专利号:WO-2021038581-A1 优先权日:2019-08-30 标题 :A one step synthesis of 2-substituted benzo[b]thiophenes 发明人:SEKAR GOVINDASAMY; POONGUZHALI ELAMVAZHUTHI 权利人:INDIAN INST TECH MADRAS 摘要:The invention pertains to a one step synthesis of 2-substituted benzo[ b ]thiophene of general formula wherein the synthesis of 2-substituted benzo[ b ]thiophenes is by reacting the starting materials substituted or unsubstituted 2-halogenobenzaldehyde and substituted or unsubstituted acetyl/phenacyl bromide with a catalyst, a sulphur source and phase transfer catalyst in an aqueous medium with atmospheric air and at temperature in the range of 25°C-30°C.
专利号:US-9873689-B2 优先权日:2014-11-07 标题:Synthesis of fatostatin based polycyclic compounds 发明人:CANTRELL JR WILLIAM R 权利人:FGH BIOTECH INC 摘要:The present invention relates to methods and strategies for large-scale synthesis of compounds having the chemical structure: n nThe R substituents are H, methyl, isopropyl, benzyl, cyclohexyl, cyclopropylmethyl, methoxy, tert-butyloxycarbonyl, methanesulfonyl, p-toluenesulfonyl, quinolinesulfonyl, or thiophenesulfonyl groups. The method comprises condensing prothionamide with a halo nitroacetophenone to form a nitrophenyl substituted thiazole, reducing the nitro group to form an amine and derivatizing the amine to produce the compound.
专利号:US-2022356182-A1 优先权日:2009-03-27 标题 :Inhibitors of hepatitis c virus replication 发明人:COBURN CRAIG A; LUDMERER STEVEN W; LIU KUN; WU HAO; SOLL RICHARD; ZHONG BIN; ZHU JIAN 权利人:MERCK SHARP & DOHME 摘要:The present invention relates to compounds of formula (I) that are useful as hepatitis C virus (HCV) NS5A inhibitors, the synthesis of such compounds, and the use of such compounds for inhibiting HCV NS5A activity, for treating or preventing HCV infections and for inhibiting HCV viral replication and/or viral production in a cell-based system.
专利号:WO-2021038452-A1 优先权日:2019-08-26 标 题 :New therapeutic agents for the treatment of haematological pathologies 发明人:CILIBRASI VINCENZO; SPANO' VIRGINIA; MONTALBANO ALESSANDRA; BARRAJA PAOLA 权利人:UNIV DEGLI STUDI DI PALERMO 摘要:The present invention relates to compounds having a tetracyclic system and the use thereof as new therapeutic agents in the treatment of acute myeloid leukemia (AML), preferably in FLT3/ITD hemizygote patients resistant to conventional therapies. The invention also relates to 5,7-dihydro-4 H -[1,3]thiazolo[4,5- e ]isoindol-2-amine compounds useful as intermediates for the synthesis of tetracyclic imidazo[2',1':2,3][1,3]thiazolo[4,5-e]isoindole compounds.
专利号:US-4230624-A 优先权日:1977-09-02 标 题 :Process for the synthesis of derivatives of the benzofuran, chromene and isochromene type 发明人:LE CORRE MAURICE; HERCOUET ALAIN; BEGASSE BEATRICE 权利人:ANVAR 摘要:The invention relates to a process for the production of therapeutic compounds of the benzofuran, chromene and isochromene type of the general formula; in which formula, R1 and R3=H, lower alkyl, aralkyl or cycloalkyl R2=H or an organic radical and when D= R1 and R3 may represent an organic radical. The process comprising the cyclization in the liquid phase and in the presence of a base a compound of the formula; in which formula; R'=an alkyl, aryl or aralkyl radical and X-=an anion.
专利号:US-11053243-B2 优先权日:2009-03-27 标 题:Inhibitors of hepatitis C virus replication 发明人:COBURN CRAIG A; LUDMERER STEVEN W; LIU KUN; WU HAO; SOIL RICHARD; ZHONG BIN; ZHU JIAN 权利人:MERCK SHARP & DOHME 摘要:The present invention relates to compounds of formula (I) that are useful as hepatitis C virus (HCV) NS5A inhibitors, the synthesis of such compounds, and the use of such compounds for inhibiting HCV NS5A activity, for treating or preventing HCV infections and for inhibiting HCV viral replication and/or viral production in a cell-based system.
参考标题:Zno/ag/fe 3 O 4 Nanoparticles Supported On Carbon Nanotubes Employing Petasites Hybridus Rhizome Water Extract: A Novel Organometallic Nanocatalyst For The Synthesis Of New Naphthyridines 作者:Zinatossadat Hossaini,Navisa Tabarsaei,Samira Khandan,Peyman Valipour,Mona Ghorchibeigi |发布日期:2021.3 摘要:Magnetic Nps As A High Performance Catalyst Was Employed For The Preparation Of Naphthyridine Derivatives In High Yields Via The Multicomponent Reactions Of Phthalaldehyde, 2‐aminoactonitrile, Activated Acetylenic Compounds, α‐haloketones, Triphenyphophine, And Ammonium Acetate In Aqueous Media At Ambient Temperature. Due To Having Isoquinoline Core, We Investigate Antioxidant Property Of Some Synthesized
合成参考文献
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