摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

(E)-4-chloro-2-(2-(2-chlorobenzylidene)hydrazinyl)pyridine | 1258542-95-8

中文名称
——
中文别名
——
英文名称
(E)-4-chloro-2-(2-(2-chlorobenzylidene)hydrazinyl)pyridine
英文别名
4-chloro-N-[(E)-(2-chlorophenyl)methylideneamino]pyridin-2-amine
(E)-4-chloro-2-(2-(2-chlorobenzylidene)hydrazinyl)pyridine化学式
CAS
1258542-95-8
化学式
C12H9Cl2N3
mdl
——
分子量
266.13
InChiKey
KKNVDVNISAVFAR-LZYBPNLTSA-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):
    4.1
  • 重原子数:
    17
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    37.3
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Palladium-Catalyzed Triazolopyridine Synthesis: Synthesis of 7-Chloro-3-(2-Chlorophenyl)-1,2,4-Triazolo[4,3-a]Pyridine
    摘要:
    Chloramine-T is thermally unstable and heating of chloramines-T beyond the temperature disclosed in this procedure should not be conducted without further safety evaluation. Hydrazine should be handled in a fume hood as it is an animal carcinogen and has been identified it as a potential human carcinogen. In addition, anhydrous hydrazine is potentially explosive, especially in contact with metals, and should only be handled as its hydrate.
    DOI:
    10.15227/orgsyn.090.0287
  • 作为产物:
    参考文献:
    名称:
    Palladium-Catalyzed Triazolopyridine Synthesis: Synthesis of 7-Chloro-3-(2-Chlorophenyl)-1,2,4-Triazolo[4,3-a]Pyridine
    摘要:
    Chloramine-T is thermally unstable and heating of chloramines-T beyond the temperature disclosed in this procedure should not be conducted without further safety evaluation. Hydrazine should be handled in a fume hood as it is an animal carcinogen and has been identified it as a potential human carcinogen. In addition, anhydrous hydrazine is potentially explosive, especially in contact with metals, and should only be handled as its hydrate.
    DOI:
    10.15227/orgsyn.090.0287
点击查看最新优质反应信息

文献信息

  • Palladium-Catalyzed Coupling of Aldehyde-Derived Hydrazones: Practical Synthesis of Triazolopyridines and Related Heterocycles
    作者:Oliver R. Thiel、Michal M. Achmatowicz、Andreas Reichelt、Robert D. Larsen
    DOI:10.1002/anie.201001999
    日期:2010.11.2
    The palladium‐catalyzed intermolecular coupling of aldehyde‐derived hydrazones with chloroazines, followed by oxidative cyclization under mild conditions afforded access to a broad variety of bicyclic heterocyclic scaffolds (see scheme) that have potential for use in drug discovery.
    钯催化的醛衍生的azo酮与氯嗪的分子间偶联,然后在温和的条件下进行氧化环化,可以使用各种各样的双环杂环骨架(参见方案),这些骨架可能会用于药物发现。
  • Imidazo- and triazolo-pyridine compounds and methods of use thereof
    申请人:Zhang Dawei
    公开号:US20080161303A1
    公开(公告)日:2008-07-03
    The present invention comprises a new class of compounds useful for the prophylaxis and treatment of protein kinase mediated diseases, including inflammation and related conditions. The compounds have a general Formula I wherein A, B, R 1 , R 2 , R 3 and R 4 are defined herein. The invention also comprises pharmaceutical compositions including one or more compounds of Formula I, uses of such compounds and compositions for treatment of P38 map kinase mediated diseases including rheumatoid arthritis, psoriasis and other inflammation disorders, as well as intermediates and processes useful for the preparation of compounds of Formula I.
    本发明涉及一类新的化合物,用于预防和治疗与蛋白激酶介导的疾病有关的疾病,包括炎症和相关病症。这些化合物具有通用的I式,其中A、B、R1、R2、R3和R4在此处被定义。该发明还涵盖包括I式中的一个或多个化合物的制药组合物,以及用于治疗P38地图激酶介导的疾病,包括类风湿性关节炎、牛皮癣和其他炎症性疾病的化合物和组合物的用途,以及用于制备I式化合物的中间体和工艺。
  • IMIDAZO- AND TRIAZOLO-PYRIDINE COMPOUNDS AND METHODS OF USE THEROF
    申请人:Amgen Inc.,
    公开号:EP2086973B1
    公开(公告)日:2012-01-25
  • US7700593B2
    申请人:——
    公开号:US7700593B2
    公开(公告)日:2010-04-20
  • [EN] IMIDAZO- AND TRIAZOLO-PYRIDINE COMPOUNDS AND METHODS OF USE THEROF<br/>[FR] COMPOSÉS D'IMIDAZO- ET DE TRIAZOLO-PYRIDINE ET LEURS PROCÉDÉS D'UTILISATION
    申请人:AMGEN INC
    公开号:WO2008045393A2
    公开(公告)日:2008-04-17
    [EN] The present invention comprises a new class of compounds useful for the prophylaxis and treatment of protein kinase mediated diseases, including inflammation and related conditions. The compounds have general Formula (I), wherein A, B, R1, R2, R3 and R4 are defined herein. The invention also comprises pharmaceutical compositions including one or more compounds of Formula (I), uses of such compounds and compositions for treatment of P38 map kinase mediated diseases including rheumatoid arthritis, psoriasis and other inflammation disorders, as well as intermediates and processes useful for the preparation of compounds of Formula (I).
    [FR] La présente invention concerne une nouvelle classe de composés utile pour la prophylaxie et le traitement de maladies favorisées par la protéine kinase, y compris l'inflammation et les états pathologiques liés. Les composés sont représentés par la formule générale (I), dans laquelle A, B, R1, R2, R3 et R4 sont tels que définis ici. L'invention concerne également des compositions pharmaceutiques incluant un ou plusieurs composé(s) représenté(s) par la formule (I), l'utilisation de ces composés et compositions pour le traitement de maladies favorisées par la P38 map kinase, y compris la polyarthrite rhumatoïde, le psoriasis et d'autres troubles inflammatoires, ainsi que des intermédiaires et des procédés utiles pour la préparation des composés représentés par la formule (I).
查看更多

同类化合物

(βS)-β-氨基-4-(4-羟基苯氧基)-3,5-二碘苯甲丙醇 (S)-(-)-7'-〔4(S)-(苄基)恶唑-2-基]-7-二(3,5-二-叔丁基苯基)膦基-2,2',3,3'-四氢-1,1-螺二氢茚 (S)-盐酸沙丁胺醇 (S)-3-(叔丁基)-4-(2,6-二甲氧基苯基)-2,3-二氢苯并[d][1,3]氧磷杂环戊二烯 (S)-2,2'-双[双(3,5-三氟甲基苯基)膦基]-4,4',6,6'-四甲氧基联苯 (S)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (R)富马酸托特罗定 (R)-(-)-盐酸尼古地平 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[((6-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-3-(叔丁基)-4-(2,6-二苯氧基苯基)-2,3-二氢苯并[d][1,3]氧杂磷杂环戊烯 (R)-2-[((二苯基膦基)甲基]吡咯烷 (N-(4-甲氧基苯基)-N-甲基-3-(1-哌啶基)丙-2-烯酰胺) (5-溴-2-羟基苯基)-4-氯苯甲酮 (5-溴-2-氯苯基)(4-羟基苯基)甲酮 (5-氧代-3-苯基-2,5-二氢-1,2,3,4-oxatriazol-3-鎓) (4S,5R)-4-甲基-5-苯基-1,2,3-氧代噻唑烷-2,2-二氧化物-3-羧酸叔丁酯 (4-溴苯基)-[2-氟-4-[6-[甲基(丙-2-烯基)氨基]己氧基]苯基]甲酮 (4-丁氧基苯甲基)三苯基溴化磷 (3aR,8aR)-(-)-4,4,8,8-四(3,5-二甲基苯基)四氢-2,2-二甲基-6-苯基-1,3-二氧戊环[4,5-e]二恶唑磷 (2Z)-3-[[(4-氯苯基)氨基]-2-氰基丙烯酸乙酯 (2S,3S,5S)-5-(叔丁氧基甲酰氨基)-2-(N-5-噻唑基-甲氧羰基)氨基-1,6-二苯基-3-羟基己烷 (2S,2''S,3S,3''S)-3,3''-二叔丁基-4,4''-双(2,6-二甲氧基苯基)-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2S)-(-)-2-{[[[[3,5-双(氟代甲基)苯基]氨基]硫代甲基]氨基}-N-(二苯基甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[[((1R,2R)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2-硝基苯基)磷酸三酰胺 (2,6-二氯苯基)乙酰氯 (2,3-二甲氧基-5-甲基苯基)硼酸 (1S,2S,3S,5S)-5-叠氮基-3-(苯基甲氧基)-2-[(苯基甲氧基)甲基]环戊醇 (1-(4-氟苯基)环丙基)甲胺盐酸盐 (1-(3-溴苯基)环丁基)甲胺盐酸盐 (1-(2-氯苯基)环丁基)甲胺盐酸盐 (1-(2-氟苯基)环丙基)甲胺盐酸盐 (-)-去甲基西布曲明 龙胆酸钠 龙胆酸叔丁酯 龙胆酸 龙胆紫 龙胆紫 齐达帕胺 齐诺康唑 齐洛呋胺 齐墩果-12-烯[2,3-c][1,2,5]恶二唑-28-酸苯甲酯 齐培丙醇 齐咪苯 齐仑太尔 黑染料 黄酮,5-氨基-6-羟基-(5CI) 黄酮,6-氨基-3-羟基-(6CI) 黄蜡,合成物 黄草灵钾盐