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N-(4-(piperidin-4-yl)-3,4-dihydro-2H-benzo[b][1,4]thiazin-6-yl)thiophene-2-carboximidamide | 1202774-38-6

中文名称
——
中文别名
——
英文名称
N-(4-(piperidin-4-yl)-3,4-dihydro-2H-benzo[b][1,4]thiazin-6-yl)thiophene-2-carboximidamide
英文别名
N'-(4-piperidin-4-yl-2,3-dihydro-1,4-benzothiazin-6-yl)thiophene-2-carboximidamide
N-(4-(piperidin-4-yl)-3,4-dihydro-2H-benzo[b][1,4]thiazin-6-yl)thiophene-2-carboximidamide化学式
CAS
1202774-38-6
化学式
C18H22N4S2
mdl
——
分子量
358.531
InChiKey
NPKJSMOIXGJKNA-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):
    3.2
  • 重原子数:
    24
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.39
  • 拓扑面积:
    107
  • 氢给体数:
    2
  • 氢受体数:
    5

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    N-(4-(piperidin-4-yl)-3,4-dihydro-2H-benzo[b][1,4]thiazin-6-yl)thiophene-2-carboximidamide盐酸 作用下, 以 甲醇乙醚 为溶剂, 以100%的产率得到N-(4-(piperidin-4-yl)-3,4-dihydro-2H-benzo[b][1,4]thiazin-6-yl)thiophene-2-carboximidamide dihydrochloride
    参考文献:
    名称:
    BENZOXAZINES, BENZOTHIAZINES, AND RELATED COMPOUNDS HAVING NOS INHIBITORY ACTIVITY
    摘要:
    本发明涉及抑制一氧化氮合酶(NOS)的苯并噁嗪,苯并噻嗪和相关化合物,特别是那些选择性地抑制神经一氧化氮合酶(nNOS)而不是其他NOS同工型的化合物。本发明的NOS抑制剂,单独或与其他药用活性剂结合使用,可用于治疗或预防各种医疗状况。
    公开号:
    US20100009975A1
  • 作为产物:
    描述:
    tert-butyl 4-(6-(thiophene-2-carboximidamido)-2H-benzo[b][1,4]thiazin-4(3H)-yl)piperidine-1-carboxylate盐酸sodium carbonate 作用下, 以 甲醇 为溶剂, 反应 0.75h, 以69.4%的产率得到N-(4-(piperidin-4-yl)-3,4-dihydro-2H-benzo[b][1,4]thiazin-6-yl)thiophene-2-carboximidamide
    参考文献:
    名称:
    BENZOXAZINES, BENZOTHIAZINES, AND RELATED COMPOUNDS HAVING NOS INHIBITORY ACTIVITY
    摘要:
    本发明涉及抑制一氧化氮合酶(NOS)的苯并噁嗪,苯并噻嗪和相关化合物,特别是那些选择性地抑制神经一氧化氮合酶(nNOS)而不是其他NOS同工型的化合物。本发明的NOS抑制剂,单独或与其他药用活性剂结合使用,可用于治疗或预防各种医疗状况。
    公开号:
    US20100009975A1
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文献信息

  • Benzoxazines, benzothiazines, and related compounds having NOS inhibitory activity
    申请人:NeurAxon, Inc.
    公开号:US08106043B2
    公开(公告)日:2012-01-31
    The present invention features benzothiazines that inhibit nitric oxide synthase (NOS), particularly those that selectively inhibit neuronal nitric oxide synthase (nNOS) in preference to other NOS isoforms, and that have the formula: The NOS inhibitors of the invention, alone or in combination with other pharmaceutically active agents, can be used for treating or preventing various medical conditions.
    本发明涉及抑制一氧化氮合酶(NOS)的苯并噻嗪,特别是那些选择性抑制神经元一氧化氮合酶(nNOS)而不是其他NOS亚型的化合物,其化学式为:本发明的NOS抑制剂可以单独或与其他药物活性剂联合使用,用于治疗或预防各种医疗状况。
  • US8106043B2
    申请人:——
    公开号:US8106043B2
    公开(公告)日:2012-01-31
  • US8618286B2
    申请人:——
    公开号:US8618286B2
    公开(公告)日:2013-12-31
  • [EN] BENZOXAZINES, BENZOTHIAZINES, AND RELATED COMPOUNDS HAVING NOS INHIBITORY ACTIVITY<br/>[FR] BENZOXAZINES, BENZOTHIAZINES ET COMPOSÉS APPARENTÉS AYANT UNE ACTIVITÉ D'INHIBITION DE NOS
    申请人:NEURAXON INC
    公开号:WO2010000073A1
    公开(公告)日:2010-01-07
    Disclosed are benzoxazines and benzothiazines of formula (I) wherein Q is O-(CHR6)1-3 or S-(CHR6)1-3; R1 and each R6 is H, optionally substituted [C1-6 alkyl, C1-4alkaryl, C1-4 alkheterocyclyl, C2-9 heterocyclyl, C3-8 cycloalkyl, C1-4 alkcycloalkyl] or - (CR1AR1B)nNR1cR1D wherein R1A, R1B, R1C, R1D are independently hydrogen, optionally substituted [C1-6 alkyl, C1-4alkaryl, C1-4 alkheterocyclyl, C2-9 heterocyclyl, C3-8 cycloalkyl, etc.] or wherein R1A and R1B combine to form =O, or wherein R1C and R1D combine to form an optionally substituted C2-9 heterocyclyl, and n is an integer between 1-6; each of R2 and R3 is H, hal, optionally substituted [C1-6 alkyl, C6-10aryl, C1-6alkaiyl, C2-9 heterocyclyl, C1-6 alkoxy, C1-6 thioalkoxy, (CH2)r2NHC(NH)R2A, CH2)r2NHC(S)NHR2A, C1-4 alkheterocyclyl] or hydroxy, wherein r2 is an integer from 0 to 2, R2A is optionally substituted [C1-6 alkyl, C6-10aryl, C^alkaryl, C2-9 heterocyclyl, C1-4 alkheterocyclyl,C1-6 thioalkoxy, C1-4 thioalkaryl, aryloyl, C1- 4thioalkheterocylyl, or amino]; each R4 and R5 is H, hal, (CH2)r2NHC(NH)R2A or CH2)r2NHC(S)NH R2A; Y1 and Y2 are together =O or Y1 and Y2 are independently H, optionally substituted [C1-6 alkyl, C6-10aryl, C1-6alkaryl, C2-9 heterocyclyl, C1-6 alkoxy, C1-6 thioalkoxy, C1-4alkheterocyclyl] or hydroxy; wherein only one of R2, R3, R4 and R5 is (CH2)r2NHC(NH)R2A or CH2)r2NHC(S)NH R2A; or a pharmaceutically acceptable salt or prodrug thereof. Said benzoxazines and benzothiazines of formula (I) inhibit nitric oxide synthase (NOS), particularly selectively inhibit neuronal nitric oxide synthase (nNOS) in preference to other NOS isoforms. The NOS inhibitors of formula (I), alone or in combinatioon with other pharmaceutically active agents, can be used for treating or preventing various medical conditions.
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同类化合物

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