbanions
  作者：Hui Geng、Pei‐Qiang Huang

  DOI：10.1002/cjoc.201900252

  日期：2019.8

  and direct transformation of carboxamides are two exciting areas that have attracted considerable attention in recent years. We report herein that secondary amides, the least reactive derivatives of carbonyl compounds, upon activated with triflic anhydride, can serve as effective hydroacylating reagents in partner with alkenes to yield ketones at ambient temperature. The method was applied to the one‐step

  烯烃的直接官能化和羧酰胺的直接转化是近年来令人瞩目的两个令人兴奋的领域。我们在此报道，仲酰胺，即羰基化合物的反应性最低的衍生物，在用三氟甲磺酸酐活化后，可以与烯烃一起作为有效的氢酰化试剂，在环境温度下产生酮。该方法已用于外消旋二氢芳基羟色酮的一步合成。在这种方法中，烯烃用作有机金属试剂的替代物，从而可以进行正交的化学选择性反应。许多烯烃（如camp烯和降冰片烯）的现成性允许一步合成酮，而传统方法则需要几个步骤。
• PHTHALIC ACID DIAMIDE DERIVATIVES FLUORINE-CONTAINING ANILINE COMPOUNDS AS STARTING MATERIAL, AGRICULTURAL AND HORTICULTURAL INSECTICIDES, AND A METHOD FOR APPLICATION OF THE INSECTICIDES
  申请人：——

  公开号：US20010041814A1

  公开（公告）日：2001-11-15

  The present invention provides a phthalic acid diamide derivative represented by the general formula (I) 1 (wherein R 1 , R 2 and R 3 are each H, C 3 -C 6 cycloalkyl group, group of the formula —A 1 —Q l or the like; X may be the same or different and are each halogen atom, nitro group, phenyl group, group of the formula —A 2 —R 7 or the like; n is 1 to 4; Y may be same or different and are each halogen atom, cyano group, phenyl group, group of the formula —A 2 —R 7 or the like; m is 1 to 5; Z 1 and Z 2 are each O or S), fluorine-containing aniline compound represented by the general formula (ST-I) as starting material for said phthalic acid diamide derivative 2 (wherein R a is halogen atom, C 1 -C 6 alkyl group or the like and R b , R c and R d is H or C 2 -C 6 perfluoroalkyl group), and an agricultural and horticultural insecticide containing said phthaldiamide derivative, as well as to provide a method for use of said insecticide. The agricultural and horticultural insecticides of the present invention show excellent activities for controlling injurious insects.

  本发明提供了一种邻苯二甲酰胺衍生物，其由通式（I）1表示（其中R1、R2和R3分别为H、C3-C6环烷基、—A1—Ql或类似基团；X可以相同也可以不同，分别为卤素原子、硝基、苯基、—A2—R7或类似基团；n为1至4；Y可以相同也可以不同，分别为卤素原子、氰基、苯基、—A2—R7或类似基团；m为1至5；Z1和Z2分别为O或S），以通式（ST-I）表示的含氟苯胺化合物作为所述邻苯二甲酰胺衍生物的起始原料2（其中Ra为卤素原子、C1-C6烷基或类似基团，而Rb、Rc和Rd为H或C2-C6全氟烷基），以及含有所述邻苯二甲酰胺衍生物的农业和园艺杀虫剂，同时提供了使用该杀虫剂的方法。本发明的农业和园艺杀虫剂对控制有害昆虫表现出优异的活性。
• Novel [1,2,4]Triazolo[4,3-a]Quinoxaline Derivative, Method For Preparing Same, And Pharmaceutical Composition For Preventing Or Treating BET Protein-Related Diseases, Containing Same As Active Ingredient
  申请人：Dong Wha Pharm. Co., Ltd.

  公开号：US20200039984A1

  公开（公告）日：2020-02-06

  Provided are a novel [1,2,4]triazolo[4,3-a]quinoxaline derivative, a method for preparing the same, and a pharmaceutical composition for preventing or treating bromodomain extra-terminal (BET) protein-related diseases including cancer and autoimmune diseases, containing the same as an active ingredient.

  提供了一种新型[1,2,4]三唑并[4,3-a]喹喔啉衍生物，一种制备该衍生物的方法，以及一种用于预防或治疗与溴结构域额外末端（BET）蛋白相关的疾病，包括癌症和自身免疫疾病的药物组合物，其中该衍生物作为活性成分。
• Phthalic acid diamide derivatives, fluorine-containing aniline compounds as starting material, agricultural and horticultural insecticides, and a method for application of the insecticides
  申请人：——

  公开号：US20030055287A1

  公开（公告）日：2003-03-20

  The present invention provides a phthalic acid diamide derivative represented by the general formula (I) 1 (wherein R 1 , R 2 and R 3 are each H, C 3 -C 6 cycloalkyl group, group of the formula -A 1 -Q l or the like; X may be the same or different and are each halogen atom, nitro group, phenyl group, group of the formula -A 2 -R 7 or the like; n is 1 to 4; Y may be same or different and are each halogen atom, cyano group, phenyl group, group of the formula -A 2 -R 7 or the like; m is 1 to 5; Z 1 and Z 2 are each O or S), fluorine-containing aniline compound represented by the general formula (ST-I) as starting material for said phthalic acid diamide derivative 2 (wherein R a is halogen atom, C 1 -C 6 alkyl group or the like and R b , R c and R d is H or C 2 -C 6 perfluoroalkyl group), and an agricultural and horticultural insecticide containing said phthaldiamide derivative, as well as to provide a method for use of said insecticide. The agricultural and horticultural insecticides of the present invention show excellent activities for controlling injurious insects.

  本发明提供了一种邻苯二甲酰胺衍生物，其表示为通式（I）1（其中R1、R2和R3分别为H、C3-C6环烷基、-A1-Ql或类似基团；X可以相同或不同，分别为卤素原子、硝基、苯基、-A2-R7或类似基团；n为1至4；Y可以相同或不同，分别为卤素原子、氰基、苯基、-A2-R7或类似基团；m为1至5；Z1和Z2分别为O或S），以及以含氟苯胺化合物为起始物质的邻苯二甲酰胺衍生物2（其中Ra为卤素原子、C1-C6烷基或类似基团，而Rb、Rc和Rd为H或C2-C6全氟烷基），以及包含所述邻苯二甲酰胺衍生物的农业和园艺杀虫剂，同时提供了使用所述杀虫剂的方法。本发明的农业和园艺杀虫剂表现出优异的控制有害昆虫的活性。
• Cycloamine ccr5 receptor antagonists
  申请人：Shiota Tatsuki

  公开号：US20070010509A1

  公开（公告）日：2007-01-11

  Remedies or prophylactics for diseases in association with CCR5 such as AIDS, rheumatoid arthritis or nephritis comprising a cyclic amine compound represented by the following formula (I), a pharmaceutically acceptable acid addition salt thereof or a pharmaceutically acceptable C 1 -C 6 alkyl addition salt thereof, as an active ingredient.

  本发明涉及与CCR5相关的疾病的治疗或预防措施，例如艾滋病、类风湿性关节炎或肾炎，包括下式（I）所表示的环状胺化合物，其药学上可接受的酸加盐或药学上可接受的C1-C6烷基加盐作为活性成分。