6-Bromoquinoline → 6-Bromoquinoline

HRID 2259052Notes

Reaction equation

HRID 2259052 reaction equation
Brc1ccc2ncccc2c1.Cc1ccc2c(cnn2C2CCCCO2)c1B(O)O>C1CCOC1.CC(=O)[O-].CC(=O)[O-].O=P([O-])([O-])[O-].[CH]1[CH][CH]C(P(c2ccccc2)c2ccccc2)[CH]1.[CH]1[CH][CH]C(P(c2ccccc2)c2ccccc2)[CH]1.[Fe].[K+].[K+].[K+].[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 3.047%HCID 792436-BromoquinolineYield 61.377%HCID 6207116,6'-BiquinolineYield 6.795%HCID 10751213HCID 10751213, compoundYield 2.021%HCID 129009568[5-Methyl-1-(oxan-2-yl)-1H-indazol-4-yl]boronic acidYield 26.759%HCID 178422846HCID 178422846, compoundYield 0%

Reagents, catalysts & solvents 4

HCID 62657Potassium Phosphate, TribasicReagentHCID 167845palladium(II) acetateCatalystHCID 178477755HCID 178477755, compoundCatalystHCID 8028TetrahydrofuranSolvent

Conditions

Temperature
100 °C

Sources & evidence

ORD record
ord-a70ce8c58b7e46f6abd91eed4778a685
Source dataset
HTE Suzuki coupling dataset

Reaction notes

Loading…