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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441285Generated: October 31, 2026

Sodium Carbonate → 4-[6-(Dimethylamino)-4-phenylpyridazin-3-yl]benzaldehyde

https://huagongshe.com/reaction/1441285

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-Formylphenylboronic AcidHCID 591073—
ReactantHCID 59164369HCID 59164369—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product4-[6-(Dimethylamino)-4-phenylpyridazin-3-yl]benzaldehydeHCID 59164367—

Reaction Conditions

Temperature110 °C

Reaction Steps

N,N-dimethyl 6-chloro-5-phenylpyridazin-3-amine (1-2; 120 mg, 0.51 mmol) was dissolved in dry dioxane (3 mL) and 4-formylphenyl boronic acid (136 mg, 0.91 mmol). 2 M aqueous Na2CO3 (0.75 mL) and palladium(0) tetrakis-triphenylphosphine (66 mg, 0.058 mmol) were then added. This mixture was degassed, the vessel sealed and heated at 110° C. for 24 hours. The cooled reaction was diluted with water and the product extracted into ethyl acetate, the extract dried over anhydrous NaSO4, filtered and evaporated. The product was purified by chromatography on silica gel and elution with a 25-65% ethyl acetate/hexane gradient to give 4-[6-(Dimethylamino)-4-phenylpyridazin-3-yl]benzaldehyde (1-3). NMR (CDCl3): δ9.98 (1H, s), 7.74 (2H, d, J=8 Hz), 7.54 (2H, d, J=8 Hz), 7.35 (3H, m), 7.19 (2H, d, J=8 Hz), 6.76 (1H, s), 3.29 (6H, s); m/e (m+1): 304.2

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07655649B2
Source datasetuspto-grants-2010_02
ORD IDord-224d1a397da645ffbdf9ef61b23f665d
Source noteuspto-grants-2010_02