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(1-(二氟甲基)-1H-吡唑-4-基)硼酸 | 1312693-57-4

中文名称
(1-(二氟甲基)-1H-吡唑-4-基)硼酸
中文别名
——
英文名称
(1-(Difluoromethyl)-1H-pyrazol-4-yl)boronic acid
英文别名
[1-(difluoromethyl)pyrazol-4-yl]boronic acid
(1-(二氟甲基)-1H-吡唑-4-基)硼酸化学式
CAS
1312693-57-4
化学式
C4H5BF2N2O2
mdl
——
分子量
161.91
InChiKey
UOXFJNMDWKLYQZ-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

计算性质

  • 辛醇/水分配系数(LogP):
    -1.04
  • 重原子数:
    11
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    58.3
  • 氢给体数:
    2
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    tert-Butyl 6-((3R,4R)-3-(tert-butoxycarbonylamino)tetrahydro-2H-pyran-4-ylamino)-4-chloro-7-fluoro-3-oxo-1H-pyrrolo[3,4-c]pyridine-2(3H)-carboxylate 、 (1-(二氟甲基)-1H-吡唑-4-基)硼酸双三苯基磷二氯化钯 acetonitrile-water 作用下, 以 1,4-二氧六环disodium;carbonate 为溶剂, 反应 0.5h, 以to give the title compound as a white solid (132 mg, 23%)的产率得到tert-Butyl 6-((3R,4R)-3-(tert-butoxycarbonylamino)tetrahydro-2H-pyran-4-ylamino)-4-(1-(difluoromethyl)-1H-pyrazol-4-yl)-7-fluoro-3-oxo-1H-pyrrolo[3,4-c]pyridine-2(3H)-carboxylate
    参考文献:
    名称:
    Fused heteroaromatic pyrrolidinones
    摘要:
    本发明涉及公式1化合物及其药学上可接受的盐,其中G,L1,L2,R1,R2,R3和R4在规范中定义。本公开还涉及制备公式1化合物的材料和方法,包含它们的药物组合物,并用于治疗涉及免疫系统和炎症的疾病、疾病和病情,包括风湿性关节炎、血液恶性肿瘤、上皮癌(即癌症)和其他抑制SYK所指示的疾病、疾病和病情。
    公开号:
    US09108970B2
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文献信息

  • FUSED HETEROAROMATIC PYRROLIDINONES
    申请人:Takeda Pharmaceutical Company Limited
    公开号:US20150336964A1
    公开(公告)日:2015-11-26
    Disclosed are compounds of Formula 1, and pharmaceutically acceptable salts thereof, wherein G, L 1 , L 2 , R 1 , R 2 , R 3 , and R 4 are defined in the specification. This disclosure also relates to materials and methods for preparing compounds of Formula 1, pharmaceutical compositions containing them, and their use for treating disorders, diseases, and conditions involving the immune system and inflammation, including rheumatoid arthritis, hematological malignancies, epithelial cancers (i.e., carcinomas), and other disorders, diseases, and conditions for which inhibition of SYK is indicated.
    本文披露了公式1的化合物及其药学上可接受的盐,其中G、L1、L2、R1、R2、R3和R4在规范中有定义。本文还涉及制备公式1化合物的材料和方法,包含它们的药物组合物,以及它们用于治疗涉及免疫系统和炎症的疾病、疾病和状况,包括类风湿性关节炎、血液恶性肿瘤、上皮癌(即癌症)和其他需要抑制SYK的疾病、疾病和状况。
  • FUSED HETEROAROMATIC PYRROLIDINONES AS SYK INHIBITORS
    申请人:Arikawa Yasuyoshi
    公开号:US20130116260A1
    公开(公告)日:2013-05-09
    Disclosed are compounds of Formula 1, and pharmaceutically acceptable salts thereof, wherein G, L 1 , L 2 , R 1 , R 2 , R 3 , and R 4 are defined in the specification. This disclosure also relates to materials and methods for preparing compounds of Formula 1, pharmaceutical compositions containing them, and their use for treating disorders, diseases, and conditions involving the immune system and inflammation, including rheumatoid arthritis, hematological malignancies, epithelial cancers (i.e., carcinomas), and other disorders, diseases, and conditions for which inhibition of SYK is indicated.
    本发明涉及式1的化合物及其药学上可接受的盐,其中G、L1、L2、R1、R2、R3和R4如规范中所定义。本公开还涉及制备式1化合物的材料和方法,包含它们的药物组合物,以及它们用于治疗涉及免疫系统和炎症的疾病、疾患和病况,包括类风湿性关节炎、血液恶性肿瘤、上皮癌(即癌症)和其他需要抑制SYK的疾病、疾患和病况。
  • Fused heteroaromatic pyrrolidinones as SYK inhibitors
    申请人:Arikawa Yasuyoshi
    公开号:US09181255B2
    公开(公告)日:2015-11-10
    Disclosed are compounds of Formula 1, and pharmaceutically acceptable salts thereof, wherein G, L1, L2, R1, R2, R3, and R4 are defined in the specification. This disclosure also relates to materials and methods for preparing compounds of Formula 1, pharmaceutical compositions containing them, and their use for treating disorders, diseases, and conditions involving the immune system and inflammation, including rheumatoid arthritis, hematological malignancies, epithelial cancers (i.e., carcinomas), and other disorders, diseases, and conditions for which inhibition of SYK is indicated.
    本发明涉及公式1的化合物及其药学上可接受的盐,其中G、L1、L2、R1、R2、R3和R4在规范中定义。本公开还涉及制备公式1化合物的材料和方法、含有它们的药物组合物以及它们用于治疗涉及免疫系统和炎症的疾病、疾病和状况,包括类风湿性关节炎、血液恶性肿瘤、上皮癌(即癌瘤)和其他需要抑制SYK的疾病、疾病和状况。
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