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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506042Generated: November 1, 2026

HCID 58266390, compound → HCID 58266744, compound

https://huagongshe.com/reaction/1506042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 58266390HCID 58266390—
ReactantHCID 58266617HCID 58266617—
SolventAcetonitrileHCID 6342—
SolventPotassium FluorideHCID 522689—
ProductHCID 58266744HCID 5826674447.4%

Reaction Conditions

Temperature100 °C

Reaction Steps

A degassed mixture of 6′-chloro-2-fluoro-5-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-[3,4′]bipyridinyl-3′-ylamine (1.99 g, 5.70 mmol), 2-bromo-5-ethyl-4,5,6,7-tetrahydrothieno[3,2-c]pyridine (1.54 g, 6.30 mmol), 1,1′-[bis(diphenylphosphino) ferrocene]dichloropalladium(II) (466 mg, 0.57 mmol) in 1N aqueous potassium fluoride solution (22.5 mL) and acetonitrile (22.5 mL) was heated under microwave irradiation at 100° C. for 30 minutes. The cooled reaction mixture was loaded onto an SCX-2 cartridge (50 g) and eluted with 2N ammonia in methanol to afford impure product as a brown solid. The resultant brown residue was purified by flash chromatography (silica, 40 g column, ISCO, 0-10% methanol in DCM) to afford the title compound as an off-white solid (1.05 g, 47%). 1H NMR (DMSO-D6, 300 MHz): 8.48 (d, J=2.4 Hz, 1H), 8.12 (dd, J=9.0, 2.6 Hz, 1H), 7.89 (s, 1H), 7.36 (s, 1H), 7.21 (s, 1H), 5.54 (s, 2H), 3.45 (s, 2H), 2.86-2.79 (m, 2H), 2.75-2.68 (m, 2H), 2.58-2.51 (m, 2H), 1.08 (t, J=7.1 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216980B2
Source datasetuspto-grants-2015_12
ORD IDord-a7db35fa73be49aaa1ef6045b60daa8b
Source noteuspto-grants-2015_12