摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

[1R,8S,9aR] 1-carbomethoxy-5-methoxy-8-phenyl-2,3,7,8,9,9a-hexahydrophenalene

中文名称
——
中文别名
——
英文名称
[1R,8S,9aR] 1-carbomethoxy-5-methoxy-8-phenyl-2,3,7,8,9,9a-hexahydrophenalene
英文别名
methyl (1R,8S,9aR)-5-methoxy-8-phenyl-2,3,7,8,9,9a-hexahydro-1H-phenalene-1-carboxylate
[1R,8S,9aR] 1-carbomethoxy-5-methoxy-8-phenyl-2,3,7,8,9,9a-hexahydrophenalene化学式
CAS
——
化学式
C22H24O3
mdl
——
分子量
336.431
InChiKey
GBYSSDBCBHTIBR-NSISKUIASA-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):
    4.5
  • 重原子数:
    25
  • 可旋转键数:
    4
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.41
  • 拓扑面积:
    35.5
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    [1R,8S,9aR] 1-carbomethoxy-5-methoxy-8-phenyl-2,3,7,8,9,9a-hexahydrophenalenesodium hydroxide 作用下, 以 甲醇乙醚 为溶剂, 生成 [1R,8S,9AR]-5-Methoxy-8-phenyl-2,3,7,8,9,9a-hexahydrophenalene-1-carboxylic acid
    参考文献:
    名称:
    Dopaminergic compounds
    摘要:
    化合物的化学式(I)的新颖化合物:##STR1##或其药学上可接受的盐、酯和酰胺,其中A为O、C、CH或CH.sub.2,n为0或1,虚线是当A为O或CH.sub.2时为单键,当A为CH或n=0时为双键,当A为C且R.sub.6和A一起形成含氮杂环时,R为氢、低碳烷基或易解离基团;R.sub.1选择自氢、卤素、低碳烷基、卤代烷基和低烷氧基;R.sub.2选择自氢、卤素、低碳烷基和卤代烷基或与R.sub.8一起形成融合环;R.sub.3为氢、烷基、烯基、炔基、环烷基、芳基或芳基烷基或与R.sub.4一起形成螺环烷基或与R.sub.5一起形成融合环烷基;R.sub.4为氢或烷基或与R.sub.3一起形成螺环烷基;R.sub.5为氢或烷基或与R.sub.3一起形成融合环烷基;R.sub.6为氢、烷基、烯基、炔基、环烷基或芳基烷基或与A一起形成融合含氮杂环或与R.sub.7或R.sub.8一起形成含氮杂环;R.sub.7为氢或烷基或与R.sub.6或R.sub.8一起形成含氮杂环;R.sub.8为氢或烷基或与R.sub.6或R.sub.7一起形成含氮杂环或与R.sub.2一起形成融合环,但R.sub.3和R.sub.4不能同时都是氢,是选择性多巴胺能作用剂,用于治疗中枢或外周神经系统中存在异常多巴胺能活性的疾病,例如,神经症、帕金森病、某些心血管疾病和成瘾行为障碍。
    公开号:
    US04994486A1
  • 作为产物:
    描述:
    (1R,8S,9AR)-1-carbomethoxy-5-methoxy-3-hydroxy-8-phenyl-7,8,9,9a-tetrahydrophenalene 、 乙酸乙酯盐酸氢气 作用下, 以 甲醇 为溶剂, 生成 [1R,8S,9aR] 1-carbomethoxy-5-methoxy-8-phenyl-2,3,7,8,9,9a-hexahydrophenalene
    参考文献:
    名称:
    Dopaminergic compounds
    摘要:
    公式(I)的新化合物:##STR1##或其药物可接受的盐、酯和酰胺,其中A是O、C、CH或CH.sub.2,n为0或1,当A为O或CH.sub.2时,虚线为单键,当A为CH或n=0时,虚线为双键,当A为C且R.sub.6和A一起形成含氮杂环时,n为0;R为氢、低级烷基或易于断裂的基团;R.sub.1选自氢、卤素、低级烷基、卤代烷基和低级烷氧基;R.sub.2选自氢、卤素、低级烷基和卤代烷基,或与R.sub.8一起形成融合环;R.sub.3选自氢、烷基、烯基、炔基、环烷基、芳基或芳基烷基,或与R.sub.4一起形成螺环烷基,或与R.sub.5一起形成融合环烷基;R.sub.4选自氢或烷基,或与R.sub.3一起形成螺环烷基;R.sub.5选自氢或烷基,或与R.sub.3一起形成融合环烷基;R.sub.6选自氢、烷基、烯基、炔基、环烷基或芳基烷基,或当A为C且n为0时,与A一起形成融合含氮杂环,或与R.sub.7或R.sub.8一起形成含氮杂环;R.sub.7选自氢或烷基,或与R.sub.6或R.sub.8一起形成含氮杂环;R.sub.8选自氢或烷基,或与R.sub.6或R.sub.7一起形成含氮杂环,或与R.sub.2一起形成融合环,但R.sub.3和R.sub.4不能同时为氢。这些化合物是选择性多巴胺能药物,并且用于治疗中枢或外周神经系统中多巴胺活动异常的疾病,例如神经疾病(如精神病、帕金森病、某些心血管疾病和成瘾行为障碍)。
    公开号:
    US04994486A1
点击查看最新优质反应信息

文献信息

  • Dopaminergic compounds
    申请人:Abbott Laboratories
    公开号:US04994486A1
    公开(公告)日:1991-02-19
    Novel compounds of Formula (I): ##STR1## or pharmaceutically acceptable salts, esters and amides thereof, wherein A is O, C, CH or CH.sub.2, n is 0 or 1, and the dotted line is a single bond when A is O or CH.sub.2 and a double bond when A is CH or when n=0, A is C and R.sub.6 and A taken together form a nitrogen-containing heterocycle; R is hydrogen, lower alkyl or a readily cleavable group; R.sub.1 is selected from hydrogen, halogen, lower alkyl, haloalkyl and lower alkoxy; R.sub.2 is selected from hydrogen, halogen, lower alkyl and haloalkyl or, taken together with R.sub.8, forms a fused ring; R.sub.3 is hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, aryl or arylalkyl or, taken together with R.sub.4, forms a spirocycloalkyl or, taken together with R.sub.5, forms a fused cycloalkyl; R.sub.4 is hydrogen or alkyl or, taken together with R.sub.3, forms a spirocycloalkyl; R.sub.5 is hydrogen or alkyl or, taken together with R.sub.3, forms a fused cycloalkyl; R.sub.6 is hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl or arylalkyl or, taken together with A when A is C and when n is 0, forms a fused nitrogen-containing heterocycle or, taken together with R.sub.7 or R.sub.8, forms a nitrogen-containing heterocycle; R.sub.7 is hydrogen or alkyl or, taken together with R.sub.6 or R.sub.8, forms a nitrogen-containing heterocycle; R.sub.8 is hydrogen or alkyl or, taken together with R.sub.6 or R.sub.7, forms a nitrogen-containing heterocycle or, taken together with R.sub.2, forms a fused ring, with the proviso that R.sub.3 and R.sub.4 cannot simultaneously both be hydrogen, are selective dopaminergic agents and are useful for treating disorders characterized by abnormal dopaminergic activity in the central or the peripheral nervous system, for example, neurological disorders such as psychoses, Parkinson's Disease, certain cardiovascular disorders and addictive behavior disorders.
    化合物的化学式(I)的新颖化合物:##STR1##或其药学上可接受的盐、酯和酰胺,其中A为O、C、CH或CH.sub.2,n为0或1,虚线是当A为O或CH.sub.2时为单键,当A为CH或n=0时为双键,当A为C且R.sub.6和A一起形成含氮杂环时,R为氢、低碳烷基或易解离基团;R.sub.1选择自氢、卤素、低碳烷基、卤代烷基和低烷氧基;R.sub.2选择自氢、卤素、低碳烷基和卤代烷基或与R.sub.8一起形成融合环;R.sub.3为氢、烷基、烯基、炔基、环烷基、芳基或芳基烷基或与R.sub.4一起形成螺环烷基或与R.sub.5一起形成融合环烷基;R.sub.4为氢或烷基或与R.sub.3一起形成螺环烷基;R.sub.5为氢或烷基或与R.sub.3一起形成融合环烷基;R.sub.6为氢、烷基、烯基、炔基、环烷基或芳基烷基或与A一起形成融合含氮杂环或与R.sub.7或R.sub.8一起形成含氮杂环;R.sub.7为氢或烷基或与R.sub.6或R.sub.8一起形成含氮杂环;R.sub.8为氢或烷基或与R.sub.6或R.sub.7一起形成含氮杂环或与R.sub.2一起形成融合环,但R.sub.3和R.sub.4不能同时都是氢,是选择性多巴胺能作用剂,用于治疗中枢或外周神经系统中存在异常多巴胺能活性的疾病,例如,神经症、帕金森病、某些心血管疾病和成瘾行为障碍。
查看更多