Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1921608Generated: October 30, 2026

Ethyl Acetate → 3-Chloro-6-(1-methyl-1H-pyrazol-4-yl)pyridazine

https://huagongshe.com/reaction/1921608

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium CarbonateHCID 10340—
Reactant1,4-DioxaneHCID 31275—
Reactant1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 2773987—
ReactantSodium chloride; waterHCID 57417360—
CatalystHCID 178418397HCID 178418397—
Product3-Chloro-6-(1-methyl-1H-pyrazol-4-yl)pyridazineHCID 5459560747%

Reaction Conditions

Temperature80 °C

Reaction Steps

A flask was charged with 3,6-dichloropyridzine (Aldrich, 297 mg, 2.0 mmol), 1-Methyl-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-1H-pyrazole (499 mg, 2.4 mmol), 2 M Na2CO3 (4 mL) and dioxane (4 mL). Argon was bubbled through the reaction for 60 seconds followed by the addition of Tetrakis(triphenylphosphine)palladium (0) (231 mg, 0.2 mmol). The reaction was heated to 80° C. overnight followed by aqueous work up using EtOAc and brine. The organic layer was dried (MgSO4) and concentrated in vacuo followed by column chromatography purification (20% Ethyl Acetate in Hexanes) resulting in the title compound as a white solid (183 mg, 47%). 1H-NMR (CD3OD): δ 8.23 (1H, s), 8.08 (1H, s), 7.84 (1H, br s), 7.34 (1H, br s), 4.00 (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173654B2
Source datasetuspto-grants-2012_05
ORD IDord-9094496d0f9d45219387845bd32716e2
Source noteuspto-grants-2012_05