6-Bromoquinoline → HCID 178422846, compound

HRID 2258813Notes

Reaction equation

HRID 2258813 reaction equation
Brc1ccc2ncccc2c1.Cc1ccc2c(cnn2C2CCCCO2)c1B(O)O>C1CCC(P(C2CCCCC2)C2CCCCC2)CC1.CC(=O)[O-].CC(=O)[O-].CO.[K+].[OH-].[Pd+2]>Cc1ccc2c(cnn2C2CCCCO2)c1.Cc1ccc2c(cnn2C2CCCCO2)c1-c1ccc2ncccc2c1.c1ccc2ncccc2c1.c1cnc2ccc(-c3ccc4ncccc4c3)cc2c1

Participants

12

Reactant 2

HCID 792436-BromoquinolineHCID 129009568[5-Methyl-1-(oxan-2-yl)-1H-indazol-4-yl]boronic acid

Product 6

HCID 7047QuinolineYield 5.041%HCID 792436-BromoquinolineYield 29.253%HCID 6207116,6'-BiquinolineYield 5.95%HCID 10751213HCID 10751213, compoundYield 2.518%HCID 129009568[5-Methyl-1-(oxan-2-yl)-1H-indazol-4-yl]boronic acidYield 10.714%HCID 178422846HCID 178422846, compoundYield 46.365%

Reagents, catalysts & solvents 4

HCID 14797Potassium HydroxideReagentHCID 75806TricyclohexylphosphineCatalystHCID 167845palladium(II) acetateCatalystHCID 887MethanolSolvent

Conditions

Temperature
100 °C

Sources & evidence

ORD record
ord-2f0fb1c8b60849baa0ea051c44b834eb
Source dataset
HTE Suzuki coupling dataset

Reaction notes

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