A Comparison of Catalysts to Promote Imidazolide Couplings Including the英文電子資料

A Comparison of Catalysts to Promote Imidazolide Couplings Including the英文電子資料

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時(shí)間:2019-06-30

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1、OrganicProcessResearch&Development2005,9,956-961FullPapersAComparisonofCatalyststoPromoteImidazolideCouplingsIncludingtheIdentificationof2-Hydroxy-5-nitropyridineasaNew,Safe,andEffectiveCatalystPeterJ.Dunn,*,2WilfriedHoffmann,2YingKang,2,3JohnC.Mitchell,3andMartinJ.Snowden3DepartmentofChemica

2、lResearchandDeVelopment,PfizerGlobalResearchandDeVelopment,Sandwich,KentCT139NJ,UnitedKingdom,andMedwaySciences,UniVersityofGreenwich,MedwayCampus,Chatham,KentME44TB,UnitedKingdomAbstract:Scheme1Fivecatalystswerecomparedwithrespecttotheirsafetyandcatalyticeffectivenessforpromotingimidazolidec

3、ouplings.Reactionrateenhancement,shocksensitivity,anddifferentialscanningcalorimetry(DSC)datawereconsideredinthisanalysis.6-Chloro-1-hydroxybenzotriazole,whichhasbeendescribedintheliteratureasasafecatalyst,wasfoundtobeshocksensitive.2-Hydroxy-5-nitropyridineisanewcatalystforthistypeofreaction

4、andwasfoundtobesafe,effective,readilyavailable,andsimilarinpricetothatofthe1-hydroxybenzo-triazole,acommoncatalystforpromotingacylationreactions.Scheme2IntroductionTheuseofN,N1-carbonyldiimidazole(CDI)asacouplingagentforamidebondformationhasrecentlybeenappliedtothelarge-scalesynthesisofanumbe

5、rofpharmaceuticalproducts,forexample,sildenafil,1darifenacin,2andsunitinib.3Inadditionasurveyof128chemicalprocessesrecentlydevelopedbyAstraZeneca,GlaxoSmithKline(GSK),andPfizerrevealedthatCDIwasthethirdmostcommonreagentOnefactorinfluencingtheincreaseduseofCDIonalargeusedforN-acylationreaction

6、sandwasusedin9outof84scaleisitsrelativelylowprice(around$8/molforalarge-examples.4Theadvantagesarethatthebyproducts,carbonscalepurchase).AlthoughCDIismoreexpensivethandioxideandimidazole,areinnocuousandthattheevolutiontraditionalamide-formingreagents,suchasthionylchlorideofcarbondioxideinform

7、ingtheimidazolide1providesaandisobutylchloroformate,insomecasesthehighyieldsdrivingforceforthereaction5,6(Scheme1).Inadditiontheandcleanenvironmentalconditionscanjustifyitsuse.imidazolebyproductcanberemovedbyanacidicwash2orAdisadvantageofCDIi

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