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3-Methoxy-7α-methylmorphinan-6-one Hydrochloride | 75764-89-5

中文名称
——
中文别名
——
英文名称
3-Methoxy-7α-methylmorphinan-6-one Hydrochloride
英文别名
3-Methoxy-7alpha-methylmorphinan-6-one Hydrochloride;(1S,9R,10R,12S)-4-methoxy-12-methyl-17-azatetracyclo[7.5.3.01,10.02,7]heptadeca-2(7),3,5-trien-13-one;hydrochloride
3-Methoxy-7α-methylmorphinan-6-one Hydrochloride化学式
CAS
75764-89-5
化学式
C18H23NO2*ClH
mdl
——
分子量
321.847
InChiKey
AKOVJGSTOWNGCL-BJLGAWORSA-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):
    2.89
  • 重原子数:
    22
  • 可旋转键数:
    1
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.61
  • 拓扑面积:
    38.3
  • 氢给体数:
    2
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    3-Methoxy-7α-methylmorphinan-6-one Hydrochloride氢溴酸碳酸氢钠 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 22.33h, 生成
    参考文献:
    名称:
    Analgesic narcotic antagonists. 4. 7-Methyl-N-(cycloalkylmethyl)-3-hydroxy morphinan-6-one and -isomorphinan-6-one
    摘要:
    3,6-Dimethoxy-7 beta, 17-dimethyl-4-hydroxy-5,6,8,14-tetradehydromorphinan (2) was converted to the 4-deoxy compound 4 and hydrolyzed to a mixture of the B/C-cis (C series) and B/C-trans (T series) isomers of 7,8-didehydromorphinan-6-one, 5. Hydrogenation of the separated isomers gave 7-methyl-6-oxo derivatives 6a. 7,8-Dimethyl-(6b) or 7-methyl-8-ethylmorphinan-6-one (6c) was prepared by reaction of 5 with lithium organocuprates. The analgesic N-methyl compounds 6 were converted to 17-(cyclopropylmethyl) or 17-(cyclobutylmethyl) derivatives 10--13. Some of these compounds had mixed profiles of narcotic agonist-antagonist effects. Studies with drug-dependent monkeys indicated that several of these compounds with an analgesic-antagonist ratio of less than 0.4 substitute for morphine.
    DOI:
    10.1021/jm00186a025
  • 作为产物:
    描述:
    17-Cyano-3-methoxy-7α-methylmorphinan-6-one 以 盐酸 为溶剂, 生成 3-Methoxy-7α-methylmorphinan-6-one Hydrochloride
    参考文献:
    名称:
    7-Methyl-8.beta.-lower alkyl or 7-methyl-8-lower alkyl B/C cis or trans
    摘要:
    揭示了具有以下结构式的7-甲基,8.beta.-较低烷基和7-甲基-8-较低烷基取代的B/C顺式或反式吗啡酮化合物:具体化合物包括在上述一般式范围内,其中R.sub.1为H或甲基,R.sub.2为环丙基甲基或环丁基甲基,R.sub.3为H,甲基,乙基或正丙基,R.sub.4为H或甲基,可用作混合镇痛剂/麻醉拮抗剂。
    公开号:
    US04230712A1
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文献信息

  • 7-Methyl-8.beta.-lower alkyl or 7-methyl-8-lower alkyl B/C cis or trans
    申请人:Miles Laboratories, Inc.
    公开号:US04230712A1
    公开(公告)日:1980-10-28
    Disclosed are 7-methyl, 8.beta.-lower alkyl and 7 methyl-8-lower alkyl substituted B/C Cis or Trans morphinan-6-one compounds characterized by the structural formula: ##STR1## Specific compounds, included within the scope of the foregoing general formula wherein R.sub.1 is H or methyl, R.sub.2 is cyclopropylmethyl or cyclobutylmethyl, R.sub.3 is H, methyl, ethyl or n-propyl and R.sub.4 is H or methyl are useful as mixed analgesics/narcotic antagonists.
    揭示了具有以下结构式的7-甲基,8.beta.-较低烷基和7-甲基-8-较低烷基取代的B/C顺式或反式吗啡酮化合物:具体化合物包括在上述一般式范围内,其中R.sub.1为H或甲基,R.sub.2为环丙基甲基或环丁基甲基,R.sub.3为H,甲基,乙基或正丙基,R.sub.4为H或甲基,可用作混合镇痛剂/麻醉拮抗剂。
  • 7-Methyl and 7-methyl-8-lower alkyl B/C cis or trans morphinan-6-one compounds, process for their preparation and pharmaceutical preparations containing them
    申请人:MILES LABORATORIES, INC.
    公开号:EP0019254B1
    公开(公告)日:1982-09-01
  • US4230712A
    申请人:——
    公开号:US4230712A
    公开(公告)日:1980-10-28
  • Analgesic narcotic antagonists. 4. 7-Methyl-N-(cycloalkylmethyl)-3-hydroxy morphinan-6-one and -isomorphinan-6-one
    作者:David L. Leland、Michael P. Kotick
    DOI:10.1021/jm00186a025
    日期:1980.12
    3,6-Dimethoxy-7 beta, 17-dimethyl-4-hydroxy-5,6,8,14-tetradehydromorphinan (2) was converted to the 4-deoxy compound 4 and hydrolyzed to a mixture of the B/C-cis (C series) and B/C-trans (T series) isomers of 7,8-didehydromorphinan-6-one, 5. Hydrogenation of the separated isomers gave 7-methyl-6-oxo derivatives 6a. 7,8-Dimethyl-(6b) or 7-methyl-8-ethylmorphinan-6-one (6c) was prepared by reaction of 5 with lithium organocuprates. The analgesic N-methyl compounds 6 were converted to 17-(cyclopropylmethyl) or 17-(cyclobutylmethyl) derivatives 10--13. Some of these compounds had mixed profiles of narcotic agonist-antagonist effects. Studies with drug-dependent monkeys indicated that several of these compounds with an analgesic-antagonist ratio of less than 0.4 substitute for morphine.
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