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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506048Generated: October 31, 2026

HCID 58266297, compound → HCID 58266787, compound

https://huagongshe.com/reaction/1506048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 58266297HCID 58266297—
ReactantHCID 58266319HCID 58266319—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
SolventPotassium FluorideHCID 522689—
ProductHCID 58266787HCID 5826678733%

Reaction Conditions

Temperature80 °C

Reaction Steps

A degassed mixture of 4,4-dimethyl-1-[4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzyl]-piperidine (836 mg, 2.5 mmol), 3-iodo-6-bromo-9H-dipyrido[2,3-b;4′,3′-d]pyrrole (500 mg, 1.3 mmol), 1,1′-[bis(diphenylphosphino)ferrocene]dichloropalladium(II) (109 mg, 0.13 mmol) in 1N aqueous potassium fluoride solution (25 mL) and acetonitrile (25 mL) was heated at 80° C. for 18 h. The cooled reaction mixture was diluted with ethyl acetate (100 mL) then washed with water (75 mL). The organic phase was separated, dried over sodium sulfate, filtered and evaporated in vacuo to afford a residue that was purified by flash chromatography (silica, 120 g column, ISCO, 0-15% methanol in DCM) to afford the title compound as an off-white solid (190 mg, 33%). 1H NMR (CDCl3 plus CD3OD, 300 MHz): 8.85 (d, J=2.2 Hz, 1H), 8.76 (d, J=2.2 Hz, 1H), 8.70 (d, J=0.9 Hz, 1H), 8.32 (d, J=0.9 Hz, 1H), 7.73 (d, J=8.0 Hz, 2H), 7.54 (d, J=8.0 Hz, 2H), 3.82 (s, 2H), 2.77-2.63 (m, 4H), 1.52 (t, J=5.6 Hz, 4H), 1.00 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216980B2
Source datasetuspto-grants-2015_12
ORD IDord-a83d9c94eadb48b19d25a418a75e57f8
Source noteuspto-grants-2015_12