6-溴烟酸置于sodium Tetrahydroborate,三氯氧磷体系中,化学反应生成2-氯-5-羟甲基吡啶 参考文献:Substituted Dipyridylethenes And-Ethynes And Key Pyridine Building Blocks 标题:Substituted Dipyridylethenes And-Ethynes And Key Pyridine Building Blocks 摘要:合成了多种新的2,5-二取代吡啶.通过还原烟酸3,氨基二甲基吡啶6的水解或5-溴吡啶12和14与丁基锂在dmf中的反应,得到了2-取代的5-醛基吡啶8,15A-B.双吡啶乙烯16A-B,E通过wadsworth-Emmons反应与吡啶基膦酸酯7合成,或者通过mcmurry反应将醛偶联形成烯烃16C-D.在双吡啶乙烯16A-D的c=c双键溴化后,经过1,2-双吡啶-1,2-二溴乙烷17A-D的消除,得到了双吡啶乙炔18A-D. Doi:10.1055/s-1994-25411
专利号:US-7919627-B2 优先权日:2005-05-02 标题:Processes for the preparation of hydroxylamines 发明人:TANG DATONG; QIU YAO-LING; KIM HEEJIN; OR YAT SUN; WANG ZHE 权利人:ENANTA PHARM INC 摘要:The present invention relates generally to novel methods for the synthesis of O-(6-pyrazol-1-yl-pyridin-3-ylmethyl)-hydroxylamine which is an essential reagent in the synthesis of one of the bridged erythromycin derivatives and their respective pharmaceutically acceptable salts in PCT Application WO 03/097659 A1. In particular, the present invention relates to processes and intermediates for the preparation of a compound of formula (Ia):
专利号:US-4285969-A 优先权日:1979-03-09 标 题:Pyrethroids 发明人:GALLI REMO; GOZZO FRANCO; PALLA OTTORINO; LONGONI ANGELO 权利人:MONTEDISON SPA 摘要:The present invention concerns new pyrethroids having a high insecticidal activity. More particularly, this invention relates to novel esters of 2,2-dimethyl-cyclopropanecarboxylic acids substituted in the 3 position; the preparation of said novel esters; the use of said novel esters as insecticides and to insecticidal compositions containing said novel esters as the active ingredient. The present invention also includes providing intermediates for the synthesis of the new pyrethroids and the process for the preparation of said intermediates.
专利号:WO-2016097345-A1 优先权日:2014-12-19 标题 :Labelled chromone derivatives 发明人:JACKSON ALEXANDER 权利人:GE HEALTHCARE LTD 摘要:The present invention relates to compounds having selective binding for MAO-B as compared with MAO-A. The invention also provides radioactive versions of these compounds, and precursor compounds for the synthesis of these radioactive compounds. The radioactive compounds of the invention are particularly useful for in vivo imaging applications.
专利号:US-2007275968-A1 优先权日:2004-09-07 标 题 :Substituted Biphenyl Derivative 发明人:KURATA HITOSHI; NISHIMATA TOYOKI; WATANABE YUKIKO; EBISAWA MASAYUKI; FUJIMOTO TEPPEI; KOBAYASHI HIDEKI 权利人:KURATA HITOSHI; NISHIMATA TOYOKI; WATANABE YUKIKO; EBISAWA MASAYUKI; FUJIMOTO TEPPEI; KOBAYASHI HIDEKI 摘要:The present invention relates to a biaryl derivative or a pharmacologically acceptable salt thereof having an excellent collagen-synthesis inhibition activity. A biaryl derivative having a structure represented by the following General Formula (I) or a pharmacologically acceptable salt thereof: n nwherein n R 1 represents a C 6 -C 10 aryl group which is substituted with one to three group(s) each independently selected from the group consisting of a group defined by formula R-L-, a di-(C 1 -C 6 alkyl)amino group, a di-(C 1 -C 6 alkyl)aminosulfonyl group, a hydroxyaminocarbonyl group, and a halogen atom, and so on; R represents a C 1 -C 6 alkyl group, and so on; L represents a sulfonyl group, an aminosulfonyl group, or a sulfonylamino group, and so on; R 2 represents a hydrogen atom, and so on; A represents a group defined by formula (II), (III), or (IV); R 3 represents a C 1 -C 6 alkyl group, and so on; and R 4 represents a C 1 -C 6 alkyl group, and so on.
专利号:CN-108689919-A 优先权日:2018-05-24 标 题:Continuous Synthesis Process of 2-Chloro-5-Chloromethylpyridine
参考标题:Investigation Of Functionalized α-Chloroalkyllithiums For A Stereospecific Reagent-Controlled Homologation Approach To The Analgesic Alkaloid (−)-Epibatidine 作者:Christopher R. Emerson,Lev N. Zakharov,Paul R. Blakemore |发布日期:2013.11.25 摘要:Respectively; α‐deuterated Isotopomers D‐18 A And D‐18 D Gave Yields Of 33 And 79 % For The Same Reaction. Double Strech Of 17 Was Pursued To Target Contiguous Stereodiads Appropriate For The Total Synthesis Of (−)‐epibatidine (15). One‐pot Double Strech Of Boronate 17 By Two Exposures To (S)‐d‐18 A (<=66 % Ee), Followed By Work‐up With Kooh, Gave The Expected Stereodiad Product In 16 % Yield (D.R.∼67:33)
合成参考文献
摘要:Croft, R. A.; Bull, J. A., Science of Synthesis Knowledge Updates, (2018) 4, 383.