4-{2-{[(tert-butyl)amino}sulfonyl}phenyl}benzoic acid | 309930-58-3

• 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: 4-{2-{[(tert-butyl)amino}sulfonyl}phenyl}benzoic acid
• 英文别名: 4-[(2-t-butylaminosulfonyl)phenyl]benzoic acid；2'-[(tert-butylamino)sulfonyl][1,1'-biphenyl]-4-carboxylic acid；4-(2-t-Butylaminosulfonylphenyl)-benzoic acid；4-[2-(tert-butylsulfamoyl)phenyl]benzoic acid
• CAS: 309930-58-3
• 化学式: C₁₇H₁₉NO₄S
• 分子量: 333.408
• InChiKey: PWVOLDMDJHZBRI-UHFFFAOYSA-N

物化性质

• 沸点：
  525.3±60.0 °C(Predicted)
• 密度：
  1.246±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3
• 重原子数：
  23
• 可旋转键数：
  5
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.24
• 拓扑面积：
  91.8
• 氢给体数：
  2
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  4-{2-{[(tert-butyl)amino}sulfonyl}phenyl}benzoic acid 在 吡啶 、 氯化亚砜 、 三甲基铝 、 三氟乙酸 、 tin(ll) chloride 作用下， 以 二氯甲烷 、 乙酸乙酯 为溶剂， 反应 32.0h， 生成 N-(5-bromo-2-pyridinyl)-(2-(4-[(2-aminosulfonyl)phenyl]phenylcarbonyl)amino)-4-aminophenylcarboxamide
  参考文献：
  名称：

  Design, synthesis, and SAR of anthranilamide-based factor Xa inhibitors incorporating substituted biphenyl P4 motifs

  摘要：

  Anthranilamides 4 and 5 were designed and synthesized as selective and orally bioavailable factor Xa inhibitors. Structural modifications aimed at lowering their lipophilicity were performed at the central phenyl ring and at the S4 binding biphenyl region by incorporating water solublizing substituents. The resulting compounds (e.g., 7, 8, 14, 30a, and 32b) are highly potent in vitro, and show improved activity in human plasma-based thrombin generation assay. (C) 2004 Published by Elsevier Ltd.

  DOI：

  10.1016/j.bmcl.2003.11.079
• 作为产物：
  描述：

  4-甲酰基苯硼酸 、 2-溴-N-叔丁基苯磺酰胺 在 四(三苯基膦)钯 sodium carbonate 、 sodium chlorite 、 sodium dihydrogenphosphate 作用下， 以 水 、 甲苯 、 2-甲基-2-丁烯 为溶剂， 反应 40.0h， 生成 4-{2-{[(tert-butyl)amino}sulfonyl}phenyl}benzoic acid
  参考文献：
  名称：

  EP1577302

  摘要：

  公开号：

文献信息

• Benzamides and related inhibitors of factor Xa
  申请人：Millennium Pharmaceuticals, Inc.

  公开号：US09108922B2

  公开（公告）日：2015-08-18

  Novel benzamide compounds including their pharmaceutically acceptable isomers, salts, hydrates, solvates and prodrug derivatives having activity against mammalian factor Xa are described. Compositions containing such compounds are also described. The compounds and compositions are useful in vitro or in vivo for preventing or treating coagulation disorders.

  描述了包括其药用可接受异构体、盐、水合物、溶剂合物和前药衍生物在内的新型苯甲酰胺化合物，具有对哺乳动物凝血因子Xa的活性。还描述了含有这些化合物的组合物。这些化合物和组合物在体外或体内用于预防或治疗凝血障碍。
• Factor xa inhibitors with aryl-amidines and derivatives, and prodrugs thereof
  申请人：——

  公开号：US20030065176A1

  公开（公告）日：2003-04-03

  The present invention relates to a compound with aryl-amidines, particularly amidinoaryl-cyclopropanes, amidinoarylmethyl-pyrroles, amidinoaryl-benzenes, amidinoaryl-pyridines, or amindonoaryl-alanines, represented by formula (1), a pharmaceutically acceptable salt, a prodrug, a hydrate, a solvate or an isomer thereof, which are inhibitors of coagulation enzyme, factor Xa (FXa). The present invention also relates to a pharmaceutical composition containing the compound, and a method of using the same as an anticoagulant agent for treatment and prevention of thrombosis disorders.

  本发明涉及一种具有芳基胺基的化合物，特别是表示为式（1）的芳基胺基环丙烷，芳基胺基甲基吡咯烷，芳基胺基苯，芳基胺基吡啶或芳基胺基丙氨酸的化合物，其为凝血酶Xa（FXa）的抑制剂，包括药用盐、前药、水合物、溶剂合物或其异构体。本发明还涉及含有该化合物的药物组合物，以及将其用作抗凝血剂治疗和预防血栓症障碍的方法。
• Aryl sulfonic pyridoxines as antiplatelet agents
  申请人：Haque Wasimul

  公开号：US20060094748A1

  公开（公告）日：2006-05-04

  Aryl sulfonic pyridoxine compounds with antiplatelet aggregation characteristics for the treatment of cardiovascular and cardiovascular related disease, are described. The methods are directed to administering pharmaceutical compositions comprising aryl sulfonic pyridoxines.

  描述了具有抗血小板聚集特性的芳基磺酸吡哆醇化合物，用于治疗心血管和心血管相关疾病。该方法涉及给予含有芳基磺酸吡哆醇的药物组合物。
• [EN] 3-AMINOCYCLOPENTANE CARBOXAMIDE DERIVATIVES<br/>[FR] DÉRIVÉS DE 3-AMINOCYCLOPENTANE CARBOXAMIDE
  申请人：MERCK PATENT GMBH

  公开号：WO2014075754A1

  公开（公告）日：2014-05-22

  Compounds of the formula (I) in which R1, R4, R, X1, X2, X3, X4, q and W have the meanings indicated in Claim 1, are inhibitors of fatty acid synthase, and can be employed, inter alia, for the treatment of diseases such as cancer, cardiovascular diseases, central nervous system injury and different forms of inflammation.

  式（I）中R1、R4、R、X1、X2、X3、X4、q和W的含义如权利要求1所示，是脂肪酸合成酶的抑制剂，可用于治疗癌症、心血管疾病、中枢神经系统损伤和不同形式的炎症等疾病。
• [EN] BENZAMIDES AND RELATED INHIBITORS OF FACTOR Xa<br/>[FR] BENZAMIDES ET INHIBITEURS ASSOCIES DU FACTEUR XA
  申请人：COR THERAPEUTICS INC

  公开号：WO2001064643A2

  公开（公告）日：2001-09-07

  Benzamide compounds of the formulae (VI) and (VII), where the variables are as defined in the claims, including their pharmaceutically acceptable isomers, salts, hydrates, solvates and prodrug derivatives having activity against mammalian factor Xa are described. Compositions containing such compounds are also described. The compounds and compositions are useful in vitro or in vivo for preventing or treating coagulation disorders.

  本文描述了公式（VI）和（VII）的苯甲酰胺化合物，其中变量如权利要求书中所定义，包括其药学上可接受的异构体、盐、水合物、溶剂合物和前药衍生物，具有对哺乳动物因子Xa的活性。还描述了含有这些化合物的组合物。这些化合物和组合物在体内或体外用于预防或治疗凝血障碍。