1-(2,3-Dichloro-phenyl)-3-methyl-urea | 90532-31-3

• 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: 1-(2,3-Dichloro-phenyl)-3-methyl-urea
• 英文别名: N-methyl-N'-(dichlorophenyl)-urea；1-(2,3-dichlorophenyl)-3-methylurea
• CAS: 90532-31-3
• 化学式: C₈H₈Cl₂N₂O
• 分子量: 219.07
• InChiKey: GCCCKLZMLIDIAX-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.9
• 重原子数：
  13
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.12
• 拓扑面积：
  41.1
• 氢给体数：
  2
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  1-(2,3-Dichloro-phenyl)-3-methyl-urea 在 palladium on activated charcoal 盐酸 、 sodium hydroxide 、 氢气 、 乙酸酐 、 sodium nitrite 作用下， 以 甲醇 、 水 、 乙酸乙酯 为溶剂， 反应 13.0h， 生成 5,6-Diamino-1-(2,3-dichloro-phenyl)-3-methyl-1H-pyrimidine-2,4-dione
  参考文献：
  名称：

  Structure and activity relationships of novel uracil derivatives as topical anti-inflammatory agents

  摘要：

  In order to create novel, topical anti-inflammatory compounds exhibiting more potent activities than lead compound CX-659S (1), we designed and synthesized various derivatives of 1 focusing on the uracil N(l)- and N(3)-substituents, and evaluated their anti-inflammatory activities via inhibition of the picryl chloride-induced contact hypersensitivity reaction (CHR) in mice. In the course of our structure and activity relationship study, we found that compounds 6k, 6q, and 6r inhibited by approximately 50% the CHR, at 0.1 mg/ear. These activities were essentially equipotent with that of Tacrolimus, a strong immunosuppressant. (C) 2003 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2003.09.012

文献信息

• Substituted ureas as herbicides
  申请人：Roussel Uclaf

  公开号：US04045209A1

  公开（公告）日：1977-08-30

  Novel urea derivatives of the formula ##STR1## wherein R and R.sub.1 are individually selected from the group consisting of hydrogen, chlorine, bromine, nitro, trifluoromethyl, lower alkyl of 1 to 6 carbon atoms and lower alkoxy of 1 to 6 carbon atoms, n is 0 or 1, X is selected from the group consisting of lower alkyl of 1 to 6 carbon atoms optionally substituted with halogen and a nitrogen heterocyclic optionally containing 1 or more other heteroatoms, Y is selected from the group consisting of hydrogen, alkyl of 1 to 4 carbon atoms and S--Z wherein Z is a nitrogen heterocyclic optionally containing 1 or more other heteroatoms and the dotted lines indicate that the compound of formula I may contain no oxygen bound to the sulfur atom or may be in sulfoxide or sulfonyl form which are useful as herbicides and thereon preparation.

  该专利描述了一种新的脲类衍生物，其化学式为##STR1##其中R和R.sub.1分别选自氢、氯、溴、硝基、三氟甲基、1至6个碳原子的低级烷基和1至6个碳原子的低级烷氧基的群组，n为0或1，X选自1至6个碳原子的低级烷基（可选地带有卤素）和一个含有1个或多个其他杂原子的氮杂环，Y选自氢、1至4个碳原子的烷基和S--Z，其中Z是一个含有1个或多个其他杂原子的氮杂环，虚线表示化合物I可能不含有氧与硫原子结合，或者可能处于亚砜或磺酰形式，这些化合物可以作为除草剂使用。
• US4045209A
  申请人：——

  公开号：US4045209A

  公开（公告）日：1977-08-30
• Structure and activity relationships of novel uracil derivatives as topical anti-inflammatory agents
  作者：Yoshiaki Isobe、Masanori Tobe、Yoshifumi Inoue、Masakazu Isobe、Masami Tsuchiya、Hideya Hayashi

  DOI：10.1016/j.bmc.2003.09.012

  日期：2003.11

  In order to create novel, topical anti-inflammatory compounds exhibiting more potent activities than lead compound CX-659S (1), we designed and synthesized various derivatives of 1 focusing on the uracil N(l)- and N(3)-substituents, and evaluated their anti-inflammatory activities via inhibition of the picryl chloride-induced contact hypersensitivity reaction (CHR) in mice. In the course of our structure and activity relationship study, we found that compounds 6k, 6q, and 6r inhibited by approximately 50% the CHR, at 0.1 mg/ear. These activities were essentially equipotent with that of Tacrolimus, a strong immunosuppressant. (C) 2003 Elsevier Ltd. All rights reserved.