发明名称 |
Method for preparing 1-(4-(4-(3,4-dichloro-2-fluorophenylamino)-7-methoxyquinazolin-6-yloxy)piperidin-1-yi)prop-2-en-1-one |
摘要 |
The present invention relates to a novel method for preparing 1-(4-(4-(3,4-dichloro-2-fluorophenylamino)-7-methoxyquinazolin-6-yloxy)piperidin-1-yl)prop-2-en-1-one in a simpler process as compared with conventional methods by allowing 4-(3,4-dichloro-2-fluorophenylamino)-7-methoxyquinazolin-6-ol to react with an N-acyl piperidine derivative in an inert polar protic solvent in the presence of a base. |
申请公布号 |
US9518043(B2) |
申请公布日期 |
2016.12.13 |
申请号 |
US201414763295 |
申请日期 |
2014.01.27 |
申请人 |
Hanmi Pharm. Co., Ltd. |
发明人 |
Bang Keuk Chan;Jung Jae Hyuk;Moon Young Ho |
分类号 |
C07D401/12;C07D239/86;C07D239/94;C07D211/46 |
主分类号 |
C07D401/12 |
代理机构 |
Marshall, Gerstein & Borun LLP |
代理人 |
Marshall, Gerstein & Borun LLP |
主权项 |
1. A method for preparing the compound of formula (I), which comprises the step of allowing the compound of formula (II) to react with the compound of formula (III) in an inert polar protic solvent in the presence of a base: wherein X is tosyloxy (OTs), mesyloxy (OMs), trifluoromethane sulfonate, fluorosulfonate or halogen; and Y is ethenyl or halogenoethyl. |
地址 |
Gyeonggi-do KR |