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4-(2-methylthiazol-4-yl)-1-piperazinecarboxylic acid tert-butyl ester | 912921-93-8

中文名称
——
中文别名
——
英文名称
4-(2-methylthiazol-4-yl)-1-piperazinecarboxylic acid tert-butyl ester
英文别名
Tert-butyl 4-(2-methylthiazol-4-yl)-1-piperazinecarboxylate;tert-butyl 4-(2-methyl-1,3-thiazol-4-yl)piperazine-1-carboxylate
4-(2-methylthiazol-4-yl)-1-piperazinecarboxylic acid tert-butyl ester化学式
CAS
912921-93-8
化学式
C13H21N3O2S
mdl
——
分子量
283.395
InChiKey
XUENGYIYDTYOBF-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):
    2.5
  • 重原子数:
    19
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.69
  • 拓扑面积:
    73.9
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    硫代乙酰胺4-(2-溴乙酰基)哌嗪-1-羧酸叔丁酯 在 silica gel 、 ethyl acetate n-hexane 作用下, 以 乙醇 为溶剂, 反应 3.0h, 以obtained in the above 1), and的产率得到4-(2-methylthiazol-4-yl)-1-piperazinecarboxylic acid tert-butyl ester
    参考文献:
    名称:
    1,4-Substituted Piperazine Derivatives
    摘要:
    化合物的化学式为(I)或其药学上可接受的盐,其中:R1代表分支的低碳原子数为3至9的烷基或类似物;R2代表含有1或2个氮原子的6元杂环芳基或类似物;R3代表氢原子,烷酰胺基或类似物;R4代表氢原子,低碳原子数的烷基或类似物;X1代表氧原子或硫原子;X2代表氧原子或单键;m表示0至4的整数。该化合物具有代谢型谷氨酸受体1的抑制作用,因此可用于治疗脑部疾病,如惊厥、急性疼痛、炎性疼痛、慢性疼痛、脑梗塞或短暂性脑缺血发作、精神障碍如精神分裂症以及焦虑和药物成瘾等疾病。
    公开号:
    US20090062293A1
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文献信息

  • 1,4-Substituted Piperazine Derivatives
    申请人:Kawamoto Hiroshi
    公开号:US20090062293A1
    公开(公告)日:2009-03-05
    A compound represented by the formula (I): or a pharmaceutically acceptable salt thereof, wherein: R 1 represents a branched lower alkyl group having from 3 to 9 carbon atoms or the like; R 2 represents a 6-membered heteroaryl group having 1 or 2 nitrogen atoms or the like; R 3 represents a hydrogen atom, an alkanoylamino group or the like; R 4 represents a hydrogen atom, a lower alkyl group or the like; X 1 represents an oxygen atom or a sulfur atom; X 2 represents an oxygen atom or a single bond; and m indicates an integer of from 0 to 4. This compound has a metabotropic glutamate receptor 1 inhibitory effect, and therefore is useful for the treatment of a brain disorder such as convulsion, acute pain, inflammatory pain, chronic pain, cerebral infraction or transient cerebral ischemic attack, a mental dysfunction such as schizophrenia, and a disease such as anxiety and drug addition.
    化合物的化学式为(I)或其药学上可接受的盐,其中:R1代表分支的低碳原子数为3至9的烷基或类似物;R2代表含有1或2个氮原子的6元杂环芳基或类似物;R3代表氢原子,烷酰胺基或类似物;R4代表氢原子,低碳原子数的烷基或类似物;X1代表氧原子或硫原子;X2代表氧原子或单键;m表示0至4的整数。该化合物具有代谢型谷氨酸受体1的抑制作用,因此可用于治疗脑部疾病,如惊厥、急性疼痛、炎性疼痛、慢性疼痛、脑梗塞或短暂性脑缺血发作、精神障碍如精神分裂症以及焦虑和药物成瘾等疾病。
  • 1,4-SUBSTITUTED PIPERAZINE DERIVATIVE
    申请人:BANYU PHARMACEUTICAL CO., LTD.
    公开号:EP1870401A1
    公开(公告)日:2007-12-26
    A compound represented by the formula (I): or a pharmaceutically acceptable salt thereof, wherein: R1 represents a branched lower alkyl group having from 3 to 9 carbon atoms or the like; R2 represents a 6-membered heteroaryl group having 1 or 2 nitrogen atoms or the like; R3 represents a hydrogen atom, an alkanoylamino group or the like; R4 represents a hydrogen atom, a lower alkyl group or the like; X1 represents an oxygen atom or a sulfur atom; X2 represents an oxygen atom or a single bond; and m indicates an integer of from 0 to 4. This compound has a metabotropic glutamate receptor 1 inhibitory effect, and therefore is useful for the treatment of a brain disorder such as convulsion, acute pain, inflammatory pain, chronic pain, cerebral infraction or transient cerebral ischemic attack, a mental dysfunction such as schizophrenia, and a disease such as anxiety and drug addition.
    式 (I) 所代表的化合物: 或其药学上可接受的盐,其中 R1 代表具有 3 至 9 个碳原子的支链低级烷基或类似基团; R2 代表具有 1 或 2 个氮原子的 6 元杂芳基或类似基团 R3 代表氢原子、烷酰氨基或类似物; R4 代表氢原子、低级烷基或类似物; X1 代表氧原子或硫原子; X2 代表氧原子或单键;以及 m 表示 0 至 4 的整数。 该化合物具有代谢型谷氨酸受体 1 抑制作用,因此可用于治疗抽搐、急性疼痛、炎症性疼痛、慢性疼痛、脑梗塞或短暂性脑缺血发作等脑部疾病,精神分裂症等精神功能障碍,以及焦虑和药物成瘾等疾病。
  • WO2006/109817
    申请人:——
    公开号:——
    公开(公告)日:——
  • US8101618B2
    申请人:——
    公开号:US8101618B2
    公开(公告)日:2012-01-24
  • 1,4-substituted piperazine derivatives
    申请人:MSD K.K.
    公开号:US08101618B2
    公开(公告)日:2012-01-24
    A compound represented by the formula (I): or a pharmaceutically acceptable salt thereof, wherein: R1 represents a branched lower alkyl group having from 3 to 9 carbon atoms or the like; R2 represents a 6-membered heteroaryl group having 1 or 2 nitrogen atoms or the like; R3 represents a hydrogen atom, an alkanoylamino group or the like; R4 represents a hydrogen atom, a lower alkyl group or the like; X1 represents an oxygen atom or a sulfur atom; X2 represents an oxygen atom or a single bond; and m indicates an integer of from 0 to 4. This compound has a metabotropic glutamate receptor 1 inhibitory effect, and therefore is useful for the treatment of a brain disorder such as convulsion, acute pain, inflammatory pain, chronic pain, cerebral infraction or transient cerebral ischemic attack, a mental dysfunction such as schizophrenia, and a disease such as anxiety and drug addition.
    化合物的化学式为(I),或其药学上可接受的盐,其中:R1代表具有3至9个碳原子的支链低级烷基或类似物;R2代表具有1或2个氮原子的6元杂环芳基基团或类似物;R3代表氢原子、烷酰氨基基团或类似物;R4代表氢原子、低级烷基或类似物;X1代表氧原子或硫原子;X2代表氧原子或单键;m表示0至4的整数。该化合物具有代谢型谷氨酸受体1的抑制作用,因此可用于治疗脑部疾病,如惊厥、急性疼痛、炎症性疼痛、慢性疼痛、脑梗死或短暂性脑缺血发作、精神障碍如精神分裂症和焦虑症以及药物成瘾等疾病。
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