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N-[2-[4-(3,4-dichlorophenyl)-1-piperazinyl]ethyl]-2-benzothiazolamine

中文名称
——
中文别名
——
英文名称
N-[2-[4-(3,4-dichlorophenyl)-1-piperazinyl]ethyl]-2-benzothiazolamine
英文别名
N-[2-[4-(3,4-dichlorophenyl)piperazin-1-yl]ethyl]-1,3-benzothiazol-2-amine
N-[2-[4-(3,4-dichlorophenyl)-1-piperazinyl]ethyl]-2-benzothiazolamine化学式
CAS
——
化学式
C19H20Cl2N4S
mdl
——
分子量
407.367
InChiKey
GJSYHSRNGCLVHN-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):
    5.6
  • 重原子数:
    26
  • 可旋转键数:
    5
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.32
  • 拓扑面积:
    59.6
  • 氢给体数:
    1
  • 氢受体数:
    5

文献信息

  • Radiolabelled alkylamino-benzothiazole and -benzoxazole derivatives and their use as D4 ligands
    申请人:JANSSEN PHARMACEUTICA N.V.
    公开号:EP1325917A1
    公开(公告)日:2003-07-09
    The present invention concerns the radiolabelled compounds of formula the N-oxide forms, the pharmaceutically acceptable acid addition salts and stereochemically isomeric forms thereof, wherein X is O or S; n is 2, 3, 4 or 5; R1 is hydrogen, C1-6alkyl, C1-6alkyloxy or halo; R2 is hydrogen, C1-6alkyl, phenyl, phenylC1-6alkyl or phenylcarbonyl; R3 and R4 each independently are selected from hydrogen, halo, nitro, C1-6alkyl, C1-6alkyloxy, haloC1-6alkyl, aminosulfonyl, mono- or di(C1-4alkyl)aminosulfonyl; or R3 and R4 may also be taken together to form a bivalent radical of formula -CH=CH-CH=CH- , characterized in that the compound has at least one halo which is a radioactive isotope of iodine, bromine or fluorine, or has at least one 11C-atom or tritium atom ; it further relates to a process of marking dopamine D4 receptor sites and a process for imaging an organ.
    本发明涉及放射性标记的式化合物 其中X为O或S;n为2、3、4或5;R1为氢、C1-6烷基、C1-6烷氧基或卤代;R2 是氢、C1-6烷基、苯基、苯基 C1-6 烷基或苯基羰基; R3 和 R4 各自独立地选自氢、卤素、硝基、C1-6烷基、C1-6烷氧基、卤代 C1-6 烷基、磺酰基、单-或二(C1-4烷基)磺酰基;或 R3 和 R4 也可以结合在一起形成式-CH=CH-CH=CH-的二价基,其特征在于该化合物具有至少一个卤素,该卤素是的放射性同位素,或具有至少一个 11C 原子或氚原子;它还涉及一种标记多巴胺 D4 受体位点的工艺和一种器官成像工艺。
  • ALKYLAMINOBENZOTHIAZOLE AND -BENZOXAZOLE DERIVATIVES
    申请人:JANSSEN PHARMACEUTICA N.V.
    公开号:EP0912533A1
    公开(公告)日:1999-05-06
  • US6103725A
    申请人:——
    公开号:US6103725A
    公开(公告)日:2000-08-15
  • US6224849B1
    申请人:——
    公开号:US6224849B1
    公开(公告)日:2001-05-01
  • [EN] ALKYLAMINOBENZOTHIAZOLE AND -BENZOXAZOLE DERIVATIVES<br/>[FR] DERIVES DE L'ALKYLAMINOBENZOTHIAZOLE ET ALKYLAMINOBENZOXAZOLE
    申请人:JANSSEN PHARMACEUTICA N.V.
    公开号:WO1997043271A1
    公开(公告)日:1997-11-20
    (EN) The present invention concerns the compounds of formula (I) the $i(N)-oxide forms, the pharmaceutically acceptable acid addition salts and stereochemically isomeric forms thereof, wherein X is O or S; n is 2, 3, 4 or 5; R1 is hydrogen, C1-6alkyl, C1-6alkyloxy or halo; R2 is hydrogen, C1-6alkyl, phenyl, phenylC1-6alkyl or phenylcarbonyl; R3 and R4 each independently are selected from hydrogen, halo, nitro, C1-6alkyl, C1-6alkyloxy, haloC1-6alkyl, aminosulfonyl, mono-or di(C1-4alkyl)aminosulfonyl; or R3 and R4 may also be taken together to form a bivalent radical of formula -CH=CH-CH=CH-; it further relates to processes for their preparation, compositions comprising them as well as their use as a medicine; compounds of formula (I) containing a radioactive isotope; a process of marking dopamine D4 receptor sites; and a process for imaging an organ are disclosed.(FR) La présente invention concerne les composés de la formule (I), les formes N-oxyde, les sels d'addition d'acide pharmaceutiquement acceptables et les formes stéréochimiquement isomériques de ces derniers. Dans la formule, X est O ou S; n est 2, 3, 4 ou 5; R1 est hydrogène, C1-6alkyle, C1-6alkyloxy ou halo; R2 est hydrogène, C1-6alkyle, phényle, phénylC1-6alkyle ou phénylcarbonyle,; R3 et R4 sont chacun indépendamment sélectionnés parmi hydrogène, halo, nitro, C1-6alkyle, C1-6alkyloxy, haloC1-6alkyle, aminosulfonyle, mono ou di(C1-4alkyl)aminosulfonyle; ou R3 et R4 peuvent être pris ensemble pour former un radical bivalent de la formule -CH=CH-CH=CH-. L'invention traite aussi de procédés pour leur préparation, de compositions les comprenant ainsi que de leur utilisation comme médicaments. L'invention a aussi pour objet des composés de la formule (I) comprenant un isotope radioactif, un procédé de marquage des sites du récepteur D4 de la dopamine et un procédé pour observer un organe par imagerie.
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