2-Amino-6-benzoyl-4,5,6,7-tetrahydro-thieno[2,3-c]pyridine-3-carboxylic acid ethyl ester | 243967-93-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 噻吩并吡啶类
• 英文名称: 2-Amino-6-benzoyl-4,5,6,7-tetrahydro-thieno[2,3-c]pyridine-3-carboxylic acid ethyl ester
• 英文别名: Ethyl 2-amino-6-benzoyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3-carboxylate；ethyl 2-amino-6-benzoyl-5,7-dihydro-4H-thieno[2,3-c]pyridine-3-carboxylate
• CAS: 243967-93-3
• 化学式: C₁₇H₁₈N₂O₃S
• 分子量: 330.408
• InChiKey: LJQMAGPFTGJEIH-UHFFFAOYSA-N

物化性质

• 熔点：
  203-205
• 沸点：
  569.6±50.0 °C(Predicted)
• 密度：
  1.318±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：
  4
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.29
• 拓扑面积：
  101
• 氢给体数：
  1
• 氢受体数：
  5

安全信息

• 危险等级：
  IRRITANT
• 海关编码：
  2934999090

反应信息

• 作为反应物：
  描述：

  乙基N-[二(甲硫基)亚甲基]甘氨酸酯 、 2-Amino-6-benzoyl-4,5,6,7-tetrahydro-thieno[2,3-c]pyridine-3-carboxylic acid ethyl ester 在 溶剂黄146 作用下， 反应 4.0h， 以40%的产率得到3,4,5,6,7,8-hexahydro-2-methylthio-4-oxo-7-phenylmethylpyrido<4',3':4,5>thieno<2,3-d>pyrimidine-3(4H)-acetic acid ethyl ester
  参考文献：
  名称：

  N-[bis(methylthio)methylene]amino Ester (BMMA): Novel Reagents for Annelation of Pyrimidine Moieties

  摘要：

  New reagents for heterocyclic annelations containing a N-[bis(methylthio)methylene]amino moiety (=BMMA) were developed and studied regarding their scope and limitations: one-pot reaction with (hetero)aromatic ortho-aminocarbonyl-type model compounds (''carbonyl'' = COOEt, COMe and CN) to a series of new benzo- or thieno-condensed pyrimidines, pyrrolo[1,2-c]pyrimidines, imidazo[1,2-c]pyrimidines and 1,2,4-triazolo[1,5-c]pyrimidines, depending on the reagent used [(MeS)(2)C=N-R with R = CH2-COOEt, CH(2)CH(2)COOEt, NH-COOEt].

  DOI：

  10.3987/com-94-s86
• 作为产物：
  描述：

  1-苯酰基-4-哌啶酮 、 氰乙酸乙酯 在 sulfur 、 三乙胺 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 生成 2-Amino-6-benzoyl-4,5,6,7-tetrahydro-thieno[2,3-c]pyridine-3-carboxylic acid ethyl ester
  参考文献：
  名称：

  Synthesis and bioactivities of novel bicyclic thiophenes and 4,5,6,7-tetrahydrothieno[2,3-c]pyridines as inhibitors of tumor necrosis factor-α (TNF-α) production

  摘要：

  We synthesized bicyclic thiophenes and 4,5,6,7-tetrahydrothieno[2,3-c]pyridine derivatives, and evaluated for their ability to inhibit LPS-stimulated production of TNF-alpha. Several compounds revealed excellent in vivo activity. Furthermore, an effective compound was found in adjuvant-induced arthritic model (AIA) of rat. (C) 2002 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(02)00332-3

文献信息

• [EN] THIENOPYRIMIDINE INHIBITORS OF ATYPICAL PROTEIN KINASE C<br/>[FR] INHIBITEURS DE TYPE THIÉNOPYRIMIDINE DE PROTÉINES KINASES C ATYPIQUES
  申请人：CANCER REC TECH LTD

  公开号：WO2013078126A1

  公开（公告）日：2013-05-30

  The present invention provides a compound of formula (I) or a salt thereof, wherein R1, R2, R3, R4, R5, R6, A, G, M, Q and X are as defined herein. A compound of formula (I) and its salts have a PKC inhibitory activity, and may be used to treat proliferative disorders.

  本发明提供了一种式（I）的化合物或其盐，其中R1、R2、R3、R4、R5、R6、A、G、M、Q和X如本文所定义。式（I）的化合物及其盐具有PKC抑制活性，并可用于治疗增生性疾病。
• [EN] MODULATORS OF PROTEIN TYROSINE PHOSPHATASES<br/>[FR] MODULATEURS DE PROTEINE-TYROSINE-PHOSPHATASES
  申请人：NOVO NORDISK A/S

  公开号：WO1999046237A1

  公开（公告）日：1999-09-16

  (EN) The present invention provides novel compounds, novel compositions, methods of their use, and methods of their manufacture, where such compounds are pharmacologically useful inhibitors of Protein Tyrosine Phosphatases (PTPases, PTPs) such as PTP1B, TC-PTP, CD45, SHP-1, SHP-2, PTP$g(a), PTP$g(e), PTP$g(m), PTP$g(d), PTP$g(s), PTP$g(z), PTP$g(b), PTPD1, PTPD2, PTPH1, PTP-MEG1, PTP-LAR, and HePTP. These compounds are indicated in the management or treatment of a broad range of diseases such as autoimmune diseases, acute and chronic inflammation, osteoporosis, various forms of cancer and malignant diseases, and type I diabetes and type II diabetes.(FR) Cette invention se rapporte à de nouveaux composés, à de nouvelles compositions, à des procédés pour leur utilisation et à des procédés pour leur fabrication, ces composés constituant des inhibiteurs pharmacologiquement utiles des protéine-tyrosine-phosphatases (PTPases, PTP) telles que PTP1B, TC-PTP, CD45, SHP-1, SHP-2, PTP$g(a), PTP$g(e), PTP$g(m), PTP$g(d), PTP$g(s), PTP$g(z), PTP$g(b), PTPD1, PTPD2, PTPH1, PTP-MEG1, PTP-LAR ET HePTP. Ces composés sont indiqués dans la prise en charge ou le traitement d'une large gamme de maladies, telles que les maladies auto-immunes, les inflammations aiguës et chroniques, l'ostéoporose, diverses formes de cancer et d'affections malignes, ainsi que le diabète de type I et le diabète de type II.

  本发明提供了新型化合物、新型组合物、它们的使用方法和制造方法，这些化合物是药理学上有用的蛋白酪氨酸磷酸酶（PTPases，PTPs）抑制剂，如PTP1B、TC-PTP、CD45、SHP-1、SHP-2、PTP $g（a）、PTP $g（e）、PTP $g（m）、PTP $g（d）、PTP $g（s）、PTP $g（z）、PTP $g（b）、PTPD1、PTPD2、PTPH1、PTP-MEG1、PTP-LAR和HePTP。这些化合物适用于治疗广泛的疾病，如自身免疫疾病、急性和慢性炎症、骨质疏松症、各种癌症和恶性疾病，以及1型和2型糖尿病的管理或治疗。
• [EN] MODULATORS OF PROTEIN TYROSINE PHOSPHATASES (PTPASES)<br/>[FR] MODULATEURS DE PROTEINE TYROSINE PHOSPHATASES (PTPASES)
  申请人：NOVO NORDISK A/S

  公开号：WO1999046267A1

  公开（公告）日：1999-09-16

  (EN) The present invention provides novel compounds, novel compositions, methods of their use, and methods of their manufacture, where such compounds are pharmacologically useful inhibitors of Protein Tyrosine Phosphatases (PTPases) such as PTP1B, CD45, SHP-1, SHP-2, PTP$g(a), LAR and HePTP or the like. The compounds are useful in the treatment of type I diabetes, type II diabetes, impaired glucose tolerance, insulin resistance, obesity, immune dysfunctions including autoimmunity diseases with dysfunctions of the coagulation system, allergic diseases including asthma, osteoporosis, proliferative disorders including cancer and psoriasis, diseases with decreased or increased synthesis or effects of growth hormone, diseases with decreased or increased synthesis of hormones or cytokines that regulate the release of/or response to growth hormone, diseases of the brain including Alzheimer's disease and schizophrenia, and infectious diseases.(FR) L'invention concerne de nouveaux composés, de nouvelles compositions, des méthodes d'utilisation et des méthodes de fabrication associées. Lesdits composés sont des inhibiteurs de protéine tyrosine phosphatases (PTPases) pharmacologiquement utiles, tels que PTP1B, CD45, SHP-1, SHP-2, PTP$g(a), LAR et HePTP ou analogues. Ces composés sont utiles dans le traitement du diabète du type I, du diabète du type II, de l'intolérance au glucose, de la résistance insulinique, de l'obésité, des dysfonctionnements immunitaires parmi lesquels les maladies auto-immunes entraînant un dysfonctionnement du système de coagulation, des maladies allergiques parmi lesquelles l'asthme, de l'ostéoporose, des troubles proliférants parmi lesquels le cancer et le psoriasis, des maladies entraînant une baisse ou une augmentation de la synthèse ou des effets des hormones de croissance, des maladies entraînant une baisse ou une augmentation de la synthèse des hormones ou cytokines qui régulent la libération d'hormones de croissance ou la réaction à ces hormones, des maladies cérébrales parmi lesquelles la maladie d'Alzheimer et la schizophrénie, et des maladies infectieuses.

  该发明提供了新型化合物、新型组合物、它们的使用方法和制备方法，其中这些化合物是药理学上有用的蛋白酪氨酸磷酸酶（PTPases）抑制剂，如PTP1B、CD45、SHP-1、SHP-2、PTP$g(a)、LAR和HePTP等。这些化合物在治疗I型糖尿病、II型糖尿病、糖耐量受损、胰岛素抵抗、肥胖症、免疫功能障碍包括自身免疫疾病与凝血系统功能障碍、包括哮喘等过敏性疾病、骨质疏松症、增生性疾病包括癌症和银屑病、生长激素合成或效应减少或增加的疾病、调节生长激素释放或响应的激素或细胞因子合成减少或增加的疾病、包括阿尔茨海默病和精神分裂症的大脑疾病以及传染性疾病中具有用处。
• Modulators of protein tyrosine phosphatases (PTPases)
  申请人：——

  公开号：US20030069267A1

  公开（公告）日：2003-04-10

  The present invention provides novel compounds, novel compositions, methods of their use, and methods of their manufacture, where such compounds are pharmacologically useful inhibitors of Protein Tyrosine Phosphatases (PTPase's) such as PTP1B, CD45, SHP-1, SHP-2, PTP&agr;, LAR and HePTP or the like. The compounds are useful in the treatment of type I diabetes, type II diabetes, impaired glucose tolerance, insulin resistance, obesity, immune dysfunctions including autoimmunity diseases with dysfunctions of the coagulation system, allergic diseases including asthma, osteoporosis, proliferative disorders including cancer and psoriasis, diseases with decreased or increased synthesis or effects of growth hormone, diseases with decreased or increased synthesis of hormones or cytokines that regulate the release of/or response to growth hormone, diseases of the brain including Alzheimer's disease and schizophrenia, and infectious diseases.

  本发明提供了新型化合物、新型组合物、它们的使用方法和制造方法，其中这些化合物是药理学上有用的蛋白酪氨酸磷酸酶（PTPase's）抑制剂，如PTP1B、CD45、SHP-1、SHP-2、PTP&agr;、LAR和HePTP等。这些化合物可用于治疗I型糖尿病、II型糖尿病、糖耐量受损、胰岛素抵抗、肥胖症、免疫功能障碍，包括凝血系统功能障碍的自身免疫性疾病、包括哮喘在内的过敏性疾病、骨质疏松症、增生性疾病，包括癌症和银屑病、合成减少或增加或对生长激素释放或响应调节的激素或细胞因子的疾病，包括阿尔茨海默病和精神分裂症的脑部疾病以及传染病。
• Thienopyrimidine Inhibitors of Atypical Protein Kinase C
  申请人：Cancer Research Technology Limited

  公开号：US20140323435A1

  公开（公告）日：2014-10-30

  The present application provides a compound of formula (I) or a salt thereof, wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , A, G, M, Q and X are as defined herein. A compound of formula (I) and its salts have aPKC inhibitory activity, and may be used to treat proliferative disorders.

  本申请提供了公式（I）的化合物或其盐，其中R1、R2、R3、R4、R5、R6、A、G、M、Q和X的定义如本文所述。公式（I）的化合物及其盐具有aPKC抑制活性，可用于治疗增殖性疾病。