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3-(N'-t-butoxycarbonylhydrazino)-1H-pyrazole-4-carboxylic acid ethyl ester | 951804-17-4

中文名称
——
中文别名
——
英文名称
3-(N'-t-butoxycarbonylhydrazino)-1H-pyrazole-4-carboxylic acid ethyl ester
英文别名
ethyl 5-[2-[(2-methylpropan-2-yl)oxycarbonyl]hydrazinyl]-1H-pyrazole-4-carboxylate
3-(N'-t-butoxycarbonylhydrazino)-1H-pyrazole-4-carboxylic acid ethyl ester化学式
CAS
951804-17-4
化学式
C11H18N4O4
mdl
——
分子量
270.288
InChiKey
IQCKSJYKBLPGRC-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):
    2.2
  • 重原子数:
    19
  • 可旋转键数:
    7
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.55
  • 拓扑面积:
    105
  • 氢给体数:
    3
  • 氢受体数:
    6

反应信息

  • 作为反应物:
    描述:
    3-(N'-t-butoxycarbonylhydrazino)-1H-pyrazole-4-carboxylic acid ethyl ester三氟乙酸盐酸 作用下, 以 二氯甲烷甲醇 为溶剂, 反应 2.0h, 生成 3-hydrazino-1H-pyrazole-4-carboxylic acid ethyl ester bishydrochloride
    参考文献:
    名称:
    2,3-DIHYDRO-IMINOISOINDOLE DERIVATIVES
    摘要:
    下列通式(1)所代表的化合物或其盐具有丝氨酸蛋白酶抑制活性,尤其对凝血因子VIIa有着卓越的抑制活性。该化合物或其盐可作为治疗和/或预防与血栓形成相关的疾病的药物。【其中,R1代表氢,R2代表可选取代的苯基等,R3代表可选取代的C6-10芳基等】。
    公开号:
    US20090270433A1
  • 作为产物:
    参考文献:
    名称:
    2,3-DIHYDRO-IMINOISOINDOLE DERIVATIVES
    摘要:
    下列通式(1)所代表的化合物或其盐具有丝氨酸蛋白酶抑制活性,尤其对凝血因子VIIa有着卓越的抑制活性。该化合物或其盐可作为治疗和/或预防与血栓形成相关的疾病的药物。【其中,R1代表氢,R2代表可选取代的苯基等,R3代表可选取代的C6-10芳基等】。
    公开号:
    US20090270433A1
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文献信息

  • Triazolone derivatives
    申请人:Clark Richard
    公开号:US20080015199A1
    公开(公告)日:2008-01-17
    A Compound represented by the following general formula (1), salts thereof or hydrates of the foregoing is a novel compound useful for treatment and/or prevention of diseases associated with thrombus formation, and which is safer with suitable physicochemical stability. [wherein R 1a , R 1b , R 1c and R 1d each independently represent hydrogen, etc.; R 2 represents optionally substituted phenyl, etc.; R 3 represents optionally substituted C6-10 aryl, etc.; and Z 1 and Z 2 each independently represent hydrogen]
    以下一般式(1)表示的化合物,其盐或上述化合物的合物是一种新型化合物,可用于治疗和/或预防与血栓形成相关的疾病,并且具有适当的物理化学稳定性,更安全。 [其中R1a,R1b,R1c和R1d分别独立表示氢等;R2表示可选择取代的苯基等;R3表示可选择取代的C6-10芳基等;Z1和Z2分别独立表示氢]
  • 2,3-dihydro-iminoisoindole derivatives
    申请人:Eisai R&D Management Co., Ltd.
    公开号:US07807690B2
    公开(公告)日:2010-10-05
    A compound represented by the following general formula (1), or a salt thereof has serine protease inhibiting activity, and particularly excellent inhibiting activity against clotting factor VIIa. This compound or a salt thereof is useful as therapeutic and/or prophylactic agents for diseases associated with thrombus formation. [wherein R1 represents hydrogen, R2 represents optionally substituted phenyl, etc., R3 represents optionally substituted C6-10 aryl, etc.].
    以下一般式(1)所代表的化合物或其盐具有丝氨酸蛋白酶抑制活性,特别是对凝血因子VIIa具有优异的抑制活性。该化合物或其盐可用作治疗和/或预防与血栓形成相关的疾病的药物。[其中R1代表氢,R2代表可选取代的苯基等,R3代表可选取代的C6-10芳基等]。
  • TRIAZOLONE DERIVATIVE
    申请人:Eisai R&D Management Co., Ltd.
    公开号:EP2000465A1
    公开(公告)日:2008-12-10
    A Compound represented by the following general formula (1), salts thereof or hydrates of the foregoing is a novel compound useful for treatment and/or prevention of diseases associated with thrombus formation, and which is safer with suitable physicochemical stability. [wherein R1a, R1b, R1c and R1d each independently represent hydrogen, etc.; R2 represents optionally substituted phenyl, etc.; R3 represents optionally substituted C6-10 aryl, etc.; and Z1 and Z2 each independently represent hydrogen]
    由以下通式(1)代表的化合物、其盐类或前述化合物的合物是一种新型化合物,可用于治疗和/或预防与血栓形成有关的疾病,且具有较高的安全性和适当的理化稳定性。 [其中 R1a、R1b、R1c 和 R1d 各自独立地代表氢等;R2 代表任选取代的苯基等;R3 代表任选取代的 C6-10 芳基等;Z1 和 Z2 各自独立地代表氢]
  • Triazolone derivative
    申请人:Eisai R&D Management Co., Ltd.
    公开号:EP2194046A1
    公开(公告)日:2010-06-09
    A Compound represented by the following general formula (1), salts thereof or hydrates of the foregoing is a novel compound useful for treatment and/or prevention of diseases associated with thrombus formation, and which is safer with suitable physicochemical stability. [wherein R1a, R1b, R1c and R1d each independently represent hydrogen, etc.; R2 represents optionally substituted phenyl, etc.; R3 represents optionally substituted C6-10 aryl, etc.; and Z1 and Z2 each independently represent hydrogen]
    由以下通式(1)代表的化合物、其盐类或前述化合物的合物是一种新型化合物,可用于治疗和/或预防与血栓形成有关的疾病,且具有更高的安全性和适当的理化稳定性。 [其中 R1a、R1b、R1c 和 R1d 各自独立地代表氢等;R2 代表任选取代的苯基等;R3 代表任选取代的 C6-10 芳基等;Z1 和 Z2 各自独立地代表氢]
  • 2,3-DIHYDROIMINOISOINDOLE DERIVATIVE
    申请人:Eisai R&D Management Co., Ltd.
    公开号:EP2202231A1
    公开(公告)日:2010-06-30
    A compound represented by the following general formula (1), or a salt thereof has serine protease inhibiting activity, and particularly excellent inhibiting activity against clotting factor VIIa. This compound or a salt thereof is useful as therapeutic and/or prophylactic agents for diseases associated with thrombus formation. [wherein R1 represents hydrogen, R2 represents optionally substituted phenyl, etc., R3 represents optionally substituted C6-10 aryl, etc.]
    由以下通式(1)代表的化合物或其盐具有丝氨酸蛋白酶抑制活性,尤其是对凝血因子 VIIa 具有极佳的抑制活性。该化合物或其盐类可作为治疗和/或预防血栓形成相关疾病的药物。 [其中 R1 代表氢,R2 代表任选取代的苯基等,R3 代表任选取代的 C6-10 芳基等。]
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