专利号:US-5455367-A 优先权日:1993-04-22 标 题:Method for the synthesis of silanes or organosilicon hydrides by the reduction of the corresponding silicon halides or organosilicon halides 发明人:KLEIN KLAUS-DIETER; KNOTT WILFRIED; KOERNER GOETZ 权利人:GOLDSCHMIDT AG TH 摘要:A method for the synthesis of silanes or organosilicon hydrides by the reduction of the corresponding silicon halides or organosilicon halides with a magnesium hydride in a liquid reaction medium is carried out by utilizing the following distinguishing features: n a) the use of non-pyrophoric, preferably autocatalytically produced, storage magnesium hydride as magnesium hydride, n b) the use of conventional ethers as reaction medium, and n c) the continuous removal of the magnesium halide formed being deposited on the surface of the magnesium hydride particles during the reaction by the action of mechanical energy or ultrasound so as to form a fresh surface.
专利号:US-8633321-B2 优先权日:2009-09-24 标 题 :Synthesis of (4-fluoro-3-piperidin-4-yl-benzyl)-carbamic acid tert-butyl ester and intermediates thereof 发明人:CHOY NAKYEN; SHAY JR JOHN J; SLEDESKI ADAM W 权利人:CHOY NAKYEN; SHAY JR JOHN J; SLEDESKI ADAM W; SANOFI AVENTIS US LLC 摘要:The present invention is an improved method for the preparation of (4-fluoro-3-pyridin-4-yl-benzyl)-carbamic acid tert-butyl ester, compound of formula I. The invention is directed to a method of synthesis for the compound of formula I in three steps, comprising formation of 5-((tert-butoxycarbonyl)aminomethyl)-2-fluorobenzeneboronic acid (compound 11), reaction of compound 11 under Suzuki coupling conditions to yield (4-fluoro-2-pyridin-4-yl-benzyl)-carbamic acid tert-butyl ester and selective hydrogenation of the aforementioned product under hydrogenation conditions yields compound I. The invention is also directed to the intermediates 5-((tert-butoxycarbonyl)amino-methyl)-2-fluorobenzeneboronic acid (compound 11), and (4-fluoro-3-pyridin-4-yl-benzyl)-carbamic acid tert-butyl ester (compound 13).
专利号:EP-0180398-A1 优先权日:1984-10-26 标 题:Synthesis of beta-lactam 发明人:OVERMAN LARRY E; OSAWA TATSUSHI 权利人:UNIV CALIFORNIA 摘要:A method of synthesizing monomeric formadelhyde imines in situ by reacting (cyanomethyl)- or (aminomethyl)-amines with organometal or Grignard reagents, and their use to synthesize 2-azetidinones (β-lactams) via reaction with enolates.
专利号:WO-2024193457-A1 优先权日:2023-03-20 标题:Preparation method of pyrrolotriazine compound 发明人:ZHENG CHENGUANG; GUO SONGJING; ZHAO REN; PAN RUI; WANG TAO; TANG PINGSHENG; JIN YEHUA; ZHU WEI; MENG YANHUA 权利人:ZHEJIANG HUAHAI PHARM CO LTD 摘要:The present invention belongs to the field of drug synthesis, and more specifically relates to a preparation method of a pyrrolotriazine compound, specifically comprising: firstly reacting compound 2 with NaH and TMSCl to protect the amino group, and then reacting with compound 3 under the action of n-butyl lithium to obtain compound 4; compound 2 can be obtained by reacting compound 1 with a bromination reagent, and compound 1 can be recovered. The method of the present invention is simple to operate, low in cost, and more conducive to industrial production.
专利号:US-2012184745-A1 优先权日:2009-09-24 标题:Synthesis of (4-fluoro-3-piperidin-4-yl-benzyl)-carbamic acid tert-butyl ester and intermediates thereof
专利号:US-9416147-B2 优先权日:2014-04-03 标题 :Preparation of silazane compound 发明人:TONOMURA YOICHI; KUBOTA TOHRU 权利人:SHINETSU CHEMICAL CO 摘要:A silazane compound useful as synthesis intermediates for paint additives, polymer modifiers, pharmaceuticals and agricultural chemicals is efficiently prepared by reaction of a halosilane compound with an amino-containing compound in a solvent which is the same silazane compound as the target product.