N-(3-bromophenyl)thieno[3,2-d]pyrimidin-4-amine

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 噻吩并嘧啶酮衍生物
• 英文名称: N-(3-bromophenyl)thieno[3,2-d]pyrimidin-4-amine
• 化学式: C₁₂H₈BrN₃S
• 分子量: 306.186
• InChiKey: IKDNMRVPNRIVPS-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.4
• 重原子数：
  17
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  66
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  3-氨基噻吩-2-甲酰胺 在 盐酸 、 三氯氧磷 作用下， 以 四氢呋喃 、 异丙醇 为溶剂， 反应 6.0h， 生成 N-(3-bromophenyl)thieno[3,2-d]pyrimidin-4-amine
  参考文献：
  名称：

  A FACILE SYNTHESIS OF NEW 4-(PHENYLAMINO)THIENO[3,2-d]PYRIMIDINES USING 3-AMINOTHIOPHENE-2-CARBOXAMIDE

  摘要：

  DOI：

  10.1515/hc.2007.13.1.33

文献信息

• N-aryl-thienopyrimidin-4-amines and analogs as activators of caspases and inducers of apoptosis and the use thereof
  申请人：Cai Xiong Sui

  公开号：US20070099877A1

  公开（公告）日：2007-05-03

  Disclosed are N-aryl-thienopyrimidin-4-amines and analogs thereof, represented by the Formulae I-II: wherein Ar and R 1 -R 4 are defined herein. The present invention relates to the discovery that compounds having Formulae I-II are activators of caspases and inducers of apoptosis. Therefore, the activators of caspases and inducers of apoptosis of this invention may be used to induce cell death in a variety of clinical conditions in which uncontrolled growth and spread of abnormal cells occurs.

  揭示了N-芳基噻吩吡嘧啶-4-胺及其类似物，由以下的式子I-II表示：其中Ar和R1-R4在此有所定义。本发明涉及发现具有式子I-II的化合物是半胱氨酸蛋白酶的激活剂和凋亡诱导剂。因此，本发明的半胱氨酸蛋白酶激活剂和凋亡诱导剂可用于诱导在各种临床病况中发生细胞死亡，这些病况中存在细胞不受控制的生长和异常细胞的扩散。
• N-arylalkyl-thienopyrimidin-4-amines and analogs as activators of caspases and inducers of apoptosis and the use thereof
  申请人：Cai Xiong Sui

  公开号：US20070099941A1

  公开（公告）日：2007-05-03

  Disclosed are N-arylalkyl-thienopyrimidin-4-amines and analogs thereof, represented by the Formula I: wherein Ar, R 1 , R 3 , R 4 , R 10 -R 12 and n are defined herein. The present invention relates to the discovery that compounds having Formula I are activators of caspases and inducers of apoptosis. Therefore, the activators of caspases and inducers of apoptosis of this invention may be used to induce cell death in a variety of clinical conditions in which uncontrolled growth and spread of abnormal cells occurs.

  揭示了N-芳基烷基噻吩嘧啶-4-胺及其类似物，其化学式如下：其中Ar、R1、R3、R4、R10-R12和n在此处定义。本发明涉及发现具有化学式I的化合物是caspase的激活剂和凋亡诱导剂。因此，本发明的caspase激活剂和凋亡诱导剂可用于诱导细胞死亡，在发生异常细胞的不受控制的生长和扩散的各种临床情况中。
• N-alkyl-N-aryl-thienopyrimidin-4-amines and analogs as activators of caspases and inducers of apoptosis and the use thereof
  申请人：Cai Xiong Sui

  公开号：US20070213305A1

  公开（公告）日：2007-09-13

  Disclosed are N-alkyl-N-aryl-thienopyrimidin-4-amines and analogs thereof, represented by the Formulae I-II: wherein Ar, R 1 -R 4 and R 10 are defined herein. The present invention relates to the discovery that compounds having Formulae I-II are activators of caspases and inducers of apoptosis. Therefore, the activators of caspases and inducers of apoptosis of this invention may be used to induce cell death in a variety of clinical conditions in which uncontrolled growth and spread of abnormal cells occurs.

  本发明涉及公开的N-烷基-N-芳基噻唑嘧啶-4-胺及其类似物，其由式I-II表示：其中Ar、R1-R4和R10如本文所定义。本发明关于发现具有式I-II的化合物是caspase的激活剂和凋亡诱导剂。因此，本发明的caspase激活剂和凋亡诱导剂可用于在多种临床情况下诱导细胞死亡，其中发生异常细胞的不受控制的生长和扩散。
• BICYCLIC COMPOUNDS CAPABLE OF INHIBITING TYROSINE KINASES OF THE EPIDERMAL GROWTH FACTOR RECEPTOR FAMILY
  申请人：WARNER-LAMBERT COMPANY

  公开号：EP0742717A1

  公开（公告）日：1996-11-20
• [EN] BICYCLIC COMPOUNDS CAPABLE OF INHIBITING TYROSINE KINASES OF THE EPIDERMAL GROWTH FACTOR RECEPTOR FAMILY<br/>[FR] COMPOSES BICYCLIQUES PERMETTANT D'INHIBER LES TYROSINE-KINASES DE LA FAMILLE DU RECEPTEUR DU FACTEUR DE CROISSANCE DE L'EPIDERME
  申请人：WARNER-LAMBERT COMPANY

  公开号：WO1995019774A1

  公开（公告）日：1995-07-27

  (EN) Epidermal growth factor inhibitors of formula (1), where: at least one, and as many as three of A-E are nitrogen, with the remaining atom(s) carbon, or any two contiguous positions in A-E taken together can be a single heteroatom, N, O or S, in which case one of the two remaining atoms must be carbon, and the other can be either carbon or nitrogen; X = O, S, NH or NR7, such that R7 = lower alkyl (1-4 carbon atoms), OH, NH2, lower alkoxy (1-4 carbon atoms) or lower monoalkylamino (1-4 carbon atoms); n = 0, 1, 2.(FR) Sont décrits des inhibiteurs du facteur de croissance de l'épiderme, de formule (1) dans laquelle au moins un, et jusqu'à trois termes parmi A-E sont azote, le ou les atome(s) restant(s) étant du carbone, ou bien deux positions contiguës quelconques dans A-E peuvent former ensemble un seul hétéroatome, N, O ou S, auquel cas l'un des deux atomes restants doit être du carbone, et l'autre peut être soit du carbone soit de l'azote; X = O, S, NH ou bien NR7, de sorte que R7 = alkyle inférieur (1-4 atomes de carbone), O, H, NH2, alcoxy inférieur (1-4 atomes de carbone) ou bien monoalkylamino inférieur (1-4 atomes de carbone); n = 0, 1, 2.