
基本信息:
- 专利标题: Process for producing 2'-(1h-tetrazol-5-yl)biphenyl-4-carbaldehyde
- 专利标题(中):制备2' - (1h-四唑-5-基)联苯-4-甲醛的方法
- 申请号:US10595122 申请日:2004-09-01
- 公开(公告)号:US20070072923A1 公开(公告)日:2007-03-29
- 发明人: Nobushige Itaya , Kozo Matsui , Yutaka Ohtani , Hiroki Ueno , Toshikazu Kaneko
- 申请人: Nobushige Itaya , Kozo Matsui , Yutaka Ohtani , Hiroki Ueno , Toshikazu Kaneko
- 专利权人: SUMITOMO CHEMICAL COMPANY, LIMITED
- 当前专利权人: SUMITOMO CHEMICAL COMPANY, LIMITED
- 优先权: JP2003-313325 20030904
- 国际申请: PCT/JP04/13014 WO 20040901
- 主分类号: A61K31/41
- IPC分类号: A61K31/41 ; C07D257/02
摘要:
The present invention provides a process for producing 2′-(1H-tetrazol-5-yl)biphenyl-4-carbaldehyde which comprises reacting 2′-cyanobiphenyl-4-carbaldehyde with a salt of azide; a process for producing a highly pure crystal of 2′-(1H-tetrazol-5-yl)biphenyl-4-carbaldehyde which comprises reacting 2′-cyanobiphenyl-4-carbaldehyde with a salt of azide, obtaining a crystal of 2′-(1H-tetrazol-5-yl)biphenyl-4-carbaldehyde, dissolving said crystal obtained and recrystallizing a highly pure crystal in tetrahydrofuran; and the like. According to the present process, 2′-(1H-tetrazol-5-yl)biphenyl-4-carbaldehyde which is useful as a synthetic intermediate of medicines can be produced in a short process at high yield and high purity.
摘要(中):
本发明提供2' - (1H-四唑-5-基)联苯-4-甲醛的制备方法,其包括使2'-氰基联苯-4-甲醛与叠氮化物的盐反应; 2' - (1H-四唑-5-基)联苯-4-甲醛的高纯度晶体的制造方法,其包括使2'-氰基联苯-4-甲醛与叠氮化物的盐反应,得到2'- (1H-四唑-5-基)联苯-4-甲醛,将所得晶体溶解并将高纯度结晶重结晶于四氢呋喃中; 等等。 根据本发明,可以以高产率和高纯度的短时间制备可用作药物合成中间体的2' - (1H-四唑-5-基)联苯-4-甲醛。
IPC结构图谱:
A | 人类生活必需 |
--A61 | 医学或兽医学;卫生学 |
----A61K | 医用、牙科用或梳妆用的配制品 |
------A61K31/00 | 含有机有效成分的医药配制品 |
--------A61K31/33 | .杂环化合物 |
----------A61K31/335 | ..仅有氧作为环杂原子的,例如制霉色基素 |
------------A61K31/41 | ...有两个或两个以上环杂原子的五元环的,其中至少有1个氮原子,例如四唑 |