CAS: 609-66-5; 2-Chlorobenzamide

上下游产品

CAS号89-98-5 邻氯苯甲醛 | CAS号873-32-5 邻氯苯腈 | CAS号201230-82-2 carbon monoxide | CAS号615-41-8 邻氯碘苯 | CAS号609-65-4 邻氯苯甲酰氯 | CAS号118-91-2 邻氯苯甲酸 | CAS号3717-28-0 邻氯苯甲醛肟 | CAS号2444-36-2 2-氯苯乙酸 | CAS号49747-51-5 2-chlorobenzoyl... | CAS号17849-38-6 2-氯苄醇 | CAS号50907-46-5 5-(2-氯苯)-1H-四唑 | CAS号3320-83-0 2-氯苯基异氰酸酯 | CAS号55-21-0 苯甲酰胺 | CAS号89-97-4 邻氯苄胺 | CAS号873-32-5 邻氯苯腈 | CAS号20668-13-7 (2-氯苯基)氨基甲酸甲酯 | CAS号22397-40-6 Oxazole,2-(2-ch... | CAS号95-51-2 2-氯苯胺 | CAS号89-98-5 邻氯苯甲醛 | CAS号72867-72-2 邻氯苯基苄基酮

邻氯苯腈置于sodium Perborate体系中,用 乙醇,水 作为反应溶剂,化学反应 0.07H,以84%的收率获得产物2-氯苯甲酰胺
参考文献:用过硼酸钠水溶液在微波促进下将腈转化为酰胺
标题:用过硼酸钠水溶液在微波促进下将腈转化为酰胺
摘要:几种芳香族和脂肪族腈,包括 α,β-双三甲基甲硅烷基腈,用四水过硼酸钠在水/乙醇 (2:1) 混合物中的微波辐照,在短时间内顺利地以高产率产生了相应的酰胺.其他官能团,如醛,在这些条件下不受影响.
DOI:10.1081/scc-100000535

专利信息

专利号:CN-118530135-A
优先权日:2024-04-22
标题:A kind of synthesis process of continuous synthesis of salicylamide

专利号:US-7179918-B2
优先权日:2001-06-11
标 题:HIV protease inhibitors, compositions containing the same, their pharmaceutical uses and materials for their synthesis
发明人：CANAN KOCH STACIE S; ALEXANDER THERESE N; BURKE BENJAMIN J; JEWELL TANYA M; KUCERA DAVID J; LINTON MARIA ANGELICA; MITCHELL JR LENNERT J; REICH SIEGFRIED H; SKALITZKY DONALD J; TATLOCK JOHN H; VARNEY MICHAEL D; VIRGIL SCOTT C; WEBBER STEPHEN E; WORLAND STEPHEN T; BARVIAN MARK; BOLTON GARY; BOYER JR FREDERICK EARL; MACHAK JEFFREY J; HOLLER TOD; MURPHY SEAN T; MELNICK MICHAEL; JOSYULA VARA PRASAD
权利人:AGOURON PHARMA
摘要:Compounds of the formula: n nwhere the formula variables are as defined herein, are disclosed that advantageously inhibit or block the biological activity of the HIV protease. These compounds, as well as pharmaceutical compositions containing these compounds, are useful for treating patients or hosts infected with the HIV virus. Intermediates and synthetic methods for preparing such compounds are also described.

专利号:US-7731932-B2
优先权日:2003-09-04
标 题 :Methods of processing nanocrystals, and compositions, devices and systems including same
发明人：SCHER ERIK C; BURETEA MIHAI A; WHITEFORD JEFFERY A; MEISEL ANDREAS P
权利人:NANOSYS INC
摘要:Methods of processing nanocrystals to remove excess free and bound organic material and particularly surfactants used during the synthesis process, and resulting nanocrystal compositions, devices and systems that are physically, electrically and chemically integratable into an end application.

专利号:US-8440842-B2
优先权日:2007-07-16
标题:Antimicrobial compounds, their synthesis and their use for treatment of mammalian infections
发明人：MOELLMANN UTE; MAKAROV VADIM; STEWART COLE T
权利人:MOELLMANN UTE; MAKAROV VADIM; STEWART COLE T; LEIBNIZ INST NATURSTOFF FORSCH
摘要:The present invention relates to compounds of Formula (I) n nor salts thereof wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , and other variables enumerated under one or more of same are as defined herein. Compounds of Formula I have activity as antimicrobial agents. Also disclosed are pharmaceutical compositions and methods of treating and preventing microbial infections in mammals, for example, a tuberculosis or leprosy infection, which employ compounds of Formula (I) or salts thereof.

专利号:SU-1739849-A3
优先权日:1987-08-03
标题 :Method for synthesis of benzamide derivatives or their pharmacologically acceptable salts

专利号:US-5021444-A
优先权日:1986-01-28
标题 :Thianaphthene derivatives
发明人：TRADA ATSUSUKE; AMEMIYA YOSHIYA; MATSUDA KEIICHI; OSHIMA TAKESHI
权利人:SANKYO CO
摘要:Compounds of formula (I): ##STR1## (wherein n is 0 or 1, R 1 and R 2 are hydrogen or alkyl, one of A 1 and A 2 is --Z--Y and the other is --W--COOH, where W and Z are alkenylene or alkylene and Y is imidazolyl or pyridyl, and the broken lines represent two single bonds or one single bond and one double bond) and their salts, esters and amides have the ability to inhibit the synthesis of thromboxane A 2 and hence are useful in the treatment of prophylaxis of thrombotic conditions. They may be prepared by introducing an imidazolyl or pyridyl group into the corresponding compound in which Y is replaced by an active group or atom.