CAS: 603-76-9; 1-Methyl-1H-Indole

上下游产品

CAS号120-72-9 吲哚 | CAS号616-38-6 碳酸二甲酯 | CAS号74-88-4 碘甲烷 | CAS号1352621-88-5 2,4,6-trichloro... | CAS号824-21-5 1-甲基吲哚啉 | CAS号5339-28-6 2-ethenyl-N-met... | CAS号74-83-9 溴甲烷 | CAS号1352334-73-6 diethyl-carbami... | CAS号81471-20-7 3-溴-1-甲基-1H-吲哚 | CAS号16136-58-6 1-甲基吲哚-2-甲酸 | CAS号1421259-27-9 N-methyl-N-((1-... | CAS号105804-97-5 (N-methylanilin... | CAS号52866-87-2 N-(tert-butylpe... | CAS号111678-54-7 2-allyl-1-methy... | CAS号112122-42-6 1-methyl-3-(1-p... | CAS号3260-62-6 N-Methylindoxyl | CAS号32387-21-6 1-甲基-3-吲哚酸 | CAS号151490-40-3 甲基(1-甲基吲哚基)-3-乙醛酸酯 | CAS号6637-11-2 2,3'-Bi-1H-indo... | CAS号1485-22-9 (1-甲基-1H-吲哚-2-基)甲醇

5-氯-1-甲基吲哚置于potassium Tert-Butylate,N,N-二甲基甲酰胺体系中,用 二甲基亚砜 作为反应溶剂,化学反应 24.0H,以96%的收率获得产物1-甲基吲哚
参考文献:可见光诱导的碱促进的芳基氟化物,氯化物,溴化物和碘化物的无过渡金属脱卤化作用
标题:可见光诱导的碱促进的芳基氟化物,氯化物,溴化物和碘化物的无过渡金属脱卤化作用
摘要:我们报告了简单有效的芳基卤化物的可见光诱导的无过渡金属氢化.可见光和碱的组合系统用于引发所需的自由基介导的氢化反应.在温和条件下,可以将多种芳基氟化物,氯化物,溴化物和碘化物还原成相应的(杂)芳烃.可以容忍各种官能团和其他杂环化合物.
DOI:10.1021/acs.Orglett.0C00827

专利信息

专利号:US-9755163-B2
优先权日:2010-04-30
标 题:Synthesis of four coordinated palladium complexes and their applications in light emitting devices thereof
发明人：LI JIAN; TURNER ERIC
权利人:ARIZONA BOARD OF REGENTS ACTING FOR AND ON BEHALF OF ARIZONA STATE UNIV; ARIZONA BOARD OF REGENTS ACTING FOR OR ON BEHALF OF ARIZONA STATE UNIV
摘要:Synthesis of four coordinated palladium complexes and their applications in light emitting devices thereof.

专利号:US-7344863-B2
优先权日:1998-03-13
标题:Methods for producing polypeptides through enhanced synthesis of encoding nucleic acid molecules
发明人：LI WU-BO; JESSEE JOEL A; SCHUSTER DAVID; XIA JIULIN; GEBEYEHU GULILAT
权利人:INVITROGEN CORP
摘要:The present invention is directed to compositions and methods for enhancing synthesis of nucleic acid molecules, particularly GC-rich nucleic acid molecules. Specifically, the invention provides compositions comprising one or more nitrogen-containing organic compounds having a formula selected from the group consisting of formula I and formula II (or salts or derivatives thereof), preferably 4-methylmorpholine N-oxide or betaine (carboxymethyltrimethylammonium), and further comprising one or more compounds selected from the group consisting of proline and an N-alkylimidazole compound, and more preferably proline, 1-methylimidazole or 4-methylimidazole. The invention further relates to methods for enhanced, high-fidelity synthesis of nucleic acid molecules, including via amplification (particularly PCR), reverse transcription, and sequencing methods. The invention also relates to nucleic acid molecules synthesized by these methods, to fragments or derivatives thereof, and to vectors and host cells comprising such nucleic acid molecules, fragments, or derivatives. The invention also relates to kits for synthesizing, amplifying, reverse transcribing or sequencing nucleic acid molecules comprising one or more of the compositions of the invention.

专利号:US-2021107859-A1
优先权日:2018-04-06
标题 :A process for the synthesis of carbon labeled organic compounds
发明人：AUDISIO DAVIDE; CANTAT THIBAULT; DESTRO GIANLUCA
权利人:COMMISSARIAT ENERGIE ATOMIQUE
摘要:A process for the synthesis of a carbon labeled organic compound containing a carbon labeled carboxyl group is described. A method of using carbon labeled organic compounds containing a carbon labeled carboxyl group according to the present disclosure; a process for manufacturing labeled pharmaceuticals and agrochemicals comprising synthesis of carbon labeled organic compounds containing a carbon labeled carboxyl group according to the present disclosure; and a process for producing tracers comprising synthesis of carbon labeled organic compounds containing a carbon labeled carboxyl group according to the present disclosure are also described.

专利号:US-2012165520-A1
优先权日:2010-12-23
标题:Process for the synthesis of prodrugs of opioids
发明人：MCGEE PAUL; GARNETT IAN; JUAN E; MANAGE A; CARNIAUX JEAN-FRANCOIS
权利人:MCGEE PAUL; GARNETT IAN; JUAN E; MANAGE A; CARNIAUX JEAN-FRANCOIS
摘要:The present invention provides a process for the synthesis of opioid prodrugs. In particular, the present invention provides a process for the synthesis of opioid prodrugs comprising: treating an opioid, in the form of a salt or a freebase, with a carbonyl synthon to form an activated intermediate and subsequently reacting the activated intermediate with an amine, in the form of a salt or a freebase.

专利号:US-5817751-A
优先权日:1994-06-23
标 题 :Method for synthesis of diketopiperazine and diketomorpholine derivatives
发明人：SZARDENINGS ANNA KATRIN; CAMPBELL DAVID
权利人:AFFYMAX TECH NV
摘要:The present invention relates to the areas of organic and medicinal chemistry. More specifically, the present invention is concerned with combinatorial and solid phase methods for the synthesis of diverse diketopiperazine derivatives, and the use of such methods to create libraries of diverse diketopiperazine derivatives. The present invention has application in the areas of chemical synthesis, the screening for new diketopiperazine derivatives having beneficial medical properties and the use of such screening to provide compositions and methods including diketopiperazine derivatives for treating disease.

专利号:EP-2586773-A1
优先权日:2011-10-27
标题 :Synthesis of Triazolopyrimidine Compounds
权利人:LEK PHARMACEUTICALS
摘要:The present invention relates to the field of organic synthesis and describes the synthesis of specific triazolopyrimidine compounds and intermediates thereof as well as related derivatives.