CAS: 17318-03-5; Magnesium 3-Fluorobenzen-1-Ide Bromide

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CAS号1073-06-9 间溴氟苯 | CAS号350-51-6 间氟苯乙烯 | CAS号1030239-93-0 (3-fluorophenyl... | CAS号396-64-5 3,3'-二氟联苯 | CAS号1030239-91-8 cyclohex-1-en-1... | CAS号402-63-1 1-(3-氟苯基)乙醇 | CAS号207917-03-1 [3-(3-fluorophe... | CAS号195528-43-9 Benzeneethanol,... | CAS号29779-02-0 3'-FLUORO-2,3,4... | CAS号708-64-5 2,2,2,3'-四氟苯乙酮

专利信息

专利号:US-9676783-B2
优先权日:2008-10-22
标 题:Method of treatment using substituted pyrazolo[1,5-A] pyrimidine compounds
发明人：HAAS JULIA; ANDREWS STEVEN W; JIANG YUTONG; ZHANG GAN
权利人:ARRAY BIOPHARMA INC
摘要:Compounds useful in the synthesis of compounds for treating pain, cancer, inflammation, neurodegenerative disease or Typanosoma cruzi infection in a mammal.

专利号:US-11420997-B2
优先权日:2018-04-13
标题:Peptide synthesis method
发明人：SUZUKI HIDEAKI; MUTO SUSUMU; FUJITA SHUJI; KUBO DAISUKE
权利人:JITSUBO CO LTD
摘要:The present invention has an object of shortening the process time and reducing use of a poor solvent for solidifying a carrier (Tag)-peptide component, by removing impurities without conducting solid-liquid separation (condensation, solid-liquid separation and drying operation) of a Tag-peptide component, in an Fmoc method using a Tag for liquid phase peptide synthesis. Provided is the peptide synthesis method that includes the following steps a-d: step a: a carrier-protected amino acid, carrier-protected peptide, or a carrier-protected amino acid amide, and an N-Fmoc-protected amino acid or an N-Fmoc-protected peptide are condensed in an organic solvent or a mixed solution of organic solvents, to obtain an N-Fmoc-carrier-protected peptide, step b: a water-soluble amine is added to the reaction solution after the condensation reaction, step c: the Fmoc group is deprotected from the protected amino group in the presence of a water-soluble amine, and step d: the reaction solution is neutralized by adding an acid, and further, by adding and washing with an acidic aqueous solution, then, by liquid-liquid separation an aqueous layer is removed to obtain an organic layer.

专利号:CN-101137646-A
优先权日:2005-01-06
标题 :Synthesis of CCR5 Receptor Antagonist

专利号:US-2006258863-A1
优先权日:2005-01-06
标题:Synthesis of CCR5 antagonists

专利号:DK-2725028-T3
优先权日:2008-10-22
标题:Substituted pyrazolo [1,5-a] pyrimidine compounds as intermediates in the synthesis of kinase inhibitors TRK

专利号:JP-2008526863-A
优先权日:2005-01-06
标 题 :Synthesis of CC5R receptor antagonists