CAS: 22710-07-2; 2,3-Dimethylpyridine 1-Oxide

相似化合物

59886-90-7 931-19-1 1073-23-0

上下游产品

CAS号583-61-9 2,3-二甲吡啶 | CAS号50-00-0 甲醛 | CAS号937-14-4 间氯过氧苯甲酸 | CAS号102625-96-7 4-methoxy-2,3-d... | CAS号59886-90-7 2,3-二甲基-4-氯吡啶-N-氧化物 | CAS号37699-43-7 2,3-二甲基-4-硝基吡啶-N-氧化物 | CAS号35392-67-7 3-methoxy-2-met... | CAS号4370-22-3 2-(氯甲基)-3-甲基吡啶盐酸盐 | CAS号193690-71-0 2-AMINO-1,6,7-T... | CAS号86604-77-5 4-甲氧基-3-甲基-2-吡啶甲醇 | CAS号57963-08-3 2-氨基-5,6-二甲基吡啶 | CAS号63071-09-0 (3-甲基吡啶-2-基)甲醇 | CAS号55589-47-4 3-甲基-2-吡啶醛

2,3-二甲基吡啶置于双氧水体系中,用 乙醇,水 用作溶剂,化学反应 6.0H,以86%的收率获得2,3-二甲基吡啶-N-氧化物
参考文献:基于聚氧钼酸酯的吡啶在温和条件下催化氧化为n-氧化物的催化系统†
标题:基于聚氧钼酸酯的吡啶在温和条件下催化氧化为n-氧化物的催化系统†
摘要:已经开发了可重复使用且有效的催化体系,用于在室温下氧化由keplerate聚氧钼酸酯({mo 132 })催化的吡啶的氧化.吡啶化合物可以在温和的条件下高产率地被氧化.
Doi:10.1039/c5Ra05196G

专利信息

专利号:US-6608202-B1
优先权日:2001-08-21
标题:Process of synthesis of a tricyclic ketone intermediate
发明人：DORAN HENRY J; O'NEILL PAT M; WILLIAMS ROBERT P
权利人:SCHERING CORP
摘要:In one embodiment, the present invention describes the synthesis of a compound of Formula III, wherein X is halogen,and intermediates therefor from easily available starting materials by a simple route.

专利号:US-9428524-B2
优先权日:2010-05-25
标 题:Synthetic process for the manufacture of ecteinascidin compounds
发明人：MARTIN LÓPEZ MA JESÚS; FRANCESCH SOLLOSO ANDRÉS; CUEVAS MARCHANTE MARIA DEL CARMEN
权利人:MARTIN LÓPEZ MA JESÚS; FRANCESCH SOLLOSO ANDRÉS; CUEVAS MARCHANTE MARIA DEL CARMEN; PHARMA MAR SA
摘要:This invention relates to compounds of formula II: wherein R 1 , R 2 , Prot SH , and Prot NH are as defined, to processes for the synthesis of ecteinascidins of formula I from compounds of formula II, and to processes for the synthesis of compounds of formula II.

专利号:US-2004110228-A1
优先权日:2002-04-01
标 题:Combinatorial organic synthesis of unique biologically active compounds
发明人：MCALPINE SHELLI R; TAYLOR RACHEL E; BOLLA MEGAN L; SEGALL ANCA M
摘要:The invention provides a method for making a combinatorial library of cyclic compounds, such as Holliday junction-trapping compounds, comprising the steps of (a) obtaining a plurality of trimers according to the generic structure X 1- X 2- X 3 , wherein X 1 , X 2 and X 3 can be independently any naturally or nonnaturally occurring amino acids or peptidomimetics thereof; (b) optionally coupling a spacer S to the trimer at either end; (c) cyclizing two trimers or trimer-spacer conjugates in a head-to-tail orientation; thereby obtaining a combinatorial library of compounds, wherein the library does not include an unmodifed or naturally occurring Holliday Junction-trapping compounds. The invention additionally provides methods macrocyclic compounds that are synergimycin derivatives.

专利号:US-2003144314-A1
优先权日:2001-08-21
标 题 :Process of synthesis of a tricyclic ketone intermediate

专利号:US-9890193-B2
优先权日:2013-06-05
标题 :Compounds having triple activities of thrombolysis, antithrombosis, and radical scavenging, synthesis, and use thereof
发明人：Peng shi qi; ZHAO MING; Wu jian hui; Wang yu ji; FENG QI QI
权利人:SHANGHAI LUMOSA THERAPEUTICS CO LTD
摘要:The present invention relates to a compound simultaneously having triple activities of thrombolysis, antithrombosis and free radical scavenging, as well as the preparation method, composition, and applications thereof. The compound is represented by the formula I shown below: n nwherein the definitions of T, Q, R 1 and R 2 are described herein. The compound of the present invention simultaneously has triple functions of thrombolysis, free radical scavenging and thrombus-targeting/antithrombosis. The present invention also relates to a pharmaceutical composition comprising the compound, and a preparation method and a nanostructure of the compound.

专利号:EP-1421068-B1
优先权日:2001-08-21
标题:A process of synthesis of a tricyclic ketone intermediate