(R)-3-(hydroxymethyl)-6-methoxy-1,2,3,4-tetrahydronaphthalen-1-one | 651013-86-4

• 分子结构分类: 有机化合物 - 苯类化合物 - 四氢化萘
• 英文名称: (R)-3-(hydroxymethyl)-6-methoxy-1,2,3,4-tetrahydronaphthalen-1-one
• 英文别名: (3R)-3-(Hydroxymethyl)-6-methoxy-3,4-dihydronaphthalen-1(2H)-one；(3R)-3-(hydroxymethyl)-6-methoxy-3,4-dihydro-2H-naphthalen-1-one
• CAS: 651013-86-4
• 化学式: C₁₂H₁₄O₃
• 分子量: 206.241
• InChiKey: SNLFPIXTPYNYRQ-MRVPVSSYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.2
• 重原子数：
  15
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.42
• 拓扑面积：
  46.5
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  (R)-3-(hydroxymethyl)-6-methoxy-1,2,3,4-tetrahydronaphthalen-1-one 在 吡啶 作用下， 以 N-甲基吡咯烷酮 为溶剂， 生成 (3R)-3-[[4-(6-fluoro-1,2-benzoxazol-3-yl)piperidin-1-yl]methyl]-6-methoxy-3,4-dihydro-2H-naphthalen-1-one
  参考文献：
  名称：

  Chemoenzymatic synthesis and binding affinity of novel (R)- and (S)-3-aminomethyl-1-tetralones, potential atypical antipsychotics

  摘要：

  A series of (R)- and (S)-3-aminomethyl-1-tetralones, conformationally constrained analogues of haloperidol, have been obtained by enzymatic resolution of the corresponding racemic 3-hydroxymethyl-1-tetralones using Pseudomonasfluorescens lipase. Their binding affinities at dopamine D-2 and serotonin 5-HT2A and 5-HT2C receptors were determined showing in some cases an atypical antipsychotic profile with Meltzer's ratio higher than 1.30. (C) 2003 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2003.11.064
• 作为产物：
  描述：

  (+/-)-2-(3-methoxybenzyl)succinic acid 1-methyl ester 在 Ru(II)-(1S,2S)-N-p-toluenesulfonyl-1,2-di-Ph-ethylenediamine manganese(IV) oxide 、 lithium aluminium tetrahydride 、 三氟乙酸 、 三氟乙酸酐 作用下， 以 四氢呋喃 、 甲醇 、 氯仿 、 丙酮 为溶剂， 反应 60.0h， 生成 (R)-3-(hydroxymethyl)-6-methoxy-1,2,3,4-tetrahydronaphthalen-1-one
  参考文献：
  名称：

  Kinetic resolution of 3-hydroxymethylbenzocycloalkanols by selective asymmetric hydrogen-transfer oxidation

  摘要：

  Kinetic resolution of 3-hydroxymethylbenzocycloalkanols was performed by selective asymmetric hydrogen-transfer oxidation using the Ru(II)-(S,S)-TsDPEN catalyst. Thus, several 3-hydroxymethyl-1-tetralols 7a-d afforded (1R,3R)-3-hydroxymethyl-1-tetralols (1R,3R)-7a-d and (S)-3-hydroxymethyl-1-tetralones (S)-9a-d, and 3-hydroxymethyl-1-indanol 7e gave (1R,3S)3-hydroxymethyl-1-indanol (1R,3S)-7e and (R)-3-hydroxymethyl-1-indanone (R)-9e, with high enantioselectivities. (C) 2003 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetasy.2003.08.016