tert-butyl N-[5-[(E)-2-(5-tert-butyl-1,3-oxazol-2-yl)ethenyl]-1,3-thiazol-2-yl]carbamate | 252661-91-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: tert-butyl N-[5-[(E)-2-(5-tert-butyl-1,3-oxazol-2-yl)ethenyl]-1,3-thiazol-2-yl]carbamate
• CAS: 252661-91-9
• 化学式: C₁₇H₂₃N₃O₃S
• 分子量: 349.454
• InChiKey: BQYTUIZAVJUJLF-BQYQJAHWSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.3
• 重原子数：
  24
• 可旋转键数：
  6
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.47
• 拓扑面积：
  106
• 氢给体数：
  1
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  tert-butyl N-[5-[(E)-2-(5-tert-butyl-1,3-oxazol-2-yl)ethenyl]-1,3-thiazol-2-yl]carbamate 在 盐酸 、 亚硝酸特丁酯 、 N,N-二异丙基乙胺 、 copper(ll) bromide 作用下， 以 1,4-二氧六环 、 N-甲基吡咯烷酮 、 甲醇 、 乙腈 为溶剂， 反应 4.0h， 生成 (R,E)-tert-butyl-3-(5-(2-(5-tert-butyloxazol-2-yl)vinyl)thiazol-2-ylamino)piperidine-1-carboxylate
  参考文献：
  名称：

  [EN] INHIBITORS OF CYCLIN-DEPENDENT KINASES
  [FR] INHIBITEURS DE KINASES CYCLINE-DÉPENDANTES

  摘要：

  公开号：

  WO2017044858A3
• 作为产物：
  描述：

  5-叔丁基-2-(氯甲基)恶唑 在 potassium tert-butylate 作用下， 以 四氢呋喃 为溶剂， 反应 0.17h， 生成 tert-butyl N-[5-[(E)-2-(5-tert-butyl-1,3-oxazol-2-yl)ethenyl]-1,3-thiazol-2-yl]carbamate
  参考文献：
  名称：

  [EN] INHIBITORS OF CYCLIN-DEPENDENT KINASES
  [FR] INHIBITEURS DE KINASES CYCLINE-DÉPENDANTES

  摘要：

  公开号：

  WO2017044858A3

文献信息

• Carbon substituted aminothiazole inhibitors of cyclin dependent kinases
  申请人：——

  公开号：US20020165259A1

  公开（公告）日：2002-11-07

  Compounds of the formula 1 and pharmaceutically acceptable salts thereof. As used in formula I, and throughout the specification, the symbols have the following meanings: R 1 ═R 2 , COR 3 , CONH 2 , CONR 2 R 3 , COOR 2 , or SO 2 R 2 ; R 2 =alkyl, cycloalkyl, heterocycloalkyl, cycloalkylalkyl, heterocycloalkylalkyl, aryl, heteroaryl, arylalkyl, heteroarylalkyl; R 3 ═H, alkyl, cycloalkyl, heterocycloalkyl, cycloalkylalkyl, heterocycloalkylalkyl, aryl, heteroaryl, arylalkyl, heteroarylalkyl; 2 , where n=0,1,2; m=1,2 but both n and m cannot be 2, or , where i, j=0 or 1 but cannot both be 1, and Y=optionally substituted alkene, alkyne, or any 2 adjacent carbon atoms of a cycloalkyl or cycloheteroalkyl ring of 3-7 atoms; R 4 =alkyl with two or more carbon atoms, cycloalkyl, heterocycloalkyl, cycloalkylalkyl, heterocycloalkylalkyl, aryl, heteroaryl, arylalkyl, heteroarylalkyl, or R 9 with the proviso that when R 1 is acetyl or propionyl and Y=alkene, then R 4 cannot be nitrofuryl or 2-quinolinyl; R 5 , R 6 , R 7 , R 8 =independently H, alkyl, cycloalkyl, heterocycloalkyl, cycloalkylalkyl, heterocycloalkylalkyl, aryl, heteroaryl, arylalkyl, heteroarylalkyl, halo, or hydroxy, alkoxy, amino, NR 12 R 13 , thio, or alkylthio with the proviso that only one such heteroatom group is bonded to any one carbon atom; R 9 = 3 where Z═O, NR 14 , S; R 10 , R 11 =independently H, alkyl, cycloalkyl, heterocycloalkyl, cycloalkylalkyl, heterocycloalkylalkyl, aryl, heteroaryl, arylalkyl, heteroarylalkyl, halo, hydroxy, alkoxy, alkylcarbonyloxy, carboxy, alkyloxycarbonyl, amino, NR 15 R 16 , carbamoyl, ureido, thio, or alkylthio; R 12 , R 13 , R 14 , R 15 , R 16 =independently H, alkyl, cycloalkyl, heterocycloalkyl, cycloalkylalkyl, heterocycloalkylalkyl, aryl, heteroaryl, arylalkyl, or heteroarylalkyl. The compounds of formula I are protein kinase inhibitors and are useful in the treatment of proliferative diseases, for example, cancer, inflammation and arthritis. They may also be useful in the treatment of Alzheimer's disease, and cardiovascular disease.

  公式1的化合物及其药学上可接受的盐。在公式I中使用的符号具有以下含义：R1═R2、COR3、CONH2、CONR2R3、COOR2或SO2R2；R2=烷基、环烷基、杂环烷基、环烷基烷基、杂环烷基烷基、芳基、杂芳基、芳基烷基、杂芳基烷基；R3═H、烷基、环烷基、杂环烷基、环烷基烷基、杂环烷基烷基、芳基、杂芳基、芳基烷基、杂芳基烷基；2，其中n=0、1、2；m=1、2，但n和m不能都为2，或者，当i、j=0或1但不能都为1时，Y=可选取代烯烃、炔烃或3-7原子的环烷基或环杂环烷基中的任意两个相邻碳原子；R4=具有两个或更多碳原子的烷基、环烷基、杂环烷基、环烷基烷基、杂环烷基烷基、芳基、杂芳基、芳基烷基、杂芳基烷基或R9，但当R1为乙酰基或丙酰基且Y=烯烃时，R4不能为硝基呋喃基或2-喹啉基；R5、R6、R7、R8=独立地为H、烷基、环烷基、杂环烷基、环烷基烷基、杂环烷基烷基、芳基、杂芳基、芳基烷基、杂芳基烷基、卤素、羟基、烷氧基、氨基、NR12R13、硫醚或烷基硫醚，但只有一个这样的杂原子基团与任何一个碳原子相结合；R9=3，其中Z═O、NR14、S；R10、R11=独立地为H、烷基、环烷基、杂环烷基、环烷基烷基、杂环烷基烷基、芳基、杂芳基、芳基烷基、杂芳基烷基、卤素、羟基、烷氧基、烷基羰氧基、羧基、烷氧羰基、氨基、NR15R16、氨基甲酰、脲基、硫醚或烷基硫醚；R12、R13、R14、R15、R16=独立地为H、烷基、环烷基、杂环烷基、环烷基烷基、杂环烷基烷基、芳基、杂芳基、芳基烷基或杂芳基烷基。公式I的化合物是蛋白激酶抑制剂，可用于治疗增生性疾病，例如癌症、炎症和关节炎。它们也可能对治疗阿尔茨海默病和心血管疾病有用。
• INHIBITORS OF CYCLIN-DEPENDENT KINASES
  申请人：Dana-Farber Cancer Institute, Inc.

  公开号：EP4019515A1

  公开（公告）日：2022-06-29

  The present invention provides novel compounds of Formulae (I'), (I), (II'), and (II), and pharmaceutically acceptable salts, solvates, hydrates, polymorphs, co-crystals, tautomers, stereoisomers, isotopically labeled derivatives, prodrugs, and compositions thereof. Also provided are methods and kits involving the inventive compounds or compositions for treating and/or preventing proliferative diseases (e.g., cancers (e.g., leukemia, acute lymphoblastic leukemia, lymphoma, Burkitt's lymphoma, melanoma, multiple myeloma, breast cancer, Ewing's sarcoma, osteosarcoma, brain cancer, ovarian cancer, neuroblastoma, lung cancer, colorectal cancer), benign neoplasms, diseases associated with angiogenesis, inflammatory diseases, autoinflammatory diseases, and autoimmune diseases) in a subject. Treatment of a subject with a proliferative disease using a compound or composition of the invention may inhibit the aberrant activity of a kinase, such as a cyclin-dependent kinase (CDK) (e.g., CDK7, CDK12, or CDK13), and therefore, induce cellular apoptosis and/or inhibit transcription in the subject.

  本发明提供了式(I')、(I)、(II')和(II)的新型化合物及其药学上可接受的盐、溶液剂、水合物、多晶型、共晶体、同分异构体、立体异构体、同位素标记的衍生物、原药及其组合物。还提供了涉及本发明化合物或组合物的方法和试剂盒，用于治疗和/或预防增殖性疾病（如癌症（如、白血病、急性淋巴细胞白血病、淋巴瘤、伯基特淋巴瘤、黑色素瘤、多发性骨髓瘤、乳腺癌、尤文氏肉瘤、骨肉瘤、脑癌、卵巢癌、神经母细胞瘤、肺癌、结直肠癌）、良性肿瘤、与血管生成相关的疾病、炎症性疾病、自身炎症性疾病和自身免疫性疾病）的方法和试剂盒。使用本发明的化合物或组合物治疗患有增殖性疾病的受试者，可抑制激酶的异常活性，如细胞周期蛋白依赖性激酶（CDK）（如CDK7、CDK12或CDK13），从而诱导细胞凋亡和/或抑制受试者的转录。
• Inhibitors of cyclin-dependent kinases
  申请人：Dana-Farber Cancer Institute, Inc.

  公开号：US11142507B2

  公开（公告）日：2021-10-12

  The present invention provides novel compounds of Formulae (I′), (I), (II′), and (II), and pharmaceutically acceptable salts, solvates, hydrates, polymorphs, co-crystals, tautomers, stereoisomers, isotopically labeled derivatives, prodrugs, and compositions thereof. Also provided are methods and kits involving the inventive compounds or compositions for treating and/or preventing proliferative diseases (e.g., cancers (e.g., leukemia, acute lymphoblastic leukemia, lymphoma, Burkitt's lymphoma, melanoma, multiple myeloma, breast cancer, Ewing's sarcoma, osteosarcoma, brain cancer, ovarian cancer, neuroblastoma, lung cancer, colorectal cancer), benign neoplasms, diseases associated with angiogenesis, inflammatory diseases, autoinflammatory diseases, and autoimmune diseases) in a subject. Treatment of a subject with a proliferative disease using a compound or composition of the invention may inhibit the aberrant activity of a kinase, such as a cyclin-dependent kinase (CDK) (e.g., CDK7, CDK12, or CDK13), and therefore, induce cellular apoptosis and/or inhibit transcription in the subject.

  本发明提供了式(I′)、(I)、(II′)和(II)的新型化合物及其药学上可接受的盐、溶液剂、水合物、多晶型、共晶体、同系物、立体异构体、同位素标记的衍生物、原药及其组合物。还提供了涉及本发明化合物或组合物的方法和试剂盒，用于治疗和/或预防增殖性疾病（如癌症（如、白血病、急性淋巴细胞白血病、淋巴瘤、伯基特淋巴瘤、黑色素瘤、多发性骨髓瘤、乳腺癌、尤文氏肉瘤、骨肉瘤、脑癌、卵巢癌、神经母细胞瘤、肺癌、结直肠癌）、良性肿瘤、与血管生成相关的疾病、炎症性疾病、自身炎症性疾病和自身免疫性疾病）的方法和试剂盒。使用本发明的化合物或组合物治疗患有增殖性疾病的受试者，可抑制激酶的异常活性，如细胞周期蛋白依赖性激酶（CDK）（如CDK7、CDK12或CDK13），从而诱导细胞凋亡和/或抑制受试者的转录。
• CARBON SUBSTITUTED AMINOTHIAZOLE INHIBITORS OF CYCLIN DEPENDENT KINASES
  申请人：BRISTOL-MYERS SQUIBB COMPANY

  公开号：EP1087951B1

  公开（公告）日：2005-02-09
• US6407124B1
  申请人：——

  公开号：US6407124B1

  公开（公告）日：2002-06-18