专利号:US-2024239799-A1 优先权日:2021-04-02 标 题:(s)-1-(5-((pyridin-3-yl)thio)pyrazin-2-yl)-4'h,6'h-spiro[piperidine-4,5'-pyrrolo [1,2-b]pyrazol]-4'-amine derivatives and similar compounds as shp2 inhibitors for the treatment of e.g. cancer 发明人:DI FABIO ROMANO; MONTALBETTI CHRISTIAN; PETROCCHI ALESSIA; GRILLO ALESSANDRO; RANDAZZO PIETRO; ROSSETTI ILARIA; CIAMMAICHELLA ALINA 权利人:C N C C S S C A R L COLLEZIONE NAZ DEI COMPOSTI CHIMICI E CENTRO SCREENING; IRBM S P A 摘要:The present invention relates to compounds of formula (I). The compounds of the formula (I) are e.g. (S)-1-(5-((pyridin-3-yl)thio) pyrazin-2-yl)-41H,6′H-spiro[piperidine-4,5′-pyrrolo[1,2-b]pyrazol]-41-amine derivatives and similar compounds. The present invention also relates to the compounds of formula (I) for use as Src homology phosphotyrosine phosphatase 2 (SHP2) inhibitors in methods of treatment of e.g. cancer, cardiovascular diseases, immunological disorders, autoimmune disorders, fibrosis, ocular disorders, systemic lupus erythematosus, diabetes, neutropenia, and combinations thereof. The present invention also relates to pharmaceutical compositions containing said compounds and to their methods of synthesis.
专利号:CN-120518668-A 优先权日:2025-05-19 标题:Synthesis method of diazinon
专利号:CN-119684131-A 优先权日:2024-12-10 标题:Continuous synthesis method of ultrasonic reinforced FOX-7
参考标题:Synthesis Of Novel C-2 Substituted Pyrimidine Nucleoside Analogs 作者:Martin Dunkel,P. Dan Cook,Oscar L. Acevedo |发布日期:1993.10 摘要:A Series Of 2-(2-Oxoalkylidene)-4(1H)-Pyrimidinone Nucleoside Analogs Were Synthesized By The Addition Of The Lithium Enolates Of Methylketones To 2,5′- And 2,2′-Anhydrouridines And To 2,5′-Anhydrothymidines. Alternatively, 2-Thiouridine Was Alkylated With Bromomethyl Ketones To Yield 2-(2-Oxoalkyl)Thio-4(1H)-Pyrimidinone Ribofuranosides In Good Yields. These Intermediates Were Subsequently Transformed
合成参考文献
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