CAS: 1075-89-4; 8-Azaspiro[4.5]Decane-7,9-Dione

相似化合物

42940-56-7 1075-89-4 21098-11-3

上下游产品

3,3-tetramethylene glutaric anhydride BUSPIRONE 8-(4-bromobutyl)-8-azaspiro[4.5]decane-7,9-dione tiospirone 8-[(Dibenzylamino)-methyl]-8-aza-spiro[4.5]decane-7,9-dione

Alkaline Earth Salt Of/the/ Methylsulfuric Acid 反应生成3,3-四亚甲基戊二酰亚胺
参考文献:Kon; Thorpe,Journal Of The Chemical Society,1919,Vol. 115,P. 702
标题:Kon; Thorpe,Journal Of The Chemical Society,1919,Vol. 115,P. 702

专利信息

专利号:US-6441189-B1
优先权日:2000-03-31
标 题 :Process for the preparation of matrix metalloproteinase inhibitors
发明人：BAILEY ANNE E; HILL DAVID R; HSIAO CHI-NUNG W; KURUKULASURIYA RAVI; WITTENBERGER STEVE; MCDERMOTT TODD; MCLAUGHLIN MAUREEN A
权利人:ABBOTT LAB
摘要:The instant invention provides a process for the synthesis of matrix metalloproteinase inhibitors.

专利号:WO-0040532-A2
优先权日:1998-12-31
标 题:Synthesis of dihydrohonokiol compositions

专利号:US-5719286-A
优先权日:1992-06-16
标 题:Process and intermediates for bis-aza-bicyclic anxiolytic agents
发明人：URBAN FRANK JOHN
权利人:PFIZER
摘要:Optically pure intermediates of formula (1) wherein the substituent B is either cis or trans to the C 9a -C 1 bond and is selected from the group consisting of --CH 2 OH, --CHO, --CH 2 OSO 2 R, --CH 2 CN, --CH(OH)CH 2 NO 2 , --CHâ•?CH--NO 2 , (2) and (3), C is selected from the group consisting of --H, (4), (5), and a nitrogen protecting group which is removable by hydrogenation or acid treatment; and wherein R is (C 1 -C 8 ) alkyl, phenyl or alkyl substituted phenyl; X is N or CH; Y is O or S and Z is H or Cl; for the synthesis of octahydro-1H-pyrido(1,2-a)pyrazinyl ethyl carboxamide anxiolytic agents.

专利号:CN-1115317-A
优先权日:1994-05-05
标 题:Improved method for large-scale synthesis of azaperidone

专利号:EP-1140756-A2
优先权日:1998-12-31
标题:Synthesis of dihydrohonokiol compositions

专利号:CN-1044474-C
优先权日:1994-05-05
标题 :Improved method for large-scale synthesis of azaperidone