1-(2-甲氧基-4-苯基甲氧基苯基)乙酮 | 56879-12-0

• 分子结构分类: 有机化合物 - 有机氧化合物
• 中文名称: 1-(2-甲氧基-4-苯基甲氧基苯基)乙酮
• 英文名称: 4-benzyloxy-2-methoxyacetophenone
• 英文别名: 1-(4-(Benzyloxy)-2-methoxyphenyl)ethanone；1-(2-methoxy-4-phenylmethoxyphenyl)ethanone
• CAS: 56879-12-0
• 化学式: C₁₆H₁₆O₃
• 分子量: 256.301
• InChiKey: BMMMQCKSIJBHKA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.3
• 重原子数：
  19
• 可旋转键数：
  5
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.19
• 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：

  1-(2-甲氧基-4-苯基甲氧基苯基)乙酮 在 正丁基锂 、 镍 、 potassium carbonate 作用下， 以 四氢呋喃 、 1,4-二氧六环 为溶剂， 反应 36.0h， 生成 6-Allyl-4-(2-benzo[1,3]dioxol-5-yl-1-methyl-ethyl)-3,6-dimethoxy-cyclohexa-2,4-dienone
  参考文献：
  名称：

  （± ） -Δ9 （12） -capnellene的全合成

  摘要：

  从2-环戊烯酮开始，标题化合物是通过[2 + 2]和[4 + 2]环加成反应的组合而合成的。

  DOI：

  10.1016/s0040-4039(00)94967-0
• 作为产物：
  描述：

  2,4-二羟基苯乙酮 在 potassium carbonate 作用下， 以 N,N-二甲基甲酰胺 、 丙酮 为溶剂， 生成 1-(2-甲氧基-4-苯基甲氧基苯基)乙酮
  参考文献：
  名称：

  A novel class of apical sodium-dependent bile acid transporter inhibitors: the amphiphilic 4-oxo-1-phenyl-1,4-dihydroquinoline derivatives

  摘要：

  A series of 4-oxo-1-phenyl-1,4-dihydroquinolines possessing a linker and an ammonio moiety were synthesized and found to inhibit the apical sodium-dependent bile acid transporter (ASBT). The potency of ASBT inhibition varied with the position and length of the linking tether. Compound 21e effectively lowered the total serum cholesterol levels in hamsters. (C) 2003 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2003.12.063

文献信息

• [EN] ESTROGEN RECEPTOR TARGETING ANTAGONISTS<br/>[FR] ANTAGONISTES CIBLANT LE RÉCEPTEUR DES OESTROGÈNES
  申请人：XAVIER UNIV OF LOUISIANA

  公开号：WO2020055973A1

  公开（公告）日：2020-03-19

  The present disclosure relates to compounds that act as antagonists via binding to the ER ligand binding domain non-covalently or covalently, or act as both antagonists and ER protein degraders, and the synthesis of the same. Further, the present disclosure teaches the utilization of such compounds in a treatment for proliferative diseases, including cancer, particularly breast cancer, and especially ER+ breast cancer.

  本公开涉及通过非共价或共价结合到ER配体结合结构域的化合物，作为拮抗剂或同时作为拮抗剂和ER蛋白降解剂，并且涉及这些化合物的合成。此外，本公开教导了利用这些化合物治疗增殖性疾病，包括癌症，特别是乳腺癌，尤其是ER+乳腺癌。
• Structural confirmation of spiroelliptin from Iryanthera elliptica by synthesis
  作者：Anselmo A. Morais、Raimundo Braz Fo、Otto R. Gottlieb

  DOI：10.1016/0031-9422(85)80049-2

  日期：1985.11

  Abstract Spiroelliptin, a spiro[cyclohexadienone-1,1′-tetralin] from Iryanthera elliptica , was synthesized by a novel process which involved the catalytic hydrogenation of the appropriate chalcone. This and other spiro[methoxycyclobexadienone-1,1′-tetralin] derivatives, obtained by the same process or by the oxidative coupling of the appropriate 1,3-diarylpropanes, were used as models in the compilation

  摘要 Spiroelliptin 是一种来自 Iryanthera elliptica 的螺[环己二烯酮-1,1'-萘满]，通过一种涉及适当查尔酮催化氢化的新工艺合成。通过相同的方法或通过适当的 1,3-二芳基丙烷的氧化偶联获得的这种和其他螺[甲氧基环苯并二烯酮-1,1'-萘满] 衍生物被用作 1 H 和 13 C NMR 数据汇编的模型允许识别三种这样的天然结构类型。
• Substituted imidazopyrimidines-pyrazines, and -triazines
  申请人：ELI LILLY AND COMPANY

  公开号：EP0113236A1

  公开（公告）日：1984-07-11

  Compounds having the formula (I) and their pharmaceutically acceptable salts, wherein one or two of A1, A2, A3, and A4 is N, and the remaining A1, A2, A3, and A4 are CH, provided that if A4 is N, then one of A1, A2, and A3 is also N, and provided that one of A1, A2, and A3 may be CX where X is halo; and each of R1, R2, and R3 is independently hydrogen, C1-C4 alkyl, C1-C4 alkoxy, allyloxy, benzyloxy, (C1-C4 alkyl) thio, (C1-C4 alkyl) sulfinyl, (C1-C4 alkyl)sulfonyl, hydroxy, halo, cyano, nitro, amino, mono- or di-(C1-C4 alkyl)amino, trifluoromethyl, or Z-Q-substituted C1-C4 alkoxy, wherein 0 is oxygen, sulfur, sulfinyl, sulfonyl, or a bond, and Z is C1-C4 alkyl, phenyl or phenyl substituted with halo, C1-C4 alkyl, C1-C4 alkoxy, hydroxy, nitro, amino, C1-C4 alkylthio, C,-C4 alkylsulfinyl, or C1-C4 alkylsulfonyl are ionotropic agents or intermediates thereto.

  具有式 (I) 的化合物 及其药学上可接受的盐类，其中 A1、A2、A3 和 A4 中的一个或两个是 N，其余的 A1、A2、A3 和 A4 是 CH，条件是如果 A4 是 N，则 A1、A2 和 A3 中的一个也是 N，并且 A1、A2 和 A3 中的一个可以是 CX，其中 X 是卤素；R1、R2 和 R3 各自独立地为氢、C1-C4 烷基、C1-C4 烷氧基、烯丙氧基、苄氧基、(C1-C4 烷基)硫基、(C1-C4 烷基)亚磺基、(C1-C4 烷基)磺酰基、羟基、卤代、氰基、硝基、氨基、单-或二-(C1-C4 烷基)氨基、三氟甲基或 Z-Q 取代的 C1-C4 烷氧基、其中 0 是氧、硫、亚砜基、磺酰基或键，Z 是 C1-C4 烷基、苯基或被卤素、C1-C4 烷基、C1-C4 烷氧基、羟基、硝基、氨基、C1-C4 烷硫基、C,-C4 烷基亚砜基或 C1-C4 烷基磺酰基取代的苯基。
• Nath, Swadhin; Bhattacharyya, Anjan; Sengupta, P. K., Journal of the Indian Chemical Society, 1983, vol. 60, p. 801 - 802
  作者：Nath, Swadhin、Bhattacharyya, Anjan、Sengupta, P. K.

  DOI：——

  日期：——
• A Short-step Convenient Synthesis of 2-Phenylbenzofuran from 3-Phenylcoumarin
  作者：Takeshi Kinoshita、Koji Ichinose

  DOI：10.3987/com-05-10424

  日期：——

  The reaction mechanism of chemical conversion of (E)-beta-[2-hydroxylphenylcthylene]benzeneethanol into 2-phenylbenzofuran by DDQ, which involves loss of one carbon unit, was characterized and described. Five naturally occurring 2-phenylbenzofurans of not only the isoflavonoid but also stilbenoid origin were synthesized by use of this chemical scheme, which proved that this new scheme is a useful tool for quick synthesis of 2-phenylbenzofurans.