CAS: 6589-55-5; α-(Methylaminomethyl)Benzyl Alcohol

上下游产品

styrene oxide methylamine formaldehyd 2-nitro-1-phenylethan-1-oldimethyl-(3-methyl-5-phenyl-[1,3,2]oxazaphospholidin-2-yl)-amine S-(2-methylamino-1-phenyl-ethyl ester)thiosulfuric acid S-(2-methylamino-1-phenyl-ethyl ester) 5-phospha-spiro[4.4]nonane4,9-dimethyl-2,7-diphenyl-1,6-dioxa-4,9-diaza-5λ5-phospha-spiro[4.4]nonane 3-methyl-5-phenyloxazolidin-2-one

📜N-Methyl-2-Hydroxy-2-Phenylethanamide置于lithium Aluminium Tetrahydride体系中,用 四氢呋喃 作为反应溶剂,化学反应 8.0H,以95.6%的收率获得产物α-(甲氨甲基)苯甲醇
参考文献:Moehre,H.; Kamper,Ch.,Pharmazie,1983,Vol. 38,# 8,P. 512-520
标题:Moehre,H.; Kamper,Ch.,Pharmazie,1983,Vol. 38,# 8,P. 512-520

专利信息

专利号:WO-0140193-A1
优先权日:1999-12-03
标题:Method for the synthesis of pyrazolines
发明人：BOLDI ARMEN M
权利人:CHEMRX ADVANCED TECHNOLOGIES I; BOLDI ARMEN M
摘要:The present invention provides a method for the synthesis of compounds of Formula (I). Also claimed are novel intermediates and their methods of synthesis.

专利号:US-4217452-A
优先权日:1974-02-09
标 题:Synthesis for the preparation of tetracyclic compounds
发明人：OLIVIE JACQUES
权利人:AKZONA INC
摘要:The invention relates to a new synthesis for the preparation of tetracyclic compounds of the general formula: ##STR1## as well as the pharmaceutically acceptable salts thereof, in which: n is the number 1 or 2, n m is the number 1, if n=2 and the number 2, if n=1, n R 1 and R 2 stand for hydrogen, hydroxy, halogen, lower alkyl (1-4 C), lower alkoxy (1-4 C) or trifluoromethyl and n R 3 represents hydrogen, alkyl (1-6 C), aralkyl (7-10 C) or an amino alkyl group (1-6 C), in which the nitrogen atom has been substituted by two alkyl groups (1-4 C), or the nitrogen atom forms part of a heterocyclic 5- or 6-membered ring, n having valuable biological properties.

专利号:US-4254031-A
优先权日:1974-02-09
标 题:Synthesis for the preparation of tetracyclic compounds
发明人：OLIVIE JACQUES
权利人:AKZONA INC
摘要:The invention relates to a new synthesis for the preparation of tetracyclic compounds of the general formula ##STR1## as well as the pharmaceutically acceptable salts thereof, in which: n is the number 1 or 2, n m is the number 1, if n=2 and the number 2, if n=1, n R 1 and R 2 stand for hydrogen, hydroxy, halogen, lower alkyl (1-4 C), lower alkoxy (1-4 C) or trifluoromethyl and n R 3 represents hydrogen, alkyl (1-6 C), aralkyl (7-10 C) or an amino alkyl group (1-6 C), in which the nitrogen atom has been substituted by two alkyl groups (1-4 C), or the nitrogen atom forms part of a heterocyclic 5- or 6-membered ring, n having valuable biological properties.

专利号:US-2018111958-A1
优先权日:2008-12-02
标 题 :Method for the synthesis of phosphorus atom modified nucleic acids

专利号:EP-1529037-A2
优先权日:2002-05-15
标 题:Synthesis of 2-alkylcysteines, 2-(hydroxylated phenyl)-4-alkylthiazoline-4-carboxylic acids and derivatives thereof

专利号:US-6417195-B1
优先权日:1999-02-22
标题 :Isoquinoline derivatives and isoquinoline combinatorial libraries
发明人：LEBL MICHAL
权利人:LION BIOSCIENCE AG
摘要:The present invention provides the synthesis of heterocyclic compounds based on the isoquinoline ring. More specifically, the invention provides novel isoquinoline derivatives as well as novel libraries comprised of such compounds.