3-碘-6,6-二甲基-环己-2-烯酮 | 1020202-99-6

• 分子结构分类: 有机化合物 - 有机氧化合物
• 中文名称: 3-碘-6,6-二甲基-环己-2-烯酮
• 英文名称: 3-iodo-6,6-dimethyl-cyclohex-2-enone
• 英文别名: 3-Iodo-6,6-dimethylcyclohex-2-enone；3-iodo-6,6-dimethylcyclohex-2-en-1-one
• CAS: 1020202-99-6
• 化学式: C₈H₁₁IO
• 分子量: 250.079
• InChiKey: GSDRNEBOVBOFGK-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2
• 重原子数：
  10
• 可旋转键数：
  0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.62
• 拓扑面积：
  17.1
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  3-碘-6,6-二甲基-环己-2-烯酮 在 sodium tetrahydroborate 、 cerium(III) chloride heptahydrate 作用下， 以 甲醇 为溶剂， 以99%的产率得到3-iodo-6,6-dimethyl-cyclohex-2-enol
  参考文献：
  名称：

  Allenyl Azide Cycloaddition Chemistry. Photochemical Initiation and CuI Mediation Leads to Improved Regioselectivity

  摘要：

  Irradiation of 2-(3-alkenyl)allenylphenyl azides in the presence of excess Cul furnished functionalized 2,3-cyclopentenylindoles in good yield with only trace amounts of competitive C-N-bonded regioisomeric products. These results represent a significant departure from the modestto-nonexistent regioselectivity that attended thermal cyclization of these allenyl azide substrates.

  DOI：

  10.1021/ol800429j
• 作为产物：
  描述：

  4,4-二甲基-1,3-环己二酮 在 碘 、 三乙胺 、 三苯基膦 作用下， 以 乙腈 为溶剂， 反应 72.0h， 以92%的产率得到3-碘-6,6-二甲基-环己-2-烯酮
  参考文献：
  名称：

  Allenyl Azide Cycloaddition Chemistry. Photochemical Initiation and CuI Mediation Leads to Improved Regioselectivity

  摘要：

  Irradiation of 2-(3-alkenyl)allenylphenyl azides in the presence of excess Cul furnished functionalized 2,3-cyclopentenylindoles in good yield with only trace amounts of competitive C-N-bonded regioisomeric products. These results represent a significant departure from the modestto-nonexistent regioselectivity that attended thermal cyclization of these allenyl azide substrates.

  DOI：

  10.1021/ol800429j

文献信息

• [EN] NOVEL CYP17 INHIBITORS/ANTIANDROGENS<br/>[FR] NOUVEAUX INHIBITEURS DE CYP17/ANTIANDROGÈNES
  申请人：ORION CORP

  公开号：WO2014202827A1

  公开（公告）日：2014-12-24

  Compounds of formula (I), wherein R1 to R8 A, B, Z1 and Z2 are as defined in the claims and pharmaceutically acceptable salts and esters thereof are disclosed. The compounds of formula (I) possess utility as androgen receptor antagonists (inhibitors) and/or cytochrome P450 monooxygenase 17a-hydroxylase/17,20-lyase (CYP17) inhibitors. The compounds are useful as medicaments in the treatment of cancer, particularly prostate cancer, and other androgen dependent conditions and diseases where androgen antagonism is desired.

  公式（I）的化合物，其中R1至R8，A，B，Z1和Z2如权利要求中所定义，并且其药用盐和酯被披露。公式（I）的化合物具有作为雄激素受体拮抗剂（抑制剂）和/或细胞色素P450单加氧酶17a-羟化酶/17,20-裂解酶（CYP17）抑制剂的效用。这些化合物在治疗癌症，特别是前列腺癌，以及其他需要雄激素拮抗作用的疾病和情况中作为药物是有用的。
• NOVEL CYP17 INHIBITORS/ANTIANDROGENS
  申请人：ORION CORPORATION

  公开号：US20160130254A1

  公开（公告）日：2016-05-12

  Compounds of formula (I) wherein R 1 to R 8 , A, B, Z 1 , and Z 2 are as defined in the claims and pharmaceutically acceptable salts and esters thereof are disclosed. The compounds of formula (I) possess utility as androgen receptor antagonists (inhibitors) and/or cytochrome P450 monooxygenase 17α-hydroxylase/17,20-lyase (CYP17) inhibitors. The compounds are useful as medicaments in the treatment of cancer, particularly prostate cancer, and other androgen dependent conditions and diseases where androgen antagonism is desired.

  公式（I）化合物的结构式中，其中R1至R8，A，B，Z1和Z2如权利要求所定义，并且其药学上可接受的盐和酯被揭示。公式（I）化合物具有作为雄激素受体拮抗剂（抑制剂）和/或细胞色素P450单加氧酶17α-羟化酶/17,20-裂解酶（CYP17）抑制剂的效用。这些化合物在治疗癌症，特别是前列腺癌和其他需要雄激素拮抗剂的疾病和病情中作为药物是有用的。
• Allenyl Azide Cycloaddition Chemistry. 2,3-Cyclopentennelated Indole Synthesis through Indolidene Intermediates
  作者：Ken S. Feldman、D. Keith Hester、Malliga R. Iyer、Paul J. Munson、Carlos Silva López、Olalla Nieto Faza

  DOI：10.1021/jo900659w

  日期：2009.7.17

  The thermal, photochemical, and photochemical/CuI-mediated cascade cyclizations of a range of substituted 1-(2-azidophenyl)-3-alkenylallenes are described. These reactions provide both 1,2- and 2,3-cyclopentennelated indole products in varying ratios. In most cases, high regioselectivity for the 2,3-annelated isomer can be achieved under the hv/CuI conditions. Computational studies of this multistep reaction support the intermediacy of indolidene intermediates whose electrocyclizations (with or without copper present) define the regioselectivity branch point in the sequence.
• US9890139B2
  申请人：——

  公开号：US9890139B2

  公开（公告）日：2018-02-13