
基本信息:
- 专利标题: PROCESS FOR PREPARING INDOL-5-OXY-QUINAZOLINE DERIVATIVES AND INTERMEDIATES
- 专利标题(中):制备吲哚-5-氧基喹唑啉衍生物和中间体的方法
- 申请号:EP07824415.9 申请日:2007-11-01
- 公开(公告)号:EP2129657A2 公开(公告)日:2009-12-09
- 发明人: ARNOTT, Euan, Alexander , CROSBY, John , EVANS, Matthew, Charles , FORD, James, Gair , JONES, Martin, Francis , LESLIE, Kevin, William , MCFARLANE, Ian, Michael , SEPENDA, George, Joseph
- 申请人: AstraZeneca AB
- 申请人地址: 151 85 Södertälje SE
- 专利权人: AstraZeneca AB
- 当前专利权人: AstraZeneca AB
- 当前专利权人地址: 151 85 Södertälje SE
- 优先权: US864036P 20061102; US957401P 20070822
- 国际公布: WO2008053221 20080508
- 主分类号: C07D209/08
- IPC分类号: C07D209/08 ; C07D239/88 ; C07D403/12 ; C07C69/732 ; C07D487/10 ; C07D207/06
摘要:
The present invention relates to chemical processes for the manufacture of certain quinazoline derivatives, or pharmaceutically acceptable salts thereof. The invention also relates to processes for the manufacture of certain intermediates useful in the manufacture of the quinazoline derivatives and to processes for the manufacture of the quinazoline derivatives utilising said intermediates. In particular, the present invention relates to chemical processes and intermediates useful in the manufacture of the compound 4-(4-fluoro-2-methylindol-5-yloxy)-6-methoxy-7-(3-pyrrolidin-1-ylpropoxy)quinazoline.
摘要(中):
本发明涉及用于制造某些喹唑啉衍生物或其药学上可接受的盐的化学方法。 本发明还涉及用于制造用于制备喹唑啉衍生物的某些中间体的方法以及利用所述中间体制备喹唑啉衍生物的方法。 具体而言,本发明涉及化学方法和用于制备化合物4-(4-氟-2-甲基吲哚-5-基氧基)-6-甲氧基-7-(3-吡咯烷-1-基丙氧基) 喹唑啉。
IPC结构图谱:
C | 化学;冶金 |
--C07 | 有机化学 |
----C07D | 杂环化合物 |
------C07D209/00 | 杂环化合物,含五元环、与其他环稠合、带1个氮原子作为惟一的杂环原子 |
--------C07D209/02 | .与一个碳环稠合 |
----------C07D209/04 | ..吲哚;氢化吲哚 |
------------C07D209/08 | ...只有氢原子或仅含氢和碳原子的基直接连在杂环的碳原子上 |