(4-isopropylphenyl)(3-pyridyl)methanol | 89667-07-2

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 异戊烯醇脂质
• 英文名称: (4-isopropylphenyl)(3-pyridyl)methanol
• 英文别名: (4-Propan-2-ylphenyl)-pyridin-3-ylmethanol
• CAS: 89667-07-2
• 化学式: C₁₅H₁₇NO
• 分子量: 227.306
• InChiKey: XVNAPWUCSVIPIL-UHFFFAOYSA-N

物化性质

• 熔点：
  107-108 °C
• 沸点：
  380.5±32.0 °C(Predicted)
• 密度：
  1.080±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.8
• 重原子数：
  17
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.27
• 拓扑面积：
  33.1
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  (4-isopropylphenyl)(3-pyridyl)methanol 生成 4-isopropylphenyl 3-pyridyl ketone
  参考文献：
  名称：

  SHINJI, TERAO;KOBEI, NISHIKAWA

  摘要：

  DOI：
• 作为产物：
  描述：

  3-溴吡啶 、 4-异丙基苯甲醛 生成 (4-isopropylphenyl)(3-pyridyl)methanol
  参考文献：
  名称：

  TEHRABI, SINDZI

  摘要：

  DOI：

文献信息

• LINCOSAMIDE DERIVATIVES AND ANTIMICROBIAL AGENTS COMPRISING THE SAME AS ACTIVE INGREDIENT
  申请人：Umemura Eijirou

  公开号：US20100184746A1

  公开（公告）日：2010-07-22

  An objective of the present invention is to provide compounds of formula (I) or their pharmacologically acceptable salts or solvates wherein A represents aryl while R 1 represents a five- or six-membered monocyclic heterocyclic group, or A represents a four- to six-membered monocyclic heterocyclic group while R 1 represents aryl or a five- or six-membered monocyclic heterocyclic group; R 2 represents a hydrogen atom or C 1-6 alkyl; R 3 represents C 1-6 alkyl or C 3-6 cycloalkyl-C 1-4 alkyl; R 4 , R 5 , and R 6 represent a hydrogen atom; R 7 represents C 1-6 alkyl; and m is 1 to 3. The compounds are novel lincosamide derivatives that have a potent activity against resistant Streptococcus pneumoniae . Further, the compounds are usable as antimicrobial agents and are useful for preventing or treating bacterial infectious diseases.

  本发明的目标是提供式（I）的化合物或其药理学上可接受的盐或溶剂，其中A代表芳基，而R1代表五元或六元单环杂环基，或A代表四至六元单环杂环基，而R1代表芳基或五元或六元单环杂环基；R2代表氢原子或C1-6烷基；R3代表C1-6烷基或C3-6环烷基-C1-4烷基；R4、R5和R6代表氢原子；R7代表C1-6烷基；m为1至3。这些化合物是新型的林可霉素衍生物，对耐药性肺炎链球菌具有强效活性。此外，这些化合物可用作抗微生物剂，对预防或治疗细菌感染性疾病有用。
• Dynamic Kinetic Resolution of Diarylmethanols with an Activated Lipoprotein Lipase
  作者：Jusuk Lee、Yeonock Oh、Yoon Kyung Choi、Eunjeong Choi、Kyungwoo Kim、Jaiwook Park、Mahn-Joo Kim

  DOI：10.1021/cs501629m

  日期：2015.2.6

  We explored the kinetic resolution of 31 different diarylmethanols with an activated lipoprotein lipase (LPL-D1) which was about 3000-fold more active than its native counterpart in organic solvent. Most of the substrates tested were accepted by LPL-D1 with good to high enantioselectivity in the kinetic resolution. Next, we explored the dynamic kinetic resolutions (DKRs) of these substrates (24 out of 31) using LPL-D1 and a ruthenium-based racemization catalyst in combination, which provided satisfactory yields (71-96%) and high enantiopurities (90-99% cc). As an illustrative example for the synthetic applications of the DKR procedure, we synthesized L-cloperastine, an antitussive drug, from phenyl-(p-trimethylsilylphenyl)methanol via DKR.
• US7867980B2
  申请人：——

  公开号：US7867980B2

  公开（公告）日：2011-01-11
• TEHRABI, SINDZI
  作者：TEHRABI, SINDZI

  DOI：——

  日期：——
• SHINJI, TERAO;KOBEI, NISHIKAWA
  作者：SHINJI, TERAO、KOBEI, NISHIKAWA

  DOI：——

  日期：——