基本信息:
- 专利标题: HYDROXYAZEPANE DERIVATIVE AND ITS SALT
- 申请号:JP19299299 申请日:1999-07-07
- 公开(公告)号:JP2001019675A 公开(公告)日:2001-01-23
- 发明人: KASAI KOICHI , OKADA KIYOSHI , SAITO SHINOBU , TOKUTAKE SHOICHI , TOBE KOUICHIROU
- 申请人: KIKKOMAN CORP
- 专利权人: KIKKOMAN CORP
- 当前专利权人: KIKKOMAN CORP
- 优先权: JP19299299 1999-07-07
- 主分类号: C07D223/08
- IPC分类号: C07D223/08 ; A61K31/00 ; A61K31/55 ; A61K31/70 ; A61K31/7042 ; A61K31/7052 ; A61P3/00 ; A61P3/10 ; A61P31/00 ; A61P31/04 ; A61P35/00 ; A61P35/04 ; A61P37/00 ; A61P37/02 ; C07H17/02
摘要:
PROBLEM TO BE SOLVED: To obtain a new compound having an excellent glucosidase inhibitory activity, useful as a therapeutic agent for diabetes by making the compound include a polyhydroxyazepane (7-membered amine). SOLUTION: This compound is shown by the formula [R1 to R4 are each H, a (substituted) alkyl or the like] such as (3S,4R, 5R,6R)-hexahydro-4- methyloxy-3,5,6-trihydroxy-1H-azepine. The compound of the formula is obtained by reacting pyranose with p-toluenesulfonyl chloride of 1-3 times as much as the molar amount of the compound in a solvent (e.g. pyridine, etc.), at -10 to 15 deg.C for about 4-48 hours to give a 6-O-arylsulfonyl pyranose and reacting the 6-O-arylsulfonylpyranose with sodium azide of 2-50 times as much as the substance in a polar solvent (e.g. water, etc.), at 50-100 deg.C for about 2-12 hours to give 6-azido-6-deoxypyranose and reducing 6-azido-6-deoxypyranose with ammonium formate in the presence of palladium-carbon at 10-100 deg.C for 3-50 hours.
信息查询:
EspacenetIPC结构图谱:
C | 化学;冶金 |
--C07 | 有机化学 |
----C07D | 杂环化合物 |
------C07D223/00 | 杂环化合物,含七元环、有1个氮原子作为惟一的杂环原子 |
--------C07D223/02 | .不与其他环稠合 |
----------C07D223/06 | ..有杂原子或有以3个键连杂原子、其中最多以1个键连卤素的碳原子,例如,酯基或腈基,直接连在环碳原子上 |
------------C07D223/08 | ...氧原子 |