N-methyl-benzamidrazone; hydrochloride | 28705-52-4

• 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: N-methyl-benzamidrazone; hydrochloride
• 英文别名: N-Methyl-benzamidrazon; Hydrochlorid；benzimidic acid 2-methylhydrazide hydrochloride；(Z)-[amino(phenyl)methylidene]-(methylamino)azanium;chloride
• CAS: 28705-52-4
• 化学式: C₈H₁₁N₃*ClH
• 分子量: 185.656
• InChiKey: ZRHHIJDMJKSOLU-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.95
• 重原子数：
  12
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.12
• 拓扑面积：
  50.4
• 氢给体数：
  3
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  N-methyl-benzamidrazone; hydrochloride 在 五氯化磷 、 三乙胺 作用下， 以 二氯甲烷 、 氯仿 、 苯 为溶剂， 反应 61.0h， 生成 Aceton-<9,10-dihydro-1,9-dimethyl-3,5,7-triphenyl-1H-1,3,2λ⁵,4-diazadiphospheto<2,1-c:2,3-c'>bis(1,2,4,3λ⁵-triazaphosphol)-10-yl>methylhydrazon-5'-oxid
  参考文献：
  名称：

  Schmidpeter, Alfred; Nayibi, Mesut; Mayer, Peter, Chemische Berichte, 1983, vol. 116, # 4, p. 1468 - 1478

  摘要：

  DOI：

文献信息

• Substituted 1,2,4-triazole derivatives
  申请人：Gruppo Lepetit S.p.A.

  公开号：US04119635A1

  公开（公告）日：1978-10-10

  New 1-alkyl-3,5-disubstituted-1,2,4-triazole derivatives of following formula I ##STR1## wherein R may represent phenyl; phenyl substituted by a radical selected from (C.sub.1-4)alkyl, e.g. methyl, ethyl, propyl, isopropyl, butyl, sec.-butyl, isobutyl or tert.-butyl, (C.sub.1-4)alkoxy, e.g. methoxy, ethoxy, propoxy, butoxy, isobutyloxy or tert.-butoxy, fluoro, chloro, bromo, nitro, amino, cyano, carbamoyl, carboxy, hydroxymethyl, methylenedioxy and trifluoromethyl; dichlorophenyl; dimethoxyphenyl; 3,4,5-trimethoxyphenyl; R.sub.1 may represent phenyl, phenyl substituted by a radical selected from (C.sub.1-4)alkyl as above defined, (C.sub.1-4)alkoxy as above defined; fluoro, chloro, bromo, hydroxymethyl, (C.sub.2-4)aliphatic acyloxymethyl, e.g. acetoxymethyl, propionyloxymethyl or butyryloxymethyl, carbamoyloxymethyl, bromomethyl and dimethylaminomethyl; dimethylphenyl; dimethoxyphenyl; phenyl contemporaneously substituted by o-hydroxymethyl and chloro; R.sub.2 represents a (C.sub.1-4)alkyl group as above defined; With the proviso that R and R.sub.1 cannot simultaneously represent phenyl; With the further proviso that, when R is phenyl, R.sub.1 cannot be p-chlorophenyl; And processes for their preparation. The compounds of the invention have CNS depressant utility. They are especially useful as sedatives and hypnotics. Some of the compounds of the invention are also useful as anxiety relieving means.

  新的1-烷基-3,5-二取代-1,2,4-三唑衍生物的化学式为I，其中R可能代表苯基；苯基被从(C.sub.1-4)烷基中选择的基团取代，例如甲基、乙基、丙基、异丙基、丁基、丙烯基、异丁基或叔丁基，(C.sub.1-4)烷氧基，例如甲氧基、乙氧基、丙氧基、丁氧基、异丁氧基或叔丁氧基，氟、氯、溴、硝基、氨基、氰基、氨甲酰基、羧基、羟甲基、亚甲二氧基和三氟甲基；二氯苯基；二甲氧基苯基；3,4,5-三甲氧基苯基；R.sub.1可能代表苯基，苯基被从上述定义的(C.sub.1-4)烷基中选择的基团取代，(C.sub.1-4)烷氧基如上所述；氟、氯、溴、羟甲基、(C.sub.2-4)脂肪酰氧甲基，例如乙酰氧甲基、丙酰氧甲基或丁酰氧甲基，氨基氧甲基、溴甲基和二甲氨基甲基；二甲基苯基；二甲氧基苯基；苯基同时被o-羟甲基和氯取代；R.sub.2代表如上所述的(C.sub.1-4)烷基基团；但R和R.sub.1不能同时代表苯基；另外规定，当R是苯基时，R.sub.1不能是对氯苯基；以及它们的制备方法。该发明的化合物具有中枢神经系统抑制作用。它们特别适用于镇静剂和催眠剂。该发明的一些化合物也可用作缓解焦虑的手段。
• Process for preparing substituted 1,2,4-triazole derivatives
  申请人：Gruppo Lepetit

  公开号：US04151169A1

  公开（公告）日：1979-04-24

  New 1-alkyl-3,5-disubstituted-1,2,4-triazole derivatives of following formula I ##STR1## wherein R may represent phenyl; phenyl substituted by a radical selected from (C.sub.1-4)alkyl, e.g. methyl, ethyl, propyl, isopropyl, butyl, sec.-butyl, isobutyl or tert.-butyl, (C.sub.1-4)alkoxy, e.g. methoxy, ethoxy, propoxy, butoxy, isobutyloxy or tert.-butoxy, fluoro, chloro, bromo, nitro, amino, cyano, carbamoyl, carboxy, hydroxymethyl, methylenedioxy and trifluoromethyl; dichlorophenyl; dimethoxyphenyl; 3,4,5-trimethoxyphenyl; R.sub.1 may represent phenyl, phenyl substituted by a radical selected from (C.sub.1-4)alkyl as above defined, (C.sub.1-4)alkoxy as above defined, fluoro, chloro, bromo, hydroxymethyl, (C.sub.2-4)aliphatic acyloxymethyl, e.g. acetoxymethyl, propionyloxymethyl or butyryloxymethyl, carbamoyloxymethyl, bromomethyl and dimethylaminomethyl; dimethylphenyl; dimethoxyphenyl; phenyl contemporaneously substituted by o-hydroxymethyl and chloro; R.sub.2 represents a (C.sub.1-4)alkyl group as above defined; with the proviso that R and R.sub.1 cannot simultaneously represent phenyl; With the further proviso that, when R is phenyl, R.sub.1 cannot be p-chlorophenyl; and processes for their preparation. The compound of the invention have CNS depressant utility. They are especially useful as sedatives and hypnotics. Some of the compounds of the invention are also useful as anxiety relieving means.

  新的1-烷基-3,5-二取代-1,2,4-三唑衍生物具有以下公式I：##STR1## 其中R可以表示苯基；苯基被从（C.sub.1-4）烷基，例如甲基，乙基，丙基，异丙基，丁基，仲丁基，异丁基或叔丁基中选择的基团取代，（C.sub.1-4）烷氧基，例如甲氧基，乙氧基，丙氧基，丁氧基，异丁氧基或叔丁氧基，氟，氯，溴，硝基，氨基，氰基，氨基甲酰，羧基，羟甲基，亚甲二氧基和三氟甲基；二氯苯基；二甲氧基苯基；3,4,5-三甲氧基苯基；R.sub.1可以表示苯基，苯基被从上述定义的（C.sub.1-4）烷基，（C.sub.1-4）烷氧基，氟，氯，溴，羟甲基，（C.sub.2-4）脂肪酰氧甲基，例如乙酰氧甲基，丙酰氧甲基或丁酰氧甲基，氨基甲酰氧甲基，溴甲基和二甲胺基甲基中选择的基团取代；二甲基苯基；二甲氧基苯基；同时被o-羟甲基和氯取代的苯基；R.sub.2代表上述定义的（C.sub.1-4）烷基。前提是R和R.sub.1不能同时表示苯基；并且当R为苯基时，R.sub.1不能是对氯苯基。其制备方法也在文中描述。该发明的化合物具有中枢神经系统抑制剂的用途。它们特别适用于镇静和催眠药。该发明的一些化合物也可用作缓解焦虑的手段。
• Khrustalev, V. A.; Solod, O. V.; Zelenin, K. N., Journal of Organic Chemistry USSR (English Translation), 1986, vol. 22, p. 444 - 453
  作者：Khrustalev, V. A.、Solod, O. V.、Zelenin, K. N.

  DOI：——

  日期：——
• Schmidpeter,A. et al., Angewandte Chemie, 1977, vol. 89, p. 554 - 555
  作者：Schmidpeter,A. et al.

  DOI：——

  日期：——
• MAJORAL J.-R.; KRAEMER R.; MPONDO TN.; NAVESN J., TETRAHEDRON LETT., 1980, 21, NO 14, 1307-1310
  作者：MAJORAL J.-R.、 KRAEMER R.、 MPONDO TN.、 NAVESN J.

  DOI：——

  日期：——