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6-溴-1H-苯并[d]咪唑-2-氨基甲酸甲酯 | 78695-17-7

中文名称
6-溴-1H-苯并[d]咪唑-2-氨基甲酸甲酯
中文别名
——
英文名称
methyl 6-bromo-1H-benzo[d]imidazol-2-ylcarbamate
英文别名
methyl N-(6-bromo-1H-benzimidazol-2-yl)carbamate
6-溴-1H-苯并[d]咪唑-2-氨基甲酸甲酯化学式
CAS
78695-17-7
化学式
C9H8BrN3O2
mdl
——
分子量
270.085
InChiKey
CLOUFUJTHZGQMB-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 密度:
    1.791±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.2
  • 重原子数:
    15
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.11
  • 拓扑面积:
    67
  • 氢给体数:
    2
  • 氢受体数:
    3

SDS

SDS:6affdd8dc4d9682acc5a1249135e9d6e
查看

反应信息

  • 作为反应物:
    描述:
    二碳酸二叔丁酯6-溴-1H-苯并[d]咪唑-2-氨基甲酸甲酯4-二甲氨基吡啶N,N-二异丙基乙胺 作用下, 以 氯仿 为溶剂, 反应 2.0h, 以58%的产率得到tert-butyl 6-bromo-2-(tert-butoxycarbonyl(methoxycarbonyl)amino)-1H-benzo[d]imidazole-1-carboxylate
    参考文献:
    名称:
    [EN] BENZOXAZEPINES AS INHIBITORS OF PI3K/m TOR AND METHODS OF THEIR USE AND MANUFACTURE
    [FR] BENZOXAZÉPINES COMME INHIBITEURS DE PI3K/M TOR, MÉTHODES D'UTILISATION ET DE FABRICATION BENZOXAZEPINES AS INHIBITORS OF PI3K/M TOR AND METHODS OF THEIR USE AND MANUFACTURE
    摘要:
    这项发明涉及式(I)的化合物:该发明提供了抑制、调节和/或调节P13K和/或mTOR的化合物,这些化合物在治疗哺乳动物的高增殖性疾病,如癌症,方面非常有用。该发明还提供了制备该化合物的方法,以及在治疗哺乳动物,特别是人类的高增殖性疾病中使用这些化合物的方法,以及含有这些化合物的药物组合物。例如,对PI3fC-α mTOR或两者都具有活性有助于其病理学和/或症状学的癌症包括乳腺癌、套细胞淋巴瘤、肾细胞癌、急性髓细胞白血病、慢性髓细胞白血病、NPM/ALK转化的间变性大细胞淋巴瘤、弥漫性大B细胞淋巴瘤、横纹肌肉瘤、卵巢癌、子宫内膜癌、宫颈癌、非小细胞肺癌、小细胞肺癌、腺癌、结肠癌、直肠癌、胃癌、肝细胞癌、黑色素瘤、胰腺癌、前列腺癌、甲状腺癌、间变性大细胞淋巴瘤、血管瘤、胶质母细胞瘤或头颈癌。
    公开号:
    WO2010138487A1
  • 作为产物:
    描述:
    1,3-二羧甲基-2-甲基-2-硫代异脲4-溴邻苯二胺甲醇乙二醇二甲醚 为溶剂, 反应 12.0h, 以77%的产率得到6-溴-1H-苯并[d]咪唑-2-氨基甲酸甲酯
    参考文献:
    名称:
    [EN] BENZOXAZEPINES AS INHIBITORS OF PI3K/m TOR AND METHODS OF THEIR USE AND MANUFACTURE
    [FR] BENZOXAZÉPINES COMME INHIBITEURS DE PI3K/M TOR, MÉTHODES D'UTILISATION ET DE FABRICATION BENZOXAZEPINES AS INHIBITORS OF PI3K/M TOR AND METHODS OF THEIR USE AND MANUFACTURE
    摘要:
    这项发明涉及式(I)的化合物:该发明提供了抑制、调节和/或调节P13K和/或mTOR的化合物,这些化合物在治疗哺乳动物的高增殖性疾病,如癌症,方面非常有用。该发明还提供了制备该化合物的方法,以及在治疗哺乳动物,特别是人类的高增殖性疾病中使用这些化合物的方法,以及含有这些化合物的药物组合物。例如,对PI3fC-α mTOR或两者都具有活性有助于其病理学和/或症状学的癌症包括乳腺癌、套细胞淋巴瘤、肾细胞癌、急性髓细胞白血病、慢性髓细胞白血病、NPM/ALK转化的间变性大细胞淋巴瘤、弥漫性大B细胞淋巴瘤、横纹肌肉瘤、卵巢癌、子宫内膜癌、宫颈癌、非小细胞肺癌、小细胞肺癌、腺癌、结肠癌、直肠癌、胃癌、肝细胞癌、黑色素瘤、胰腺癌、前列腺癌、甲状腺癌、间变性大细胞淋巴瘤、血管瘤、胶质母细胞瘤或头颈癌。
    公开号:
    WO2010138487A1
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文献信息

  • [EN] BENZOXAZEPINES AS INHIBITORS OF PI3K/m TOR AND METHODS OF THEIR USE AND MANUFACTURE<br/>[FR] BENZOXAZÉPINES COMME INHIBITEURS DE PI3K/M TOR, MÉTHODES D'UTILISATION ET DE FABRICATION BENZOXAZEPINES AS INHIBITORS OF PI3K/M TOR AND METHODS OF THEIR USE AND MANUFACTURE
    申请人:EXELIXIS INC
    公开号:WO2010138487A1
    公开(公告)日:2010-12-02
    The invention is directed to Compounds of Formula (I): the invention provides compounds that inhibit, regulate, and/or modulate P13K and/or mTOR that are useful in the treatment of hyperproliferative diseases, such as cancer, in mammals. This invention also provides methods of making the compound methods of using such compounds in the treatment of hyperproliferative diseases in mammals, especially humans, and to pharmaceutical compositions containing such compounds. For example, cancer in which activity against PI3fC-alph mTOR, or both contributes to its pathology and/or symptomatology include breast cancer mantle cell lymphoma, renal cell carcinoma, acute myelogenous leukemia, chronic myelogenous leukemia, NPM/ALK- transformed anaplastic large cell lymphoma, diffu large B cell lymphoma, rhabdomyosarcoma, ovarian cancer, endometrial cancer, cervic cancer, non small cell lung carcinoma, small cell lung carcinoma, adenocarcinoma, col cancer, rectal cancer, gastric carcinoma, hepatocellular carcinoma, melanoma, pancreat cancer, prostate carcinoma, thyroid carcinoma, anaplastic large cell lymphoma, hemangiom glioblastoma, or head and neck cancer.
    这项发明涉及式(I)的化合物:该发明提供了抑制、调节和/或调节P13K和/或mTOR的化合物,这些化合物在治疗哺乳动物的高增殖性疾病,如癌症,方面非常有用。该发明还提供了制备该化合物的方法,以及在治疗哺乳动物,特别是人类的高增殖性疾病中使用这些化合物的方法,以及含有这些化合物的药物组合物。例如,对PI3fC-α mTOR或两者都具有活性有助于其病理学和/或症状学的癌症包括乳腺癌、套细胞淋巴瘤、肾细胞癌、急性髓细胞白血病、慢性髓细胞白血病、NPM/ALK转化的间变性大细胞淋巴瘤、弥漫性大B细胞淋巴瘤、横纹肌肉瘤、卵巢癌、子宫内膜癌、宫颈癌、非小细胞肺癌、小细胞肺癌、腺癌、结肠癌、直肠癌、胃癌、肝细胞癌、黑色素瘤、胰腺癌、前列腺癌、甲状腺癌、间变性大细胞淋巴瘤、血管瘤、胶质母细胞瘤或头颈癌。
  • Benzoxazepines as Inhibitors of PI3K/mTOR and Methods of Their Use and Manufacture
    申请人:Aay Naing
    公开号:US20120258953A1
    公开(公告)日:2012-10-11
    The invention is directed to Compounds of Formula (I): the invention provides compounds that inhibit, regulate, and/or modulate P13K and/or mTOR that are useful in the treatment of hyperproliferative diseases, such as cancer, in mammals. This invention also provides methods of making the compound methods of using such compounds in the treatment of hyperproliferative diseases in mammals, especially humans, and to pharmaceutical compositions containing such compounds. For example, cancer in which activity against PI3fC-alph mTOR, or both contributes to its pathology and/or symptomatology include breast cancer mantle cell lymphoma, renal cell carcinoma, acute myelogenous leukemia, chronic myelogenous leukemia, NPM/ALK-transformed anaplastic large cell lymphoma, diffu large B cell lymphoma, rhabdomyosarcoma, ovarian cancer, endometrial cancer, cervic cancer, non small cell lung carcinoma, small cell lung carcinoma, adenocarcinoma, col cancer, rectal cancer, gastric carcinoma, hepatocellular carcinoma, melanoma, pancreat cancer, prostate carcinoma, thyroid carcinoma, anaplastic large cell lymphoma, hemangiom glioblastoma, or head and neck cancer.
    本发明涉及化合物I式的化合物:本发明提供了一种抑制、调节和/或调节P13K和/或mTOR的化合物,其在哺乳动物中治疗增殖过度性疾病,如癌症方面非常有用。本发明还提供了制备该化合物的方法,使用这些化合物在哺乳动物中治疗增殖过度性疾病的方法,特别是人类,并提供了包含这些化合物的制药组合物。例如,对于活性针对PI3fC-alph mTOR或两者都对其病理和/或症状学产生贡献的癌症,包括乳腺癌、曼托细胞淋巴瘤、肾细胞癌、急性髓性白血病、慢性髓性白血病、NPM / ALK转化的间变性大细胞淋巴瘤、弥漫性大B细胞淋巴瘤、横纹肌肉瘤、卵巢癌、子宫内膜癌、宫颈癌、非小细胞肺癌、小细胞肺癌、腺癌、结肠癌、直肠癌、胃癌、肝细胞癌、黑色素瘤、胰腺癌、前列腺癌、甲状腺癌、间变性大细胞淋巴瘤、血管瘤、胶质母细胞瘤或头颈癌。
  • Benzoxazepines as Inhibitors of PI3K/mTOR and Methods of Their use and Manufacture
    申请人:Rice Kenneth D.
    公开号:US20140024637A1
    公开(公告)日:2014-01-23
    The invention is directed to Compounds of Formula I: and pharmaceutically acceptable salts or solvates thereof, as well as methods of making and using the compounds.
    本发明涉及式I的化合物,以及其药学上可接受的盐或溶剂化物,以及制备和使用该化合物的方法。
  • Benzoxazepines as inhibitors of PI3K/mTOR and methods of their use and manufacture
    申请人:Aay Naing
    公开号:US08637499B2
    公开(公告)日:2014-01-28
    The invention is directed to Compounds of Formula (I): the invention provides compounds that inhibit, regulate, and/or modulate P13K and/or mTOR that are useful in the treatment of hyperproliferative diseases, such as cancer, in mammals. This invention also provides methods of making the compound methods of using such compounds in the treatment of hyperproliferative diseases in mammals, especially humans, and to pharmaceutical compositions containing such compounds. For example, cancer in which activity against PI3fC-alph mTOR, or both contributes to its pathology and/or symptomatology include breast cancer mantle cell lymphoma, renal cell carcinoma, acute myelogenous leukemia, chronic myelogenous leukemia, NPM/ALK-transformed anaplastic large cell lymphoma, diffu large B cell lymphoma, rhabdomyosarcoma, ovarian cancer, endometrial cancer, cervic cancer, non small cell lung carcinoma, small cell lung carcinoma, adenocarcinoma, col cancer, rectal cancer, gastric carcinoma, hepatocellular carcinoma, melanoma, pancreat cancer, prostate carcinoma, thyroid carcinoma, anaplastic large cell lymphoma, hemangiom glioblastoma, or head and neck cancer.
    本发明涉及式(I)的化合物:本发明提供了抑制,调节和/或调节P13K和/或mTOR的化合物,这些化合物对于哺乳动物(特别是人类)的高增殖性疾病的治疗非常有用,例如癌症。本发明还提供制备该化合物的方法,使用这种化合物治疗哺乳动物(特别是人类)的高增殖性疾病的方法,以及含有这种化合物的制药组合物。例如,对于PI3fC-alph mTOR或两者都对其病理学和/或症状学产生影响的癌症包括乳腺癌,曼托细胞淋巴瘤,肾细胞癌,急性髓性白血病,慢性髓性白血病,NPM / ALK转化的间变性大细胞淋巴瘤,弥漫性大B细胞淋巴瘤,横纹肌肉瘤,卵巢癌,子宫内膜癌,宫颈癌,非小细胞肺癌,小细胞肺癌,腺癌,结肠癌,直肠癌,胃癌,肝细胞癌,黑色素瘤,胰腺癌,前列腺癌,甲状腺癌,间变性大细胞淋巴瘤,血管瘤,胶质母细胞瘤或头颈癌。
  • BENZOXAZEPINES AS INHIBITORS OF PI3K/m TOR AND METHODS OF THEIR USE AND MANUFACTURE
    申请人:Exelixis, Inc.
    公开号:EP2435426B1
    公开(公告)日:2013-05-22
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