4-(2-chloropyrimidin-4-yl)thiomorpholine | 56032-11-2

• 分子结构分类: 有机化合物 - 有机氮化合物
• 英文名称: 4-(2-chloropyrimidin-4-yl)thiomorpholine
• CAS: 56032-11-2
• 化学式: C₈H₁₀ClN₃S
• mdl: MFCD16712444
• 分子量: 215.706
• InChiKey: RPWSDNURTKMYOG-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2
• 重原子数：
  13
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  54.3
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  4-(2-chloropyrimidin-4-yl)thiomorpholine 在 盐酸 、 potassium carbonate 、 溶剂黄146 、 potassium iodide 作用下， 以 N,N-二甲基甲酰胺 、 正丁醇 为溶剂， 反应 14.0h， 生成 N-(4-(3-(piperidin-1-yl)propoxy)phenyl)-4-thiomorpholinopyrimidin-2-amine
  参考文献：
  名称：

  Discovery and SAR studies of novel 2-anilinopyrimidine-based selective inhibitors against triple-negative breast cancer cell line MDA-MB-468

  摘要：

  Triple-negative breast cancers (TNBCs) are characterized as an invasive and intractable subtype of breast cancers. Overexpression of epidermal growth factor receptor (EGFR) has been considered to be an important target for TNBC therapy, but efficacies of EGFR inhibitors in clinical trials are elusive. In this study, novel series of 2-anilinopyrimidines were synthesized in an effort to identify selective inhibitors against an EGFR-overexpressing TNBC cell line. Biological evaluation demonstrated that compounds 21 and 38, with a 4-methylpiperidine group and a high ClogP value, exhibited good potency and selectivity for the TNBC cell line. This study has provided evidence to support further development of 2-anilinopyrimidine-based TNBC selective inhibitors and investigation of the targets of compounds 21 and 38.

  DOI：

  10.1016/j.bmcl.2018.11.010
• 作为产物：
  描述：

  硫代吗啉 、 2,4-二氯嘧啶 以 乙醇 为溶剂， 生成 4-(2-chloropyrimidin-4-yl)thiomorpholine
  参考文献：
  名称：

  SAR优化研究了一系列新型的2-苯胺基嘧啶类化合物作为针对三阴性乳腺癌细胞MDA-MB-468的选择性抑制剂。

  摘要：

  三阴性乳腺癌（TNBC）约占乳腺癌病例的15％，并且表现出侵略性的临床行为。在这项研究中，我们基于先前报道的化合物1的结构设计和合成了两个系列的2-苯胺基嘧啶，它们可作为基础样TNBC细胞系MDA-MB-468的选择性抑制剂。通过对1的精细调节，发现嘧啶核4位的环状和无环胺对于选择性至关重要。对类似物的结构-活性关系的广泛分析表明，丙基链末端的氨基烷基易于修饰。在新合成的类似物中，带有4-氯哌啶和环己基的化合物38被发现是最有效和最具选择性的，

  DOI：

  10.1016/j.bmcl.2019.126752

文献信息

• [EN] PYRIMIDINE COMPOUNDS THAT INHIBIT ANAPLASTIC LYMPHOMA KINASE<br/>[FR] COMPOSÉS PYRIMIDINE QUI INHIBENT LA KINASE DU LYMPHOME ANAPLASIQUE
  申请人：AMGEN INC

  公开号：WO2011143033A1

  公开（公告）日：2011-11-17

  Compounds of Formula I are useful inhibitors of anaplastic lymphoma kinase. Compounds of Formula I have the following structure: where the definitions of the variables are provided herein.

  Formula I的化合物是一种有用的间变性淋巴瘤激酶抑制剂。Formula I的化合物具有以下结构：变量的定义在此提供。
• SAR optimization studies on a novel series of 2-anilinopyrimidines as selective inhibitors against triple-negative breast cancer cell line MDA-MB-468
  作者：Jeyun Jo、Heegyu Kim、Ji Youn Oh、Soyeong Kim、Yeong Hye Park、Hyeonjin Choi、Jee-Yeong Jeong、Young-Suk Jung、Hwayoung Yun

  DOI：10.1016/j.bmcl.2019.126752

  日期：2019.12

  synthesized two series of 2-anilinopyrimidines based on the structure of our previously reported compound 1 that act as a selective inhibitor of the basal-like TNBC cell line MDA-MB-468. Through the fine-tuning of 1, cyclic and acyclic amines at 4-position of the pyrimidine core were turned out to be crucial for the selectivity. An extensive analysis of structure-activity relationships of the analogs revealed

  三阴性乳腺癌（TNBC）约占乳腺癌病例的15％，并且表现出侵略性的临床行为。在这项研究中，我们基于先前报道的化合物1的结构设计和合成了两个系列的2-苯胺基嘧啶，它们可作为基础样TNBC细胞系MDA-MB-468的选择性抑制剂。通过对1的精细调节，发现嘧啶核4位的环状和无环胺对于选择性至关重要。对类似物的结构-活性关系的广泛分析表明，丙基链末端的氨基烷基易于修饰。在新合成的类似物中，带有4-氯哌啶和环己基的化合物38被发现是最有效和最具选择性的，
• 2,4,5,6-Tetrasubstituted pyrimidines and salts thereof
  申请人：Boehringer Ingelheim GmbH

  公开号：US03975384A1

  公开（公告）日：1976-08-17

  Compounds of the formula ##SPC1## Wherein R.sub.1 is alkoxy of 1 to 3 carbon atoms, morpholino, thiomorpholino, 1-oxido-thiomorpholino, 1,1-dioxido-thiomorpholino, or ##EQU1## where A is hydrogen, alkanoyl of 1 to 4 carbon atoms, alkenoyl of 2 to 4 carbon atoms, methoxy-(alkanoyl of 1 to 4 carbon atoms), carboxyl-(alkanoyl of 1 to 4 carbon atoms), acetyl-(alkanoyl of 1 to 4 carbon atoms), methoxy-(alkenoyl of 2 to 4 carbon atoms), carboxyl-(alkenoyl of 2 to 4 carbon atoms), acetyl-(alkenoyl of 2 to 4 carbon atoms), aminocarbonyl, mono(alkyl of 1 to 4 carbon atoms)-aminocarbonyl, di-(alkyl of 1 to 4 carbon atoms)-aminocarbonyl, methoxymethylaminocarbonyl, pyridinoyl, salicyloyl, furanoyl, or (alkyl of 1 to 3 carbon atoms)-sulfonyl, R.sub.2 is morpholino, thiomorpholino, 1-oxido-thiomorpholino, 1,1-dioxido-thiomorpholino, piperazino or N'-[acetyl-(alkanoyl of 1 to 3 arbon atoms)]-piperazino, R.sub.3 is hydrogen, chlorine, bromine, nitro, cyano, formyl, acetyl or carbalkoxy of 2 to 4 carbon atoms, and R.sub.4 is hydrogen, chlorine, bromine, cyano, carbalkoxy of 2 to 4 carbon atoms, alkyl of 1 to 6 carbon atoms, mono(carbalkoxy of 2 to 4 carbon atoms)-alkyl of 1 to 6 carbon atoms, di(carbalkoxy of 2 to 4 carbon atoms)-alkyl of 1 to 6 carbon atoms, hydroxyl, allyloxy, alkoxy of 1 to 6 carbon atoms, mercapto, allylmercapto, (alkyl of 1 to 6 carbon atoms)-mercapto, 1-oxidothiomorpholino, or --NHB where B is hydrogen, alkyl of 1 to 3 carbon atoms, cyclohexyl, phenyl, chloro-phenyl, carboxy-phenyl, carbomethoxy-phenyl or pyridyl, And non-toxic, pharmacologically acceptable acid addition salts thereof; the compounds as well as the salts are useful as antithrombotics.

  化合物的公式为##SPC1##其中R.sub.1是1到3个碳原子的烷氧基，吗啡基，硫环氧基，1-氧代硫环氧基，1,1-二氧代硫环氧基或##EQU1##其中A是氢，1到4个碳原子的烷酰基，2到4个碳原子的烯酰基，甲氧基-(1到4个碳原子的烷酰基)，羧基-(1到4个碳原子的烷酰基)，乙酰基-(1到4个碳原子的烷酰基)，甲氧基-(2到4个碳原子的烯酰基)，羧基-(2到4个碳原子的烯酰基)，乙酰基-(2到4个碳原子的烯酰基)，氨基甲酰基，单(1到4个碳原子的烷基)-氨基甲酰基，双(1到4个碳原子的烷基)-氨基甲酰基，甲氧基甲基氨基甲酰基，吡啶酰基，水杨酰基，呋喃酰基或(1到3个碳原子的烷基)-磺酰基，R.sub.2是吗啡基，硫环氧基，1-氧代硫环氧基，1,1-二氧代硫环氧基，哌嗪基或N'-[乙酰-(1到3个碳原子的烷酰基)]-哌嗪基，R.sub.3是氢，氯，溴，硝基，氰基，甲酰基，乙酰基或2到4个碳原子的羧基烷氧基，R.sub.4是氢，氯，溴，氰基，2到4个碳原子的羧基烷氧基，1到6个碳原子的烷基，单(2到4个碳原子的羧基烷氧基)-1到6个碳原子的烷基，双(2到4个碳原子的羧基烷氧基)-1到6个碳原子的烷基，羟基，丙烯氧基，1到6个碳原子的烷氧基，硫醇基，丙烯硫醇基，(1到6个碳原子的烷基)-硫醇基，1-氧代硫环氧基或--NHB，其中B是氢，1到3个碳原子的烷基，环己基，苯基，氯苯基，羧基苯基，甲氧基苯基或吡啶基，以及其无毒、药理学上可接受的酸盐；这些化合物和盐作为抗血栓剂具有用处。
• US3932387A
  申请人：——

  公开号：US3932387A

  公开（公告）日：1976-01-13
• US3975384A
  申请人：——

  公开号：US3975384A

  公开（公告）日：1976-08-17