您的位置: 首页 > 农业专利 > 详情页

取代螺環酮縮醇衍生物、及其做為糖尿病治療藥之使用
专利权人:
CHUGAI SEIYAKU KABUSHIKI KAISHA
发明人:
SATO, TSUTOMU,佐藤勉,HONDA, KIYOFUMI,本田清史,KAWAI, TAKAHIRO,河合隆博,AHN, KOO HYEON,安球铉,安球鉉
申请号:
TW096124510
公开号:
TWI403516B
申请日:
2007.07.05
申请国别(地区):
TW
年份:
2013
代理人:
摘要:
The present invention provides a compound represented by Formula (II): wherein R 1 is a chlorine atom, a fluorine atom, a methyl group or an ethynyl group; Ar is a group represented by the following Formula (a), Formula (b), Formula (c) or Formula (d): wherein R 2 is a C 1-6 alkyl group which may be substituted with one or more halogen atoms, a C 1-6 alkoxy group which may be substituted with one or more halogen atoms, a C 1-3 alkylthio group, a halogen atom, a C 1-3 alkylcarbonyl group or a C 2-5 alkynyl group which may be substituted with -OR 4 ; R 3 is a hydrogen atom or a C 1-3 alkyl group; R 4 is a hydrogen atom or a C 1-3 alkyl group; provided that Ar is a group represented by Formula (a) when R 1 is a fluorine atom, methyl group or an ethynyl group, and that R 2 is methoxy group, an ethoxy group, an isopropyl group, a propyl group, a trifluoromethyl group, a trifluoromethoxy group, 2-fluoroethyl group or 1-propynyl group when R 1 is a methyl group or a pharmaceutically acceptable salt or a solvate thereof and a pharmaceutical agent, a pharmaceutical composition and so on comprising the compound.根據本發明可提供以下式(II)所示化合物,或做為醫藥可被容許之其鹽或其媒合物,以及含該化合物之醫藥、醫藥組成物等者,[式中R1係氯原子、氟原子、甲基或乙炔基;Ar係示以下式(a)、式(b)、式(c)或式(d)所示基;R2係可被1以上之鹵素原子所取代之C1-6烷基,可被1以上之鹵素原子所取代之C1-6烷氧基、C1-3烷硫基、鹵素原子、C1-3烷羰基、或可被-OR4所取代之C2-5炔基;R3係氫原子或C1-3烷基;R4係氫原子或C1-3烷基;惟R1為氟原子、甲基或乙炔基時,Ar係式(a)所示基;且R1為甲基時,R2係甲氧基、乙氧基、異丙基、丙基、三氟化甲基、三氟化甲氧基、2-氟化乙基、或1-丙炔基]。
来源网站:
中国工程科技知识中心
来源网址:
http://www.ckcest.cn/home/

意 见 箱

匿名:登录

个人用户登录

找回密码

第三方账号登录

忘记密码

个人用户注册

必须为有效邮箱
6~16位数字与字母组合
6~16位数字与字母组合
请输入正确的手机号码

信息补充