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1-deoxy-Δ8-tetrahydrocannabinyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane | 1227828-17-2

中文名称
——
中文别名
——
英文名称
1-deoxy-Δ8-tetrahydrocannabinyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
英文别名
4,4,5,5-tetramethyl-2-((6aR,10aR)-6,6,9-trimethyl-3-pentyl-6a,7,10,10a-tetrahydro-6H-benzo[c]chromen-1-yl)-1,3,2-dioxaborolane;2-[(6aR,10aR)-6,6,9-trimethyl-3-pentyl-6a,7,10,10a-tetrahydrobenzo[c]chromen-1-yl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
1-deoxy-Δ8-tetrahydrocannabinyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane化学式
CAS
1227828-17-2
化学式
C27H41BO3
mdl
——
分子量
424.432
InChiKey
AKWGAUCEMVTORZ-NHCUHLMSSA-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):
    6.33
  • 重原子数:
    31
  • 可旋转键数:
    5
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.7
  • 拓扑面积:
    27.7
  • 氢给体数:
    0
  • 氢受体数:
    3

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    1-deoxy-Δ8-tetrahydrocannabinyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolanecopper(ll) bromide 作用下, 以 甲醇 为溶剂, 反应 10.0h, 以75%的产率得到JWH-460
    参考文献:
    名称:
    1-Bromo-3-(1′,1′-dimethylalkyl)-1-deoxy-Δ8-tetrahydrocannabinols: New selective ligands for the cannabinoid CB2 receptor
    摘要:
    Delta(8)-Tetrahydrocannabinol (26), 3-(1',1'-dimethylbutyl)- (12), 3-(1',1'-dimethylpentyl)- (13), 3-(1',1'-dimethylhexyl)- (14) and 3-(1',1'-dimethylheptyl)-Delta(8)-tetrahydrocannabinol (15) have been converted into the corresponding 1-bromo-1-deoxy-Delta(8)-tetrahydrocannabinols (25, 8-11). This was accomplished using a protocol developed in our laboratory in which the trifluoromethanesulfonate of a phenol undergoes palladium mediated coupling with pinacolborane. Reaction of this dioxaborolane with aqueous-methanolic copper(II) bromide provides the aryl bromide. The affinities of these bromo cannabinoids for the cannabinoid CB1 and CB2 receptors were determined. All of these compounds showed selectivity for the CB2 receptor and one of them, 1-bromo-1-deoxy-3-(1',1'-dimethylhexyl)-Delta(8)-tetrahydrocannabinol (10), exhibits 52-fold selectivity for this receptor with good (28 nM) affinity. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2010.09.061
  • 作为产物:
    描述:
    Δ8-tetrahydrocannabinyl trifluoromethanesulfonate频那醇硼烷1,1'-双(二苯膦基)二茂铁二氯化钯(II)二氯甲烷复合物三乙胺 作用下, 以 乙腈 为溶剂, 以65%的产率得到1-deoxy-Δ8-tetrahydrocannabinyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
    参考文献:
    名称:
    1-Bromo-3-(1′,1′-dimethylalkyl)-1-deoxy-Δ8-tetrahydrocannabinols: New selective ligands for the cannabinoid CB2 receptor
    摘要:
    Delta(8)-Tetrahydrocannabinol (26), 3-(1',1'-dimethylbutyl)- (12), 3-(1',1'-dimethylpentyl)- (13), 3-(1',1'-dimethylhexyl)- (14) and 3-(1',1'-dimethylheptyl)-Delta(8)-tetrahydrocannabinol (15) have been converted into the corresponding 1-bromo-1-deoxy-Delta(8)-tetrahydrocannabinols (25, 8-11). This was accomplished using a protocol developed in our laboratory in which the trifluoromethanesulfonate of a phenol undergoes palladium mediated coupling with pinacolborane. Reaction of this dioxaborolane with aqueous-methanolic copper(II) bromide provides the aryl bromide. The affinities of these bromo cannabinoids for the cannabinoid CB1 and CB2 receptors were determined. All of these compounds showed selectivity for the CB2 receptor and one of them, 1-bromo-1-deoxy-3-(1',1'-dimethylhexyl)-Delta(8)-tetrahydrocannabinol (10), exhibits 52-fold selectivity for this receptor with good (28 nM) affinity. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2010.09.061
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文献信息

  • FLUORINATION OF ORGANIC COMPOUNDS
    申请人:Ritter Tobias
    公开号:US20110312903A1
    公开(公告)日:2011-12-22
    Methods for fluorinating organic compounds are described herein.
    本文描述了有机化合物氟化的方法。
  • Fluorination of organic compounds
    申请人:Ritter Tobias
    公开号:US09024093B2
    公开(公告)日:2015-05-05
    Methods for fluorinating organic compounds are described herein.
    本文描述了有机化合物氟化的方法。
  • 1-Bromo-3-(1′,1′-dimethylalkyl)-1-deoxy-Δ8-tetrahydrocannabinols: New selective ligands for the cannabinoid CB2 receptor
    作者:John W. Huffman、Seon A. Hepburn、Nataliya Lyutenko、Alicia L.S. Thompson、Jenny L. Wiley、Dana E. Selley、Billy R. Martin
    DOI:10.1016/j.bmc.2010.09.061
    日期:2010.11.15
    Delta(8)-Tetrahydrocannabinol (26), 3-(1',1'-dimethylbutyl)- (12), 3-(1',1'-dimethylpentyl)- (13), 3-(1',1'-dimethylhexyl)- (14) and 3-(1',1'-dimethylheptyl)-Delta(8)-tetrahydrocannabinol (15) have been converted into the corresponding 1-bromo-1-deoxy-Delta(8)-tetrahydrocannabinols (25, 8-11). This was accomplished using a protocol developed in our laboratory in which the trifluoromethanesulfonate of a phenol undergoes palladium mediated coupling with pinacolborane. Reaction of this dioxaborolane with aqueous-methanolic copper(II) bromide provides the aryl bromide. The affinities of these bromo cannabinoids for the cannabinoid CB1 and CB2 receptors were determined. All of these compounds showed selectivity for the CB2 receptor and one of them, 1-bromo-1-deoxy-3-(1',1'-dimethylhexyl)-Delta(8)-tetrahydrocannabinol (10), exhibits 52-fold selectivity for this receptor with good (28 nM) affinity. (C) 2010 Elsevier Ltd. All rights reserved.
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