0000000000237692

AUTHOR

Tobias Lucas

0000-0003-3043-5411

showing 12 related works from this author

Six-Step Gram-Scale Synthesis of the Human Immunodeficiency Virus Integrase Inhibitor Dolutegravir Sodium

2021

This is the accepted manuscript version of the work published in its final form as Dietz, Jule-Philipp; Lucas, Tobias; Groß, Jonathan; Seitel, Sebastian; Brauer, Jan; Ferenc, Dorota; Gupton, B. Frank; Opatz, Till. Organic Process Research & Development; Volume: 25; Issue: 11; Pages: 1898-1910; https://doi.org/10.1021/acs.oprd.1c00139. Deposited by shareyourpaper.org and openaccessbutton.org. We've taken reasonable steps to ensure this content doesn't violate copyright. However, if you think it does you can request a takedown by emailing help@openaccessbutton.org.

Scale (ratio)ChemistryOrganic ChemistryHuman immunodeficiency virus (HIV)medicineIntegrase inhibitorDolutegravir sodiumPhysical and Theoretical Chemistrymedicine.disease_causeGeneralLiterature_REFERENCE(e.g.dictionariesencyclopediasglossaries)VirologyGramOrganic Process Research & Development
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A concise route to MK-4482 (EIDD-2801) from cytidine.

2020

A two-step route to MK-4482 (EIDD-2801, 1) was developed consisting of an esterification and hydroxamination of cytidine. The selective acylation and direct amination eliminate the need for protecting and activating groups and proceed in overall yield of 75%, a significant advancement over the reported yield of 17%. The step count is reduced from five transformations to two, and expensive uridine is replaced with the more available cytidine.

010405 organic chemistryAcylationMetals and AlloysCytidineGeneral ChemistryCytidine010402 general chemistryHydroxylamines01 natural sciencesCombinatorial chemistryCatalysisUridine0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsAcylationchemistry.chemical_compoundKineticschemistryYield (chemistry)Materials ChemistryCeramics and CompositesStep countAminationChemical communications (Cambridge, England)
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Glucose as an Eco‐Friendly Reductant in a One‐Pot Synthesis of 2,3‐Dihydroquinazolin‐4(1 H )‐ones

2020

SUSTENTABILIDADEChemistryOrganic ChemistryOne-pot synthesisBiomassOrganic chemistryPhysical and Theoretical ChemistryEnvironmentally friendlyEuropean Journal of Organic Chemistry
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Visible Light Enables Aerobic Iodine Catalyzed Glycosylation

2019

chemistry.chemical_compoundGlycosylationCarbohydrate chemistryChemistryOrganic Chemistrychemistry.chemical_elementPhysical and Theoretical ChemistryPhotochemistryIodineCatalysisVisible spectrumEuropean Journal of Organic Chemistry
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Front Cover: Glucose as an Eco‐Friendly Reductant in a One‐Pot Synthesis of 2,3‐Dihydroquinazolin‐4(1 H )‐ones (Eur. J. Org. Chem. 41/2020)

2020

Front coverChemistryOrganic ChemistryOne-pot synthesisOrganic chemistryPhysical and Theoretical ChemistryEnvironmentally friendlyEuropean Journal of Organic Chemistry
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Six-Step Gram Scale Synthesis of the HIV Integrase Inhibitor Dolutegravir Sodium

2021

A short and practical synthesis for preparing the active pharmaceutical ingredient dolutegravir sodium was investigated. The convergent strategy developed herein starts from 3-(R)-amino-1- butanol and builds up the BC ring system in 76% isolated yield over four steps. Ring A was constructed by a one-pot 1,4-addition to diethyl-(2E/Z)-2-(ethoxymethylidene)-3-oxobutandioate and subsequent MgBr2·OEt2-mediated regioselective cyclization. Amide formation with 2,4- difluorobenzylamine was either performed from the carboxylic acid or through aminolysis of the corresponding ester precursor. Final salt formation afforded dolutegravir sodium in 48–51% isolated yield (HPLC-purity: 99.7–99.9%) over six…

Active ingredientchemistry.chemical_classificationbiologyChemistryStereochemistryCarboxylic acidButanolRegioselectivityIntegrasechemistry.chemical_compoundAminolysisYield (chemistry)Amidebiology.protein
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Front Cover: Visible Light Enables Aerobic Iodine Catalyzed Glycosylation (Eur. J. Org. Chem. 28/2019)

2019

chemistry.chemical_compoundFront coverGlycosylationchemistryOrganic Chemistrychemistry.chemical_elementPhysical and Theoretical ChemistryPhotochemistryIodineVisible spectrumCatalysisEuropean Journal of Organic Chemistry
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Synthesis of 4-amino-5-fluoropyrimidines and 5-amino-4-fluoropyrazoles from a β-fluoroenolate salt

2020

A synthesis of fluorinated pyrimidines under mild conditions from amidine hydrochlorides and the recently described potassium 2-cyano-2-fluoroethenolate was developed. A broad substrate scope was tested and mostly excellent yields were obtained. The synthesis of fluorinated aminopyrazoles from the same fluorinated precursor could be demonstrated but proceeded with lower efficiency.

chemistry.chemical_classificationcyclizationfluorinated heterocyclesChemistrypyrimidinesPotassiumOrganic Chemistrychemistry.chemical_elementSalt (chemistry)Substrate (chemistry)Combinatorial chemistryFull Research PaperpyrazolesAmidinelcsh:QD241-441Chemistrychemistry.chemical_compoundlcsh:Organic chemistryfluorineFluorinelcsh:Qlcsh:ScienceBeilstein Journal of Organic Chemistry
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Total synthesis and biological evaluation of seven new anti-inflammatory oxacyclododecindione-type macrolactones

2020

Through variation of our previously published total synthesis of two highly active anti-inflammatory macrolactones from the oxacyclododecindione family (J. Tauber, M. Rohr, T. Walter, G. Erkel and T. Opatz, Org. Biomol. Chem., 2015, 13, 7813-7821), seven new representatives of this compound class were prepared. Substitution of the 14-hydroxy group in oxacyclododecindione with a methyl substituent provided a readily accessible non-natural analogue which has similar pharmacological properties to the scarcely available natural product. Since the producible amount of substance is therefore no longer restricted by low fermentation yields, extensive in vivo studies become possible for the first t…

Macrocyclic CompoundsNatural productStereochemistryOrganic ChemistrySubstituentTotal synthesisBiochemistrychemistry.chemical_compoundchemistryIn vivoSide chainBioassayFermentationPhysical and Theoretical ChemistryIC50Organic & Biomolecular Chemistry
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CCDC 1998325: Experimental Crystal Structure Determination

2020

Related Article: Carina Weber, Nina Vierengel, Thorsten Walter, Torsten Behrendt, Tobias Lucas, Gerhard Erkel, Till Opatz|2020|Org.Biomol.Chem.|18|5906|doi:10.1039/D0OB00958J

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters(E)-14-chloro-1113-dihydroxy-4559-tetramethyl-4567-tetrahydro-2H-benzo[d][1]oxacyclododecine-210(1H)-dioneExperimental 3D Coordinates
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CCDC 1998326: Experimental Crystal Structure Determination

2020

Related Article: Carina Weber, Nina Vierengel, Thorsten Walter, Torsten Behrendt, Tobias Lucas, Gerhard Erkel, Till Opatz|2020|Org.Biomol.Chem.|18|5906|doi:10.1039/D0OB00958J

(E)-1113-bis(benzyloxy)-9-ethyl-455-trimethyl-4567-tetrahydro-2H-benzo[d][1]oxacyclododecine-210(1H)-dioneSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1998324: Experimental Crystal Structure Determination

2020

Related Article: Carina Weber, Nina Vierengel, Thorsten Walter, Torsten Behrendt, Tobias Lucas, Gerhard Erkel, Till Opatz|2020|Org.Biomol.Chem.|18|5906|doi:10.1039/D0OB00958J

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters(E)-1113-bis(benzyloxy)-4559-tetramethyl-4567-tetrahydro-2H-benzo[d][1]oxacyclododecine-210(1H)-dione unknown solvateExperimental 3D Coordinates
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