专利号:CN-108863834-A 优先权日:2018-08-13 标题:A new method for the synthesis of 2-fluoro-1,3-dicarbonyl compounds
专利号:US-10570157-B2 优先权日:2015-07-30 标 题 :Cyclic diarylboron derivatives as NLRP3 inflammasome inhibitors 发明人:BROUGH DAVID; ALLAN STUART MCRAE; FREEMAN SALLY; BALDWIN ALEX GEORGE 权利人:UNIV MANCHESTER 摘要:Inhibitor compounds are disclosed. The compounds are effective in the treatment of diseases or conditions in which interleukin 1 β activity is implicated. Methods of synthesis of the compounds, as well as pharmaceutical compositions comprising the compounds are also disclosed.
专利号:US-2002002286-A1 优先权日:2000-02-09 标 题:Solid-phase process for making indole compounds 发明人:KETCHA DANIEL MICHAEL; WILSON LAWRENCE JOSEPH 摘要:The subject invention involves a solid-phase process for the synthesis of indole compounds comprising the steps: n (a) treating an amino resin with diketene to provide a resin-bound acetoacetamide; n (b) treating the product from Step (a) with a primary amine in the presence of a dehydrating agent to provide a resin-bound enaminone; n (c) treating the product from Step (b) with a 1,4-benzoquinone, and releasing the resulting indole product from the resin.
专利号:US-6388093-B1 优先权日:2001-01-05 标 题:Syntheses for preparing 1,4-diketopyrrolo [3,4-c]pyrroles 发明人:CHAMBERLAIN TERRENCE R; THORNLEY CRAIG 权利人:SUN CHEMICAL CORP 摘要:A synthesis for preparing asymmetrical 1,4-diketopyrrolo[3,4-c]pyrroles involving: (a) reacting a β-ketoamide with a strong base; (b) halogenating the same or a different β-ketoamide; (c) reacting the reaction products of step (a) and (b) to form a succinamide; and (d) heating the succinamide in the presence of a Lewis Acid. Symmetrical 1,4-diketopyrrolo [3,4-c]pyrroles are synthesized by oxidatively dimerizing the reaction product of step (b) to form a succinamide; and heating the succinamide in the presence of a Lewis Acid.
专利号:US-2004215010-A1 优先权日:2000-06-13 标 题 :Universal solid supports for solid phase oligosynthesis and methods for their preparation and use 发明人:KUMAREV VIKTOR 权利人:KUMAREV VIKTOR 摘要:This invention pertains to solid-phase oligosynthesis, and more particularly to universal solid supports for solid-phase oligonucleotide synthesis, methods for their preparation, and methods for their use. One aspect of the invention pertains to a method for the preparation of a universal solid support suitable for use in solid-phase oligosynthesis, which method comprises the steps of: (a) reacting a pendant functional group (e.g., —NH2) of a solid support (e.g., CPG) with a linker reagent (e g., oxalyl chloride), thereby forming a pendant linker group (e.g., —C(â•?O)Cl); (b) removing at least a portion of excess unreacted linker reagent by evaporation (e.g., using a rotavapor apparatus); and, (c) reacting said pendant linker group with a cyclic reagent (e.g., protected inosine), thereby forming a pendant cyclic group.
专利号:CN-108863834-B 优先权日:2018-08-13 标题:Novel synthesis method of 2-fluoro-1, 3-dicarbonyl compound