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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1822399Generated: November 1, 2026

Hydrochloric Acid → HCID 54739227, compound

https://huagongshe.com/reaction/1822399

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Fluorophenylboronic acidHCID 285645—
ReactantN-{[2-[(4-Bromophenyl)methyl]-5-hydroxy-6-(1-methylethyl)-3-oxo-2,3-dihydro-4-pyridazinyl]carbonyl}glycineHCID 54739228—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 54739227HCID 5473922740.4%

Reaction Steps

To a 5 ml microwave tube was added N-{[2-[(4-bromophenyl)methyl]-5-hydroxy-6-(1-methylethyl)-3-oxo-2,3-dihydro-4-pyridazinyl]carbonyl}glycine (example 61, 40 mg, 0.094 mmol), 4-fluorobenzeneboronic acid (14 mg, 0.10 mmol), potassium carbonate (40 mg, 0.290 mmol), and tetrakis(triphenylphosphine)palladium (0) (6 mg, 5 μmol) in 1,4-Dioxane (1.5 ml) and Water (0.500 ml). The mixture was irradiated at 100° C. for 20 minutes, diluted with water (5 ml), acidified with 1N HCl (2 ml), and extracted with ethyl acetate (20 ml). The organic phase was washed with brine, dried over MgSO4, filtered, and solvents removed under reduced pressure. The crude residue was purified by HPLC chromatography (ODS silica, gradient 15-95% acetonitrile/water (0.1% TFA)) to afford the title compound (16.6 mg, 0.038 mmol, 40% yield) as a white powder. 1H NMR (400 MHz, DMSO-d6) d ppm 15.88 (s, 1H), 12.99 (br. s., 1H), 10.20 (t, J=5.56 Hz, 1H), 7.65-7.74 (m, 2H), 7.62 (d, J=8.08 Hz, 2H), 7.39 (d, J=8.34 Hz, 2H), 7.23-7.33 (m, 2H), 5.29 (s, 2H), 4.10 (d, J=5.81 Hz, 2H), 3.20 (sept, J=6.78 Hz, 1H), 1.22 (d, J=6.82 Hz, 6H). MS (ES+) m/e 440 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07608621B2
Source datasetuspto-grants-2009_10
ORD IDord-4e11170a560744d4a0025253d4206641
Source noteuspto-grants-2009_10