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5,6-Dichlorothiazolo(4,5-b)pyrazine | 66490-66-2

中文名称
——
中文别名
——
英文名称
5,6-Dichlorothiazolo(4,5-b)pyrazine
英文别名
5,6-dichloro-[1,3]thiazolo[4,5-b]pyrazine
5,6-Dichlorothiazolo(4,5-b)pyrazine化学式
CAS
66490-66-2
化学式
C5HCl2N3S
mdl
——
分子量
206.055
InChiKey
IIBKVHMVAIFESG-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):
    2.8
  • 重原子数:
    11
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    66.9
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    原甲酸三乙酯3-amino-5,6-dichloropyrazine-2-thiol 在 petroleum-ether 作用下, 反应 20.0h, 以to give 7.7 g的产率得到5,6-Dichlorothiazolo(4,5-b)pyrazine
    参考文献:
    名称:
    Microbicidal/fungicidal thiazolopyrazines
    摘要:
    具有抑制微生物生长活性的噻唑吡嗪的化学式为##STR1##其中X为--Br,--Cl或F,R为--H或--CH.sub.3-x Y.sub.x,Y为--Br,--Cl或F,x为0,1,2或3。这些化合物还可用作制备高活性抗微生物三环化合物的中间体。
    公开号:
    US04075207A1
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文献信息

  • Chemokine Receptor Antagonist and Medical Use Thereof
    申请人:Habashita Hiromu
    公开号:US20070254886A1
    公开(公告)日:2007-11-01
    The present invention relates to a compound represented by formula (I), a salt thereof, an N-oxide thereof, a solvate thereof or a prodrug thereof, and medical use thereof (the symbols in the formula are as described in the specification). The compound represented by formula (I) has chemokine receptor (especially in CCR4 and/or CCR5) antagonistic activity. Therefore it is useful for prevention and/or treatment of a chemokine receptor-mediated disease such as inflammatory and/or allergic diseases [systemic inflammatory response syndrome (SIRS), anaphylaxis, anaphylactoid reaction, allergic angiitis, transplant rejection reaction, hepatitis, nephritis, nephropathy, pancreatitis, rhinitis, arthritis, inflammatory ocular disease, inflammatory bowel disease, disease in cerebro and/or circulatory system, respiratory disease, dermatosis, autoimmune disease, and the like], infection [viral disease (human immunodeficiency virus infection, acquired immunodeficiency syndrome, SARS, etc.), and the like], and the like.
    本发明涉及一种由公式(I)表示的化合物,其盐、N-氧化物、溶剂化物或前药,以及其医药用途(公式中的符号如说明书所述)。公式(I)表示的化合物具有趋化因子受体(尤其是在CCR4和/或CCR5中)拮抗活性。因此,它对于预防和/或治疗趋化因子受体介导的疾病,如炎症和/或过敏性疾病[全身性炎症反应综合征(SIRS)、过敏性休克、过敏性反应、过敏性血管炎、移植排斥反应、肝炎、肾炎、肾病、胰腺炎、鼻炎、关节炎、炎症性眼部疾病、炎症性肠病、脑和/或循环系统疾病、呼吸系统疾病、皮肤病、自身免疫性疾病等]、感染[病毒性疾病(人类免疫缺陷病毒感染、获得性免疫缺陷综合征、SARS等)等]等非常有用。
  • CHEMOKINE RECEPTOR ANTAGONIST AND MEDICAL USE THEREOF
    申请人:HABASHITA Hiromu
    公开号:US20100266539A1
    公开(公告)日:2010-10-21
    The present invention relates to a compound represented by formula (I), a salt thereof, an N-oxide thereof, a solvate thereof or a prodrug thereof, and medical use thereof (the symbols in the formula are as described in the specification). The compound represented by formula (I) has chemokine receptor (especially in CCR4 and/or CCR5) antagonistic activity. Therefore it is useful for prevention and/or treatment of a chemokine receptor-mediated disease such as inflammatory and/or allergic diseases [systemic inflammatory response syndrome (SIRS), anaphylaxis, anaphylactoid reaction, allergic angiitis, transplant rejection reaction, hepatitis, nephritis, nephropathy, pancreatitis, rhinitis, arthritis, inflammatory ocular disease, inflammatory bowel disease, disease in cerebro and/or circulatory system, respiratory disease, dermatosis, autoimmune disease, and the like], infection [viral disease (human immunodeficiency virus infection, acquired immunodeficiency syndrome, SARS, etc.), and the like], and the like.
    本发明涉及一种由式(I)所表示的化合物,其盐、N-氧化物、溶剂化物或前药,以及其医药用途(式中符号如规范所述)。由式(I)所表示的化合物具有趋化因子受体(特别是在CCR4和/或CCR5中)的拮抗活性。因此,它对于预防和/或治疗趋化因子受体介导的疾病,如炎症和/或过敏性疾病[全身性炎症反应综合征(SIRS)、过敏反应、过敏性血管炎、移植排斥反应、肝炎、肾炎、肾病、胰腺炎、鼻炎、关节炎、炎症性眼病、炎症性肠病、脑和/或循环系统疾病、呼吸道疾病、皮肤病、自身免疫性疾病等]、感染[病毒性疾病(人类免疫缺陷病毒感染、获得性免疫缺陷综合征、SARS等)等]等具有用处。
  • US4075207A
    申请人:——
    公开号:US4075207A
    公开(公告)日:1978-02-21
  • US4172133A
    申请人:——
    公开号:US4172133A
    公开(公告)日:1979-10-23
  • US7732442B2
    申请人:——
    公开号:US7732442B2
    公开(公告)日:2010-06-08
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