CAS: 16532-79-9; 4-Bromophenylacetonitrile

相似化合物

1878-68-8 27200-79-9 74860-13-2

上下游产品

CAS号773837-37-9 sodium cyanide | CAS号589-15-1 对溴溴苄 | CAS号143-33-9 氰化钠 | CAS号19158-51-1 4-甲苯磺酰氰 | CAS号501325-59-3 p-bromobenzyl a... | CAS号55883-45-9 1-bromo-4-(iodo... | CAS号10442-39-4 氰化四丁基胺 | CAS号130534-91-7 1-bromo-4-((met... | CAS号873-75-6 4-溴苄醇 | CAS号101422-55-3 3,4-bis(4-bromo... | CAS号1032528-06-5 1-(4-(4,4,5,5-四... | CAS号52787-14-1 4-甲酸甲酯苯乙酸甲酯 | CAS号41841-16-1 4-溴苯乙酸甲酯 | CAS号76469-88-0 对氰甲基苯甲酸甲酯 | CAS号4654-39-1 4-溴苯乙醇 | CAS号3277-79-0 (4-bromophenyl)... | CAS号143407-75-4 sodium,(6R,7R)-... | CAS号147111-30-6 2-(4-溴苯基)乙烷硫代酰胺 | CAS号143433-72-1 sodium,(6R,7R)-...

β-Methoxy Bromostyrene置于三甲基氯硅烷,氨,碘,Sodium Iodide体系中,用 水,乙腈 用作溶剂,化学反应 7.0H,反应生成对溴苯乙腈
参考文献:在无金属氰化物条件下通过 Wittig 反应从醛中一锅法制备 C1-同系化脂肪腈
标题:在无金属氰化物条件下通过 Wittig 反应从醛中一锅法制备 C1-同系化脂肪腈
摘要:通过用(甲氧基甲基)三苯基鏻叶立德处理芳香族和脂肪族醛,然后用 Ptsoh(ts = 对甲苯磺酰基)水解所得甲基乙烯基醚并用分子碘处理,实现了获得 C1 同系脂肪腈的一锅法和氨水在无金属氰化物条件下.使用本方法成功地获得了新戊基型腈,这些方法不能通过将新戊醇转化为甲苯磺酸盐并用金属氰化物处理的常规方法获得.
Doi:10.1002/ejoc.201700277

专利信息

专利号:US-9834556-B2
优先权日:2014-03-24
标题 :Process of preparing 3-(3-(4-aminocyclobutyl)phenyl)-5-phenyl-3H-imidazo[4,5-B]pyridin-2-YL)pyridin-2-amine
发明人：BATES CRAIG; CHEN JIAN-XIE; MAO JIANMIN; REED DAVID P
权利人:ARQULE INC
摘要:The present invention is directed to a processes for the synthesis of 3-(3-(4-(1-aminocyclobutyl)phenyl)-5-phenyl-3H-imidazo[4,5-b]pyridin-2-yl)pyridin-2-amine:

专利号:US-8754259-B2
优先权日:2008-08-15
标 题 :Synthesis of cyclohexane derivatives useful as sensates in consumer products
发明人：YELM KENNETH EDWARD; BUNKE GREGORY MARK; HAUGHT JOHN CHRISTIAN
权利人:PROCTER & GAMBLE; PROCTER & GAMBLE
摘要:The present invention provides synthetic routes for preparing various isomers of cyclohexane-based coolants, such as menthyl esters and menthanecarboxamide derivatives, in particular those substituted at the amide nitrogen, for example with an aromatic ring or aryl moiety. Such structures have high cooling potency and long lasting sensory effect, which make them useful in a wide variety of consumer products. One synthetic route involves a copper catalyzed coupling of a primary menthanecarboxamide with an aryl halide, such reaction working best in the presence of potassium phosphate and water. Using this synthetic route, specific isomers can be prepared including the menthanecarboxamide isomer having the same configuration as l-menthol and new isomers such as a neoisomer having opposite stereochemistry at the carboxamide (C-1) position. The neoisomer unexpectedly has potent and long lasting cooling effect. Preparation schemes for neoisomers of other menthyl derivatives which are useful as coolants, including esters, ethers, carboxy esters and other N-substituted carboxamides are also provided.

专利号:US-8895741-B2
优先权日:2003-06-03
标 题:Process for the synthesis of biaryl oxazolidinones
发明人：WU YUSHENG; CHEN SHILI; CHEN YI; HANSELMANN ROGER; LOU RONGLIANG; ZHOU JIACHENG
权利人:WU YUSHENG; CHEN SHILI; CHEN YI; HANSELMANN ROGER; LOU RONGLIANG; ZHOU JIACHENG; MELINTA THERAPEUTICS INC
摘要:The present invention relates to processes for the preparation of biaryl oxazolidinones. These compounds are useful as anti-infective, anti-proliferative, anti-inflammatory, and prokinetic agents.

专利号:US-9018249-B2
优先权日:2011-09-13
标题 :SGLT inhibitors
发明人：JAIN RAJESH; TREHAN SANJAY; DAS JAGATTARAN; NANDA GURMEET KAUR; THUNGATHURTHI SASTRY V R S; SINGH NISHAN; SHARMA SUDHIR KUMAR
权利人:JAIN RAJESH; TREHAN SANJAY; DAS JAGATTARAN; NANDA GURMEET KAUR; THUNGATHURTHI SASTRY V R S; SINGH NISHAN; SHARMA SUDHIR KUMAR; PANACEA BIOTEC LTD
摘要:The present invention relates to novel compounds of Formula I, their pharmaceutically acceptable derivatives, tautomeric forms, isomers, polymorphs, prodrugs, metabolites, salts or solvates thereof. The invention also relates to the processes for the synthesis of novel compounds of Formula I, their pharmaceutically acceptable derivatives, tautomeric forms, isomers, polymorphs, prodrugs, metabolites, salts or solvates thereof. The present invention also provides pharmaceutical compositions comprising novel compounds of Formula I and methods of treating or preventing one or more conditions or diseases that may be regulated or normalized via inhibition of Sodium Glucose Cotransporter-2 (SGLT-2).

专利号:US-2010022772-A1
优先权日:2003-06-03
标 题:Process for the synthesis of biaryl oxazolidnones

专利号:CN-105568312-B
优先权日:2016-01-06
标题:A kind of method of indirect electrocatalytic synthesis of 2-arylpyrrole compound