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8-phenyl-1,4-dioxaspiro[4.5]decan-8-amine hydrochloride | 65619-74-1

中文名称
——
中文别名
——
英文名称
8-phenyl-1,4-dioxaspiro[4.5]decan-8-amine hydrochloride
英文别名
4-Amino-4-phenylcyclohexanone ethylene ketal hydrochloride;8-phenyl-1,4-dioxaspiro[4.5]decan-8-amine;hydrochloride
8-phenyl-1,4-dioxaspiro[4.5]decan-8-amine hydrochloride化学式
CAS
65619-74-1
化学式
C14H19NO2*ClH
mdl
——
分子量
269.771
InChiKey
FVXOGNXUZZJKFT-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):
    2.58
  • 重原子数:
    18
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.57
  • 拓扑面积:
    44.5
  • 氢给体数:
    2
  • 氢受体数:
    3

反应信息

点击查看最新优质反应信息

文献信息

  • 4-Amino-4-phenylcyclohexanone ketal compositions and process of use
    申请人:The Upjohn Company
    公开号:US04065573A1
    公开(公告)日:1977-12-27
    A class of new 4-amino-4-arylcyclohexanones, their ketals, and acid addition salts have been synthesized and found to be useful for relieving pain in animals. Their analgesic activity appears to be of high order, and in addition some exhibit narcotic antagonist activity that is useful in modifying the cardiovascular, respiratory, and behavioral depression caused by other analgesics. Several show mixed analgesic and narcotic antagonist activity. Preferred compounds of the class are 4-(m-hydroxyphenyl)-4-dimethylaminocyclohexanone ethylene ketal, and 4-(m-hydroxyphenyl)-4-(n-butylmethylamino)cyclohexanone ethylene ketal as free bases and as their hydrochloride salts. Processes for synthesis and intermediates are described. Unit dosage forms and therapeutic treatments are disclosed.
    一类新的4-基-4-芳基环己酮,它们的缩醛和酸盐已经合成,并发现对于缓解动物的疼痛很有用。它们的镇痛活性似乎是很高的,并且一些还表现出对镇痛引起的心血管、呼吸和行为抑制有用的麻醉拮抗活性。其中几种显示出混合的镇痛和麻醉拮抗活性。该类化合物的首选化合物是4-(间羟基苯基)-4-二甲氨基环己酮二醚缩醛,以及4-(间羟基苯基)-4-(正丁基甲基基)环己酮二醚缩醛,作为游离碱和其盐酸盐形式。描述了合成和中间体的过程。披露了单位剂量形式和治疗方法。
  • [EN] 3-((HETERO-)ARYL)-8-AMINO-2-OXO-1,3-DIAZA-SPIRO-[4.5]-DECANE DERIVATIVES<br/>[FR] DÉRIVÉS DE 3-((HÉTÉRO-)ARYL)-8-AMINO-2-OXO-1,3-DIAZA-SPIRO-[4.5]-DÉCANE
    申请人:GRUENENTHAL GMBH
    公开号:WO2017121647A1
    公开(公告)日:2017-07-20
    The invention relates to 3-((hetero-)aryl)-8-amino-2-oxo-1,3-diaza-spiro-[4.5]-decane derivatives, their preparation and their use in medicine, particularly in the treatment of pain.
    本发明涉及3-(杂)芳基-8-基-2-氧代-1,3-二氮杂螺[4.5]癸烷生物,它们的制备方法以及它们在医药中的应用,特别是在治疗疼痛方面的应用。
  • 3-(Carboxyethyl)-8-Amino-2-Oxo-1,3-Diaza-Spiro-[4.5]-Decane Derivatives
    申请人:Gruenenthal GmbH
    公开号:US20170197919A1
    公开(公告)日:2017-07-13
    The invention relates to 3-(carboxyethyl)-8-amino-2-oxo-1,3-diazaspiro-[4.5]-decane derivatives, their preparation and their use in medicine, particularly in the treatment of pain.
    这项发明涉及3-(羧乙基)-8-基-2-氧代-1,3-二氮杂螺[4.5]-癸烷生物,它们的制备以及它们在医学中的应用,特别是在疼痛治疗中的应用。
  • [EN] 3-((HETERO-)ARYL)-ALKYL-8-AMINO-2-OXO-1,3-DIAZA-SPIRO-[4.5]-DECANE DERIVATIVES<br/>[FR] DÉRIVÉS DE 3-((HÉTÉRO-)ARYL)-ALKYL-8-AMINO-2-OXO-1,3-DIAZA-SPIRO-[4.5]-DÉCANE
    申请人:GRUENENTHAL GMBH
    公开号:WO2017121648A1
    公开(公告)日:2017-07-20
    The invention relates to 3-((hetero-)aryl)-alkyl-8-amino-2-oxo-1,3-diaza-spiro-[4.5]-decane derivatives, their preparation and their use in medicine, particularly in the treatment of pain.
    这项发明涉及3-((杂-)芳基)-烷基-8-基-2-氧代-1,3-二氮杂-螺[4.5]-癸烷生物,它们的制备以及它们在医学中的应用,特别是在疼痛治疗中的应用。
  • 4-Amino-4-aryl-cyclohexanones
    申请人:The Upjohn Company
    公开号:US04460604A1
    公开(公告)日:1984-07-17
    A class of 4-amine-4-arylcyclohexanones, their ketals, and acid addition salts have been synthesized and found to be useful for relieving pain in animals. Their analgesic activity appears to be of high order, and in addition some exhibit narcotic antagonist activity that is useful in modifying the cardiovascular, respiratory, and behavioral depression caused by other analgesics. Several show mixed analgesic and narcotic antagonist activity. Preferred compounds of the class are 4-(m-hydroxyphenyl)-4-dimethylaminocyclohexanone ethylene ketal, and 4-(m-hydroxyphenyl)-4-(n-butylmethylamino)cyclohexanone ethylene ketal as free bases and as their hydrochloride salts. Processes for synthesis and intermediates are described. Unit dosage forms and therapeutic treatments are disclosed.
    一类4-基-4-芳基环己酮及其缩酮和酸加成盐已经被合成,并发现它们对动物缓解疼痛非常有用。它们的镇痛活性似乎是很高的,此外,一些化合物还表现出镇痛拮抗活性,对于调节其他镇痛药物引起的心血管、呼吸和行为抑制非常有用。几种化合物显示出混合的镇痛和镇痛拮抗活性。该类化合物中的优选化合物是4-(间羟基苯基)-4-二甲氨基环己酮乙烯缩酮和4-(间羟基苯基)-4-(正丁基甲基基)环己酮乙烯缩酮,作为自由碱和它们的盐酸盐。描述了合成和中间体的过程。公制剂量形式和治疗方法也被披露。
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