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(R)-N-[5-methyl-8-(4-methylpiperazin-1-yl)-1,2,3,4-tetrahydro-2-naphtyl]-4-morpholinobenzamide monohydrobromide | 285996-93-2

中文名称
——
中文别名
——
英文名称
(R)-N-[5-methyl-8-(4-methylpiperazin-1-yl)-1,2,3,4-tetrahydro-2-naphtyl]-4-morpholinobenzamide monohydrobromide
英文别名
(R)-N-[5-methyl-8-(4-methylpiperazin-1-yl)-1,2,3,4-tetrahydro-2-naphthyl]-4-morpholinobenzamide monohydrobromide;N-[(2R)-5-methyl-8-(4-methylpiperazin-1-yl)-1,2,3,4-tetrahydronaphthalen-2-yl]-4-morpholin-4-ylbenzamide;hydrobromide
(R)-N-[5-methyl-8-(4-methylpiperazin-1-yl)-1,2,3,4-tetrahydro-2-naphtyl]-4-morpholinobenzamide monohydrobromide化学式
CAS
285996-93-2
化学式
BrH*C27H36N4O2
mdl
——
分子量
529.52
InChiKey
OEEVRGHITZQMTH-VZYDHVRKSA-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):
    3.45
  • 重原子数:
    34
  • 可旋转键数:
    4
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.52
  • 拓扑面积:
    48
  • 氢给体数:
    2
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    AR-A000002咪唑氢溴酸溶剂黄146乙醇 作用下, 以 乙醇 为溶剂, 反应 10.0h, 以gives 533 g (92%) of (R)-N-[5-methyl-8-(4-methylpiperazin-1-yl)-1,2,3,4-tetrahydro-2-naphtyl]-4-morpholinobenzamide monohydrobromide Form A的产率得到(R)-N-[5-methyl-8-(4-methylpiperazin-1-yl)-1,2,3,4-tetrahydro-2-naphtyl]-4-morpholinobenzamide monohydrobromide
    参考文献:
    名称:
    Form of (R)-N-[5-methyl-8-(4-methylpiperazin-1-yl)-1,2,3,4-tetrahydro-2-naphthyl]-4-morpholinobenzamide
    摘要:
    本发明涉及一种新型的血清素H5-HT1B受体拮抗剂,即(R)-N-[5-甲基-8-(4-甲基哌嗪-1-基)-1,2,2,4-四氢-2-萘基]-4-吗啉基苯甲酰胺的一种盐的新型形式,称为(R)-N-[5-甲基-8-(4-甲基哌嗪-1-基)-1,2,3,4-四氢-2-萘基]-4-吗啉基苯甲酰胺单一溴化氢酸盐A形式。本发明还涉及制备该A形式的工艺,该形式在适当的制药配方后具有潜在的医疗用途,特别是在中枢神经系统疾病、过度活跃的膀胱或血管痉挛或肿瘤生长控制方面。
    公开号:
    US06706710B2
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文献信息

  • Novel form of (r)-n-[5-methyl-8-(4-methylpiperazin-1-yl)-1,2,3,4-tetrahydro-2-naphthyl]-4-morpholinobenzamide
    申请人:——
    公开号:US20030166653A1
    公开(公告)日:2003-09-04
    This invention relates to a novel form of a serotonin h5-HT 1B -receptor antagonist, namely a novel form of a salt of (R)-N-[5-methyl-8-(4-methylpiperazin-1-yl)-1,2,3,4-tetrahydro-2-naphtyl]-4-morpholinobenzamide referred to as (R)-N-[5-methyl-8-(4-methylpiperazin-1-yl)-1,2,3,4-tetrahydro-2-naphtyl]-4-morpholinobenzamide monohydrobromide Form A. The invention also relates to processes for preparation of said of Form A, which form has a potential use after suitable pharmaceutical formulation in medical treatment, preferably in CNS disorders, over active bladder or vasospam, or growth control of tumors.
    本发明涉及一种新型的血清素h5-HT1B受体拮抗剂,即(R)-N-[5-甲基-8-(4-甲基哌嗪-1-基)-1,2,3,4-四氢-2-基]-4-吗啉基苯甲酰胺的盐的新型形式,称为(R)-N-[5-甲基-8-(4-甲基哌嗪-1-基)-1,2,3,4-四氢-2-基]-4-吗啉基苯甲酰胺单盐酸A型。本发明还涉及制备该A型形式的方法,该形式在适当的药物制剂后具有潜在的医疗用途,优选用于中枢神经系统疾病、过度活跃的膀胱或血管痉挛或肿瘤生长控制等方面。
  • New oral immediated release dosage form
    申请人:Eriksson Patrik
    公开号:US20060034911A1
    公开(公告)日:2006-02-16
    The present invention relates to a solid oral immediate release dosage form of a pharmaceutically active compound, N-[(1,2,3,4-tetrahydro-5-methyl-8-(4-methylpiperazin-1-yl)-2-naphthyl]-4-morpholinobenzamide, in the form of the free base or pharmaceutically acceptable salts thereof. The invention further relates to processes for preparing said dosage form, the use of said dosage form and a method of prevention and/or treatment of CNS disorders and related medical disturbances using said dosage form.
    本发明涉及一种药物活性化合物N-[(1,2,3,4-四氢-5-甲基-8-(4-甲基哌嗪-1-基)-2-基]-4-吗啉苯甲酰胺的固体口服速释剂型,其形式为游离碱或其药学上可接受的盐。本发明进一步涉及制备所述剂型的工艺、所述剂型的用途以及使用所述剂型预防和/或治疗中枢神经系统紊乱及相关医疗干扰的方法。
  • MORPHOLINOBENZAMIDE SALTS
    申请人:AstraZeneca AB
    公开号:EP1149083A1
    公开(公告)日:2001-10-31
  • NOVEL FORM OF (R)- i N /i - 5-METHYL-8-(4-METHYLPIPERAZIN-1-YL)-1,2,3,4-TETRAHYDRO-2-NAPHTHYL]-4-MORPHOLINOBENZAMIDE
    申请人:AstraZeneca AB
    公开号:EP1305303A1
    公开(公告)日:2003-05-02
  • METHOD OF USING AMINOCYANOPYRIDINE COMPOUNDS AS MITOGEN ACTIVATED PROTEIN KINASE-ACTIVATED PROTEIN KINASE-2 INHIBITORS
    申请人:Pharmacia Corporation
    公开号:EP1569645A2
    公开(公告)日:2005-09-07
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