CAS: 67-03-8; 3-((4-Amino-2-Methylpyrimidin-5-yl)Methyl)-5-(2-Hydroxyethyl)-4-Methylthiazol-3-Ium Chloride Hydrochloride

相似化合物

6779-97-1 3419-28-1 1037-29-2

上下游产品

CAS号137-00-8 4-甲基-5-噻唑乙醇 | CAS号73-66-5 4-Pyrimidinamin... | CAS号13051-49-5 5-乙酰氧基-3-氯-2-戊酮 | CAS号31375-19-6 Pyrimido[4,5-D]... | CAS号55289-66-2 (4-oxo-3-sulfan... | CAS号31375-20-9 N-[(4-amino-2-m... | CAS号663179-26-8 2-ethoxy-3-chlo... | CAS号64-18-6 甲酸 | CAS号7732-18-5 水 | CAS号24361-62-4 1-(4-amino-2-me... | CAS号490-82-4 硫代硫胺素 | CAS号299-35-4 硫代硫胺素 | CAS号94-75-7 2,4-二氯苯氧乙酸 | CAS号532-43-4 硝酸硫胺 | CAS号59-58-5 丙舒硫胺 | CAS号58-56-0 吡哆醇盐酸盐 | CAS号59-43-8 维生素 B1 | CAS号15743-04-1 Thiamine Sulfate | CAS号15666-52-1 3-[(4-Amino-2-m... | CAS号137-00-8 4-甲基-5-噻唑乙醇

(4-Amino-2-Methyl-Pyrimidin-5-Ylmethyl)-Dicarbothioamidoic Acid-(1-Acetyl-3-Hydroxy-Propyl Ester)置于盐酸,双氧水体系中,用 水 作为反应溶剂,化学反应 20.0H,以94.7%的收率获得产物盐酸硫胺
参考文献:一种氯化噻唑鎓盐酸盐的合成工艺
标题:一种氯化噻唑鎓盐酸盐的合成工艺
摘要:本发明提供了一种氯化噻唑鎓盐酸盐的合成工艺,其包括如下步骤:将硫代盐酸硫胺和盐酸,加入三口烧瓶中,放入冷冻槽中降温到零下10oc;慢慢加入双氧水,温度控制在零下10oc;双氧水加入结束,保温反应20小时;保温结束后,过滤分离氯化噻唑鎓盐酸盐,用甲醇清洗,烘干得氯化噻唑鎓盐酸盐成品.本发明具有缩短工艺路线,节省反应时间,降低生产成本,减少含盐废水排放等优点.

专利信息

专利号:US-9732272-B2
优先权日:2010-12-28
标 题:Synthesis of highly fluorescent GSH-CDTE nanoparticles (quantum dots)
发明人：PEREZ DONOSO JOSE MANUEL; MONRAS CHARLES JUAN PABLO; OSORIO-ROMAN IGOR ORLANDO; VASQUEZ GUZMAN CLAUDIO CHRISITAN
权利人:UNIV SANTIAGO CHILE
摘要:The invention relates to a method for the synthesis of glutathione-capped cadmium-telluride (GSH-CdTe) quantum dots in an aqueous medium, including the steps of: a) preparing a precursor solution of cadmium in a citrate buffer; b) adding glutathione (GSH) to the preceding mixture via strong agitation; c) adding a telluride (potassium or sodium telluride) oxyanion as a telluride donor to the preceding mixture; d) allowing the preceding mixture to react; and e) stopping the reaction by incubation at low temperature.

专利号:US-12391691-B2
优先权日:2018-11-16
标题:Synthesis of key intermediate of KRAS G12C inhibitor compound
发明人：PARSONS ANDREW THOMAS; COCHRAN BRIAN MCNEIL; POWAZINIK IV WILLIAM; CAPORINI MARC ANTHONY
权利人:AMGEN INC
摘要:The present invention relates to an improved, efficient, scalable process to prepare intermediate compounds, such as compound 5M, having the structure n nuseful for the synthesis of compounds that target KRAS G12C mutations, such as

专利号:US-2025206736-A1
优先权日:2019-11-14
标题 :Synthesis of kras g12c inhibitor compound
发明人：CORBETT MICHAEL THOMAS; CAILLE SEBASTIEN
权利人:AMGEN INC
摘要:The present disclosure relates to an improved, efficient, scalable process to prepare intermediate compounds, such as 2-isopropyl-4-methylpyridin-3-amine, useful for the synthesis of compounds, such as Compound 9, for the treatment of KRAS G12C mutated cancers.

专利号:US-5344775-A
优先权日:1991-11-15
标题 :Synthesis of taxanes in culture using pseudocalluscells
发明人：SMITH RICHARD J
权利人:ESCAGENETICS CORP
摘要:A method of synthesis of taxanes from pseudocallus of Taxus species, particularly T. baccata , and methods for pseudocallus production are described. Pseudocallus of the invention can be distinguished from callus tissue and cell suspensions by (1) its unique morphology which is characterized by an amorphous aggregation of cells lacking both differentiated tissues and clearly defined meristematic zones; by (2) very poor intercellular adhesion resulting in marked tissue friability; and by (3) relatively high initial rate of mass doubling. Production of taxanes is achieved by culturing the pseudocallus on support culture medium.

专利号:US-2017268027-A1
优先权日:2014-12-22
标题:Method for synthesis of fatty acids
发明人：CESCUT JULIEN; URIBELARREA JEAN-LOUIS; GUILLOUET STEPHANE; MOLINA-JOUVE CAROLE; SAGNAK RANA
权利人:INST NAT DES SCIENCES APPLIQUEES DE TOULOUSE; CENTRE NAT RECH SCIENT; AGRONOMIQUE INST NAT RECH; FIDOP (FONDS DE DEV DES FILIERES DES OLEAGINEUX ET DES PROTEAGINEUX)
摘要:Disclosed is a method for synthesis of fatty acids by culturing a eukaryotic microorganism from the fungi kingdom, that is naturally oleaginous or rendered oleaginous. The culture is performed in the presence a fatty acid synthase inhibitor in the culture medium.

专利号:WO-2025038767-A1
优先权日:2023-08-14
标 题:Cell-free synthesis platform for synthetically dimierized, clickable fragment antigen-binding (fab) fragments
发明人：THAMES ARIEL; RISCHE CLAYTON; JEWETT MICHAEL; BOCHNER BRUCE
权利人:UNIV NORTHWESTERN
摘要:Disclosed are components, systems, methods, and kits for synthesis of diamerized, clickable antigen binding fragments, such as Fab fragments, and uses thereof. The components, systems, methods, and kits disclosed herein utilize cell-free protein synthesis (CFPS) systems and methods to produce clickable antigen binding fragments.