4,4-dimethyl-2-(4'-methoxymethoxymethylbiphenyl-2-yl)oxazoline | 158144-37-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 4,4-dimethyl-2-(4'-methoxymethoxymethylbiphenyl-2-yl)oxazoline
• 英文别名: 2-[2-[4-(methoxymethoxymethyl)phenyl]phenyl]-4,4-dimethyl-5H-1,3-oxazole
• CAS: 158144-37-7
• 化学式: C₂₀H₂₃NO₃
• 分子量: 325.408
• InChiKey: KJZAALDXFRLHPX-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.3
• 重原子数：
  24
• 可旋转键数：
  6
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.35
• 拓扑面积：
  40
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  4,4-dimethyl-2-(4'-methoxymethoxymethylbiphenyl-2-yl)oxazoline 在 盐酸 、 sodium hydroxide 、 phosphorus tribromide 、 硫酸 、 碳酸氢钠 作用下， 以 吡啶 、 甲醇 、 乙醇 、 正己烷 、 水 为溶剂， 生成 4'-溴甲基-2-甲酸甲酯联苯
  参考文献：
  名称：

  Process for the preparation of imidazopyridine derivatives, and

  摘要：

  本发明提供了一种工业上有利的制备2-烷基-3-(联苯基-4-基)甲基-3H-咪唑并[4,5-b]吡啶衍生物的方法，该衍生物如下式(II)所示，是一种抗肾素II受体拮抗剂的前体，可用作降压药物，联苯衍生物是吡啶衍生物的取代基的前体，提供了其制备方法以及用于制备联苯衍生物的中间体：##STR1## 根据本发明，可以通过酰胺化、N-烷基化和还原环化，以高产率制备2-烷基-3-(联苯基-4-基)甲基-3H-咪唑并[4,5-b]吡啶衍生物。在随后进行的步骤中，引入的5-位卤代基作为对硝化的保护基可以同时被消除。因此，这一方法在工业上具有优势。此外，本发明的联苯衍生物在产物的反应性和纯度方面表现出色，因此是适合工业生产的中间体。

  公开号：

  US05554757A1
• 作为产物：
  描述：

  2-(2-甲氧基苯基)-4,4-二甲基-2-噁唑啉 、 4-bromobenzyl-methoxymethyl ether 在 ammonium chloride 、 magnesium 作用下， 以 四氢呋喃 为溶剂， 以96%的产率得到4,4-dimethyl-2-(4'-methoxymethoxymethylbiphenyl-2-yl)oxazoline
  参考文献：
  名称：

  Process for the preparation of imidazopyridine derivatives, and

  摘要：

  本发明提供了一种工业上有利的制备2-烷基-3-(联苯基-4-基)甲基-3H-咪唑并[4,5-b]吡啶衍生物的方法，该衍生物如下式(II)所示，是一种抗肾素II受体拮抗剂的前体，可用作降压药物，联苯衍生物是吡啶衍生物的取代基的前体，提供了其制备方法以及用于制备联苯衍生物的中间体：##STR1## 根据本发明，可以通过酰胺化、N-烷基化和还原环化，以高产率制备2-烷基-3-(联苯基-4-基)甲基-3H-咪唑并[4,5-b]吡啶衍生物。在随后进行的步骤中，引入的5-位卤代基作为对硝化的保护基可以同时被消除。因此，这一方法在工业上具有优势。此外，本发明的联苯衍生物在产物的反应性和纯度方面表现出色，因此是适合工业生产的中间体。

  公开号：

  US05554757A1

文献信息

• Intermediates for imidazopyridines
  申请人：Eisai Co., Ltd.

  公开号：US05618969A1

  公开（公告）日：1997-04-08

  The present invention provides an industrially advantageous process for preparing a 2-alkyl-3-(biphenyl-4-yl)methyl-3H-imidazo[4,5-b]pyridine derivative represented by the following formula (II) which is a precursor of an antagonist against an angiotensin II receptor useful as an antihypertensive drug, a biphenyl derivative which is a precursor of the substituent of the pyridine derivative, a process for the preparation thereof, and an intermediate useful for the preparation of the biphenyl derivative: ##STR1##

  本发明提供了一种工业上有利的制备2-烷基-3-(联苯基-4-基)甲基-3H-咪唑[4,5-b]吡啶衍生物的方法，该衍生物 represented by the following formula (II) ，是一种抗高血压药物的血管紧张素 II 受体拮抗剂的前体，一种用于制备吡啶衍生物取代基的联苯衍生物前体，以及一种用于制备联苯衍生物的中间体：##STR1##
• Intermediates for imidazopyridine derivatives
  申请人：Eisai Co., Ltd.

  公开号：US05700938A1

  公开（公告）日：1997-12-23

  The present invention provides an industrially advantageous process for preparing a 2-alkyl-3-(biphenyl-4-yl)methyl-3H-imidazo\x9b4,5-b!pyridine derivative represented by the following formula (II) which is a precursor of an antagonist against an angiotensin II receptor useful as an antihypertensive drug, a biphenyl derivative which is a precursor of the substituent of the pyridine derivative, a process for the preparation thereof, and an intermediate useful for the preparation of the biphenyl derivative: ##STR1## The 2-alkyl-3-(biphenyl-4-yl)methyl-3H-imidazo\x9b4,5-b!pyridine derivative can be prepared in a high yield according to the present invention from a 2-amino-5-halogeno-3-nitropyridine derivative through amidation, N-alkylation and reductive cyclization. The halogen atom introduced at the 5-position as a protective group against nitration can be eliminated simultaneously in the step which is conducted thereafter. Thus, this process is industrially advantageous. Further, the biphenyl derivative of the present invention is excellent in reactivity and purity of the product, thus being an intermediate suitable for the industrial production.

  本发明提供了一种工业上有利的制备2-烷基-3-(联苯基-4-基)甲基-3H-咪唑[4,5-b]吡啶衍生物的方法，该衍生物由以下式子(II)表示，是一种抗肾素II受体拮抗剂的前体，可用作降压药物，联苯衍生物是吡啶衍生物取代基的前体，提供了其制备方法和用于制备联苯衍生物的中间体：##STR1## 根据本发明，可以通过酰胺化，N-烷基化和还原环化从2-氨基-5-卤代-3-硝基吡啶衍生物高收率地制备2-烷基-3-(联苯基-4-基)甲基-3H-咪唑[4,5-b]吡啶衍生物。在随后进行的步骤中，引入的5位卤素原子作为对硝化的保护基可以同时消除。因此，这个过程具有工业上的优点。此外，本发明的联苯衍生物在反应性和产物纯度方面都很优秀，因此是适用于工业生产的中间体。
• Process for the preparation of biphenyl containing intermediates useful
  申请人：Eisai Co., Ltd.

  公开号：US05557002A1

  公开（公告）日：1996-09-17

  The present invention provides an industrially advantageous process for preparing a 2-alkyl-3-(biphenyl-4-yl)methyl-3H-imidazo[4,5-b]pyridine derivative represented by the following formula (II) which is a precursor of an antagonist against an angiotensin II receptor useful as an antihypertensive drug, a biphenyl derivative which is a precursor of the substituent of the pyridine derivative, a process for the preparation thereof, and an intermediate useful for the preparation of the biphenyl derivative: ##STR1## The 2-alkyl-3-(biphenyl-4-yl)methyl-3H-imidazo[4,5-b]pyridine derivative can be prepared in a high yield according to the present invention from a 2-amino-5-halogeno-3-nitropyridine derivative through amidation, N-alkylation and reductive cyclization. The halogen atom introduced at the 5-position as a protective group against nitration can be eliminated simultaneously in the step which is conducted thereafter. Thus, this process is industrially advantageous. Further, the biphenyl derivative of the present invention is excellent in reactivity and purity of the product, thus being an intermediate suitable for the industrial production.

  本发明提供了一种工业上有利的制备2-烷基-3-(联苯基-4-基)甲基-3H-咪唑[4,5-b]吡啶衍生物的方法，该衍生物表示为以下式子(II)，是一种抗高血压药物的血管紧张素II受体拮抗剂的前体，联苯衍生物是吡啶衍生物取代基的前体，本发明还提供了其制备方法和用于制备联苯衍生物的中间体：##STR1## 根据本发明，可以通过酰胺化、N-烷基化和还原性环化从2-氨基-5-卤代-3-硝基吡啶衍生物高产率制备2-烷基-3-(联苯基-4-基)甲基-3H-咪唑[4,5-b]吡啶衍生物。在随后进行的步骤中，引入5-位的卤原子作为对硝化的保护基，可以同时消除卤原子。因此，这个过程是工业上有利的。此外，本发明的联苯衍生物在反应性和产物纯度方面都非常优秀，因此是适合工业生产的中间体。
• Intermediates for substituted biphenylmethylmidazopyridine angiotensin
  申请人：Eisai Co., Ltd.

  公开号：US05559236A1

  公开（公告）日：1996-09-24

  The present invention provides an industrially advantageous process for preparing a 2-alkyl-3-(biphenyl-4-yl)methyl-3H-imidazo[4,5-b]pyridine derivative represented by the following formula (II) which is a precursor of an antagonist against an angiotensin II receptor useful as an antihypertensive drug, a biphenyl derivative which is a precursor of the substituent of the pyridine derivative, a process for the preparation thereof, and an intermediate useful for the preparation of the biphenyl derivative: ##STR1## The 2-alkyl-3-(biphenyl-4-yl)methyl-3H-imidazo-[4,5-b]pyridine derivative can be prepared in a high yield according to the present invention from a 2-amino-5-halogeno-3-nitropyridine derivative through amidation, N-alkylation and reductive cyclization. The halogen atom introduced at the 5-position as a protective group against nitration can be eliminated simultaneously in the step which is conducted thereafter. Thus, this process is industrially advantageous. Further, the biphenyl derivative of the present invention is excellent in reactivity and purity of the product, thus being an intermediate suitable for the industrial production.

  本发明提供了一种工业上有利的制备2-烷基-3-(联苯基-4-基)甲基-3H-咪唑[4,5-b]吡啶衍生物的过程，该衍生物表示为以下公式(II)，该衍生物是一种抗高血压药物的血管紧张素II受体拮抗剂的前体，联苯衍生物是吡啶衍生物的取代基的前体，其制备过程和用于制备联苯衍生物的中间体：##STR1## 2-烷基-3-(联苯基-4-基)甲基-3H-咪唑[4,5-b]吡啶衍生物可以按照本发明从2-氨基-5-卤代-3-硝基吡啶衍生物经过酰胺化、N-烷基化和还原环化的步骤高产率制备。在随后进行的步骤中，引入到5位的卤原子作为硝化的保护基可以同时消除。因此，这个过程在工业上具有优势。此外，本发明的联苯衍生物在反应性和产品纯度方面表现出色，因此是适合工业生产的中间体。
• Sulfonyloxy-biphenylcarboxylic ester derivatives which are intermediates
  申请人：Eisai Co., Ltd.

  公开号：US05587504A1

  公开（公告）日：1996-12-24

  The present invention provides an industrially advantageous process for preparing a 2-alkyl-3-(biphenyl-4-yl)methyl-3H-imidazo[4,5-b]pyridine derivative represented by the following formula (II) which is a precursor of an antagonist against an angiotensin II receptor useful as an antihypertensive drug, a biphenyl derivative which is a precursor of the substituent of the pyridine derivative, a process for the preparation thereof, and an intermediate useful for the preparation of the biphenyl derivative: ##STR1## The 2-alkyl-3-(biphenyl-4-yl)methyl-3H-imidazo[4,5-b]pyridine derivative can be prepared in a high yield according to the present invention from a 2-amino-5-halogeno-3-nitropyridine derivative through amidation, N-alkylation and reductive cyclization.

  本发明提供了一种工业上有利的制备2-烷基-3-(联苯基-4-基)甲基-3H-咪唑[4,5-b]吡啶衍生物的方法，其表示为以下公式(II)，该衍生物是一种抗血管紧张素II受体拮抗剂的前体，可用作降压药物，联苯衍生物是吡啶衍生物取代基的前体，提供了其制备方法以及制备联苯衍生物的中间体：##STR1## 通过酰胺化、N-烷基化和还原环化，可以根据本发明从2-氨基-5-卤代-3-硝基吡啶衍生物高产地制备2-烷基-3-(联苯基-4-基)甲基-3H-咪唑[4,5-b]吡啶衍生物。