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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993364Generated: October 30, 2026

Nitrogen → HCID 57445398, compound

https://huagongshe.com/reaction/1993364

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantPotassium CarbonateHCID 11430—
Reactant9-Benzyl-9-borabicyclo(3.3.1)nonaneHCID 4150924—
Reactant3-Chloro-6-(3-fluoro-4-methoxyphenyl)pyridazineHCID 20398284—
CatalystHCID 178477754HCID 178477754—
SolventDimethylformamideHCID 6228—
ProductHCID 57445398HCID 57445398—

Reaction Conditions

Temperature65 °C

Reaction Steps

A solution of 3-chloro-6-(3-fluoro-4-methoxy-phenyl)-pyridazine (Step 1, 2.0 g, 8.38 mmol), B-benzyl-9-BBN (0.5 mL in THF, 20 mL) and K2CO3 (3.5 g, 25.1 mmol) in 30 mL of DMF was degassed with N2 for 5 min. Cat. Pd(DPPF)Cl2 (731 mg, 1 mmol) was then added and the reaction was heated at 65° C. for 3 h (preheated oil bath). The mixture was poured into ice water and extracted with 50 mL 2×EtOAc. The combined organic phases were washed with 50 mL of brine and dried over Na2SO4. The solution was concentrated in vacuo and the crude was purified by silica gel column chromatograph (50% EtOAc/Hexane to EtOAc) to give light yellow solid. MS (ESI pos. ion) m/z: 295.3 (M+H). Calc'd Exact Mass for C18H15FN2O: 294.32.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652009B2
Source datasetuspto-grants-2010_01
ORD IDord-b95c7908c6174fc394e4e6df1b1d58b7
Source noteuspto-grants-2010_01