575484-83-2 + 24313-88-0 = 841290-80-0 反应条件:1.1 Reagents: Trifluoroacetic Acid Solvents: Methanol; Overnight,100 °C 标题:Design,Synthesis Of Diaminopyrimidine Inhibitors Targeting Ige- And Igg-Mediated Activation Of Fc Receptor Signaling 作者:Argade,Ankush; Bhamidipati,Somasekhar; Li,Hui; Sylvain,Catherine; Clough,Jeffrey; Et Al 参考文献:Bioorganic & Medicinal Chemistry Letters 日期:2015 卷标:25(10) 页码:2122-2128]
575484-83-2 + 24313-88-0 = 841290-80-0 + 1294007-59-2 + 946572-80-1 反应条件:1.1 Solvents: N-Methyl-2-Pyrrolidone,Water; Rt -> 120 °C; 10 H,120 °C; 120 °C -> 65 °C1.2 Reagents: Sodium Hydroxide Solvents: Water; Ph 8.5,65 °C; 65 °C -> 20 °C; 6 H,20 °C 标题:Real-Time Monitoring And Control Of Critical Process Impurities During The Manufacture Of Fostamatinib Disodium 作者:Hart,Richard; Herring,Adam; Howell,Gareth P.; Mckeever-Abbas,Ben; Pedge,Nicholas; Et Al 参考文献:Organic Process Research & Development 日期:2015 卷标:19(4) 页码:537-542
📜在 Phosphatase From Bovine Intestinal Mucosa,Magnesium Chloride体系中,化学反应生成 6-[[5-氟-2-[(3,4,5-三甲氧基苯基)氨基]-4-嘧啶基]氨基]-2,2-二甲基-2H-吡啶并[3,2-B]-1,4-噁嗪-3(4H)-酮 参考文献:Metabolism Of Fostamatinib,The Oral Methylene Phosphate Prodrug Of The Spleen Tyrosine Kinase Inhibitor R406 In Humans: Contribution Of Hepatic And Gut Bacterial Processes To The Overall Biotransformation 标题:Metabolism Of Fostamatinib,The Oral Methylene Phosphate Prodrug Of The Spleen Tyrosine Kinase Inhibitor R406 In Humans: Contribution Of Hepatic And Gut Bacterial Processes To The Overall Biotransformation 摘要:化反应. DOI:10.1124/dmd.110.032151
专利号:US-2025289827-A1 优先权日:2022-12-02 标 题:Morphic forms of a mutant braf degrader and methods of manufacture thereof 发明人:YU ROBERT T; HE MINSHENG; SCHNADERBECK MATTHEW J; KREGER BRIDGET; POLLOCK ROY MACFARLANE; JIANG SIYI; LI MEIQI; CHEN BOLU; LU JIANNAN 权利人:C4 THERAPEUTICS INC 摘要:Advantageous isolated morphic forms of (3R)-3-[6-[2-cyano-3-[[ethyl(methyl)sulfamoyl]amino]-6-fluorophenoxy]-4-oxoquinazolin-3-yl]-8-[2-[1-[3-(2,4-dioxo-1,3-diazinan-1-yl)-5-fluoro-1-methylindazol-6-yl]-4-hydroxypiperidin-4-yl]acetyl]-1-oxa-8-azaspiro[4.5]decane (Compound 1), which is a mutant BRAF degrader, and methods to prepare Compound 1 morphic forms for therapeutic applications are provided in the invention. The invention also provides improved methods for the synthesis of Compound 1, new pharmaceutical compositions comprising Compound 1, and new uses of Compound 1.
专利号:US-8299242-B2 优先权日:2009-07-02 标 题 :Synthesis of 2,4-pyrimidinediamines
专利号:US-8481724-B2 优先权日:2009-07-02 标题:Synthesis of 2,4-pyrimidinediamines
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