专利号:US-8710210-B2 优先权日:2010-06-30 标题:Method of using N-thio compounds for oligonucleotide synthesis 发明人:HE YIGANG; SOROKIN VICTOR; MAZUR WIESLAW ADAM 权利人:HE YIGANG; SOROKIN VICTOR; MAZUR WIESLAW ADAM; GIRINDUS AMERICA INC 摘要:A method for synthesizing an oligonucleotide which comprises using a sulfurizing agent of general formula (I) for sulfurizing at least one phosphorus internucleotide linkage of a precursor of the oligonucleotide, wherein R is an aryl group or a heteroaryl group, which is bonded to the S-atom through an annular carbon atom; and R 1 and R 2 are independently organic residues, preferably a C1-C20 hydrocarbon residue. The method may further comprise purifying the oligonucleotide. Also included is a process for the synthesis of the sulfurizing agent.
专利号:US-4774331-A 优先权日:1986-08-22 标 题:Process for ortho-cyanation of phenols or phenylamines 发明人:ADACHI MAKOTO; MATSUMURA HIROMU; SUGASAWA TSUTOMU 权利人:SHIONOGI & CO 摘要:A process for ortho-cyanation of phenols or phenylamines which comprises reacting a phenyl compound having a hydroxy group or an optionally substituted amino or cyclic amino group, of which the ortho position is vacant, with trichloroacetonitrile, a C1-C5 alkyl thiocyanate or a C6 - C12 aryl thiocyanate in the presence of a boron trihalide and treating the resultant product with an alkali is provided, and said process is useful in the synthesis of intermediates for medicinals or pesticides.
专利号:US-4857645-A 优先权日:1986-11-06 标 题:Process for introducing a thiocarboxylic ester group at the orthoposition of phenols or phenylamines 发明人:MAKOTO ADACHI; MATSUMURA HIROMU; SUGASAWA TSUTOMU 权利人:SHIONOGI & CO 摘要:A process for introducing thiocarboxylic ester at ortho-position of phenols or phenylamines which comprises reacting a phenyl compound having group or optionally substituted amino or cyclic amino group, of which at least one ortho-position is vacant, with C 1 -C 5 alkyl thiocyanate, C 7 -C 13 aralkyl thiocyanate or C 6 -C 12 aryl thiocyanate in the presence of a boron trihalide and hydrolyzing the resultant product under acidic conditions is provided, and said process is useful in the synthesis of medicinals, pesticides and dyes.
专利号:US-7087783-B2 优先权日:2000-05-29 标 题 :Method for preparing nitrogen-containing compounds 发明人:EMURA TAKASHI; HANEISHI TSUYOSHI 权利人:CHUGAI PHARMACEUTICAL CO LTD 摘要:A synthesis method which comprises reacting NH group-containing compounds with thiocyanates, cyanamides, nitriles or esters in the presence of a silylating agent to synthesize the corresponding nitrogen-containing addition or substitution products. This method not only enables the direct and efficient synthesis of nitrogen-containing compounds including isothioureas, guanidines, amidines and amides, but it also has a wide range of applications and is suitable for large-scale synthesis.
专利号:US-5629394-A 优先权日:1992-12-17 标 题 :Direct synthesis by living cationic polymerization of nitrogen-containing polymers 发明人:CHERADAME HERVE M; CHEN FRANK J; STANAT JON E R; NGUYEN HUNG A; TABAR BEHROOZ R 权利人:EXXON CHEMICAL PATENTS INC 摘要:A method is provided for the direct synthesis by living cationic polymerization of novel polymeric materials functionalized with desirable nitrogen-containing functional groups such as terminal azido, cyano, carbonylamino, cyanato, thiocyanato or thiocarbonylamino groups. Polymerization and functionalization occur in a substantially simultaneous manner. All necessary reactants for the functionalization are present when polymerization is initiated. The nitrogen-containing functional group is provided as a part of a molecule having a release moiety which is preferably resonance stabilized or a tertiary alkyl type and which acts to aid the nitrogen-containing species in functioning as a leaving group.
专利号:US-8501954-B2 优先权日:2008-07-29 标题:Asymmetric process for making substituted 2-amino-thiazolones 发明人:CAILLE SEB; CUI SHENG; WANG XIANG; FAUL MARGARET 权利人:CAILLE SEB; CUI SHENG; WANG XIANG; FAUL MARGARET; AMGEN INC 摘要:The invention provides two process for synthesizing substituted aminothiazolone compounds as inhibitors of 11-β-hydroxy steroid dehydrogenase type 1. The processes allow the stereoselective synthesis of the desired compounds without the use of stoichiometric amounts of chiral catalysts.
摘要:U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals., NX#02865 摘要:Journal of Industrial Hygiene and Toxicology., 18(310), 1936 摘要:Naunyn-Schmiedeberg's Archiv fuer Experimentelle Pathologie und Pharmakologie., 150(257), 1930 摘要:Budavari, S. (ed.). The Merck Index - Encyclopedia of Chemicals, Drugs and Biologicals. Rahway, NJ: Merck and Co., Inc., 1989., p. 1469 摘要:Franke C et al; Chemosphere 29: 1501-14 (1994)