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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870640Generated: October 31, 2026

Potassium Carbonate → HCID 86696334, compound

https://huagongshe.com/reaction/870640

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Aminomethylphenylboronic acid hydrochlorideHCID 2734311—
ReactantHCID 86696333HCID 86696333—
CatalystHCID 178418476HCID 178418476—
SolventMethanolHCID 887—
SolventAcetonitrile--water (1/1)HCID 18373917—
ProductHCID 86696334HCID 86696334—

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of (3-bromo-imidazo[1,2-b]pyridazin-6-yl)-(3-phenyl-propyl)-amine (100 mg, 0.3 mmol), (4-aminomethylphenyl)boronic acid hydrochloride (67 mg, 0.36 mmol), K2CO3 (124 mg, 0.9 mmol) and dichlorobis(triphenylphosphine)palladium(II) (11 mg, 0.015 mmol) in MeCN/water (3.6 ml/0.9 ml) was heated in a microwave at 150° C. for 20 min. The reaction mixture was diluted with MeOH (2 ml) and filtered. The filtrate was subjected to preparative HPLC to give the titled compound as AcOH salt (29.9 mg). 1H NMR (400 MHz, METHANOL-d4) δ ppm 1.93 (s, 3H) 1.99-2.09 (m, 2H) 2.70-2.80 (m, 2H) 3.41 (t, J=6.95 Hz, 2H) 4.14 (s, 2H) 6.74 (d, J=9.60 Hz, 1H) 7.15-7.29 (m, 5H) 7.53 (d, J=8.34 Hz, 2H) 7.64 (d, J=9.60 Hz, 1H) 7.80 (s, 1H) 8.24 (d, J=8.59 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969565B2
Source datasetuspto-grants-2015_03
ORD IDord-33b948aed1c649b1b706f8ed39dc7708
Source noteuspto-grants-2015_03